ClinVar for Gene (Select 999) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3224194	NM_004360.5(CDH1):c.954C>A (p.Thr318=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224193	NM_004360.5(CDH1):c.939C>A (p.Asp313Glu)	CDH1 (D313E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224192	NM_004360.5(CDH1):c.889A>C (p.Asn297His)	CDH1 (N297H)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224191	NM_004360.5(CDH1):c.855A>T (p.Thr285=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224190	NM_004360.5(CDH1):c.828dup (p.Pro277fs)	CDH1 (P277fs)	Duplication (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3224189	NM_004360.5(CDH1):c.811G>T (p.Val271Phe)	CDH1 (V271F)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224188	NM_004360.5(CDH1):c.762T>C (p.Asp254=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224187	NM_004360.5(CDH1):c.755T>C (p.Val252Ala)	CDH1 (V252A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224186	NM_004360.5(CDH1):c.731A>T (p.Asp244Val)	CDH1 (D244V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224184	NM_004360.5(CDH1):c.469G>C (p.Val157Leu)	CDH1 (V157L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224183	NM_004360.5(CDH1):c.454_457del (p.Gln152fs)	CDH1 (Q152fs)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3224182	NM_004360.5(CDH1):c.2629G>T (p.Gly877Ter)	CDH1 (G222* +3 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224180	NM_004360.5(CDH1):c.2558C>G (p.Ser853Ter)	CDH1 (S198* +3 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224179	NM_004360.5(CDH1):c.2547CTC[1] (p.Ser851del)	CDH1 (S196del +3 more)	Microsatellite (inframe_deletion +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224178	NM_004360.5(CDH1):c.2548T>C (p.Ser850Pro)	CDH1 (S195P +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224177	NM_004360.5(CDH1):c.2502C>G (p.Asp834Glu)	CDH1 (D179E +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224176	NM_004360.5(CDH1):c.2475G>T (p.Pro825=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224175	NM_004360.5(CDH1):c.2437G>A (p.Glu813Lys)	CDH1 (E158K +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224174	NM_004360.5(CDH1):c.2421T>G (p.Ile807Met)	CDH1 (I152M +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224173	NM_004360.5(CDH1):c.2338C>T (p.Pro780Ser)	CDH1 (P125S +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224172	NM_004360.5(CDH1):c.2335C>A (p.Arg779=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224169	NM_004360.5(CDH1):c.2211C>T (p.Val737=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224168	NM_004360.5(CDH1):c.2169G>C (p.Leu723=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224167	NM_004360.5(CDH1):c.2103C>G (p.Val701=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224166	NM_004360.5(CDH1):c.20G>A (p.Ser7Asn)	CDH1 (S7N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224165	NM_004360.5(CDH1):c.2078G>A (p.Gly693Asp)	CDH1 (G177D +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224162	NM_004360.5(CDH1):c.1937-1G>C	CDH1	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224161	NM_004360.5(CDH1):c.190C>A (p.Gln64Lys)	CDH1 (Q64K)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224160	NM_004360.5(CDH1):c.1863C>T (p.Pro621=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224159	NM_004360.5(CDH1):c.1809T>C (p.Cys603=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224158	NM_004360.5(CDH1):c.1790C>A (p.Pro597His)	CDH1 (P536H +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224157	NM_004360.5(CDH1):c.1722T>A (p.Val574=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224155	NM_004360.5(CDH1):c.1683C>T (p.Tyr561=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224154	NM_004360.5(CDH1):c.1681T>C (p.Tyr561His)	CDH1 (Y45H +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224153	NM_004360.5(CDH1):c.1650G>A (p.Arg550=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224152	NM_004360.5(CDH1):c.1596G>T (p.Trp532Cys)	CDH1 (W16C +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224151	NM_004360.5(CDH1):c.1582G>A (p.Asp528Asn)	CDH1 (D12N +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224150	NM_004360.5(CDH1):c.1571G>C (p.Arg524Pro)	CDH1 (R463P +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224149	NM_004360.5(CDH1):c.1530C>A (p.Ala510=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224148	NM_004360.5(CDH1):c.1523A>G (p.Tyr508Cys)	CDH1 (Y447C +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224147	NM_004360.5(CDH1):c.1493A>T (p.Asp498Val)	CDH1 (D437V +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224145	NM_004360.5(CDH1):c.1450C>T (p.Pro484Ser)	CDH1 (P423S +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224144	NM_004360.5(CDH1):c.1347G>C (p.Gln449His)	CDH1 (Q388H +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224143	NM_004360.5(CDH1):c.1283A>G (p.Asn428Ser)	CDH1 (N428S)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3224142	NM_004360.5(CDH1):c.1280C>G (p.Thr427Arg)	CDH1 (T427R)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224137	NM_004360.5(CDH1):c.1139A>T (p.Tyr380Phe)	CDH1 (Y380F)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3224136	NM_004360.5(CDH1):c.1133C>T (p.Thr378Ile)	CDH1 (T378I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3141066	NM_004360.5(CDH1):c.2042T>C (p.Leu681Ser)	CDH1 (L26S +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076087	NM_004360.5(CDH1):c.-7G>A	CDH1	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076086	NM_004360.5(CDH1):c.-20C>T	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076085	NM_004360.5(CDH1):c.-11C>T	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3066086	NM_004360.5(CDH1):c.1712-2A>G	CDH1	Single nucleotide variant (splice acceptor variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3064696	NM_004360.5(CDH1):c.1697T>G (p.Ile566Arg)	CDH1 (I505R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3063909	NM_004360.5(CDH1):c.2186T>G (p.Leu729Arg)	CDH1 (L213R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063808	NC_000016.9:g.(68857530_68862076)_(68863701_68867192)dup	CDH1	Duplication	Malignant tumor of breast	GLikely pathogenic
Select item 3063446	GRCh37/hg19 16q22.1(chr16:67583728-69977397)x3	ACD, C16orf86 +48 more	Copy number gain	not specified	GUncertain significance
Select item 3061882	NM_004360.5(CDH1):c.164-8_164-3del	CDH1	Deletion (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3048835	NM_004360.5(CDH1):c.-9C>A	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	CDH1-related condition	GLikely benign
Select item 3046276	NM_004360.5(CDH1):c.-10C>A	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	CDH1-related condition	GLikely benign
Select item 3024037	NM_004360.5(CDH1):c.311A>G (p.Asp104Gly)	CDH1 (D104G)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3020733	NM_004360.5(CDH1):c.1344G>A (p.Gln448=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 3018885	NM_004360.5(CDH1):c.1223C>A (p.Ala408Glu)	CDH1 (A408E)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3018335	NM_004360.5(CDH1):c.2378G>A (p.Ser793Asn)	CDH1 (S277N +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3018015	NM_004360.5(CDH1):c.2337G>T (p.Arg779=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 3015076	NM_004360.5(CDH1):c.1621G>A (p.Ala541Thr)	CDH1 (A25T +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 3009011	NM_004360.5(CDH1):c.1138-19A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 3008993	NM_004360.5(CDH1):c.2296-7T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 3003601	NM_004360.5(CDH1):c.387+5G>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2998991	NM_004360.5(CDH1):c.362A>G (p.His121Arg)	CDH1 (H121R)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2997476	NM_004360.5(CDH1):c.1513A>G (p.Ile505Val)	CDH1 (I444V +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2993742	NM_004360.5(CDH1):c.2450C>A (p.Ala817Glu)	CDH1 (A756E +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2989173	NM_004360.5(CDH1):c.1956G>T (p.Leu652Phe)	CDH1 (L136F +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2988816	NM_004360.5(CDH1):c.143G>C (p.Arg48Thr)	CDH1 (R48T)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2985312	NM_004360.5(CDH1):c.2165-11C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2984791	NM_004360.5(CDH1):c.187C>A (p.Arg63=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2981980	NM_004360.5(CDH1):c.1330T>C (p.Phe444Leu)	CDH1 (F444L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2979540	NM_004360.5(CDH1):c.1437T>G (p.Asp479Glu)	CDH1 (D479E +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2973458	NM_004360.5(CDH1):c.163+11G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2972165	NM_004360.5(CDH1):c.972A>C (p.Gly324=)	CDH1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2970628	NM_004360.5(CDH1):c.2165-11dup	CDH1	Duplication (intron variant)	Hereditary diffuse gastric adenocarcinoma	GBenign
Select item 2968987	NM_004360.5(CDH1):c.806G>C (p.Gly269Ala)	CDH1 (G269A)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2957126	NM_004360.5(CDH1):c.1608T>C (p.Asn536=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2955358	NM_004360.5(CDH1):c.2648A>G (p.Ter883Trp)	CDH1	Single nucleotide variant (stop lost)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2918553	NM_004360.5(CDH1):c.2340T>C (p.Pro780=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2916919	NM_004360.5(CDH1):c.2443C>T (p.Leu815=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2915573	NM_004360.5(CDH1):c.1320+18C>T	CDH1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2915498	NM_004360.5(CDH1):c.2600A>C (p.Asn867Thr)	CDH1 (N351T +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2915497	NM_004360.5(CDH1):c.1864A>G (p.Asn622Asp)	CDH1 (N106D +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2913251	NM_004360.5(CDH1):c.135C>G (p.His45Gln)	CDH1 (H45Q)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2910019	NM_004360.5(CDH1):c.1565+18T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2907493	NM_004360.5(CDH1):c.576C>A (p.Ile192=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2906629	NM_004360.5(CDH1):c.1320+17_1320+18insTAAGATG	CDH1	Insertion (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2903389	NM_004360.5(CDH1):c.2314C>T (p.Leu772=)	CDH1	Single nucleotide variant (synonymous variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2902584	NM_004360.5(CDH1):c.163+10C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2898644	NM_004360.5(CDH1):c.1009-20T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2897774	NM_004360.5(CDH1):c.2636G>A (p.Gly879Asp)	CDH1 (G224D +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2897055	NM_004360.5(CDH1):c.1936+9C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GLikely benign
Select item 2884511	NM_004360.5(CDH1):c.584A>G (p.Gln195Arg)	CDH1 (Q195R)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2880910	NM_004360.5(CDH1):c.1858C>G (p.Pro620Ala)	CDH1 (P620A +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2879117	NM_004360.5(CDH1):c.2408A>G (p.Asn803Ser)	CDH1 (N803S +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance

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