ClinVar for Gene (Select 7694) - ClinVar

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Links from Gene

Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3194020	NM_007134.1(ZNF135):c.32G>A (p.Gly11Asp)	ZNF135 (G11D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194019	NM_001289401.2(ZNF135):c.221C>T (p.Ala74Val)	ZNF135 (A32V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194017	NM_001289401.2(ZNF135):c.1952A>G (p.Lys651Arg)	ZNF135 (K609R +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3194016	NM_001289401.2(ZNF135):c.1828G>A (p.Asp610Asn)	ZNF135 (D568N +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194015	NM_001289401.2(ZNF135):c.1588G>T (p.Ala530Ser)	ZNF135 (A488S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194014	NM_001289401.2(ZNF135):c.1490A>G (p.Asn497Ser)	ZNF135 (N497S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3194013	NM_001289401.2(ZNF135):c.1147G>A (p.Glu383Lys)	ZNF135 (E383K +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194012	NM_001289401.2(ZNF135):c.946C>T (p.His316Tyr)	ZNF135 (H328Y +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2615285	NM_001289401.2(ZNF135):c.1384G>A (p.Gly462Arg)	ZNF135 (G420R +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2608314	NM_001289401.2(ZNF135):c.247G>A (p.Val83Met)	ZNF135 (V83M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592154	NM_001289401.2(ZNF135):c.541A>G (p.Thr181Ala)	ZNF135 (T205A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570437	NM_001289401.2(ZNF135):c.1427G>A (p.Arg476Gln)	ZNF135 (R476Q +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2569713	NM_001289401.2(ZNF135):c.1285C>T (p.Arg429Trp)	ZNF135 (R387W +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2568996	NM_001289401.2(ZNF135):c.572G>A (p.Gly191Glu)	ZNF135 (G191E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544144	NM_001289401.2(ZNF135):c.1834G>A (p.Gly612Arg)	ZNF135 (G636R +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2543145	NM_001289401.2(ZNF135):c.712G>A (p.Gly238Arg)	ZNF135 (G238R +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2514526	NM_001289401.2(ZNF135):c.1640A>G (p.Glu547Gly)	ZNF135 (E547G +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2472087	NM_001289401.2(ZNF135):c.1384G>C (p.Gly462Arg)	ZNF135 (G474R +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2465407	NM_001289401.2(ZNF135):c.179C>T (p.Pro60Leu)	ZNF135 (P18L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410977	NM_001289401.2(ZNF135):c.1460T>C (p.Ile487Thr)	ZNF135 (I445T +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2380496	NM_001289401.2(ZNF135):c.386C>G (p.Thr129Ser)	ZNF135 (T153S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378617	NM_001289401.2(ZNF135):c.878C>T (p.Thr293Ile)	ZNF135 (T293I +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2375537	NM_001289401.2(ZNF135):c.1355C>T (p.Ser452Leu)	ZNF135 (S410L +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2360253	NM_001289401.2(ZNF135):c.477G>C (p.Gln159His)	ZNF135 (Q159H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359968	NM_001289401.2(ZNF135):c.149T>C (p.Leu50Pro)	ZNF135 (L50P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352721	NM_001289401.2(ZNF135):c.173C>T (p.Pro58Leu)	ZNF135 (P16L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339123	NM_001289401.2(ZNF135):c.1522T>C (p.Ser508Pro)	ZNF135 (S520P +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2335844	NM_007134.1(ZNF135):c.31G>A (p.Gly11Ser)	ZNF135 (G11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330655	NM_001289401.2(ZNF135):c.850C>T (p.Pro284Ser)	ZNF135 (P308S +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2307041	NM_001289401.2(ZNF135):c.1030C>T (p.His344Tyr)	ZNF135 (H302Y +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2281208	NM_001289401.2(ZNF135):c.574A>C (p.Thr192Pro)	ZNF135 (T204P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248036	NM_001289401.2(ZNF135):c.394C>T (p.His132Tyr)	ZNF135 (H90Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228599	NM_001289401.2(ZNF135):c.764C>T (p.Ser255Leu)	ZNF135 (S255L +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2222911	NM_001289401.2(ZNF135):c.1541G>A (p.Arg514Gln)	ZNF135 (R514Q +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 1177145	t(10;19)(q26.13;q13.43)	FGFR2, ZNF135	Translocation	Glioblastoma	GUncertain significance
Select item 808656	NM_001289401.2(ZNF135):c.1731G>A (p.Pro577=)	ZNF135	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 787146	NM_001289401.2(ZNF135):c.645A>G (p.Lys215=)	ZNF135 (M108V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 785647	NM_001289401.2(ZNF135):c.1612A>G (p.Ile538Val)	ZNF135 (I496V +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GBenign
Select item 781540	NM_001289401.2(ZNF135):c.1845T>C (p.Phe615=)	ZNF135	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GBenign
Select item 781539	NM_001289401.2(ZNF135):c.1788C>T (p.His596=)	ZNF135	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GBenign
Select item 781538	NM_001289401.2(ZNF135):c.462G>A (p.Thr154=)	ZNF135	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 746583	NM_001289401.2(ZNF135):c.589G>T (p.Glu197Ter)	ZNF135 (E155* +3 more)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely benign
Select item 726932	NM_001289401.2(ZNF135):c.196C>T (p.Leu66=)	ZNF135	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 726216	NM_001289401.2(ZNF135):c.-58G>C	ZNF135 (G16R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 724935	NM_001289401.2(ZNF135):c.1158G>A (p.Glu386=)	ZNF135	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 689096	GRCh37/hg19 19q13.43(chr19:58369898-58590859)x3	C19orf18, ZNF135 +7 more	Copy number gain	not provided	GUncertain significance
Select item 688389	GRCh37/hg19 19q13.43(chr19:58092045-58686148)x3	C19orf18, ZIK1 +21 more	Copy number gain	not provided	GUncertain significance
Select item 687845	GRCh37/hg19 19q13.43(chr19:58369898-58590924)x3	C19orf18, ZNF135 +7 more	Copy number gain	not provided	GUncertain significance
Select item 685397	GRCh37/hg19 19q13.43(chr19:57952073-58661581)x3	C19orf18, VN1R1 +29 more	Copy number gain	not provided	GUncertain significance
Select item 564606	GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	ZNF548, ZNF549 +157 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 442403	GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3	A1BG, AURKC +64 more	Copy number gain	See cases	GUncertain significance
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 253827	GRCh37/hg19 19q13.43(chr19:58458999-58929684)x3	ZNF329, ZNF135 +14 more	Copy number gain	See cases	GUncertain significance
Select item 153721	GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	A1BG, A1BG-AS1 +547 more	Copy number gain	See cases	GPathogenic
Select item 153557	GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3	A1BG, A1BG-AS1 +179 more	Copy number gain	See cases	GUncertain significance
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	A1BG, A1BG-AS1 +782 more	Copy number gain	See cases	GPathogenic
Select item 144762	GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	SSC5D, SYT5 +553 more	Copy number gain	See cases	GPathogenic
Select item 144709	GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	TMC4, TMEM150B +537 more	Copy number gain	See cases	GPathogenic
Select item 59128	GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3	A1BG, A1BG-AS1 +215 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	MIR10394, MIR125A +806 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064933, LOC130064934 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	ZBTB45, ZFP28 +1081 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LILRA4, LILRA5 +761 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 66