Related gene-specific medical variations for Gene (Select 8600) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3006663	NM_003701.4(TNFSF11):c.417C>T (p.His139=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970106	NM_003701.4(TNFSF11):c.75G>A (p.Pro25=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2913780	NM_003701.4(TNFSF11):c.306A>G (p.Thr102=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2871216	NM_003701.4(TNFSF11):c.525C>A (p.Ile175=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867011	NM_003701.4(TNFSF11):c.402C>A (p.Ile134=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865096	NM_003701.4(TNFSF11):c.414G>A (p.Gln138=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2847224	NM_003701.4(TNFSF11):c.387+19T>C	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2831767	NM_003701.4(TNFSF11):c.99G>A (p.Pro33=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2827644	NM_003701.4(TNFSF11):c.114G>A (p.Pro38=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2798978	NM_003701.4(TNFSF11):c.434-11C>T	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2778917	NM_003701.4(TNFSF11):c.220-11C>T	TNFSF11, LOC126861752	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2772810	NM_003701.4(TNFSF11):c.387+7C>T	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2751685	NM_003701.4(TNFSF11):c.220-7T>C	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2727597	NM_003701.4(TNFSF11):c.60C>T (p.Gly20=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2697473	NM_003701.4(TNFSF11):c.434-18G>A	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2634819	NM_003701.4(TNFSF11):c.387+1G>A	LOC126861752, TNFSF11	Single nucleotide variant (splice donor variant)	TNFSF11-related condition	GUncertain significance
Select item 2613572	NM_003701.4(TNFSF11):c.47A>G (p.Glu16Gly)	LOC130009662, TNFSF11 (E16G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2531255	NM_003701.4(TNFSF11):c.413A>T (p.Gln138Leu)	LOC126861753, TNFSF11 (Q138L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488609	NM_003701.4(TNFSF11):c.326C>T (p.Thr109Ile)	LOC126861752, TNFSF11 (T36I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2437134	NM_003701.4(TNFSF11):c.2T>C (p.Met1Thr)	LOC130009662, TNFSF11 (M1T)	Single nucleotide variant (missense variant +2 more)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 2321959	NM_003701.4(TNFSF11):c.143T>A (p.Met48Lys)	LOC130009662, TNFSF11 (M48K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2191611	NM_003701.4(TNFSF11):c.84C>T (p.Gly28=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2182091	NM_003701.4(TNFSF11):c.84C>G (p.Gly28=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2115286	NM_003701.4(TNFSF11):c.268A>G (p.Ile90Val)	LOC126861752, TNFSF11 (I90V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2092573	NM_003701.4(TNFSF11):c.388-8T>G	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2087750	NM_003701.4(TNFSF11):c.432A>G (p.Lys144=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2066471	NM_003701.4(TNFSF11):c.16A>G (p.Arg6Gly)	LOC130009662, TNFSF11 (R6G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2063425	NM_003701.4(TNFSF11):c.152C>T (p.Ala51Val)	LOC130009662, TNFSF11 (A51V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2044087	NM_003701.4(TNFSF11):c.344C>T (p.Ser115Leu)	LOC126861752, TNFSF11 (S42L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2018234	NM_003701.4(TNFSF11):c.246T>C (p.Asp82=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2012206	NM_003701.4(TNFSF11):c.138C>A (p.Arg46=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2008357	NM_003701.4(TNFSF11):c.291A>C (p.Ala97=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2003341	NM_003701.4(TNFSF11):c.532+17T>C	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1973339	NM_003701.4(TNFSF11):c.53T>C (p.Met18Thr)	LOC130009662, TNFSF11 (M18T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1965583	NM_003701.4(TNFSF11):c.37C>G (p.Arg13Gly)	LOC130009662, TNFSF11 (R13G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1962162	NM_003701.4(TNFSF11):c.9C>G (p.Arg3=)	LOC130009662, TNFSF11	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 1952011	NM_003701.4(TNFSF11):c.125C>G (p.Pro42Arg)	LOC130009662, TNFSF11 (P42R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1949000	NM_003701.4(TNFSF11):c.13A>G (p.Ser5Gly)	LOC130009662, TNFSF11 (S5G)	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 1933780	NM_003701.4(TNFSF11):c.387+20G>A	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1932149	NM_003701.4(TNFSF11):c.58G>A (p.Gly20Ser)	LOC130009662, TNFSF11 (G20S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1926500	NM_003701.4(TNFSF11):c.387+13_387+14delinsGA	LOC126861752, TNFSF11	Indel (intron variant)	not provided	GUncertain significance
Select item 1924143	NM_003701.4(TNFSF11):c.532+10A>G	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1923644	NM_003701.4(TNFSF11):c.403G>T (p.Val135Phe)	LOC126861753, TNFSF11 (V62F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1908113	NM_003701.4(TNFSF11):c.102G>A (p.Pro34=)	LOC130009662, TNFSF11	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 1696233	NM_003701.4(TNFSF11):c.350G>A (p.Arg117Lys)	LOC126861752, TNFSF11 (R117K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1667117	NM_003701.4(TNFSF11):c.132C>T (p.Ala44=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1655179	NM_003701.4(TNFSF11):c.114G>T (p.Pro38=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1646928	NM_003701.4(TNFSF11):c.9C>A (p.Arg3=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1640382	NM_003701.4(TNFSF11):c.72C>A (p.Ala24=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1628998	NM_003701.4(TNFSF11):c.393A>G (p.Leu131=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1624527	NM_003701.4(TNFSF11):c.324T>C (p.Asp108=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1621646	NM_003701.4(TNFSF11):c.354A>G (p.Arg118=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1614338	NM_003701.4(TNFSF11):c.24C>T (p.Tyr8=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1602415	NM_003701.4(TNFSF11):c.434-11C>G	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1596545	NM_003701.4(TNFSF11):c.220-9C>T	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1589625	NM_003701.4(TNFSF11):c.30G>A (p.Lys10=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1586069	NM_003701.4(TNFSF11):c.480T>C (p.Leu160=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	TNFSF11-related condition +1 more	GLikely benign
Select item 1564948	NM_003701.4(TNFSF11):c.78C>T (p.His26=)	LOC130009662, TNFSF11	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 1549015	NM_003701.4(TNFSF11):c.468G>A (p.Lys156=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1535022	NM_003701.4(TNFSF11):c.420C>T (p.Ile140=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1524135	NM_003701.4(TNFSF11):c.140C>T (p.Ser47Phe)	TNFSF11, LOC130009662 (S47F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1519296	NM_003701.4(TNFSF11):c.3G>A (p.Met1Ile)	LOC130009662, TNFSF11 (M1I)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1516096	NM_003701.4(TNFSF11):c.101C>A (p.Pro34Gln)	LOC130009662, TNFSF11 (P34Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1515522	NM_003701.4(TNFSF11):c.81G>C (p.Glu27Asp)	LOC130009662, TNFSF11 (E27D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1507289	NM_003701.4(TNFSF11):c.292G>C (p.Asp98His)	LOC126861752, TNFSF11 (D98H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1480778	NM_003701.4(TNFSF11):c.79G>A (p.Glu27Lys)	LOC130009662, TNFSF11 (E27K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1474050	NM_003701.4(TNFSF11):c.92A>T (p.His31Leu)	TNFSF11, LOC130009662 (H31L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1465669	NM_003701.4(TNFSF11):c.28A>G (p.Lys10Glu)	TNFSF11, LOC130009662 (K10E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1465276	NM_003701.4(TNFSF11):c.353G>T (p.Arg118Ile)	LOC126861752, TNFSF11 (R118I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1462118	NM_003701.4(TNFSF11):c.470G>A (p.Arg157Lys)	LOC126861753, TNFSF11 (R157K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1443796	NM_003701.4(TNFSF11):c.478C>T (p.Leu160Phe)	TNFSF11, LOC126861753 (L160F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1422743	NM_003701.4(TNFSF11):c.79G>C (p.Glu27Gln)	LOC130009662, TNFSF11 (E27Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1417724	NM_003701.4(TNFSF11):c.2T>A (p.Met1Lys)	LOC130009662, TNFSF11 (M1K)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1414339	NM_003701.4(TNFSF11):c.308C>T (p.Thr103Ile)	LOC126861752, TNFSF11 (T103I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1410746	NM_003701.4(TNFSF11):c.514G>A (p.Ala172Thr)	LOC126861753, TNFSF11 (A99T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1409770	NM_003701.4(TNFSF11):c.30G>C (p.Lys10Asn)	LOC130009662, TNFSF11 (K10N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1397727	NM_003701.4(TNFSF11):c.154C>G (p.Leu52Val)	LOC130009662, TNFSF11 (L52V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1396652	NM_003701.4(TNFSF11):c.254A>G (p.His85Arg)	LOC126861752, TNFSF11 (H12R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1386384	NM_003701.4(TNFSF11):c.484G>A (p.Ala162Thr)	LOC126861753, TNFSF11 (A162T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1382923	NM_003701.4(TNFSF11):c.64_65delinsAG (p.Pro22Ser)	LOC130009662, TNFSF11 (P22S)	Indel (intron variant +1 more)	not provided	GUncertain significance
Select item 1345678	NM_003701.4(TNFSF11):c.53T>A (p.Met18Lys)	LOC130009662, TNFSF11 (M18K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1183681	NM_003701.4(TNFSF11):c.220-94G>A	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1177514	NM_003701.4(TNFSF11):c.2T>G (p.Met1Arg)	LOC130009662, TNFSF11 (M1R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1137585	NM_003701.4(TNFSF11):c.433+19A>T	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1053667	NM_003701.4(TNFSF11):c.434C>T (p.Ala145Val)	LOC126861753, TNFSF11 (A145V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1023946	NM_003701.4(TNFSF11):c.110C>G (p.Ala37Gly)	LOC130009662, TNFSF11 (A37G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1012150	NM_003701.4(TNFSF11):c.263A>G (p.Tyr88Cys)	LOC126861752, TNFSF11 (Y15C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 884198	NM_003701.4(TNFSF11):c.520G>A (p.Asp174Asn)	LOC126861753, TNFSF11 (D101N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 884197	NM_003701.4(TNFSF11):c.435G>A (p.Ala145=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	Autosomal recessive osteopetrosis 2 +1 more	GConflicting classifications of pathogenicity
Select item 884196	NM_003701.4(TNFSF11):c.433+13C>G	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 884144	NM_003701.4(TNFSF11):c.-147C>T	LOC130009662, TNFSF11	Single nucleotide variant (intron variant +1 more)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 882482	NM_003701.4(TNFSF11):c.420C>G (p.Ile140Met)	LOC126861753, TNFSF11 (I67M +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive osteopetrosis 2 +1 more	GConflicting classifications of pathogenicity
Select item 880857	NM_003701.4(TNFSF11):c.-7G>C	LOC130009662, TNFSF11	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 880856	NM_003701.4(TNFSF11):c.-94C>T	LOC130009662, TNFSF11	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 880855	NM_003701.4(TNFSF11):c.-104C>T	LOC130009662, TNFSF11	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal recessive osteopetrosis 2	GUncertain significance
Select item 764537	NM_003701.4(TNFSF11):c.66C>G (p.Pro22=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 719202	NM_003701.4(TNFSF11):c.434-9C>T	LOC126861753, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 718598	NM_003701.4(TNFSF11):c.101C>G (p.Pro34Arg)	LOC130009662, TNFSF11 (P34R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 716176	NM_003701.4(TNFSF11):c.396A>G (p.Gln132=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	Autosomal recessive osteopetrosis 2 +2 more	GBenign
Select item 501658	NM_003701.4(TNFSF11):c.83G>A (p.Gly28Asp)	LOC130009662, TNFSF11 (G28D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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