ClinVar Miner

List of variants in gene TRIP12 studied for autosomal dominant non-syndromic intellectual disability

Included ClinVar conditions (47):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_001348323.3(TRIP12):c.2651-25C>T rs4972915 0.81767
NM_001348323.3(TRIP12):c.2736A>G (p.Thr912=) rs13018957 0.38821
NM_001348323.3(TRIP12):c.2651-39A>C rs4973229 0.38648
NM_001348323.3(TRIP12):c.3482+15G>A rs6720868 0.36718
NM_001348323.3(TRIP12):c.703A>G (p.Ile235Val) rs780999801 0.00003
NM_001348323.3(TRIP12):c.989C>T (p.Ser330Leu) rs779389307 0.00002
NM_001348323.3(TRIP12):c.2038A>G (p.Asn680Asp) rs772399122 0.00001
NM_001348323.3(TRIP12):c.2071G>T (p.Val691Phe) rs1305168076 0.00001
NM_001348323.3(TRIP12):c.4253G>A (p.Arg1418Lys) rs1157793506 0.00001
NM_001348323.3(TRIP12):c.5938A>G (p.Ser1980Gly) rs749300014 0.00001
NM_001348323.3(TRIP12):c.748G>A (p.Ala250Thr) rs539119124 0.00001
NM_001348323.3(TRIP12):c.78A>C (p.Gln26His) rs1046355070 0.00001
NM_001348323.3(TRIP12):c.983A>C (p.Glu328Ala) rs986636922 0.00001
NM_001348323.3(TRIP12):c.1012C>T (p.Gln338Ter)
NM_001348323.3(TRIP12):c.1037A>G (p.Lys346Arg) rs2056267716
NM_001348323.3(TRIP12):c.1090C>T (p.Arg364Trp)
NM_001348323.3(TRIP12):c.1133+21del rs11373804
NM_001348323.3(TRIP12):c.1160G>A (p.Arg387Lys) rs2054983988
NM_001348323.3(TRIP12):c.1177C>T (p.Arg393Cys)
NM_001348323.3(TRIP12):c.137C>T (p.Pro46Leu) rs2060290263
NM_001348323.3(TRIP12):c.1381C>A (p.Pro461Thr) rs771031325
NM_001348323.3(TRIP12):c.1510C>T (p.Gln504Ter)
NM_001348323.3(TRIP12):c.1651C>T (p.Arg551Ter) rs1553636520
NM_001348323.3(TRIP12):c.1684C>T (p.Arg562Ter) rs1575419803
NM_001348323.3(TRIP12):c.1787_1800del (p.Met596fs)
NM_001348323.3(TRIP12):c.1823C>T (p.Ala608Val)
NM_001348323.3(TRIP12):c.1922C>T (p.Thr641Met)
NM_001348323.3(TRIP12):c.2009C>T (p.Thr670Ile)
NM_001348323.3(TRIP12):c.2065C>T (p.Gln689Ter)
NM_001348323.3(TRIP12):c.2096A>G (p.Asn699Ser)
NM_001348323.3(TRIP12):c.2273G>A (p.Cys758Tyr)
NM_001348323.3(TRIP12):c.2378_2379insT (p.Val794fs) rs2154275777
NM_001348323.3(TRIP12):c.2396A>G (p.Lys799Arg)
NM_001348323.3(TRIP12):c.2625_2629del (p.Asn876fs)
NM_001348323.3(TRIP12):c.2679_2685del (p.Asp893fs)
NM_001348323.3(TRIP12):c.2764_2767dup (p.Ser923Ter)
NM_001348323.3(TRIP12):c.2776G>T (p.Gly926Ter) rs2154270715
NM_001348323.3(TRIP12):c.3088_3089del (p.Gly1030fs)
NM_001348323.3(TRIP12):c.3166C>T (p.Gln1056Ter) rs1575203936
NM_001348323.3(TRIP12):c.3204dup (p.Gly1069fs) rs1553620494
NM_001348323.3(TRIP12):c.3206+408T>G rs1461598857
NM_001348323.3(TRIP12):c.3207-7T>C
NM_001348323.3(TRIP12):c.3208C>T (p.Arg1070Ter) rs1575161164
NM_001348323.3(TRIP12):c.329A>G (p.Asn110Ser)
NM_001348323.3(TRIP12):c.3399C>G (p.Asn1133Lys)
NM_001348323.3(TRIP12):c.3434G>T (p.Gly1145Val) rs2154266281
NM_001348323.3(TRIP12):c.3482+1G>A rs1553616463
NM_001348323.3(TRIP12):c.3490dup (p.Ile1164fs) rs2043184881
NM_001348323.3(TRIP12):c.3671_3672del (p.Val1223_Ser1224insTer) rs1553614300
NM_001348323.3(TRIP12):c.3725T>C (p.Leu1242Pro) rs2154264253
NM_001348323.3(TRIP12):c.3774G>T (p.Glu1258Asp) rs1268798250
NM_001348323.3(TRIP12):c.3782T>C (p.Leu1261Ser)
NM_001348323.3(TRIP12):c.3808del (p.Ser1270fs) rs2042881907
NM_001348323.3(TRIP12):c.3816+2T>A
NM_001348323.3(TRIP12):c.3835A>G (p.Ile1279Val) rs764732335
NM_001348323.3(TRIP12):c.3869del (p.Leu1290fs)
NM_001348323.3(TRIP12):c.3968+1G>A rs1553612358
NM_001348323.3(TRIP12):c.399dup (p.Pro134fs) rs2060119917
NM_001348323.3(TRIP12):c.4108G>A (p.Val1370Ile)
NM_001348323.3(TRIP12):c.4216-2A>G
NM_001348323.3(TRIP12):c.4277A>G (p.His1426Arg)
NM_001348323.3(TRIP12):c.4317del (p.Gln1440fs)
NM_001348323.3(TRIP12):c.4318C>T (p.Gln1440Ter)
NM_001348323.3(TRIP12):c.4368dup (p.Asn1457fs) rs2041642562
NM_001348323.3(TRIP12):c.4609A>G (p.Ile1537Val)
NM_001348323.3(TRIP12):c.4610T>C (p.Ile1537Thr)
NM_001348323.3(TRIP12):c.4642CTT[1] (p.Leu1550del)
NM_001348323.3(TRIP12):c.4726del (p.Ser1576fs) rs2154256586
NM_001348323.3(TRIP12):c.4789A>G (p.Ile1597Val)
NM_001348323.3(TRIP12):c.4838+2T>G rs2040714903
NM_001348323.3(TRIP12):c.4861A>C (p.Thr1621Pro)
NM_001348323.3(TRIP12):c.4864C>T (p.Arg1622Trp) rs1320218400
NM_001348323.3(TRIP12):c.488A>T (p.Gln163Leu) rs1295583557
NM_001348323.3(TRIP12):c.4904G>A (p.Arg1635Gln) rs2154255374
NM_001348323.3(TRIP12):c.4928C>A (p.Thr1643Asn) rs2154255362
NM_001348323.3(TRIP12):c.4986T>A (p.Asp1662Glu) rs1468657712
NM_001348323.3(TRIP12):c.5009G>A (p.Arg1670Gln) rs1553602821
NM_001348323.3(TRIP12):c.5030C>T (p.Ala1677Val)
NM_001348323.3(TRIP12):c.5259_5276delinsAAATGATATG (p.Leu1754fs) rs2154245501
NM_001348323.3(TRIP12):c.5308A>G (p.Met1770Val) rs1428800056
NM_001348323.3(TRIP12):c.5429C>T (p.Ser1810Leu) rs2036612429
NM_001348323.3(TRIP12):c.5452_5453delinsAAACAAATTGTAAATTGTACCA (p.Pro1818fs)
NM_001348323.3(TRIP12):c.5459dup (p.Ala1821fs) rs2036605188
NM_001348323.3(TRIP12):c.5675del (p.Asn1892fs)
NM_001348323.3(TRIP12):c.5801C>T (p.Pro1934Leu)
NM_001348323.3(TRIP12):c.586_587del (p.Ser196fs) rs1553704327
NM_001348323.3(TRIP12):c.6034A>G (p.Thr2012Ala) rs1574632490
NM_001348323.3(TRIP12):c.6096_6109dup (p.Tyr2037Ter)
NM_001348323.3(TRIP12):c.6122C>T (p.Pro2041Leu) rs2032214426
NM_001348323.3(TRIP12):c.6126_6128delinsTT (p.Tyr2043fs)
NM_001348323.3(TRIP12):c.6184C>T (p.Gln2062Ter) rs1387893497
NM_001348323.3(TRIP12):c.638_639del (p.Arg213fs)
NM_001348323.3(TRIP12):c.692G>C (p.Gly231Ala)
NM_001348323.3(TRIP12):c.935T>G (p.Val312Gly)
NM_001348323.3(TRIP12):c.964C>A (p.Pro322Thr)

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