ClinVar Miner

List of variants studied for Clark-Baraitser syndrome

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_001348323.3(TRIP12):c.2651-25C>T rs4972915 0.81444
NM_001348323.3(TRIP12):c.2651-39A>C rs4973229 0.38913
NM_001348323.3(TRIP12):c.2736A>G (p.Thr912=) rs13018957 0.38821
NM_001348323.3(TRIP12):c.3482+15G>A rs6720868 0.36169
NM_001348323.3(TRIP12):c.1922C>T (p.Thr641Met) rs142882915 0.00092
NM_001348323.3(TRIP12):c.1823C>T (p.Ala608Val) rs139703319 0.00021
NM_001348323.3(TRIP12):c.4610T>C (p.Ile1537Thr) rs201067731 0.00005
NM_001348323.3(TRIP12):c.1177C>T (p.Arg393Cys) rs899545454 0.00004
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.2009C>T (p.Thr670Ile) rs2047157169 0.00001
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.2096A>G (p.Asn699Ser) rs762183066 0.00001
NM_001348323.3(TRIP12):c.2273G>A (p.Cys758Tyr) rs1386605432 0.00001
NM_001348323.3(TRIP12):c.3207-7T>C rs776422458 0.00001
NM_001348323.3(TRIP12):c.329A>G (p.Asn110Ser) rs772882161 0.00001
NM_001348323.3(TRIP12):c.3782T>C (p.Leu1261Ser) rs1417292516 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.964C>A (p.Pro322Thr) rs138526427 0.00001
NM_001348323.3(TRIP12):c.983A>C (p.Glu328Ala) rs986636922 0.00001
NM_001348323.3(TRIP12):c.1012C>T (p.Gln338Ter) rs2475891095
NM_001348323.3(TRIP12):c.1037A>G (p.Lys346Arg) rs2056267716
NM_001348323.3(TRIP12):c.1090C>T (p.Arg364Trp) rs2056255401
NM_001348323.3(TRIP12):c.1133+21del rs11373804
NM_001348323.3(TRIP12):c.1160G>A (p.Arg387Lys) rs2054983988
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.1439G>C (p.Gly480Ala)
NM_001348323.3(TRIP12):c.1486G>A (p.Ala496Thr) rs2049053255
NM_001348323.3(TRIP12):c.1510C>T (p.Gln504Ter) rs2473013696
NM_001348323.3(TRIP12):c.1604C>T (p.Thr535Met)
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) rs2472696414
NM_001348323.3(TRIP12):c.1987-4dup
NM_001348323.3(TRIP12):c.2065C>T (p.Gln689Ter) rs2472430261
NM_001348323.3(TRIP12):c.2071G>A (p.Val691Ile)
NM_001348323.3(TRIP12):c.2090T>A (p.Leu697His)
NM_001348323.3(TRIP12):c.225-11T>C
NM_001348323.3(TRIP12):c.2293G>A (p.Val765Ile)
NM_001348323.3(TRIP12):c.2378_2379insT (p.Val794fs) rs2154275777
NM_001348323.3(TRIP12):c.2396A>G (p.Lys799Arg) rs1444131578
NM_001348323.3(TRIP12):c.2477T>C (p.Ile826Thr)
NM_001348323.3(TRIP12):c.2624del (p.Pro875fs) rs2472099492
NM_001348323.3(TRIP12):c.2625_2629del (p.Asn876fs) rs2472099074
NM_001348323.3(TRIP12):c.2679_2685del (p.Asp893fs) rs2471982038
NM_001348323.3(TRIP12):c.2764_2767dup (p.Ser923Ter) rs2471975615
NM_001348323.3(TRIP12):c.2776G>T (p.Gly926Ter) rs2154270715
NM_001348323.3(TRIP12):c.3014T>G (p.Val1005Gly)
NM_001348323.3(TRIP12):c.3088_3089del (p.Gly1030fs) rs2471836738
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.3208C>T (p.Arg1070Ter) rs1575161164
NM_001348323.3(TRIP12):c.3399C>G (p.Asn1133Lys) rs2471614177
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.3551del (p.Asn1184fs)
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.3808del (p.Ser1270fs) rs2042881907
NM_001348323.3(TRIP12):c.3816+2T>A rs2471479385
NM_001348323.3(TRIP12):c.3835A>G (p.Ile1279Val) rs764732335
NM_001348323.3(TRIP12):c.3869del (p.Leu1290fs) rs2471401877
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) rs1332901100
NM_001348323.3(TRIP12):c.4216-2A>G rs2471181256
NM_001348323.3(TRIP12):c.4277A>G (p.His1426Arg) rs1367634297
NM_001348323.3(TRIP12):c.4317del (p.Gln1440fs) rs2471174164
NM_001348323.3(TRIP12):c.4318C>T (p.Gln1440Ter) rs1559428905
NM_001348323.3(TRIP12):c.4368dup (p.Asn1457fs) rs2041642562
NM_001348323.3(TRIP12):c.4609A>G (p.Ile1537Val) rs1242181004
NM_001348323.3(TRIP12):c.4642CTT[1] (p.Leu1550del) rs2471034166
NM_001348323.3(TRIP12):c.4726del (p.Ser1576fs) rs2154256586
NM_001348323.3(TRIP12):c.4789A>G (p.Ile1597Val) rs2470983247
NM_001348323.3(TRIP12):c.4838+2T>G rs2040714903
NM_001348323.3(TRIP12):c.4861A>C (p.Thr1621Pro) rs2470918350
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.4996-12_4996-2del rs2470807328
NM_001348323.3(TRIP12):c.5009G>A (p.Arg1670Gln) rs1553602821
NM_001348323.3(TRIP12):c.5030C>T (p.Ala1677Val) rs2470804912
NM_001348323.3(TRIP12):c.5114C>T (p.Pro1705Leu) rs2470377269
NM_001348323.3(TRIP12):c.5231A>G (p.Tyr1744Cys) rs2470347391
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.5429dup (p.His1811fs)
NM_001348323.3(TRIP12):c.5452_5453delinsAAACAAATTGTAAATTGTACCA (p.Pro1818fs) rs2470271582
NM_001348323.3(TRIP12):c.5459dup (p.Ala1821fs) rs2036605188
NM_001348323.3(TRIP12):c.5538_5566del (p.Glu1846fs)
NM_001348323.3(TRIP12):c.564T>A (p.Ser188Arg)
NM_001348323.3(TRIP12):c.5675del (p.Asn1892fs) rs2470100391
NM_001348323.3(TRIP12):c.5801C>T (p.Pro1934Leu) rs747501109
NM_001348323.3(TRIP12):c.586_587del (p.Ser196fs) rs1553704327
NM_001348323.3(TRIP12):c.5884C>T (p.His1962Tyr) rs2469796407
NM_001348323.3(TRIP12):c.6034A>G (p.Thr2012Ala) rs1574632490
NM_001348323.3(TRIP12):c.6096_6109dup (p.Tyr2037Ter) rs2469687265
NM_001348323.3(TRIP12):c.6122C>T (p.Pro2041Leu) rs2032214426
NM_001348323.3(TRIP12):c.6126_6128delinsTT (p.Tyr2043fs) rs2469686275
NM_001348323.3(TRIP12):c.6184C>T (p.Gln2062Ter) rs1387893497
NM_001348323.3(TRIP12):c.638_639del (p.Arg213fs) rs2475946632
NM_001348323.3(TRIP12):c.692G>C (p.Gly231Ala) rs372749816
NM_001348323.3(TRIP12):c.740C>T (p.Ser247Leu)
NM_001348323.3(TRIP12):c.835G>A (p.Ala279Thr)
NM_001348323.3(TRIP12):c.8A>C (p.Asn3Thr) rs746096308
NM_001348323.3(TRIP12):c.935T>G (p.Val312Gly) rs2475899699

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