ClinVar Miner

List of variants in gene CHD3 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 150
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HGVS dbSNP gnomAD frequency
NM_001005273.3(CHD3):c.3417G>T (p.Gly1139=) rs61753146 0.00115
NM_001005273.3(CHD3):c.5798C>T (p.Ala1933Val) rs140448992 0.00008
NM_001005273.3(CHD3):c.1612C>G (p.Pro538Ala) rs761557613 0.00003
NM_001005273.3(CHD3):c.341A>C (p.Lys114Thr) rs376670741 0.00001
NM_001005273.3(CHD3):c.5971C>T (p.Arg1991Ter) rs1971670741 0.00001
NM_001005273.3(CHD3):c.100+1G>A
NM_001005273.3(CHD3):c.103A>G (p.Lys35Glu)
NM_001005273.3(CHD3):c.1198G>A (p.Ala400Thr)
NM_001005273.3(CHD3):c.121C>A (p.Leu41Met)
NM_001005273.3(CHD3):c.1331A>T (p.Glu444Val)
NM_001005273.3(CHD3):c.1421G>A (p.Cys474Tyr)
NM_001005273.3(CHD3):c.1501A>G (p.Thr501Ala)
NM_001005273.3(CHD3):c.1503+6T>C
NM_001005273.3(CHD3):c.1523G>C (p.Arg508Pro)
NM_001005273.3(CHD3):c.1534A>C (p.Ile512Leu)
NM_001005273.3(CHD3):c.1546C>T (p.Arg516Trp)
NM_001005273.3(CHD3):c.1555G>A (p.Glu519Lys)
NM_001005273.3(CHD3):c.155G>A (p.Arg52Gln)
NM_001005273.3(CHD3):c.1565T>C (p.Val522Ala)
NM_001005273.3(CHD3):c.1571T>C (p.Val524Ala)
NM_001005273.3(CHD3):c.1598A>T (p.Asn533Ile)
NM_001005273.3(CHD3):c.1613C>G (p.Pro538Arg)
NM_001005273.3(CHD3):c.1637C>T (p.Ser546Leu)
NM_001005273.3(CHD3):c.1643G>A (p.Arg548Gln) rs2151518787
NM_001005273.3(CHD3):c.1655T>A (p.Val552Asp)
NM_001005273.3(CHD3):c.1681C>T (p.His561Tyr)
NM_001005273.3(CHD3):c.1747C>T (p.Arg583Trp)
NM_001005273.3(CHD3):c.202C>T (p.Arg68Cys)
NM_001005273.3(CHD3):c.2095AAG[6] (p.Lys703_Glu704insLys)
NM_001005273.3(CHD3):c.2152C>G (p.Pro718Ala) rs2151560373
NM_001005273.3(CHD3):c.2197G>A (p.Gly733Arg)
NM_001005273.3(CHD3):c.2238G>T (p.Trp746Cys)
NM_001005273.3(CHD3):c.2242C>T (p.Arg748Cys)
NM_001005273.3(CHD3):c.2243G>A (p.Arg748His)
NM_001005273.3(CHD3):c.2450C>T (p.Thr817Met)
NM_001005273.3(CHD3):c.2467C>T (p.Arg823Trp) rs1970056398
NM_001005273.3(CHD3):c.2474T>G (p.Ile825Ser) rs2151564258
NM_001005273.3(CHD3):c.2551G>A (p.Ala851Thr)
NM_001005273.3(CHD3):c.2660G>A (p.Arg887Gln)
NM_001005273.3(CHD3):c.2695C>T (p.Leu899Phe) rs1970159341
NM_001005273.3(CHD3):c.2698A>G (p.Asn900Asp) rs2151572474
NM_001005273.3(CHD3):c.2755C>T (p.Leu919=)
NM_001005273.3(CHD3):c.2794G>A (p.Glu932Lys)
NM_001005273.3(CHD3):c.2806A>G (p.Asn936Asp) rs2151574702
NM_001005273.3(CHD3):c.2890A>G (p.Met964Val)
NM_001005273.3(CHD3):c.2897G>A (p.Arg966Gln) rs1555611692
NM_001005273.3(CHD3):c.292G>A (p.Gly98Arg)
NM_001005273.3(CHD3):c.301C>T (p.Arg101Trp)
NM_001005273.3(CHD3):c.3050C>T (p.Ser1017Leu)
NM_001005273.3(CHD3):c.3055C>T (p.Leu1019Phe)
NM_001005273.3(CHD3):c.3070G>T (p.Asp1024Tyr)
NM_001005273.3(CHD3):c.3115G>A (p.Ala1039Thr)
NM_001005273.3(CHD3):c.3133C>A (p.Leu1045Ile)
NM_001005273.3(CHD3):c.3299G>A (p.Gly1100Asp)
NM_001005273.3(CHD3):c.3312G>C (p.Glu1104Asp) rs2151596943
NM_001005273.3(CHD3):c.3313C>T (p.Arg1105Cys)
NM_001005273.3(CHD3):c.3314G>A (p.Arg1105His)
NM_001005273.3(CHD3):c.3337G>A (p.Ala1113Thr) rs1274980815
NM_001005273.3(CHD3):c.3338C>T (p.Ala1113Val)
NM_001005273.3(CHD3):c.3358G>A (p.Asp1120Asn) rs1350258866
NM_001005273.3(CHD3):c.3362G>A (p.Arg1121Gln) rs1567860112
NM_001005273.3(CHD3):c.3397C>T (p.Leu1133Phe)
NM_001005273.3(CHD3):c.3421C>A (p.Leu1141Met)
NM_001005273.3(CHD3):c.3437C>T (p.Ala1146Val) rs2151600297
NM_001005273.3(CHD3):c.3496-3C>T rs2151603234
NM_001005273.3(CHD3):c.3540G>A (p.Met1180Ile)
NM_001005273.3(CHD3):c.3559C>T (p.Arg1187Cys) rs2151603656
NM_001005273.3(CHD3):c.3563C>T (p.Ala1188Val)
NM_001005273.3(CHD3):c.3652G>T (p.Gly1218Cys)
NM_001005273.3(CHD3):c.3655T>G (p.Ser1219Ala) rs2151604360
NM_001005273.3(CHD3):c.3759T>G (p.Ile1253Met)
NM_001005273.3(CHD3):c.3763T>G (p.Tyr1255Asp)
NM_001005273.3(CHD3):c.3781G>T (p.Ala1261Ser)
NM_001005273.3(CHD3):c.3805G>C (p.Asp1269His)
NM_001005273.3(CHD3):c.3839A>G (p.Asn1280Ser)
NM_001005273.3(CHD3):c.3877G>A (p.Val1293Met)
NM_001005273.3(CHD3):c.3877G>T (p.Val1293Leu)
NM_001005273.3(CHD3):c.3894+8G>A
NM_001005273.3(CHD3):c.3895A>G (p.Ile1299Val) rs2151615075
NM_001005273.3(CHD3):c.3909G>C (p.Glu1303Asp) rs2151615191
NM_001005273.3(CHD3):c.3911G>A (p.Arg1304Gln)
NM_001005273.3(CHD3):c.4054G>A (p.Ala1352Thr) rs2151615882
NM_001005273.3(CHD3):c.4061A>T (p.Gln1354Leu)
NM_001005273.3(CHD3):c.4070A>G (p.Gln1357Arg)
NM_001005273.3(CHD3):c.4078C>G (p.Gln1360Glu)
NM_001005273.3(CHD3):c.4129C>T (p.Arg1377Cys)
NM_001005273.3(CHD3):c.4142G>T (p.Arg1381Leu) rs1165994865
NM_001005273.3(CHD3):c.4249C>T (p.Arg1417Trp)
NM_001005273.3(CHD3):c.4250G>A (p.Arg1417Gln)
NM_001005273.3(CHD3):c.4321G>T (p.Val1441Leu)
NM_001005273.3(CHD3):c.4325G>A (p.Arg1442Gln)
NM_001005273.3(CHD3):c.4345G>C (p.Glu1449Gln) rs1970875545
NM_001005273.3(CHD3):c.4355T>C (p.Phe1452Ser)
NM_001005273.3(CHD3):c.4364A>G (p.Tyr1455Cys)
NM_001005273.3(CHD3):c.4372T>G (p.Leu1458Val)
NM_001005273.3(CHD3):c.4385A>C (p.His1462Pro)
NM_001005273.3(CHD3):c.4424C>T (p.Ala1475Val)
NM_001005273.3(CHD3):c.4453C>T (p.Arg1485Cys)
NM_001005273.3(CHD3):c.4475T>C (p.Ile1492Thr)
NM_001005273.3(CHD3):c.4487C>T (p.Ser1496Phe)
NM_001005273.3(CHD3):c.4595C>T (p.Ser1532Phe)
NM_001005273.3(CHD3):c.4651T>C (p.Cys1551Arg) rs960431387
NM_001005273.3(CHD3):c.4654A>T (p.Thr1552Ser)
NM_001005273.3(CHD3):c.4670C>G (p.Thr1557Ser)
NM_001005273.3(CHD3):c.4709C>G (p.Pro1570Arg) rs199768991
NM_001005273.3(CHD3):c.4738G>A (p.Glu1580Lys)
NM_001005273.3(CHD3):c.4778T>C (p.Met1593Thr)
NM_001005273.3(CHD3):c.4782G>C (p.Glu1594Asp)
NM_001005273.3(CHD3):c.4910A>G (p.Asp1637Gly)
NM_001005273.3(CHD3):c.4945G>A (p.Glu1649Lys)
NM_001005273.3(CHD3):c.4970A>T (p.Asp1657Val)
NM_001005273.3(CHD3):c.5026+3A>C
NM_001005273.3(CHD3):c.5056C>A (p.Pro1686Thr)
NM_001005273.3(CHD3):c.5059G>A (p.Gly1687Arg)
NM_001005273.3(CHD3):c.5113C>T (p.Pro1705Ser)
NM_001005273.3(CHD3):c.5167T>A (p.Trp1723Arg)
NM_001005273.3(CHD3):c.5303A>T (p.Gln1768Leu)
NM_001005273.3(CHD3):c.5339C>T (p.Ala1780Val) rs2151661582
NM_001005273.3(CHD3):c.533C>A (p.Pro178His)
NM_001005273.3(CHD3):c.5341A>C (p.Asn1781His)
NM_001005273.3(CHD3):c.5401G>C (p.Glu1801Gln)
NM_001005273.3(CHD3):c.5404C>A (p.Gln1802Lys)
NM_001005273.3(CHD3):c.5408C>T (p.Ala1803Val)
NM_001005273.3(CHD3):c.541C>T (p.Pro181Ser)
NM_001005273.3(CHD3):c.5431C>T (p.Arg1811Trp)
NM_001005273.3(CHD3):c.5438C>T (p.Ala1813Val) rs1336103222
NM_001005273.3(CHD3):c.5465C>A (p.Pro1822Gln) rs752113004
NM_001005273.3(CHD3):c.5481G>A (p.Met1827Ile)
NM_001005273.3(CHD3):c.5500G>A (p.Ala1834Thr)
NM_001005273.3(CHD3):c.556A>G (p.Met186Val) rs2151493103
NM_001005273.3(CHD3):c.5575G>A (p.Ala1859Thr)
NM_001005273.3(CHD3):c.5578G>A (p.Val1860Ile)
NM_001005273.3(CHD3):c.5657T>C (p.Leu1886Pro) rs1971515823
NM_001005273.3(CHD3):c.5677G>A (p.Ala1893Thr)
NM_001005273.3(CHD3):c.5701C>T (p.Arg1901Cys)
NM_001005273.3(CHD3):c.578G>T (p.Trp193Leu)
NM_001005273.3(CHD3):c.5813C>A (p.Ala1938Glu)
NM_001005273.3(CHD3):c.5815C>G (p.Pro1939Ala)
NM_001005273.3(CHD3):c.5822_5823delinsCA (p.Gly1941Ala)
NM_001005273.3(CHD3):c.582A>C (p.Arg194Ser)
NM_001005273.3(CHD3):c.5850C>T (p.Tyr1950=)
NM_001005273.3(CHD3):c.5897C>G (p.Pro1966Arg)
NM_001005273.3(CHD3):c.5917G>C (p.Glu1973Gln) rs1064795926
NM_001005273.3(CHD3):c.5935_5936delinsAA (p.Ala1979Lys)
NM_001005273.3(CHD3):c.5957A>G (p.Asp1986Gly)
NM_001005273.3(CHD3):c.5969C>T (p.Pro1990Leu)
NM_001005273.3(CHD3):c.694_696del (p.Thr232del)
NM_001005273.3(CHD3):c.704C>A (p.Ala235Glu) rs1969176834
NM_001005273.3(CHD3):c.737C>T (p.Pro246Leu)
NM_001005273.3(CHD3):c.784G>A (p.Glu262Lys)

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