ClinVar Miner

List of variants in gene CHST3 reported as uncertain significance by Invitae

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Total variants: 112
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HGVS dbSNP gnomAD frequency
NM_004273.5(CHST3):c.980A>C (p.Asp327Ala) rs573403001 0.00029
NM_004273.5(CHST3):c.1324G>A (p.Ala442Thr) rs776562348 0.00011
NM_004273.5(CHST3):c.518C>T (p.Ser173Phe) rs751961615 0.00010
NM_004273.5(CHST3):c.1044C>G (p.Ile348Met) rs3740128 0.00009
NM_004273.5(CHST3):c.269T>C (p.Leu90Pro) rs138203946 0.00006
NM_004273.5(CHST3):c.276C>A (p.Ser92Arg) rs777858428 0.00005
NM_004273.5(CHST3):c.475T>A (p.Phe159Ile) rs145538723 0.00004
NM_004273.5(CHST3):c.1184C>T (p.Pro395Leu) rs756147851 0.00003
NM_004273.5(CHST3):c.244G>A (p.Glu82Lys) rs368468468 0.00003
NM_004273.5(CHST3):c.320T>A (p.Met107Lys) rs765024887 0.00003
NM_004273.5(CHST3):c.7A>G (p.Lys3Glu) rs199515173 0.00003
NM_004273.5(CHST3):c.1076C>T (p.Pro359Leu) rs1193910975 0.00002
NM_004273.5(CHST3):c.1166C>T (p.Ala389Val) rs766952355 0.00002
NM_004273.5(CHST3):c.1242C>G (p.Ile414Met) rs1004650270 0.00002
NM_004273.5(CHST3):c.133A>T (p.Ile45Leu) rs756821052 0.00002
NM_004273.5(CHST3):c.1414G>A (p.Glu472Lys) rs779698260 0.00002
NM_004273.5(CHST3):c.334G>A (p.Glu112Lys) rs751470049 0.00002
NM_004273.5(CHST3):c.1031A>G (p.Asn344Ser) rs777739643 0.00001
NM_004273.5(CHST3):c.182A>G (p.Asp61Gly) rs1362350248 0.00001
NM_004273.5(CHST3):c.202G>A (p.Ala68Thr) rs142556853 0.00001
NM_004273.5(CHST3):c.295T>A (p.Leu99Met) rs1446955235 0.00001
NM_004273.5(CHST3):c.311A>G (p.Glu104Gly) rs148801316 0.00001
NM_004273.5(CHST3):c.313C>G (p.Pro105Ala) rs747226832 0.00001
NM_004273.5(CHST3):c.340G>C (p.Glu114Gln) rs759393390 0.00001
NM_004273.5(CHST3):c.398G>A (p.Arg133His) rs767508669 0.00001
NM_004273.5(CHST3):c.466G>A (p.Gly156Ser) rs202107912 0.00001
NM_004273.5(CHST3):c.538A>T (p.Asn180Tyr) rs1249561246 0.00001
NM_004273.5(CHST3):c.544G>A (p.Ala182Thr) rs745523940 0.00001
NM_004273.5(CHST3):c.655A>G (p.Met219Val) rs779793827 0.00001
NM_004273.5(CHST3):c.665G>A (p.Arg222Gln) rs1437776489 0.00001
NM_004273.5(CHST3):c.757G>A (p.Gly253Ser) rs200988207 0.00001
NM_004273.5(CHST3):c.790T>C (p.Cys264Arg) rs1459673649 0.00001
NM_004273.5(CHST3):c.793C>G (p.Arg265Gly) rs760987231 0.00001
NM_004273.5(CHST3):c.853C>T (p.Pro285Ser) rs868146865 0.00001
NM_004273.5(CHST3):c.862G>A (p.Glu288Lys) rs903606184 0.00001
NM_004273.5(CHST3):c.869C>G (p.Pro290Arg) rs768963465 0.00001
NM_004273.5(CHST3):c.922G>T (p.Ala308Ser) rs1840062598 0.00001
NM_004273.5(CHST3):c.994G>A (p.Gly332Ser) rs971956671 0.00001
NM_004273.5(CHST3):c.100G>A (p.Val34Ile)
NM_004273.5(CHST3):c.1036G>A (p.Glu346Lys)
NM_004273.5(CHST3):c.1042A>C (p.Ile348Leu) rs2131776087
NM_004273.5(CHST3):c.1058A>C (p.Glu353Ala) rs2131776149
NM_004273.5(CHST3):c.1109G>A (p.Arg370His) rs1355385307
NM_004273.5(CHST3):c.1109G>C (p.Arg370Pro) rs1355385307
NM_004273.5(CHST3):c.1151A>G (p.Glu384Gly)
NM_004273.5(CHST3):c.1165G>A (p.Ala389Thr)
NM_004273.5(CHST3):c.1169G>A (p.Gly390Asp)
NM_004273.5(CHST3):c.11G>A (p.Gly4Glu) rs1840033319
NM_004273.5(CHST3):c.1204C>G (p.Gln402Glu)
NM_004273.5(CHST3):c.1264T>C (p.Ser422Pro)
NM_004273.5(CHST3):c.1276G>A (p.Glu426Lys) rs1223108562
NM_004273.5(CHST3):c.1304A>G (p.Lys435Arg)
NM_004273.5(CHST3):c.1318_1327del (p.Val440fs)
NM_004273.5(CHST3):c.1367C>A (p.Ala456Glu)
NM_004273.5(CHST3):c.1394G>A (p.Arg465His) rs569940449
NM_004273.5(CHST3):c.1420G>A (p.Gly474Ser)
NM_004273.5(CHST3):c.162G>C (p.Gln54His)
NM_004273.5(CHST3):c.196G>A (p.Asp66Asn) rs964738146
NM_004273.5(CHST3):c.19T>A (p.Leu7Met) rs2131772503
NM_004273.5(CHST3):c.268C>T (p.Leu90Phe)
NM_004273.5(CHST3):c.296T>C (p.Leu99Ser)
NM_004273.5(CHST3):c.2T>C (p.Met1Thr)
NM_004273.5(CHST3):c.307G>A (p.Val103Met)
NM_004273.5(CHST3):c.316G>A (p.Ala106Thr)
NM_004273.5(CHST3):c.322G>A (p.Glu108Lys)
NM_004273.5(CHST3):c.328G>A (p.Ala110Thr)
NM_004273.5(CHST3):c.347A>G (p.Glu116Gly) rs2131774439
NM_004273.5(CHST3):c.34C>T (p.Arg12Trp)
NM_004273.5(CHST3):c.368C>T (p.Pro123Leu)
NM_004273.5(CHST3):c.377C>A (p.Pro126Gln) rs371091098
NM_004273.5(CHST3):c.377C>T (p.Pro126Leu)
NM_004273.5(CHST3):c.37G>A (p.Asp13Asn)
NM_004273.5(CHST3):c.386C>A (p.Ala129Glu)
NM_004273.5(CHST3):c.386C>T (p.Ala129Val)
NM_004273.5(CHST3):c.394C>G (p.Arg132Gly) rs766145797
NM_004273.5(CHST3):c.395G>A (p.Arg132Gln)
NM_004273.5(CHST3):c.422C>T (p.Thr141Met) rs267606735
NM_004273.5(CHST3):c.430G>A (p.Gly144Ser) rs1360950889
NM_004273.5(CHST3):c.434C>T (p.Ser145Phe)
NM_004273.5(CHST3):c.442G>T (p.Val148Leu)
NM_004273.5(CHST3):c.445G>A (p.Gly149Ser)
NM_004273.5(CHST3):c.449A>C (p.Glu150Ala) rs1840053078
NM_004273.5(CHST3):c.467G>A (p.Gly156Asp)
NM_004273.5(CHST3):c.469A>G (p.Asn157Asp)
NM_004273.5(CHST3):c.505G>A (p.Glu169Lys)
NM_004273.5(CHST3):c.527C>T (p.Pro176Leu)
NM_004273.5(CHST3):c.530G>C (p.Gly177Ala)
NM_004273.5(CHST3):c.535G>A (p.Ala179Thr)
NM_004273.5(CHST3):c.571G>A (p.Val191Met) rs774652828
NM_004273.5(CHST3):c.582G>C (p.Gln194His)
NM_004273.5(CHST3):c.582G>T (p.Gln194His) rs759873741
NM_004273.5(CHST3):c.597C>A (p.Asp199Glu)
NM_004273.5(CHST3):c.613C>T (p.His205Tyr)
NM_004273.5(CHST3):c.634G>A (p.Glu212Lys) rs371650865
NM_004273.5(CHST3):c.635A>T (p.Glu212Val) rs1840057080
NM_004273.5(CHST3):c.677G>T (p.Arg226Leu) rs1287871626
NM_004273.5(CHST3):c.688G>A (p.Glu230Lys) rs774599785
NM_004273.5(CHST3):c.697G>A (p.Val233Ile)
NM_004273.5(CHST3):c.726C>A (p.Phe242Leu) rs764522356
NM_004273.5(CHST3):c.773C>G (p.Thr258Arg) rs1840059581
NM_004273.5(CHST3):c.791G>A (p.Cys264Tyr)
NM_004273.5(CHST3):c.812C>T (p.Ala271Val)
NM_004273.5(CHST3):c.845T>A (p.Phe282Tyr)
NM_004273.5(CHST3):c.84_98dup (p.Val32_Ile33insMetValPheValVal)
NM_004273.5(CHST3):c.85G>T (p.Val29Phe) rs751067074
NM_004273.5(CHST3):c.874C>G (p.Leu292Val) rs1474879888
NM_004273.5(CHST3):c.877G>T (p.Asp293Tyr)
NM_004273.5(CHST3):c.901C>T (p.Arg301Cys)
NM_004273.5(CHST3):c.916G>A (p.Val306Met) rs1564532505
NM_004273.5(CHST3):c.928C>A (p.Arg310Ser)
NM_004273.5(CHST3):c.929G>C (p.Arg310Pro)
NM_004273.5(CHST3):c.976G>A (p.Asp326Asn)

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