Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.72008135G>ACA470284547CHST3c.1104G>A (p.Leu368=)
dbSNP gnomAD v4
10g.72008135G>CCA470284550CHST3c.1104G>C (p.Leu368=)
10g.72008135G=CA1918976755CHST3c.1104G= (p.Leu368=)
10g.72008135G>TCA470284552CHST3c.1104G>T (p.Leu368=)
gnomAD v4
10g.72008136G>ACA377150927CHST3c.1105G>A (p.Val369Met)
dbSNP gnomAD v2
10g.72008136G>CCA377150930CHST3c.1105G>C (p.Val369Leu)
10g.72008136G=CA1918976756CHST3c.1105G= (p.Val369=)
10g.72008136G>TCA377150931CHST3c.1105G>T (p.Val369Leu)
10g.72008137T>ACA377150932CHST3c.1106T>A (p.Val369Glu)
10g.72008137T>CCA377150934CHST3c.1106T>C (p.Val369Ala)
10g.72008137T>GCA377150936CHST3c.1106T>G (p.Val369Gly)
10g.72008138G>ACA470284555CHST3c.1107G>A (p.Val369=)
dbSNP
10g.72008138G>CCA470284557CHST3c.1107G>C (p.Val369=)
10g.72008138G=CA1918976757CHST3c.1107G= (p.Val369=)
10g.72008138G>TCA470284558CHST3c.1107G>T (p.Val369=)
COSMIC
10g.72008139C>ACA377150941CHST3c.1108C>A (p.Arg370Ser)
10g.72008139C=CA1918976758CHST3c.1108C= (p.Arg370=)
10g.72008139C>GCA377150944CHST3c.1108C>G (p.Arg370Gly)
gnomAD v4
10g.72008139C>TCA377150945CHST3c.1108C>T (p.Arg370Cys)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.72008140G>ACA377150946CHST3c.1109G>A (p.Arg370His)
ClinVar dbSNP gnomAD v4
10g.72008140G>CCA377150953CHST3c.1109G>C (p.Arg370Pro)
ClinVar dbSNP gnomAD v4
10g.72008140G=CA1918976759CHST3c.1109G= (p.Arg370=)
10g.72008140G>TCA377150949CHST3c.1109G>T (p.Arg370Leu)
dbSNP gnomAD v2 gnomAD v4
10g.72008141C>ACA470284561CHST3c.1110C>A (p.Arg370=)
10g.72008141C>GCA470284564CHST3c.1110C>G (p.Arg370=)
10g.72008141C>TCA470284562CHST3c.1110C>T (p.Arg370=)
10g.72008142T>ACA377150969CHST3c.1111T>A (p.Tyr371Asn)
10g.72008142T>CCA377150987CHST3c.1111T>C (p.Tyr371His)
dbSNP gnomAD v2 gnomAD v4
10g.72008142T>GCA377150975CHST3c.1111T>G (p.Tyr371Asp)
10g.72008142T=CA1918976760CHST3c.1111T= (p.Tyr371=)
10g.72008143A>CCA377150994CHST3c.1112A>C (p.Tyr371Ser)
10g.72008143A>GCA377150996CHST3c.1112A>G (p.Tyr371Cys)
gnomAD v4 COSMIC
10g.72008143A>TCA377151001CHST3c.1112A>T (p.Tyr371Phe)
10g.72008144C>ACA377151017CHST3c.1113C>A (p.Tyr371Ter)
dbSNP
10g.72008144C=CA1918976761CHST3c.1113C= (p.Tyr371=)
10g.72008144C>GCA377151023CHST3c.1113C>G (p.Tyr371Ter)
10g.72008144C>TCA470284568CHST3c.1113C>T (p.Tyr371=)
10g.72008145G>ACA253726CHST3c.1114G>A (p.Glu372Lys)
ClinVar dbSNP gnomAD v4
10g.72008145G>CCA377151036CHST3c.1114G>C (p.Glu372Gln)
10g.72008145G=CA1918976762CHST3c.1114G= (p.Glu372=)
10g.72008145G>TCA377151046CHST3c.1114G>T (p.Glu372Ter)
10g.72008146A>CCA377151049CHST3c.1115A>C (p.Glu372Ala)
10g.72008146A>GCA377151050CHST3c.1115A>G (p.Glu372Gly)
10g.72008146A>TCA377151051CHST3c.1115A>T (p.Glu372Val)
10g.72008147G>ACA470284574CHST3c.1116G>A (p.Glu372=)
ClinVar gnomAD v4
10g.72008147G>CCA377151061CHST3c.1116G>C (p.Glu372Asp)
10g.72008147G=CA1918976763CHST3c.1116G= (p.Glu372=)
10g.72008147G>TCA377151055CHST3c.1116G>T (p.Glu372Asp)
dbSNP gnomAD v4
10g.72008148G>ACA377151066CHST3c.1117G>A (p.Asp373Asn)
10g.72008148G>CCA377151067CHST3c.1117G>C (p.Asp373His)
10g.72008148G>TCA377151068CHST3c.1117G>T (p.Asp373Tyr)
gnomAD v4
10g.72008149A>CCA377151071CHST3c.1118A>C (p.Asp373Ala)
10g.72008149A>GCA377151073CHST3c.1118A>G (p.Asp373Gly)
gnomAD v4
10g.72008149A>TCA377151075CHST3c.1118A>T (p.Asp373Val)
10g.72008150C>ACA377151092CHST3c.1119C>A (p.Asp373Glu)
10g.72008150C>GCA377151103CHST3c.1119C>G (p.Asp373Glu)
gnomAD v4
10g.72008150C>TCA470284577CHST3c.1119C>T (p.Asp373=)
gnomAD v4
10g.72008151G>ACA377151107CHST3c.1120G>A (p.Val374Met)
gnomAD v4
10g.72008151G>CCA377151110CHST3c.1120G>C (p.Val374Leu)
10g.72008151G=CA1918976764CHST3c.1120G= (p.Val374=)
10g.72008151G>TCA377151113CHST3c.1120G>T (p.Val374Leu)
dbSNP gnomAD v2 gnomAD v4
10g.72008151_72008171dupCA2609583234CHST3c.1120_1140dup (p.Gln380_Lys381insValAlaArgGlyProLeuGln)
gnomAD v4
10g.72008152T>ACA377151138CHST3c.1121T>A (p.Val374Glu)
10g.72008152T>CCA377151128CHST3c.1121T>C (p.Val374Ala)
dbSNP gnomAD v2 gnomAD v4
10g.72008152T>GCA377151124CHST3c.1121T>G (p.Val374Gly)
10g.72008152T=CA1918976765CHST3c.1121T= (p.Val374=)
10g.72008153G>ACA470284581CHST3c.1122G>A (p.Val374=)
10g.72008153G>CCA470284582CHST3c.1122G>C (p.Val374=)
10g.72008153G>TCA470284583CHST3c.1122G>T (p.Val374=)
10g.72008153_72008154insCTCA2609583270CHST3c.1122_1123insCT (p.Ala375LeufsTer20)
gnomAD v4
10g.72008154G>ACA377151143CHST3c.1123G>A (p.Ala375Thr)
10g.72008154G>CCA377151146CHST3c.1123G>C (p.Ala375Pro)
10g.72008154G>TCA377151148CHST3c.1123G>T (p.Ala375Ser)
10g.72008155C>ACA377151151CHST3c.1124C>A (p.Ala375Glu)
10g.72008155C>GCA377151152CHST3c.1124C>G (p.Ala375Gly)
10g.72008155C>TCA377151153CHST3c.1124C>T (p.Ala375Val)
gnomAD v4
10g.72008156_72008157delCA2502195260CHST3c.1125_1126del (p.Gly377AlafsTer?)
10g.72008156A=CA1918976766CHST3c.1125A= (p.Ala375=)
10g.72008156A>CCA470284588CHST3c.1125A>C (p.Ala375=)
10g.72008156A>GCA470284589CHST3c.1125A>G (p.Ala375=)
dbSNP gnomAD v3 gnomAD v4
10g.72008156A>TCA470284590CHST3c.1125A>T (p.Ala375=)
10g.72008156_72008162delCA2609583303CHST3c.1125_1131del (p.Gly377CysfsTer15)
gnomAD v4
10g.72008157C>ACA377151156CHST3c.1126C>A (p.Arg376Ser)
10g.72008157C=CA1918976767CHST3c.1126C= (p.Arg376=)
10g.72008157C>GCA377151158CHST3c.1126C>G (p.Arg376Gly)
10g.72008157C>TCA377151168CHST3c.1126C>T (p.Arg376Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008158G>ACA377151176CHST3c.1127G>A (p.Arg376His)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.72008158G>CCA377151178CHST3c.1127G>C (p.Arg376Pro)
10g.72008158G=CA1918976768CHST3c.1127G= (p.Arg376=)
10g.72008158G>TCA377151179CHST3c.1127G>T (p.Arg376Leu)
gnomAD v4
10g.72008159C>ACA470284593CHST3c.1128C>A (p.Arg376=)
10g.72008159C=CA1918976769CHST3c.1128C= (p.Arg376=)
10g.72008159C>GCA209479366CHST3c.1128C>G (p.Arg376=)
dbSNP
10g.72008159C>TCA470284594CHST3c.1128C>T (p.Arg376=)
ClinVar dbSNP gnomAD v4
10g.72008160G>ACA377151185CHST3c.1129G>A (p.Gly377Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.72008160G>CCA377151181CHST3c.1129G>C (p.Gly377Arg)
gnomAD v4
10g.72008160G=CA1918976770CHST3c.1129G= (p.Gly377=)
10g.72008160G>TCA377151183CHST3c.1129G>T (p.Gly377Trp)
10g.72008161G>ACA377151188CHST3c.1130G>A (p.Gly377Glu)
10g.72008161G>CCA377151196CHST3c.1130G>C (p.Gly377Ala)
10g.72008161G>TCA377151202CHST3c.1130G>T (p.Gly377Val)
gnomAD v4
10g.72008162G>ACA470284595CHST3c.1131G>A (p.Gly377=)
10g.72008162G>CCA470284597CHST3c.1131G>C (p.Gly377=)
10g.72008162G=CA1918976771CHST3c.1131G= (p.Gly377=)
10g.72008162G>TCA470284598CHST3c.1131G>T (p.Gly377=)
dbSNP gnomAD v2 gnomAD v4
10g.72008162_72008163dupCA2513611549CHST3c.1131_1132dup (p.Pro378ArgfsTer17)
10g.72008163C>ACA377151210CHST3c.1132C>A (p.Pro378Thr)
10g.72008163C>GCA377151213CHST3c.1132C>G (p.Pro378Ala)
10g.72008163C>TCA377151216CHST3c.1132C>T (p.Pro378Ser)
gnomAD v4
10g.72008164C>ACA377151222CHST3c.1133C>A (p.Pro378Gln)
dbSNP gnomAD v4
10g.72008164C=CA1918976772CHST3c.1133C= (p.Pro378=)
10g.72008164C>GCA377151229CHST3c.1133C>G (p.Pro378Arg)
10g.72008164C>TCA377151238CHST3c.1133C>T (p.Pro378Leu)
gnomAD v4 COSMIC
10g.72008165G>ACA209479368CHST3c.1134G>A (p.Pro378=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008165G>CCA470284601CHST3c.1134G>C (p.Pro378=)
10g.72008165G=CA1918976773CHST3c.1134G= (p.Pro378=)
10g.72008165G>TCA470284602CHST3c.1134G>T (p.Pro378=)
gnomAD v4
10g.72008166C>ACA377151242CHST3c.1135C>A (p.Leu379Met)
10g.72008166C=CA1918976774CHST3c.1135C= (p.Leu379=)
10g.72008166C>GCA377151247CHST3c.1135C>G (p.Leu379Val)
10g.72008166C>TCA5548207CHST3c.1135C>T (p.Leu379=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008167T>ACA377151260CHST3c.1136T>A (p.Leu379Gln)
10g.72008167T>CCA377151265CHST3c.1136T>C (p.Leu379Pro)
gnomAD v4
10g.72008167T>GCA377151256CHST3c.1136T>G (p.Leu379Arg)
gnomAD v4
10g.72008168G>ACA470284606CHST3c.1137G>A (p.Leu379=)
gnomAD v4
10g.72008168G>CCA470284607CHST3c.1137G>C (p.Leu379=)
10g.72008168G>TCA470284608CHST3c.1137G>T (p.Leu379=)
gnomAD v4
10g.72008169C>ACA377151269CHST3c.1138C>A (p.Gln380Lys)
10g.72008169C=CA1918976775CHST3c.1138C= (p.Gln380=)
10g.72008169C>GCA377151266CHST3c.1138C>G (p.Gln380Glu)
COSMIC
10g.72008169C>TCA377151275CHST3c.1138C>T (p.Gln380Ter)
dbSNP gnomAD v4
10g.72008170A>CCA377151279CHST3c.1139A>C (p.Gln380Pro)
10g.72008170A>GCA377151280CHST3c.1139A>G (p.Gln380Arg)
10g.72008170A>TCA377151281CHST3c.1139A>T (p.Gln380Leu)
10g.72008171G>ACA470284613CHST3c.1140G>A (p.Gln380=)
10g.72008171G>CCA377151285CHST3c.1140G>C (p.Gln380His)
10g.72008171G>TCA377151287CHST3c.1140G>T (p.Gln380His)
10g.72008172A>CCA377151288CHST3c.1141A>C (p.Lys381Gln)
10g.72008172A>GCA377151289CHST3c.1141A>G (p.Lys381Glu)
10g.72008172A>TCA377151294CHST3c.1141A>T (p.Lys381Ter)
10g.72008173delCA2609583419CHST3c.1142del (p.Lys381ArgfsTer13)
gnomAD v4
10g.72008173A>CCA377151300CHST3c.1142A>C (p.Lys381Thr)
gnomAD v4
10g.72008173A>GCA377151313CHST3c.1142A>G (p.Lys381Arg)
10g.72008173A>TCA377151317CHST3c.1142A>T (p.Lys381Met)
10g.72008174G>ACA470284615CHST3c.1143G>A (p.Lys381=)
ClinVar dbSNP COSMIC
10g.72008174G>CCA377151319CHST3c.1143G>C (p.Lys381Asn)
10g.72008174G>TCA377151318CHST3c.1143G>T (p.Lys381Asn)
10g.72008175G>ACA377151323CHST3c.1144G>A (p.Ala382Thr)
10g.72008175G>CCA377151332CHST3c.1144G>C (p.Ala382Pro)
10g.72008175G>TCA377151334CHST3c.1144G>T (p.Ala382Ser)
gnomAD v4
10g.72008176C>ACA377151336CHST3c.1145C>A (p.Ala382Asp)
dbSNP gnomAD v2 gnomAD v4
10g.72008176C=CA1918976776CHST3c.1145C= (p.Ala382=)
10g.72008176C>GCA377151337CHST3c.1145C>G (p.Ala382Gly)
10g.72008176C>TCA377151339CHST3c.1145C>T (p.Ala382Val)
10g.72008177_72008178delCA2563961136CHST3c.1146_1147del (p.Glu384AspfsTer?)
10g.72008177C>ACA470284621CHST3c.1146C>A (p.Ala382=)
10g.72008177C>GCA470284622CHST3c.1146C>G (p.Ala382=)
10g.72008177C>TCA470284623CHST3c.1146C>T (p.Ala382=)
gnomAD v4
10g.72008178C>ACA377151358CHST3c.1147C>A (p.Arg383Ser)
10g.72008178C=CA1918976777CHST3c.1147C= (p.Arg383=)
10g.72008178C>GCA377151362CHST3c.1147C>G (p.Arg383Gly)
dbSNP gnomAD v2 gnomAD v4
10g.72008178C>TCA377151364CHST3c.1147C>T (p.Arg383Cys)
dbSNP gnomAD v3 gnomAD v4
10g.72008181_72008197delCA2573145449CHST3c.1150_1166del (p.Glu384ArgfsTer?)
ClinVar dbSNP
10g.72008179G>ACA5548208CHST3c.1148G>A (p.Arg383His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008179G>CCA377151365CHST3c.1148G>C (p.Arg383Pro)
dbSNP
10g.72008179G=CA1918976778CHST3c.1148G= (p.Arg383=)
10g.72008179G>TCA377151367CHST3c.1148G>T (p.Arg383Leu)
10g.72008180C>ACA470284627CHST3c.1149C>A (p.Arg383=)
gnomAD v4
10g.72008180C=CA1918976779CHST3c.1149C= (p.Arg383=)
10g.72008180C>GCA470284628CHST3c.1149C>G (p.Arg383=)
gnomAD v4
10g.72008180C>TCA470284629CHST3c.1149C>T (p.Arg383=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.72008180_72008181insTGCA2519056411CHST3c.1149_1150insTG (p.Glu384TrpfsTer11)
10g.72008181G>ACA377151374CHST3c.1150G>A (p.Glu384Lys)
gnomAD v4
10g.72008181G>CCA377151376CHST3c.1150G>C (p.Glu384Gln)
10g.72008181G>TCA377151372CHST3c.1150G>T (p.Glu384Ter)
10g.72008182A>CCA377151378CHST3c.1151A>C (p.Glu384Ala)
10g.72008182A>GCA377151380CHST3c.1151A>G (p.Glu384Gly)
ClinVar
10g.72008182A>TCA377151383CHST3c.1151A>T (p.Glu384Val)
10g.72008183G>ACA470284632CHST3c.1152G>A (p.Glu384=)
10g.72008183G>CCA377151393CHST3c.1152G>C (p.Glu384Asp)
10g.72008183G>TCA377151406CHST3c.1152G>T (p.Glu384Asp)
gnomAD v4
10g.72008184A=CA1918976780CHST3c.1153A= (p.Met385=)
10g.72008184A>CCA377151411CHST3c.1153A>C (p.Met385Leu)
10g.72008184A>GCA377151413CHST3c.1153A>G (p.Met385Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008184A>TCA377151414CHST3c.1153A>T (p.Met385Leu)
10g.72008185T>ACA377151415CHST3c.1154T>A (p.Met385Lys)
10g.72008185T>CCA377151416CHST3c.1154T>C (p.Met385Thr)
10g.72008185T>GCA377151418CHST3c.1154T>G (p.Met385Arg)
10g.72008186G>ACA377151422CHST3c.1155G>A (p.Met385Ile)
10g.72008186G>CCA377151425CHST3c.1155G>C (p.Met385Ile)
10g.72008186G=CA1918976781CHST3c.1155G= (p.Met385=)
10g.72008186G>TCA377151421CHST3c.1155G>T (p.Met385Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.72008187T>ACA377151432CHST3c.1156T>A (p.Tyr386Asn)
10g.72008187T>CCA377151441CHST3c.1156T>C (p.Tyr386His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008187T>GCA377151445CHST3c.1156T>G (p.Tyr386Asp)
10g.72008187T=CA1918976782CHST3c.1156T= (p.Tyr386=)
10g.72008188A>CCA377151448CHST3c.1157A>C (p.Tyr386Ser)
10g.72008188A>GCA377151450CHST3c.1157A>G (p.Tyr386Cys)
10g.72008188A>TCA377151456CHST3c.1157A>T (p.Tyr386Phe)
gnomAD v4
10g.72008189C>ACA377151457CHST3c.1158C>A (p.Tyr386Ter)
10g.72008189C=CA1918976783CHST3c.1158C= (p.Tyr386=)
10g.72008189C>GCA377151458CHST3c.1158C>G (p.Tyr386Ter)
10g.72008189C>TCA470284645CHST3c.1158C>T (p.Tyr386=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.72008190C>ACA377151460CHST3c.1159C>A (p.Arg387Ser)
dbSNP gnomAD v2 gnomAD v4
10g.72008190C=CA1918976784CHST3c.1159C= (p.Arg387=)
10g.72008190C>GCA377151462CHST3c.1159C>G (p.Arg387Gly)
10g.72008190C>TCA377151463CHST3c.1159C>T (p.Arg387Cys)
dbSNP gnomAD v2 gnomAD v4
10g.72008191G>ACA5548209CHST3c.1160G>A (p.Arg387His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008191G>CCA377151467CHST3c.1160G>C (p.Arg387Pro)
gnomAD v4
10g.72008191G=CA1918976785CHST3c.1160G= (p.Arg387=)
10g.72008191G>TCA377151469CHST3c.1160G>T (p.Arg387Leu)
10g.72008192C>ACA470284652CHST3c.1161C>A (p.Arg387=)
gnomAD v4
10g.72008192C>GCA470284651CHST3c.1161C>G (p.Arg387=)
10g.72008192C>TCA470284650CHST3c.1161C>T (p.Arg387=)
gnomAD v4
10g.72008193T>ACA377151471CHST3c.1162T>A (p.Phe388Ile)
10g.72008193T>CCA5548210CHST3c.1162T>C (p.Phe388Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008193T>GCA377151470CHST3c.1162T>G (p.Phe388Val)
10g.72008193T=CA1918976786CHST3c.1162T= (p.Phe388=)
10g.72008194T>ACA377151478CHST3c.1163T>A (p.Phe388Tyr)
10g.72008194T>CCA377151474CHST3c.1163T>C (p.Phe388Ser)
10g.72008194T>GCA377151476CHST3c.1163T>G (p.Phe388Cys)
10g.72008195C>ACA377151481CHST3c.1164C>A (p.Phe388Leu)
10g.72008195C=CA1918976787CHST3c.1164C= (p.Phe388=)
10g.72008195C>GCA377151483CHST3c.1164C>G (p.Phe388Leu)
10g.72008195C>TCA5548211CHST3c.1164C>T (p.Phe388=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.72008196G>ACA377151488CHST3c.1165G>A (p.Ala389Thr)
ClinVar gnomAD v4
10g.72008196G>CCA377151486CHST3c.1165G>C (p.Ala389Pro)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.72008196G=CA1918976788CHST3c.1165G= (p.Ala389=)
10g.72008196G>TCA209479377CHST3c.1165G>T (p.Ala389Ser)
dbSNP gnomAD v4
10g.72008197C>ACA377151492CHST3c.1166C>A (p.Ala389Asp)
10g.72008197C=CA1918976789CHST3c.1166C= (p.Ala389=)
10g.72008197C>GCA377151494CHST3c.1166C>G (p.Ala389Gly)
10g.72008197C>TCA5548212CHST3c.1166C>T (p.Ala389Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008198C>ACA470284665CHST3c.1167C>A (p.Ala389=)
gnomAD v4
10g.72008198C=CA1918976790CHST3c.1167C= (p.Ala389=)
10g.72008198C>GCA470284668CHST3c.1167C>G (p.Ala389=)
10g.72008198C>TCA470284667CHST3c.1167C>T (p.Ala389=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.72008199G>ACA377151497CHST3c.1168G>A (p.Gly390Ser)
gnomAD v4 COSMIC
10g.72008199G>CCA377151500CHST3c.1168G>C (p.Gly390Arg)
dbSNP gnomAD v3 gnomAD v4
10g.72008199G=CA1918976791CHST3c.1168G= (p.Gly390=)
10g.72008199G>TCA377151504CHST3c.1168G>T (p.Gly390Cys)
gnomAD v4
10g.72008200G>ACA377151506CHST3c.1169G>A (p.Gly390Asp)
ClinVar gnomAD v4
10g.72008200G>CCA209479381CHST3c.1169G>C (p.Gly390Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008200G=CA1918976792CHST3c.1169G= (p.Gly390=)
10g.72008200G>TCA377151507CHST3c.1169G>T (p.Gly390Val)
10g.72008201C>ACA470284670CHST3c.1170C>A (p.Gly390=)
gnomAD v4
10g.72008201C=CA1918976793CHST3c.1170C= (p.Gly390=)
10g.72008201C>GCA470284671CHST3c.1170C>G (p.Gly390=)
10g.72008201C>TCA470284672CHST3c.1170C>T (p.Gly390=)
dbSNP gnomAD v2 gnomAD v4
10g.72008202A>CCA377151508CHST3c.1171A>C (p.Ile391Leu)
10g.72008202A>GCA377151509CHST3c.1171A>G (p.Ile391Val)
10g.72008202A>TCA377151511CHST3c.1171A>T (p.Ile391Phe)
10g.72008203T>ACA377151513CHST3c.1172T>A (p.Ile391Asn)
10g.72008203T>CCA377151515CHST3c.1172T>C (p.Ile391Thr)
gnomAD v4
10g.72008203T>GCA377151517CHST3c.1172T>G (p.Ile391Ser)
10g.72008204C>ACA202345CHST3c.1173C>A (p.Ile391=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008204C=CA1918976794CHST3c.1173C= (p.Ile391=)
10g.72008204C>GCA377151521CHST3c.1173C>G (p.Ile391Met)
10g.72008204C>TCA470284679CHST3c.1173C>T (p.Ile391=)
dbSNP
10g.72008208delCA645561185CHST3c.1177del (p.Leu393Ter)
ClinVar dbSNP gnomAD v4 COSMIC
10g.72008205C>ACA5548213CHST3c.1174C>A (p.Pro392Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008205C=CA1918976795CHST3c.1174C= (p.Pro392=)
10g.72008205C>GCA377151526CHST3c.1174C>G (p.Pro392Ala)
10g.72008205C>TCA377151528CHST3c.1174C>T (p.Pro392Ser)
10g.72008205_72008206insACCA2565414752CHST3c.1174_1175insAC (p.Pro392HisfsTer3)
10g.72008206C>ACA377151534CHST3c.1175C>A (p.Pro392His)
10g.72008206C=CA1918976796CHST3c.1175C= (p.Pro392=)
10g.72008206C>GCA209479385CHST3c.1175C>G (p.Pro392Arg)
dbSNP gnomAD v4
10g.72008206C>TCA377151532CHST3c.1175C>T (p.Pro392Leu)
dbSNP gnomAD v2 gnomAD v4
10g.72008207C>ACA470284684CHST3c.1176C>A (p.Pro392=)
10g.72008207C=CA1918976797CHST3c.1176C= (p.Pro392=)
10g.72008207C>GCA470284686CHST3c.1176C>G (p.Pro392=)
gnomAD v4
10g.72008207C>TCA470284687CHST3c.1176C>T (p.Pro392=)
dbSNP gnomAD v2 gnomAD v4
10g.72008208C>ACA377151535CHST3c.1177C>A (p.Leu393Met)
gnomAD v4
10g.72008208C>GCA377151536CHST3c.1177C>G (p.Leu393Val)
10g.72008208C>TCA470284689CHST3c.1177C>T (p.Leu393=)
10g.72008208_72008209delinsCTCA1918976798CHST3c.1177_1178delinsCT (p.Leu393=)
10g.72008209delCA1918976799CHST3c.1178del (p.Leu393ArgfsTer?)
dbSNP
10g.72008209T>ACA377151537CHST3c.1178T>A (p.Leu393Gln)
10g.72008209T>CCA377151539CHST3c.1178T>C (p.Leu393Pro)
gnomAD v4
10g.72008209T>GCA377151541CHST3c.1178T>G (p.Leu393Arg)
10g.72008209_72008210delCA2504443631CHST3c.1178_1179del (p.Leu393HisfsTer?)
10g.72008210G>ACA470284694CHST3c.1179G>A (p.Leu393=)
gnomAD v4
10g.72008210G>CCA470284696CHST3c.1179G>C (p.Leu393=)
gnomAD v4
10g.72008210G>TCA470284697CHST3c.1179G>T (p.Leu393=)
gnomAD v4
10g.72008211A=CA1918976800CHST3c.1180A= (p.Thr394=)
10g.72008211A>CCA5548214CHST3c.1180A>C (p.Thr394Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.72008211A>GCA377151545CHST3c.1180A>G (p.Thr394Ala)
dbSNP gnomAD v3 gnomAD v4
10g.72008211A>TCA377151547CHST3c.1180A>T (p.Thr394Ser)
dbSNP gnomAD v2 gnomAD v4
10g.72008212C>ACA377151550CHST3c.1181C>A (p.Thr394Asn)
10g.72008212C=CA1918976801CHST3c.1181C= (p.Thr394=)
10g.72008212C>GCA377151552CHST3c.1181C>G (p.Thr394Ser)
10g.72008212C>TCA377151554CHST3c.1181C>T (p.Thr394Ile)
dbSNP gnomAD v2
10g.72008213C>ACA5548215CHST3c.1182C>A (p.Thr394=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.72008213C=CA1918976802CHST3c.1182C= (p.Thr394=)
10g.72008213C>GCA470284698CHST3c.1182C>G (p.Thr394=)
10g.72008213C>TCA5548216CHST3c.1182C>T (p.Thr394=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008214C>ACA377151563CHST3c.1183C>A (p.Pro395Thr)
gnomAD v4
10g.72008214C=CA1918976803CHST3c.1183C= (p.Pro395=)
10g.72008214C>GCA377151566CHST3c.1183C>G (p.Pro395Ala)
10g.72008214C>TCA209479391CHST3c.1183C>T (p.Pro395Ser)
dbSNP gnomAD v4
10g.72008215C>ACA377151569CHST3c.1184C>A (p.Pro395Gln)
gnomAD v4
10g.72008215C=CA1918976804CHST3c.1184C= (p.Pro395=)
10g.72008215C>GCA377151571CHST3c.1184C>G (p.Pro395Arg)
10g.72008215C>TCA5548217CHST3c.1184C>T (p.Pro395Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.72008216G>ACA470283833CHST3c.1185G>A (p.Pro395=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.72008216G>CCA470283835CHST3c.1185G>C (p.Pro395=)
10g.72008216G=CA1918976805CHST3c.1185G= (p.Pro395=)
10g.72008216G>TCA470283836CHST3c.1185G>T (p.Pro395=)
ClinVar gnomAD v4
10g.72008217C>ACA377151577CHST3c.1186C>A (p.Gln396Lys)
gnomAD v4
10g.72008217C>GCA377151578CHST3c.1186C>G (p.Gln396Glu)
10g.72008217C>TCA377151581CHST3c.1186C>T (p.Gln396Ter)
gnomAD v4
10g.72008218A=CA1918976806CHST3c.1187A= (p.Gln396=)
10g.72008218A>CCA377151585CHST3c.1187A>C (p.Gln396Pro)
10g.72008218A>GCA209479393CHST3c.1187A>G (p.Gln396Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.72008218A>TCA377151586CHST3c.1187A>T (p.Gln396Leu)
10g.72008219G>ACA470283846CHST3c.1188G>A (p.Gln396=)
gnomAD v4
10g.72008219G>CCA377151590CHST3c.1188G>C (p.Gln396His)
gnomAD v4
10g.72008219G>TCA377151592CHST3c.1188G>T (p.Gln396His)
gnomAD v4
10g.72008220G>ACA377151595CHST3c.1189G>A (p.Val397Met)
dbSNP gnomAD v2 gnomAD v4
10g.72008220G>CCA377151598CHST3c.1189G>C (p.Val397Leu)
10g.72008220G=CA1918976807CHST3c.1189G= (p.Val397=)
10g.72008220G>TCA377151600CHST3c.1189G>T (p.Val397Leu)
gnomAD v4
10g.72008221T>ACA377151602CHST3c.1190T>A (p.Val397Glu)
10g.72008221T>CCA377151603CHST3c.1190T>C (p.Val397Ala)
dbSNP gnomAD v3 gnomAD v4
10g.72008221T>GCA209479396CHST3c.1190T>G (p.Val397Gly)
dbSNP
10g.72008221T=CA1918976808CHST3c.1190T= (p.Val397=)
10g.72008222G>ACA10604626CHST3c.1191G>A (p.Val397=)
ClinVar dbSNP gnomAD v4
10g.72008222G>CCA470283855CHST3c.1191G>C (p.Val397=)
10g.72008222G=CA1918976809CHST3c.1191G= (p.Val397=)
10g.72008222G>TCA470283858CHST3c.1191G>T (p.Val397=)
gnomAD v4
10g.72008223G>ACA377151609CHST3c.1192G>A (p.Glu398Lys)
gnomAD v4
10g.72008223G>CCA377151613CHST3c.1192G>C (p.Glu398Gln)
10g.72008223G>TCA377151611CHST3c.1192G>T (p.Glu398Ter)
gnomAD v4 COSMIC
10g.72008224A>CCA377151617CHST3c.1193A>C (p.Glu398Ala)
10g.72008224A>GCA377151620CHST3c.1193A>G (p.Glu398Gly)
10g.72008224A>TCA377151618CHST3c.1193A>T (p.Glu398Val)
10g.72008225A>CCA377151623CHST3c.1194A>C (p.Glu398Asp)
10g.72008225A>GCA470283867CHST3c.1194A>G (p.Glu398=)
10g.72008225A>TCA377151625CHST3c.1194A>T (p.Glu398Asp)
10g.72008226G>ACA377151627CHST3c.1195G>A (p.Asp399Asn)
10g.72008226G>CCA377151629CHST3c.1195G>C (p.Asp399His)
dbSNP gnomAD v3 gnomAD v4
10g.72008226G=CA1918976810CHST3c.1195G= (p.Asp399=)
10g.72008226G>TCA377151631CHST3c.1195G>T (p.Asp399Tyr)
gnomAD v4
10g.72008227A>CCA377151635CHST3c.1196A>C (p.Asp399Ala)
10g.72008227A>GCA377151638CHST3c.1196A>G (p.Asp399Gly)
10g.72008227A>TCA377151641CHST3c.1196A>T (p.Asp399Val)
10g.72008228C>ACA377151643CHST3c.1197C>A (p.Asp399Glu)
gnomAD v4
10g.72008228C=CA1918976811CHST3c.1197C= (p.Asp399=)
10g.72008228C>GCA377151645CHST3c.1197C>G (p.Asp399Glu)
10g.72008228C>TCA5548218CHST3c.1197C>T (p.Asp399=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.72008229T>ACA377151653CHST3c.1198T>A (p.Trp400Arg)
10g.72008229T>CCA377151651CHST3c.1198T>C (p.Trp400Arg)
gnomAD v4
10g.72008229T>GCA377151649CHST3c.1198T>G (p.Trp400Gly)
gnomAD v4
10g.72008230G>ACA377151656CHST3c.1199G>A (p.Trp400Ter)
gnomAD v4
10g.72008230G>CCA377151657CHST3c.1199G>C (p.Trp400Ser)
10g.72008230G>TCA377151658CHST3c.1199G>T (p.Trp400Leu)
gnomAD v4
10g.72008231G>ACA377151659CHST3c.1200G>A (p.Trp400Ter)
gnomAD v4
10g.72008231G>CCA377151660CHST3c.1200G>C (p.Trp400Cys)
10g.72008231G>TCA377151661CHST3c.1200G>T (p.Trp400Cys)
gnomAD v4
10g.72008232A>CCA377151662CHST3c.1201A>C (p.Ile401Leu)
10g.72008232A>GCA377151663CHST3c.1201A>G (p.Ile401Val)
10g.72008232A>TCA377151664CHST3c.1201A>T (p.Ile401Phe)
10g.72008233T>ACA377151665CHST3c.1202T>A (p.Ile401Asn)
gnomAD v4
10g.72008233T>CCA377151666CHST3c.1202T>C (p.Ile401Thr)
gnomAD v4
10g.72008233T>GCA377151667CHST3c.1202T>G (p.Ile401Ser)
10g.72008234C>ACA470283890CHST3c.1203C>A (p.Ile401=)
gnomAD v4
10g.72008234C>GCA377151668CHST3c.1203C>G (p.Ile401Met)
10g.72008234C>TCA470283894CHST3c.1203C>T (p.Ile401=)
gnomAD v4
10g.72008235C>ACA377151671CHST3c.1204C>A (p.Gln402Lys)
gnomAD v4
10g.72008235C>GCA377151669CHST3c.1204C>G (p.Gln402Glu)
ClinVar
10g.72008235C>TCA377151670CHST3c.1204C>T (p.Gln402Ter)
gnomAD v4

Number of alleles fetched