Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49451591G>ACA234287MMUTc.1207C>T (p.Arg403Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49451591G>CCA3846942MMUTc.1207C>G (p.Arg403Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451591G=CA1627389333MMUTc.1207C= (p.Arg403=)
6g.49451591G>TCA450606476MMUTc.1207C>A (p.Arg403=)
gnomAD v4
6g.49451592A=CA1627389334MMUTc.1206T= (p.Ala402=)
6g.49451592A>CCA3846943MMUTc.1206T>G (p.Ala402=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451592A>GCA450606478MMUTc.1206T>C (p.Ala402=)
ClinVar gnomAD v4
6g.49451592A>TCA450606480MMUTc.1206T>A (p.Ala402=)
6g.49451593G>ACA364398892MMUTc.1205C>T (p.Ala402Val)
dbSNP gnomAD v2 gnomAD v4
6g.49451593G>CCA3846944MMUTc.1205C>G (p.Ala402Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451593G=CA1627389335MMUTc.1205C= (p.Ala402=)
6g.49451593G>TCA364398891MMUTc.1205C>A (p.Ala402Asp)
6g.49451594C>ACA364398893MMUTc.1204G>T (p.Ala402Ser)
6g.49451594C>GCA364398894MMUTc.1204G>C (p.Ala402Pro)
6g.49451594C>TCA364398895MMUTc.1204G>A (p.Ala402Thr)
gnomAD v4
6g.49451595A>CCA364398896MMUTc.1203T>G (p.Ser401Arg)
6g.49451595A>GCA450606489MMUTc.1203T>C (p.Ser401=)
6g.49451595A>TCA364398897MMUTc.1203T>A (p.Ser401Arg)
6g.49451596C>ACA364398898MMUTc.1202G>T (p.Ser401Ile)
6g.49451596C>GCA364398899MMUTc.1202G>C (p.Ser401Thr)
6g.49451596C>TCA364398900MMUTc.1202G>A (p.Ser401Asn)
gnomAD v4
6g.49451596_49451597delinsCTCA1627389336MMUTc.1201_1202delinsAG (p.Ser401=)
6g.49451597T>ACA364398901MMUTc.1201A>T (p.Ser401Cys)
6g.49451597T>CCA364398902MMUTc.1201A>G (p.Ser401Gly)
6g.49451597T>GCA364398903MMUTc.1201A>C (p.Ser401Arg)
6g.49451600delCA825477395MMUTc.1201del (p.Ser401ValfsTer30)
dbSNP
6g.49451598T>ACA364398904MMUTc.1200A>T (p.Lys400Asn)
6g.49451598T>CCA450606500MMUTc.1200A>G (p.Lys400=)
6g.49451598T>GCA364398905MMUTc.1200A>C (p.Lys400Asn)
6g.49451599T>ACA364398908MMUTc.1199A>T (p.Lys400Ile)
6g.49451599T>CCA364398907MMUTc.1199A>G (p.Lys400Arg)
6g.49451599T>GCA364398906MMUTc.1199A>C (p.Lys400Thr)
6g.49451600T>ACA364398909MMUTc.1198A>T (p.Lys400Ter)
ClinVar dbSNP
6g.49451600T>CCA364398910MMUTc.1198A>G (p.Lys400Glu)
6g.49451600T>GCA364398911MMUTc.1198A>C (p.Lys400Gln)
6g.49451600T=CA1627389337MMUTc.1198A= (p.Lys400=)
6g.49451600_49451602delinsTCACA1627389338MMUTc.1196_1198delinsTGA (p.Val399=)
6g.49451601C>ACA450606509MMUTc.1197G>T (p.Val399=)
ClinVar
6g.49451601C>GCA450606511MMUTc.1197G>C (p.Val399=)
6g.49451601C>TCA450606513MMUTc.1197G>A (p.Val399=)
6g.49451603_49451604delCA567155985MMUTc.1196_1197del (p.Val399GlufsTer24)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451602A>CCA364398912MMUTc.1196T>G (p.Val399Gly)
6g.49451602A>GCA364398913MMUTc.1196T>C (p.Val399Ala)
gnomAD v4
6g.49451602A>TCA364398914MMUTc.1196T>A (p.Val399Glu)
6g.49451603C>ACA364398915MMUTc.1195G>T (p.Val399Leu)
6g.49451603C>GCA364398916MMUTc.1195G>C (p.Val399Leu)
6g.49451603C>TCA364398917MMUTc.1195G>A (p.Val399Met)
gnomAD v4
6g.49451604A>CCA450606520MMUTc.1194T>G (p.Thr398=)
6g.49451604A>GCA450606521MMUTc.1194T>C (p.Thr398=)
6g.49451604A>TCA450606522MMUTc.1194T>A (p.Thr398=)
6g.49451605G>ACA364398918MMUTc.1193C>T (p.Thr398Ile)
gnomAD v4
6g.49451605G>CCA364398919MMUTc.1193C>G (p.Thr398Ser)
6g.49451605G>TCA364398920MMUTc.1193C>A (p.Thr398Asn)
6g.49451606T>ACA364398921MMUTc.1192A>T (p.Thr398Ser)
6g.49451606T>CCA364398922MMUTc.1192A>G (p.Thr398Ala)
gnomAD v4 COSMIC
6g.49451606T>GCA364398923MMUTc.1192A>C (p.Thr398Pro)
gnomAD v4
6g.49451607T>ACA450606531MMUTc.1191A>T (p.Pro397=)
6g.49451607T>CCA450606532MMUTc.1191A>G (p.Pro397=)
6g.49451607T>GCA450606533MMUTc.1191A>C (p.Pro397=)
ClinVar dbSNP gnomAD v4
6g.49451608G>ACA3846945MMUTc.1190C>T (p.Pro397Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451608G>CCA364398925MMUTc.1190C>G (p.Pro397Arg)
6g.49451608G=CA1627389339MMUTc.1190C= (p.Pro397=)
6g.49451608G>TCA364398924MMUTc.1190C>A (p.Pro397Gln)
6g.49451609delCA2679046693MMUTc.1190del (p.Pro397GlnfsTer3)
gnomAD v4
6g.49451609G>ACA364398926MMUTc.1189C>T (p.Pro397Ser)
6g.49451609G>CCA364398927MMUTc.1189C>G (p.Pro397Ala)
6g.49451609G>TCA364398928MMUTc.1189C>A (p.Pro397Thr)
6g.49451610C>ACA364398929MMUTc.1188G>T (p.Leu396Phe)
6g.49451610C>GCA364398930MMUTc.1188G>C (p.Leu396Phe)
6g.49451610C>TCA450606541MMUTc.1188G>A (p.Leu396=)
6g.49451611A>CCA364398931MMUTc.1187T>G (p.Leu396Trp)
6g.49451611A>GCA364398932MMUTc.1187T>C (p.Leu396Ser)
6g.49451611A>TCA364398933MMUTc.1187T>A (p.Leu396Ter)
6g.49451612A>CCA364398934MMUTc.1186T>G (p.Leu396Val)
6g.49451612A>GCA450606549MMUTc.1186T>C (p.Leu396=)
6g.49451612A>TCA364398935MMUTc.1186T>A (p.Leu396Met)
gnomAD v4
6g.49451613A>CCA450606552MMUTc.1185T>G (p.Gly395=)
6g.49451613A>GCA450606554MMUTc.1185T>C (p.Gly395=)
6g.49451613A>TCA450606555MMUTc.1185T>A (p.Gly395=)
gnomAD v4
6g.49451614C>ACA364398936MMUTc.1184G>T (p.Gly395Val)
gnomAD v4
6g.49451614C=CA1627389340MMUTc.1184G= (p.Gly395=)
6g.49451614C>GCA364398937MMUTc.1184G>C (p.Gly395Ala)
6g.49451614C>TCA3846946MMUTc.1184G>A (p.Gly395Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451615C>ACA364398940MMUTc.1183G>T (p.Gly395Cys)
6g.49451615C>GCA364398938MMUTc.1183G>C (p.Gly395Arg)
6g.49451615C>TCA364398939MMUTc.1183G>A (p.Gly395Ser)
6g.49451616C>ACA364398941MMUTc.1182G>T (p.Leu394Phe)
6g.49451616C=CA1627389341MMUTc.1182G= (p.Leu394=)
6g.49451616C>GCA364398942MMUTc.1182G>C (p.Leu394Phe)
6g.49451616C>TCA3846947MMUTc.1182G>A (p.Leu394=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451617A>CCA364398943MMUTc.1181T>G (p.Leu394Trp)
6g.49451617A>GCA364398944MMUTc.1181T>C (p.Leu394Ser)
6g.49451617A>TCA364398945MMUTc.1181T>A (p.Leu394Ter)
6g.49451619dupCA10575868MMUTc.1181dup (p.Leu394PhefsTer30)
ClinVar dbSNP gnomAD v4
6g.49451618A>CCA364398946MMUTc.1180T>G (p.Leu394Val)
6g.49451618A>GCA450606570MMUTc.1180T>C (p.Leu394=)
ClinVar dbSNP
6g.49451618A>TCA364398947MMUTc.1180T>A (p.Leu394Met)
6g.49451619A>CCA450606577MMUTc.1179T>G (p.Ala393=)
6g.49451619A>GCA450606574MMUTc.1179T>C (p.Ala393=)
6g.49451619A>TCA450606575MMUTc.1179T>A (p.Ala393=)
6g.49451620G>ACA364398948MMUTc.1178C>T (p.Ala393Val)
gnomAD v4
6g.49451620G>CCA364398949MMUTc.1178C>G (p.Ala393Gly)
6g.49451620G>TCA364398950MMUTc.1178C>A (p.Ala393Asp)
6g.49451621C>ACA364398951MMUTc.1177G>T (p.Ala393Ser)
6g.49451621C>GCA364398953MMUTc.1177G>C (p.Ala393Pro)
6g.49451621C>TCA364398952MMUTc.1177G>A (p.Ala393Thr)
6g.49451622T>ACA364398954MMUTc.1176A>T (p.Glu392Asp)
6g.49451622T>CCA450606585MMUTc.1176A>G (p.Glu392=)
6g.49451622T>GCA364398955MMUTc.1176A>C (p.Glu392Asp)
6g.49451623T>ACA364398956MMUTc.1175A>T (p.Glu392Val)
6g.49451623T>CCA364398957MMUTc.1175A>G (p.Glu392Gly)
6g.49451623T>GCA364398958MMUTc.1175A>C (p.Glu392Ala)
6g.49451624C>ACA364398959MMUTc.1174G>T (p.Glu392Ter)
COSMIC
6g.49451624C>GCA364398960MMUTc.1174G>C (p.Glu392Gln)
6g.49451624C>TCA364398961MMUTc.1174G>A (p.Glu392Lys)
6g.49451625A>CCA364398962MMUTc.1173T>G (p.Asp391Glu)
6g.49451625A>GCA450606595MMUTc.1173T>C (p.Asp391=)
6g.49451625A>TCA364398963MMUTc.1173T>A (p.Asp391Glu)
gnomAD v4
6g.49451626T>ACA364398964MMUTc.1172A>T (p.Asp391Val)
6g.49451626T>CCA364398965MMUTc.1172A>G (p.Asp391Gly)
6g.49451626T>GCA364398966MMUTc.1172A>C (p.Asp391Ala)
6g.49451626_49451627delinsACA2580074726MMUTc.1171_1172delinsT (p.Asp391LeufsTer9)
ClinVar
6g.49451627C>ACA364398967MMUTc.1171G>T (p.Asp391Tyr)
6g.49451627C>GCA364398968MMUTc.1171G>C (p.Asp391His)
6g.49451627C>TCA364398969MMUTc.1171G>A (p.Asp391Asn)
gnomAD v4
6g.49451628A=CA1627389342MMUTc.1170T= (p.Phe390=)
6g.49451628A>CCA364398970MMUTc.1170T>G (p.Phe390Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451628A>GCA450606603MMUTc.1170T>C (p.Phe390=)
6g.49451628A>TCA364398971MMUTc.1170T>A (p.Phe390Leu)
6g.49451629A>CCA364398972MMUTc.1169T>G (p.Phe390Cys)
6g.49451629A>GCA364398973MMUTc.1169T>C (p.Phe390Ser)
gnomAD v4
6g.49451629A>TCA364398974MMUTc.1169T>A (p.Phe390Tyr)
6g.49451630A>CCA364398975MMUTc.1168T>G (p.Phe390Val)
6g.49451630A>GCA364398976MMUTc.1168T>C (p.Phe390Leu)
6g.49451630A>TCA364398977MMUTc.1168T>A (p.Phe390Ile)
6g.49451632_49451634delCA2679046694MMUTc.1166_1168del (p.Ser389del)
gnomAD v4
6g.49451631A=CA1627389343MMUTc.1167T= (p.Ser389=)
6g.49451631A>CCA450606611MMUTc.1167T>G (p.Ser389=)
6g.49451631A>GCA450606612MMUTc.1167T>C (p.Ser389=)
6g.49451631A>TCA450606613MMUTc.1167T>A (p.Ser389=)
dbSNP
6g.49451632G>ACA364398978MMUTc.1166C>T (p.Ser389Phe)
6g.49451632G>CCA364398979MMUTc.1166C>G (p.Ser389Cys)
gnomAD v4
6g.49451632G>TCA364398980MMUTc.1166C>A (p.Ser389Tyr)
6g.49451633A=CA1627389344MMUTc.1165T= (p.Ser389=)
6g.49451633A>CCA364398981MMUTc.1165T>G (p.Ser389Ala)
6g.49451633A>GCA364398982MMUTc.1165T>C (p.Ser389Pro)
dbSNP
6g.49451633A>TCA364398983MMUTc.1165T>A (p.Ser389Thr)
6g.49451634A=CA1627389345MMUTc.1164T= (p.Asn388=)
6g.49451634A>CCA364398984MMUTc.1164T>G (p.Asn388Lys)
6g.49451634A>GCA450606614MMUTc.1164T>C (p.Asn388=)
ClinVar dbSNP gnomAD v4
6g.49451634A>TCA10575869MMUTc.1164T>A (p.Asn388Lys)
ClinVar dbSNP
6g.49451635T>ACA364398985MMUTc.1163A>T (p.Asn388Ile)
6g.49451635T>CCA364398986MMUTc.1163A>G (p.Asn388Ser)
gnomAD v4
6g.49451635T>GCA364398987MMUTc.1163A>C (p.Asn388Thr)
6g.49451636T>ACA364398988MMUTc.1162A>T (p.Asn388Tyr)
6g.49451636T>CCA3846948MMUTc.1162A>G (p.Asn388Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451636T>GCA364398989MMUTc.1162A>C (p.Asn388His)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451636T=CA1627389346MMUTc.1162A= (p.Asn388=)
6g.49451637T>ACA450606615MMUTc.1161A>T (p.Thr387=)
6g.49451637T>CCA450606617MMUTc.1161A>G (p.Thr387=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49451637T>GCA450606616MMUTc.1161A>C (p.Thr387=)
6g.49451637T=CA1627389347MMUTc.1161A= (p.Thr387=)
6g.49451641_49451642delCA2578717902MMUTc.1160_1161del (p.Thr387LysfsTer4)
6g.49451638G>ACA364398992MMUTc.1160C>T (p.Thr387Ile)
ClinVar dbSNP
6g.49451638G>CCA364398990MMUTc.1160C>G (p.Thr387Arg)
6g.49451638G=CA1627389348MMUTc.1160C= (p.Thr387=)
6g.49451638G>TCA364398991MMUTc.1160C>A (p.Thr387Lys)
ClinVar dbSNP gnomAD v4
6g.49451639T>ACA364398993MMUTc.1159A>T (p.Thr387Ser)
6g.49451639T>CCA364398994MMUTc.1159A>G (p.Thr387Ala)
6g.49451639T>GCA364398995MMUTc.1159A>C (p.Thr387Pro)
ClinVar dbSNP gnomAD v4
6g.49451639T=CA1627389349MMUTc.1159A= (p.Thr387=)
6g.49451640G>ACA450606618MMUTc.1158C>T (p.His386=)
6g.49451640G>CCA364398996MMUTc.1158C>G (p.His386Gln)
6g.49451640G>TCA364398997MMUTc.1158C>A (p.His386Gln)
COSMIC
6g.49451641T>ACA364398998MMUTc.1157A>T (p.His386Leu)
6g.49451641T>CCA138796375MMUTc.1157A>G (p.His386Arg)
dbSNP gnomAD v2 gnomAD v4
6g.49451641T>GCA364398999MMUTc.1157A>C (p.His386Pro)
ClinVar
6g.49451641T=CA1627389350MMUTc.1157A= (p.His386=)
6g.49451642G>ACA364399000MMUTc.1156C>T (p.His386Tyr)
6g.49451642G>CCA364399001MMUTc.1156C>G (p.His386Asp)
6g.49451642G=CA1627389351MMUTc.1156C= (p.His386=)
6g.49451642G>TCA364399002MMUTc.1156C>A (p.His386Asn)
ClinVar dbSNP gnomAD v4
6g.49451643C>ACA364399003MMUTc.1155G>T (p.Leu385Phe)
6g.49451643C>GCA364399004MMUTc.1155G>C (p.Leu385Phe)
gnomAD v4
6g.49451643C>TCA450606619MMUTc.1155G>A (p.Leu385=)
ClinVar dbSNP
6g.49451644A>CCA364399005MMUTc.1154T>G (p.Leu385Trp)
gnomAD v4
6g.49451644A>GCA364399006MMUTc.1154T>C (p.Leu385Ser)
gnomAD v4
6g.49451644A>TCA364399007MMUTc.1154T>A (p.Leu385Ter)
6g.49451646delCA2679046696MMUTc.1154del (p.Leu385CysfsTer15)
gnomAD v4
6g.49451645_49451646delCA2695206528MMUTc.1153_1154del (p.Leu385AlafsTer6)
6g.49451645A>CCA364399008MMUTc.1153T>G (p.Leu385Val)
6g.49451645A>GCA450606621MMUTc.1153T>C (p.Leu385=)
6g.49451645A>TCA364399009MMUTc.1153T>A (p.Leu385Met)
6g.49451646A>CCA450606622MMUTc.1152T>G (p.Ser384=)
ClinVar dbSNP
6g.49451646A>GCA450606623MMUTc.1152T>C (p.Ser384=)
6g.49451646A>TCA450606624MMUTc.1152T>A (p.Ser384=)
6g.49451647G>ACA364399012MMUTc.1151C>T (p.Ser384Phe)
dbSNP
6g.49451647G>CCA364399011MMUTc.1151C>G (p.Ser384Cys)
6g.49451647G=CA1627389352MMUTc.1151C= (p.Ser384=)
6g.49451647G>TCA364399010MMUTc.1151C>A (p.Ser384Tyr)
6g.49451648A>CCA364399013MMUTc.1150T>G (p.Ser384Ala)
6g.49451648A>GCA364399015MMUTc.1150T>C (p.Ser384Pro)
6g.49451648A>TCA364399014MMUTc.1150T>A (p.Ser384Thr)
6g.49451649C>ACA364399016MMUTc.1149G>T (p.Gln383His)
6g.49451649C=CA1627389353MMUTc.1149G= (p.Gln383=)
6g.49451649C>GCA364399017MMUTc.1149G>C (p.Gln383His)
6g.49451649C>TCA450606626MMUTc.1149G>A (p.Gln383=)
6g.49451650T>ACA364399018MMUTc.1148A>T (p.Gln383Leu)
6g.49451650T>CCA364399019MMUTc.1148A>G (p.Gln383Arg)
dbSNP COSMIC
6g.49451650T>GCA364399020MMUTc.1148A>C (p.Gln383Pro)
6g.49451650T=CA1627389354MMUTc.1148A= (p.Gln383=)
6g.49451650dupCA3846949MMUTc.1148dup (p.Ser384ValfsTer8)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451650_49451651delCA2573140874MMUTc.1147_1148del (p.Gln383ValfsTer8)
ClinVar dbSNP
6g.49451651G>ACA364399021MMUTc.1147C>T (p.Gln383Ter)
COSMIC
6g.49451651G>CCA364399022MMUTc.1147C>G (p.Gln383Glu)
6g.49451651G>TCA364399023MMUTc.1147C>A (p.Gln383Lys)
6g.49451652A>CCA450606628MMUTc.1146T>G (p.Thr382=)
6g.49451652A>GCA450606630MMUTc.1146T>C (p.Thr382=)
6g.49451652A>TCA450606629MMUTc.1146T>A (p.Thr382=)
ClinVar dbSNP gnomAD v4
6g.49451653G>ACA364399024MMUTc.1145C>T (p.Thr382Ile)
6g.49451653G>CCA364399025MMUTc.1145C>G (p.Thr382Ser)
6g.49451653G>TCA364399026MMUTc.1145C>A (p.Thr382Asn)
6g.49451654T>ACA364399027MMUTc.1144A>T (p.Thr382Ser)
6g.49451654T>CCA364399028MMUTc.1144A>G (p.Thr382Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451654T>GCA364399029MMUTc.1144A>C (p.Thr382Pro)
6g.49451654T=CA1627389355MMUTc.1144A= (p.Thr382=)
6g.49451655C>ACA450606631MMUTc.1143G>T (p.Gly381=)
6g.49451655C=CA1627389356MMUTc.1143G= (p.Gly381=)
6g.49451655C>GCA450606632MMUTc.1143G>C (p.Gly381=)
6g.49451655C>TCA450606633MMUTc.1143G>A (p.Gly381=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49451657delCA2679046697MMUTc.1143del (p.Thr382LeufsTer18)
gnomAD v4
6g.49451656C>ACA364399032MMUTc.1142G>T (p.Gly381Val)
ClinVar dbSNP
6g.49451656C=CA1627389357MMUTc.1142G= (p.Gly381=)
6g.49451656C>GCA364399031MMUTc.1142G>C (p.Gly381Ala)
6g.49451656C>TCA364399030MMUTc.1142G>A (p.Gly381Glu)
6g.49451657C>ACA364399033MMUTc.1141G>T (p.Gly381Trp)
6g.49451657C>GCA364399034MMUTc.1141G>C (p.Gly381Arg)
6g.49451657C>TCA364399035MMUTc.1141G>A (p.Gly381Arg)
ClinVar gnomAD v4
6g.49451658T>ACA450606635MMUTc.1140A>T (p.Gly380=)
6g.49451658T>CCA450606634MMUTc.1140A>G (p.Gly380=)
6g.49451658T>GCA450606636MMUTc.1140A>C (p.Gly380=)
6g.49451659C>ACA364399036MMUTc.1139G>T (p.Gly380Val)
6g.49451659C=CA1627389358MMUTc.1139G= (p.Gly380=)
6g.49451659C>GCA364399037MMUTc.1139G>C (p.Gly380Ala)
6g.49451659C>TCA3846950MMUTc.1139G>A (p.Gly380Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451660C>ACA364399038MMUTc.1138G>T (p.Gly380Ter)
6g.49451660C>GCA364399039MMUTc.1138G>C (p.Gly380Arg)
6g.49451660C>TCA364399040MMUTc.1138G>A (p.Gly380Arg)
6g.49451661A>CCA364399041MMUTc.1137T>G (p.Phe379Leu)
6g.49451661A>GCA450606637MMUTc.1137T>C (p.Phe379=)
6g.49451661A>TCA364399042MMUTc.1137T>A (p.Phe379Leu)
6g.49451663delCA2695206529MMUTc.1137del (p.Phe379LeufsTer21)
6g.49451662A=CA1627389359MMUTc.1136T= (p.Phe379=)
6g.49451662A>CCA3846951MMUTc.1136T>G (p.Phe379Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451662A>GCA364399043MMUTc.1136T>C (p.Phe379Ser)
6g.49451662A>TCA364399044MMUTc.1136T>A (p.Phe379Tyr)
6g.49451663A>CCA364399047MMUTc.1135T>G (p.Phe379Val)
6g.49451663A>GCA364399046MMUTc.1135T>C (p.Phe379Leu)
6g.49451663A>TCA364399045MMUTc.1135T>A (p.Phe379Ile)
6g.49451664T>ACA450606639MMUTc.1134A>T (p.Val378=)
6g.49451664T>CCA3846952MMUTc.1134A>G (p.Val378=)
dbSNP ExAC gnomAD v2
6g.49451664T>GCA450606640MMUTc.1134A>C (p.Val378=)
6g.49451664T=CA1627389360MMUTc.1134A= (p.Val378=)
6g.49451665A>CCA364399048MMUTc.1133T>G (p.Val378Gly)
6g.49451665A>GCA364399049MMUTc.1133T>C (p.Val378Ala)
6g.49451665A>TCA364399050MMUTc.1133T>A (p.Val378Glu)
6g.49451666C>ACA364399051MMUTc.1132G>T (p.Val378Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451666C=CA1627389361MMUTc.1132G= (p.Val378=)
6g.49451666C>GCA364399052MMUTc.1132G>C (p.Val378Leu)
6g.49451666C>TCA364399053MMUTc.1132G>A (p.Val378Ile)
dbSNP gnomAD v2 gnomAD v4
6g.49451670_49451672delCA2770993687MMUTc.1130_1132del (p.Ala377del)
6g.49451667T>ACA450606641MMUTc.1131A>T (p.Ala377=)
6g.49451667T>CCA450606642MMUTc.1131A>G (p.Ala377=)
ClinVar dbSNP
6g.49451667T>GCA450606643MMUTc.1131A>C (p.Ala377=)
6g.49451668G>ACA364399054MMUTc.1130C>T (p.Ala377Val)
6g.49451668G>CCA364399055MMUTc.1130C>G (p.Ala377Gly)
6g.49451668G=CA1627389362MMUTc.1130C= (p.Ala377=)
6g.49451668G>TCA115263MMUTc.1130C>A (p.Ala377Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
6g.49451669C>ACA364399056MMUTc.1129G>T (p.Ala377Ser)
6g.49451669C>GCA364399057MMUTc.1129G>C (p.Ala377Pro)
6g.49451669C>TCA364399058MMUTc.1129G>A (p.Ala377Thr)
gnomAD v4
6g.49451670T>ACA450606644MMUTc.1128A>T (p.Ala376=)
6g.49451670T>CCA450606645MMUTc.1128A>G (p.Ala376=)
gnomAD v4
6g.49451670T>GCA450606646MMUTc.1128A>C (p.Ala376=)
6g.49451670_49451672delinsTGCCA1627389363MMUTc.1126_1128delinsGCA (p.Ala376=)
6g.49451671G>ACA364399061MMUTc.1127C>T (p.Ala376Val)
6g.49451671G>CCA364399059MMUTc.1127C>G (p.Ala376Gly)
6g.49451671G>TCA364399060MMUTc.1127C>A (p.Ala376Glu)
6g.49451671_49451672delCA658683443MMUTc.1126_1127del (p.Ala376SerfsTer15)
ClinVar dbSNP gnomAD v4
6g.49451672C>ACA364399062MMUTc.1126G>T (p.Ala376Ser)
6g.49451672C=CA1627389364MMUTc.1126G= (p.Ala376=)
6g.49451672C>GCA364399063MMUTc.1126G>C (p.Ala376Pro)
6g.49451672C>TCA364399064MMUTc.1126G>A (p.Ala376Thr)
dbSNP gnomAD v2 gnomAD v4
6g.49451673C>ACA364399065MMUTc.1125G>T (p.Met375Ile)
6g.49451673C=CA1627389365MMUTc.1125G= (p.Met375=)
6g.49451673C>GCA364399066MMUTc.1125G>C (p.Met375Ile)
6g.49451673C>TCA3846953MMUTc.1125G>A (p.Met375Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451674A>CCA364399067MMUTc.1124T>G (p.Met375Arg)
6g.49451674A>GCA364399068MMUTc.1124T>C (p.Met375Thr)
gnomAD v3 gnomAD v4
6g.49451674A>TCA364399069MMUTc.1124T>A (p.Met375Lys)
6g.49451675T>ACA364399070MMUTc.1123A>T (p.Met375Leu)
6g.49451675T>CCA364399071MMUTc.1123A>G (p.Met375Val)
gnomAD v4
6g.49451675T>GCA364399072MMUTc.1123A>C (p.Met375Leu)
6g.49451676T>ACA450606647MMUTc.1122A>T (p.Ala374=)
6g.49451676T>CCA450606648MMUTc.1122A>G (p.Ala374=)
6g.49451676T>GCA450606649MMUTc.1122A>C (p.Ala374=)
6g.49451677G>ACA364399075MMUTc.1121C>T (p.Ala374Val)
6g.49451677G>CCA364399073MMUTc.1121C>G (p.Ala374Gly)
6g.49451677G>TCA364399074MMUTc.1121C>A (p.Ala374Glu)
6g.49451678C>ACA364399076MMUTc.1120G>T (p.Ala374Ser)
6g.49451678C>GCA364399078MMUTc.1120G>C (p.Ala374Pro)
6g.49451678C>TCA364399077MMUTc.1120G>A (p.Ala374Thr)
gnomAD v4
6g.49451679T>ACA364399079MMUTc.1119A>T (p.Glu373Asp)
6g.49451679T>CCA3846954MMUTc.1119A>G (p.Glu373=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451679T>GCA364399080MMUTc.1119A>C (p.Glu373Asp)
6g.49451679T=CA1627389366MMUTc.1119A= (p.Glu373=)
6g.49451680T>ACA364399081MMUTc.1118A>T (p.Glu373Val)
6g.49451680T>CCA364399082MMUTc.1118A>G (p.Glu373Gly)
ClinVar dbSNP
6g.49451680T>GCA364399084MMUTc.1118A>C (p.Glu373Ala)
6g.49451681C>ACA364399086MMUTc.1117G>T (p.Glu373Ter)
COSMIC
6g.49451681C>GCA364399088MMUTc.1117G>C (p.Glu373Gln)
6g.49451681C>TCA364399090MMUTc.1117G>A (p.Glu373Lys)
6g.49451682T>ACA450606651MMUTc.1116A>T (p.Ile372=)
6g.49451682T>CCA3846955MMUTc.1116A>G (p.Ile372Met)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451682T>GCA450606650MMUTc.1116A>C (p.Ile372=)
6g.49451682T=CA1627389367MMUTc.1116A= (p.Ile372=)
6g.49451683A=CA1627389368MMUTc.1115T= (p.Ile372=)
6g.49451683A>CCA364399096MMUTc.1115T>G (p.Ile372Arg)
6g.49451683A>GCA3846956MMUTc.1115T>C (p.Ile372Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451683A>TCA364399093MMUTc.1115T>A (p.Ile372Lys)
6g.49451683_49451706delCA913110642MMUTc.1092_1115del (p.Tyr364Ter)
6g.49451683_49451706delinsATTGCAGTACGGACAATATTATTGCA1627389369MMUTc.1092_1115delinsCAATAATATTGTCCGTACTGCAAT (p.Tyr364=)
6g.49451684T>ACA364399098MMUTc.1114A>T (p.Ile372Leu)
6g.49451684T>CCA3846957MMUTc.1114A>G (p.Ile372Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451684T>GCA364399101MMUTc.1114A>C (p.Ile372Leu)
6g.49451684T=CA1627389370MMUTc.1114A= (p.Ile372=)
6g.49451685_49451707delCA567155986MMUTc.1092_1114del (p.Asn365ArgfsTer19)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451685T>ACA450606652MMUTc.1113A>T (p.Ala371=)
6g.49451685T>CCA450606654MMUTc.1113A>G (p.Ala371=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
6g.49451685T>GCA450606653MMUTc.1113A>C (p.Ala371=)
ClinVar dbSNP gnomAD v4
6g.49451685T=CA1627389371MMUTc.1113A= (p.Ala371=)
6g.49451686G>ACA364399106MMUTc.1112C>T (p.Ala371Val)
ClinVar
6g.49451686G>CCA364399108MMUTc.1112C>G (p.Ala371Gly)
6g.49451686G>TCA364399109MMUTc.1112C>A (p.Ala371Glu)
6g.49451687C>ACA364399111MMUTc.1111G>T (p.Ala371Ser)
6g.49451687C>GCA364399113MMUTc.1111G>C (p.Ala371Pro)
6g.49451687C>TCA364399115MMUTc.1111G>A (p.Ala371Thr)
gnomAD v4
6g.49451688A>CCA450606655MMUTc.1110T>G (p.Thr370=)
6g.49451688A>GCA450606656MMUTc.1110T>C (p.Thr370=)
dbSNP gnomAD v4
6g.49451688A>TCA450606657MMUTc.1110T>A (p.Thr370=)
6g.49451689G>ACA364399118MMUTc.1109C>T (p.Thr370Ile)
6g.49451689G>CCA364399120MMUTc.1109C>G (p.Thr370Ser)
6g.49451689G>TCA364399122MMUTc.1109C>A (p.Thr370Asn)
6g.49451690T>ACA364399127MMUTc.1108A>T (p.Thr370Ser)
6g.49451690T>CCA364399125MMUTc.1108A>G (p.Thr370Ala)
ClinVar gnomAD v4
6g.49451690T>GCA312765MMUTc.1108A>C (p.Thr370Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451690T=CA1627389372MMUTc.1108A= (p.Thr370=)
6g.49451691A>CCA450606658MMUTc.1107T>G (p.Arg369=)
6g.49451691A>GCA450606659MMUTc.1107T>C (p.Arg369=)
gnomAD v4 COSMIC
6g.49451691A>TCA450606660MMUTc.1107T>A (p.Arg369=)
6g.49451691dupCA1139659593MMUTc.1107dup (p.Thr370TyrfsTer22)
ClinVar dbSNP

Number of alleles fetched