Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25004891_25007522dupCA10575788ARXc.1120-82_1469dup
ClinVar
Xg.25007298_25007303delinsGAGGGACA2420207075ARXc.1256_1261delinsTCCCTC (p.Phe419=)
Xg.25007303_25007307delCA1139667343ARXc.1256_1260del (p.Phe419SerfsTer?)
ClinVar dbSNP
Xg.25007301G>ACA412611390ARXc.1258C>T (p.Pro420Ser)
dbSNP gnomAD v3 gnomAD v4
Xg.25007301G>CCA412611391ARXc.1258C>G (p.Pro420Ala)
Xg.25007301G=CA2420207078ARXc.1258C= (p.Pro420=)
Xg.25007301G>TCA412611392ARXc.1258C>A (p.Pro420Thr)
gnomAD v4
Xg.25007302G>ACA515947072ARXc.1257C>T (p.Phe419=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25007302G>CCA412611393ARXc.1257C>G (p.Phe419Leu)
Xg.25007302G=CA2420207079ARXc.1257C= (p.Phe419=)
Xg.25007302G>TCA412611394ARXc.1257C>A (p.Phe419Leu)
gnomAD v4
Xg.25007303A>CCA412611395ARXc.1256T>G (p.Phe419Cys)
Xg.25007303A>GCA412611396ARXc.1256T>C (p.Phe419Ser)
Xg.25007303A>TCA412611397ARXc.1256T>A (p.Phe419Tyr)
Xg.25007304A>CCA412611398ARXc.1255T>G (p.Phe419Val)
Xg.25007304A>GCA412611399ARXc.1255T>C (p.Phe419Leu)
Xg.25007304A>TCA412611400ARXc.1255T>A (p.Phe419Ile)
Xg.25007305G>ACA515947073ARXc.1254C>T (p.Pro418=)
Xg.25007305G>CCA515947074ARXc.1254C>G (p.Pro418=)
Xg.25007305G>TCA515947075ARXc.1254C>A (p.Pro418=)
gnomAD v4
Xg.25007306G>ACA412611403ARXc.1253C>T (p.Pro418Leu)
Xg.25007306G>CCA412611402ARXc.1253C>G (p.Pro418Arg)
ClinVar dbSNP
Xg.25007306G=CA2420207080ARXc.1253C= (p.Pro418=)
Xg.25007306G>TCA412611401ARXc.1253C>A (p.Pro418His)
gnomAD v4
Xg.25007307G>ACA412611404ARXc.1252C>T (p.Pro418Ser)
ClinVar
Xg.25007307G>CCA412611405ARXc.1252C>G (p.Pro418Ala)
Xg.25007307G>TCA412611406ARXc.1252C>A (p.Pro418Thr)
Xg.25007308G>ACA515947076ARXc.1251C>T (p.Ser417=)
gnomAD v4
Xg.25007308G>CCA412611407ARXc.1251C>G (p.Ser417Arg)
Xg.25007308G>TCA412611408ARXc.1251C>A (p.Ser417Arg)
Xg.25007309C>ACA412611409ARXc.1250G>T (p.Ser417Ile)
gnomAD v4
Xg.25007309C>GCA412611410ARXc.1250G>C (p.Ser417Thr)
Xg.25007309C>TCA412611411ARXc.1250G>A (p.Ser417Asn)
gnomAD v4
Xg.25007310T>ACA412611412ARXc.1249A>T (p.Ser417Cys)
Xg.25007310T>CCA412611413ARXc.1249A>G (p.Ser417Gly)
gnomAD v4
Xg.25007310T>GCA412611414ARXc.1249A>C (p.Ser417Arg)
Xg.25007311G>ACA515947242ARXc.1248C>T (p.Ala416=)
ClinVar gnomAD v4
Xg.25007311G>CCA515947243ARXc.1248C>G (p.Ala416=)
Xg.25007311G>TCA515947244ARXc.1248C>A (p.Ala416=)
Xg.25007312G>ACA412611415ARXc.1247C>T (p.Ala416Val)
gnomAD v4
Xg.25007312G>CCA10373822ARXc.1247C>G (p.Ala416Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007312G=CA2420207081ARXc.1247C= (p.Ala416=)
Xg.25007312G>TCA412611416ARXc.1247C>A (p.Ala416Asp)
gnomAD v4
Xg.25007313C>ACA412611418ARXc.1246G>T (p.Ala416Ser)
Xg.25007313C>GCA412611419ARXc.1246G>C (p.Ala416Pro)
gnomAD v4
Xg.25007313C>TCA412611417ARXc.1246G>A (p.Ala416Thr)
gnomAD v4
Xg.25007314G>ACA515947250ARXc.1245C>T (p.Asp415=)
ClinVar dbSNP gnomAD v4
Xg.25007314G>CCA412611420ARXc.1245C>G (p.Asp415Glu)
Xg.25007314G>TCA412611421ARXc.1245C>A (p.Asp415Glu)
dbSNP gnomAD v4
Xg.25007315T>ACA412611422ARXc.1244A>T (p.Asp415Val)
Xg.25007315T>CCA412611423ARXc.1244A>G (p.Asp415Gly)
COSMIC
Xg.25007315T>GCA412611424ARXc.1244A>C (p.Asp415Ala)
Xg.25007316C>ACA412611425ARXc.1243G>T (p.Asp415Tyr)
Xg.25007316C>GCA412611426ARXc.1243G>C (p.Asp415His)
Xg.25007316C>TCA412611427ARXc.1243G>A (p.Asp415Asn)
Xg.25007317C>ACA515947258ARXc.1242G>T (p.Leu414=)
gnomAD v4
Xg.25007317C>GCA515947260ARXc.1242G>C (p.Leu414=)
Xg.25007317C>TCA515947259ARXc.1242G>A (p.Leu414=)
gnomAD v4
Xg.25007318A>CCA412611428ARXc.1241T>G (p.Leu414Arg)
Xg.25007318A>GCA412611429ARXc.1241T>C (p.Leu414Pro)
gnomAD v4
Xg.25007318A>TCA412611430ARXc.1241T>A (p.Leu414Gln)
Xg.25007319G>ACA515947262ARXc.1240C>T (p.Leu414=)
Xg.25007319G>CCA412611431ARXc.1240C>G (p.Leu414Val)
ClinVar
Xg.25007319G>TCA412611432ARXc.1240C>A (p.Leu414Met)
gnomAD v4
Xg.25007320G>ACA515947265ARXc.1239C>T (p.Tyr413=)
ClinVar gnomAD v4
Xg.25007320G>CCA412611433ARXc.1239C>G (p.Tyr413Ter)
Xg.25007320G>TCA412611434ARXc.1239C>A (p.Tyr413Ter)
gnomAD v4
Xg.25007321T>ACA412611435ARXc.1238A>T (p.Tyr413Phe)
Xg.25007321T>CCA412611436ARXc.1238A>G (p.Tyr413Cys)
dbSNP
Xg.25007321T>GCA412611437ARXc.1238A>C (p.Tyr413Ser)
Xg.25007321T=CA2420207082ARXc.1238A= (p.Tyr413=)
Xg.25007322A>CCA412611438ARXc.1237T>G (p.Tyr413Asp)
Xg.25007322A>GCA412611439ARXc.1237T>C (p.Tyr413His)
gnomAD v4
Xg.25007322A>TCA412611440ARXc.1237T>A (p.Tyr413Asn)
Xg.25007323G>ACA515947269ARXc.1236C>T (p.Pro412=)
dbSNP gnomAD v3 gnomAD v4
Xg.25007323G>CCA515947270ARXc.1236C>G (p.Pro412=)
dbSNP gnomAD v2 gnomAD v4
Xg.25007323G=CA2420207083ARXc.1236C= (p.Pro412=)
Xg.25007323G>TCA515947271ARXc.1236C>A (p.Pro412=)
gnomAD v4
Xg.25007324G>ACA412611441ARXc.1235C>T (p.Pro412Leu)
Xg.25007324G>CCA412611442ARXc.1235C>G (p.Pro412Arg)
gnomAD v4
Xg.25007324G>TCA412611443ARXc.1235C>A (p.Pro412His)
gnomAD v4
Xg.25007325G>ACA412611444ARXc.1234C>T (p.Pro412Ser)
dbSNP
Xg.25007325G>CCA412611445ARXc.1234C>G (p.Pro412Ala)
Xg.25007325G>TCA412611446ARXc.1234C>A (p.Pro412Thr)
gnomAD v4
Xg.25007326G>ACA515947276ARXc.1233C>T (p.Ser411=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25007326G>CCA412611448ARXc.1233C>G (p.Ser411Arg)
Xg.25007326G=CA2420207084ARXc.1233C= (p.Ser411=)
Xg.25007326G>TCA412611447ARXc.1233C>A (p.Ser411Arg)
gnomAD v4
Xg.25007327C>ACA412611449ARXc.1232G>T (p.Ser411Ile)
gnomAD v4
Xg.25007327C>GCA412611451ARXc.1232G>C (p.Ser411Thr)
Xg.25007327C>TCA412611450ARXc.1232G>A (p.Ser411Asn)
gnomAD v4
Xg.25007328T>ACA412611452ARXc.1231A>T (p.Ser411Cys)
Xg.25007328T>CCA412611453ARXc.1231A>G (p.Ser411Gly)
gnomAD v4
Xg.25007328T>GCA412611454ARXc.1231A>C (p.Ser411Arg)
Xg.25007329G>ACA515947281ARXc.1230C>T (p.Leu410=)
gnomAD v4
Xg.25007329G>CCA515947282ARXc.1230C>G (p.Leu410=)
ClinVar
Xg.25007329G>TCA515947283ARXc.1230C>A (p.Leu410=)
gnomAD v4
Xg.25007330A>CCA412611455ARXc.1229T>G (p.Leu410Arg)
Xg.25007330A>GCA412611456ARXc.1229T>C (p.Leu410Pro)
Xg.25007330A>TCA412611457ARXc.1229T>A (p.Leu410His)
Xg.25007331G>ACA412611458ARXc.1228C>T (p.Leu410Phe)
Xg.25007331G>CCA412611459ARXc.1228C>G (p.Leu410Val)
Xg.25007331G>TCA412611460ARXc.1228C>A (p.Leu410Ile)
gnomAD v4
Xg.25007332C>ACA515947288ARXc.1227G>T (p.Pro409=)
gnomAD v4
Xg.25007332C=CA2420207085ARXc.1227G= (p.Pro409=)
Xg.25007332C>GCA515947289ARXc.1227G>C (p.Pro409=)
Xg.25007332C>TCA515947291ARXc.1227G>A (p.Pro409=)
gnomAD v4
Xg.25007333G>ACA412611461ARXc.1226C>T (p.Pro409Leu)
gnomAD v4
Xg.25007333G>CCA412611462ARXc.1226C>G (p.Pro409Arg)
Xg.25007333G=CA2420207087ARXc.1226C= (p.Pro409=)
Xg.25007333G>TCA412611463ARXc.1226C>A (p.Pro409Gln)
ClinVar dbSNP gnomAD v4
Xg.25007339_25007342dupCA2420207086ARXc.1223_1226dup (p.Leu410ProfsTer?)
ClinVar dbSNP
Xg.25007334G>ACA412611466ARXc.1225C>T (p.Pro409Ser)
gnomAD v4
Xg.25007334G>CCA412611464ARXc.1225C>G (p.Pro409Ala)
Xg.25007334G>TCA412611465ARXc.1225C>A (p.Pro409Thr)
gnomAD v4
Xg.25007335G>ACA515947297ARXc.1224C>T (p.His408=)
Xg.25007335G>CCA412611467ARXc.1224C>G (p.His408Gln)
Xg.25007335G>TCA412611468ARXc.1224C>A (p.His408Gln)
gnomAD v4
Xg.25007336T>ACA412611469ARXc.1223A>T (p.His408Leu)
Xg.25007336T>CCA412611470ARXc.1223A>G (p.His408Arg)
Xg.25007336T>GCA412611471ARXc.1223A>C (p.His408Pro)
gnomAD v4
Xg.25007337G>ACA412611472ARXc.1222C>T (p.His408Tyr)
Xg.25007337G>CCA412611473ARXc.1222C>G (p.His408Asp)
Xg.25007337G>TCA412611474ARXc.1222C>A (p.His408Asn)
Xg.25007338G>ACA515947308ARXc.1221C>T (p.Thr407=)
dbSNP gnomAD v3 gnomAD v4
Xg.25007338G>CCA515947305ARXc.1221C>G (p.Thr407=)
Xg.25007338G=CA2420207088ARXc.1221C= (p.Thr407=)
Xg.25007338G>TCA515947303ARXc.1221C>A (p.Thr407=)
gnomAD v4
Xg.25007339G>ACA412611475ARXc.1220C>T (p.Thr407Ile)
gnomAD v4
Xg.25007339G>CCA412611476ARXc.1220C>G (p.Thr407Ser)
Xg.25007339G>TCA412611477ARXc.1220C>A (p.Thr407Asn)
gnomAD v4
Xg.25007340T>ACA412611480ARXc.1219A>T (p.Thr407Ser)
Xg.25007340T>CCA412611479ARXc.1219A>G (p.Thr407Ala)
dbSNP gnomAD v3 gnomAD v4
Xg.25007340T>GCA412611478ARXc.1219A>C (p.Thr407Pro)
Xg.25007341G>ACA515947315ARXc.1218C>T (p.Ala406=)
Xg.25007341G>CCA515947313ARXc.1218C>G (p.Ala406=)
Xg.25007341G>TCA515947312ARXc.1218C>A (p.Ala406=)
gnomAD v4
Xg.25007342G>ACA412611483ARXc.1217C>T (p.Ala406Val)
Xg.25007342G>CCA412611481ARXc.1217C>G (p.Ala406Gly)
Xg.25007342G>TCA412611482ARXc.1217C>A (p.Ala406Asp)
gnomAD v4
Xg.25007343C>ACA412611484ARXc.1216G>T (p.Ala406Ser)
gnomAD v4
Xg.25007343C=CA2420207089ARXc.1216G= (p.Ala406=)
Xg.25007343C>GCA412611485ARXc.1216G>C (p.Ala406Pro)
Xg.25007343C>TCA294727ARXc.1216G>A (p.Ala406Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25007344G>ACA515947322ARXc.1215C>T (p.Ser405=)
gnomAD v4
Xg.25007344G>CCA515947319ARXc.1215C>G (p.Ser405=)
Xg.25007344G>TCA515947320ARXc.1215C>A (p.Ser405=)
gnomAD v4
Xg.25007345G>ACA412611488ARXc.1214C>T (p.Ser405Phe)
gnomAD v4
Xg.25007345G>CCA412611487ARXc.1214C>G (p.Ser405Cys)
Xg.25007345G>TCA412611486ARXc.1214C>A (p.Ser405Tyr)
gnomAD v4
Xg.25007346A>CCA412611489ARXc.1213T>G (p.Ser405Ala)
Xg.25007346A>GCA412611490ARXc.1213T>C (p.Ser405Pro)
gnomAD v4
Xg.25007346A>TCA412611491ARXc.1213T>A (p.Ser405Thr)
gnomAD v4
Xg.25007347G>ACA515947323ARXc.1212C>T (p.Leu404=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007347G>CCA515947324ARXc.1212C>G (p.Leu404=)
gnomAD v4
Xg.25007347G=CA2420207090ARXc.1212C= (p.Leu404=)
Xg.25007347G>TCA515947325ARXc.1212C>A (p.Leu404=)
gnomAD v4
Xg.25007348A>CCA412611492ARXc.1211T>G (p.Leu404Arg)
Xg.25007348A>GCA412611493ARXc.1211T>C (p.Leu404Pro)
gnomAD v4
Xg.25007348A>TCA412611494ARXc.1211T>A (p.Leu404His)
Xg.25007349G>ACA412611495ARXc.1210C>T (p.Leu404Phe)
Xg.25007349G>CCA412611497ARXc.1210C>G (p.Leu404Val)
Xg.25007349G>TCA412611496ARXc.1210C>A (p.Leu404Ile)
gnomAD v4
Xg.25007350C>ACA515947327ARXc.1209G>T (p.Pro403=)
gnomAD v4
Xg.25007350C=CA2420207091ARXc.1209G= (p.Pro403=)
Xg.25007350C>GCA515947328ARXc.1209G>C (p.Pro403=)
ClinVar dbSNP gnomAD v4
Xg.25007350C>TCA515947329ARXc.1209G>A (p.Pro403=)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25007351G>ACA412611498ARXc.1208C>T (p.Pro403Leu)
gnomAD v4
Xg.25007351G>CCA412611499ARXc.1208C>G (p.Pro403Arg)
Xg.25007351G>TCA412611500ARXc.1208C>A (p.Pro403Gln)
gnomAD v4
Xg.25007352G>ACA412611501ARXc.1207C>T (p.Pro403Ser)
Xg.25007352G>CCA412611502ARXc.1207C>G (p.Pro403Ala)
Xg.25007352G>TCA412611503ARXc.1207C>A (p.Pro403Thr)
gnomAD v4
Xg.25007353C>ACA515947334ARXc.1206G>T (p.Gly402=)
dbSNP gnomAD v3 gnomAD v4
Xg.25007353C=CA2420207092ARXc.1206G= (p.Gly402=)
Xg.25007353C>GCA515947335ARXc.1206G>C (p.Gly402=)
Xg.25007353C>TCA515947336ARXc.1206G>A (p.Gly402=)
dbSNP gnomAD v4
Xg.25007356delCA2573158494ARXc.1206del (p.Pro403ArgfsTer?)
ClinVar dbSNP gnomAD v4
Xg.25007354C>ACA412611504ARXc.1205G>T (p.Gly402Val)
Xg.25007354C>GCA412611505ARXc.1205G>C (p.Gly402Ala)
Xg.25007354C>TCA412611506ARXc.1205G>A (p.Gly402Glu)
Xg.25007355C>ACA412611507ARXc.1204G>T (p.Gly402Trp)
ClinVar gnomAD v4
Xg.25007355C=CA2420207093ARXc.1204G= (p.Gly402=)
Xg.25007355C>GCA412611508ARXc.1204G>C (p.Gly402Arg)
Xg.25007355C>TCA412611509ARXc.1204G>A (p.Gly402Arg)
ClinVar dbSNP gnomAD v4
Xg.25007356C>ACA515947339ARXc.1203G>T (p.Pro401=)
gnomAD v4
Xg.25007356C=CA2420207094ARXc.1203G= (p.Pro401=)
Xg.25007356C>GCA515947340ARXc.1203G>C (p.Pro401=)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.25007356C>TCA515947341ARXc.1203G>A (p.Pro401=)
gnomAD v4
Xg.25007357G>ACA412611511ARXc.1202C>T (p.Pro401Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25007357G>CCA412611512ARXc.1202C>G (p.Pro401Arg)
Xg.25007357G=CA2420207095ARXc.1202C= (p.Pro401=)
Xg.25007357G>TCA412611510ARXc.1202C>A (p.Pro401Gln)
gnomAD v4
Xg.25007358G>ACA412611513ARXc.1201C>T (p.Pro401Ser)
gnomAD v4 COSMIC
Xg.25007358G>CCA412611514ARXc.1201C>G (p.Pro401Ala)
gnomAD v4
Xg.25007358G>TCA412611515ARXc.1201C>A (p.Pro401Thr)
gnomAD v4
Xg.25007359G>ACA515947343ARXc.1200C>T (p.Phe400=)
gnomAD v4
Xg.25007359G>CCA412611516ARXc.1200C>G (p.Phe400Leu)
Xg.25007359G>TCA412611517ARXc.1200C>A (p.Phe400Leu)
gnomAD v4
Xg.25007360A>CCA412611518ARXc.1199T>G (p.Phe400Cys)
Xg.25007360A>GCA412611519ARXc.1199T>C (p.Phe400Ser)
gnomAD v4
Xg.25007360A>TCA412611520ARXc.1199T>A (p.Phe400Tyr)
gnomAD v4
Xg.25007361A>CCA412611521ARXc.1198T>G (p.Phe400Val)
Xg.25007361A>GCA412611522ARXc.1198T>C (p.Phe400Leu)
gnomAD v4
Xg.25007361A>TCA412611523ARXc.1198T>A (p.Phe400Ile)
Xg.25007362G>ACA515947350ARXc.1197C>T (p.Pro399=)
gnomAD v4
Xg.25007362G>CCA515947349ARXc.1197C>G (p.Pro399=)
Xg.25007362G>TCA515947348ARXc.1197C>A (p.Pro399=)
gnomAD v4
Xg.25007363G>ACA412611524ARXc.1196C>T (p.Pro399Leu)
Xg.25007363G>CCA412611525ARXc.1196C>G (p.Pro399Arg)
Xg.25007363G>TCA412611526ARXc.1196C>A (p.Pro399His)
gnomAD v4
Xg.25007364G>ACA412611529ARXc.1195C>T (p.Pro399Ser)
gnomAD v4
Xg.25007364G>CCA412611528ARXc.1195C>G (p.Pro399Ala)
Xg.25007364G>TCA412611527ARXc.1195C>A (p.Pro399Thr)
gnomAD v4
Xg.25007365C>ACA515947356ARXc.1194G>T (p.Leu398=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007365C=CA2420207096ARXc.1194G= (p.Leu398=)
Xg.25007365C>GCA515947359ARXc.1194G>C (p.Leu398=)
Xg.25007365C>TCA515947357ARXc.1194G>A (p.Leu398=)
gnomAD v4
Xg.25007366A>CCA412611530ARXc.1193T>G (p.Leu398Arg)
Xg.25007366A>GCA412611531ARXc.1193T>C (p.Leu398Pro)
gnomAD v4
Xg.25007366A>TCA412611532ARXc.1193T>A (p.Leu398Gln)
Xg.25007367G>ACA515947360ARXc.1192C>T (p.Leu398=)
gnomAD v4
Xg.25007367G>CCA412611533ARXc.1192C>G (p.Leu398Val)
Xg.25007367G>TCA412611534ARXc.1192C>A (p.Leu398Met)
gnomAD v4
Xg.25007368C>ACA515947361ARXc.1191G>T (p.Gly397=)
gnomAD v4
Xg.25007368C>GCA515947362ARXc.1191G>C (p.Gly397=)
Xg.25007368C>TCA515947363ARXc.1191G>A (p.Gly397=)
gnomAD v4
Xg.25007369C>ACA412611535ARXc.1190G>T (p.Gly397Val)
gnomAD v4
Xg.25007369C>GCA412611536ARXc.1190G>C (p.Gly397Ala)
Xg.25007369C>TCA412611537ARXc.1190G>A (p.Gly397Glu)
gnomAD v4
Xg.25007370C>ACA412611538ARXc.1189G>T (p.Gly397Trp)
gnomAD v4
Xg.25007370C=CA2420207097ARXc.1189G= (p.Gly397=)
Xg.25007370C>GCA412611539ARXc.1189G>C (p.Gly397Arg)
gnomAD v4
Xg.25007370C>TCA412611540ARXc.1189G>A (p.Gly397Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007371A>CCA515947368ARXc.1188T>G (p.Pro396=)
Xg.25007371A>GCA515947369ARXc.1188T>C (p.Pro396=)
gnomAD v4
Xg.25007371A>TCA515947370ARXc.1188T>A (p.Pro396=)
Xg.25007371_25007372delinsAGCA2420207098ARXc.1187_1188delinsCT (p.Pro396=)
Xg.25007372G>ACA412611541ARXc.1187C>T (p.Pro396Leu)
gnomAD v4
Xg.25007372G>CCA412611542ARXc.1187C>G (p.Pro396Arg)
Xg.25007372G=CA2420207099ARXc.1187C= (p.Pro396=)
Xg.25007372G>TCA412611543ARXc.1187C>A (p.Pro396His)
dbSNP gnomAD v4
Xg.25007377dupCA658682663ARXc.1187dup (p.Gly397TrpfsTer?)
ClinVar dbSNP
Xg.25007377delCA641364597ARXc.1187del (p.Pro396LeufsTer?)
dbSNP gnomAD v2 gnomAD v4 COSMIC
Xg.25007374_25007381delCA2740092069ARXc.1180_1187del (p.His394TrpfsTer?)
ClinVar
Xg.25007373G>ACA412611544ARXc.1186C>T (p.Pro396Ser)
dbSNP gnomAD v4
Xg.25007373G>CCA10373823ARXc.1186C>G (p.Pro396Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007373G=CA2420207100ARXc.1186C= (p.Pro396=)
Xg.25007373G>TCA327732621ARXc.1186C>A (p.Pro396Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007374G>ACA515947374ARXc.1185C>T (p.Pro395=)
ClinVar
Xg.25007374G>CCA515947375ARXc.1185C>G (p.Pro395=)
gnomAD v4
Xg.25007374G>TCA515947377ARXc.1185C>A (p.Pro395=)
gnomAD v4
Xg.25007375G>ACA412611545ARXc.1184C>T (p.Pro395Leu)
Xg.25007375G>CCA412611546ARXc.1184C>G (p.Pro395Arg)
Xg.25007375G>TCA412611547ARXc.1184C>A (p.Pro395His)
gnomAD v4
Xg.25007376G>ACA412611548ARXc.1183C>T (p.Pro395Ser)
dbSNP gnomAD v4
Xg.25007376G>CCA412611549ARXc.1183C>G (p.Pro395Ala)
Xg.25007376G=CA2420207101ARXc.1183C= (p.Pro395=)
Xg.25007376G>TCA412611550ARXc.1183C>A (p.Pro395Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007377G>ACA327732622ARXc.1182C>T (p.His394=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007377G>CCA412611552ARXc.1182C>G (p.His394Gln)
Xg.25007377G=CA2420207102ARXc.1182C= (p.His394=)
Xg.25007377G>TCA412611551ARXc.1182C>A (p.His394Gln)
gnomAD v3 gnomAD v4
Xg.25007378T>ACA412611553ARXc.1181A>T (p.His394Leu)
Xg.25007378T>CCA412611554ARXc.1181A>G (p.His394Arg)
gnomAD v4
Xg.25007378T>GCA412611555ARXc.1181A>C (p.His394Pro)
dbSNP
Xg.25007379G>ACA412611556ARXc.1180C>T (p.His394Tyr)
gnomAD v4
Xg.25007379G>CCA412611557ARXc.1180C>G (p.His394Asp)
Xg.25007379G>TCA412611558ARXc.1180C>A (p.His394Asn)
gnomAD v4
Xg.25007380G>ACA515947381ARXc.1179C>T (p.Thr393=)
gnomAD v4 COSMIC
Xg.25007380G>CCA515947383ARXc.1179C>G (p.Thr393=)
Xg.25007380G>TCA515947382ARXc.1179C>A (p.Thr393=)
gnomAD v4
Xg.25007381G>ACA412611559ARXc.1178C>T (p.Thr393Ile)
gnomAD v4
Xg.25007381G>CCA412611561ARXc.1178C>G (p.Thr393Ser)
Xg.25007381G>TCA412611560ARXc.1178C>A (p.Thr393Asn)
gnomAD v4
Xg.25007382T>ACA412611562ARXc.1177A>T (p.Thr393Ser)
Xg.25007382T>CCA412611563ARXc.1177A>G (p.Thr393Ala)
Xg.25007382T>GCA412611564ARXc.1177A>C (p.Thr393Pro)
Xg.25007383C>ACA412611565ARXc.1176G>T (p.Gln392His)
gnomAD v4
Xg.25007383C>GCA412611566ARXc.1176G>C (p.Gln392His)
Xg.25007383C>TCA515947387ARXc.1176G>A (p.Gln392=)
Xg.25007384T>ACA412611567ARXc.1175A>T (p.Gln392Leu)
gnomAD v4
Xg.25007384T>CCA412611568ARXc.1175A>G (p.Gln392Arg)
gnomAD v4
Xg.25007384T>GCA412611569ARXc.1175A>C (p.Gln392Pro)
Xg.25007385G>ACA412611570ARXc.1174C>T (p.Gln392Ter)
gnomAD v4
Xg.25007385G>CCA412611571ARXc.1174C>G (p.Gln392Glu)
Xg.25007385G>TCA412611572ARXc.1174C>A (p.Gln392Lys)
gnomAD v4 COSMIC
Xg.25007386C>ACA515947390ARXc.1173G>T (p.Ala391=)
gnomAD v4
Xg.25007386C=CA2420207103ARXc.1173G= (p.Ala391=)
Xg.25007386C>GCA515947392ARXc.1173G>C (p.Ala391=)
Xg.25007386C>TCA515947391ARXc.1173G>A (p.Ala391=)
ClinVar dbSNP gnomAD v4
Xg.25007387G>ACA412611573ARXc.1172C>T (p.Ala391Val)
gnomAD v4
Xg.25007387G>CCA412611575ARXc.1172C>G (p.Ala391Gly)
dbSNP gnomAD v2
Xg.25007387G=CA2420207104ARXc.1172C= (p.Ala391=)
Xg.25007387G>TCA412611574ARXc.1172C>A (p.Ala391Glu)
gnomAD v4 COSMIC
Xg.25007388C>ACA412611576ARXc.1171G>T (p.Ala391Ser)
gnomAD v4
Xg.25007388C=CA2420207105ARXc.1171G= (p.Ala391=)
Xg.25007388C>GCA412611578ARXc.1171G>C (p.Ala391Pro)
Xg.25007388C>TCA412611577ARXc.1171G>A (p.Ala391Thr)
dbSNP gnomAD v2 gnomAD v4
Xg.25007389G>ACA10373824ARXc.1170C>T (p.Gly390=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25007389G>CCA515947399ARXc.1170C>G (p.Gly390=)
gnomAD v4
Xg.25007389G=CA2420207106ARXc.1170C= (p.Gly390=)
Xg.25007389G>TCA515947400ARXc.1170C>A (p.Gly390=)
gnomAD v4
Xg.25007390C>ACA412611579ARXc.1169G>T (p.Gly390Val)
gnomAD v4
Xg.25007390C=CA2420207107ARXc.1169G= (p.Gly390=)
Xg.25007390C>GCA412611580ARXc.1169G>C (p.Gly390Ala)
Xg.25007390C>TCA412611581ARXc.1169G>A (p.Gly390Asp)
dbSNP gnomAD v2 gnomAD v4
Xg.25007391C>ACA412611582ARXc.1168G>T (p.Gly390Cys)
gnomAD v4
Xg.25007391C>GCA412611583ARXc.1168G>C (p.Gly390Arg)
Xg.25007391C>TCA412611584ARXc.1168G>A (p.Gly390Ser)
gnomAD v4
Xg.25007392T>ACA515947403ARXc.1167A>T (p.Ala389=)
Xg.25007392T>CCA515947404ARXc.1167A>G (p.Ala389=)
gnomAD v4
Xg.25007392T>GCA515947405ARXc.1167A>C (p.Ala389=)
gnomAD v4
Xg.25007393G>ACA412611585ARXc.1166C>T (p.Ala389Val)
gnomAD v4
Xg.25007393G>CCA412611586ARXc.1166C>G (p.Ala389Gly)
gnomAD v4
Xg.25007393G>TCA412611587ARXc.1166C>A (p.Ala389Glu)
gnomAD v4
Xg.25007394C>ACA412611590ARXc.1165G>T (p.Ala389Ser)
gnomAD v4
Xg.25007394C=CA2420207108ARXc.1165G= (p.Ala389=)
Xg.25007394C>GCA412611589ARXc.1165G>C (p.Ala389Pro)
Xg.25007394C>TCA412611588ARXc.1165G>A (p.Ala389Thr)
ClinVar gnomAD v4
Xg.25007395delCA2820110004ARXc.1165del (p.Ala389GlnfsTer?)
Xg.25007395C>ACA412611591ARXc.1164G>T (p.Lys388Asn)
gnomAD v4
Xg.25007395C>GCA412611592ARXc.1164G>C (p.Lys388Asn)
gnomAD v4
Xg.25007395C>TCA515947408ARXc.1164G>A (p.Lys388=)
gnomAD v4
Xg.25007397_25007398insTGCTTCA213345ARXc.1164_1165insCAAAG (p.Ala389GlnfsTer?)
ClinVar dbSNP
Xg.25007396T>ACA412611593ARXc.1163A>T (p.Lys388Met)
gnomAD v4
Xg.25007396T>CCA412611594ARXc.1163A>G (p.Lys388Arg)
Xg.25007396T>GCA412611595ARXc.1163A>C (p.Lys388Thr)
Xg.25007397delCA2579637355ARXc.1163del (p.Lys388ArgfsTer?)
gnomAD v4
Xg.25007397T>ACA412611596ARXc.1162A>T (p.Lys388Ter)
Xg.25007397T>CCA412611597ARXc.1162A>G (p.Lys388Glu)
gnomAD v4
Xg.25007397T>GCA412611598ARXc.1162A>C (p.Lys388Gln)
Xg.25007398C>ACA412611599ARXc.1161G>T (p.Glu387Asp)
gnomAD v4
Xg.25007398C=CA2420207109ARXc.1161G= (p.Glu387=)
Xg.25007398C>GCA412611600ARXc.1161G>C (p.Glu387Asp)
ClinVar
Xg.25007398C>TCA515947417ARXc.1161G>A (p.Glu387=)
dbSNP gnomAD v4
Xg.25007399T>ACA412611602ARXc.1160A>T (p.Glu387Val)
Xg.25007399T>CCA412611603ARXc.1160A>G (p.Glu387Gly)
gnomAD v4
Xg.25007399T>GCA412611601ARXc.1160A>C (p.Glu387Ala)
Xg.25007400C>ACA412611604ARXc.1159G>T (p.Glu387Ter)
gnomAD v4
Xg.25007400C>GCA412611605ARXc.1159G>C (p.Glu387Gln)
gnomAD v4
Xg.25007400C>TCA412611606ARXc.1159G>A (p.Glu387Lys)
gnomAD v4
Xg.25007402delCA2693353353ARXc.1159del (p.Glu387ArgfsTer?)
gnomAD v4
Xg.25007401C>ACA515947424ARXc.1158G>T (p.Arg386=)
ClinVar gnomAD v4
Xg.25007401C=CA2420207110ARXc.1158G= (p.Arg386=)
Xg.25007401C>GCA515947423ARXc.1158G>C (p.Arg386=)
Xg.25007401C>TCA515947425ARXc.1158G>A (p.Arg386=)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched