Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.7568529A=CA1608623089DSPc.1359A= (p.Pro453=)
6g.7568529A>CCA448521988DSPc.1359A>C (p.Pro453=)
6g.7568529A>GCA448521989DSPc.1359A>G (p.Pro453=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7568529A>TCA448521990DSPc.1359A>T (p.Pro453=)
6g.7568530G>ACA362676557DSPc.1360G>A (p.Asp454Asn)
6g.7568530G>CCA362676559DSPc.1360G>C (p.Asp454His)
6g.7568530G>TCA362676560DSPc.1360G>T (p.Asp454Tyr)
COSMIC
6g.7568531A=CA1608623091DSPc.1361A= (p.Asp454=)
6g.7568531A>CCA362676561DSPc.1361A>C (p.Asp454Ala)
dbSNP gnomAD v3 gnomAD v4
6g.7568531A>GCA362676562DSPc.1361A>G (p.Asp454Gly)
6g.7568531A>TCA362676563DSPc.1361A>T (p.Asp454Val)
6g.7568532C>ACA027756DSPc.1362C>A (p.Asp454Glu)
dbSNP ExAC gnomAD v2
6g.7568532C=CA1608623096DSPc.1362C= (p.Asp454=)
6g.7568532C>GCA362676566DSPc.1362C>G (p.Asp454Glu)
dbSNP gnomAD v3 gnomAD v4
6g.7568532C>TCA448521996DSPc.1362C>T (p.Asp454=)
ClinVar dbSNP
6g.7568533T>ACA362676567DSPc.1363T>A (p.Tyr455Asn)
6g.7568533T>CCA362676569DSPc.1363T>C (p.Tyr455His)
6g.7568533T>GCA362676571DSPc.1363T>G (p.Tyr455Asp)
6g.7568534A=CA1608623100DSPc.1364A= (p.Tyr455=)
6g.7568534A>CCA362676576DSPc.1364A>C (p.Tyr455Ser)
6g.7568534A>GCA362676577DSPc.1364A>G (p.Tyr455Cys)
dbSNP gnomAD v3 gnomAD v4
6g.7568534A>TCA362676573DSPc.1364A>T (p.Tyr455Phe)
6g.7568535C>ACA362676580DSPc.1365C>A (p.Tyr455Ter)
6g.7568535C>GCA362676579DSPc.1365C>G (p.Tyr455Ter)
6g.7568535C>TCA448522014DSPc.1365C>T (p.Tyr455=)
ClinVar
6g.7568536A=CA1608623116DSPc.1366A= (p.Arg456=)
6g.7568536A>CCA448522016DSPc.1366A>C (p.Arg456=)
dbSNP gnomAD v3 gnomAD v4
6g.7568536A>GCA362676581DSPc.1366A>G (p.Arg456Gly)
6g.7568536A>TCA362676582DSPc.1366A>T (p.Arg456Ter)
6g.7568537G>ACA362676583DSPc.1367G>A (p.Arg456Lys)
6g.7568537G>CCA362676584DSPc.1367G>C (p.Arg456Thr)
6g.7568537G>TCA362676586DSPc.1367G>T (p.Arg456Ile)
6g.7568538A>CCA362676587DSPc.1368A>C (p.Arg456Ser)
6g.7568538A>GCA448522021DSPc.1368A>G (p.Arg456=)
6g.7568538A>TCA362676588DSPc.1368A>T (p.Arg456Ser)
6g.7568539A>CCA362676589DSPc.1369A>C (p.Ser457Arg)
6g.7568539A>GCA362676590DSPc.1369A>G (p.Ser457Gly)
6g.7568539A>TCA362676591DSPc.1369A>T (p.Ser457Cys)
6g.7568540G>ACA362676592DSPc.1370G>A (p.Ser457Asn)
ClinVar
6g.7568540G>CCA362676593DSPc.1370G>C (p.Ser457Thr)
6g.7568540G>TCA362676594DSPc.1370G>T (p.Ser457Ile)
6g.7568541C>ACA362676597DSPc.1371C>A (p.Ser457Arg)
gnomAD v4
6g.7568541C>GCA362676595DSPc.1371C>G (p.Ser457Arg)
6g.7568541C>TCA448522042DSPc.1371C>T (p.Ser457=)
6g.7568542A=CA1608623121DSPc.1372A= (p.Asn458=)
6g.7568542A>CCA362676599DSPc.1372A>C (p.Asn458His)
dbSNP
6g.7568542A>GCA362676601DSPc.1372A>G (p.Asn458Asp)
6g.7568542A>TCA362676602DSPc.1372A>T (p.Asn458Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7568543A>CCA362676603DSPc.1373A>C (p.Asn458Thr)
6g.7568543A>GCA362676604DSPc.1373A>G (p.Asn458Ser)
gnomAD v4
6g.7568543A>TCA362676605DSPc.1373A>T (p.Asn458Ile)
6g.7568544T>ACA362676608DSPc.1374T>A (p.Asn458Lys)
6g.7568544T>CCA448522054DSPc.1374T>C (p.Asn458=)
6g.7568544T>GCA362676609DSPc.1374T>G (p.Asn458Lys)
gnomAD v4
6g.7568545A>CCA362676613DSPc.1375A>C (p.Lys459Gln)
6g.7568545A>GCA362676614DSPc.1375A>G (p.Lys459Glu)
6g.7568545A>TCA362676615DSPc.1375A>T (p.Lys459Ter)
6g.7568546A>CCA362676620DSPc.1376A>C (p.Lys459Thr)
6g.7568546A>GCA362676621DSPc.1376A>G (p.Lys459Arg)
6g.7568546A>TCA362676622DSPc.1376A>T (p.Lys459Ile)
6g.7568547A>CCA362676623DSPc.1377A>C (p.Lys459Asn)
6g.7568547A>GCA448522070DSPc.1377A>G (p.Lys459=)
6g.7568547A>TCA362676624DSPc.1377A>T (p.Lys459Asn)
6g.7568548C>ACA362676625DSPc.1378C>A (p.Pro460Thr)
6g.7568548C=CA1608623123DSPc.1378C= (p.Pro460=)
6g.7568548C>GCA027784DSPc.1378C>G (p.Pro460Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568548C>TCA362676626DSPc.1378C>T (p.Pro460Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7568549C>ACA362676635DSPc.1379C>A (p.Pro460His)
6g.7568549C=CA1608623133DSPc.1379C= (p.Pro460=)
6g.7568549C>GCA362676637DSPc.1379C>G (p.Pro460Arg)
6g.7568549C>TCA027800DSPc.1379C>T (p.Pro460Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568550C>ACA448522081DSPc.1380C>A (p.Pro460=)
6g.7568550C=CA1608623139DSPc.1380C= (p.Pro460=)
6g.7568550C>GCA448522082DSPc.1380C>G (p.Pro460=)
gnomAD v4
6g.7568550C>TCA448522083DSPc.1380C>T (p.Pro460=)
ClinVar dbSNP gnomAD v4
6g.7568550_7568553delinsCATTCA1608623137DSPc.1380_1383delinsCATT (p.Pro460=)
6g.7568551A>CCA362676638DSPc.1381A>C (p.Ile461Leu)
6g.7568551A>GCA362676639DSPc.1381A>G (p.Ile461Val)
gnomAD v4
6g.7568551A>TCA362676641DSPc.1381A>T (p.Ile461Phe)
6g.7568554_7568556delCA004913DSPc.1384_1386del (p.Ile462del)
ClinVar dbSNP
6g.7568552T>ACA362676644DSPc.1382T>A (p.Ile461Asn)
6g.7568552T>CCA362676645DSPc.1382T>C (p.Ile461Thr)
ClinVar dbSNP gnomAD v4
6g.7568552T>GCA362676649DSPc.1382T>G (p.Ile461Ser)
6g.7568552T=CA1608623145DSPc.1382T= (p.Ile461=)
6g.7568553T>ACA448522090DSPc.1383T>A (p.Ile461=)
6g.7568553T>CCA448522093DSPc.1383T>C (p.Ile461=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7568553T>GCA362676652DSPc.1383T>G (p.Ile461Met)
6g.7568553T=CA1608623149DSPc.1383T= (p.Ile461=)
6g.7568554A>CCA362676656DSPc.1384A>C (p.Ile462Leu)
6g.7568554A>GCA362676655DSPc.1384A>G (p.Ile462Val)
6g.7568554A>TCA362676654DSPc.1384A>T (p.Ile462Phe)
6g.7568554_7568555delinsATCA1608623151DSPc.1384_1385delinsAT (p.Ile462=)
6g.7568555T>ACA362676657DSPc.1385T>A (p.Ile462Asn)
6g.7568555T>CCA362676658DSPc.1385T>C (p.Ile462Thr)
6g.7568555T>GCA362676660DSPc.1385T>G (p.Ile462Ser)
gnomAD v4
6g.7568556delCA913187583DSPc.1386del (p.Leu463SerfsTer22)
ClinVar dbSNP
6g.7568556T>ACA448522098DSPc.1386T>A (p.Ile462=)
6g.7568556T>CCA448522104DSPc.1386T>C (p.Ile462=)
dbSNP gnomAD v4
6g.7568556T>GCA362676661DSPc.1386T>G (p.Ile462Met)
6g.7568556T=CA1608623159DSPc.1386T= (p.Ile462=)
6g.7568556_7568559delCA2677222923DSPc.1386_1389del (p.Leu463GlufsTer21)
ClinVar gnomAD v4
6g.7568557C>ACA362676673DSPc.1387C>A (p.Leu463Ile)
6g.7568557C>GCA362676674DSPc.1387C>G (p.Leu463Val)
6g.7568557C>TCA362676675DSPc.1387C>T (p.Leu463Phe)
6g.7568558T>ACA362676678DSPc.1388T>A (p.Leu463His)
6g.7568558T>CCA362676681DSPc.1388T>C (p.Leu463Pro)
ClinVar dbSNP
6g.7568558T>GCA362676685DSPc.1388T>G (p.Leu463Arg)
6g.7568558T=CA1608623163DSPc.1388T= (p.Leu463=)
6g.7568559C>ACA448522116DSPc.1389C>A (p.Leu463=)
6g.7568559C>GCA448522118DSPc.1389C>G (p.Leu463=)
6g.7568559C>TCA448522120DSPc.1389C>T (p.Leu463=)
6g.7568560A>CCA448522122DSPc.1390A>C (p.Arg464=)
6g.7568560A>GCA362676692DSPc.1390A>G (p.Arg464Gly)
6g.7568560A>TCA362676694DSPc.1390A>T (p.Arg464Ter)
6g.7568561G>ACA362676697DSPc.1391G>A (p.Arg464Lys)
6g.7568561G>CCA362676707DSPc.1391G>C (p.Arg464Thr)
6g.7568561G>TCA362676700DSPc.1391G>T (p.Arg464Ile)
6g.7568562A=CA1608623173DSPc.1392A= (p.Arg464=)
6g.7568562A>CCA362676709DSPc.1392A>C (p.Arg464Ser)
ClinVar dbSNP
6g.7568562A>GCA448522137DSPc.1392A>G (p.Arg464=)
6g.7568562A>TCA362676712DSPc.1392A>T (p.Arg464Ser)
6g.7568563G>ACA362676715DSPc.1393G>A (p.Ala465Thr)
6g.7568563G>CCA362676717DSPc.1393G>C (p.Ala465Pro)
6g.7568563G>TCA362676719DSPc.1393G>T (p.Ala465Ser)
6g.7568564C>ACA362676721DSPc.1394C>A (p.Ala465Asp)
6g.7568564C>GCA362676723DSPc.1394C>G (p.Ala465Gly)
6g.7568564C>TCA362676724DSPc.1394C>T (p.Ala465Val)
6g.7568568_7568569delCA2677222928DSPc.1398_1399del (p.Cys467Ter)
gnomAD v4
6g.7568565T>ACA448522153DSPc.1395T>A (p.Ala465=)
6g.7568565T>CCA027834DSPc.1395T>C (p.Ala465=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568565T>GCA027851DSPc.1395T>G (p.Ala465=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568565T=CA1608623187DSPc.1395T= (p.Ala465=)
6g.7568566C>ACA362676731DSPc.1396C>A (p.Leu466Ile)
6g.7568566C>GCA362676733DSPc.1396C>G (p.Leu466Val)
6g.7568566C>TCA362676736DSPc.1396C>T (p.Leu466Phe)
ClinVar
6g.7568567T>ACA362676742DSPc.1397T>A (p.Leu466His)
6g.7568567T>CCA004921DSPc.1397T>C (p.Leu466Pro)
ClinVar dbSNP
6g.7568567T>GCA362676745DSPc.1397T>G (p.Leu466Arg)
6g.7568567T=CA1608623198DSPc.1397T= (p.Leu466=)
6g.7568568C>ACA448522161DSPc.1398C>A (p.Leu466=)
6g.7568568C=CA1608623209DSPc.1398C= (p.Leu466=)
6g.7568568C>GCA448522165DSPc.1398C>G (p.Leu466=)
ClinVar dbSNP gnomAD v4
6g.7568568C>TCA448522167DSPc.1398C>T (p.Leu466=)
COSMIC
6g.7568569T>ACA362676746DSPc.1399T>A (p.Cys467Ser)
6g.7568569T>CCA362676748DSPc.1399T>C (p.Cys467Arg)
6g.7568569T>GCA362676747DSPc.1399T>G (p.Cys467Gly)
6g.7568570G>ACA362676749DSPc.1400G>A (p.Cys467Tyr)
dbSNP gnomAD v3 gnomAD v4
6g.7568570G>CCA362676751DSPc.1400G>C (p.Cys467Ser)
6g.7568570G>TCA362676753DSPc.1400G>T (p.Cys467Phe)
6g.7568571T>ACA362676756DSPc.1401T>A (p.Cys467Ter)
6g.7568571T>CCA448522172DSPc.1401T>C (p.Cys467=)
gnomAD v4
6g.7568571T>GCA362676758DSPc.1401T>G (p.Cys467Trp)
6g.7568572G>ACA362676764DSPc.1402G>A (p.Asp468Asn)
6g.7568572G>CCA362676767DSPc.1402G>C (p.Asp468His)
6g.7568572G>TCA362676769DSPc.1402G>T (p.Asp468Tyr)
6g.7568573A>CCA362676773DSPc.1403A>C (p.Asp468Ala)
6g.7568573A>GCA362676774DSPc.1403A>G (p.Asp468Gly)
6g.7568573A>TCA362676777DSPc.1403A>T (p.Asp468Val)
6g.7568574C>ACA362676779DSPc.1404C>A (p.Asp468Glu)
6g.7568574C=CA1608623215DSPc.1404C= (p.Asp468=)
6g.7568574C>GCA362676781DSPc.1404C>G (p.Asp468Glu)
6g.7568574C>TCA448522191DSPc.1404C>T (p.Asp468=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7568575delCA448522197DSPc.1405del (p.Tyr469ThrfsTer16)
6g.7568575T>ACA362676784DSPc.1405T>A (p.Tyr469Asn)
6g.7568575T>CCA362676785DSPc.1405T>C (p.Tyr469His)
6g.7568575T>GCA362676787DSPc.1405T>G (p.Tyr469Asp)
6g.7568576A>CCA362676790DSPc.1406A>C (p.Tyr469Ser)
6g.7568576A>GCA362676798DSPc.1406A>G (p.Tyr469Cys)
6g.7568576A>TCA362676800DSPc.1406A>T (p.Tyr469Phe)
6g.7568577C>ACA362676802DSPc.1407C>A (p.Tyr469Ter)
6g.7568577C>GCA362676803DSPc.1407C>G (p.Tyr469Ter)
6g.7568577C>TCA448522207DSPc.1407C>T (p.Tyr469=)
6g.7568578A=CA1608623221DSPc.1408A= (p.Lys470=)
6g.7568578A>CCA362676804DSPc.1408A>C (p.Lys470Gln)
gnomAD v4
6g.7568578A>GCA362676805DSPc.1408A>G (p.Lys470Glu)
dbSNP
6g.7568578A>TCA362676806DSPc.1408A>T (p.Lys470Ter)
6g.7568579A>CCA362676808DSPc.1409A>C (p.Lys470Thr)
6g.7568579A>GCA362676809DSPc.1409A>G (p.Lys470Arg)
6g.7568579A>TCA362676812DSPc.1409A>T (p.Lys470Ile)
6g.7568580A=CA1608623223DSPc.1410A= (p.Lys470=)
6g.7568580A>CCA362676814DSPc.1410A>C (p.Lys470Asn)
6g.7568580A>GCA448522216DSPc.1410A>G (p.Lys470=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7568580A>TCA362676817DSPc.1410A>T (p.Lys470Asn)
6g.7568581C>ACA362676819DSPc.1411C>A (p.Gln471Lys)
6g.7568581C=CA1608623228DSPc.1411C= (p.Gln471=)
6g.7568581C>GCA362676822DSPc.1411C>G (p.Gln471Glu)
6g.7568581C>TCA362676825DSPc.1411C>T (p.Gln471Ter)
6g.7568581_7568582insTCA915944142DSPc.1411_1412insT (p.Gln471LeufsTer8)
ClinVar dbSNP
6g.7568582A=CA1608623234DSPc.1412A= (p.Gln471=)
6g.7568582A>CCA362676829DSPc.1412A>C (p.Gln471Pro)
6g.7568582A>GCA027864DSPc.1412A>G (p.Gln471Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568582A>TCA362676833DSPc.1412A>T (p.Gln471Leu)
6g.7568583A=CA1608623248DSPc.1413A= (p.Gln471=)
6g.7568583A>CCA362676835DSPc.1413A>C (p.Gln471His)
6g.7568583A>GCA027899DSPc.1413A>G (p.Gln471=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568583A>TCA362676848DSPc.1413A>T (p.Gln471His)
6g.7568584G>ACA362676850DSPc.1414G>A (p.Asp472Asn)
ClinVar dbSNP
6g.7568584G>CCA362676853DSPc.1414G>C (p.Asp472His)
6g.7568584G>TCA362676854DSPc.1414G>T (p.Asp472Tyr)
6g.7568585A>CCA362676857DSPc.1415A>C (p.Asp472Ala)
6g.7568585A>GCA362676856DSPc.1415A>G (p.Asp472Gly)
6g.7568585A>TCA362676855DSPc.1415A>T (p.Asp472Val)
6g.7568585_7568586insCCAAACACACCCAACCA2769905262DSPc.1415_1416insCCAAACACACCCAAC (p.Asp472_Gln473insGlnThrHisProThr)
6g.7568585_7568586insACCAAACACACCCAACCA2769905261DSPc.1415_1416insACCAAACACACCCAAC (p.Asp472GlufsTer12)
6g.7568586T>ACA362676858DSPc.1416T>A (p.Asp472Glu)
gnomAD v4
6g.7568586T>CCA448522238DSPc.1416T>C (p.Asp472=)
dbSNP
6g.7568586T>GCA362676860DSPc.1416T>G (p.Asp472Glu)
ClinVar dbSNP
6g.7568586T=CA1608623255DSPc.1416T= (p.Asp472=)
6g.7568587C>ACA362676862DSPc.1417C>A (p.Gln473Lys)
ClinVar
6g.7568587C>GCA362676868DSPc.1417C>G (p.Gln473Glu)
6g.7568587C>TCA362676865DSPc.1417C>T (p.Gln473Ter)
COSMIC
6g.7568588A=CA1608623285DSPc.1418A= (p.Gln473=)
6g.7568588A>CCA362676870DSPc.1418A>C (p.Gln473Pro)
6g.7568588A>GCA027921DSPc.1418A>G (p.Gln473Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568588A>TCA362676873DSPc.1418A>T (p.Gln473Leu)
6g.7568589G>ACA448522255DSPc.1419G>A (p.Gln473=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7568589G>CCA362676887DSPc.1419G>C (p.Gln473His)
6g.7568589G=CA1608623299DSPc.1419G= (p.Gln473=)
6g.7568589G>TCA362676889DSPc.1419G>T (p.Gln473His)
6g.7568590G>ACA362676893DSPc.1419+1G>A (n.1419+1G>A)
6g.7568590G>CCA362676902DSPc.1419+1G>C (n.1419+1G>C)
6g.7568590G>TCA362676900DSPc.1419+1G>T (n.1419+1G>T)
6g.7568591T>ACA362676903DSPc.1419+2T>A (n.1419+2T>A)
6g.7568591T>CCA362676907DSPc.1419+2T>C (n.1419+2T>C)
6g.7568591T>GCA362676912DSPc.1419+2T>G (n.1419+2T>G)
6g.7568594G>CCA133956112DSPc.1419+5G>C (n.1419+5G>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7568594G=CA1608623303DSPc.1419+5G= (n.1419+5G=)
6g.7568594_7568595insAGTTTTAGAGGAGATCA1608623304DSPc.1419+5_1419+6insAGTTTTAGAGGAGAT (n.1419+5_1419+6insAGTTTTAGAGGAGAT)
dbSNP
6g.7568595T>CCA565103535DSPc.1419+6T>C (n.1419+6T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7568595T=CA1608623308DSPc.1419+6T= (n.1419+6T=)
6g.7568596A=CA1608623316DSPc.1419+7A= (n.1419+7A=)
6g.7568596A>GCA133956115DSPc.1419+7A>G (n.1419+7A>G)
dbSNP gnomAD v4
6g.7568596A>TCA028035DSPc.1419+7A>T (n.1419+7A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568598T>GCA2677223009DSPc.1419+9T>G (n.1419+9T>G)
gnomAD v4
6g.7568599C=CA1608623319DSPc.1419+10C= (n.1419+10C=)
6g.7568599C>GCA027936DSPc.1419+10C>G (n.1419+10C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568600A>CCA2677223010DSPc.1419+11A>C (n.1419+11A>C)
gnomAD v4
6g.7568603T>CCA565103536DSPc.1419+14T>C (n.1419+14T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7568603T=CA1608623325DSPc.1419+14T= (n.1419+14T=)
6g.7568604A=CA1608623327DSPc.1419+15A= (n.1419+15A=)
6g.7568604A>CCA027953DSPc.1419+15A>C (n.1419+15A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568606A=CA1608623332DSPc.1419+17A= (n.1419+17A=)
6g.7568606A>GCA027974DSPc.1419+17A>G (n.1419+17A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568607A=CA1608623338DSPc.1419+18A= (n.1419+18A=)
6g.7568607A>CCA027983DSPc.1419+18A>C (n.1419+18A>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568608T>GCA2677223070DSPc.1419+19T>G (n.1419+19T>G)
gnomAD v4
6g.7568610A=CA1608623340DSPc.1419+21A= (n.1419+21A=)
6g.7568610A>CCA565103537DSPc.1419+21A>C (n.1419+21A>C)
dbSNP gnomAD v2 gnomAD v4
6g.7568610A>GCA2677223077DSPc.1419+21A>G (n.1419+21A>G)
gnomAD v4
6g.7568611T>ACA028002DSPc.1419+22T>A (n.1419+22T>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568611T>CCA1608623348DSPc.1419+22T>C (n.1419+22T>C)
dbSNP gnomAD v4
6g.7568611T=CA1608623345DSPc.1419+22T= (n.1419+22T=)
6g.7568613C>ACA2578524314DSPc.1419+24C>A (n.1419+24C>A)
gnomAD v4
6g.7568613C=CA1608623351DSPc.1419+24C= (n.1419+24C=)
6g.7568613C>TCA1608623352DSPc.1419+24C>T (n.1419+24C>T)
dbSNP gnomAD v4
6g.7568613_7568615delinsCAACA1608623350DSPc.1419+24_1419+26delinsCAA (n.1419+24_1419+26delinsCAA)
6g.7568614A=CA1608623357DSPc.1419+25A= (n.1419+25A=)
6g.7568614A>CCA2578524315DSPc.1419+25A>C (n.1419+25A>C)
gnomAD v4
6g.7568614A>GCA1608623354DSPc.1419+25A>G (n.1419+25A>G)
dbSNP gnomAD v4
6g.7568616_7568617delCA004928DSPc.1419+27_1419+28del (n.1419+27_1419+28del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7568615A>GCA2677223126DSPc.1419+26A>G (n.1419+26A>G)
gnomAD v4
6g.7568617A=CA1608623360DSPc.1419+28A= (n.1419+28A=)
6g.7568617A>TCA028022DSPc.1419+28A>T (n.1419+28A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7568618G>ACA2677223132DSPc.1419+29G>A (n.1419+29G>A)
gnomAD v4
6g.7568621T>CCA2677223133DSPc.1419+32T>C (n.1419+32T>C)
gnomAD v4
6g.7568623C=CA1608623368DSPc.1419+34C= (n.1419+34C=)
6g.7568623C>TCA565103538DSPc.1419+34C>T (n.1419+34C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7568625C>TCA2578524316DSPc.1419+36C>T (n.1419+36C>T)
gnomAD v4
6g.7568627G>ACA2677223135DSPc.1419+38G>A (n.1419+38G>A)
gnomAD v4
6g.7568629_7568631delinsCTTCA1608623370DSPc.1419+40_1419+42delinsCTT (n.1419+40_1419+42delinsCTT)

Number of alleles fetched