Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154957061G>ACA255113F8c.1648C>T (p.Arg550Cys)
c.*1524C>T (n.*1524C>T)
c.1543C>T (p.Arg515Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.154957061G>CCA255114F8c.1648C>G (p.Arg550Gly)
c.*1524C>G (n.*1524C>G)
c.1543C>G (p.Arg515Gly)
ClinVar dbSNP
Xg.154957061G=CA2466845345F8c.1648C= (p.Arg550=)
c.*1524C= (n.*1524C=)
c.1543C= (p.Arg515=)
Xg.154957061G>TCA414911841F8c.1648C>A (p.Arg550Ser)
c.*1524C>A (n.*1524C>A)
c.1543C>A (p.Arg515Ser)
Xg.154957062G>ACA519358613F8c.1647C>T (p.Thr549=)
c.*1523C>T (n.*1523C>T)
c.1542C>T (p.Thr514=)
Xg.154957062G>CCA519358614F8c.1647C>G (p.Thr549=)
c.*1523C>G (n.*1523C>G)
c.1542C>G (p.Thr514=)
Xg.154957062G>TCA519358616F8c.1647C>A (p.Thr549=)
c.*1523C>A (n.*1523C>A)
c.1542C>A (p.Thr514=)
Xg.154957063G>ACA10568425F8c.1646C>T (p.Thr549Ile)
c.*1522C>T (n.*1522C>T)
c.1541C>T (p.Thr514Ile)
dbSNP ExAC gnomAD v2
Xg.154957063G>CCA414911844F8c.1646C>G (p.Thr549Ser)
c.*1522C>G (n.*1522C>G)
c.1541C>G (p.Thr514Ser)
Xg.154957063G=CA2466845346F8c.1646C= (p.Thr549=)
c.*1522C= (n.*1522C=)
c.1541C= (p.Thr514=)
Xg.154957063G>TCA414911846F8c.1646C>A (p.Thr549Asn)
c.*1522C>A (n.*1522C>A)
c.1541C>A (p.Thr514Asn)
dbSNP
Xg.154957064T>ACA414911850F8c.1645A>T (p.Thr549Ser)
c.*1521A>T (n.*1521A>T)
c.1540A>T (p.Thr514Ser)
Xg.154957064T>CCA414911851F8c.1645A>G (p.Thr549Ala)
c.*1521A>G (n.*1521A>G)
c.1540A>G (p.Thr514Ala)
Xg.154957064T>GCA414911848F8c.1645A>C (p.Thr549Pro)
c.*1521A>C (n.*1521A>C)
c.1540A>C (p.Thr514Pro)
Xg.154957065C>ACA519358622F8c.1644G>T (p.Leu548=)
c.*1520G>T (n.*1520G>T)
c.1539G>T (p.Leu513=)
gnomAD v4
Xg.154957065C>GCA519358626F8c.1644G>C (p.Leu548=)
c.*1520G>C (n.*1520G>C)
c.1539G>C (p.Leu513=)
Xg.154957065C>TCA519358624F8c.1644G>A (p.Leu548=)
c.*1520G>A (n.*1520G>A)
c.1539G>A (p.Leu513=)
Xg.154957066A>CCA414911852F8c.1643T>G (p.Leu548Arg)
c.*1519T>G (n.*1519T>G)
c.1538T>G (p.Leu513Arg)
Xg.154957066A>GCA16609330F8c.1643T>C (p.Leu548Pro)
c.*1519T>C (n.*1519T>C)
c.1538T>C (p.Leu513Pro)
Xg.154957066A>TCA414911854F8c.1643T>A (p.Leu548Gln)
c.*1519T>A (n.*1519T>A)
c.1538T>A (p.Leu513Gln)
Xg.154957067G>ACA519358632F8c.1642C>T (p.Leu548=)
c.*1518C>T (n.*1518C>T)
c.1537C>T (p.Leu513=)
Xg.154957067G>CCA414911856F8c.1642C>G (p.Leu548Val)
c.*1518C>G (n.*1518C>G)
c.1537C>G (p.Leu513Val)
COSMIC COSMIC
Xg.154957067G>TCA414911858F8c.1642C>A (p.Leu548Met)
c.*1518C>A (n.*1518C>A)
c.1537C>A (p.Leu513Met)
Xg.154957068G>ACA519358636F8c.1641C>T (p.Cys547=)
c.*1517C>T (n.*1517C>T)
c.1536C>T (p.Cys512=)
Xg.154957068G>CCA414911863F8c.1641C>G (p.Cys547Trp)
c.*1517C>G (n.*1517C>G)
c.1536C>G (p.Cys512Trp)
Xg.154957068G>TCA414911860F8c.1641C>A (p.Cys547Ter)
c.*1517C>A (n.*1517C>A)
c.1536C>A (p.Cys512Ter)
Xg.154957069C>ACA414911866F8c.1640G>T (p.Cys547Phe)
c.*1516G>T (n.*1516G>T)
c.1535G>T (p.Cys512Phe)
dbSNP
Xg.154957069C=CA2466845347F8c.1640G= (p.Cys547=)
c.*1516G= (n.*1516G=)
c.1535G= (p.Cys512=)
Xg.154957069C>GCA414911869F8c.1640G>C (p.Cys547Ser)
c.*1516G>C (n.*1516G>C)
c.1535G>C (p.Cys512Ser)
Xg.154957069C>TCA414911871F8c.1640G>A (p.Cys547Tyr)
c.*1516G>A (n.*1516G>A)
c.1535G>A (p.Cys512Tyr)
dbSNP
Xg.154957070A=CA2466845348F8c.1639T= (p.Cys547=)
c.*1515T= (n.*1515T=)
c.1534T= (p.Cys512=)
Xg.154957070A>CCA414911873F8c.1639T>G (p.Cys547Gly)
c.*1515T>G (n.*1515T>G)
c.1534T>G (p.Cys512Gly)
Xg.154957070A>GCA414911874F8c.1639T>C (p.Cys547Arg)
c.*1515T>C (n.*1515T>C)
c.1534T>C (p.Cys512Arg)
ClinVar dbSNP
Xg.154957070A>TCA10568426F8c.1639T>A (p.Cys547Ser)
c.*1515T>A (n.*1515T>A)
c.1534T>A (p.Cys512Ser)
dbSNP ExAC
Xg.154957071C>ACA519358649F8c.1638G>T (p.Arg546=)
c.*1514G>T (n.*1514G>T)
c.1533G>T (p.Arg511=)
Xg.154957071C=CA2466845349F8c.1638G= (p.Arg546=)
c.*1514G= (n.*1514G=)
c.1533G= (p.Arg511=)
Xg.154957071C>GCA519358650F8c.1638G>C (p.Arg546=)
c.*1514G>C (n.*1514G>C)
c.1533G>C (p.Arg511=)
COSMIC COSMIC
Xg.154957071C>TCA519358653F8c.1638G>A (p.Arg546=)
c.*1514G>A (n.*1514G>A)
c.1533G>A (p.Arg511=)
dbSNP gnomAD v2 gnomAD v4
Xg.154957072C>ACA414911876F8c.1637G>T (p.Arg546Leu)
c.*1513G>T (n.*1513G>T)
c.1532G>T (p.Arg511Leu)
Xg.154957072C=CA2466845350F8c.1637G= (p.Arg546=)
c.*1513G= (n.*1513G=)
c.1532G= (p.Arg511=)
Xg.154957072C>GCA414911879F8c.1637G>C (p.Arg546Pro)
c.*1513G>C (n.*1513G>C)
c.1532G>C (p.Arg511Pro)
Xg.154957072C>TCA10568427F8c.1637G>A (p.Arg546Gln)
c.*1513G>A (n.*1513G>A)
c.1532G>A (p.Arg511Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
Xg.154957073G>ACA255112F8c.1636C>T (p.Arg546Trp)
c.*1512C>T (n.*1512C>T)
c.1531C>T (p.Arg511Trp)
ClinVar dbSNP gnomAD v4
Xg.154957073G>CCA414911881F8c.1636C>G (p.Arg546Gly)
c.*1512C>G (n.*1512C>G)
c.1531C>G (p.Arg511Gly)
Xg.154957073G=CA2466845351F8c.1636C= (p.Arg546=)
c.*1512C= (n.*1512C=)
c.1531C= (p.Arg511=)
Xg.154957073G>TCA519358660F8c.1636C>A (p.Arg546=)
c.*1512C>A (n.*1512C>A)
c.1531C>A (p.Arg511=)
dbSNP gnomAD v4
Xg.154957074A>CCA519358665F8c.1635T>G (p.Pro545=)
c.*1511T>G (n.*1511T>G)
c.1530T>G (p.Pro510=)
Xg.154957074A>GCA519358663F8c.1635T>C (p.Pro545=)
c.*1511T>C (n.*1511T>C)
c.1530T>C (p.Pro510=)
Xg.154957074A>TCA519358661F8c.1635T>A (p.Pro545=)
c.*1511T>A (n.*1511T>A)
c.1530T>A (p.Pro510=)
COSMIC COSMIC
Xg.154957075G>ACA414911884F8c.1634C>T (p.Pro545Leu)
c.*1510C>T (n.*1510C>T)
c.1529C>T (p.Pro510Leu)

Number of alleles fetched