Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154956961T>ACA414911610F8c.1748A>T (p.Asn583Ile)
c.*1624A>T (p.=)
c.1643A>T (p.Asn548Ile)
Xg.154956961T>CCA10568415F8c.1748A>G (p.Asn583Ser)
c.*1624A>G (p.=)
c.1643A>G (p.Asn548Ser)
ClinVar dbSNP ExAC gnomAD
Xg.154956961T>GCA414911611F8c.1748A>C (p.Asn583Thr)
c.*1624A>C (p.=)
c.1643A>C (p.Asn548Thr)
Xg.154956961T=CA2466845303F8c.1748A= (p.Asn583=)
c.*1624A= (p.=)
c.1643A= (p.Asn548=)
Xg.154956962T>ACA414911612F8c.1747A>T (p.Asn583Tyr)
c.*1623A>T (p.=)
c.1642A>T (p.Asn548Tyr)
Xg.154956962T>CCA414911613F8c.1747A>G (p.Asn583Asp)
c.*1623A>G (p.=)
c.1642A>G (p.Asn548Asp)
Xg.154956962T>GCA337332843F8c.1747A>C (p.Asn583His)
c.*1623A>C (p.=)
c.1642A>C (p.Asn548His)
dbSNP
Xg.154956962T=CA2466845304F8c.1747A= (p.Asn583=)
c.*1623A= (p.=)
c.1642A= (p.Asn548=)
Xg.154956963T>ACA519358217F8c.1746A>T (p.Gly582=)
c.*1622A>T (p.=)
c.1641A>T (p.Gly547=)
Xg.154956963T>CCA519358215F8c.1746A>G (p.Gly582=)
c.*1622A>G (p.=)
c.1641A>G (p.Gly547=)
Xg.154956963T>GCA519358214F8c.1746A>C (p.Gly582=)
c.*1622A>C (p.=)
c.1641A>C (p.Gly547=)
Xg.154956964C>ACA414911615F8c.1745G>T (p.Gly582Val)
c.*1621G>T (p.=)
c.1640G>T (p.Gly547Val)
Xg.154956964C>GCA414911616F8c.1745G>C (p.Gly582Ala)
c.*1621G>C (p.=)
c.1640G>C (p.Gly547Ala)
Xg.154956964C>TCA414911614F8c.1745G>A (p.Gly582Glu)
c.*1621G>A (p.=)
c.1640G>A (p.Gly547Glu)
COSMIC COSMIC
Xg.154956965C>ACA414911617F8c.1744G>T (p.Gly582Ter)
c.*1620G>T (p.=)
c.1639G>T (p.Gly547Ter)
Xg.154956965C>GCA414911618F8c.1744G>C (p.Gly582Arg)
c.*1620G>C (p.=)
c.1639G>C (p.Gly547Arg)
Xg.154956965C>TCA414911619F8c.1744G>A (p.Gly582Arg)
c.*1620G>A (p.=)
c.1639G>A (p.Gly547Arg)
Xg.154956966T>ACA414911620F8c.1743A>T (p.Arg581Ser)
c.*1619A>T (p.=)
c.1638A>T (p.Arg546Ser)
Xg.154956966T>CCA519358226F8c.1743A>G (p.Arg581=)
c.*1619A>G (p.=)
c.1638A>G (p.Arg546=)
Xg.154956966T>GCA414911621F8c.1743A>C (p.Arg581Ser)
c.*1619A>C (p.=)
c.1638A>C (p.Arg546Ser)
Xg.154956967C>ACA414911622F8c.1742G>T (p.Arg581Ile)
c.*1618G>T (p.=)
c.1637G>T (p.Arg546Ile)
COSMIC COSMIC
Xg.154956967C>GCA414911623F8c.1742G>C (p.Arg581Thr)
c.*1618G>C (p.=)
c.1637G>C (p.Arg546Thr)
Xg.154956967C>TCA414911624F8c.1742G>A (p.Arg581Lys)
c.*1618G>A (p.=)
c.1637G>A (p.Arg546Lys)
Xg.154956968T>ACA414911625F8c.1741A>T (p.Arg581Ter)
c.*1617A>T (p.=)
c.1636A>T (p.Arg546Ter)
Xg.154956968T>CCA414911626F8c.1741A>G (p.Arg581Gly)
c.*1617A>G (p.=)
c.1636A>G (p.Arg546Gly)
Xg.154956968T>GCA519358235F8c.1741A>C (p.Arg581=)
c.*1617A>C (p.=)
c.1636A>C (p.Arg546=)
Xg.154956969T>ACA414911627F8c.1740A>T (p.Gln580His)
c.*1616A>T (p.=)
c.1635A>T (p.Gln545His)
Xg.154956969T>CCA519358238F8c.1740A>G (p.Gln580=)
c.*1616A>G (p.=)
c.1635A>G (p.Gln545=)
Xg.154956969T>GCA414911628F8c.1740A>C (p.Gln580His)
c.*1616A>C (p.=)
c.1635A>C (p.Gln545His)
Xg.154956970T>ACA414911631F8c.1739A>T (p.Gln580Leu)
c.*1615A>T (p.=)
c.1634A>T (p.Gln545Leu)
Xg.154956970T>CCA414911629F8c.1739A>G (p.Gln580Arg)
c.*1615A>G (p.=)
c.1634A>G (p.Gln545Arg)
Xg.154956970T>GCA414911630F8c.1739A>C (p.Gln580Pro)
c.*1615A>C (p.=)
c.1634A>C (p.Gln545Pro)
Xg.154956971G>ACA414911632F8c.1738C>T (p.Gln580Ter)
c.*1614C>T (p.=)
c.1633C>T (p.Gln545Ter)
Xg.154956971G>CCA414911633F8c.1738C>G (p.Gln580Glu)
c.*1614C>G (p.=)
c.1633C>G (p.Gln545Glu)
Xg.154956971G>TCA414911634F8c.1738C>A (p.Gln580Lys)
c.*1614C>A (p.=)
c.1633C>A (p.Gln545Lys)
Xg.154956972A>CCA414911635F8c.1737T>G (p.Asp579Glu)
c.*1613T>G (p.=)
c.1632T>G (p.Asp544Glu)
Xg.154956972A>GCA519358248F8c.1737T>C (p.Asp579=)
c.*1613T>C (p.=)
c.1632T>C (p.Asp544=)
Xg.154956972A>TCA414911636F8c.1737T>A (p.Asp579Glu)
c.*1613T>A (p.=)
c.1632T>A (p.Asp544Glu)
Xg.154956973T>ACA414911637F8c.1736A>T (p.Asp579Val)
c.*1612A>T (p.=)
c.1631A>T (p.Asp544Val)
Xg.154956973T>CCA414911638F8c.1736A>G (p.Asp579Gly)
c.*1612A>G (p.=)
c.1631A>G (p.Asp544Gly)
Xg.154956973T>GCA414911639F8c.1736A>C (p.Asp579Ala)
c.*1612A>C (p.=)
c.1631A>C (p.Asp544Ala)
Xg.154956974C>ACA414911640F8c.1735G>T (p.Asp579Tyr)
c.*1611G>T (p.=)
c.1630G>T (p.Asp544Tyr)
Xg.154956974C>GCA414911641F8c.1735G>C (p.Asp579His)
c.*1611G>C (p.=)
c.1630G>C (p.Asp544His)
Xg.154956974C>TCA414911642F8c.1735G>A (p.Asp579Asn)
c.*1611G>A (p.=)
c.1630G>A (p.Asp544Asn)
Xg.154956975T>ACA519358260F8c.1734A>T (p.Val578=)
c.*1610A>T (p.=)
c.1629A>T (p.Val543=)
Xg.154956975T>CCA519358262F8c.1734A>G (p.Val578=)
c.*1610A>G (p.=)
c.1629A>G (p.Val543=)
Xg.154956975T>GCA519358264F8c.1734A>C (p.Val578=)
c.*1610A>C (p.=)
c.1629A>C (p.Val543=)
Xg.154956975_154956977delinsTACCA2466845305F8c.1732_1734delinsGTA (p.Val578=)
c.*1608_*1610delinsGTA (p.=)
c.1627_1629delinsGTA (p.Val543=)
Xg.154956976A>CCA414911643F8c.1733T>G (p.Val578Gly)
c.*1609T>G (p.=)
c.1628T>G (p.Val543Gly)
Xg.154956976A>GCA414911645F8c.1733T>C (p.Val578Ala)
c.*1609T>C (p.=)
c.1628T>C (p.Val543Ala)

Number of alleles fetched