Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.165046898T>ACA355052170SIc.1830A>T (p.Glu610Asp)
c.1731A>T (p.Glu577Asp)
3g.165046898T>CCA436706660SIc.1830A>G (p.Glu610=)
c.1731A>G (p.Glu577=)
gnomAD v4
3g.165046898T>GCA355052171SIc.1830A>C (p.Glu610Asp)
c.1731A>C (p.Glu577Asp)
3g.165046899T>ACA355052172SIc.1829A>T (p.Glu610Val)
c.1730A>T (p.Glu577Val)
3g.165046899T>CCA355052173SIc.1829A>G (p.Glu610Gly)
c.1730A>G (p.Glu577Gly)
3g.165046899T>GCA355052174SIc.1829A>C (p.Glu610Ala)
c.1730A>C (p.Glu577Ala)
3g.165046900C>ACA355052177SIc.1828G>T (p.Glu610Ter)
c.1729G>T (p.Glu577Ter)
3g.165046900C=CA1417400335SIc.1828G= (p.Glu610=)
c.1729G= (p.Glu577=)
3g.165046900C>GCA355052176SIc.1828G>C (p.Glu610Gln)
c.1729G>C (p.Glu577Gln)
3g.165046900C>TCA355052175SIc.1828G>A (p.Glu610Lys)
c.1729G>A (p.Glu577Lys)
ClinVar dbSNP
3g.165046901C>ACA355052179SIc.1827G>T (p.Trp609Cys)
c.1728G>T (p.Trp576Cys)
3g.165046901C=CA1417400338SIc.1827G= (p.Trp609=)
c.1728G= (p.Trp576=)
3g.165046901C>GCA355052178SIc.1827G>C (p.Trp609Cys)
c.1728G>C (p.Trp576Cys)
3g.165046901C>TCA2690935SIc.1827G>A (p.Trp609Ter)
c.1728G>A (p.Trp576Ter)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.165046902C>ACA355052180SIc.1826G>T (p.Trp609Leu)
c.1727G>T (p.Trp576Leu)
ClinVar gnomAD v4
3g.165046902C>GCA355052182SIc.1826G>C (p.Trp609Ser)
c.1727G>C (p.Trp576Ser)
3g.165046902C>TCA355052181SIc.1826G>A (p.Trp609Ter)
c.1727G>A (p.Trp576Ter)
COSMIC COSMIC
3g.165046903A=CA1417400343SIc.1825T= (p.Trp609=)
c.1726T= (p.Trp576=)
3g.165046903A>CCA355052183SIc.1825T>G (p.Trp609Gly)
c.1726T>G (p.Trp576Gly)
3g.165046903A>GCA355052184SIc.1825T>C (p.Trp609Arg)
c.1726T>C (p.Trp576Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.165046903A>TCA355052185SIc.1825T>A (p.Trp609Arg)
c.1726T>A (p.Trp576Arg)
3g.165046904T>ACA436706662SIc.1824A>T (p.Ser608=)
c.1725A>T (p.Ser575=)
dbSNP gnomAD v4
3g.165046904T>CCA436706661SIc.1824A>G (p.Ser608=)
c.1725A>G (p.Ser575=)
dbSNP
3g.165046904T>GCA2690936SIc.1824A>C (p.Ser608=)
c.1725A>C (p.Ser575=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.165046904T=CA1417400345SIc.1824A= (p.Ser608=)
c.1725A= (p.Ser575=)
3g.165046905G>ACA355052186SIc.1823C>T (p.Ser608Leu)
c.1724C>T (p.Ser575Leu)
gnomAD v4
3g.165046905G>CCA355052187SIc.1823C>G (p.Ser608Ter)
c.1724C>G (p.Ser575Ter)
3g.165046905G>TCA355052188SIc.1823C>A (p.Ser608Ter)
c.1724C>A (p.Ser575Ter)
3g.165046906A>CCA355052189SIc.1822T>G (p.Ser608Ala)
c.1723T>G (p.Ser575Ala)
3g.165046906A>GCA355052190SIc.1822T>C (p.Ser608Pro)
c.1723T>C (p.Ser575Pro)
gnomAD v4
3g.165046906A>TCA355052191SIc.1822T>A (p.Ser608Thr)
c.1723T>A (p.Ser575Thr)
3g.165046907A=CA1417400350SIc.1821T= (p.Ala607=)
c.1722T= (p.Ala574=)
3g.165046907A>CCA436706665SIc.1821T>G (p.Ala607=)
c.1722T>G (p.Ala574=)
3g.165046907A>GCA436706664SIc.1821T>C (p.Ala607=)
c.1722T>C (p.Ala574=)
gnomAD v4
3g.165046907A>TCA436706663SIc.1821T>A (p.Ala607=)
c.1722T>A (p.Ala574=)
dbSNP gnomAD v3 gnomAD v4
3g.165046908G>ACA355052194SIc.1820C>T (p.Ala607Val)
c.1721C>T (p.Ala574Val)
gnomAD v4
3g.165046908G>CCA355052193SIc.1820C>G (p.Ala607Gly)
c.1721C>G (p.Ala574Gly)
3g.165046908G>TCA355052192SIc.1820C>A (p.Ala607Asp)
c.1721C>A (p.Ala574Asp)
gnomAD v4
3g.165046909C>ACA355052195SIc.1819G>T (p.Ala607Ser)
c.1720G>T (p.Ala574Ser)
3g.165046909C>GCA355052196SIc.1819G>C (p.Ala607Pro)
c.1720G>C (p.Ala574Pro)
gnomAD v4
3g.165046909C>TCA355052197SIc.1819G>A (p.Ala607Thr)
c.1720G>A (p.Ala574Thr)
gnomAD v4
3g.165046910A>CCA436706666SIc.1818T>G (p.Thr606=)
c.1719T>G (p.Thr573=)
3g.165046910A>GCA436706668SIc.1818T>C (p.Thr606=)
c.1719T>C (p.Thr573=)
3g.165046910A>TCA436706667SIc.1818T>A (p.Thr606=)
c.1719T>A (p.Thr573=)
COSMIC
3g.165046911G>ACA2690937SIc.1817C>T (p.Thr606Ile)
c.1718C>T (p.Thr573Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.165046911G>CCA355052198SIc.1817C>G (p.Thr606Ser)
c.1718C>G (p.Thr573Ser)
gnomAD v4
3g.165046911G=CA1417400353SIc.1817C= (p.Thr606=)
c.1718C= (p.Thr573=)
3g.165046911G>TCA355052199SIc.1817C>A (p.Thr606Asn)
c.1718C>A (p.Thr573Asn)
dbSNP gnomAD v2 gnomAD v4
3g.165046912T>ACA355052200SIc.1816A>T (p.Thr606Ser)
c.1717A>T (p.Thr573Ser)
3g.165046912T>CCA355052201SIc.1816A>G (p.Thr606Ala)
c.1717A>G (p.Thr573Ala)

Number of alleles fetched