Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.39022784A>TCA297272SOS1n.1524T>A
c.411T>A (p.Ser137Arg)
n.1865T>A
n.1651T>A
c.1533T>A (p.Ser511Arg)
c.1644T>A (p.Ser548Arg)
c.1737T>A (p.Ser579Arg)
c.1623T>A (p.Ser541Arg)
c.1620T>A (p.Ser540Arg)
c.1473T>A (p.Ser491Arg)
c.579T>A (p.Ser193Arg)
ClinVar dbSNP
2g.39022784A=CA1246139530SOS1n.1524T=
c.411T= (p.Ser137=)
n.1865T=
n.1651T=
c.1533T= (p.Ser511=)
c.1644T= (p.Ser548=)
c.1737T= (p.Ser579=)
c.1623T= (p.Ser541=)
c.1620T= (p.Ser540=)
c.1473T= (p.Ser491=)
c.579T= (p.Ser193=)
dbSNP

Number of alleles fetched