Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43120144T>GCA008989RETc.2275T>G (p.Ser759Ala)
n.2245T>G
n.2236T>G
c.2671T>G (p.Ser891Ala)
c.*1265T>G (n.*1265T>G)
c.*20T>G (n.*20T>G)
c.1909T>G (p.Ser637Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.43120144T=CA1905819918RETc.2275T= (p.Ser759=)
n.2245T=
n.2236T=
c.2671T= (p.Ser891=)
c.*1265T= (n.*1265T=)
c.*20T= (n.*20T=)
c.1909T= (p.Ser637=)
dbSNP

Number of alleles fetched