Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43120185C>ACA040485RETc.2316C>A (p.Ser772=)
n.2286C>A
n.2277C>A
c.2712C>A (p.Ser904=)
c.*1306C>A (n.*1306C>A)
c.*61C>A (n.*61C>A)
c.1950C>A (p.Ser650=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.43120185C>GCA009034RETc.2316C>G (p.Ser772=)
n.2286C>G
n.2277C>G
c.2712C>G (p.Ser904=)
c.*1306C>G (n.*1306C>G)
c.*61C>G (n.*61C>G)
c.1950C>G (p.Ser650=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.43120185C>TCA469029015RETc.2316C>T (p.Ser772=)
n.2286C>T
n.2277C>T
c.2712C>T (p.Ser904=)
c.*1306C>T (n.*1306C>T)
c.*61C>T (n.*61C>T)
c.1950C>T (p.Ser650=)
dbSNP

Number of alleles fetched