Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.72350518C>GCA16044204HEXAc.805G>C (p.Gly269Arg)
c.413-4193G>C (p.=)
n.738G>C (p.=)
c.838G>C (p.Gly280Arg)
c.*215G>C (p.=)
n.677G>C
c.*326G>C (p.=)
n.6209G>C
n.1306G>C
n.847G>C
ClinVar dbSNP
15g.72350518C>TCA116500HEXAc.805G>A (p.Gly269Ser)
c.413-4193G>A (p.=)
n.738G>A (p.=)
c.838G>A (p.Gly280Ser)
c.*215G>A (p.=)
n.677G>A
c.*326G>A (p.=)
n.6209G>A
n.1306G>A
n.847G>A
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched