Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.156759301G>CCA362009512SGCDc.784G>C (p.Glu262Gln)
c.781G>C (p.Glu261Gln)
 dbSNP gnomAD v4
5g.156759301G>ACA340753SGCDc.784G>A (p.Glu262Lys)
c.781G>A (p.Glu261Lys)
 ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched