Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862969G>CCA16602548ABL1c.813G>C (p.Gln271His)
c.756G>C (p.Gln252His)
ClinVar dbSNP COSMIC
9g.130862969G>ACA467496369ABL1c.813G>A (p.Gln271=)
c.756G>A (p.Gln252=)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862969G>TCA16602549ABL1c.813G>T (p.Gln271His)
c.756G>T (p.Gln252His)
ClinVar dbSNP COSMIC

Number of alleles fetched