Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130872903C>TCA467395081ABL1c.1008C>T (p.Phe336=)
c.951C>T (p.Phe317=)
dbSNP gnomAD v4
9g.130872903C>GCA16602555ABL1c.1008C>G (p.Phe336Leu)
c.951C>G (p.Phe317Leu)
ClinVar dbSNP COSMIC
9g.130872903C>ACA16602554ABL1c.1008C>A (p.Phe336Leu)
c.951C>A (p.Phe317Leu)
ClinVar dbSNP COSMIC

Number of alleles fetched