Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130873027T>CCA16602581ABL1c.1132T>C (p.Phe378Leu)
c.1075T>C (p.Phe359Leu)
ClinVar dbSNP
9g.130873027T>GCA16602557ABL1c.1132T>G (p.Phe378Val)
c.1075T>G (p.Phe359Val)
ClinVar dbSNP COSMIC
9g.130873027T>ACA16602580ABL1c.1132T>A (p.Phe378Ile)
c.1075T>A (p.Phe359Ile)
ClinVar dbSNP COSMIC

Number of alleles fetched