Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.53906876T>G | CA344603 | PRKCG | c.2075T>G (p.Val692Gly) n.1476T>G c.1967T>G (p.Val656Gly) c.1166T>G (p.Val389Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53906876T>C | CA9640768 | PRKCG | c.2075T>C (p.Val692Ala) n.1476T>C c.1967T>C (p.Val656Ala) c.1166T>C (p.Val389Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53906876T>A | CA407420670 | PRKCG | c.2075T>A (p.Val692Glu) n.1476T>A c.1967T>A (p.Val656Glu) c.1166T>A (p.Val389Glu) | dbSNP gnomAD v2 gnomAD v4 |