Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.89333553G>A | CA10602212 | POLG,POLGARF | c.202C>T (p.Gln68Ter) c.257C>T (p.Ala86Val) n.400C>T | ClinVar dbSNP gnomAD v4 |
15 | g.89333553G= | CA2194572970 | POLG,POLGARF | c.202C= (p.Gln68=) c.257C= (p.Ala86=) n.400C= | dbSNP |