Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.133354713A>G | CA16605654 | SURF1 | c.269T>C (p.Leu90Pro) n.215T>C c.-59T>C (n.-59T>C) | ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4 |
9 | g.133354713A= | CA1882636590 | SURF1 | c.269T= (p.Leu90=) n.215T= c.-59T= (n.-59T=) | dbSNP |