| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.9094987C>T | CA127863 | A2M,KLRG1 | c.2111G>A (p.Arg704His) n.348+6563G>A c.430G>A (n.430G>A) c.1811G>A (p.Arg604His) c.1661G>A (p.Arg554His) c.*34-30387C>T (n.*34-30387C>T) c.*33+36821C>T (n.*33+36821C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.9094987C= | CA2015339309 | A2M,KLRG1 | c.2111G= (p.Arg704=) n.348+6563G= c.430G= (n.430G=) c.1811G= (p.Arg604=) c.1661G= (p.Arg554=) c.*34-30387C= (n.*34-30387C=) c.*33+36821C= (n.*33+36821C=) | dbSNP |