| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.9079755C>T | CA127860 | A2M,KLRG1 | c.2915G>A (p.Cys972Tyr) n.270G>A n.451+10157G>A n.349-7034G>A c.2615G>A (p.Cys872Tyr) c.2465G>A (p.Cys822Tyr) c.*33+21589C>T (n.*33+21589C>T) | ClinVar dbSNP gnomAD v4 |
| 12 | g.9079755C= | CA2015332159 | A2M,KLRG1 | c.2915G= (p.Cys972=) n.270G= n.451+10157G= n.349-7034G= c.2615G= (p.Cys872=) c.2465G= (p.Cys822=) c.*33+21589C= (n.*33+21589C=) | dbSNP |