| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.73418244G>A | CA127974 | ALB | c.1585G>A (p.Glu529Lys) c.1240G>A (p.Glu414Lys) c.1009G>A (p.Glu337Lys) c.*864G>A (n.*864G>A) n.239G>A c.1135G>A (p.Glu379Lys) n.1132G>A c.1118G>A c.946G>A (p.Glu316Lys) | ClinVar dbSNP COSMIC |
| 4 | g.73418244G>C | CA357244978 | ALB | c.1585G>C (p.Glu529Gln) c.1240G>C (p.Glu414Gln) c.1009G>C (p.Glu337Gln) c.*864G>C (n.*864G>C) n.239G>C c.1135G>C (p.Glu379Gln) n.1132G>C c.1118G>C c.946G>C (p.Glu316Gln) | dbSNP |
| 4 | g.73418244G= | CA1468146932 | ALB | c.1585G= (p.Glu529=) c.1240G= (p.Glu414=) c.1009G= (p.Glu337=) c.*864G= (n.*864G=) n.239G= c.1135G= (p.Glu379=) n.1132G= c.1118G= c.946G= (p.Glu316=) | dbSNP |