Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.3732998G>A | CA549687 | TP73 | c.1587G>A (p.Ala529=) c.1542G>A (p.Ala514=) c.1830G>A (p.Ala610=) c.*236G>A (n.*236G>A) c.*253G>A (n.*253G>A) c.1683G>A (p.Ala561=) c.1617G>A (p.Ala539=) n.989G>A c.1440G>A (p.Ala480=) c.1395G>A (p.Ala465=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
1 | g.3732998G= | CA1140174352 | TP73 | c.1587G= (p.Ala529=) c.1542G= (p.Ala514=) c.1830G= (p.Ala610=) c.*236G= (n.*236G=) c.*253G= (n.*253G=) c.1683G= (p.Ala561=) c.1617G= (p.Ala539=) n.989G= c.1440G= (p.Ala480=) c.1395G= (p.Ala465=) | dbSNP |