Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673535C>G | CA397835662 | TP53 | c.993G>C (p.Gln331His) c.597G>C (p.Gln199His) c.714G>C (p.Gln238His) c.972G>C (p.Gln324His) c.782+646G>C (n.782+646G>C) c.53G>C c.876G>C (p.Gln292His) c.516G>C (p.Gln172His) c.960G>C (p.Gln320His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535C>T | CA10590137 | TP53 | c.993G>A (p.Gln331=) c.597G>A (p.Gln199=) c.714G>A (p.Gln238=) c.972G>A (p.Gln324=) c.782+646G>A (n.782+646G>A) c.53G>A c.876G>A (p.Gln292=) c.516G>A (p.Gln172=) c.960G>A (p.Gln320=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535C>A | CA287486501 | TP53 | c.993G>T (p.Gln331His) c.597G>T (p.Gln199His) c.714G>T (p.Gln238His) c.972G>T (p.Gln324His) c.782+646G>T (n.782+646G>T) c.53G>T c.876G>T (p.Gln292His) c.516G>T (p.Gln172His) c.960G>T (p.Gln320His) | dbSNP COSMIC COSMIC COSMIC COSMIC |