Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673802C>G | CA10580917 | TP53 | c.818G>C (p.Arg273Pro) c.422G>C (p.Arg141Pro) c.539G>C (p.Arg180Pro) c.797G>C (p.Arg266Pro) c.782+379G>C (n.782+379G>C) c.701G>C (p.Arg234Pro) c.341G>C (p.Arg114Pro) c.785G>C (p.Arg262Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673802C>T | CA000434 | TP53 | c.818G>A (p.Arg273His) c.422G>A (p.Arg141His) c.539G>A (p.Arg180His) c.797G>A (p.Arg266His) c.782+379G>A (n.782+379G>A) c.701G>A (p.Arg234His) c.341G>A (p.Arg114His) c.785G>A (p.Arg262His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673802C>A | CA001530 | TP53 | c.818G>T (p.Arg273Leu) c.422G>T (p.Arg141Leu) c.539G>T (p.Arg180Leu) c.797G>T (p.Arg266Leu) c.782+379G>T (n.782+379G>T) c.701G>T (p.Arg234Leu) c.341G>T (p.Arg114Leu) c.785G>T (p.Arg262Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |