Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112450335C>T | CA261555 | PTPN11 | c.155C>T (p.Thr52Ile) c.152C>T (p.Thr51Ile) | ClinVar dbSNP gnomAD v4 COSMIC |
12 | g.112450335C>G | CA386777440 | PTPN11 | c.155C>G (p.Thr52Ser) c.152C>G (p.Thr51Ser) | dbSNP COSMIC |
12 | g.112450335C>A | CA386777437 | PTPN11 | c.155C>A (p.Thr52Asn) c.152C>A (p.Thr51Asn) | dbSNP |