Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112452972A>G | CA16455939 | PTPN11 | c.333-223A>G (n.333-223A>G) c.330-223A>G (n.330-223A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.112452972A>T | CA2063742947 | PTPN11 | c.333-223A>T (n.333-223A>T) c.330-223A>T (n.330-223A>T) | dbSNP |