Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.6778468A>T | CA202297 | BMP2 | c.570A>T (p.Arg190Ser) c.102A>T (p.Arg34Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.6778468A>G | CA509817765 | BMP2 | c.570A>G (p.Arg190=) c.102A>G (p.Arg34=) | dbSNP |
20 | g.6778468A= | CA2348112131 | BMP2 | c.570A= (p.Arg190=) c.102A= (p.Arg34=) | dbSNP |