Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.52397583G>A | CA199725 | THSD1 | c.670C>T (p.Arg224Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
13 | g.52397583G>C | CA6992161 | THSD1 | c.670C>G (p.Arg224Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.52397583G= | CA2091759483 | THSD1 | c.670C= (p.Arg224=) | dbSNP |