Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.34256250T>A | CA399059946 | CCL2 | c.105T>A (p.Cys35Ter) n.966T>A n.43T>A | dbSNP gnomAD v4 |
17 | g.34256250T>C | CA8495435 | CCL2 | c.105T>C (p.Cys35=) n.966T>C n.43T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.34256250T= | CA2256959952 | CCL2 | c.105T= (p.Cys35=) n.966T= n.43T= | dbSNP |