Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.46373906C>G | CA2354770 | CCR5,CCR5AS | c.1004C>G (p.Ala335Gly) n.392-2489G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.46373906C>T | CA119358 | CCR5,CCR5AS | c.1004C>T (p.Ala335Val) n.392-2489G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.46373906C= | CA1362082836 | CCR5,CCR5AS | c.1004C= (p.Ala335=) n.392-2489G= | dbSNP |