Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.46357717G>A | CA119415 | CCR2 | c.190G>A (p.Val64Ile) n.315-400G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.46357717G= | CA1362075544 | CCR2 | c.190G= (p.Val64=) n.315-400G= | dbSNP |
3 | g.46357717G>T | CA352466533 | CCR2 | c.190G>T (p.Val64Phe) n.315-400G>T | dbSNP gnomAD v4 |