Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.132334853C>A | CA446335133 | MIR3936HG,SLC22A4 | c.1182C>A (p.Thr394=) n.634G>T c.654C>A (p.Thr218=) c.906C>A (p.Thr302=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.132334853C>G | CA3403605 | MIR3936HG,SLC22A4 | c.1182C>G (p.Thr394=) n.634G>C c.654C>G (p.Thr218=) c.906C>G (p.Thr302=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.132334853C>T | CA446335143 | MIR3936HG,SLC22A4 | c.1182C>T (p.Thr394=) n.634G>A c.654C>T (p.Thr218=) c.906C>T (p.Thr302=) | dbSNP |