Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135817964T>G | CA348607139 | LCT | c.1084A>C (p.Ile362Leu) | dbSNP gnomAD v4 |
2 | g.135817964T>C | CA1888447 | LCT | c.1084A>G (p.Ile362Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817964T>A | CA348607138 | LCT | c.1084A>T (p.Ile362Phe) | dbSNP |
2 | g.135817964T= | CA1290835002 | LCT | c.1084A= (p.Ile362=) | dbSNP |