Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.99583418G>A | CA440328604 | MTTP | c.294G>A (p.Glu98=) c.45G>A (p.Glu15=) c.*384G>A (n.*384G>A) c.324G>A (p.Glu108=) c.375G>A (p.Glu125=) c.*357G>A (n.*357G>A) | dbSNP |
4 | g.99583418G>C | CA3021799 | MTTP | c.294G>C (p.Glu98Asp) c.45G>C (p.Glu15Asp) c.*384G>C (n.*384G>C) c.324G>C (p.Glu108Asp) c.375G>C (p.Glu125Asp) c.*357G>C (n.*357G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.99583418G>T | CA102617498 | MTTP | c.294G>T (p.Glu98Asp) c.45G>T (p.Glu15Asp) c.*384G>T (n.*384G>T) c.324G>T (p.Glu108Asp) c.375G>T (p.Glu125Asp) c.*357G>T (n.*357G>T) | dbSNP |