Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.141972905G>A | CA4520156 | MGAM,OR9A4,TAS2R38 | c.-3+26908G>A (n.-3+26908G>A) c.785C>T (p.Ala262Val) c.*25-13491G>A (n.*25-13491G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.141972905G= | CA115857 | MGAM,OR9A4,TAS2R38 | c.-3+26908G= (n.-3+26908G=) c.785C= (p.Ala262=) c.*25-13491G= (n.*25-13491G=) | dbSNP |
7 | g.141972905G>C | CA369564139 | MGAM,OR9A4,TAS2R38 | c.-3+26908G>C (n.-3+26908G>C) c.785C>G (p.Ala262Gly) c.*25-13491G>C (n.*25-13491G>C) | dbSNP |
7 | g.141972905G>T | CA369564138 | MGAM,OR9A4,TAS2R38 | c.-3+26908G>T (n.-3+26908G>T) c.785C>A (p.Ala262Asp) c.*25-13491G>T (n.*25-13491G>T) | dbSNP |