Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.39247226C>G | CA9426137 | IFNL4 | c.448G>C (p.Ala150Pro) c.447G>C (p.Ser149=) c.422+242G>C (n.422+242G>C) c.232G>C (p.Ala78Pro) c.304G>C (p.Ala102Pro) n.725G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.39247226C>A | CA507655560 | IFNL4 | c.448G>T (p.Ala150Ser) c.447G>T (p.Ser149=) c.422+242G>T (n.422+242G>T) c.232G>T (p.Ala78Ser) c.304G>T (p.Ala102Ser) n.725G>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.39247226C>T | CA507655561 | IFNL4 | c.448G>A (p.Ala150Thr) c.447G>A (p.Ser149=) c.422+242G>A (n.422+242G>A) c.232G>A (p.Ala78Thr) c.304G>A (p.Ala102Thr) n.725G>A | dbSNP gnomAD v4 |
19 | g.39247226C= | CA2335423393 | IFNL4 | c.448G= (p.Ala150=) c.447G= (p.Ser149=) c.422+242G= (n.422+242G=) c.232G= (p.Ala78=) c.304G= (p.Ala102=) n.725G= | dbSNP |