Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.39247226C>GCA9426137IFNL4c.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
19g.39247226C>ACA507655560IFNL4c.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
19g.39247226C>TCA507655561IFNL4c.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
19g.39247226C=CA2335423393IFNL4c.448G= (p.Ala150=)
c.447G= (p.Ser149=)
c.422+242G= (n.422+242G=)
c.232G= (p.Ala78=)
c.304G= (p.Ala102=)
n.725G=
dbSNP

Number of alleles fetched