Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51915293G>TCA16613819ACVRL1c.571G>T (p.Glu191Ter)
c.841G>T (p.Glu281Ter)
c.319G>T (p.Glu107Ter)
c.883G>T (p.Glu295Ter)
c.52G>T (p.Glu18Ter)
ClinVar dbSNP gnomAD v4
12g.51915293G>CCA384900515ACVRL1c.571G>C (p.Glu191Gln)
c.841G>C (p.Glu281Gln)
c.319G>C (p.Glu107Gln)
c.883G>C (p.Glu295Gln)
c.52G>C (p.Glu18Gln)
dbSNP gnomAD v3 gnomAD v4
12g.51915293G>ACA6573006ACVRL1c.571G>A (p.Glu191Lys)
c.841G>A (p.Glu281Lys)
c.319G>A (p.Glu107Lys)
c.883G>A (p.Glu295Lys)
c.52G>A (p.Glu18Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.51915293G=CA2036269446ACVRL1c.571G= (p.Glu191=)
c.841G= (p.Glu281=)
c.319G= (p.Glu107=)
c.883G= (p.Glu295=)
c.52G= (p.Glu18=)
dbSNP

Number of alleles fetched