Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.72021211G>ACA126901DHODHc.605G>A (p.Gly202Asp)
n.1485-1954G>A
n.522G>A
n.314-1954G>A
c.514-2934G>A
c.521G>A (p.Gly174Asp)
c.197G>A (p.Gly66Asp)
c.176G>A (p.Gly59Asp)
c.278G>A (p.Gly93Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.72021211G>CCA126900DHODHc.605G>C (p.Gly202Ala)
n.1485-1954G>C
n.522G>C
n.314-1954G>C
c.514-2934G>C
c.521G>C (p.Gly174Ala)
c.197G>C (p.Gly66Ala)
c.176G>C (p.Gly59Ala)
c.278G>C (p.Gly93Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched