Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.75733629G>TCA16040778ACADMc.387+1G>T (p.=)
c.399+1G>T (p.=)
c.279+1G>T (p.=)
c.486+1G>T (p.=)
c.-100+707G>T (p.=)
c.*54+707G>T (p.=)
c.*171+1G>T (p.=)
c.*155+1G>T (p.=)
n.296+707G>T
c.118+5141G>T (p.=)
c.*151+1G>T (p.=)
c.286+707G>T (p.=)
ClinVar dbSNP COSMIC COSMIC
1g.75733629G>ACA16040777ACADMc.387+1G>A (p.=)
c.399+1G>A (p.=)
c.279+1G>A (p.=)
c.486+1G>A (p.=)
c.-100+707G>A (p.=)
c.*54+707G>A (p.=)
c.*171+1G>A (p.=)
c.*155+1G>A (p.=)
n.296+707G>A
c.118+5141G>A (p.=)
c.*151+1G>A (p.=)
c.286+707G>A (p.=)
ClinVar dbSNP

Number of alleles fetched