Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.75740069T>CCA24627662ACADMc.558T>C (p.Asn186=)
c.570T>C (p.Asn190=)
c.450T>C (p.Asn150=)
c.657T>C (p.Asn219=)
c.-10T>C (p.=)
c.*144T>C (p.=)
c.*342T>C (p.=)
c.*326T>C (p.=)
n.331T>C
n.467T>C
c.*55T>C (p.=)
c.*322T>C (p.=)
c.*142T>C (p.=)
dbSNP
1g.75740069T>ACA247000ACADMc.558T>A (p.Asn186Lys)
c.570T>A (p.Asn190Lys)
c.450T>A (p.Asn150Lys)
c.657T>A (p.Asn219Lys)
c.-10T>A (p.=)
c.*144T>A (p.=)
c.*342T>A (p.=)
c.*326T>A (p.=)
n.331T>A
n.467T>A
c.*55T>A (p.=)
c.*322T>A (p.=)
c.*142T>A (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched