Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.75734850G>ACA252830ACADMc.447G>A (p.Met149Ile)
n.2571G>A
n.1409G>A
c.*215G>A (p.=)
c.31-5130G>A (p.=)
c.*213G>A (p.=)
c.*410G>A (p.=)
n.207+1928G>A
c.*31G>A (p.=)
n.3736G>A
c.286+1928G>A (p.=)
c.*361G>A (p.=)
c.*110G>A (p.=)
c.*114G>A (p.=)
c.*231G>A (p.=)
c.*314G>A (p.=)
c.*211G>A (p.=)
n.804G>A
c.*54+1928G>A (p.=)
n.669G>A
c.189G>A (p.Met63Ile)
n.1063G>A
c.546G>A (p.Met182Ile)
c.459G>A (p.Met153Ile)
n.220G>A
n.356G>A
c.119-5130G>A (p.=)
c.339G>A (p.Met113Ile)
c.-100+1928G>A (p.=)
ClinVar dbSNP
1g.75734850G>TCA913107ACADMc.447G>T (p.Met149Ile)
n.2571G>T
n.1409G>T
c.*215G>T (p.=)
c.31-5130G>T (p.=)
c.*213G>T (p.=)
c.*410G>T (p.=)
n.207+1928G>T
c.*31G>T (p.=)
n.3736G>T
c.286+1928G>T (p.=)
c.*361G>T (p.=)
c.*110G>T (p.=)
c.*114G>T (p.=)
c.*231G>T (p.=)
c.*314G>T (p.=)
c.*211G>T (p.=)
n.804G>T
c.*54+1928G>T (p.=)
n.669G>T
c.189G>T (p.Met63Ile)
n.1063G>T
c.546G>T (p.Met182Ile)
c.459G>T (p.Met153Ile)
n.220G>T
n.356G>T
c.119-5130G>T (p.=)
c.339G>T (p.Met113Ile)
c.-100+1928G>T (p.=)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched