Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.73173663A>TCA225022PSEN1c.436A>T (p.Met146Leu)
c.424A>T (p.Met142Leu)
c.160A>T (p.Met54Leu)
n.436A>T (p.Met146Leu)
n.424A>T (p.Met142Leu)
c.*380A>T (p.=)
ClinVar dbSNP
14g.73173663A>GCA258120PSEN1c.436A>G (p.Met146Val)
c.424A>G (p.Met142Val)
c.160A>G (p.Met54Val)
n.436A>G (p.Met146Val)
n.424A>G (p.Met142Val)
c.*380A>G (p.=)
ClinVar dbSNP
14g.73173663A>CCA341490PSEN1c.436A>C (p.Met146Leu)
c.424A>C (p.Met142Leu)
c.160A>C (p.Met54Leu)
n.436A>C (p.Met146Leu)
n.424A>C (p.Met142Leu)
c.*380A>C (p.=)
ClinVar dbSNP

Number of alleles fetched