Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66481830T>CCA16602654MAP2K1c.578T>C (p.Leu193Pro)
c.644T>C (p.Leu215Pro)
c.497T>C (p.Leu166Pro)
c.569-5398T>C (n.569-5398T>C)
n.1002T>C
c.695T>C (p.Leu232Pro)
c.569-3164T>C (n.569-3164T>C)
c.500T>C (p.Leu167Pro)
c.116T>C (p.Leu39Pro)
c.566T>C (p.Leu189Pro)
ClinVar dbSNP
15g.66481830T>ACA392936369MAP2K1c.578T>A (p.Leu193His)
c.644T>A (p.Leu215His)
c.497T>A (p.Leu166His)
c.569-5398T>A (n.569-5398T>A)
n.1002T>A
c.695T>A (p.Leu232His)
c.569-3164T>A (n.569-3164T>A)
c.500T>A (p.Leu167His)
c.116T>A (p.Leu39His)
c.566T>A (p.Leu189His)
dbSNP

Number of alleles fetched