Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.165992302G>ACA285192SCN1Ac.4973C>T (p.Thr1658Met)
c.4889C>T (p.Thr1630Met)
c.4940C>T (p.Thr1647Met)
n.176-23311G>A
c.4970C>T (p.Thr1657Met)
c.4937C>T (p.Thr1646Met)
c.4691C>T (p.Thr1564Met)
c.4886C>T (p.Thr1629Met)
c.2531C>T (p.Thr844Met)
n.5409C>T
n.5423C>T
n.5395C>T
n.4889C>T (p.Thr1630Met)
ClinVar dbSNP COSMIC COSMIC COSMIC
2g.165992302G>CCA284994SCN1Ac.4973C>G (p.Thr1658Arg)
c.4889C>G (p.Thr1630Arg)
c.4940C>G (p.Thr1647Arg)
n.176-23311G>C
c.4970C>G (p.Thr1657Arg)
c.4937C>G (p.Thr1646Arg)
c.4691C>G (p.Thr1564Arg)
c.4886C>G (p.Thr1629Arg)
c.2531C>G (p.Thr844Arg)
n.5409C>G
n.5423C>G
n.5395C>G
n.4889C>G (p.Thr1630Arg)
ClinVar dbSNP

Number of alleles fetched