Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.96287959C>ACA261210SNRNP200c.3269G>T (p.Arg1090Leu)
n.386G>T
ClinVar dbSNP
2g.96287959C>TCA1778496SNRNP200c.3269G>A (p.Arg1090Gln)
n.386G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.96287959C=CA1272537754SNRNP200c.3269G= (p.Arg1090=)
n.386G=
dbSNP

Number of alleles fetched