Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.151289853C>TCA1088645ZNF687c.2810C>T (p.Pro937Leu)
c.1618C>T
c.*112C>T (n.*112C>T)
c.2837C>T (p.Pro946Leu)
c.2633C>T (p.Pro878Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.151289853C>GCA072935ZNF687c.2810C>G (p.Pro937Arg)
c.1618C>G
c.*112C>G (n.*112C>G)
c.2837C>G (p.Pro946Arg)
c.2633C>G (p.Pro878Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.151289853C>ACA1088644ZNF687c.2810C>A (p.Pro937His)
c.1618C>A
c.*112C>A (n.*112C>A)
c.2837C>A (p.Pro946His)
c.2633C>A (p.Pro878His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched