Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.159316780C>ACA3538673IL12Bc.262G>T (p.Val88Phe)
c.*387G>T (n.*387G>T)
c.892G>T (p.Val298Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.159316780C=CA1595015835IL12Bc.262G= (p.Val88=)
c.*387G= (n.*387G=)
c.892G= (p.Val298=)
 dbSNP

Number of alleles fetched