Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.144415295G>ACA116329SLC39A4c.599C>T (p.Pro200Leu)
c.524C>T (p.Pro175Leu)
c.317C>T (p.Pro106Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.144415295G>CCA372624654SLC39A4c.599C>G (p.Pro200Arg)
c.524C>G (p.Pro175Arg)
c.317C>G (p.Pro106Arg)
dbSNP gnomAD v4
8g.144415295G=CA1826307691SLC39A4c.599C= (p.Pro200=)
c.524C= (p.Pro175=)
c.317C= (p.Pro106=)
dbSNP

Number of alleles fetched