Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142179G>TCA357019VHLc.332G>T (p.Ser111Ile)
ClinVar dbSNP COSMIC
3g.10142179G>CCA351751328VHLc.332G>C (p.Ser111Thr)
dbSNP
3g.10142179G>ACA357091VHLc.332G>A (p.Ser111Asn)
ClinVar dbSNP gnomAD v4 COSMIC
3g.10142179G=CA1345066522VHLc.332G= (p.Ser111=)
dbSNP

Number of alleles fetched