Most severe consequence
12
Missense variant
Alleles
A/G|Ancestral: A|Highest population MAF: < 0.01
Location
Chromosome 15:48411229 (forward strand)|View in location tab
Co-located variant
HGMD-PUBLIC CM117734
Evidence status 
HGVS names
This variant has 10 HGVS names - Show
Synonyms
Uniprot VAR_066011
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 4 transcripts.
