Most severe consequence
12
Missense variant
Alleles
G/A|Ancestral: G|MAF: 0.02 (A)|Highest population MAF: 0.13
Location
Chromosome 10:133273262 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 16 HGVS names - Show
Synonyms
Uniprot VAR_061735
Genotyping chips
This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_ExomeChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 10 transcripts and has 2504 sample genotypes.
