Most severe consequence
12
Missense variant
Alleles
C/T|Ancestral: C|MAF: 0.01 (T)|Highest population MAF: 0.05
Location
Chromosome 10:133273956 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 20 HGVS names - Show
Synonyms
Uniprot VAR_059760
Genotyping chips
This variant has assays on: 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 14 transcripts and has 2507 sample genotypes.
