Most severe consequence
12
Missense variant
Alleles
T/G|Ancestral: T|Highest population MAF: < 0.01
Location
Chromosome 1:150578489 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 12 HGVS names - Show
Synonyms
Uniprot VAR_054157
Genotyping chips
This variant has assays on: Illumina_ExomeChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 5 transcripts and 1 regulatory feature.
