Most severe consequence
12
Missense variant
Alleles
T/C|Ancestral: T|Highest population MAF: < 0.01
Location
Chromosome 22:43129265 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 5 HGVS names - Show
Synonyms
Uniprot VAR_029180
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 3 transcripts, 1 regulatory feature, has 1 sample genotype and is mentioned in 1 citation.
