Most severe consequence
12
Missense variant
Alleles
G/T|Ancestral: G
Location
Chromosome 22:17738107 (forward strand)|View in location tab
HGVS names
This variant has 37 HGVS names - Show
Synonyms
Uniprot VAR_025332
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 15 transcripts and has 1 sample genotype.
