Most severe consequence
12
Missense variant
Alleles
G/T|Ancestral: G|Highest population MAF: < 0.01
Location
Chromosome 19:1399019 (forward strand)|View in location tab
Co-located variants
COSMIC COSM3281262, COSM3281261
Evidence status 
HGVS names
This variant has 14 HGVS names - Show
Synonyms
Uniprot VAR_075298
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 21 transcripts.
