Most severe consequence
13
missense variant
Alleles
G/A/T|Highest population MAF: 0.28
Change tolerance
CADD: A:15.36, T:14.75
Location
Chromosome 11:193146 (forward strand)|VCF:11 193146 rs61736219 G A,T
Co-located variant
COSMIC COSV57292313
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Genotyping chips
This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 2 transcripts.
