Most severe consequence
22
synonymous variant
Alleles
C/T|Highest population MAF: 0.12
Change tolerance
CADD: T:6.205
Location
Chromosome 11:194441 (forward strand)|VCF:11 194441 rs61997072 C T
Co-located variant
COSMIC COSV57293255
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Genotyping chips
This variant has assays on: Illumina_HumanOmni5, Illumina_HumanOmni2.5
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 and is mentioned in 1 citation.
