Most severe consequence
13
missense variant
Alleles
C/G/T|Ancestral: C|Highest population MAF: < 0.01
Change tolerance
CADD: G:26.7, T:29.1
Location
Chromosome 12:103246597 (forward strand)|VCF:12 103246597 rs62508698 C G,T
Co-located variants
COSMIC COSV61016380 ; HGMD-PUBLIC CM890094
Evidence status 
Clinical significance
HGVS names
This variant has 12 HGVS names - Show
Synonyms
This variant has 8 synonyms - Show
Genotyping chips
This variant has assays on: Illumina_HumanOmni1-Quad
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 3 transcripts, is associated with 6 phenotypes and is mentioned in 19 citations.
Description from SNPedia
Description not available [More information from SNPedia]