Most severe consequence
28
intron variant
Alleles
T/A/C|Ancestral: T|Highest population MAF: 0.49
Change tolerance
CADD: A:8.210, C:8.788|GERP: -0.66
Location
Chromosome 14:73342516 (forward strand)|VCF:14 73342516 rs12586996 T A,C
Co-located variant
COSMIC COSV61832429
Evidence status 
HGVS names
This variant has 18 HGVS names - Show
Synonyms
ClinGen Allele Registry CA2146547742 (A), CA15815175 (C)
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 8 transcripts and has 3009 sample genotypes.
