Most severe consequence
4
stop gained
Alleles
C/A/G/T|Ancestral: C
Change tolerance
CADD: A:35, G:18.61, T:22.2|GERP: -0.21
Location
Chromosome 16:23635180 (forward strand)|VCF:16 23635180 rs1060502785 C A,G,T
Co-located variants
COSMIC COSV55171183, COSV105056633
Evidence status 
Clinical significance
HGVS names
This variant has 21 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 3 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]
