Most severe consequence
4
stop gained
Alleles
G/A/C/T|Ancestral: G|Highest population MAF: < 0.01
Change tolerance
CADD: A:34, C:16.08, T:16.78|GERP: -0.07
Location
Chromosome 16:23635498 (forward strand)|VCF:16 23635498 rs1060502788 G A,C,T
Co-located variants
HGMD-PUBLIC CM1614211 ; dbSNP rs886039738 (G/-) ; COSMIC COSV55167570
Evidence status 
Clinical significance
HGVS names
This variant has 21 HGVS names - Show
Synonyms
This variant has 6 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 7 phenotypes and is mentioned in 3 citations.
Description from SNPedia
Description not available [More information from SNPedia]
