Most severe consequence
4
stop gained
Alleles
G/A/C/T|Ancestral: G
Change tolerance
CADD: A:31, C:27.8, T:42
Location
Chromosome 13:49033886 (forward strand)|VCF:13 49033886 rs137853295 G A,C,T
Co-located variants
COSMIC COSV57314492, COSV57302098 ; HGMD-PUBLIC CM920604
Evidence status 
Clinical significance
HGVS names
This variant has 18 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 2 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]