Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 17:72122794 (forward strand) | View in location tab

Co-located

with COSMIC COSM437264 (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 4 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2829 sample genotypes and is associated with 1 phenotype.

Variant displays