Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 11:119278181 (forward strand) | View in location tab

Co-located

with COSMIC COSM34053 (T/G), COSM34052 (T/C) ; HGMD-PUBLIC CM105459, CM099544

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 2 transcripts and is associated with 3 phenotypes.

Variant displays