Original source

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

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

Chromosome 4:73404394 (forward strand) | View in location tab

Co-located

with COSMIC COSM3605659 (C/T) ; HGMD-PUBLIC CM900010

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB MalmoI

This variant has 21 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays