Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: < 0.01 (A)
Location

Chromosome 4:154606833 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4404169 ; HGMD-PUBLIC CM900316

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays