This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: 0.29 (A)
Location

Chromosome 7:55161562 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3721608 ; HGMD-PUBLIC CM942312

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 7 synonyms - Show

HGVS names

This variant has 48 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 24 transcripts, has 3857 sample genotypes, is associated with 1 phenotype and is mentioned in 33 citations.

Variant displays