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: 0.01 (C)
Location

Chromosome 12:40320043 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1361433, COSM1361432 ; HGMD-PUBLIC CM084928

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_ExomeChip

About this variant

This variant overlaps 12 transcripts, has 2506 sample genotypes, is associated with 1 phenotype and is mentioned in 11 citations.

Variant displays