This variant has been flagged

None of the variant alleles match the reference allele (G)

Original source

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

A/C | Ancestral: G | Ambiguity code: M
Note: The reference base for this variant (A) does not match the Ensembl reference base (G) at this location.

Chromosome 12:40294866 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 836 sample genotypes and is mentioned in 1 citation.

Variant displays