This variant has been flagged

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

Original source

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

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

Chromosome 12:56663421 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3190098, rs386513775

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad

About this variant

This variant overlaps 14 transcripts and has 2 sample genotypes.

Variant displays