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

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

Chromosome 4:154586093 (forward strand)|View in location tab

Most severe consequence
Stop gained
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 10 transcripts and has 270 sample genotypes.

Variant displays