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 16:20336704 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 10 transcripts and has 268 sample genotypes.

Variant displays