This variant has been flagged

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

Original source

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

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

Chromosome 3:184375988 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 32 transcripts and has 2 sample genotypes.

Variant displays