This variant has been flagged

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

Original source

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

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

Chromosome 1:148808592 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB NC_000001.9:g.143787132G>A

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 12 transcripts and 1 regulatory feature.

Variant displays