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

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.

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

Most severe consequence
Missense variant
Evidence status


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