This variant has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 7:55200351 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_019299

HGVS names

This variant has 36 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts, has 86 sample genotypes and is mentioned in 2 citations.

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