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 22:36292060 (forward strand) | View in location tab


with HGMD-PUBLIC CM014588, CM002373, CM010348

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 7 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, is associated with 7 phenotypes and is mentioned in 6 citations.

Variant displays