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

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

Chromosome 10:43113621 (forward strand) | View in location tab


with HGMD-PUBLIC CM020766, CM961242, CM961243

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 39 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, is associated with 6 phenotypes and is mentioned in 3 citations.

Variant displays