Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)

Chromosome 10:87863158 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

Clinical significance


ClinVar SCV000149471

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays