Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 5:35873559 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1695579

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB IL7R_617G_A_031511

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and is associated with 1 phenotype.

Variant displays