Original source

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

C/T|Ancestral: C|Ambiguity code: Y

Chromosome 5:35871070 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3615740 ; HGMD-PUBLIC CM002997 ; PhenCode IL7Rbase_D0050:g.15116C>T (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 3504, 2010_April_001_028_IL7R_146661_0005

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 2 phenotypes.

Variant displays