Original source

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

T/G|Ancestral: T|Ambiguity code: K

Chromosome 11:36576118 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM961218 ; PhenCode RAG1base_HSRAG1:g.2926T>G (T/G)

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 5134, 2010_April_001_266_RAG1_179615_0003

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays