Original source

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

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

Chromosome 11:36575624 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM961216 ; PhenCode RAG1base_HSRAG1:g.2432G>T (G/T)

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 5133, 2010_April_001_265_RAG1_179615_0002

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 2 phenotypes.

Variant displays