Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

A/G | Ancestral: A | Ambiguity code: R

Chromosome 11:36576039 (forward strand) | View in location tab


with COSMIC COSM314666 (A/T) ; HGMD-PUBLIC CM981697 ; PhenCode RAG1base_HSRAG1:g.2847A>G (A/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variant displays