Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 11:36575514 (forward strand) | View in location tab


with COSMIC COSM1470480 (G/A) ; HGMD-PUBLIC CM981696 ; PhenCode RAG1base_RAG1_DNA:g.8502G>A (G/A), RAG1base_HSRAG1:g.2322G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 5 phenotypes.

Variation displays