Original source

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

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

Chromosome 11:36574985 (forward strand) | View in location tab


with COSMIC COSM415610 (C/A), COSM542386 (C/T) ; HGMD-PUBLIC CM981695 ; PhenCode RAG1base_RAG1_DNA:g.7973C>T (C/T), RAG1base_HSRAG1:g.1793C>T (C/T)

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

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

Variation displays