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 11:36575825 (forward strand) | View in location tab


with HGMD-PUBLIC CM010080 ; PhenCode RAG1base_RAG1_DNA:g.8813C>T (C/T), RAG1base_HSRAG1:g.2633C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays