Original source

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

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

Chromosome 11:36575174 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010078 ; PhenCode RAG1base_HSRAG1:g.1982C>T (C/T), RAG1base_RAG1_DNA:g.8162C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_025982

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

Variation displays