Original source

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

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

Chromosome 11:119278181 (forward strand) | View in location tab

Co-located

with COSMIC COSM34052 (T/C), COSM34053 (T/G) ; HGMD-PUBLIC CM099544, CM105459

Most severe consequence
Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays