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 | MAF: < 0.01 (T)
Location

Chromosome 7:140015766 (forward strand) | View in location tab

Co-located

with COSMIC COSM129632 (C/T)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_014160

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays