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 | MAF: 0.46 (T)

Chromosome 7:155458738 (forward strand) | View in location tab


with COSMIC COSM3762526 (C/T)

Most severe consequence
Evidence status


Uniprot VAR_021985

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 1366 individual genotypes and is mentioned in 4 citations.

Variation displays