Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.23 (C)
Location

Chromosome 5:161854239 (forward strand) | View in location tab

Co-located

with COSMIC COSM4003435 (T/C)

Most severe consequence
Evidence status

Clinical significance

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

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2614 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays