Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 17:61480239 (forward strand) | View in location tab

Co-located

with COSMIC COSM3755736 (C/T)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3726 individual genotypes and is mentioned in 4 citations.

Variation displays