Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 19:16482518 (forward strand) | View in location tab

Co-located

with COSMIC COSM2150999 (C/T)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

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 5 transcripts and has 2806 individual genotypes.

Variation displays