Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (C)
Location

Chromosome 19:8974328 (forward strand) | View in location tab

Co-located

with COSMIC COSM3933274 (T/C), COSM3933273 (T/C)

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

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

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3766 sample genotypes.

Variant displays