This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: G | Ambiguity code: N | MAF: 0.19 (G)
Location

Chromosome 19:40757498 (forward strand) | View in location tab

Co-located

with COSMIC COSM4000739 (A/G)

Most severe consequence
 
Missense variant
Evidence status

This variant has 45 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 30 transcripts and has 4068 sample genotypes.

Variant displays