Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.23 (A)
Location

Chromosome 16:55697923 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754933 (G/A), COSM3754932 (G/A)

Most severe consequence
Evidence status

Synonyms

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

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 3748 individual genotypes and is mentioned in 21 citations.

Variation displays