Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 19:15184323 (forward strand) | View in location tab

Co-located

with COSMIC COSM4131311 (G/A), COSM4131312 (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs57387743

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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 3817 sample genotypes and is mentioned in 3 citations.

Variant displays