Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.02 (A)
Location

Chromosome 5:1279324 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3723835

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_198253.2:c.2097C>T

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 6 transcripts, has 2595 sample genotypes and is associated with 1 phenotype.

Variant displays