Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 12:40298488 (forward strand)|View in location tab

Co-located variants

COSMIC COSM693216 ; HGMD-PUBLIC CS053469

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_198578.3:c.3342A>G

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts, has 1 sample genotype, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays