Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.46 (C)
Location

Chromosome 3:52799789 (forward strand) | View in location tab

Co-located

with COSMIC COSM1617893 (C/A), COSM1617892 (C/A)

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2690 sample genotypes and is mentioned in 1 citation.

Variant displays