Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)
Location

Chromosome 1:237678090 (forward strand) | View in location tab

Co-located

with COSMIC COSM3751034 (A/G), COSM3751033 (A/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2508 sample genotypes, is associated with 3 phenotypes and is mentioned in 6 citations.

Variant displays