Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.42 (C)
Location

Chromosome 3:49887507 (forward strand) | View in location tab

Co-located

with COSMIC COSM3736321 (T/C), COSM3736322 (T/C)

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 12 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2688 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays