Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 5:228281 (forward strand) | View in location tab

Co-located

with COSMIC COSM247233 (G/C)

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 1 sample genotype.

Variant displays