Original source

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

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

Chromosome 4:154606868 (forward strand) | View in location tab

Co-located

with COSMIC COSM3409117 (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000004.10:g.155747470G>A

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and is associated with 1 phenotype.

Variant displays