Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

COSMIC COSM3409117

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000004.10:g.155747470G>A

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 11 transcripts.

Variant displays