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 18:52752126 (forward strand) | View in location tab

Co-located

with COSMIC COSM106533 (G/A)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000018.8:g.48532494G>A

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

About this variant

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

Somatic mutation displays