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 19:41978041 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3389055 ; HGMD-PUBLIC CM042305

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_152296.3:c.1838C>T, 5376

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays