Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 19:41970405 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4537615 ; HGMD-PUBLIC CM042308

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5381, SCV000053410, NM_152296.3:c.2401G>T

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, is associated with 4 phenotypes and is mentioned in 2 citations.

Variant displays