Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 10:23193805 (forward strand)|View in location tab

Co-located variants

COSMIC COSM917084 ; HGMD-PUBLIC CM043069

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14692, 2010_April_001_090_PTF1A_607194_0001

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and is associated with 2 phenotypes.

Variant displays