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 14:36662968 (forward strand)|View in location tab

Co-located variants

COSMIC COSM39639 ; HGMD-PUBLIC CM032984

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_056_PAX9_167416_0008, 4529

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays