Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 12:114385521 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971438, CM109115

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_122_TBX5_601620_0003, 10322

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays