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 22:29668405 (forward strand) | View in location tab

Co-located

with COSMIC COSM1717398 (C/T) ; HGMD-PUBLIC CM941102

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_062_NF2_607379_0010, 14818

This variant has 27 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variant displays