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 22:29661313 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1578860, COSM22000 ; HGMD-PUBLIC CD931032, CM930515

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14817, 2009_August_001_061_NF2_607379_0009

HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays