Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 22:29681443 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1142979 ; HGMD-PUBLIC CM941107

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_070_NF2_607379_0015, 14823

HGVS names

This variant has 26 HGVS names - Show

About this variant

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

Variant displays