Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 22:30057302 (forward strand) | View in location tab

Co-located

with COSMIC COSM22000 (C/T), COSM1578860 (C/T) ; HGMD-PUBLIC CD931032, CM930515

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14817, 2009_August_001_061_NF2_607379_0009

This variation has 29 HGVS names - click the plus to show

Variation displays