Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14817, 2009_August_001_061_NF2_607379_0009

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

Variation displays