Genomic variant #0000322055

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6943128_6943130dup
DNA change (hg38) -
Published as ZNF215:NM_001004684.1:c.895_896insCAA, NM_013250.2:c.-5115_-5114insCAA
ISCN -
DB-ID OR2D3_000001
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Leiden




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
OR2D3 NM_001004684.1 ?/. - c.896_898dup VUS - -