Variant #0000691174 (NC_000011.9:g.6943128_6943130dup, ZNF215(NM_013250.2):c.-5114_-5112dup)

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.6943128_6943130dup
DNA change (hg38) -
Published as OR2D3(NM_001004684.1):c.895_896insCAA (p.(Pro299_Met300insThr)), OR2D3(NM_001004684.1):c.896_898dupCAA (p.P299_M300insT)
ISCN -
DB-ID OR2D3_000001 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2D3 NM_001004684.1 ?/. - c.896_898dup r.(?) p.(Pro299_Met300insThr)
ZNF215 NM_013250.2 ?/. - c.-5114_-5112dup r.(?) p.(=)