Variant #0000688118 (NC_000001.10:g.248059817_248059818del, NM_001001957.2:c.929_930del (OR2W3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.248059817_248059818del
DNA change (hg38) -
Published as OR2W3(NM_001001957.2):c.929_930delAG (p.E310Afs*?)
ISCN -
DB-ID OR2W3_000014
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2W3 NM_001001957.2 +/. - c.929_930del r.(?) p.(Glu310AlafsTer?)


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