Variant #0000960987 (NC_000001.10:g.248802253_248802255dup, NM_001001827.1:c.308_310dup (OR2T35))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.248802253_248802255dup
DNA change (hg38) -
Published as OR2T35(NM_001001827.2):c.308_310dupTCT (p.F103dup)
ISCN -
DB-ID OR2T35_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2T35 NM_001001827.1 -?/. - c.308_310dup r.(?) p.(Phe103dup)


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