Variant #0001031919 (NC_000001.10:g.248129487G>A, NM_001004491.1:c.854G>A (OR2AK2))

Chromosome 1
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.248129487G>A
DNA change (hg38) -
Published as OR2AK2(NM_001004491.1):c.854G>A (p.(Arg285Gln))
ISCN -
DB-ID OR2AK2_000010
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
OR2L8 NM_001001963.1 ?/. - c.*16389G>A r.(=) p.(=)
OR2AK2 NM_001004491.1 ?/. - c.854G>A r.(?) p.(Arg285Gln)
OR2L2 NM_001004686.2 ?/. - c.-72083G>A r.(?) p.(=)
OR2L3 NM_001004687.1 ?/. - c.-94497G>A r.(?) p.(=)
OR2L5 NM_001258284.1 ?/. - c.-55763G>A r.(?) p.(=)
OR2L13 NM_175911.2 ?/. - c.-144+28801G>A r.(=) p.(=)


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