Variant #0000973860 (NC_000001.10:g.248129501G>A, NM_001004491.1:c.868G>A (OR2AK2))

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.248129501G>A
DNA change (hg38) -
Published as OR2AK2(NM_001004491.1):c.868G>A (p.(Ala290Thr))
ISCN -
DB-ID OR2AK2_000008
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) 0.00193 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 2024-04-19 20:20:39 +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.*16403G>A r.(=) p.(=)
OR2AK2 NM_001004491.1 -?/. - c.868G>A r.(?) p.(Ala290Thr)
OR2L2 NM_001004686.2 -?/. - c.-72069G>A r.(?) p.(=)
OR2L3 NM_001004687.1 -?/. - c.-94483G>A r.(?) p.(=)
OR2L5 NM_001258284.1 -?/. - c.-55749G>A r.(?) p.(=)
OR2L13 NM_175911.2 -?/. - c.-144+28815G>A r.(=) p.(=)


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