Variant #0000973856 (NC_000001.10:g.248128983A>T, NM_001004491.1:c.350A>T (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.248128983A>T
DNA change (hg38) -
Published as OR2AK2(NM_001004491.1):c.350A>T (p.(Tyr117Phe))
ISCN -
DB-ID OR2AK2_000004
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) 0.00148 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2L8 NM_001001963.1 -?/. - c.*15885A>T r.(=) p.(=)
OR2AK2 NM_001004491.1 -?/. - c.350A>T r.(?) p.(Tyr117Phe)
OR2L2 NM_001004686.2 -?/. - c.-72587A>T r.(?) p.(=)
OR2L3 NM_001004687.1 -?/. - c.-95001A>T r.(?) p.(=)
OR2L5 NM_001258284.1 -?/. - c.-56267A>T r.(?) p.(=)
OR2L13 NM_175911.2 -?/. - c.-144+28297A>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.