Variant #0000506836 (NC_000001.10:g.248224344C>T, NM_001004491.1:c.*94703C>T (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.248224344C>T
DNA change (hg38) g.248061042C>T
Published as OR2L3(NM_001004687.1):c.361C>T (p.R121C)
ISCN -
DB-ID OR2AK2_000001
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2L8 NM_001001963.1 ?/. - c.*111246C>T r.(=) p.(=)
OR2AK2 NM_001004491.1 ?/. - c.*94703C>T r.(=) p.(=)
OR2L2 NM_001004686.2 ?/. - c.*21836C>T r.(=) p.(=)
OR2L3 NM_001004687.1 ?/. - c.361C>T r.(?) p.(Arg121Cys)
OR2L5 NM_001258284.1 ?/. - c.*38156C>T r.(=) p.(=)
OR2L13 NM_175911.2 ?/. - c.-143-37609C>T r.(=) p.(=)


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