Variant #0000991074 (NC_000001.10:g.247921099C>T, NM_012353.2:c.610G>A (OR1C1))

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.247921099C>T
DNA change (hg38) -
Published as OR1C1(NM_012353.2):c.610G>A (p.(Gly204Ser))
ISCN -
DB-ID OR1C1_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) 0.0001 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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR11L1 NM_001001959.1 ?/. - c.*83131G>A r.(=) p.(=)
OR14A16 NM_001001966.1 ?/. - c.*57003G>A r.(=) p.(=)
OR6F1 NM_001005286.1 ?/. - c.-45042G>A r.(?) p.(=)
OR13G1 NM_001005487.1 ?/. - c.-84756G>A r.(?) p.(=)
OR1C1 NM_012353.2 ?/. - c.610G>A r.(?) p.(Gly204Ser)
TRIM58 NM_015431.3 ?/. - c.-99450C>T r.(?) p.(=)


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