Variant #0000999047 (NC_000011.9:g.4661514G>A, NM_001004751.2:c.494G>A (OR51D1))

Chromosome 11
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.4661514G>A
DNA change (hg38) -
Published as OR51D1(NM_001004751.2):c.494G>A (p.(Gly165Glu))
ISCN -
DB-ID OR51D1_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
OR51D1 NM_001004751.2 ?/. - c.494G>A r.(?) p.(Gly165Glu)
OR51E1 NM_152430.3 ?/. - c.-3786G>A r.(?) p.(=)


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