Variant #0000992721 (NC_000002.11:g.240969461G>A, NM_004544.3:c.-4743C>T (NDUFA10))

Chromosome 2
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.240969461G>A
DNA change (hg38) -
Published as OR6B2(NM_001005853.1):c.386C>T (p.(Pro129Leu))
ISCN -
DB-ID NDUFA10_000022
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) 0.00053 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     
OR6B2 NM_001005853.1 ?/. - c.386C>T r.(?) p.(Pro129Leu)
NDUFA10 NM_004544.3 ?/. - c.-4743C>T r.(?) p.(=)


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