Variant #0001042693 (NC_000019.9:g.14674625G>A, NM_004146.5:c.*2320C>T (NDUFB7))

Chromosome 19
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.14674625G>A
DNA change (hg38) -
Published as TECR(NM_138501.6):c.177G>A (p.(Leu59=))
ISCN -
DB-ID NDUFB7_000005
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) 7.0E-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 2025-05-05 21:14:00 +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     
NDUFB7 NM_004146.5 ?/. - c.*2320C>T r.(=) p.(=)
TECR NM_138501.5 ?/. - c.177G>A r.(?) p.(=)


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