Variant #0000983236 (NC_000019.9:g.1391005G>A, NM_024407.4:c.364G>A (NDUFS7))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1391005G>A
DNA change (hg38) -
Published as NDUFS7(NM_001363602.2):c.364G>A (p.V122M), NDUFS7(NM_024407.5):c.364G>A (p.(Val122Met), p.V122M)
ISCN -
DB-ID NDUFS7_000007 See all 5 reported entries
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) 5.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS7 NM_024407.4 +?/. - c.364G>A r.(?) p.(Val122Met)


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