Variant #0001035240 (NC_000005.9:g.52978961_52978966dup, NM_002495.2:c.438_443dup (NDUFS4))

Chromosome 5
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.52978961_52978966dup
DNA change (hg38) -
Published as NDUFS4(NM_002495.4):c.438_443dup (p.(Asp146_Ile147dup))
ISCN -
DB-ID NDUFS4_000016
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) Retrieve
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS4 NM_002495.2 ?/. - c.438_443dup r.(?) p.(Asp146_Ile147dup)


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