Variant #0000983675 (NC_000019.9:g.5893196_5893197del, NM_175614.4:c.*1559_*1560del (NDUFA11))

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.5893196_5893197del
DNA change (hg38) -
Published as NDUFA11(NM_001193375.3):c.421_422del (p.(Val141Thrfs*286))
ISCN -
DB-ID NDUFA11_000019
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 2024-04-19 20:27:30 +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     
NDUFA11 NM_175614.4 ?/. - c.*1559_*1560del r.(=) p.(=)


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