Variant #0000624398 (NC_000023.10:g.119005316_119005321del, NDUFA1(NM_004541.3):c.-559_-554del)

Chromosome X
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.119005316_119005321del
DNA change (hg38) g.119871353_119871358del
Published as RNF113A(NM_006978.3):c.265_270delGAGGAA (p.E89_E90del)
ISCN -
DB-ID NDUFA1_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFA1 NM_004541.3 ?/. - c.-559_-554del r.(?) p.(=)
RNF113A NM_006978.2 ?/. - c.265_270del r.(?) p.(Glu89_Glu90del)