View genomic variant #0000021762

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.97338648T>A
Published as -
GERP -
Segregation -
DB-ID NDUFAF4_000022
MSCV MSCV_0021762
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFAF4 00000953 NM_014165.3 0000021762 ./. - - c.*332A>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000273464;
Chromosome 6:97338648..97338648
Allele frequencies from TGP 0.29133
ClinVar Allele ID 309128
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1
HGVS variant names NC 000006.11:g.97338648T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10627825
Gene symbol:Gene id. NDUFAF4:29078
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 10499008
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None