View genomic variant #0000021769

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.97339088C>T
Published as -
GERP -
Segregation -
DB-ID NDUFAF4_000036
MSCV MSCV_0021769
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.89217 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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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 0000021769 ./. - - c.420G>A p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000117706; RCV000328919; RCV000676774; RCV001778735;
Chromosome 6:97339088..97339088
Allele frequencies from ESP 0.89217
Allele frequencies from ExAC 0.89442
Allele frequencies from TGP 0.93391
ClinVar Allele ID 135138
Disease database name and identifier MONDO:MONDO:0032620, MedGen:C4748778, OMIM:618237|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 15|Mitochondrial complex I deficiency, nuclear type 1|not specified|not provided
HGVS variant names NC 000006.11:g.97339088C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA153855
Gene symbol:Gene id. NDUFAF4:29078
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 11402
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002711805;
Chromosome 6:97339088..97339089
ClinVar Allele ID 2028465
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000006.11:g.97339088 97339089delinsTC
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Indel
Sequence Ontology for variant type SO:1000032
Gene symbol:Gene id. NDUFAF4:29078
Molecular consequence SO:0001583|missense variant
Allele origin germline
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