View genomic variant #0000021768

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.97339078A>G
Published as -
GERP -
Segregation -
DB-ID NDUFAF4_000035
MSCV MSCV_0021768
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.46924 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 0000021768 ./. - - c.430T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000117707; RCV000271558; RCV000676773; RCV001778736;
Chromosome 6:97339078..97339078
Allele frequencies from ESP 0.46924
Allele frequencies from ExAC 0.51783
Allele frequencies from TGP 0.51498
ClinVar Allele ID 135139
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.97339078A>G
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:CA153857
Gene symbol:Gene id. NDUFAF4:29078
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 6684
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