View genomic variant #0000026543

Chromosome 6
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.97345671C>G
Published as -
GERP -
Segregation -
DB-ID NDUFAF4_000042
MSCV -
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 Lishuang Shen




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 0000026543 ./. - - c.7G>C p.(Ala3Pro) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000591072; RCV000754577;
Chromosome 6:97345671..97345671
ClinVar Allele ID 490691
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0032620, MedGen:C4748778, OMIM:618237
ClinVar preferred disease name not provided|Mitochondrial complex 1 deficiency, nuclear type 15
HGVS variant names NC 000006.11:g.97345671C>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA365281646|OMIM:611776.0002
Gene symbol:Gene id. NDUFAF4:29078|LOC129996857:129996857
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1554197721
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