View genomic variant #0000001202

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.97344666A>G
Published as -
GERP 3.930
Segregation -
DB-ID NDUFAF4_000001 See all 2 reported entries
MSCV MSCV_0001202
dbSNP ID rs63751061
Frequency -
Sources ; clinVar; Ensembl;
Reference 18179882
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.
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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 0000001202 +/+ - 2/3 c.194T>C p.(Leu65Pro) probably_damaging(1) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV000000826;
Chromosome 6:97344666..97344666
ClinVar Allele ID 15829
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name Mitochondrial complex I deficiency
HGVS variant names NC 000006.11:g.97344666A>G
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA114514|OMIM:611776.0001|UniProtKB:Q9P032#VAR 044329
Gene symbol:Gene id. NDUFAF4:29078
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 63751061
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