View genomic variant #0000019379

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207013834_207013835insA
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000038
MSCV MSCV_0019379
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

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS1 00000204 NM_001199981.1 0000019379 ./. - - c.154-15_154-14insT p.(=) - - - -
NDUFS1 00000202 NM_001199982.1 0000019379 ./. - - c.6-1277_6-1276insT p.(=) - - - -
NDUFS1 00000203 NM_001199983.1 0000019379 ./. - - c.91-15_91-14insT p.(=) - - - -
NDUFS1 00000206 NM_001199984.1 0000019379 ./. - - c.304-15_304-14insT p.(=) - - - -
NDUFS1 00000205 NM_005006.6 0000019379 ./. - - c.262-15_262-14insT p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000268364; RCV000360707; RCV002057638;
Chromosome 2:207013834..207013835
ClinVar Allele ID 287274
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MedGen:CN517202
ClinVar preferred disease name Mitochondrial complex I deficiency|Leigh syndrome|not provided
HGVS variant names NC 000002.11:g.207013845dup
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(1)
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA2070832
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 34184317
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000307662; RCV000364669; RCV001522963;
Chromosome 2:207013835..207013835
ClinVar Allele ID 287257
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency|not provided|Leigh syndrome
HGVS variant names NC 000002.11:g.207013845del
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(2)
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA2070831
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 34184317
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