View genomic variant #0000019373

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207011696_207011698del
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000007 See all 2 reported entries
MSCV MSCV_0000854
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 0000019373 ./. - - c.558_560del p.(Ile187del) - - - -
NDUFS1 00000202 NM_001199982.1 0000019373 ./. - - c.333_335del p.(Ile112del) - - - -
NDUFS1 00000203 NM_001199983.1 0000019373 ./. - - c.495_497del p.(Ile166del) - - - -
NDUFS1 00000206 NM_001199984.1 0000019373 ./. - - c.708_710del p.(Ile237del) - - - -
NDUFS1 00000205 NM_005006.6 0000019373 ./. - - c.666_668del p.(Ile223del) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000015298;
Chromosome 2:207011696..207011698
ClinVar Allele ID 29269
Disease database name and identifier MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 5
HGVS variant names NC 000002.11:g.207011698 207011700del
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA123812|OMIM:157655.0001
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001822|inframe deletion
Allele origin germline
dbSNP ID 397515383
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002083097;
Chromosome 2:207011698..207011698
ClinVar Allele ID 1585141
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.207011698G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 906676893
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