View genomic variant #0000019367

Chromosome 2
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.207008763C>A
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000045
MSCV MSCV_0019367
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.50961 View details
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 0000019367 ./. - - c.858G>T p.(=) - - - -
NDUFS1 00000202 NM_001199982.1 0000019367 ./. - - c.633G>T p.(=) - - - -
NDUFS1 00000203 NM_001199983.1 0000019367 ./. - - c.795G>T p.(=) - - - -
NDUFS1 00000206 NM_001199984.1 0000019367 ./. - - c.1008G>T p.(=) - - - -
NDUFS1 00000205 NM_005006.6 0000019367 ./. - - c.966G>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000117710; RCV000328157; RCV000385000; RCV000676273; RCV001778738;
Chromosome 2:207008763..207008763
Allele frequencies from ESP 0.50961
Allele frequencies from TGP 0.46226
ClinVar Allele ID 135142
Disease database name and identifier MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 5|Mitochondrial complex I deficiency, nuclear type 1|not specified|not provided|Leigh syndrome
HGVS variant names NC 000002.11:g.207008763C>A
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:CA153862
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 1127566
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002213345;
Chromosome 2:207008763..207008763
ClinVar Allele ID 1559630
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.207008763C>T
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 1127566
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