View genomic variant #0000025782

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.206994967C>T
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000051
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

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 0000025782 ./. - - c.1446-1G>A p.? - - - -
NDUFS1 00000202 NM_001199982.1 0000025782 ./. - - c.1221-1G>A p.? - - - -
NDUFS1 00000203 NM_001199983.1 0000025782 ./. - - c.1383-1G>A p.? - - - -
NDUFS1 00000206 NM_001199984.1 0000025782 ./. - - c.1596-1G>A p.? - - - -
NDUFS1 00000205 NM_005006.6 0000025782 ./. - - c.1554-1G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000778153;
Chromosome 2:206994967..206994967
ClinVar Allele ID 619933
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.206994967C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001574|splice acceptor variant
Allele origin germline
dbSNP ID 1056433452
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