View genomic variant #0000019338

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.206988062_206988063insA
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000047
MSCV MSCV_0019338
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 0000019338 ./. - - c.*846_*847insT p.(=) - - - -
NDUFS1 00000202 NM_001199982.1 0000019338 ./. - - c.*846_*847insT p.(=) - - - -
NDUFS1 00000203 NM_001199983.1 0000019338 ./. - - c.*846_*847insT p.(=) - - - -
NDUFS1 00000206 NM_001199984.1 0000019338 ./. - - c.*846_*847insT p.(=) - - - -
NDUFS1 00000205 NM_005006.6 0000019338 ./. - - c.*846_*847insT p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000271891; RCV000364348;
Chromosome 2:206988062..206988063
ClinVar Allele ID 287223
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency|Leigh syndrome
HGVS variant names NC 000002.11:g.206988074dup
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA10613950
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 58253838
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000329565; RCV000367850;
Chromosome 2:206988063..206988063
ClinVar Allele ID 284147
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency|Leigh syndrome
HGVS variant names NC 000002.11:g.206988074del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA10612141
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 58253838
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