View genomic variant #0000023490

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.47002089G>A
Published as -
GERP -
Segregation -
DB-ID NDUFB11_000001
MSCV MSCV_0023490
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

2 entries on 1 page. Showing entries 1 - 2.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFB11 00000956 NM_001135998.2 0000023490 ./. - - c.262C>T p.(Arg88*) - - - -
NDUFB11 00000957 NM_019056.6 0000023490 ./. - - c.262C>T p.(Arg88*) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000170490; RCV000240620; RCV000346231; RCV000763626;
Chromosome X:47002089..47002089
ClinVar Allele ID 188131
Disease database name and identifier MONDO:MONDO:0024552, MedGen:C0796070, OMIM:309801, Orphanet:2556|MONDO:MONDO:0010494, MedGen:C4225421, OMIM:300952, Orphanet:2556|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:CN517202|Human Phenotype Ontology:HP:0005152, MONDO:MONDO:0010771, MedGen:C1708371, OMIM:500000, Orphanet:137675
ClinVar preferred disease name Linear skin defects with multiple congenital anomalies 1|Linear skin defects with multiple congenital anomalies 3|Mitochondrial complex I deficiency, nuclear type 1|not provided|Histiocytoid cardiomyopathy
HGVS variant names NC 000023.10:g.47002089G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA199656|OMIM:300403.0001
Gene symbol:Gene id. NDUFB11:54539
Molecular consequence SO:0001587|nonsense
Allele origin
dbSNP ID 786205225
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