View genomic variant #0000023489

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.47001817C>T
Published as -
GERP -
Segregation -
DB-ID NDUFB11_000002
MSCV MSCV_0023489
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.
Legend  

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 0000023489 ./. - - c.361G>A p.(Glu121Lys) - - - -
NDUFB11 00000957 NM_019056.6 0000023489 ./. - - c.391G>A p.(Glu131Lys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000412600; RCV000487272; RCV002272220;
Chromosome X:47001817..47001817
ClinVar Allele ID 359054
Disease database name and identifier MONDO:MONDO:0010494, MedGen:C4225421, OMIM:300952, Orphanet:2556|MONDO:MONDO:0026721, MedGen:C4746985, OMIM:301021|MedGen:CN517202
ClinVar preferred disease name Linear skin defects with multiple congenital anomalies 3|Mitochondrial complex 1 deficiency, nuclear type 30|not provided
HGVS variant names NC 000023.10:g.47001817C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16042217|OMIM:300403.0003
Gene symbol:Gene id. NDUFB11:54539
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1057519073
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