View genomic variant #0000019699

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.240960689_240960690insATT
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000037
MSCV MSCV_0019699
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

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFA10 00000183 NM_004544.3 0000019699 ./. - - c.384_385insAAT p.(Ser128_Tyr129insAsn) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000412484;
Chromosome 2:240960689..240960690
ClinVar Allele ID 359100
Disease database name and identifier MONDO:MONDO:0032626, MedGen:C4748796, OMIM:618243
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 22
HGVS variant names NC 000002.11:g.240960690 240960691insTTA
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Variant clinical sources reported ClinGen:CA16044169|OMIM:603835.0004
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 1057519415
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