View genomic variant #0000019253

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.74372361_74372362insT
Published as -
GERP -
Segregation -
DB-ID BOLA3_000006
MSCV MSCV_0019253
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     
BOLA3 00000055 NM_001035505.1 0000019253 ./. - - c.123_124insA p.(Glu42Argfs*13) - - - -
BOLA3 00000056 NM_212552.2 0000019253 ./. - - c.123_124insA p.(Glu42Argfs*13) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000024012;
Chromosome 2:74372361..74372362
ClinVar Allele ID 39977
Disease database name and identifier MONDO:MONDO:0013675, MedGen:C3280378, OMIM:614299, Orphanet:401874
ClinVar preferred disease name Multiple mitochondrial dysfunctions syndrome 2
HGVS variant names NC 000002.11:g.74372364dup
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA351345|OMIM:613183.0001
Gene symbol:Gene id. BOLA3:388962
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 869320737
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