View genomic variant #0000019252

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.74372349G>A
Published as -
GERP -
Segregation -
DB-ID BOLA3_000005
MSCV MSCV_0019252
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 View details
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     
BOLA3 00000055 NM_001035505.1 0000019252 ./. - - c.136C>T p.(Arg46*) - - - -
BOLA3 00000056 NM_212552.2 0000019252 ./. - - c.136C>T p.(Arg46*) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000210081; RCV001568158;
Chromosome 2:74372349..74372349
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 226292
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0013675, MedGen:C3280378, OMIM:614299, Orphanet:401874
ClinVar preferred disease name not provided|Multiple mitochondrial dysfunctions syndrome 2
HGVS variant names NC 000002.11:g.74372349G>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:CA352436|OMIM:613183.0002
Gene symbol:Gene id. BOLA3:388962
Molecular consequence SO:0001587|nonsense
Allele origin
dbSNP ID 143492730
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