View genomic variant #0000019251

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74372348C>T
Published as -
GERP -
Segregation -
DB-ID BOLA3_000004
MSCV MSCV_0019251
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00031 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 0000019251 ./. - - c.137G>A p.(Arg46Gln) - - - -
BOLA3 00000056 NM_212552.2 0000019251 ./. - - c.137G>A p.(Arg46Gln) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000324798; RCV002051844;
Chromosome 2:74372348..74372348
Allele frequencies from ESP 0.00031
Allele frequencies from ExAC 0.00034
ClinVar Allele ID 290565
Disease database name and identifier MONDO:MONDO:0013675, MedGen:C3280378, OMIM:614299, Orphanet:401874|MedGen:CN517202
ClinVar preferred disease name Multiple mitochondrial dysfunctions syndrome 2|not provided
HGVS variant names NC 000002.11:g.74372348C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1719496
Gene symbol:Gene id. BOLA3:388962
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 144366005
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