View genomic variant #0000021348

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.130522806_130522807insG
Published as -
GERP -
Segregation -
DB-ID LYRM7_000003
MSCV MSCV_0021348
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
LYRM7 00002189 NM_181705.2 0000021348 ./. - - c.244+4_244+5insG p.? - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000208754;
Chromosome 5:130522806..130522807
ClinVar Allele ID 224860
Disease database name and identifier MONDO:MONDO:0014364, MedGen:C4014440, OMIM:615838
ClinVar preferred disease name Mitochondrial complex III deficiency nuclear type 8
HGVS variant names NC 000005.9:g.130522807dup
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:CA352197|OMIM:615831.0002
Gene symbol:Gene id. LYRM7:90624
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 869025602
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