View genomic variant #0000021345

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.130515842G>A
Published as -
GERP -
Segregation -
DB-ID LYRM7_000004
MSCV MSCV_0021345
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 0000021345 ./. - - c.73G>A p.(Asp25Asn) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000122742;
Chromosome 5:130515842..130515842
ClinVar Allele ID 139382
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.130515842G>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA163124|OMIM:615831.0001|UniProtKB:Q5U5X0#VAR 071187
Gene symbol:Gene id. LYRM7:90624
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 587777433
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