View genomic variant #0000025732

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.44184584G>T
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000128
MSCV -
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 Lishuang Shen




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     
LRPPRC 00000168 NM_133259.3 0000025732 ./. - - c.1589C>A p.(Ser530*) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000665443; RCV002530656;
Chromosome 2:44184584..44184584
ClinVar Allele ID 542130
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472
ClinVar preferred disease name not provided|Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
HGVS variant names NC 000002.11:g.44184584G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. LRPPRC:10128|LOC129388857:129388857
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 775735922
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