View genomic variant #0000025737

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.44200942T>G
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000133
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 0000025737 ./. - - c.1253A>C p.(Asn418Thr) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000199058; RCV002515406; RCV002517226;
Chromosome 2:44200942..44200942
Allele frequencies from ESP 0.00008
ClinVar Allele ID 210850
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN169374|MedGen:CN517202
ClinVar preferred disease name Inborn genetic diseases|not specified|not provided
HGVS variant names NC 000002.11:g.44200942T>C
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:CA323597
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 373908553
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000523785; RCV000667875; RCV003323585;
Chromosome 2:44200942..44200942
ClinVar Allele ID 443251
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472|MedGen:CN517202
ClinVar preferred disease name not specified|Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type|not provided
HGVS variant names NC 000002.11:g.44200942T>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1639049
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 373908553
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