View genomic variant #0000025736

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.44200932A>G
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000132
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 0000025736 ./. - - c.1261+2T>C p.? - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000667170;
Chromosome 2:44200932..44200932
ClinVar Allele ID 542278
Disease database name and identifier MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472
ClinVar preferred disease name Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
HGVS variant names NC 000002.11:g.44200932A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001575|splice donor variant
Allele origin unknown
dbSNP ID 1553410852
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