View genomic variant #0000019154

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.44206964C>T
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000058
MSCV MSCV_0019154
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.
Legend  

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 0000019154 ./. - - c.469+1G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000804658;
Chromosome 2:44206964..44206964
ClinVar Allele ID 650932
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.44206964C>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 germline
dbSNP ID 1060499785
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000454266; RCV002522742;
Chromosome 2:44206964..44206964
ClinVar Allele ID 389196
Disease database name and identifier MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472|MedGen:CN517202
ClinVar preferred disease name Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type|not provided
HGVS variant names NC 000002.11:g.44206964C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16609552
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001575|splice donor variant
Allele origin germline
dbSNP ID 1060499785
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