View genomic variant #0000019134

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.44174907T>C
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000077
MSCV MSCV_0019134
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00062 View details
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     
LRPPRC 00000168 NM_133259.3 0000019134 ./. - - c.1928A>G p.(His643Arg) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000362182; RCV000676634;
Chromosome 2:44174907..44174907
Allele frequencies from ESP 0.00062
Allele frequencies from ExAC 0.00078
ClinVar Allele ID 210841
Disease database name and identifier MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472|MedGen:C3661900
ClinVar preferred disease name Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type|not provided
HGVS variant names NC 000002.11:g.44174907T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA319900
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 148575027
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