View genomic variant #0000019157

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.44209544G>A
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000061
MSCV MSCV_0019157
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.
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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 0000019157 ./. - - c.179C>T p.(Ala60Val) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000356535; RCV002523135; RCV002519979;
Chromosome 2:44209544..44209544
Allele frequencies from ExAC 0.00010
Allele frequencies from TGP 0.00020
ClinVar Allele ID 287126
Disease database name and identifier MedGen:C3661900|MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472
ClinVar preferred disease name not provided|Inborn genetic diseases|Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
HGVS variant names NC 000002.11:g.44209544G>A
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:CA1639442
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 546399905
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