View genomic variant #0000019143

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.44190783T>C
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000086
MSCV MSCV_0019143
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01884 View details
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 0000019143 ./. - - c.1432A>G p.(Thr478Ala) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000126651; RCV000223987; RCV001001626;
Chromosome 2:44190783..44190783
Allele frequencies from ESP 0.01884
Allele frequencies from ExAC 0.00564
Allele frequencies from TGP 0.02356
ClinVar Allele ID 141844
Disease database name and identifier MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type|not specified|not provided
HGVS variant names NC 000002.11:g.44190783T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA291968|UniProtKB:P42704#VAR 052935
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 35035668
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