View genomic variant #0000019135

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.44175293G>A
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000078
MSCV MSCV_0019135
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02092 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 0000019135 ./. - - c.1888C>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000126654; RCV000270035; RCV000946606;
Chromosome 2:44175293..44175293
Allele frequencies from ESP 0.02092
Allele frequencies from ExAC 0.00617
Allele frequencies from TGP 0.02516
ClinVar Allele ID 141847
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472
ClinVar preferred disease name not specified|not provided|Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
HGVS variant names NC 000002.11:g.44175293G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA291972
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 35881858
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