View genomic variant #0000019139

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.44177705G>A
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000082
MSCV MSCV_0019139
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 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 0000019139 ./. - - c.1677+7C>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000321679; RCV001443264;
Chromosome 2:44177705..44177705
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00013
ClinVar Allele ID 289909
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Leigh syndrome
HGVS variant names NC 000002.11:g.44177705G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1638839
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 374995996
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