View genomic variant #0000000831

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.55894142T>C
Published as -
GERP 5.560
Segregation -
DB-ID PNPT1_000001 See all 2 reported entries
MSCV MSCV_0000831
dbSNP ID rs397514598
Frequency -
Sources ; clinvar;
Reference 23084291
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
PNPT1 00000264 NM_033109.4 0000000831 +/+ - 13/28 c.1160A>G p.(Gln387Arg) probably_damaging(0.987) missense_variant - deleterious(0.01)
PNPT1 00000265 XM_005264629.1 0000000831 +/+ - 13/28 c.920A>G p.(Gln307Arg) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000033022;
Chromosome 2:55894142..55894142
ClinVar Allele ID 48400
Disease database name and identifier MONDO:MONDO:0013977, MedGen:C4706283, OMIM:614932, Orphanet:319514
ClinVar preferred disease name Combined oxidative phosphorylation defect type 13
HGVS variant names NC 000002.11:g.55894142T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA130566|OMIM:610316.0001|UniProtKB:Q8TCS8#VAR 069248
Gene symbol:Gene id. PNPT1:87178
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 397514598
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