View genomic variant #0000019174

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.55874556C>G
Published as -
GERP -
Segregation -
DB-ID PNPT1_000006
MSCV MSCV_0019174
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

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 0000019174 ./. - - c.1528G>C p.(Ala510Pro) - - - -
PNPT1 00000265 XM_005264629.1 0000019174 ./. - - c.1288G>C p.(Ala430Pro) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000239707; RCV002518548;
Chromosome 2:55874556..55874556
ClinVar Allele ID 247641
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0013977, MedGen:C4706283, OMIM:614932, Orphanet:319514
ClinVar preferred disease name not provided|Combined oxidative phosphorylation defect type 13
HGVS variant names NC 000002.11:g.55874556C>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10586243|OMIM:610316.0012
Gene symbol:Gene id. PNPT1:87178
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 879255657
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