View genomic variant #0000019175

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.55874559C>T
Published as -
GERP -
Segregation -
DB-ID PNPT1_000007
MSCV MSCV_0019175
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00115 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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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 0000019175 ./. - - c.1525G>A p.(Val509Ile) - - - -
PNPT1 00000265 XM_005264629.1 0000019175 ./. - - c.1285G>A p.(Val429Ile) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000191121; RCV000196452; RCV000766604; RCV000845061; RCV003152596; RCV002514095;
Chromosome 2:55874559..55874559
Allele frequencies from ESP 0.00115
Allele frequencies from ExAC 0.00075
ClinVar Allele ID 205732
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN169374|MONDO:MONDO:0013977, MedGen:C4706283, OMIM:614932, Orphanet:319514|MONDO:MONDO:0012103, MedGen:C1837518, OMIM:608703, Orphanet:101111|MONDO:MONDO:0013978, MedGen:C1824925, OMIM:614934, Orphanet:90636|MedGen:C3661900
ClinVar preferred disease name Inborn genetic diseases|not specified|Combined oxidative phosphorylation defect type 13|Spinocerebellar ataxia type 25|Autosomal recessive nonsyndromic hearing loss 70|not provided
HGVS variant names NC 000002.11:g.55874559C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(5)|Benign(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA250389
Gene symbol:Gene id. PNPT1:87178
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 146571352
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