View genomic variant #0000019172

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.55873563del
Published as -
GERP -
Segregation -
DB-ID PNPT1_000004
MSCV MSCV_0019172
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 0000019172 ./. - - c.1661del p.(Ile554Lysfs*15) - - - -
PNPT1 00000265 XM_005264629.1 0000019172 ./. - - c.1421del p.(Ile474Lysfs*15) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000591053;
Chromosome 2:55873563..55873563
ClinVar Allele ID 489747
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.55873563del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA658795798
Gene symbol:Gene id. PNPT1:87178
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 1553493871
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