View genomic variant #0000002945

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.3870280C>A
Published as -
GERP 1.850
Segregation -
DB-ID PANK2_000008
MSCV MSCV_0002945
dbSNP ID rs137852969
Frequency -
Sources ; clinvar;
Reference 16240131
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
PANK2 00003255 NM_024960.4 0000002945 +/+ - - c.-246+729C>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000004823;
Chromosome 20:3870280..3870280
ClinVar Allele ID 19600
Disease database name and identifier MONDO:MONDO:0009319, MedGen:C0018523, OMIM:234200, Orphanet:157850
ClinVar preferred disease name Pigmentary pallidal degeneration
HGVS variant names NC 000020.10:g.3870280C>A
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:CA253224|Genetic Testing Registry (GTR):GTR000556333|OMIM:606157.0015
Gene symbol:Gene id. PANK2:80025|LOC130065345:130065345
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 137852969
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001338030; RCV003331121;
Chromosome 20:3870280..3870280
ClinVar Allele ID 1034694
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009319, MedGen:C0018523, OMIM:234200, Orphanet:157850
ClinVar preferred disease name not specified|Pigmentary pallidal degeneration
HGVS variant names NC 000020.10:g.3870280C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. PANK2:80025|LOC130065345:130065345
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 137852969
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