View genomic variant #0000002948

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.3888800C>T
Published as -
GERP 3.660
Segregation -
DB-ID PANK2_000003
MSCV MSCV_0002948
dbSNP ID rs137852962
Frequency -
Sources ; clinvar;
Reference 11479594
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.
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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 0000002948 +/+ - - c.-18C>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000004811;
Chromosome 20:3888800..3888800
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 19590
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.3888800C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA253212|Genetic Testing Registry (GTR):GTR000556333|OMIM:606157.0005|UniProtKB:Q9BZ23#VAR 015159
Gene symbol:Gene id. PANK2:80025
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 137852962
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