View genomic variant #0000002950

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.3899342G>A
Published as -
GERP 5.120
Segregation -
DB-ID PANK2_000005
MSCV MSCV_0002950
dbSNP ID rs137852959
Frequency -
Sources ; clinvar;
Reference 11479594
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 View details
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 0000002950 +/+ - 6/7 c.688G>A p.(Gly230Arg) probably_damaging(1) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV000004807; RCV000004808; RCV000132732; RCV000190815; RCV000224470; RCV001588799; RCV002496261;
Chromosome 20:3899342..3899342
Allele frequencies from ExAC 0.00010
ClinVar Allele ID 19587
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0009319, MedGen:C0018523, OMIM:234200, Orphanet:157850|MONDO:MONDO:0011798, MedGen:C1846582, OMIM:607236, Orphanet:157855|MedGen:CN517202|Human Phenotype Ontology:HP:0000547, MONDO:MONDO:0019200, MeSH:D012174, MedGen:C0035334, OMIM:268000, OMIM:PS268000, Orphanet:791|MedGen:C2751506
ClinVar preferred disease name Inborn genetic diseases|Pigmentary pallidal degeneration|Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration|not provided|Retinitis pigmentosa|Neurodegeneration with brain iron accumulation 1, atypical
HGVS variant names NC 000020.10:g.3899342G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA116915|Genetic Testing Registry (GTR):GTR000556333|OMIM:606157.0002|UniProtKB:Q9BZ23#VAR 015168
Gene symbol:Gene id. PANK2:80025
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 137852959
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