View genomic variant #0000015301
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
Type |
- |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53662722_53662723insGC |
Published as |
- |
GERP |
- |
Segregation |
- |
DB-ID |
CPT2_000018 |
MSCV |
MSCV_0015301 |
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
ClinVar @ MSeqDR | RCVaccession | RCV000409793; RCV000410888; RCV000411956; RCV001042031; RCV001570857; RCV003475976; | Chromosome | 1:53662722..53662723 | ClinVar Allele ID | 357116 | Disease database name and identifier | MedGen:C3661900|MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0013633, MedGen:C3280160, OMIM:614212, Orphanet:263524|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305|MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157 | ClinVar preferred disease name | not provided|Carnitine palmitoyl transferase II deficiency, myopathic form|Carnitine palmitoyl transferase II deficiency, neonatal form|Encephalopathy, acute, infection-induced, susceptibility to, 4|Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyltransferase II deficiency | HGVS variant names | NC 000001.10:g.53662723GC[3] | ClinVar review status | criteria provided, multiple submitters, no conflicts | Clinical Significance | Pathogenic/Likely pathogenic | Variant type | Microsatellite | Sequence Ontology for variant type | SO:0000289 | Variant clinical sources reported | ClinGen:CA858892|Genetic Testing Registry (GTR):GTR000604056|OMIM:600650.0014 | Gene symbol:Gene id. | CPT2:1376|LOC129930561:129930561 | Molecular consequence | SO:0001589|frameshift variant | Allele origin | germline | dbSNP ID | 754363068 | Variant Flags | : |
ClinVar @ MSeqDR as full content XML tree
ClinVar @ MSeqDR | RCVaccession | RCV001467775; | Chromosome | 1:53662723..53662723 | Allele frequencies from ExAC | 0.00009 | ClinVar Allele ID | 1110700 | Disease database name and identifier | MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157 | ClinVar preferred disease name | Carnitine palmitoyltransferase II deficiency | HGVS variant names | NC 000001.10:g.53662723G>A | ClinVar review status | criteria provided, single submitter | Clinical Significance | Likely benign | Variant type | single nucleotide variant | Sequence Ontology for variant type | SO:0001483 | Gene symbol:Gene id. | CPT2:1376|LOC129930561:129930561 | Molecular consequence | SO:0001819|synonymous variant | Allele origin | germline | dbSNP ID | 773734918 | 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
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