View genomic variant #0000015395

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.76199310del
Published as -
GERP -
Segregation -
DB-ID ACADM_000084
MSCV MSCV_0015395
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
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     
ACADM 00000384 NM_000016.4 0000015395 ./. - - c.384del p.? - - - -
ACADM 00000383 NM_001127328.1 0000015395 ./. - - c.396del p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000169015; RCV000383616;
Chromosome 1:76199310..76199310
ClinVar Allele ID 186629
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0008721, MedGen:C0220710, OMIM:201450, Orphanet:42
ClinVar preferred disease name not provided|Medium-chain acyl-coenzyme A dehydrogenase deficiency
HGVS variant names NC 000001.10:g.76199314del
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(8)|Uncertain significance(1)
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA273882
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001575|splice donor variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 786204424
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000354099; RCV000701018;
Chromosome 1:76199311..76199311
ClinVar Allele ID 265252
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0008721, MedGen:C0220710, OMIM:201450, Orphanet:42
ClinVar preferred disease name not provided|Medium-chain acyl-coenzyme A dehydrogenase deficiency
HGVS variant names NC 000001.10:g.76199311G>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
Variant clinical sources reported ClinGen:CA10603782
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 886042076
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