View genomic variant #0000015403

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.76200518_76200521del
Published as -
GERP -
Segregation -
DB-ID ACADM_000092
MSCV MSCV_0015403
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

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 0000015403 ./. - - c.430_433del p.(Lys144Ilefs*5) - - - -
ACADM 00000383 NM_001127328.1 0000015403 ./. - - c.442_445del p.(Lys148Ilefs*5) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000409112; RCV000498380;
Chromosome 1:76200518..76200521
ClinVar Allele ID 357136
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.76200519 76200522del
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA16040779
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001589|frameshift variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 1057517356
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002287741; RCV003326625;
Chromosome 1:76200518..76200518
ClinVar Allele ID 1706666
Disease database name and identifier MedGen:C3661900|Human Phenotype Ontology:HP:0003119, Human Phenotype Ontology:HP:0003611, MedGen:C4025650
ClinVar preferred disease name not provided|Abnormal circulating lipid concentration
HGVS variant names NC 000001.10:g.76200518A>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001587|nonsense, SO:0001627|intron variant
Allele origin germline
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