View genomic variant #0000017995

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.7123443C>A
Published as -
GERP -
Segregation -
DB-ID ACADVL_000175
MSCV MSCV_0017995
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

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACADVL 00000390 NM_000018.3 0000017995 ./. - - c.65C>A p.(Ser22*) - - - -
ACADVL 00000391 NM_001033859.2 0000017995 ./. - - c.65C>A p.(Ser22*) - - - -
ACADVL 00000388 NM_001270447.1 0000017995 ./. - - c.134C>A p.(Ser45*) - - - -
ACADVL 00000389 NM_001270448.1 0000017995 ./. - - c.-164C>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000152732; RCV000985184;
Chromosome 17:7123443..7123443
ClinVar Allele ID 177423
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name not provided|Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7123443C>A
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA233425
Gene symbol:Gene id. ACADVL:37|LOC130060113:130060113
Molecular consequence SO:0001587|nonsense, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 727503788
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002037005;
Chromosome 17:7123443..7123443
ClinVar Allele ID 1395916
Disease database name and identifier MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7123443C>G
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
Gene symbol:Gene id. ACADVL:37|LOC130060113:130060113
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 727503788
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003110861;
Chromosome 17:7123443..7123443
ClinVar Allele ID 1940547
Disease database name and identifier MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names NC 000017.10:g.7123443C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. ACADVL:37|LOC130060113:130060113
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR 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