View genomic variant #0000002657

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.7127342G>A
Published as -
GERP 5.740
Segregation -
DB-ID ACADVL_000033
MSCV MSCV_0002657
dbSNP ID rs200366828
Frequency -
Sources ; Ensembl;
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 0000002657 ?/? - 14/20 c.1388G>A p.? probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000391 NM_001033859.2 0000002657 ?/? - 13/19 c.1322G>A p.(Gly441Glu) probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000388 NM_001270447.1 0000002657 ?/? - 15/21 c.1457G>A p.(Gly486Glu) probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000389 NM_001270448.1 0000002657 ?/? - 13/19 c.1160G>A p.(Gly387Glu) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000522607; RCV000809103;
Chromosome 17:7127342..7127342
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 445886
Disease database name and identifier MedGen:C3661900|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.7127342G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Likely pathogenic(3)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8338091
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 200366828
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