View genomic variant #0000005195

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.7127184G>A
Published as -
GERP 5.770
Segregation -
DB-ID ACADVL_000003 See all 3 reported entries
MSCV MSCV_0005195
dbSNP ID rs2309689
Frequency -
Sources ; ensembl;
Reference 20301763;20060901;9546340;23757202;8845838
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 0000005195 ./. - 13/20 c.1322G>A p.(Gly441Asp) probably_damaging(1) missense_variant - deleterious(0)
ACADVL 00000391 NM_001033859.2 0000005195 ./. - 12/19 c.1256G>A p.(Gly419Asp) probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000388 NM_001270447.1 0000005195 ./. - 14/21 c.1391G>A p.(Gly464Asp) probably_damaging(0.999) missense_variant - deleterious(0)
ACADVL 00000389 NM_001270448.1 0000005195 ./. - 12/19 c.1094G>A p.(Gly365Asp) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000020072; RCV000077903;
Chromosome 17:7127184..7127184
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 33868
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.7127184G>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:CA220193|OMIM:609575.0009|UniProtKB:P49748#VAR 000354
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 2309689
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000989694;
Chromosome 17:7127184..7127184
ClinVar Allele ID 791824
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.7127184G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 2309689
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