View genomic variant #0000005197

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.7127326T>C
Published as -
GERP 5.740
Segregation -
DB-ID ACADVL_000006 See all 3 reported entries
MSCV MSCV_0005197
dbSNP ID rs118204017
Frequency -
Sources ; ensembl;
Reference 9709714
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 0000005197 ./. - 14/20 c.1372T>C p.(Phe458Leu) probably_damaging(0.926) missense_variant - tolerated(0.3)
ACADVL 00000391 NM_001033859.2 0000005197 ./. - 13/19 c.1306T>C p.(Phe436Leu) probably_damaging(0.994) missense_variant - tolerated(0.28)
ACADVL 00000388 NM_001270447.1 0000005197 ./. - 15/21 c.1441T>C p.(Phe481Leu) probably_damaging(0.994) missense_variant - tolerated(0.57)
ACADVL 00000389 NM_001270448.1 0000005197 ./. - 13/19 c.1144T>C p.(Phe382Leu) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000001699; RCV001731269;
Chromosome 17:7127326..7127326
ClinVar Allele ID 16671
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.7127326T>C
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA251907|OMIM:609575.0012|UniProtKB:P49748#VAR 010103
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 118204017
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