View genomic variant #0000005200

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.7127955G>A
Published as -
GERP 1.580
Segregation -
DB-ID ACADVL_000009 See all 3 reported entries
MSCV MSCV_0005200
dbSNP ID rs113994171
Frequency -
Sources ; ensembl;
Reference 20301763
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
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 0000005200 ./. - - c.1679-6G>A p.(=) - - - -
ACADVL 00000391 NM_001033859.2 0000005200 ./. - - c.1613-6G>A p.(=) - - - -
ACADVL 00000388 NM_001270447.1 0000005200 ./. - - c.1748-6G>A p.(=) - - - -
ACADVL 00000389 NM_001270448.1 0000005200 ./. - - c.1451-6G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000031857; RCV000185730;
Chromosome 17:7127955..7127955
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00004
Allele frequencies from TGP 0.00020
ClinVar Allele ID 33871
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.7127955G>A
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:CA312281
Gene symbol:Gene id. ACADVL:37
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 113994171
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