View genomic variant #0000015360

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.76194174G>T
Published as -
GERP -
Segregation -
DB-ID ACADM_000136
MSCV MSCV_0015360
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

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACADM 00000384 NM_000016.4 0000015360 ./. - - c.118+1G>T p.? - - - -
ACADM 00000383 NM_001127328.1 0000015360 ./. - - c.130+1G>T p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000410407;
Chromosome 1:76194174..76194174
ClinVar Allele ID 357129
Disease database name and identifier MONDO:MONDO:0008721, MedGen:C0220710, OMIM:201450, Orphanet:42
ClinVar preferred disease name Medium-chain acyl-coenzyme A dehydrogenase deficiency
HGVS variant names NC 000001.10:g.76194174G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16040772
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001575|splice donor variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 113887538
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