View genomic variant #0000015341

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.76190111T>C
Published as -
GERP -
Segregation -
DB-ID ACADM_000149
MSCV MSCV_0015341
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 0000015341 ./. - - c.-362T>C p.(=) - - - -
ACADM 00000383 NM_001127328.1 0000015341 ./. - - c.-362T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000316956; RCV001594933;
Chromosome 1:76190111..76190111
Allele frequencies from TGP 0.08786
ClinVar Allele ID 281807
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0008721, MedGen:C0220710, OMIM:201450, Orphanet:42
ClinVar preferred disease name not provided|Medium-chain acyl-coenzyme A dehydrogenase deficiency
HGVS variant names NC 000001.10:g.76190111T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10610739
Gene symbol:Gene id. ACADM:34
Allele origin germline
dbSNP ID 1251076
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