View genomic variant #0000000056

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.76226985T>C
Published as -
GERP 5.210
Segregation -
DB-ID ACADM_000011 See all 2 reported entries
MSCV MSCV_0000056
dbSNP ID rs121434275
Frequency -
Sources ; clinvar;
Reference 1684086
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 0000000056 +/+ - 11/12 c.1124T>C p.(Ile375Thr) probably_damaging(0.975) missense_variant - deleterious(0)
ACADM 00000383 NM_001127328.1 0000000056 +/+ - 11/12 c.1136T>C p.(Ile379Thr) probably_damaging(0.996) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000003772;
Chromosome 1:76226985..76226985
ClinVar Allele ID 18628
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.76226985T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA252826|OMIM:607008.0004|UniProtKB:P11310#VAR 000327
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121434275
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