View genomic variant #0000015365

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.76198337G>A
Published as -
GERP -
Segregation -
DB-ID ACADM_000107
MSCV MSCV_0015365
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00246 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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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 0000015365 ./. - - c.127G>A p.(Glu43Lys) - - - -
ACADM 00000383 NM_001127328.1 0000015365 ./. - - c.139G>A p.(Glu47Lys) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000077881; RCV000176959; RCV002251961; RCV003226190; RCV003415841;
Chromosome 1:76198337..76198337
Allele frequencies from ESP 0.00246
Allele frequencies from ExAC 0.00225
Allele frequencies from TGP 0.00200
ClinVar Allele ID 98168
Disease database name and identifier .|MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0008721, MedGen:C0220710, OMIM:201450, Orphanet:42|.
ClinVar preferred disease name ACADM-related condition|not specified|not provided|Medium-chain acyl-coenzyme A dehydrogenase deficiency|See cases
HGVS variant names NC 000001.10:g.76198337G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(3)|Uncertain significance(8)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA220170
Gene symbol:Gene id. ACADM:34
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 147559466
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