RGD:405104462 Rat Genome Database

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Variant: RGD:405104462 -  Homo sapiens

RGD ID: 405104462
ClinVar ID: CV2897628
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ETHE1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 44,031,239
GRCh38 19 43,527,087
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014297.5:c.81+10G>C
NG_199012.1:g.25C>G
NG_008141.1:g.5158G>C
NC_000019.9:g.44031239C>G
More... 		07/25/2023 intron variant likely benign Encephalopathy, petechiae, and ethylmalonic aciduria; EPEMA syndrome; Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV2897628Humanethylmalonic encephalopathy  IAGP 8554872ClinVar Annotator: match by term: Ethylmalonic encephalopathyClinVarPMID:28492532
Gene Symbol:ETHE1
Accession:XM_005258687
Location:5UTRS;EXON

Gene Symbol:ETHE1
Accession:NM_001320868
Location:5UTRS;INTRON

Gene Symbol:ETHE1
Accession:NM_014297
Location:INTRON

Gene Symbol:ETHE1
Accession:NM_001320869
Location:INTRON

Gene Symbol:ETHE1
Accession:NM_001320867
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003497739 CLINVAR
MedGen C1865349 CLINVAR
NCBI Gene ETHE1 CLINVAR
OMIM 602473 CLINVAR
  608451 CLINVAR