RGD:14746619 Rat Genome Database

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Variant: RGD:14746619 -  Homo sapiens

RGD ID: 14746619
RS ID: rs1591361903
ClinVar ID: CV654081
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACAT1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 108,004,534
GRCh38 11 108,133,807
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000019.4:c.121-13T>A
NG_009888.2:g.22103T>A
NC_000011.10:g.108133807T>A
NC_000011.9:g.108004534T>A
More... 		05/05/2019 intron variant pathogenic 2-methyl-3-hydroxybutyricacidemia; 3-ketothiolase deficiency; 3-oxothiolase deficiency; Alpha-methylacetoaceticaciduria; Beta ketothiolase deficiency; Mitochondrial acetoacetyl-CoA Thiolase deficiency
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ACAT1
Accession:NM_001386691
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386679
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386688
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386685
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386687
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386689
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386690
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386682
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386686
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386681
Location:5UTRS;INTRON

Gene Symbol:ACAT1
Accession:NM_001386678
Location:INTRON

Gene Symbol:ACAT1
Accession:NM_001386677
Location:INTRON

Gene Symbol:ACAT1
Accession:NM_000019
Location:INTRON

Gene Symbol:ACAT1
Accession:NR_170163
Location:INTRON;NON-CODING

Gene Symbol:ACAT1
Accession:NR_170162
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28393214   PMID:31268215  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000844772 CLINVAR
dbSNP (RS) rs1591361903 CLINVAR
MedGen C1536500 CLINVAR
NCBI Gene ACAT1 CLINVAR
OMIM 203750 CLINVAR
  607809 CLINVAR
SNOMED CT 124258007 CLINVAR