rs200892543 Rat Genome Database

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Variant: rs200892543 -  Homo sapiens

RGD ID: 15147872
RS ID: rs200892543
ClinVar ID: CV744109
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACAT2  TCP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 160,199,686
GRCh38 6 159,778,654
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001008897.2:c.*391C>T
NM_030752.3:c.*391C>T
NM_005891.3:c.1024-5G>A
NM_001303253.1:c.1111-5G>A
More... 		04/11/2018 3 prime utr variant likely benign none provided

Gene Symbol:TCP1
Accession:NM_001008897
Location:3UTRS;EXON

Gene Symbol:TCP1
Accession:NM_030752
Location:3UTRS;EXON

Gene Symbol:ACAT2
Accession:NM_005891
Location:INTRON

Gene Symbol:ACAT2
Accession:NM_001303253
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000900609 CLINVAR
dbSNP (RS) rs200892543 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACAT2 CLINVAR
  TCP1 CLINVAR
OMIM 100678 CLINVAR
  186980 CLINVAR