RGD:11659785 Rat Genome Database

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Variant: RGD:11659785 -  Homo sapiens

RGD ID: 11659785
RS ID: rs886048691
ClinVar ID: CV315290
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A22  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 791,070
GRCh38 11 791,070
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023407.1:g.12200T>A
NC_000011.10:g.791070A>T
NC_000011.9:g.791070A>T
NM_001191061.2:c.*845T>A
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC25A22
Accession:NM_001191061
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_047427601
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_011520370
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_047427599
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_011520369
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:NM_001191060
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_024448687
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_024448688
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_047427600
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_024448689
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:NM_024698
Location:3UTRS;EXON

Gene Symbol:SLC25A22
Accession:XM_011520371
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000361194 CLINVAR
dbSNP (RS) rs886048691 CLINVAR
MedGen C0270855 CLINVAR
NCBI Gene SLC25A22 CLINVAR
OMIM 609302 CLINVAR
SNOMED CT 44423001 CLINVAR