RGD:28868861 Rat Genome Database

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Variant: RGD:28868861 -  Homo sapiens

RGD ID: 28868861
RS ID: rs551904948
ClinVar ID: CV868856
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A22  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 791,694
GRCh38 11 791,694
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001191060.2:c.*221C>G
NM_001191061.2:c.*221C>G
NM_024698.5:c.*221C>G
NM_024698.6:c.*221C>G
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC25A22
Accession:XM_024448689
Location:3UTRS;EXON

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

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

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

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

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

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

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

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

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

Gene Symbol:SLC25A22
Accession:NM_001191061
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001112776 CLINVAR
dbSNP (RS) rs551904948 CLINVAR
MedGen C0270855 CLINVAR
NCBI Gene SLC25A22 CLINVAR
OMIM 609302 CLINVAR
SNOMED CT 44423001 CLINVAR