RGD:13509659 Rat Genome Database

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Variant: RGD:13509659 -  Homo sapiens

RGD ID: 13509659
RS ID: rs1555204095
ClinVar ID: CV482029
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBK1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 64,875,610
GRCh38 12 64,481,830
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.64481830A>G
NC_000012.11:g.64875610A>G
NM_013254.4:c.813-12A>G
NM_013254.3:c.813-12A>G
More... 		11/02/2017 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:TBK1
Accession:XM_005268809
Location:INTRON

Gene Symbol:TBK1
Accession:NM_013254
Location:INTRON

Gene Symbol:TBK1
Accession:XM_005268810
Location:INTRON

Gene Symbol:TBK1
Accession:XR_007063071
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000578578 CLINVAR
dbSNP (RS) rs1555204095 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene TBK1 CLINVAR
OMIM 604834 CLINVAR