RGD:14741172 Rat Genome Database

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Variant: RGD:14741172 -  Homo sapiens

RGD ID: 14741172
RS ID: rs1586261589
ClinVar ID: CV663203
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC112268030  RAD21  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 117,861,181
GRCh38 8 116,848,942
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006265.3:c.1704+4T>C
NG_032862.1:g.30925T>C
NC_000008.11:g.116848942A>G
NC_000008.10:g.117861181A>G
More... 		03/23/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LOC112268030
Accession:XR_002956724
Location:EXON;NON-CODING

Gene Symbol:RAD21
Accession:NM_006265
Location:INTRON

Gene Symbol:LOC112268030
Accession:XR_007061065
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000840657 CLINVAR
dbSNP (RS) rs1586261589 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene RAD21 CLINVAR
OMIM 606462 CLINVAR