RGD:15170459 Rat Genome Database

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Variant: RGD:15170459 -  Homo sapiens

RGD ID: 15170459
RS ID: rs373147022
ClinVar ID: CV745409
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GK  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 30,671,741
GRCh38 X 30,653,624
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008178.1:g.5266G>A
NC_000023.11:g.30653624G>A
NC_000023.10:g.30671741G>A
LRG_848t1:c.78+9G>A
More... 		02/07/2018 intron variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GK
Accession:NM_001128127
Location:INTRON

Gene Symbol:GK
Accession:NM_001205019
Location:INTRON

Gene Symbol:GK
Accession:NM_001399987
Location:INTRON

Gene Symbol:GK
Accession:XM_006724483
Location:INTRON

Gene Symbol:GK
Accession:NM_203391
Location:INTRON

Gene Symbol:GK
Accession:XM_011545491
Location:INTRON

Gene Symbol:GK
Accession:XM_011545492
Location:INTRON

Gene Symbol:GK
Accession:NM_000167
Location:INTRON

Gene Symbol:GK
Accession:NR_174375
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174369
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174374
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174373
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174372
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174370
Location:INTRON;NON-CODING

Gene Symbol:GK
Accession:NR_174371
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000905270 CLINVAR
  RCV003950645 CLINVAR
dbSNP (RS) rs373147022 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GK CLINVAR
OMIM 300474 CLINVAR