RGD:150485063 Rat Genome Database

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Variant: RGD:150485063 -  Homo sapiens

RGD ID: 150485063
RS ID: rs4617310
ClinVar ID: CV1273934
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GK  GK-AS1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 30,725,794
GRCh38 X 30,707,677
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_848t1:c.894+79C>T
LRG_848t2:c.876+79C>T
NC_000023.11:g.30707677C>T
NC_000023.10:g.30725794C>T
More... 		05/12/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GK-AS1
Accession:NR_046603
Location:EXON;NON-CODING

Gene Symbol:GK
Accession:NM_001205019
Location:INTRON

Gene Symbol:GK
Accession:NM_203391
Location:INTRON

Gene Symbol:GK
Accession:NM_001128127
Location:INTRON

Gene Symbol:GK
Accession:NM_000167
Location:INTRON

Gene Symbol:GK
Accession:XM_006724483
Location:INTRON

Gene Symbol:GK
Accession:XM_011545491
Location:INTRON

Gene Symbol:GK
Accession:XM_011545492
Location:INTRON

Gene Symbol:GK
Accession:NM_001399987
Location:INTRON

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

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

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

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

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001698634 CLINVAR
dbSNP (RS) rs4617310 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GK CLINVAR
  GK-AS1 CLINVAR
OMIM 300474 CLINVAR