RGD:13525200 Rat Genome Database

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Variant: RGD:13525200 -  Homo sapiens

RGD ID: 13525200
RS ID: rs1364324227
ClinVar ID: CV507131
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DLG4  LOC126862479  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 7,099,904
GRCh38 17 7,196,585
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000017.10:g.7099904G>C
NM_001365.3:c.1213-10C>G
NC_000017.11:g.7196585G>C
NG_008391.3:g.28465C>G
More... 		04/20/2017 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:DLG4
Accession:NM_001365
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001128827
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001321075
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001321077
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001321076
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001321074
Location:INTRON

Gene Symbol:DLG4
Accession:NM_001369566
Location:INTRON

Gene Symbol:DLG4
Accession:NR_135527
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000602835 CLINVAR
dbSNP (RS) rs1364324227 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DLG4 CLINVAR
  LOC126862479 CLINVAR
OMIM 602887 CLINVAR