RGD:12899602 Rat Genome Database

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Variant: RGD:12899602 -  Homo sapiens

RGD ID: 12899602
RS ID: rs1064794361
ClinVar ID: CV411455
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DLG3  DLG3-AS1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 69,674,171
GRCh38 X 70,454,321
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021120.4:c.1405+5G>C
NG_015849.2:g.14467G>C
NM_021120.2:c.1405+5G>C
NG_015849.1:g.14467G>C
More... 		07/26/2022 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:DLG3
Accession:XM_005262248
Location:5UTRS;INTRON

Gene Symbol:DLG3
Accession:XM_017029324
Location:INTRON

Gene Symbol:DLG3
Accession:NM_020730
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441884
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441883
Location:INTRON

Gene Symbol:DLG3
Accession:NM_001166278
Location:INTRON

Gene Symbol:DLG3
Accession:XM_011530883
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441887
Location:INTRON

Gene Symbol:DLG3
Accession:NM_021120
Location:INTRON

Gene Symbol:DLG3
Accession:XM_006724625
Location:INTRON

Gene Symbol:DLG3
Accession:XM_006724626
Location:INTRON

Gene Symbol:DLG3
Accession:XM_017029322
Location:INTRON

Gene Symbol:DLG3
Accession:XM_017029325
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441888
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441885
Location:INTRON

Gene Symbol:DLG3
Accession:XM_017029323
Location:INTRON

Gene Symbol:DLG3
Accession:XM_047441886
Location:INTRON

Gene Symbol:DLG3
Accession:XM_017029327
Location:INTRON

Gene Symbol:DLG3-AS1
Accession:NR_046586
Location:INTRON;NON-CODING

Gene Symbol:DLG3-AS1
Accession:NR_109801
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000480576 CLINVAR
dbSNP (RS) rs1064794361 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene DLG3 CLINVAR
  DLG3-AS1 CLINVAR
OMIM 300189 CLINVAR