RGD:15157954 Rat Genome Database

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Variant: RGD:15157954 -  Homo sapiens

RGD ID: 15157954
RS ID: rs199537326
ClinVar ID: CV745399
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCX  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 110,574,278
GRCh38 X 111,331,050
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000555.3:c.1052-9T>C
NM_001195553.2:c.809-9T>C
NM_001369370.1:c.809-9T>C
NM_001369371.1:c.809-9T>C
More... 		05/22/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DCX
Accession:NM_178151
Location:INTRON

Gene Symbol:DCX
Accession:NM_000555
Location:INTRON

Gene Symbol:DCX
Accession:NM_001369373
Location:INTRON

Gene Symbol:DCX
Accession:NM_001369371
Location:INTRON

Gene Symbol:DCX
Accession:NM_001369370
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DCX
Accession:NM_001369374
Location:INTRON

Gene Symbol:DCX
Accession:NM_178153
Location:INTRON

Gene Symbol:DCX
Accession:NM_001195553
Location:INTRON

Gene Symbol:DCX
Accession:NM_001369372
Location:INTRON

Gene Symbol:DCX
Accession:NM_001410715
Location:INTRON

Gene Symbol:DCX
Accession:NM_178152
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000902636 CLINVAR
dbSNP (RS) rs199537326 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DCX CLINVAR
OMIM 300121 CLINVAR