RGD:150415360 Rat Genome Database

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Variant: RGD:150415360 -  Homo sapiens

RGD ID: 150415360
RS ID: rs145191840
ClinVar ID: CV1192509
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DDX3X  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 41,193,434
GRCh38 X 41,334,181
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363819.1:c.-1975G>A
NC_000023.10:g.41193434G>A
NR_126094.2:n.20G>A
NR_126093.1:n.874G>A
More... 		07/27/2018 5 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DDX3X
Accession:NM_001356
Location:5UTRS;EXON

Gene Symbol:DDX3X
Accession:XM_011543892
Location:5UTRS;EXON

Gene Symbol:DDX3X
Accession:NM_001363819
Location:5UTRS;EXON

Gene Symbol:DDX3X
Accession:NM_001193416
Location:5UTRS;EXON

Gene Symbol:DDX3X
Accession:NM_001193417
Location:5UTRS;EXON

Gene Symbol:DDX3X
Accession:NR_126094
Location:EXON;NON-CODING

Gene Symbol:DDX3X
Accession:NR_126093
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001567950 CLINVAR
dbSNP (RS) rs145191840 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DDX3X CLINVAR
OMIM 300160 CLINVAR