RGD:402500736 Rat Genome Database

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Variant: RGD:402500736 -  Homo sapiens

RGD ID: 402500736
ClinVar ID: CV3170548
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRIP4  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 64,690,030
GRCh38 15 64,397,831
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321924.2:c.-73+13T>G
NM_016213.5:c.618+13T>G
NG_046848.1:g.15028T>G
NC_000015.10:g.64397831T>G
More... 		04/21/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRIP4
Accession:NM_001321924
Location:5UTRS;INTRON

Gene Symbol:TRIP4
Accession:NM_016213
Location:INTRON

Gene Symbol:TRIP4
Accession:NR_135855
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003877921 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRIP4 CLINVAR
OMIM 604501 CLINVAR