RGD:405109778 Rat Genome Database

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Variant: RGD:405109778 -  Homo sapiens

RGD ID: 405109778
ClinVar ID: CV2898671
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRIM28  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 59,061,099
GRCh38 19 58,549,732
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_046945.1:g.10264C>G
NC_000019.10:g.58549732C>G
NC_000019.9:g.59061099C>G
NM_005762.3:c.1983-5C>G
More... 		01/31/2024 intron variant benign|likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRIM28
Accession:NM_005762
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003557615 CLINVAR
  RCV003981000 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRIM28 CLINVAR
OMIM 601742 CLINVAR