RGD:405014061 Rat Genome Database

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Variant: RGD:405014061 -  Homo sapiens

RGD ID: 405014061
ClinVar ID: CV2997684
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASET2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 167,356,491
GRCh38 6 166,943,003
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003730.6:c.332+16T>C
NG_016280.2:g.18587T>C
NC_000006.12:g.166943003A>G
NC_000006.11:g.167356491A>G
 01/08/2024 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RNASET2
Accession:NM_003730
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003694148 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RNASET2 CLINVAR
OMIM 612944 CLINVAR