RGD:156330294 Rat Genome Database

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Variant: RGD:156330294 -  Homo sapiens

RGD ID: 156330294
ClinVar ID: CV2180942
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASET2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 167,344,611
GRCh38 6 166,931,123
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016280.2:g.30467A>G
NC_000006.12:g.166931123T>C
NC_000006.11:g.167344611T>C
NM_003730.6:c.493-5A>G
 04/08/2022 intron variant uncertain significance 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 RCV003047169 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RNASET2 CLINVAR
OMIM 612944 CLINVAR