RGD:155798684 Rat Genome Database

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Variant: RGD:155798684 -  Homo sapiens

RGD ID: 155798684
ClinVar ID: CV1860751
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NCR3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 31,560,670
GRCh38 6 31,592,893
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_147130.3:c.-172G>A
NG_021176.1:g.5093G>A
NC_000006.12:g.31592893C>T
NC_000006.11:g.31560670C>T
More... 		12/06/2022 5 prime utr variant pathogenic
Disease Annotations     Click to see Annotation Detail View
malaria  (IAGP)


Variant Details
Variant Transcripts
Gene Symbol:NCR3
Accession:XM_011514459
Location:5UTRS;EXON

Gene Symbol:NCR3
Accession:NM_001145466
Location:5UTRS;EXON

Gene Symbol:NCR3
Accession:XM_006715049
Location:5UTRS;EXON

Gene Symbol:NCR3
Accession:NM_147130
Location:5UTRS;EXON

Gene Symbol:NCR3
Accession:NM_001145467
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002467393 CLINVAR
MedGen C1970029 CLINVAR
NCBI Gene NCR3 CLINVAR
OMIM 611550 CLINVAR