RGD:407511756 Rat Genome Database

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Variant: RGD:407511756 -  Homo sapiens

RGD ID: 407511756
ClinVar ID: CV3463408
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIDD1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 802,328
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_145886.4:c.1043G>A
NM_145887.4:c.1043G>A
NG_023407.1:g.942G>A
NC_000011.10:g.802328C>T
More... 		03/31/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004648148 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene PIDD1 CLINVAR
OMIM 605247 CLINVAR