rs28360884 Rat Genome Database

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Variant: rs28360884 -  Homo sapiens

RGD ID: 150440882
RS ID: rs28360884
ClinVar ID: CV1265472
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIDD1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 802,902
GRCh38 11 802,902
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_145887.4:c.710-11A>C
NG_023407.1:g.368A>C
NC_000011.10:g.802902T>G
NC_000011.9:g.802902T>G
More... 		02/13/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIDD1
Accession:XM_047427245
Location:5UTRS;EXON

Gene Symbol:PIDD1
Accession:XM_011520213
Location:5UTRS;INTRON

Gene Symbol:PIDD1
Accession:XM_047427246
Location:5UTRS;INTRON

Gene Symbol:PIDD1
Accession:NM_145887
Location:INTRON

Gene Symbol:PIDD1
Accession:NM_145886
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_005253006
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_005253005
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_011520212
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_011520210
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_011520209
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427240
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427239
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427238
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427243
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427242
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427241
Location:INTRON

Gene Symbol:PIDD1
Accession:XM_047427244
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001679175 CLINVAR
dbSNP (RS) rs28360884 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIDD1 CLINVAR
OMIM 605247 CLINVAR