RGD:14739921 Rat Genome Database

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Variant: RGD:14739921 -  Homo sapiens

RGD ID: 14739921
RS ID: rs1586148685
ClinVar ID: CV655871
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 94,929,272
GRCh38 8 93,917,044
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001161781.2:c.-219C>T
NM_001161780.2:c.-40C>T
NM_018444.4:c.-80C>T
NG_012233.1:g.5111C>T
More...
03/19/2018 5 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDP1
Accession:NM_018444
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:NM_001161780
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:NM_001161779
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:NM_001161781
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:XM_047421905
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:XM_047421907
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:XM_047421906
Location:5UTRS;EXON

Gene Symbol:PDP1
Accession:XM_017013588
Location:INTRON

Gene Symbol:PDP1
Accession:XM_047421909
Location:INTRON

Gene Symbol:PDP1
Accession:XM_047421904
Location:INTRON

Gene Symbol:PDP1
Accession:XM_047421908
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000840112 CLINVAR
dbSNP (RS) rs1586148685 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene PDP1 CLINVAR
OMIM 605993 CLINVAR