RGD:150464127 Rat Genome Database

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Variant: RGD:150464127 -  Homo sapiens

RGD ID: 150464127
RS ID: rs77851303
ClinVar ID: CV1214886
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLD1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 171,329,981
GRCh38 3 171,612,191
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001130081.3:c.2768+88A>G
NM_002662.5:c.2882+88A>G
NG_029851.1:g.203304A>G
NC_000003.12:g.171612191T>C
More... 		05/15/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PLD1
Accession:NM_002662
Location:INTRON

Gene Symbol:PLD1
Accession:XM_011512898
Location:INTRON

Gene Symbol:PLD1
Accession:XM_011512899
Location:INTRON

Gene Symbol:PLD1
Accession:XM_011512897
Location:INTRON

Gene Symbol:PLD1
Accession:XM_005247534
Location:INTRON

Gene Symbol:PLD1
Accession:XM_017006624
Location:INTRON

Gene Symbol:PLD1
Accession:XM_047448318
Location:INTRON

Gene Symbol:PLD1
Accession:XM_005247533
Location:INTRON

Gene Symbol:PLD1
Accession:XM_047448316
Location:INTRON

Gene Symbol:PLD1
Accession:NM_001130081
Location:INTRON

Gene Symbol:PLD1
Accession:XM_047448317
Location:INTRON

Gene Symbol:PLD1
Accession:XR_007095693
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001613882 CLINVAR
dbSNP (RS) rs77851303 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLD1 CLINVAR
OMIM 602382 CLINVAR