RGD:8633412 Rat Genome Database

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Variant: RGD:8633412 -  Homo sapiens

RGD ID: 8633412
ClinVar ID: CV88627
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTPRD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 8,465,675
GRCh38 9 8,465,675
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001171025.1:c.2242C>T
NM_130393.3:c.2257C>T
NM_001040712.2:c.2263C>T
NM_130391.3:c.2272C>T
More... 		synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:PTPRD
Accession:XM_017014966
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_024447625
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001377946
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423641
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423655
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014980
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_006716817
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014982
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001377958
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001377947
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423653
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423654
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423643
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_006716825
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014958
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014979
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423658
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423657
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423650
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423646
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014974
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_130393
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014965
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423659
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014970
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014968
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423649
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423645
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423642
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014967
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423647
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_002839
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001040712
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_006716827
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001378058
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014972
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423644
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_130391
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014963
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014964
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014978
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423660
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423656
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_001171025
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014961
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014971
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014976
Location:INTRON

Gene Symbol:PTPRD
Accession:NM_130392
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_006716823
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014969
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014977
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_017014983
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423651
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423652
Location:INTRON

Gene Symbol:PTPRD
Accession:XM_047423648
Location:INTRON

Variant Samples