RGD:597782864 Rat Genome Database

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Variant: RGD:597782864 -  Homo sapiens

RGD ID: 597782864
ClinVar ID: CV3585228
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTPN7  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 202,128,535
GRCh38 1 202,159,407
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001364877.2:c.-5T>G
NM_001364878.1:c.-5T>G
NM_002832.4:c.-5T>G
NM_080588.3:c.113T>G
More... 		10/11/2024 5 prime utr variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004854041 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PTPN7 CLINVAR
OMIM 176889 CLINVAR