RGD:401926617 Rat Genome Database

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Variant: RGD:401926617 -  Homo sapiens

RGD ID: 401926617
ClinVar ID: CV2827520
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: PTPRG  PTPRG-AS1  
Reference Nucleotide: -
Variant Nucleotide: TTTTTTTTTTTTTTTTTTTTTTT
Position
Assembly Chr Position
GRCh37 3 62,267,214
GRCh38 3 62,281,539
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001375471.1:c.3679-12_3679-11insTTTTTTTTTTTTTTTTTTTTTTT
NM_002841.4:c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTT
NC_000003.12:g.62281551_62281552insTTTTTTTTTTTTTTTTTTTTTTT
NC_000003.11:g.62267226_62267227insTTTTTTTTTTTTTTTTTTTTTTT
 04/01/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.


Database
Acc Id
Source(s)
ClinVar RCV003437890 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PTPRG CLINVAR
  PTPRG-AS1 CLINVAR
OMIM 176886 CLINVAR