RGD:151235157 Rat Genome Database

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Variant: RGD:151235157 -  Homo sapiens

RGD ID: 151235157
RS ID: rs1402130017
ClinVar ID: CV1318418
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 89,623,325
GRCh38 10 87,863,568
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_1087:g.4870C>G
NG_007466.2:g.5131G>C
NC_000010.11:g.87863568G>C
LRG_311:g.5131G>C
More... 		06/13/2023 uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001794741 CLINVAR
dbSNP (RS) rs1402130017 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR