RGD:152078612 Rat Genome Database

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Variant: RGD:152078612 -  Homo sapiens

RGD ID: 152078612
RS ID: rs1858339251
ClinVar ID: CV1666623
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,361
GRCh38 10 87,863,604
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_1087:g.4834C>A
LRG_311:g.5167G>T
NG_033079.1:g.4834C>A
NG_007466.2:g.5167G>T
More... 		01/10/2023 uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002210968 CLINVAR
dbSNP (RS) rs1858339251 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR