RGD:151350976 Rat Genome Database

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Variant: RGD:151350976 -  Homo sapiens

RGD ID: 151350976
RS ID: rs376448795
ClinVar ID: CV1323229
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STK11  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 1,220,366
GRCh38 19 1,220,367
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_319t1:c.465-6C>G
NM_000455.5:c.465-6C>G
LRG_319:g.35961C>G
NG_007460.2:g.35961C>G
More... 		05/17/2021 intron variant uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:STK11
Accession:NM_000455
Location:INTRON

Gene Symbol:STK11
Accession:NM_001407255
Location:INTRON

Gene Symbol:STK11
Accession:NR_176325
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001805557 CLINVAR
dbSNP (RS) rs376448795 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene STK11 CLINVAR
OMIM 602216 CLINVAR
SNOMED CT 699346009 CLINVAR