RGD:155717506 Rat Genome Database

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Variant: RGD:155717506 -  Homo sapiens

RGD ID: 155717506
ClinVar ID: CV1822983
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STK11  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 1,221,208
GRCh38 19 1,221,209
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_319t1:c.735-4G>T
NM_000455.5:c.735-4G>T
LRG_319:g.36803G>T
NG_007460.2:g.36803G>T
More... 		09/14/2022 intron variant likely benign 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 Information

Database Acc Id Source(s)
ClinVar RCV002380262 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene STK11 CLINVAR
OMIM 602216 CLINVAR
SNOMED CT 699346009 CLINVAR