RGD:11606592 Rat Genome Database

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Variant: RGD:11606592 -  Homo sapiens

RGD ID: 11606592
RS ID: rs13096
ClinVar ID: CV316700
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KRAS  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 25,359,841
GRCh38 12 25,206,907
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.25206907T>C
NC_000012.11:g.25359841T>C
NM_004985.3:c.*2888A>G
LRG_344t2:c.*3009A>G
More... 		06/14/2016 3 prime utr variant likely benign Noonan's syndrome; Pseudo-Turner syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KRAS
Accession:NM_001369786
Location:3UTRS;EXON

Gene Symbol:KRAS
Accession:NM_001369787
Location:3UTRS;EXON

Gene Symbol:KRAS
Accession:XM_047428826
Location:3UTRS;EXON

Gene Symbol:KRAS
Accession:NM_004985
Location:3UTRS;EXON

Gene Symbol:KRAS
Accession:NM_033360
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000333153 CLINVAR
dbSNP (RS) rs13096 CLINVAR
MedGen C0028326 CLINVAR
NCBI Gene KRAS CLINVAR
OMIM 190070 CLINVAR
SNOMED CT 205824006 CLINVAR