RGD:11659329 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:11659329 -  Homo sapiens

RGD ID: 11659329
RS ID: rs886049187
ClinVar ID: CV316702
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KRAS  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 25,360,404
GRCh38 12 25,207,470
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.25207470C>T
NC_000012.11:g.25360404C>T
NM_004985.3:c.*2325G>A
LRG_344t1:c.*2325G>A
More...
06/14/2016 3 prime utr variant uncertain significance Noonan's syndrome; Pseudo-Turner syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KRAS
Accession:NM_004985
Location:3UTRS;EXON

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

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

Gene Symbol:KRAS
Accession:NM_001369786
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000356994 CLINVAR
dbSNP (RS) rs886049187 CLINVAR
MedGen C0028326 CLINVAR
NCBI Gene KRAS CLINVAR
OMIM 190070 CLINVAR
SNOMED CT 205824006 CLINVAR