RGD:11603114 Rat Genome Database

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Variant: RGD:11603114 -  Homo sapiens

RGD ID: 11603114
RS ID: rs140837295
ClinVar ID: CV318664
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CBL  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 119,174,579
GRCh38 11 119,303,869
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_608t1:c.*4088C>T
LRG_608:g.102590C>T
NG_016808.1:g.102590C>T
NC_000011.10:g.119303869C>T
More... 		01/13/2018 3 prime utr variant benign|likely benign CBL MUTATION-ASSOCIATED SYNDROME; CBL SYNDROME; Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia; NOONAN SYNDROME-LIKE DISORDER WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CBL
Accession:NM_005188
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000296681 CLINVAR
dbSNP (RS) rs140837295 CLINVAR
MedGen C3150803 CLINVAR
NCBI Gene CBL CLINVAR
OMIM 165360 CLINVAR
  613563 CLINVAR