RGD:15184297 Rat Genome Database

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Variant: RGD:15184297 -  Homo sapiens

RGD ID: 15184297
RS ID: rs141989882
ClinVar ID: CV709611
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSF2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 131,410,577
GRCh38 5 132,074,884
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000758.4:c.276C>T
NG_033024.1:g.6093C>T
NC_000005.10:g.132074884C>T
NC_000005.9:g.131410577C>T
More...
07/06/2018 synonymous variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CSF2
Accession:NM_000758
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 92
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MWLQSLLLLGTVACSISAPARSPSPSTQPWEHVNAIQEARRLLNLSRDTAAEMNETVEVISEMFDLQEPTCLQTRLELYK
QGLRGSLTKLKGPLTMMASHYKQHCPPTPETSCATQIITFESFKENLKDFLLVIPFDCWEPVQE*

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000975079 CLINVAR
dbSNP (RS) rs141989882 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CSF2 CLINVAR
OMIM 138960 CLINVAR