rs372529945 Rat Genome Database

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Variant: rs372529945 -  Homo sapiens

RGD ID: 15117649
RS ID: rs372529945
ClinVar ID: CV760334
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DLL4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 41,222,813
GRCh38 15 40,930,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.9:g.41222813C>T
NM_019074.3:c.337-10C>T
NC_000015.10:g.40930615C>T
LRG_1268:g.6283C>T
More... 		03/09/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DLL4
Accession:NM_019074
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000917832 CLINVAR
dbSNP (RS) rs372529945 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DLL4 CLINVAR
OMIM 605185 CLINVAR