RGD:14741198 Rat Genome Database

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Variant: RGD:14741198 -  Homo sapiens

RGD ID: 14741198
ClinVar ID: CV671844
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: JAG1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 10,644,666
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000020.11:g.10664018C>G
NC_000020.10:g.10644666C>G
NM_000214.2:c.388-4G>C
03/30/2018 likely benign

Variant Details
Variant Transcripts
Gene Symbol:JAG1
Accession:NM_000214
Location:INTRON

Variant Samples