RGD:15148442 Rat Genome Database

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Variant: RGD:15148442 -  Homo sapiens

RGD ID: 15148442
RS ID: rs770742362
ClinVar ID: CV759459
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NOTCH4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 32,180,412
GRCh38 6 32,212,635
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.32212635G>A
NM_004557.4:c.2527-8C>T
NG_028190.1:g.16433C>T
NC_000006.11:g.32180412G>A
More... 		05/07/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NOTCH4
Accession:NM_004557
Location:INTRON

Gene Symbol:NOTCH4
Accession:NR_134950
Location:INTRON;NON-CODING

Gene Symbol:NOTCH4
Accession:NR_134949
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000923097 CLINVAR
dbSNP (RS) rs770742362 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NOTCH4 CLINVAR
OMIM 164951 CLINVAR