RGD:150458122 Rat Genome Database

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Variant: RGD:150458122 -  Homo sapiens

RGD ID: 150458122
RS ID: rs114816309
ClinVar ID: CV1237171
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NOTCH4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 32,182,875
GRCh38 6 32,215,098
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004557.4:c.2021+128A>G
NG_028190.1:g.13970A>G
NC_000006.12:g.32215098T>C
NC_000006.11:g.32182875T>C
 05/25/2021 intron variant 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 Information

Database Acc Id Source(s)
ClinVar RCV001648850 CLINVAR
dbSNP (RS) rs114816309 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NOTCH4 CLINVAR
OMIM 164951 CLINVAR