RGD:150428669 Rat Genome Database

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Variant: RGD:150428669 -  Homo sapiens

RGD ID: 150428669
RS ID: rs12001608
ClinVar ID: CV1187448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124902310  NOTCH1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 139,410,570
GRCh38 9 136,516,118
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017617.5:c.1556-24C>T
LRG_1122:g.34669C>T
NG_007458.1:g.34669C>T
NC_000009.12:g.136516118G>A
More... 		07/08/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NOTCH1
Accession:NM_017617
Location:INTRON

Gene Symbol:NOTCH1
Accession:XM_011518717
Location:INTRON

Gene Symbol:LOC124902310
Accession:XR_007061865
Location:INTRON;NON-CODING

Gene Symbol:LOC124902310
Accession:XR_007061864
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001562566 CLINVAR
dbSNP (RS) rs12001608 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NOTCH1 CLINVAR
OMIM 190198 CLINVAR