RGD:126909081 Rat Genome Database

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Variant: RGD:126909081 -  Homo sapiens

RGD ID: 126909081
RS ID: rs2149008276
ClinVar ID: CV1052552
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAGT1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 77,086,398
GRCh38 X 77,830,901
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_353t1:c.998-6C>G
NM_001367916.1:c.902-6C>G
NM_032121.5:c.998-6C>G
LRG_353:g.69668C>G
More... 		04/17/2020 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MAGT1
Accession:NM_001367916
Location:INTRON

Gene Symbol:MAGT1
Accession:NM_032121
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001368221 CLINVAR
dbSNP (RS) rs2149008276 CLINVAR
MedGen C3275445 CLINVAR
NCBI Gene MAGT1 CLINVAR
OMIM 300715 CLINVAR
  300853 CLINVAR