RGD:26914474 Rat Genome Database

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Variant: RGD:26914474 -  Homo sapiens

RGD ID: 26914474
RS ID: rs1941875791
ClinVar ID: CV851895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEN1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 64,575,577
GRCh38 11 64,808,105
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001370259.2:c.446-6C>A
LRG_509:g.8190C>A
NG_033040.1:g.137C>A
NG_008929.1:g.8190C>A
More... 		01/28/2019 intron variant uncertain significance Endocrine adenomatosis multiple; MEA I; MEN 1; MEN I; Wermer syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MEN1
Accession:NM_001370261
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407144
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407146
Location:INTRON

Gene Symbol:MEN1
Accession:NM_000244
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370251
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370259
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407151
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370260
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407150
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130801
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407149
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130804
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370263
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407142
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130803
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130799
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017766
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407143
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130802
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407152
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130800
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370262
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407145
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407147
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407148
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017768
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017767
Location:INTRON

Gene Symbol:MEN1
Accession:NR_176284
Location:INTRON;NON-CODING

Gene Symbol:MEN1
Accession:NR_176286
Location:INTRON;NON-CODING

Gene Symbol:MEN1
Accession:NR_176287
Location:INTRON;NON-CODING

Gene Symbol:MEN1
Accession:NR_176285
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001054998 CLINVAR
dbSNP (RS) rs1941875791 CLINVAR
MedGen C0025267 CLINVAR
NCBI Gene MEN1 CLINVAR
OMIM 131100 CLINVAR
  613733 CLINVAR
SNOMED CT 30664006 CLINVAR