RGD:25326753 Rat Genome Database

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Variant: RGD:25326753 -  Homo sapiens

RGD ID: 25326753
RS ID: rs1592648530
ClinVar ID: CV815505
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEN1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 64,575,019
GRCh38 11 64,807,547
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_130799.2:c.783+5G>A
NM_001370259.2:c.783+5G>A
LRG_509:g.8748G>A
NG_033040.1:g.695G>A
More... 		11/13/2018 intron variant uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MEN1
Accession:NM_130799
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407146
Location:INTRON

Gene Symbol:MEN1
Accession:NM_000244
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407150
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130801
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130800
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407148
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017768
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370263
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370262
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407145
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017766
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370251
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407142
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407144
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407149
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370259
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407147
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370260
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407151
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001370261
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407143
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130804
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:XM_017017767
Location:INTRON

Gene Symbol:MEN1
Accession:NM_001407152
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130802
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEN1
Accession:NM_130803
Location:INTRON

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

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001026855 CLINVAR
dbSNP (RS) rs1592648530 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MEN1 CLINVAR
OMIM 613733 CLINVAR
SNOMED CT 699346009 CLINVAR