RGD:152031164 Rat Genome Database

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Variant: RGD:152031164 -  Homo sapiens

RGD ID: 152031164
RS ID: rs2123144086
ClinVar ID: CV1548638
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNAP25  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 10,277,709
GRCh38 20 10,297,061
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001322902.2:c.407+11T>A
NM_001322903.2:c.407+11T>A
NM_001322904.2:c.407+11T>A
NM_001322905.2:c.407+11T>A
More... 		11/24/2021 intron variant likely benign MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:SNAP25
Accession:NM_001322904
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322903
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001424415
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322902
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_003081
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322908
Location:INTRON

Gene Symbol:SNAP25
Accession:XM_047440391
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001424416
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_130811
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322905
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322906
Location:INTRON

Gene Symbol:SNAP25
Accession:XM_017028022
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322910
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322907
Location:INTRON

Gene Symbol:SNAP25
Accession:NM_001322909
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002086302 CLINVAR
dbSNP (RS) rs2123144086 CLINVAR
MedGen C4225364 CLINVAR
NCBI Gene SNAP25 CLINVAR
OMIM 600322 CLINVAR
  616330 CLINVAR