rs115215815 Rat Genome Database

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Variant: rs115215815 -  Homo sapiens

RGD ID: 15115935
RS ID: rs115215815
ClinVar ID: CV778861
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FMN2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 240,286,653
GRCh38 1 240,123,353
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020066.4:c.1782+8G>A
NM_001305424.2:c.1782+8G>A
NM_001348094.2:c.1782+8G>A
NM_020066.5:c.1782+8G>A
More... 		12/31/2019 intron variant benign FMN2-related condition; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FMN2
Accession:XM_017001840
Location:INTRON

Gene Symbol:FMN2
Accession:NM_001348094
Location:INTRON

Gene Symbol:FMN2
Accession:NM_001305424
Location:INTRON

Gene Symbol:FMN2
Accession:XM_011544237
Location:INTRON

Gene Symbol:FMN2
Accession:XM_017001841
Location:INTRON

Gene Symbol:FMN2
Accession:XM_017001837
Location:INTRON

Gene Symbol:FMN2
Accession:NM_020066
Location:INTRON

Gene Symbol:FMN2
Accession:XM_047425620
Location:INTRON

Gene Symbol:FMN2
Accession:XM_017001838
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000961943 CLINVAR
  RCV003960718 CLINVAR
dbSNP (RS) rs115215815 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FMN2 CLINVAR
OMIM 606373 CLINVAR