RGD:15109735 Rat Genome Database

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Variant: RGD:15109735 -  Homo sapiens

RGD ID: 15109735
RS ID: rs766290203
ClinVar ID: CV758822
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GPSM2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 109,440,258
GRCh38 1 108,897,636
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321039.3:c.414+9G>A
NM_001321038.2:c.414+9G>A
NM_013296.5:c.414+9G>A
NG_028108.2:g.27287G>A
More... 		04/13/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GPSM2
Accession:XM_047418723
Location:INTRON

Gene Symbol:GPSM2
Accession:NM_001321039
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_047418724
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_017001098
Location:INTRON

Gene Symbol:GPSM2
Accession:NM_013296
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_011541303
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_011541302
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_017001097
Location:INTRON

Gene Symbol:GPSM2
Accession:XM_006710589
Location:INTRON

Gene Symbol:GPSM2
Accession:NM_001321038
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000916394 CLINVAR
dbSNP (RS) rs766290203 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GPSM2 CLINVAR
OMIM 609245 CLINVAR