RGD:152161457 Rat Genome Database

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Variant: RGD:152161457 -  Homo sapiens

RGD ID: 152161457
RS ID: rs906377309
ClinVar ID: CV1606163
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SYT2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 202,568,332
GRCh38 1 202,599,204
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001136504.1:c.1053+14G>T
NM_177402.5:c.1053+14G>T
NG_041776.1:g.116220G>T
NC_000001.11:g.202599204C>A
More... 		10/27/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SYT2
Accession:XM_011509192
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000312
Location:INTRON

Gene Symbol:SYT2
Accession:NM_001136504
Location:INTRON

Gene Symbol:SYT2
Accession:NM_177402
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000310
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000311
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000309
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000313
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002181007 CLINVAR
dbSNP (RS) rs906377309 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SYT2 CLINVAR
OMIM 600104 CLINVAR