RGD:13509719 Rat Genome Database

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Variant: RGD:13509719 -  Homo sapiens

RGD ID: 13509719
RS ID: rs759167957
ClinVar ID: CV481577
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SYT2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 202,569,605
GRCh38 1 202,600,477
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_041776.1:g.114947C>G
NC_000001.10:g.202569605G>C
NC_000001.11:g.202600477G>C
NM_001136504.1:c.802-3C>G
More... 		11/14/2017 intron variant uncertain significance none provided

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

Gene Symbol:SYT2
Accession:XM_017000313
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000310
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000309
Location:INTRON

Gene Symbol:SYT2
Accession:NM_001136504
Location:INTRON

Gene Symbol:SYT2
Accession:NM_177402
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000311
Location:INTRON

Gene Symbol:SYT2
Accession:XM_017000312
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000578687 CLINVAR
dbSNP (RS) rs759167957 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SYT2 CLINVAR
OMIM 600104 CLINVAR