RGD:15105471 Rat Genome Database

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Variant: RGD:15105471 -  Homo sapiens

RGD ID: 15105471
RS ID: rs116399728
ClinVar ID: CV779374
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SYCE1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 135,371,661
GRCh38 10 133,558,157
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_130784.4:c.211+10G>A
NM_001143763.2:c.319+10G>A
NM_001143764.3:c.319+10G>A
NG_052008.1:g.15119G>A
More... 		12/31/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SYCE1
Accession:NM_001143764
Location:INTRON

Gene Symbol:SYCE1
Accession:NM_001143763
Location:INTRON

Gene Symbol:SYCE1
Accession:NM_130784
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000959893 CLINVAR
dbSNP (RS) rs116399728 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SYCE1 CLINVAR
OMIM 611486 CLINVAR