RGD:15128512 Rat Genome Database

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Variant: RGD:15128512 -  Homo sapiens

RGD ID: 15128512
RS ID: rs182480080
ClinVar ID: CV759169
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SESTD1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 179,977,444
GRCh38 2 179,112,717
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_178123.5:c.1961+7G>A
NC_000002.12:g.179112717C>T
NC_000002.11:g.179977444C>T
NM_178123.4:c.1961+7G>A
 07/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SESTD1
Accession:XM_011512141
Location:INTRON

Gene Symbol:SESTD1
Accession:XM_047446273
Location:INTRON

Gene Symbol:SESTD1
Accession:XM_047446274
Location:INTRON

Gene Symbol:SESTD1
Accession:XM_047446275
Location:INTRON

Gene Symbol:SESTD1
Accession:NM_178123
Location:INTRON

Gene Symbol:SESTD1
Accession:XR_007084411
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000919665 CLINVAR
dbSNP (RS) rs182480080 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SESTD1 CLINVAR