RGD:152127432 Rat Genome Database

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Variant: RGD:152127432 -  Homo sapiens

RGD ID: 152127432
RS ID: rs2109034292
ClinVar ID: CV1530274
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEPSECS  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 25,157,816
GRCh38 4 25,156,194
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_016955.4:c.390T>C
NG_028222.1:g.9389T>C
NC_000004.12:g.25156194A>G
NC_000004.11:g.25157816A>G
More... 		01/13/2021 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEPSECS
Accession:XM_011513848
Location:EXON

Gene Symbol:SEPSECS
Accession:NM_001410714
Location:EXON

Gene Symbol:SEPSECS
Accession:NM_016955
Location:EXON

Gene Symbol:SEPSECS
Accession:XM_011513847
Location:EXON

Gene Symbol:SEPSECS
Accession:XM_011513846
Location:EXON

Gene Symbol:
Accession:
Location:EXON

Gene Symbol:SEPSECS
Accession:XM_047415762
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002198867 CLINVAR
dbSNP (RS) rs2109034292 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEPSECS CLINVAR
OMIM 613009 CLINVAR