RGD:152107059 Rat Genome Database

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Variant: RGD:152107059 -  Homo sapiens

RGD ID: 152107059
RS ID: rs188601318
ClinVar ID: CV1639120
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEPSECS  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 25,128,983
GRCh38 4 25,127,361
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.25127361C>G
NM_016955.4:c.1027-4G>C
NG_028222.1:g.38222G>C
NC_000004.11:g.25128983C>G
10/31/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEPSECS
Accession:NM_016955
Location:INTRON

Gene Symbol:SEPSECS
Accession:XM_011513848
Location:INTRON

Gene Symbol:SEPSECS
Accession:XM_011513846
Location:INTRON

Gene Symbol:SEPSECS
Accession:XM_011513847
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SEPSECS
Accession:XM_047415762
Location:INTRON

Gene Symbol:SEPSECS
Accession:NM_001410714
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002152546 CLINVAR
dbSNP (RS) rs188601318 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEPSECS CLINVAR
OMIM 613009 CLINVAR