RGD:11594104 Rat Genome Database

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Variant: RGD:11594104 -  Homo sapiens

RGD ID: 11594104
RS ID: rs13109061
ClinVar ID: CV298091
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEPSECS  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 25,124,746
GRCh38 4 25,123,124
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028222.1:g.42459A>G
NC_000004.12:g.25123124T>C
NC_000004.11:g.25124746T>C
NM_016955.4:c.*807A>G
More... 		06/14/2016 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SEPSECS
Accession:NM_016955
Location:3UTRS;EXON

Gene Symbol:SEPSECS
Accession:XM_011513846
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:SEPSECS
Accession:XM_011513848
Location:3UTRS;EXON

Gene Symbol:SEPSECS
Accession:XM_047415762
Location:3UTRS;EXON

Gene Symbol:SEPSECS
Accession:NM_001410714
Location:3UTRS;EXON

Gene Symbol:SEPSECS
Accession:XM_011513847
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355435 CLINVAR
dbSNP (RS) rs13109061 CLINVAR
MedGen C3151140 CLINVAR
NCBI Gene SEPSECS CLINVAR
OMIM 613009 CLINVAR
  613811 CLINVAR