rs73794525 Rat Genome Database

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Variant: rs73794525 -  Homo sapiens

RGD ID: 150442067
RS ID: rs73794525
ClinVar ID: CV1233637
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SERAC1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 158,571,941
GRCh38 6 158,150,909
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032861.4:c.129-320G>A
NG_032889.1:g.22372G>A
NC_000006.12:g.158150909C>T
NC_000006.11:g.158571941C>T
 07/07/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SERAC1
Accession:XM_006715586
Location:5UTRS;INTRON

Gene Symbol:SERAC1
Accession:XM_011536198
Location:5UTRS;INTRON

Gene Symbol:SERAC1
Accession:XM_047419421
Location:INTRON

Gene Symbol:SERAC1
Accession:NM_032861
Location:INTRON

Gene Symbol:SERAC1
Accession:XM_024446573
Location:INTRON

Gene Symbol:SERAC1
Accession:NR_073096
Location:INTRON;NON-CODING

Gene Symbol:SERAC1
Accession:XR_007059349
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001645325 CLINVAR
dbSNP (RS) rs73794525 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SERAC1 CLINVAR
OMIM 614725 CLINVAR