rs112885868 Rat Genome Database

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Variant: rs112885868 -  Homo sapiens

RGD ID: 150509610
RS ID: rs112885868
ClinVar ID: CV1229938
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C12orf57  LOC127823546  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 7,053,121
GRCh38 12 6,943,958
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301834.1:c.-15-149G>A
NM_001301836.2:c.13+296G>A
NG_008047.1:g.24496G>A
NG_034262.1:g.5142G>A
More... 		03/28/2021 intron variant benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Variant Details
Variant Transcripts
Gene Symbol:C12orf57
Accession:NM_001301834
Location:5UTRS;INTRON

Gene Symbol:C12orf57
Accession:NM_001301838
Location:INTRON

Gene Symbol:C12orf57
Accession:NM_138425
Location:INTRON

Gene Symbol:C12orf57
Accession:NM_001301836
Location:INTRON

Gene Symbol:C12orf57
Accession:NM_001301837
Location:INTRON

Gene Symbol:C12orf57
Accession:NR_126035
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001636518 CLINVAR
dbSNP (RS) rs112885868 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C12orf57 CLINVAR
OMIM 615140 CLINVAR