rs115350072 Rat Genome Database

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Variant: rs115350072 -  Homo sapiens

RGD ID: 150514071
RS ID: rs115350072
ClinVar ID: CV1228040
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GATC  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 120,897,772
GRCh38 12 120,459,969
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_176818.3:c.*10T>G
NC_000012.12:g.120459969T>G
NC_000012.11:g.120897772T>G
NR_033684.2:n.556T>G
 05/04/2021 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GATC
Accession:NM_176818
Location:3UTRS;EXON

Gene Symbol:GATC
Accession:NR_033684
Location:EXON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001638318 CLINVAR
dbSNP (RS) rs115350072 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GATC CLINVAR
OMIM 617210 CLINVAR