rs73215991 Rat Genome Database

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Variant: rs73215991 -  Homo sapiens

RGD ID: 150481691
RS ID: rs73215991
ClinVar ID: CV1258963
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 132,181,494
GRCh38 3 132,462,650
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001329126.2:c.1770+127T>G
NM_015268.4:c.1770+127T>G
NG_051045.1:g.50124T>G
NC_000003.12:g.132462650T>G
More... 		07/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNAJC13
Accession:XM_047447820
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447819
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_015268
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001686093 CLINVAR
dbSNP (RS) rs73215991 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR