rs6778925 Rat Genome Database

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Variant: rs6778925 -  Homo sapiens

RGD ID: 150511137
RS ID: rs6778925
ClinVar ID: CV1229366
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 132,175,779
GRCh38 3 132,456,935
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.1349+103C>A
NM_015268.4:c.1349+103C>A
NG_051045.1:g.44409C>A
NC_000003.12:g.132456935C>A
More... 		07/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNAJC13
Accession:XM_047447819
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447820
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_015268
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001637294 CLINVAR
dbSNP (RS) rs6778925 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR