rs3762674 Rat Genome Database

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Variant: rs3762674 -  Homo sapiens

RGD ID: 150450737
RS ID: rs3762674
ClinVar ID: CV1254148
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 132,235,022
GRCh38 3 132,516,178
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015268.4:c.5486-244G>T
NM_001329126.2:c.5501-244G>T
NG_051045.1:g.103652G>T
NC_000003.12:g.132516178G>T
More... 		07/09/2018 intron variant benign none provided

Gene Symbol:DNAJC13
Accession:NM_015268
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447819
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447820
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001667786 CLINVAR
dbSNP (RS) rs3762674 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR