rs138029604 Rat Genome Database

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Variant: rs138029604 -  Homo sapiens

RGD ID: 150459754
RS ID: rs138029604
ClinVar ID: CV1268386
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: DNAJC13  
Reference Nucleotide: -
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 132,193,459
GRCh38 3 132,474,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015268.4:c.2292-316dup
NM_001329126.2:c.2307-316dup
NG_051045.1:g.62090dup
NC_000003.12:g.132474616dup
More... 		12/05/2020 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001693383 CLINVAR
dbSNP (RS) rs138029604 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR