RGD:405264412 Rat Genome Database

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Variant: RGD:405264412 -  Homo sapiens

RGD ID: 405264412
ClinVar ID: CV3185315
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 132,244,637
GRCh38 3 132,525,793
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015268.4:c.6240+4T>C
NM_001329126.2:c.6255+4T>C
NG_051045.1:g.113267T>C
NC_000003.12:g.132525793T>C
More... 		12/01/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447819
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447820
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_015268
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV003885879 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR