rs139279002 Rat Genome Database

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Variant: rs139279002 -  Homo sapiens

RGD ID: 150421312
RS ID: rs139279002
ClinVar ID: CV1194434
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DLAT  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 111,904,513
GRCh38 11 112,033,789
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001372042.1:c.325+259C>T
NM_001372040.1:c.406+259C>T
NM_001372038.1:c.508+259C>T
NM_001372037.1:c.619+259C>T
More...
06/12/2019 intron variant likely benign none provided

Gene Symbol:DLAT
Accession:NM_001372037
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372038
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372031
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372035
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372041
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372034
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372042
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372036
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001931
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372033
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372040
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372039
Location:INTRON

Gene Symbol:DLAT
Accession:NM_001372032
Location:INTRON

Gene Symbol:DLAT
Accession:NR_164072
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV001570492 CLINVAR
dbSNP (RS) rs139279002 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DLAT CLINVAR
OMIM 608770 CLINVAR