rs139204615 Rat Genome Database

rs139204615 Rat Genome Database

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Variant: rs139204615 - Homo sapiens

RGD ID:

150481830

RS ID:

rs139204615

ClinVar ID:

CV1209859

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

DLAT

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	11	111,909,853
GRCh38	11	112,039,129

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_001372042.1:c.514-115G>A NM_001372040.1:c.595-115G>A NM_001372039.1:c.661-115G>A NM_001372041.1:c.661-115G>A More...	07/15/2018	intron variant	likely benign	none provided

Gene Symbol:	DLAT
Accession:	NM_001372036
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372038
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372034
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372037
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372040
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372035
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372039
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372032
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372033
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372042
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372031
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001931
Location:	INTRON

Gene Symbol:	DLAT
Accession:	NM_001372041
Location:	INTRON

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

ClinVar GRCh37	ClinVar GRCh38

Database	Acc Id	Source(s)
ClinVar	RCV001590557	CLINVAR
dbSNP (RS)	rs139204615	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	DLAT	CLINVAR
OMIM	608770	CLINVAR