RGD:150444685 Rat Genome Database

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Variant: RGD:150444685 -  Homo sapiens

RGD ID: 150444685
RS ID: rs13335900
ClinVar ID: CV1288058
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NDE1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 15,784,903
GRCh38 16 15,691,046
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001143979.2:c.524-98G>A
NM_017668.3:c.524-98G>A
NG_021210.1:g.52780G>A
NC_000016.10:g.15691046G>A
More... 		06/26/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NDE1
Accession:NM_001143979
Location:INTRON

Gene Symbol:NDE1
Accession:NM_017668
Location:INTRON

Gene Symbol:NDE1
Accession:XM_005255396
Location:INTRON

Gene Symbol:NDE1
Accession:XM_006720897
Location:INTRON

Gene Symbol:NDE1
Accession:XM_006720900
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023353
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023349
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023354
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023355
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023352
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023350
Location:INTRON

Gene Symbol:NDE1
Accession:XM_017023357
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434261
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434259
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434264
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434260
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434258
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434267
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434262
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434263
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434265
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434266
Location:INTRON

Gene Symbol:NDE1
Accession:XM_047434268
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001725780 CLINVAR
dbSNP (RS) rs13335900 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NDE1 CLINVAR
OMIM 609449 CLINVAR