RGD:150486333 Rat Genome Database

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Variant: RGD:150486333 -  Homo sapiens

RGD ID: 150486333
RS ID: rs75032008
ClinVar ID: CV1274036
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TAPT1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 16,215,855
GRCh38 4 16,214,232
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_153365.3:c.200-334A>G
NG_033259.1:g.17307A>G
NC_000004.12:g.16214232T>C
NC_000004.11:g.16215855T>C
 05/01/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TAPT1
Accession:XM_011513816
Location:5UTRS;INTRON

Gene Symbol:TAPT1
Accession:XM_047449754
Location:5UTRS;INTRON

Gene Symbol:TAPT1
Accession:XM_047449755
Location:5UTRS;INTRON

Gene Symbol:TAPT1
Accession:NM_153365
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_011513812
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_011513817
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_047449756
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_047449757
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_047449759
Location:INTRON

Gene Symbol:TAPT1
Accession:XM_047449758
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001698915 CLINVAR
dbSNP (RS) rs75032008 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TAPT1 CLINVAR
OMIM 612758 CLINVAR