RGD:11645298 Rat Genome Database

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Variant: RGD:11645298 -  Homo sapiens

RGD ID: 11645298
RS ID: rs886048535
ClinVar ID: CV328606
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TPP1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 6,634,365
GRCh38 11 6,613,134
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008653.1:g.11328T>G
NC_000011.10:g.6613134A>C
NC_000011.9:g.6634365A>C
NM_000391.4:c.*1412T>G
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TPP1
Accession:NM_000391
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000264580 CLINVAR
dbSNP (RS) rs886048535 CLINVAR
MedGen CN239323 CLINVAR
NCBI Gene TPP1 CLINVAR
OMIM 607998 CLINVAR