RGD:11544490 Rat Genome Database

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Variant: RGD:11544490 -  Homo sapiens

RGD ID: 11544490
RS ID: rs1345186
ClinVar ID: CV251060
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TP63  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 189,604,160
GRCh38 3 189,886,371
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.12:g.189886371T>C
NC_000003.11:g.189604160T>C
NM_001329964.2:c.1344-23T>C
NM_001329146.2:c.813-23T>C
More... 		03/03/2015 intron variant benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:TP63
Accession:NM_001114981
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329964
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114979
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329146
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114980
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329145
Location:INTRON

Gene Symbol:TP63
Accession:NM_003722
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329149
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329144
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329150
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114982
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114978
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329148
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000243865 CLINVAR
  RCV001651179 CLINVAR
dbSNP (RS) rs1345186 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene TP63 CLINVAR
OMIM 603273 CLINVAR