RGD:150435598 Rat Genome Database

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Variant: RGD:150435598 -  Homo sapiens

RGD ID: 150435598
RS ID: rs7624324
ClinVar ID: CV1233901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TP63  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 189,586,876
GRCh38 3 189,869,087
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_428t1:c.1130-237T>C
NM_001329148.2:c.1118-237T>C
NM_001114979.2:c.1130-237T>C
NM_001114980.2:c.848-237T>C
More... 		07/07/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TP63
Accession:NM_001114982
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329964
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329144
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114979
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114980
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329145
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114981
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329148
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329146
Location:INTRON

Gene Symbol:TP63
Accession:NM_003722
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114978
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329149
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329150
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001644028 CLINVAR
dbSNP (RS) rs7624324 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TP63 CLINVAR
OMIM 603273 CLINVAR