RGD:150412358 Rat Genome Database

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Variant: RGD:150412358 -  Homo sapiens

RGD ID: 150412358
RS ID: rs57935694
ClinVar ID: CV1176298
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC111162620  TP63  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 189,348,936
GRCh38 3 189,631,147
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_055551.1:g.544C>T
NC_000003.12:g.189631147C>T
NC_000003.11:g.189348936C>T
NM_001329964.2:c.56+33909C>T
More... 		02/28/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TP63
Accession:NM_001329150
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329148
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114978
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114981
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114980
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329149
Location:INTRON

Gene Symbol:TP63
Accession:NM_003722
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114982
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329144
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329964
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329145
Location:INTRON

Gene Symbol:TP63
Accession:NM_001114979
Location:INTRON

Gene Symbol:TP63
Accession:NM_001329146
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001547502 CLINVAR
dbSNP (RS) rs57935694 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC111162620 CLINVAR
  TP63 CLINVAR
OMIM 603273 CLINVAR