RGD:11646809 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:11646809 -  Homo sapiens

RGD ID: 11646809
RS ID: rs886053516
ClinVar ID: CV346183
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126862483  TP53  WRAP53  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 7,590,768
GRCh38 17 7,687,450
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_375:g.6380G>C
NG_028245.1:g.6380G>C
NC_000017.11:g.7687450G>C
NC_000017.10:g.7590768G>C
More...
01/12/2018 2kb upstream variant|5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TP53
Accession:NM_001126112
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_000546
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001126113
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001126114
Location:5UTRS;EXON

Gene Symbol:WRAP53
Accession:NM_001143991
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001126118
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001276761
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001276760
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001276695
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001276696
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001407269
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001407268
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001407262
Location:5UTRS;EXON

Gene Symbol:TP53
Accession:NM_001407263
Location:5UTRS;EXON

Gene Symbol:WRAP53
Accession:NM_001143990
Location:5UTRS;INTRON

Gene Symbol:TP53
Accession:NR_176326
Location:EXON;NON-CODING

Gene Symbol:TP53
Accession:NM_001126115
Location:INTRON

Gene Symbol:TP53
Accession:NM_001126117
Location:INTRON

Gene Symbol:TP53
Accession:NM_001126116
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_018081
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143992
Location:INTRON

Gene Symbol:TP53
Accession:NM_001276697
Location:INTRON

Gene Symbol:TP53
Accession:NM_001276699
Location:INTRON

Gene Symbol:TP53
Accession:NM_001276698
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407265
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407264
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407266
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407267
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407270
Location:INTRON

Gene Symbol:TP53
Accession:NM_001407271
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000272984 CLINVAR
  RCV001126970 CLINVAR
dbSNP (RS) rs886053516 CLINVAR
MedGen C1835398 CLINVAR
  CN239315 CLINVAR
NCBI Gene LOC126862483 CLINVAR
  TP53 CLINVAR
  WRAP53 CLINVAR
OMIM 151623 CLINVAR
  191170 CLINVAR
  612661 CLINVAR