RGD:11609609 Rat Genome Database

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Variant: RGD:11609609 -  Homo sapiens

RGD ID: 11609609
ClinVar ID: CV312613
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPS1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 116,421,962
GRCh38 8 115,409,734
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012383.3:g.264268G>T
NC_000008.11:g.115409734C>A
NC_000008.10:g.116421962C>A
NM_014112.2:c.*4289G>T
More...
06/14/2016 3 prime utr variant benign

Variant Details
Variant Transcripts
Gene Symbol:TRPS1
Accession:NM_014112
Location:3UTRS;EXON

Gene Symbol:TRPS1
Accession:NM_001282902
Location:3UTRS;EXON

Gene Symbol:TRPS1
Accession:NM_001282903
Location:3UTRS;EXON

Gene Symbol:TRPS1
Accession:NM_001330599
Location:3UTRS;EXON

Variant Samples