RGD:11601805 Rat Genome Database

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Variant: RGD:11601805 -  Homo sapiens

RGD ID: 11601805
ClinVar ID: CV312680
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 116,425,635
GRCh38 8 115,413,407
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.260595G>A
NC_000008.11:g.115413407C>T
NC_000008.10:g.116425635C>T
NM_014112.2:c.*616G>A
More... 		06/14/2016 3 prime utr variant likely 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