RGD:11611474 Rat Genome Database

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Variant: RGD:11611474 -  Homo sapiens

RGD ID: 11611474
ClinVar ID: CV312656
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPS1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 116,424,165
GRCh38 8 115,411,937
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.262065G>T
NC_000008.11:g.115411937C>A
NC_000008.10:g.116424165C>A
NM_014112.2:c.*2086G>T
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