RGD:150472062 Rat Genome Database

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Variant: RGD:150472062 -  Homo sapiens

RGD ID: 150472062
RS ID: rs3917190
ClinVar ID: CV1236279
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGFB3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 76,431,792
GRCh38 14 75,965,449
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001329938.2:c.754+139A>G
NM_001329939.2:c.754+139A>G
NM_003239.5:c.754+139A>G
LRG_399:g.21301A>G
More... 		06/23/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TGFB3
Accession:NM_003239
Location:INTRON

Gene Symbol:TGFB3
Accession:NM_001329938
Location:INTRON

Gene Symbol:TGFB3
Accession:NM_001329939
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001651364 CLINVAR
dbSNP (RS) rs3917190 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TGFB3 CLINVAR
OMIM 190230 CLINVAR