RGD:11622384 Rat Genome Database

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Variant: RGD:11622384 -  Homo sapiens

RGD ID: 11622384
RS ID: rs116586110
ClinVar ID: CV339317
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGFB3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 76,424,706
GRCh38 14 75,958,363
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_399:g.28387T>C
NG_011715.1:g.28387T>C
NC_000014.9:g.75958363A>G
NC_000014.8:g.76424706A>G
More...
06/19/2018 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TGFB3
Accession:NM_003239
Location:3UTRS;EXON

Gene Symbol:TGFB3
Accession:NM_001329939
Location:3UTRS;EXON

Gene Symbol:TGFB3
Accession:NM_001329938
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001593961 CLINVAR
dbSNP (RS) rs116586110 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TGFB3 CLINVAR
OMIM 190230 CLINVAR