RGD:14730797 Rat Genome Database

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Variant: RGD:14730797 -  Homo sapiens

RGD ID: 14730797
RS ID: rs3917175
ClinVar ID: CV666641
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGFB3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 76,437,763
GRCh38 14 75,971,420
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.516+135T>C
NG_011715.1:g.15330T>C
NC_000014.9:g.75971420A>G
NC_000014.8:g.76437763A>G
More... 		06/16/2018 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 RCV000835839 CLINVAR
dbSNP (RS) rs3917175 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TGFB3 CLINVAR
OMIM 190230 CLINVAR