RGD:14716474 Rat Genome Database

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Variant: RGD:14716474 -  Homo sapiens

RGD ID: 14716474
RS ID: rs1059363
ClinVar ID: CV655490
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127398176  TFG  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 100,428,460
GRCh38 3 100,709,616
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006070.5:c.-149G>C
NM_001007565.2:c.-44+185G>C
NG_027821.2:g.5327G>C
NC_000003.12:g.100709616G>C
More... 		06/20/2018 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TFG
Accession:XM_006713472
Location:5UTRS;EXON

Gene Symbol:TFG
Accession:XM_017005527
Location:5UTRS;EXON

Gene Symbol:TFG
Accession:NM_001195479
Location:5UTRS;EXON

Gene Symbol:TFG
Accession:NM_006070
Location:5UTRS;EXON

Gene Symbol:TFG
Accession:XM_005247066
Location:5UTRS;INTRON

Gene Symbol:TFG
Accession:XM_047447243
Location:5UTRS;INTRON

Gene Symbol:TFG
Accession:NM_001007565
Location:5UTRS;INTRON

Gene Symbol:TFG
Accession:NM_001195478
Location:5UTRS;INTRON

Gene Symbol:TFG
Accession:XM_047447242
Location:INTRON

Gene Symbol:TFG
Accession:XM_047447244
Location:INTRON

Gene Symbol:TFG
Accession:XM_011512334
Location:INTRON

Gene Symbol:TFG
Accession:XM_047447241
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829742 CLINVAR
dbSNP (RS) rs1059363 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TFG CLINVAR
OMIM 602498 CLINVAR