RGD:14733285 Rat Genome Database

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Variant: RGD:14733285 -  Homo sapiens

RGD ID: 14733285
RS ID: rs114709278
ClinVar ID: CV659442
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TFG  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 100,464,009
GRCh38 3 100,745,165
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001195478.2:c.820+234T>C
NM_001007565.2:c.820+234T>C
NM_006070.6:c.820+234T>C
NG_027821.2:g.40876T>C
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TFG
Accession:XM_047447243
Location:INTRON

Gene Symbol:TFG
Accession:XM_047447241
Location:INTRON

Gene Symbol:TFG
Accession:NM_006070
Location:INTRON

Gene Symbol:TFG
Accession:NM_001195479
Location:INTRON

Gene Symbol:TFG
Accession:XM_011512334
Location:INTRON

Gene Symbol:TFG
Accession:XM_047447244
Location:INTRON

Gene Symbol:TFG
Accession:XM_005247066
Location:INTRON

Gene Symbol:TFG
Accession:XM_017005527
Location:INTRON

Gene Symbol:TFG
Accession:NM_001007565
Location:INTRON

Gene Symbol:TFG
Accession:XM_006713472
Location:INTRON

Gene Symbol:TFG
Accession:NM_001195478
Location:INTRON

Gene Symbol:TFG
Accession:XM_047447242
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000837032 CLINVAR
dbSNP (RS) rs114709278 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TFG CLINVAR
OMIM 602498 CLINVAR