RGD:150406875 Rat Genome Database

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Variant: RGD:150406875 -  Homo sapiens

RGD ID: 150406875
RS ID: rs146255276
ClinVar ID: CV1195490
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBC1D20  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 419,620
GRCh38 20 438,976
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.10:g.419620G>A
NG_034082.1:g.28578C>T
NC_000020.11:g.438976G>A
NM_144628.4:c.956+132C>T
06/28/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TBC1D20
Accession:NM_144628
Location:INTRON

Gene Symbol:TBC1D20
Accession:NR_111901
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001572160 CLINVAR
dbSNP (RS) rs146255276 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TBC1D20 CLINVAR
OMIM 611663 CLINVAR