RGD:150423179 Rat Genome Database

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Variant: RGD:150423179 -  Homo sapiens

RGD ID: 150423179
RS ID: rs192618416
ClinVar ID: CV1185552
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBC1D20  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 421,059
GRCh38 20 440,415
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_144628.4:c.627-26G>C
NG_034082.1:g.27139G>C
NC_000020.11:g.440415C>G
NC_000020.10:g.421059C>G
 07/21/2018 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 RCV001554980 CLINVAR
dbSNP (RS) rs192618416 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TBC1D20 CLINVAR
OMIM 611663 CLINVAR