RGD:13541158 Rat Genome Database

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Variant: RGD:13541158 -  Homo sapiens

RGD ID: 13541158
RS ID: rs199842533
ClinVar ID: CV506115
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TUBB3  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 90,001,130
GRCh38 16 89,934,722
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_027810.1:g.17714T>G
NC_000016.10:g.89934722T>G
NC_000016.9:g.90001130T>G
NM_006086.4:c.278-7T>G
More... 		09/13/2022 intron variant benign|likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:TUBB3
Accession:NM_001197181
Location:INTRON

Gene Symbol:TUBB3
Accession:NM_006086
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000615760 CLINVAR
  RCV002528721 CLINVAR
dbSNP (RS) rs199842533 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene TUBB3 CLINVAR
OMIM 602661 CLINVAR