RGD:14725097 Rat Genome Database

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Variant: RGD:14725097 -  Homo sapiens

RGD ID: 14725097
RS ID: rs77681059
ClinVar ID: CV668577
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TUBB3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 90,000,044
GRCh38 16 89,933,636
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006086.4:c.277+58C>T
NM_001197181.2:c.61+58C>T
NG_027810.1:g.16628C>T
NC_000016.10:g.89933636C>T
More... 		06/16/2018 intron variant benign 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 Information

Database Acc Id Source(s)
ClinVar RCV000833280 CLINVAR
dbSNP (RS) rs77681059 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TUBB3 CLINVAR
OMIM 602661 CLINVAR