RGD:150441125 Rat Genome Database

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Variant: RGD:150441125 -  Homo sapiens

RGD ID: 150441125
RS ID: rs74497017
ClinVar ID: CV1220269
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBX18  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 85,469,801
GRCh38 6 84,760,083
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001080508.3:c.599+172G>A
NG_046956.1:g.9648G>A
NC_000006.12:g.84760083C>T
NC_000006.11:g.85469801C>T
 06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TBX18
Accession:NM_001080508
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001610253 CLINVAR
dbSNP (RS) rs74497017 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TBX18 CLINVAR
OMIM 604613 CLINVAR