RGD:407506154 Rat Genome Database

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Variant: RGD:407506154 -  Homo sapiens

RGD ID: 407506154
ClinVar ID: CV3478469
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TAAR9  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 132,859,593
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_175057.4:c.165T>G
NC_000006.12:g.132538454T>G
NC_000006.11:g.132859593T>G
NM_175057.3:c.165T>G
More...
04/01/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004671033 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TAAR9 CLINVAR
OMIM 608282 CLINVAR