RGD:401920924 Rat Genome Database

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Variant: RGD:401920924 -  Homo sapiens

RGD ID: 401920924
ClinVar ID: CV2820703
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TAAR9  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 132,860,343
GRCh38 6 132,539,204
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.132539204T>C
NC_000006.11:g.132860343T>C
NP_778227.3:p.Ala305=
NM_175057.4:c.915T>C
 03/01/2023 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TAAR9
Accession:NM_175057
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 305
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MVNNFSQAEAVELCYKNVNESCIKTPYSPGPRSILYAVLGFGAVLAAFGNLLVMIAILHFKQLHTPTNFLIASLACADFL
VGVTVMPFSTVRSVESCWYFGDSYCKFHTCFDTSFCFASLFHLCCISVDRYIAVTDPLTYPTKFTVSVSGICIVLSWFFS
VTYSFSIFYTGANEEGIEELVVALTCVGGCQAPLNQNWVLLCFLLFFIPNVAMVFIYSKIFLVAKHQARKIESTASQAQS
SSESYKERVAKRERKAAKTLGIAMAAFLVSWLPYLVDAVIDAYMNFITPPYVYEILVWCVYYNSAMNPLIYAFFYQWFGK
AIKLIVSGKVLRTDSSTTNLFSEEVETD*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003432047 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TAAR9 CLINVAR
OMIM 608282 CLINVAR