RGD:405743679 Rat Genome Database

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Variant: RGD:405743679 -  Homo sapiens

RGD ID: 405743679
ClinVar ID: CV3331193
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TAAR9  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 132,860,392
GRCh38 6 132,539,253
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.964A>G
NC_000006.12:g.132539253A>G
NC_000006.11:g.132860392A>G
NM_175057.3:c.964A>G
More... 		12/27/2023 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:TAAR9
Accession:NM_175057
Location:EXON
Amino Acid Prediction: I to V (nonsynonymous)
Amino Acid Position: 322
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MVNNFSQAEAVELCYKNVNESCIKTPYSPGPRSILYAVLGFGAVLAAFGNLLVMIAILHFKQLHTPTNFLIASLACADFL
VGVTVMPFSTVRSVESCWYFGDSYCKFHTCFDTSFCFASLFHLCCISVDRYIAVTDPLTYPTKFTVSVSGICIVLSWFFS
VTYSFSIFYTGANEEGIEELVVALTCVGGCQAPLNQNWVLLCFLLFFIPNVAMVFIYSKIFLVAKHQARKIESTASQAQS
SSESYKERVAKRERKAAKTLGIAMAAFLVSWLPYLVDAVIDAYMNFITPPYVYEILVWCVYYNSAMNPLIYAFFYQWFGK
AVKLIVSGKVLRTDSSTTNLFSEEVETD*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004466104 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TAAR9 CLINVAR
OMIM 608282 CLINVAR