RGD:401887420 Rat Genome Database

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Variant: RGD:401887420 -  Homo sapiens

RGD ID: 401887420
ClinVar ID: CV2773448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR10A3  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 7,960,582
GRCh38 11 7,939,035
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001003745.2:c.486G>T
NC_000011.10:g.7939035C>A
NC_000011.9:g.7960582C>A
NM_001003745.1:c.486G>T
More... 		07/12/2023 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:OR10A3
Accession:NM_001003745
Location:EXON
Amino Acid Prediction: W to C (nonsynonymous)
Amino Acid Position: 162
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKRQNQSCVVEFILLGFSNFPELQVQLFGVFLVIYVVTLMGNAIITVIISLNQSLHVPMYLFLLNLSVVEVSFSAVITPE
MLVVLSTEKTMISFVGCFAQMYFILLFGGTECFLLGAMAYDRFAAICHPLNYPVIMNRGVFMKLVIFSWISGIMVATVQT
TCVFSFPFCGPNEINHLFCETPPVLELVCADTFLFEIYAFTGTILIVMVPFLLILLSYIRVLFAILKMPSTTGRQKAFST
CASHLTSVTLFYGTANMTYLQPKSGYSPETKKLISLAYTLLTPLLNPLIYSLRNSEMKRTLIKLWRRKVILHTF*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004354084 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene OR10A3 CLINVAR