RGD:15166630 Rat Genome Database

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Variant: RGD:15166630 -  Homo sapiens

RGD ID: 15166630
RS ID: rs11535718
ClinVar ID: CV701639
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR10G9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 123,893,988
GRCh38 11 124,023,281
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001001953.1:c.269C>T
NC_000011.10:g.124023281C>T
NC_000011.9:g.123893988C>T
NP_001001953.1:p.Ala90Val
 06/22/2017 missense variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:OR10G9
Accession:NM_001001953
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 90
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSKTSLVTAFILTGLPHAPGLDAPLFGIFLVVYVLTVLGNLLILLVIRVDSHLHTPMYYFLTNLSFIDMWFSTVTVPKML
MTLVSPSGRVISFHSCVAQLYFFHFLGSTECFLYTVMSYDRYLAISYPLRYTSMMSGSRCALLATSTWLSGSLHSAVQTI
LTFHLPYCGPNQIQHYLCDAPPILKLACADTSANEMVIFVDIGLVASGCFLLIVLSYVSIVCSILRIHTSEGRHRAFQTC
ASHCIVVLCFFVPCVFIYLRPGSRDVVDGVVAIFYTVLTPLLNPVVYTLRNKEVKKAVLKLRDKVAHSQGE*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000948879 CLINVAR
dbSNP (RS) rs11535718 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene OR10G9 CLINVAR