RGD:8626938 Rat Genome Database

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Variant: RGD:8626938 -  Homo sapiens

RGD ID: 8626938
ClinVar ID: CV82082
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR10G9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 123,894,507
GRCh38 11 124,023,800
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.8:g.123399717C>T
NM_001001953.1:c.788C>T
NC_000011.10:g.124023800C>T
NC_000011.9:g.123894507C>T
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR10G9
Accession:NM_001001953
Location:EXON
Amino Acid Prediction: S to F (nonsynonymous)
Amino Acid Position: 263
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSKTSLVTAFILTGLPHAPGLDAPLFGIFLVVYVLTVLGNLLILLVIRVDSHLHTPMYYFLTNLSFIDMWFSTVTVPKML
MTLVSPSGRAISFHSCVAQLYFFHFLGSTECFLYTVMSYDRYLAISYPLRYTSMMSGSRCALLATSTWLSGSLHSAVQTI
LTFHLPYCGPNQIQHYLCDAPPILKLACADTSANEMVIFVDIGLVASGCFLLIVLSYVSIVCSILRIHTSEGRHRAFQTC
ASHCIVVLCFFVPCVFIYLRPGFRDVVDGVVAIFYTVLTPLLNPVVYTLRNKEVKKAVLKLRDKVAHSQGE*
Variant Samples