RGD:8633914 Rat Genome Database

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Variant: RGD:8633914 -  Homo sapiens

RGD ID: 8633914
ClinVar ID: CV89130
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR8D1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 124,180,459
GRCh38 11 124,310,563
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001002917.1:c.204C>T
NC_000011.10:g.124310563G>A
NC_000011.9:g.124180459G>A
NP_001002917.1:p.Phe68=
More... 		synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR8D1
Accession:NM_001002917
Location:EXON
Amino Acid Prediction: F to L (nonsynonymous)
Amino Acid Position: 68
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTMENYSMAAQFVLDGLTQQAELQLPLFLLFLGIYVVTVVGNLGMILLIAVSPLLHTPMYYFLSSLSLVDFCYSSVITPK
MLVNFLGKKNTILYSECMVQLFFFVVFVVAEGYLLTAMAYDRYVAICSPLLYNAIMSSWVCSLLVLAAFFLGFLSALTHT
SAMMKLSFCKSHIINHYFCDVLPLLNLSCSNTHLNELLLFIIAGFNTLVPTLAVAVSYAFILYSILHIRSSEGRSKAFGT
CSSHLMAVVIFFGSITFMYFKPPSSNSLDQEKVSSVFYTTVIPMLNPLIYSLRNKDVKKALRKVLVGK*
Variant Samples