RGD:8634770 Rat Genome Database

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Variant: RGD:8634770 -  Homo sapiens

RGD ID: 8634770
ClinVar ID: CV89990
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR9K2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 55,523,785
GRCh38 12 55,130,001
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.10:g.53810052C>T
NM_001005243.1:c.233C>T
NC_000012.12:g.55130001C>T
NC_000012.11:g.55523785C>T
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR9K2
Accession:NM_001005243
Location:EXON
Amino Acid Prediction: P to L (nonsynonymous)
Amino Acid Position: 56
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGDRGTSNHSEMTDFILAGFRVRPELHILLFLLFLFVYAMILLGNVGMMTIIMTDLRLNTPMYFFLGNLSFIDLFYSSVI
EPKAMINFWSENKSISFAGCVAQLFLFALLIVTEGFLLAAMAYDRFIAICNPLLYSVQMSTRLCTQLVAGSYFCGCISSV
IQTSMTFTLSFCASRAVDHFYCDSRPLQRLSCSDLFIHRMISFSLSCIIILPTIIVIIVSYMYIVSTVLKIHSTEGHKKA
FSTCSSHLGVVSVLYGAVFFMYLTPDRFPELSKVASLCYSLVTPMLNPLIYSLRNKDVQEALKKFLEKKNIIL*
Variant Samples