RGD:8634781 Rat Genome Database

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Variant: RGD:8634781 -  Homo sapiens

RGD ID: 8634781
ClinVar ID: CV90001
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR6C76  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 55,820,070
GRCh38 12 55,426,286
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.54106337C>T
NM_001005183.1:c.33C>T
NC_000012.12:g.55426286C>T
NC_000012.11:g.55820070C>T
More... 		synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR6C76
Accession:NM_001005183
Location:EXON
Amino Acid Prediction: I to I (synonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKNRTSVTDFILLGLTDNPQLQVVIFSFLFLTYVLSVTGNLTIISLTLLDSHLKTPMYFFLRNFSLEISFTSVCNPRFLI
SILTGDKSISYNACAAQLFFFIFLGSTEFFLLASMSYDCYVAICKPLHYTTIMSDRICYQLIISSWLAGFLVIFPPLAMG
LQLDFCDSNVIDHFTCDSAPLLQISCTDTSTLELMSFILALFTLISTLILVILSYTYIIRTILRIPSAQQRKKAFSTCSS
HVIVVSISYGSCIFMYVKTSAKEGVALTKGVAILNTSVAPMLNPFIYTLRNQQVKQAFKDVLRKISHKKKKH*
Variant Samples