RGD:8630979 Rat Genome Database

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Variant: RGD:8630979 -  Homo sapiens

RGD ID: 8630979
ClinVar ID: CV86135
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR5H15  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 97,888,234
GRCh38 3 98,169,390
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001005515.1:c.691G>A
NC_000003.12:g.98169390G>A
NC_000003.11:g.97888234G>A
NP_001005515.1:p.Asp231Asn
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR5H15
Accession:NM_001005515
Location:EXON
Amino Acid Prediction: D to N (nonsynonymous)
Amino Acid Position: 231
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEEENATLLTEFVLTGFLYQPQWKIPLFLAFLVIYLITIMGNLGLIAVIWKDPHLHIPMYLLLGNLAFVDAWISSTVTPK
MLNNFLAKSKMISLSECKIQFFSIAIGVTTECFLLATMAYDRYVAICKPLLYPAIMTNGLCIRLLILSYIAGILHALIHE
GFLFRLTFCNSNIVHHIYCDTIPLSKISCTDSSINFLMVFIFSGSIQVFSIVTILISYTFVLFTVLEKKSNKGVRKAFST
CGAHLFSVCLYYGPLLLMYVGPASPQADGQNMVEPLFYTVIIPLLNPIIYSLRNKQVIVSFIKMLKRNVKVSY*
Variant Samples