RGD:8633906 Rat Genome Database

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Variant: RGD:8633906 -  Homo sapiens

RGD ID: 8633906
ClinVar ID: CV89122
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR10G4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 123,886,691
GRCh38 11 124,015,984
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001004462.1:c.410G>A
NC_000011.10:g.124015984G>A
NC_000011.9:g.123886691G>A
NP_001004462.1:p.Gly137Glu
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:OR10G4
Accession:NM_001004462
Location:EXON
Amino Acid Prediction: G to E (nonsynonymous)
Amino Acid Position: 137
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSNASLVTAFILTGLPHAPGLDALLFGIFLVVYVLTVLGNLLILLVIRVDSHLHTPMYYFLTNLSFIDMWFSTVTVPKML
MTLVSPSGRAISFHSCVAQLYFFHFLGSTECFLYTVMSYDRYLAISYPLRYTSMMSESRCALLATGTWLSGSLHSAVQTI
LTFHLPYCGPNQIQHYFCDAPPILKLACADTSANVMVIFVDIGIVASGCFVLIVLSYVSIVCSILRIRTSDGRRRAFQTC
ASHCIVVLCFFVPCVVIYLRPGSMDAMDGVVAIFYTVLTPLLNPVVYTLRNKEVKKAVLKLRDKVAHPQRK*
Variant Samples