RGD:155973362 Rat Genome Database

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Variant: RGD:155973362 -  Homo sapiens

RGD ID: 155973362
ClinVar ID: CV2224610
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OR51B5  OR51B6  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 5,372,966
GRCh38 11 5,351,736
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_001004750.1:p.Pro77Ser
NM_001005567.3:c.-359-4826G>A
NM_001004750.1:c.229C>T
NC_000011.10:g.5351736C>T
More... 		07/06/2021 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:OR51B5
Accession:NM_001005567
Location:5UTRS;INTRON

Gene Symbol:OR51B6
Accession:NM_001004750
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 77
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGLNKSASTFQLTGFPGMEKAHHWIFIPLLAAYISILLGNGTLLFLIRNDHNLHEPMYYFLAMLAATDLGVTLTTMSTVL
GVLWLDHREIGHGACFSQAYFIHTLSVMESGVLLAMAYDCFITIRSPLRYTSILTNTQVMKIGVRVLTRAGLSIMPIVVR
LHWFPYCRSHVLSHAFCLHQDVIKLACADITFNRLYPVVVLFAMVLLDFLIIFFSYILILKTVMGIGSGGERAKALNTCV
SHICCILVFYVTVVCLTFIHRFGKHVPHVVHITMSYIHFLFPPFMNPFIYSIKTKQIQSGILRLFSLPHSRA*

Gene Symbol:OR51B5
Accession:NM_001395252
Location:INTRON

Gene Symbol:OR51B5
Accession:NR_038321
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004098178 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene OR51B5 CLINVAR
  OR51B6 CLINVAR