RGD:8632877 Rat Genome Database

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Variant: RGD:8632877 -  Homo sapiens

RGD ID: 8632877
ClinVar ID: CV88092
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GPR20  LOC127460573  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 142,366,983
GRCh38 8 141,356,883
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005293.2:c.1041C>T
NC_000008.11:g.141356883G>A
NC_000008.10:g.142366983G>A
NP_005284.2:p.Ala347=
More... 		synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:GPR20
Accession:NM_005293
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 347
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MPSVSPAGPSAGAVPNATAVTTVRTNASGLEVPLFHLFARLDEELHGTFPGLWLALMAVHGAIFLAGLVLNGLALYVFCC
RTRAKTPSVIYTINLVVTDLLVGLSLPTRFAVYYGARGCLRCAFPHVLGYFLNMHCSILFLTCICVDRYLAIVRPEGSRR
CRQPACARAVCAFVWLAAGAVTLSVLGVTGSRPCCRVFALTVLEFLLPLLVISVFTGRIMCALSRPGLLHQGRQRRVRAM
QLLLTVLIIFLVCFTPFHARQVAVALWPDMPHHTSLVVYHVAVTLSSLNSCMDPIVYCFVTSGFQATVRGLFGQHGEREP
SSGDVVSMHRSSKGSGRHHILSAGPHALTQALANGPEA*
Variant Samples