RGD:8633793 Rat Genome Database

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Variant: RGD:8633793 -  Homo sapiens

RGD ID: 8633793
ClinVar ID: CV89009
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP2C8  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 96,829,083
GRCh38 10 95,069,326
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001198854.1:c.-105G>A
NM_001198853.1:c.-172G>A
NM_001198855.1:c.-234G>A
NM_000770.3:c.77G>A
More... 		missense|missense variant|5 prime utr variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:CYP2C8
Accession:NM_001198853
Location:5UTRS;EXON

Gene Symbol:CYP2C8
Accession:NM_001198854
Location:5UTRS;EXON

Gene Symbol:CYP2C8
Accession:NM_001198855
Location:5UTRS;EXON

Gene Symbol:CYP2C8
Accession:NM_000770
Location:EXON
Amino Acid Prediction: R to K (nonsynonymous)
Amino Acid Position: 26
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEPFVVLVLCLSFMLLFSLWRQSCRKRKLPPGPTPLPIIGNMLQIDVKDICKSFTNFSKVYGPVFTVYFGMNPIVVFHGY
EAVKEALIDNGEEFSGRGNSPISQRITKGLGIISSNGKRWKEIRRFSLTTLRNFGMGKRSIEDRVQEEAHCLVEELRKTK
ASPCDPTFILGCAPCNVICSVVFQKRFDYKDQNFLTLMKRFNENFRILNSPWIQVCNNFPLLIDCFPGTHNKVLKNVALT
RSYIREKVKEHQASLDVNNPRDFIDCFLIKMEQEKDNQKSEFNIENLVGTVADLFVAGTETTSTTLRYGLLLLLKHPEVT
AKVQEEIDHVIGRHRSPCMQDRSHMPYTDAVVHEIQRYSDLVPTGVPHAVTTDTKFRNYLIPKGTTIMALLTSVLHDDKE
FPNPNIFDPGHFLDKNGNFKKSDYFMPFSAGKRICAGEGLARMELFLFLTTILQNFNLKSVDDLKNLNTTAVTKGIVSLP
PSYQICFIPV*
Variant Samples