RGD:15160308 Rat Genome Database

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Variant: RGD:15160308 -  Homo sapiens

RGD ID: 15160308
RS ID: rs112447740
ClinVar ID: CV717662
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GPR101  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 136,113,099
GRCh38 X 137,030,940
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1000t1:c.735G>A
NM_054021.2:c.735G>A
LRG_1000:g.8056G>A
NG_016367.2:g.8056G>A
More... 		12/31/2019 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GPR101
Accession:NM_054021
Location:EXON
Amino Acid Prediction: E to E (synonymous)
Amino Acid Position: 245
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTSTCTNSTRESNSSHTCMPLSKMPISLAHGIIRSTVLVIFLAASFVGNIVLALVLQRKPQLLQVTNRFIFNLLVTDLLQ
ISLVAPWVVATSVPLFWPLNSHFCTALVSLTHLFAFASVNTIVVVSVDRYLSIIHPLSYPSKMTQRRGYLLLYGTWIVAI
LQSTPPLYGWGQAAFDERNALCSMIWGASPSYTILSVVSFIVIPLIVMIACYSVVFCAARRQHALLYNVKRHSLEVRVKD
CVENEDEEGAEKKEEFQDESEFRRQHEGEVKAKEGRMEAKDGSLKAKEGSTGTSESSVEARGSEEVRESSTVASDGSMEG
KEGSTKVEENSMKADKGRTEVNQCSIDLGEDDMEFGEDDINFSEDDVEAVNIPESLPPSRRNSNSNPPLPRCYQCKAAKV
IFIIIFSYVLSLGPYCFLAVLAVWVDVETQVPQWVITIIIWLFFLQCCIHPYVYGYMHKTIKKEIQDMLKKFFCKEKPPK
EDSHPDLPGTEGGTEGKIVPSYDSATFP*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000969875 CLINVAR
dbSNP (RS) rs112447740 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GPR101 CLINVAR
OMIM 300393 CLINVAR