RGD:156026453 Rat Genome Database

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Variant: RGD:156026453 -  Homo sapiens

RGD ID: 156026453
ClinVar ID: CV2242355
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GLP1R  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 39,016,648
GRCh38 6 39,048,872
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002062.5:c.32C>A
NC_000006.12:g.39048872C>A
NC_000006.11:g.39016648C>A
NR_136562.2:n.92C>A
More... 		09/16/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:GLP1R
Accession:NM_002062
Location:EXON
Amino Acid Prediction: A to E (nonsynonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAGAPGPLRLELLLLGMVGRAGPRPQGATVSLWETVQKWREYRRQCQRSLTEDPPPATDLFCNRTFDEYACWPDGEPGSF
VNVSCPWYLPWASSVPQGHVYRFCTAEGLWLQKDNSSLPWRDLSECEESKRGERSSPEEQLLFLYIIYTVGYALSFSALV
IASAILLGFRHLHCTRNYIHLNLFASFILRALSVFIKDAALKWMYSTAAQQHQWDGLLSYQDSLSCRLVFLLMQYCVAAN
YYWLLVEGVYLYTLLAFSVLSEQWIFRLYVSIGWGVPLLFVVPWGIVKYLYEDEGCWTRNSNMNYWLIIRLPILFAIGVN
FLIFVRVICIVVSKLKANLMCKTDIKCRLAKSTLTLIPLLGTHEVIFAFVMDEHARGTLRFIKLFTELSFTSFQGLMVAI
LYCFVNNEVQLEFRKSWERWRLEHLHIQRDSSMKPLKCPTSSLSSGATAGSSMYTATCQASCS*

Gene Symbol:GLP1R
Accession:NR_136563
Location:EXON;NON-CODING

Gene Symbol:GLP1R
Accession:NR_136562
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004111362 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene GLP1R CLINVAR
OMIM 138032 CLINVAR