Transcript #00007153

Transcript name transcript variant 1
Gene name GRM8 (glutamate receptor, metabotropic 8)
Chromosome 7
Transcript - NCBI ID NM_000845.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000836.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

161 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-12C>T r.(=) p.(=)
?/? c.-6G>A r.(=) p.(=)
?/? c.10G>A r.(?) p.(Glu4Lys)
?/? c.20G>A r.(?) p.(Arg7Gln)
?/? c.35C>A r.(?) p.(Pro12His)
?/? c.54C>T r.(=) p.(=)
?/? c.59A>G r.(?) p.(Lys20Arg)
?/? c.79A>G r.(?) p.(Met27Val)
?/? c.96C>G r.(?) p.(His32Gln)
?/? c.147G>T r.(=) p.(=)
?/? c.151C>A r.(?) p.(Leu51Ile)
?/? c.165C>T r.(=) p.(=)
?/? c.168A>G r.(=) p.(=)
?/? c.222C>T r.(=) p.(=)
?/? c.256A>T r.(?) p.(Ile86Phe)
?/? c.264G>A r.(=) p.(=)
?/? c.269C>T r.(?) p.(Pro90Leu)
?/? c.310G>A r.(?) p.(Asp104Asn)
?/? c.351A>C r.(=) p.(=)
?/? c.353C>T r.(?) p.(Thr118Ile)
?/? c.357C>T r.(=) p.(=)
?/? c.358G>A r.(?) p.(Val120Met)
?/? c.386C>T r.(?) p.(Ser129Leu)
?/? c.433G>A r.(?) p.(Asp145Asn)
?/? c.446G>T r.(?) p.(Gly149Val)
?/? c.471C>T r.(=) p.(=)
?/? c.472G>A r.(?) p.(Val158Met)
?/? c.478A>G r.(?) p.(Ile160Val)
?/? c.511-42A>C r.(=) p.(=)
?/? c.511-27T>A r.(=) p.(=)
?/? c.511-16A>G r.(=) p.(=)
?/? c.583G>A r.(?) p.(Val195Met)
?/? c.585G>T r.(=) p.(=)
?/? c.628G>A r.(?) p.(Val210Met)
?/? c.690C>T r.(=) p.(=)
?/? c.693T>C r.(=) p.(=)
?/? c.727+38G>A r.(=) p.(=)
?/? c.727+48273_727+48274insG r.(=) p.(=)
?/? c.727+48277G>A r.(=) p.(=)
?/? c.727+48322T>C N/A N/A
?/? c.727+48393C>T N/A N/A
?/? c.727+48408C>T N/A N/A
?/? c.728-50A>G r.(=) p.(=)
?/? c.728-38C>T r.(=) p.(=)
?/? c.759C>T r.(=) p.(=)
?/? c.764G>A r.(?) p.(Arg255His)
?/? c.768A>T r.(?) p.(Glu256Asp)
?/? c.794T>C r.(?) p.(Ile265Thr)
?/? c.846C>T r.(=) p.(=)
?/? c.853G>A r.(?) p.(Asp285Asn)
?/? c.863+39G>C r.(=) p.(=)
?/? c.864-38A>G r.(=) p.(=)
?/? c.864-25G>A r.(=) p.(=)
?/? c.864-13T>C r.(=) p.(=)
?/? c.864-12T>G r.(=) p.(=)
?/? c.877G>A r.(?) p.(Ala293Thr)
?/? c.895C>A r.(?) p.(Gln299Lys)
?/? c.899G>C r.(?) p.(Ser300Thr)
?/? c.905A>G r.(?) p.(His302Arg)
?/? c.924A>G r.(=) p.(=)
?/? c.1003C>T r.(?) p.(Arg335*)
?/? c.1012A>G r.(?) p.(Ile338Val)
?/? c.1013T>A r.(?) p.(Ile338Asn)
?/? c.1019-11C>G r.(=) p.(=)
?/? c.1041C>A r.(?) p.(Ser347Arg)
?/? c.1085T>A r.(?) p.(Phe362Tyr)
?/? c.1155A>C r.(=) p.(=)
?/? c.1156+26T>C r.(=) p.(=)
?/? c.1156+47T>C r.(=) p.(=)
?/? c.1157-52C>G r.(=) p.(=)
?/? c.1157-39C>G r.(=) p.(=)
?/? c.1157-24G>A r.(=) p.(=)
?/? c.1157-16C>A r.(=) p.(=)
?/? c.1157-3C>A r.spl? p.?
?/? c.1165C>T r.(?) p.(Arg389*)
?/? c.1188T>C r.(=) p.(=)
?/? c.1200A>G r.(=) p.(=)
?/? c.1274C>A r.(?) p.(Pro425His)
?/? c.1282A>G r.(?) p.(Ile428Val)
?/? c.1303A>G r.(?) p.(Ser435Gly)
?/? c.1343C>G r.(?) p.(Ala448Gly)
?/? c.1357+12C>T r.(=) p.(=)
?/? c.1357+27A>G r.(=) p.(=)
?/? c.1358-5T>C r.spl? p.?
?/? c.1358-4A>G r.spl? p.?
?/? c.1386T>C r.(=) p.(=)
?/? c.1409G>A r.(?) p.(Arg470His)
?/? c.1444_1445insA r.(?) p.(Ser482Lysfs*26)
?/? c.1452G>A r.(=) p.(=)
?/? c.1464C>T r.(=) p.(=)
?/? c.1486C>A r.(?) p.(His496Asn)
?/? c.1494+10G>A r.(=) p.(=)
?/? c.1494+13A>G r.(=) p.(=)
?/? c.1494+21A>G r.(=) p.(=)
?/? c.1495-26G>A r.(=) p.(=)
?/? c.1495-9T>C r.(=) p.(=)
?/? c.1534C>G r.(?) p.(Pro512Ala)
?/? c.1538C>T r.(?) p.(Ala513Val)
?/? c.1539G>A r.(=) p.(=)
?/? c.1584G>A r.(=) p.(=)
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