Transcript #00008940 (NM_007327.3, GRIN1 gene)

Transcript name transcript variant NR1-3
Gene name GRIN1 (glutamate receptor, ionotropic, N-methyl D-aspartate 1)
Chromosome 9
Transcript - NCBI ID NM_007327.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_015566.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.? r.(?) p.?
+/. - c.? r.(?) p.?
-?/. - c.264C>T r.(?) p.(Tyr88=)
+/. - c.352G>A r.(?) p.(Val118Met)
-?/. i c.393+37G>A r.(=) p.(=)
-?/. i c.393+37G>A r.(=) p.(=)
-?/. - c.394-1095T>A r.(=) p.(=)
./. - c.416G>A r.(?) p.(Arg139His)
?/. - c.466C>G r.(?) p.(Arg156Gly)
-?/. - c.510C>A r.(?) p.(Asp170Glu)
?/. - c.520C>G r.(?) p.(Arg174Gly)
?/. - c.524C>T r.(?) p.(Ala175Val)
-?/. - c.531G>A r.(?) p.(Gln177=)
?/. - c.536G>A r.(?) p.(Arg179His)
-?/. - c.567C>G r.(?) p.(Ser189=)
?/. - c.588G>C r.(?) p.(Gln196His)
?/. - c.614C>T r.(?) p.(Thr205Met)
+/. - c.649C>T r.(?) p.(Arg217Trp)
+/. - c.649C>T r.(?) p.(Arg217Trp)
-?/. - c.654C>T r.(?) p.(Val218=)
?/. - c.660C>T r.(?) p.(Ile220=)
+/. - c.679G>C r.(?) p.(Asp227His)
+/. - c.679G>C r.(?) p.(Asp227His)
?/. - c.679G>C r.(?) p.(Asp227His)
+?/. 5 c.679G>C r.(?) p.(Asp227His)
+?/. 5 c.679G>C r.(?) p.(Asp227His)
-?/. - c.693A>C r.(?) p.(Val231=)
-?/. - c.693A>C r.(?) p.(Val231=)
-?/. - c.780C>T r.(?) p.(Arg260=)
-/. - c.789A>G r.(?) p.(Pro263=)
-/. - c.789A>G r.(?) p.(Pro263=)
-/. - c.789A>G r.(?) p.(Pro263=)
-?/. - c.793+5G>A r.spl? p.?
-/. - c.855G>A r.(?) p.(Val285=)
-?/. - c.864G>A r.(?) p.(Val288=)
?/. - c.952G>C r.(?) p.(Gly318Arg)
?/. - c.952G>C r.(?) p.(Gly318Arg)
-?/. - c.968+15C>T r.(=) p.(=)
?/. - c.1045G>T r.(?) p.(Ala349Ser)
./. - c.1066del r.(?) p.(Leu356Cysfs*43)
-?/. - c.1121C>T r.(?) p.(Pro374Leu)
+?/. - c.1191A>C r.(?) p.(Arg397Ser)
-?/. I c.1197+27T>G r.(=) p.(=)
?/. - c.1252G>A r.(?) p.(Gly418Arg)
?/. - c.1255A>G r.(?) p.(Thr419Ala)
?/. - c.1288C>T r.(?) p.(Pro430Ser)
-?/. i c.1339+36G>C r.(=) p.(=)
-?/. i c.1339+36G>C r.(=) p.(=)
-?/. - c.1340-4C>A r.spl? p.?
+/. - c.1422C>A r.(?) p.(Tyr474Ter)
-/. i c.1467+8G>A r.(=) p.(=)
-/. - c.1467+8G>A r.(=) p.(=)
-/. - c.1467+8G>A r.(=) p.(=)
-/. i c.1467+8G>A r.(=) p.(=)
-?/. - c.1513C>T r.(?) p.(Leu505=)
+?/. - c.1518del r.(?) p.(Ser507Alafs*6)
-/. - c.1548G>A r.(=) p.(=)
-?/. - c.1548G>A r.(?) p.(Pro516=)
-/. - c.1548G>A r.(=) p.(=)
?/. - c.1566G>C r.(?) p.(Glu522Asp)
-/. - c.1584G>A r.(?) p.(Glu528=)
+?/. - c.1592A>G r.(?) p.(Lys531Arg)
+/. - c.1643G>A r.(?) p.(Arg548Gln)
+?/. - c.1643G>A r.(?) p.(Arg548Gln)
+/. - c.1645A>C r.(?) p.(Ser549Arg)
+/. - c.1645A>G r.(?) p.(Ser549Gly)
+/. - c.1652T>C r.(?) p.(Leu551Pro)
+/. - c.1656C>A r.(?) p.(Asp552Glu)
+/. - c.1656C>A r.(?) p.(Asp552Glu)
+/. - c.1658C>T r.(?) p.(Ser553Leu)
+/. - c.1666C>T r.(?) p.(Gln556*)
+/. - c.1666C>T r.(?) p.(Gln556*)
+/. - c.1666C>T r.(?) p.(Gln556*)
+?/. - c.1667A>G r.(?) p.(Gln556Arg)
+/. - c.1670C>G r.(?) p.(Pro557Arg)
+/. - c.1676A>G r.(?) p.(Gln559Arg)
+/. - c.1676A>G r.(?) p.(Gln559Arg)
+/. 12 c.1679_1681dup r.(?) p.(Ser560dup)
+/. 12 c.1679_1681dup r.(?) p.Ser560dup
+/. - c.1852G>C r.(?) p.(Gly618Arg)
+?/. - c.1852G>C r.(?) p.(Gly618Arg)
+/. - c.1854_1859dup r.(?) p.(Ile619_Gly620dup)
+/. - c.1858G>A r.(?) p.(Gly620Arg)
-?/. - c.1864+10C>T r.(=) p.(=)
-?/. i c.1864+17C>T r.(=) p.(=)
-?/. i c.1864+17C>T r.(=) p.(=)
+?/. - c.1912G>A r.(?) p.(Gly638Ser)
+/. - c.1913G>C r.(?) p.(Gly638Ala)
+/. - c.1913G>C r.(?) p.(Gly638Ala)
+/. - c.1923G>A r.(?) p.(Met641Ile)
+/. - c.1933G>T r.(?) p.(Ala645Ser)
+/. - c.1940A>C r.(?) p.(Tyr647Ser)
+/. - c.1940A>G r.(?) p.(Tyr647Cys)
+/. - c.1949A>T r.(?) p.(Asn650Ile)
+/. - c.1950C>G r.(?) p.(Asn650Lys)
?/. - c.1955C>A r.(?) p.(Ala652Glu)
+?/. - c.1957G>A r.(?) p.(Ala653Thr)
+?/. - c.1972G>T r.(?) p.(Asp658Tyr)
+/. - c.1975C>T r.(?) p.(Arg659Trp)
+?/. - c.1976G>A r.(?) p.(Arg659Gln)
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