Transcript #00020634 (NM_006772.2, SYNGAP1 gene)

Transcript name synaptic Ras GTPase activating protein 1
Gene name SYNGAP1 (synaptic Ras GTPase activating protein 1)
Chromosome 6
Transcript - NCBI ID NM_006772.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006763.2
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

230 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-3580_-3579del r.(?) p.(=)
?/. - c.-3353G>A r.(?) p.(=)
-?/. - c.-2155A>G r.(?) p.(=)
+/. - c.-194_(1530_?)[0] r.0 p.0
+/. - c.0 r.0 p.0
+/. - c.0 r.0 p.0
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.55del r.(?) p.(Ala19Profs*50)
+?/. - c.67+2T>C r.spl? p.?
-/. - c.68-79T>G r.(=) p.(=)
-?/. - c.84T>C r.(?) p.(Ser28=)
./. - c.84T>C r.(=) p.(=)
-/. - c.84T>C r.(?) p.(Ser28=)
+?/. - c.91C>T r.(?) p.(Arg31Ter)
?/. - c.163C>A r.(?) p.(Gln55Lys)
-?/. - c.189+371C>A r.(=) p.(=)
./. - c.198C>T r.(=) p.(=)
-?/. - c.216G>C r.(?) p.(Arg72=)
+/? 3 c.283dup r.(?) p.(His95Profs*5)
-/. - c.296-282C>T r.(=) p.(=)
-/. - c.296-160C>T r.(=) p.(=)
-?/. - c.296-8C>T r.(=) p.(=)
-?/. - c.296-4C>T r.spl? p.?
+/? 4 c.321_324del r.(?) p.(Lys108Valfs*25)
+?/. - c.(322_325del) r.(?) p.(Lys108Valfs*25)
+/. - c.333del r.(?) p.(Lys114SerfsTer20)
+/. - c.333del r.(?) p.(Lys114SerfsTer20)
?/. - c.346T>C r.(?) p.(Tyr116His)
?/. - c.388-3C>G r.spl? p.?
+?/. - c.389-2A>T r.spl p.?
+/. - c.403C>T r.(?) p.(Arg135Ter)
+/. - c.403C>T r.(?) p.(Arg135*)
+/? 5 c.412A>T r.(?) p.(Lys138*)
+?/. - c.427C>T r.(?) p.(Arg143*)
+/. - c.427C>T r.(?) p.(Arg143Ter)
+/. - c.431_434del r.(?) p.(Thr144Serfs*29)
-?/. - c.447A>G r.(?) p.(Lys149=)
+?/. 5 c.478del r.(?) p.(Leu160Cysfs*14)
+/. - c.490C>T r.(?) p.(Arg164*)
+?/. - c.509G>A r.(?) p.(Arg170Gln)
./. - c.509G>A r.(?) p.(Arg170Gln)
+?/. - c.509G>A r.(?) p.(Arg170Gln)
+?/. - c.509G>C r.(?) p.(Arg170Pro)
+?/. - c.509G>T r.(?) p.(Arg170Leu)
+/? 5i c.510-1G>A r.spl p.?
./. - c.510-1G>A r.spl? p.?
+/. - c.510-1G>A r.spl? p.?
+/. - c.535del r.(?) p.(Glu179Serfs*9)
-?/. - c.540A>T r.(?) p.(Ser180=)
+?/. - c.564_583del r.(?) p.(Pro189IlefsTer7)
+/. - c.599T>A r.(?) p.(Leu200*)
-?/. - c.603T>G r.(?) p.(Asp201Glu)
+?/. - c.651del r.(?) p.(Glu217Aspfs*6)
+/. - c.664-1G>C r.spl? p.?
?/. - c.692T>C r.(?) p.(Phe231Ser)
-?/. - c.708G>T r.(?) p.(Ala236=)
+/. 7 c.739C>T r.(?) p.(Gln247Ter)
./. - c.762+32C>T r.(=) p.(=)
-/. - c.762+119T>A r.(=) p.(=)
+/. - c.800^801G>A r.(?) p.(Trp267*)
?/. - c.812C>T r.(?) p.(Ala271Val)
?/. - c.814C>T r.(?) p.(Arg272Trp)
?/. - c.827C>T r.(?) p.(Pro276Leu)
?/. - c.916G>A r.(?) p.(Val306Ile)
+?/. - c.968T>C r.(?) p.(Leu323Pro)
?/. - c.970C>T r.(?) p.(Arg324Trp)
+?/. 8 c.1030G>A r.(?) p.(Gly344Ser)
+/. 8 c.1043_1044del r.(?) p.(Val348Alafs*70)
+/? 8 c.1084T>C r.(?) p.(Trp362Arg)
?/. - c.1090C>G r.(?) p.(Pro364Ala)
./. - c.1152C>T r.(=) p.(=)
./. - c.1158G>A r.(=) p.(=)
+?/. - c.1167del r.(?) p.(Gly391AlafsTer12)
?/. - c.1193C>T r.(?) p.(Pro398Leu)
?/. - c.1199T>G r.(?) p.(Val400Gly)
+?/. - c.1210G>C r.(?) p.(Ala404Pro)
+/? 8 c.1253_1254del r.(?) p.(Lys418Argfs*54)
?/. 8 c.1258T>C r.(?) p.(Phe420Leu)
?/. - c.1292T>C r.(?) p.(Leu431Pro)
-?/. - c.1312G>A r.(?) p.(Ala438Thr)
+?/. - c.1387-2del r.spl p.?
./. - c.1491T>C r.(=) p.(=)
-?/. - c.1491T>C r.(?) p.(Tyr497=)
+/. - c.1515C>G r.(?) p.(Tyr505Ter)
-/. - c.1531+52C>T r.(=) p.(=)
./. - c.1531+52C>T r.(=) p.(=)
./. - c.1536A>G r.(=) p.(=)
+/. - c.1549_1554del r.(?) p.(Leu517_Tyr518del)
+/. - c.1572C>A r.(?) p.(Cys524*)
-?/. - c.1581C>T r.(?) p.(Asp527=)
+?/. 10 c.1591_1592del r.(?) p.(Cys531HisfsTer17)
+?/. 10 c.1630C>T r.? p.(Arg544*)
?/. - c.1639T>C r.(?) p.(Cys547Arg)
?/. - c.1648G>C r.(?) p.(Ala550Pro)
-?/. - c.1660G>A r.(?) p.(Val554Met)
+/. - c.1676+2T>C r.spl? p.?
-/. - c.1676+199del r.(=) p.(=)
+?/. - c.1685C>T r.(?) p.(Pro562Leu)
+/? 11 c.1685C>T r.(?) p.(Pro562Leu)
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