Transcript #00005068 (NM_020549.4, CHAT gene)

Transcript name transcript variant M
Gene name CHAT (choline O-acetyltransferase)
Chromosome 10
Transcript - NCBI ID NM_020549.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_065574.3
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-3362C>A r.(?) p.(=)
+?/. - c.-3058A>G r.(?) p.(=)
?/. - c.-2429G>C r.(?) p.(=)
+/. - c.-2361del r.(?) p.(=)
?/. - c.-2287G>A r.(?) p.(=)
?/. - c.-2258G>C r.(?) p.(=)
-?/. - c.-1866C>T r.(?) p.(=)
-/. - c.-10T>G r.(?) p.(=)
?/. _1_15_ c.-153_*58{2} r.? p.?
+/. - c.0 r.0 p.0
+?/. - c.3G>A r.(?) p.(Met1?)
+?/. - c.3G>A r.(?) p.(Met1?)
-/. - c.141C>G r.(?) p.(Asp47Glu)
-?/. - c.287-442C>T r.(=) p.(=)
-/. - c.358G>A r.(?) p.(Ala120Thr)
+/. 2 c.358G>A r.(?) p.(?)
?/. - c.388-26C>A r.(=) p.(=)
+/. 3 c.406G>A r.(?) p.(Val136Met)
+/. 3 c.406G>A r.(?) p.(Val136Met)
+/. 3 c.406G>A r.(?) p.(Val136Met)
+/. 3 c.406G>A r.(?) p.(Val136Met)
+/. 3 c.406G>A r.(?) p.(Val136Met)
-?/. - c.414G>C r.(?) p.(=)
+/. - c.418C>T r.(?) p.(Gln140*)
?/. - c.487C>T r.(?) p.(Arg163Trp)
?/. - c.487C>T r.(?) p.(Arg163Trp)
+/. 3 c.522_523dup r.0 p.0
+/. 4 c.580G>C r.spl? p.(Val194Leu)
+/. 4 c.605T>G r.(?) p.(Met202Arg)
?/. 4 c.619C>G r.(?) p.(Arg207Gly)
+?/. 4 c.620G>A r.(?) p.(Arg207His)
+/. 4 c.629T>C r.(?) p.(Leu210Pro)
+/. 4 c.629T>C r.(?) p.(Leu210Pro)
+/. 4 c.629T>C r.(?) p.(Leu210Pro)
+/. 4 c.631C>G r.(?) p.(Pro211Ala)
+/. 4 c.631C>G r.(?) p.(Pro211Ala)
+/. 4 c.678_684del r.(?) p.(Gly227Metfs*4)
+/. - c.698+60C>T r.(=) p.(=)
?/. - c.699-122_699-57dup r.(?) p.(=)
+/. 5 c.703G>A r.(?) p.(Ala235Thr)
-?/. - c.711C>G r.(?) p.(Ser237Arg)
-/. - c.727C>T r.(?) p.(Leu243Phe)
-/. - c.727C>T r.(?) p.(Leu243Phe)
-/. - c.727C>T r.(?) p.(Leu243Phe)
-/. - c.727C>T r.(?) p.(Leu243Phe)
-/. - c.753-26C>T r.(=) p.(=)
+?/. - c.850G>A r.(?) p.(Gly284Ser)
+/. 6 c.914T>C r.(?) p.(Ile305Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1007T>C r.(?) p.(Ile336Thr)
+/. 7 c.1061C>T r.(?) p.(Thr354Met)
?/. - c.1061C>T r.(?) p.(Thr354Met)
+/. 7 c.1061C>T r.(?) p.(Thr354Met)
+?/. 7 c.1102C>G r.(?) p.(Leu368Val)
-/. - c.1112-83G>T r.(=) p.(=)
-?/. - c.1135G>C r.(?) p.(Asp379His)
-?/. - c.1198G>A r.(?) p.(Asp400Asn)
-?/. - c.1198G>A r.(?) p.(Asp400Asn)
+?/. 7 c.1231G>A r.(?) p.(Gly411Arg)
-?/. - c.1248C>T r.(?) p.(=)
+/. 8 c.1249G>A r.(?) p.(Gly417Arg)
+/. 8 c.1249G>A r.(?) p.(Gly417Arg)
+/. 8 c.1258C>T r.(?) p.(Arg420Cys)
+/. 8 c.1262G>C r.(?) p.(Trp421Ser)
+?/. - c.1267G>A r.(?) p.(Asp423Asn)
?/. 8 c.1267G>A r.(?) p.(Asp423Asn)
?/. - c.1288G>A r.(?) p.(Val430Met)
?/. - c.1288G>A r.(?) p.(Val430Met)
+?/. - c.1288G>A r.(?) p.(Val430Met)
?/. - c.1288G>A r.(?) p.(Val430Met)
+?/. 7 c.1300G>A r.(?) p.(Gly434Ser)
+/. 9 c.1321G>A r.(?) p.(Glu441Lys)
+/. 9 c.1321G>A r.(?) p.(Glu441Lys)
-?/. - c.1372C>T r.(?) p.(Leu458Phe)
-?/. - c.1372C>T r.(?) p.(Leu458Phe)
-?/. - c.1372C>T r.(?) p.(Leu458Phe)
-/. - c.1381= r.(=) p.(Met461=)
?/. - c.1426G>A r.(?) p.(Glu476Lys)
+/. 10 c.1444A>G r.(?) p.(Arg482Gly)
+/. 10 c.1444A>G r.(?) p.(Arg482Gly)
+/. 10 c.1444A>G r.(?) p.(Arg482Gly)
?/. - c.1460G>T r.(?) p.(Cys487Phe)
+/. 10 c.1492T>C r.(?) p.(Ser498Pro)
+/. 10 c.1493C>T r.(?) p.(Ser498Leu)
+/. 10 c.1493C>T r.(?) p.(Ser498Leu)
+?/. 11 c.1505T>C r.(?) p.(Leu502Pro)
+/. 11 c.1516G>T r.(?) p.(Val506Leu)
+/. 11 c.1516G>T r.(?) p.(Val506Leu)
+/. 11 c.1516G>T r.(?) p.(Val506Leu)
+/. 11 c.1516G>T r.(?) p.(Val506Leu)
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