Transcript #00024098 (NM_005901.5, SMAD2 gene)

Transcript name transcript variant 1
Gene name SMAD2 (SMAD family member 2)
Chromosome 18
Transcript - NCBI ID NM_005901.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_005892.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-01-18 11:31:51 +01:00 (CET)
Date last edited N/A


Variants

66 entries on 1 page. Showing entries 1 - 66.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-53-120A>G r.(=) p.(=)
?/. - c.10A>G r.(?) p.(Ile4Val)
-?/. - c.162A>G r.(?) p.(Lys54=)
?/. - c.170G>A r.(?) p.(Arg57Gln)
-?/. - c.236+410G>A r.(=) p.(=)
?/. - c.237-12A>G r.(=) p.(=)
-?/. - c.237-5C>T r.spl? p.?
?/. - c.327-2A>T r.spl? p.?
?/. - c.341G>A r.(?) p.(Arg114His)
?/. - c.368T>G r.(?) p.(Leu123Trp)
-?/. - c.393A>G r.(?) p.(=)
?/. - c.436A>G r.(?) p.(Ile146Val)
?/. - c.437T>C r.(?) p.(Ile146Thr)
?/. - c.448G>A r.(?) p.(Glu150Lys)
?/. - c.448G>A r.(?) p.(Glu150Lys)
?/. - c.448G>A r.(?) p.(Glu150Lys)
-?/. - c.520+146A>T r.(=) p.(=)
-?/. - c.521-42T>C r.(=) p.(=)
-?/. - c.521-30C>T r.(=) p.(=)
-/. - c.521-16del r.(=) p.(=)
?/. - c.559C>A r.(?) p.(Leu187Ile)
?/. - c.610A>C r.(?) p.(Thr204Pro)
+?/. - c.612dup r.(?) p.(Asn205Ter)
-?/. - c.656-119A>G r.(=) p.(=)
-?/. - c.690A>T r.(?) p.(Gly230=)
?/. - c.711G>C r.(?) p.(Leu237Phe)
-?/. - c.711G>C r.(?) p.(Leu237Phe)
?/. - c.711G>C r.(?) p.(Leu237Phe)
?/. - c.720T>A r.(?) p.(Ser240Arg)
-?/. - c.730+10del r.(=) p.(=)
-/. - c.730+10dup r.(=) p.(=)
-/. - c.730+11T>A r.(=) p.(=)
-?/. - c.731-170G>C r.(=) p.(=)
?/. - c.757_759del r.(?) p.(Thr253del)
-?/. - c.784+150T>C r.(=) p.(=)
-?/. - c.784+245T>C r.(=) p.(=)
-/. - c.785-802_785-801del r.(=) p.(=)
-?/. - c.785-259C>T r.(=) p.(=)
-?/. - c.785-47T>A r.(=) p.(=)
-?/. - c.785-20_785-18del r.(=) p.(=)
-?/. - c.785-18dup r.(=) p.(=)
-?/. - c.785-17A>C r.(=) p.(=)
-?/. - c.789A>G r.(?) p.(Leu263=)
?/. - c.790C>T r.(?) p.(Gln264*)
-/. - c.828G>A r.(?) p.(Ser276=)
./. - c.919A>G r.(?) p.(Asn307Asp)
+/. - c.935G>C r.(?) p.(Cys312Ser)
+?/. - c.954T>A r.(?) p.(Asn318Lys)
-/. - c.997+18T>G r.(=) p.(=)
-?/. - c.998-18A>G r.(=) p.(=)
-?/. - c.1044G>A r.(?) p.(Glu348=)
+?/. - c.1082A>C r.(?) p.(Asn361Thr)
-?/. - c.1136-10T>C r.(=) p.(=)
+?/. - c.1163A>G r.(?) p.(Gln388Arg)
+?/. 10 c.1163A>G r.(?) p.(Gln388Arg)
+?/. 10 c.1163A>G r.(?) p.(Gln388Arg)
+?/. - c.1190C>A r.(?) p.(Ser397Tyr)
-?/. - c.1245A>G r.(?) p.(Arg415=)
?/. - c.1279C>T r.(?) p.(Arg427*)
-/. - c.1280+16T>C r.(=) p.(=)
-?/. - c.1287G>A r.(?) p.(Gln429=)
+?/. - c.1346T>C r.(?) p.(Leu449Ser)
+?/. 11 c.1346T>C r.(?) p.(Leu449Ser)
+?/. - c.1369G>A r.(?) p.(Gly457Arg)
+?/. 11 c.1369G>A r.(?) p.(Gly457Arg)
?/. - c.1400C>T r.(?) p.(Ser467Leu)
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