Transcript #00018902 (NM_001041.3, SI gene)

Transcript name sucrase-isomaltase (alpha-glucosidase)
Gene name SI (sucrase-isomaltase (alpha-glucosidase))
Chromosome 3
Transcript - NCBI ID NM_001041.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001032.2
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

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.43G>T r.(?) p.(Val15Phe)
-/. - c.43G>T r.(?) p.(Val15Phe)
+/. 4 c.273_274del r.(?) p.(Gly92Leufs*8)
+/. 4 c.273_274del r.(?) p.(Gly92Leufs*8)
+/. 4 c.273_274del r.(?) p.(Gly92Leufs*8)
-?/. - c.355A>T r.(?) p.(Met119Leu)
-/. - c.374-11del r.(=) p.(=)
?/. - c.653G>T r.(?) p.(Gly218Val)
-/. - c.691A>G r.(?) p.(Thr231Ala)
-/. - c.691A>G r.(?) p.(Thr231Ala)
-?/. - c.740A>G r.(?) p.(Lys247Arg)
+/. - c.787C>T r.(?) p.(Arg263*)
-?/. - c.825C>T r.(?) p.(Tyr275=)
-?/. - c.876C>T r.(?) p.(Phe292=)
?/. - c.1043C>T r.(?) p.(Pro348Leu)
?/. - c.1111G>A r.(?) p.(Val371Met)
-/. - c.1146+13A>C r.(=) p.(=)
-/. - c.1146+13A>C r.(=) p.(=)
-/. - c.1437C>T r.(?) p.(Asn479=)
-/. - c.1437C>T r.(?) p.(Asn479=)
?/. - c.1498G>T r.(?) p.(Asp500Tyr)
+/. - c.1512+6T>C r.(=) p.(=)
?/. - c.1533C>G r.(?) p.(Ser511Arg)
-/. - c.1715+99G>T r.(=) p.(=)
+?/. - c.1730T>G r.(?) p.(Val577Gly)
+?/. - c.1730T>G r.(?) p.(Val577Gly)
+/. - c.1730T>G r.(?) p.(Val577Gly)
+?/. - c.1730T>G r.(?) p.(Val577Gly)
+?/. - c.1780T>C r.(?) p.(Ser594Pro)
-/. - c.1797G>T r.(?) p.(Ala599=)
-/. - c.1797G>T r.(?) p.(Ala599=)
?/. - c.1846A>G r.(?) p.(Ile616Val)
?/. - c.1888-3T>A r.spl? p.?
-/. - c.1888del r.(?) p.(Val630Leufs*60)
?/. - c.2320A>G r.(?) p.(Arg774Gly)
?/. - c.2320A>G r.(?) p.(Arg774Gly)
-?/. - c.2343T>C r.(?) p.(Tyr781=)
-?/. - c.2395A>G r.(?) p.(Ile799Val)
?/. - c.2599T>C r.(?) p.(Tyr867His)
?/. - c.2736+2T>A r.spl? p.?
-/. - c.2737-11dup r.(=) p.(=)
-?/. - c.2737-5C>A r.spl? p.?
?/. - c.2834C>A r.(?) p.(Pro945Gln)
-?/. - c.2849C>A r.(?) p.(Ala950Glu)
-?/. - c.2892G>A r.(?) p.(Thr964=)
?/. - c.2923T>C r.(?) p.(Tyr975His)
-?/. - c.2923T>C r.(?) p.(Tyr975His)
?/. - c.2923T>C r.(?) p.(Tyr975His)
-?/. - c.2923T>C r.(?) p.(Tyr975His)
-?/. - c.2923T>C r.(?) p.(Tyr975His)
+/. - c.3218G>A r.(?) p.(Gly1073Asp)
+?/. - c.3218G>A r.(?) p.(Gly1073Asp)
-?/. - c.3234G>A r.(?) p.(Arg1078=)
-?/. - c.3246A>G r.(?) p.(Gly1082=)
?/. - c.3389C>T r.(?) p.(Thr1130Ile)
?/. - c.3557G>A r.(?) p.(Arg1186His)
-?/. - c.3634-5dup r.spl? p.?
-?/. - c.3720G>A r.(?) p.(Arg1240=)
-?/. - c.3733G>A r.(?) p.(Ala1245Thr)
-/. - c.3888+19C>T r.(=) p.(=)
-/. - c.3888+19C>T r.(=) p.(=)
-?/. - c.3905G>C r.(?) p.(Gly1302Ala)
?/. - c.3914C>T r.(?) p.(Thr1305Ile)
?/. - c.3914C>T r.(?) p.(Thr1305Ile)
-?/. - c.3955G>A r.(?) p.(Val1319Ile)
-?/. - c.4008A>G r.(?) p.(Pro1336=)
-/. - c.4026A>G r.(?) p.(Thr1342=)
-/. - c.4026A>G r.(?) p.(Thr1342=)
?/. - c.4133T>G r.(?) p.(Ile1378Ser)
?/. - c.4240G>A r.(?) p.(Glu1414Lys)
-?/. - c.4240G>A r.(?) p.(Glu1414Lys)
-?/. - c.4542T>C r.(?) p.(Gly1514=)
-/. - c.4569G>A r.(?) p.(Met1523Ile)
-/. - c.4569G>A r.(?) p.(Met1523Ile)
?/. - c.4573T>C r.(?) p.(Tyr1525His)
+/. - c.4573T>C r.(?) p.(Tyr1525His)
?/. - c.4586A>G r.(?) p.(Asp1529Gly)
-?/. - c.4721C>G r.(?) p.(Thr1574Ser)
-/. - c.4927-19C>T r.(=) p.(=)
-?/. - c.4951G>A r.(?) p.(Val1651Ile)
-?/. - c.5096A>C r.(?) p.(Asn1699Thr)
-?/. - c.5193T>C r.(?) p.(Ser1731=)
-?/. - c.5279G>T r.(?) p.(Gly1760Val)
?/. - c.5279G>T r.(?) p.(Gly1760Val)
-?/. - c.5301G>A r.(?) p.(Thr1767=)
-?/. - c.5363C>T r.(?) p.(Thr1788Met)
-?/. - c.5403C>T r.(?) p.(Asp1801=)
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