Transcript #00024204 (NM_001048166.1, STIL gene)

Transcript name transcript variant 1
Gene name STIL (SCL/TAL1 interrupting locus)
Chromosome 1
Transcript - NCBI ID NM_001048166.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001041631.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-11-28 12:52:34 +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.45-1G>A r.spl? p.?
?/. - c.45G>T r.(?) p.(Arg15Ser)
?/. - c.53C>G r.(?) p.(Ser18*)
?/. - c.227C>T r.(?) p.(Ser76Leu)
-/. - c.257C>T r.(?) p.(Ala86Val)
-/. - c.257C>T r.(?) p.(Ala86Val)
-/. - c.257C>T r.(?) p.(Ala86Val)
?/. - c.310C>G r.(?) p.(Arg104Gly)
-?/. - c.428T>C r.(?) p.(Val143Ala)
?/. - c.520C>T r.(?) p.(His174Tyr)
-?/. - c.573A>G r.(?) p.(Ala191=)
+?/. - c.575C>T r.(?) p.(Ala192Val)
-?/. - c.1036C>T r.(?) p.(Pro346Ser)
-?/. - c.1051A>G r.(?) p.(Ile351Val)
-/. - c.1055G>A r.(?) p.(Arg352His)
?/. - c.1057del r.(?) p.(Cys353ValfsTer3)
-?/. - c.1069G>A r.(?) p.(Ala357Thr)
-?/. - c.1120T>C r.(?) p.(Phe374Leu)
-?/. - c.1136C>T r.(?) p.(Ser379Phe)
+/. - c.1226G>C r.(?) p.(Ser409Thr)
+?/. - c.1229C>G r.(?) p.(Pro410Arg)
?/. - c.1229C>G r.(?) p.(Pro410Arg)
+?/. 11 c.1231C>G r.(?) p.(His411Asp)
-/. - c.1452C>G r.(?) p.(Ser484=)
-/. - c.1452C>G r.(?) p.(Ser484=)
-?/. - c.1455G>C r.(?) p.(Leu485Phe)
+/. - c.1455G>C r.(?) p.(Leu485Phe)
?/. - c.1700C>T r.(?) p.(Pro567Leu)
?/. - c.1700C>T r.(?) p.(Pro567Leu)
-?/. - c.1839A>G r.(?) p.(Gln613=)
-/. - c.2017A>G r.(?) p.(Ser673Gly)
-?/. - c.2070A>T r.(?) p.(Ser690=)
-?/. - c.2175C>T r.(?) p.(Phe725=)
-/. - c.2218-17G>A r.(=) p.(=)
+/. - c.2354_2355dup r.(?) p.(Lys786GlufsTer4)
?/. - c.2362G>A r.(?) p.(Val788Ile)
?/. - c.2362G>A r.(?) p.(Val788Ile)
-?/. - c.2384-13A>G r.(=) p.(=)
+/. - c.2393T>G r.(?) p.(Leu798Trp)
-?/. - c.2454C>T r.(?) p.(Thr818=)
-/. - c.2615+27A>G r.(=) p.(=)
-/. - c.2954A>G r.(?) p.(His985Arg)
-/. - c.2954A>G r.(?) p.(His985Arg)
-/. - c.2954A>G r.(?) p.(His985Arg)
-?/. - c.3037C>T r.(?) p.(Pro1013Ser)
?/. - c.3061C>T r.(?) p.(His1021Tyr)
-?/. - c.3276C>T r.(?) p.(Asp1092=)
-?/. - c.3333T>C r.(?) p.(Ile1111=)
+?/. 17 c.3370A>G r.(?) p.(Met1124Val)
-?/. - c.3378A>G r.(?) p.(Arg1126=)
-?/. - c.3430G>A r.(?) p.(Asp1144Asn)
-/. - c.3486T>C r.(?) p.(Pro1162=)
-/. - c.3486T>C r.(?) p.(Pro1162=)
-/. - c.3486T>C r.(?) p.(Pro1162=)
?/. - c.3487G>A r.(?) p.(Glu1163Lys)
?/. - c.3515C>T r.(?) p.(Ser1172Phe)
?/. - c.3551G>C r.(?) p.(Cys1184Ser)
+?/. - c.3552_3553del r.(?) p.(Cys1184*)
+?/. - c.3598A>G r.(?) p.(Thr1200Ala)
?/. - c.3694C>T r.(?) p.(Arg1232Ter)
?/. - c.3700G>A r.(?) p.(Gly1234Arg)
?/. - c.3713T>G r.(?) p.(Phe1238Cys)
?/. - c.3776C>A r.(?) p.(Pro1259His)
-?/. - c.3786G>A r.(?) p.(Thr1262=)
+?/. - c.3838C>T r.(?) p.(Arg1280Cys)
?/. - c.3849G>T r.(?) p.(Gln1283His)
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