Transcript #00025524 (NM_020706.2, SCAF4 gene)

Transcript name transcript variant 1
Gene name SCAF4 (SR-related CTD-associated factor 4)
Chromosome 21
Transcript - NCBI ID NM_020706.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_065757.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-06-09 17:43:04 +02:00 (CEST)
Date last edited N/A


Variants

80 entries on 1 page. Showing entries 1 - 80.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.31-955G>C r.(=) p.(=)
?/. - c.31-796A>G r.(=) p.(=)
?/. - c.31-255C>T r.(=) p.(=)
?/. - c.159+1G>A r.spl? p.?
+?/. - c.175A>T r.(?) p.(Lys59*)
+/. 4i c.321+1G>T r.[193_321del,114_321del,?] p.?
-?/. - c.322-7G>A r.(=) p.(=)
?/. - c.407C>T r.(?) p.(Ala136Val)
?/. - c.453_456del r.(?) p.(Asn151LysfsTer8)
+/. - c.453_456del r.(?) p.(Asn151Lysfs*8)
?/. - c.768del r.(?) p.(Phe257Leufs*89)
+?/. - c.783G>T r.783g>u p.Leu261Phe
-?/. - c.868C>A r.(?) p.(Pro290Thr)
-?/. - c.876C>T r.(?) p.(Ala292=)
?/. - c.937C>T r.(?) p.(Pro313Ser)
-?/. - c.1021T>C r.(?) p.(Phe341Leu)
+/. - c.1028del r.(?) p.(Pro343Hisfs*3)
-?/. - c.1058T>C r.(?) p.(Met353Thr)
?/. - c.1147G>A r.(?) p.(Val383Met)
-?/. - c.1159A>G r.(?) p.(Thr387Ala)
?/. - c.1264C>G r.(?) p.(Gln422Glu)
?/. - c.1277G>A r.(?) p.(Arg426Gln)
+/. - c.1301C>A r.1301c>a p.Ser434*
+?/. - c.1313dup r.(?) p.(Ala439Serfs*11)
-?/. - c.1382G>A r.(?) p.(Arg461His)
+/. - c.1423C>T r.(?) p.(Arg475*)
+?/. - c.1450C>T r.(?) p.(Arg484*)
?/. - c.1457_1458del r.(?) p.(Lys486Argfs*49)
+?/. 12 c.1457_1458del r.(1457_1458del) p.(Lys486ArgfsTer49)
+?/. 12 c.1457_1460del r.(?) p.(Lys486Argfs*12)
+?/. - c.1471C>T r.(?) p.(Arg491*)
+?/. 13 c.1585G>T r.(?) p.(Glu529*)
+?/. - c.1614+1G>C r.spl? p.?
+?/. 13i c.1614+1G>C r.spl p.?
+/. - c.1649dup r.(?) p.(Met550Ilefs*4)
+?/. - c.1693C>T r.(?) p.(Arg565*)
+/. - c.1812G>A r.(?) p.(Trp604*)
+/. - c.1889G>A r.1889g>a p.Trp630*
-?/. - c.1916A>G r.(?) p.(Asn639Ser)
-?/. - c.1974A>G r.(?) p.(Ile658Met)
?/. - c.2005A>G r.(?) p.(Ile669Val)
-?/. - c.2091G>A r.(?) p.(Pro697=)
?/. - c.2116A>G r.(?) p.(Ile706Val)
-?/. - c.2210-5del r.spl? p.?
?/. - c.2287A>C r.(?) p.(Ile763Leu)
+?/. - c.2375del r.(?) p.(Ala792Valfs*11)
-?/. - c.2489-3T>C r.spl? p.?
-?/. - c.2562C>T r.(?) p.(Pro854=)
?/. - c.2648C>T r.(?) p.(Pro883Leu)
?/. - c.2732C>T r.(?) p.(Pro911Leu)
?/. - c.2751G>T r.(?) p.(Arg917Ser)
-?/. - c.2793A>G r.(?) p.(Pro931=)
-?/. - c.2796G>T r.(?) p.(Gly932=)
-?/. - c.2877_2879del r.(?) p.(Gln966del)
?/. - c.2891_2899del r.(?) p.(Gln964_Gln966del)
-?/. - c.3083G>A r.(?) p.(Arg1028His)
-?/. - c.3119G>A r.(?) p.(Arg1040Gln)
?/. - c.3200_3201del r.(?) p.(Glu1067Valfs*3)
+?/. - c.3200_3201del r.(?) p.(Glu1067Valfs*3)
-?/. - c.3217G>A r.(?) p.(Glu1073Lys)
?/. - c.3227G>A r.(?) p.(Arg1076Gln)
-?/. - c.3254_3257del r.(?) p.(Asp1085Glyfs*18)
?/. - c.3371_3372del r.(?) p.(Glu1124Valfs*4)
-?/. - c.3394T>A r.(?) p.(Ser1132Thr)
?/. - c.3394T>A r.(?) p.(Ser1132Thr)
+?/. - c.*2843C>G r.(=) p.(=)
+/. - c.*2852A>G r.(=) p.(=)
-?/. - c.*2863A>T r.(=) p.(=)
-?/. - c.*2863A>T r.(=) p.(=)
-?/. - c.*2863A>T r.(=) p.(=)
-?/. - c.*2878T>C r.(=) p.(=)
+/. - c.*4040A>G r.(=) p.(=)
?/. - c.*4083T>C r.(=) p.(=)
+?/. - c.*4112G>A r.(=) p.(=)
?/. - c.*4886_*4888del r.(=) p.(=)
-?/. - c.*4904G>A r.(=) p.(=)
-?/. - c.*4961G>A r.(=) p.(=)
-?/. - c.*4964G>A r.(=) p.(=)
-?/. - c.*4967G>A r.(=) p.(=)
-?/. - c.*4970A>G r.(=) p.(=)
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