Transcript #00025729 (NM_001170629.1, CHD8 gene)

Transcript name transcript variant 1
Gene name CHD8 (chromodomain helicase DNA binding protein 8)
Chromosome 14
Transcript - NCBI ID NM_001170629.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001164100.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-08-11 14:04:13 +02:00 (CEST)
Date last edited N/A


Variants

214 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.-776224_*65596del r.0 p.0
?/. - c.-171G>A r.(?) p.(=)
-?/. - c.27C>T r.(?) p.(Phe9=)
+/. - c.58_59del r.(?) p.(Leu20Aspfs*2)
?/. - c.68A>C r.(?) p.(Asp23Ala)
-?/. - c.145A>G r.(?) p.(Met49Val)
-?/. - c.262G>A r.(?) p.(Glu88Lys)
-?/. - c.312G>C r.(?) p.(Gln104His)
?/. - c.386T>C r.(?) p.(Leu129Pro)
-?/. - c.456A>G r.(?) p.(Pro152=)
-?/. - c.456A>G r.(?) p.(Pro152=)
+/. - c.470del r.(?) p.(Pro157LeufsTer50)
?/. - c.710G>A r.(?) p.(Arg237His)
?/. - c.715G>A r.(?) p.(Val239Ile)
?/. - c.856C>T r.(?) p.(Arg286Cys)
-?/. - c.871C>T r.(?) p.(Leu291Phe)
?/. - c.871C>T r.(?) p.(Leu291Phe)
-?/. - c.871C>T r.(?) p.(Leu291Phe)
+?/. - c.898C>T r.(?) p.(Gln300*)
?/. - c.982A>G r.(?) p.(Lys328Glu)
?/. - c.1053C>G r.(?) p.(Ile351Met)
?/. E-3 c.1053C>G r.(?) p.(Ile351Met)
?/. 3 c.1053C>G r.(?) p.(Ile351Met)
-?/. - c.1076C>T r.(?) p.(Ser359Leu)
-?/. - c.1091C>G r.(?) p.(Pro364Arg)
+/. - c.1123_1124del r.(?) p.(Leu375Valfs*45)
-?/. - c.1166G>A r.(?) p.(Ser389Asn)
+/. - c.1184del r.(?) p.(Ser395Ter)
?/. - c.1210C>T r.(?) p.(Pro404Ser)
?/. - c.1252G>A r.(?) p.(Val418Ile)
-?/. - c.1296A>G r.(?) p.(Ser432=)
-?/. - c.1315C>T r.(?) p.(His439Tyr)
?/. - c.1315C>T r.(?) p.(His439Tyr)
-?/. - c.1319C>T r.(?) p.(Ser440Leu)
-?/. - c.1323G>C r.(?) p.(Gly441=)
-?/. - c.1437C>T r.(?) p.(Asn479=)
?/. - c.1601+6T>A r.(=) p.(=)
+/. - c.1638dup r.(?) p.(Asn547*)
+/. - c.1690C>T r.(?) p.(Arg564Ter)
?/. - c.1899+5G>A r.spl? p.?
+?/. - c.1968+1G>A r.spl p.?
-?/. - c.1968+6G>A r.(=) p.(=)
?/. - c.2008G>C r.(?) p.(Val670Leu)
+/. - c.2024+5G>A r.spl? p.?
-?/. - c.2024+8A>T r.(=) p.(=)
?/. - c.2098C>T r.(?) p.(Arg700Cys)
?/. - c.2111A>G r.(?) p.(Lys704Arg)
?/. - c.2111A>G r.(?) p.(Lys704Arg)
+?/. - c.2140G>T r.(?) p.(Glu714Ter)
?/. - c.2143-3T>G r.spl? p.?
+?/. - c.2252G>T r.(?) p.(Trp751Leu)
-?/. - c.2300T>C r.(?) p.(Val767Ala)
+/. - c.2303_2321delinsGGCCCAGTGCTTGGCCAG r.(?) p.(Asp768GlyfsTer21)
?/. - c.2317C>G r.(?) p.(Arg773Gly)
-?/. - c.2318G>A r.(?) p.(Arg773Gln)
?/. - c.2318G>A r.(?) p.(Arg773Gln)
?/. - c.2364+2T>C r.spl? p.?
?/. - c.2484C>T r.(?) p.(Asn828=)
?/. - c.2617A>G r.(?) p.(Asn873Asp)
-?/. - c.2652G>A r.(?) p.(Met884Ile)
+/. 13i c.2730+4A>G r.2486_2487ins[GTGG;2486+5_2487-1] p.Gln830fs
+?/. - c.2731-2A>G r.spl? p.?
+/. - c.2801_2804del r.(?) p.(Cys934LeufsTer19)
-?/. - c.2812C>T r.(?) p.(Arg938Cys)
+/. - c.2907+1G>T r.spl p.?
+?/. - c.2950del r.(?) p.(Val984Ter)
+/. - c.3022del r.(?) p.(Asp1008Thrfs*21)
+?/. - c.3050del r.(?) p.(Gln1017ArgfsTer12)
?/. - c.3193T>G r.(?) p.(Leu1065Val)
+?/. - c.3226G>T r.(?) p.(Ala1076Ser)
+/. - c.3308-1G>C r.[3307_3308ins[3308-66_3308-2;c],3308_3379del] p.[Gly1103Valfs*3,Ala1104Hisfs*12]
+/. - c.3340G>T r.(?) p.(Glu1114Ter)
?/. - c.3404T>G r.(?) p.(Leu1135Arg)
?/. - c.3464_3466del r.(?) p.(Phe1155del)
+/. - c.3512A>C r.(?) p.(Gln1171Pro)
+/. - c.3518+1G>T r.spl p.?
+/. - c.3562C>T r.(?) p.(Arg1188Ter)
+?/. - c.3562C>T r.(?) p.(Arg1188Ter)
?/. - c.3581G>A r.(?) p.(Arg1194His)
+/. - c.3628C>T r.(?) p.(Arg1210Trp)
+/. - c.3638del r.(?) p.(Gly1213AspfsTer40)
?/. - c.3643G>C r.(?) p.(Gly1215Arg)
+?/. - c.3754G>A r.(?) p.(Val1252Met)
+?/. - c.3882+1G>A r.spl? p.?
+?/. 20 c.3994C>T r.(?) p.(Gln1332*)
+?/. - c.4009C>T r.(?) p.(Arg1337Ter)
?/. - c.4009C>T r.(?) p.(Arg1337Ter)
?/. - c.4062+5G>C r.spl? p.?
?/. - c.4156G>C r.(?) p.(Asp1386His)
+/. - c.4204C>T r.(?) p.(Arg1402Ter)
+/. - c.4204C>T r.(?) p.(Arg1402Ter)
?/. - c.4216C>T r.(?) p.(Arg1406Cys)
-?/. - c.4245C>T r.(?) p.(Asp1415=)
?/. - c.4315_4317del r.(?) p.(His1439del)
?/. - c.4322A>G r.(?) p.(Tyr1441Cys)
+/. - c.4367A>G r.(?) p.(Tyr1456Cys)
+/. - c.4378C>T r.(?) p.(Arg1460*)
+/. - c.4384C>T r.(?) p.(Arg1462*)
?/. - c.4405C>T r.(?) p.(Arg1469Cys)
+?/. - c.4414C>T r.(?) p.(Arg1472Ter)
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