Transcript #00000408 (NM_153252.4, BRWD3 gene)

Transcript name bromodomain and WD repeat domain containing 3
Gene name BRWD3 (bromodomain and WD repeat domain containing 3)
Chromosome X
Transcript - NCBI ID NM_153252.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_694984.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.14C>G r.(?) p.(Pro5Arg)
-?/. - c.33G>A r.(?) p.(Glu11=)
-?/. - c.33G>A r.(?) p.(Glu11=)
?/. - c.67G>C r.(?) p.(Gly23Arg)
-?/. - c.94C>T r.(?) p.(Leu32=)
+?/. - c.100C>T r.(?) p.(Gln34*)
?/. - c.121-163_121-162del r.(=) p.(=)
?/. - c.121-163_121-162del r.(=) p.(=)
?/. - c.121-162del r.(=) p.(=)
?/. - c.121-162del r.(=) p.(=)
?/. - c.331+123G>A r.(=) p.(=)
?/. - c.331+123G>A r.(=) p.(=)
-?/. - c.348A>G r.(?) p.(Leu116=)
?/. - c.445G>A r.(?) p.(Ala149Thr)
?/. - c.460G>A r.(?) p.(Gly154Ser)
+?/. - c.568C>T r.(?) p.(Arg190Ter)
-?/. - c.573C>T r.(?) p.(Ser191=)
+?/. - c.591+1G>A r.spl? p.?
?/. - c.592-47_592-45dup r.(=) p.(=)
?/. - c.592-47_592-45dup r.(=) p.(=)
?/. - c.592-47_592-45dup r.(=) p.(=)
?/. - c.592-47_592-45dup r.(=) p.(=)
-?/. - c.597A>C r.(?) p.(Ser199=)
+?/. - c.696T>A r.(?) p.(Tyr232*)
?/. - c.778C>A r.(?) p.(Leu260Ile)
?/. - c.814-167G>A r.(=) p.(=)
?/. - c.814-167G>A r.(=) p.(=)
-/. - c.814-4dup r.spl? p.?
-?/. - c.915A>G r.(?) p.(Arg305=)
?/. - c.917A>G r.(?) p.(Asp306Gly)
?/. 10 c.946dup r.(?) p.(Arg316Lysfs*22)
?/. - c.1085C>T r.(?) p.(Thr362Met)
?/. - c.1087-100dup r.(=) p.(=)
?/. - c.1087-23G>C r.(=) p.(=)
?/. - c.1087-23G>C r.(=) p.(=)
?/. - c.1102G>C r.(?) p.(Val368Leu)
-?/. - c.1118A>G r.(?) p.(Asn373Ser)
?/. - c.1118A>G r.(?) p.(Asn373Ser)
?/. - c.1118A>G r.(?) p.(Asn373Ser)
?/. - c.1128-152T>G r.(=) p.(=)
-?/. - c.1131A>G r.(?) p.(Leu377=)
-?/. - c.1307C>T r.(?) p.(Thr436Ile)
?/. - c.1500A>C r.(?) p.(Lys500Asn)
?/. - c.1650+220A>G r.(=) p.(=)
?/. - c.1650+220A>G r.(=) p.(=)
?/. - c.1685G>A r.(?) p.(Arg562His)
-?/. - c.1758T>A r.(?) p.(Pro586=)
?/. - c.2044+4_2044+7del r.spl? p.?
-?/. - c.2151G>A r.(?) p.(Arg717=)
?/. - c.2165C>A r.(?) p.(Thr722Asn)
+/. - c.2187G>A r.(?) p.(Trp729*)
-?/. - c.2325+5G>A r.spl? p.?
-?/. - c.2325+5G>A r.spl? p.?
-?/. - c.2604A>G r.(?) p.(Leu868=)
?/. - c.2729G>C r.(?) p.(Gly910Ala)
?/. - c.2773C>T r.(?) p.(Pro925Ser)
-?/. - c.2784C>A r.(?) p.(Ile928=)
+?/. - c.2800C>T r.(?) p.(Arg934Ter)
+/. - c.3307G>T r.(?) p.(Glu1103Ter)
-?/. - c.3429A>G r.(?) p.(Arg1143=)
?/. - c.3433G>A r.(?) p.(Glu1145Lys)
?/. - c.3433G>A r.(?) p.(Glu1145Lys)
?/. - c.3433G>A r.(?) p.(Glu1145Lys)
?/. - c.3433G>A r.(?) p.(Glu1145Lys)
+?/. - c.3436G>T r.(?) p.(Glu1146*)
?/. - c.3469C>T r.(?) p.(Leu1157Phe)
?/. - c.3481+136G>T r.(=) p.(=)
?/. - c.3481+136G>T r.(=) p.(=)
-?/. - c.3482-4G>C r.spl? p.?
?/. - c.3658T>C r.(?) p.(Phe1220Leu)
+?/. - c.3791del r.(?) p.(Ser1264Ilefs*13)
-/. - c.3863= r.(=) p.(Arg1288=)
?/. - c.3863A>G - p.(Lys1288Arg)
?/. - c.3863A>G - p.(Lys1288Arg)
?/. - c.3865-101_3865-98del r.(=) p.(=)
?/. - c.3865-101_3865-96del r.(=) p.(=)
?/. - c.3865-99_3865-98del r.(=) p.(=)
?/. - c.3865-93_3865-92del r.(=) p.(=)
+/. - c.4067C>A r.(?) p.(Ser1356Ter)
?/. - c.4339C>T r.(?) p.(Arg1447Trp)
?/. - c.4339C>T r.(?) p.(Arg1447Trp)
?/. - c.4339C>T r.(?) p.(Arg1447Trp)
-?/. - c.4377A>G r.(?) p.(Leu1459=)
?/. - c.4394C>G r.(?) p.(Pro1465Arg)
-?/. - c.4471A>G r.(?) p.(Thr1491Ala)
+?/. - c.4585C>T r.(?) p.(Arg1529Ter)
+?/. - c.4655-1G>T r.spl? p.?
?/. 41 c.4786A>G r.(?) p.(Lys1596Glu)
-?/. - c.5101G>A r.(?) p.(Gly1701Arg)
-?/. - c.5101G>A r.(?) p.(Gly1701Arg)
-?/. - c.5101G>A r.(?) p.(Gly1701Arg)
-?/. - c.5130G>T r.(?) p.(Gly1710=)
?/. - c.5173C>T r.(?) p.(Arg1725Ter)
?/. - c.5174G>A r.(?) p.(Arg1725Gln)
?/. - c.5248A>T r.(?) p.(Arg1750Ter)
-?/. - c.5263A>C r.(?) p.(Arg1755=)
-?/. - c.5292T>A r.(?) p.(Asp1764Glu)
?/. - c.*3850G>C r.(=) p.(=)
?/. - c.*3850G>C r.(=) p.(=)
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