Transcript #00005003 (NM_007186.3, CEP250 gene)

Transcript name centrosomal protein 250kDa
Gene name CEP250 (centrosomal protein 250kDa)
Chromosome 20
Transcript - NCBI ID NM_007186.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_009117.2
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

106 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.243+11C>T r.(=) p.(=)
?/. - c.247C>T r.(?) p.(Pro83Ser)
?/. - c.327G>T r.(?) p.(Arg109Ser)
-?/. - c.353C>T r.(?) p.(Thr118Ile)
-?/. - c.353C>T r.(?) p.(Thr118Ile)
./. - c.361C>T r.(?) p.(Arg121*)
-?/. - c.384C>T r.(?) p.(Asp128=)
+/. - c.493-1G>A r.spl? p.?
?/. - c.493-1G>A r.spl p.?
?/. - c.527G>A r.(?) p.(Arg176His)
?/. - c.545G>A r.(?) p.(Arg182Gln)
+/. - c.562C>T r.(?) p.(Arg188*)
+/. - c.562C>T r.(?) p.(Arg188*)
+/. - c.562C>T r.(?) p.(Arg188*)
-?/. - c.777A>G r.(?) p.(Glu259=)
-?/. - c.777A>G r.(?) p.(Glu259=)
-?/. - c.798G>A r.(?) p.(Glu266=)
?/. - c.851G>A r.(?) p.(Arg284Gln)
-?/. - c.859G>A r.(?) p.(Glu287Lys)
-/. - c.936A>G r.(?) p.(Thr312=)
-?/. - c.936A>G r.(?) p.(Thr312=)
-?/. - c.1001C>T r.(?) p.(Ala334Val)
-?/. - c.1050+7G>A r.(=) p.(=)
?/. - c.1113G>A r.(?) p.(Leu371=)
+?/. - c.1164del r.(?) p.(Thr389LeufsTer7)
?/. - c.1174C>T r.(?) p.(Arg392Cys)
-?/. - c.1200G>A r.(?) p.(Gln400=)
-?/. - c.1210-14C>T r.(=) p.(=)
-?/. - c.1213C>T r.(?) p.(Leu405=)
?/. - c.1256T>G r.(?) p.(Leu419Trp)
-?/. - c.1437G>A r.(?) p.(Leu479=)
?/. - c.1550C>T r.(?) p.(Ala517Val)
-/. - c.1679G>A r.(?) p.(Arg560Lys)
+?/. 16 c.1826C>T r.(?) p.(Ala609Val)
-?/. - c.1827G>A r.(?) p.(Ala609=)
-?/. - c.2006A>G r.(?) p.(Gln669Arg)
?/. - c.2120C>T r.(?) p.(Thr707Met)
+/. - c.2155C>T r.(?) p.(Arg719*)
?/. - c.2216C>T r.(?) p.(Ala739Val)
+/. - c.2512del r.(?) p.(Gln838LysfsTer18)
-?/. - c.2526T>G r.(?) p.(=)
-?/. - c.2686A>G r.(?) p.(Thr896Ala)
?/. - c.2740_2741del r.(?) p.(Ser914CysfsTer76)
?/. - c.2775G>T r.(?) p.(Lys925Asn)
-?/. - c.2829T>C r.(?) p.(Asp943=)
?/. - c.2920C>T r.(?) p.(Gln974Ter)
-?/. - c.3237A>G r.(?) p.(Gln1079=)
+?/. - c.3273_3289del r.(?) p.(Ala1092ArgfsTer19)
-?/. - c.3306+8C>G r.(=) p.(=)
-?/. - c.3307-10T>C r.(=) p.(=)
+?/. - c.3337A>T r.(?) p.(Lys1113*)
-/. - c.3381G>A r.(?) p.(Glu1127=)
-?/. - c.3402G>A r.(?) p.(Thr1134=)
+/. - c.3463C>T r.(?) p.(Arg1155*)
+/. 26 c.3463C>T r.(?) p.(Arg1155*)
+/. - c.3463C>T r.(?) p.(Arg1155*)
+/. - c.3463C>T r.(?) p.(Arg1155*)
+/. - c.3463C>T r.(?) p.(Arg1155*)
+/. - c.3463C>T r.(?) p.(Arg1155*)
-/. - c.3629C>T r.(?) p.(Ala1210Val)
-?/. - c.3629C>T r.(?) p.(Ala1210Val)
-/. - c.3899-10_3899-9dup r.(=) p.(=)
-/. - c.3906C>T r.(?) p.(Ser1302=)
-?/. - c.3967G>A r.(?) p.(Ala1323Thr)
-/. - c.3967G>A r.(?) p.(Ala1323Thr)
+/. - c.4006C>T r.(?) p.(Arg1336Ter)
+?/. - c.4006C>T r.(?) p.(Arg1336*)
+/. - c.4039C>T r.(?) p.(Gln1347Ter)
-/. - c.4365G>A r.(?) p.(Lys1455=)
+/. - c.4388_4389del r.(?) p.(Leu1463ArgfsTer23)
?/. - c.4567G>A r.(?) p.(Val1523Ile)
-?/. - c.4861C>A r.(?) p.(Leu1621Met)
-?/. - c.4866A>G r.(?) p.(=)
-?/. - c.4931G>A r.(?) p.(Arg1644Lys)
?/. - c.4960G>A r.(?) p.(Glu1654Lys)
-/. - c.5570G>A r.(?) p.(Arg1857His)
+/. - c.5579_5580dup r.(?) p.(Leu1861SerfsTer33)
?/. - c.5644G>T r.(?) p.(Val1882Phe)
-?/. - c.5790G>A r.(?) p.(Gln1930=)
-?/. - c.5798C>T r.(?) p.(Ala1933Val)
-?/. - c.5850G>A r.(?) p.(Gln1950=)
?/. - c.5932C>T r.(?) p.(Gln1978Ter)
+/. - c.5959C>T r.(?) p.(Gln1987Ter)
+/. - c.5959C>T r.(?) p.(Gln1987Ter)
-?/. - c.5974C>T r.(?) p.(Arg1992Cys)
?/. - c.5974C>T r.(?) p.(Arg1992Cys)
?/. - c.6038G>A r.(?) p.(Arg2013Gln)
?/. - c.6118C>G r.(?) p.(Leu2040Val)
-?/. - c.6150G>A r.(?) p.(Glu2050=)
-/. - c.6157C>T r.(?) p.(His2053Tyr)
?/. - c.6238C>G r.(?) p.(Leu2080Val)
-?/. - c.6304A>G r.(?) p.(Thr2102Ala)
-/. - c.6358A>G r.(?) p.(Asn2120Asp)
-?/. - c.6424G>T r.(?) p.(Asp2142Tyr)
?/. - c.6451_6462del r.(?) p.(Glu2151_Arg2154del)
?/. - c.6451_6462del r.(?) p.(Glu2151_Arg2154del)
?/. - c.6532C>T r.(?) p.(Leu2178Phe)
?/. - c.6557G>T r.(?) p.(Ser2186Ile)
-?/. - c.6613G>A r.(?) p.(Asp2205Asn)
-?/. - c.6751-7C>T r.(=) p.(=)
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