Transcript #00025820 (NM_001194998.1, CEP152 gene)

Transcript name transcript variant 1
Gene name CEP152 (centrosomal protein 152kDa)
Chromosome 15
Transcript - NCBI ID NM_001194998.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001181927.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2023-03-14 15:26:27 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-94A>G r.(?) p.(=)
-/. - c.-26A>T r.(?) p.(=)
-/. - c.-24A>T r.(?) p.(=)
?/. - c.4T>A r.(?) p.(Ser2Thr)
-?/. - c.35T>C r.(?) p.(Val12Ala)
?/. - c.85G>A r.(?) p.(Glu29Lys)
-?/. - c.87+27dup r.(=) p.(=)
-?/. - c.88-7G>A r.(=) p.(=)
-?/. - c.158A>G r.(?) p.(Tyr53Cys)
-/. - c.161C>T r.(?) p.(Ser54Leu)
-?/. - c.171C>T r.(?) p.(Ser57=)
-/. - c.191+11G>A r.(=) p.(=)
-/. - c.191+11G>A r.(=) p.(=)
-?/. - c.261+8T>G r.(=) p.(=)
?/. - c.262-3T>C r.spl? p.?
-?/. - c.318A>G r.(?) p.(Glu106=)
-?/. - c.344G>A r.(?) p.(Arg115Gln)
-?/. - c.344G>A r.(?) p.(Arg115Gln)
?/. - c.392G>T r.(?) p.(Gly131Val)
-?/. - c.398G>C r.(?) p.(Ser133Thr)
+/. - c.467dup r.(?) p.(Gln157SerfsTer6)
+/. - c.467dup r.(?) p.(Gln157SerfsTer6)
?/. - c.501T>G r.(?) p.(Asn167Lys)
-?/. - c.567G>A r.(?) p.(Pro189=)
-?/. - c.644G>A r.(?) p.(Ser215Asn)
-?/. - c.644G>A r.(?) p.(Ser215Asn)
?/. - c.667C>T r.(?) p.(Gln223Ter)
+/. - c.667C>T r.(?) p.(Gln223Ter)
+/. - c.667C>T r.(?) p.(Gln223Ter)
-?/. - c.678A>G r.(?) p.(Leu226=)
?/. - c.685A>C r.(?) p.(Asn229His)
-/. - c.691+9C>T r.(=) p.(=)
-/. - c.691+9C>T r.(=) p.(=)
-?/. - c.767T>C r.(?) p.(Ile256Thr)
-?/. - c.767T>C r.(?) p.(Ile256Thr)
-/. - c.833-4G>A r.spl? p.?
-/. - c.833-4G>A r.spl? p.?
-/. - c.833-4G>A r.spl? p.?
-?/. - c.925A>C r.(?) p.(Lys309Gln)
-?/. - c.925A>C r.(?) p.(Lys309Gln)
?/. - c.962A>G r.(?) p.(Asn321Ser)
?/. - c.962A>G r.(?) p.(Asn321Ser)
-/. - c.972+19G>A r.(=) p.(=)
?/. - c.981G>C r.(?) p.(Lys327Asn)
-?/. - c.982A>C r.(?) p.(Lys328Gln)
-?/. - c.982A>C r.(?) p.(Lys328Gln)
-?/. - c.1110C>T r.(?) p.(Tyr370=)
-?/. - c.1180A>G r.(?) p.(Ile394Val)
-?/. - c.1180A>G r.(?) p.(Ile394Val)
?/. - c.1190G>A r.(?) p.(Arg397His)
+?/. - c.1421T>G r.(?) p.(Leu474*)
?/. - c.1550T>A r.(?) p.(Val517Asp)
?/. - c.1655G>A r.(?) p.(Arg552His)
-?/. - c.1782+3A>T r.spl? p.?
+?/. - c.1797del r.(?) p.(Ser600Glnfs*46)
+/. - c.1908+1G>T r.spl? p.?
-/. - c.2000A>G r.(?) p.(Lys667Arg)
-?/. - c.2000A>G r.(?) p.(Lys667Arg)
+/. - c.2000A>G r.(?) p.(Lys667Arg)
-/. - c.2019-13G>A r.(=) p.(=)
+/. - c.2034T>G r.(?) p.(Tyr678Ter)
+/. - c.2034T>G r.(?) p.(Tyr678*)
?/. - c.2068C>T r.(?) p.(Arg690Cys)
-?/. - c.2076C>T r.(?) p.(Ser692=)
+/. - c.2085_2086insG r.(?) p.(Lys696GlufsTer11)
+/. - c.2147+1G>A r.spl? p.?
-?/. - c.2147+10A>C r.(=) p.(=)
+?/. - c.2148-17G>A r.(=) p.(=)
+?/. - c.2174_2176del r.(?) p.(Glu725del)
-?/. - c.2262G>A r.(?) p.(Glu754=)
-/. - c.2378G>T r.(?) p.(Ser793Ile)
-?/. - c.2378G>T r.(?) p.(Ser793Ile)
?/. - c.2491G>A r.(?) p.(Ala831Thr)
?/. - c.2518G>A r.(?) p.(Glu840Lys)
-/. - c.2740C>G r.(?) p.(Leu914Val)
-/. - c.2740C>G r.(?) p.(Leu914Val)
-?/. - c.2804A>G r.(?) p.(Gln935Arg)
?/. - c.2828A>G r.(?) p.(Glu943Gly)
-?/. - c.2835C>G r.(?) p.(Val945=)
-?/. - c.2878T>C r.(?) p.(Trp960Arg)
?/. - c.2878T>C r.(?) p.(Trp960Arg)
+/. - c.2959C>T r.(?) p.(Arg987*)
?/. - c.2984C>T r.(?) p.(Ala995Val)
+?/. - c.3016del r.(?) p.(Thr1006LeufsTer15)
-?/. - c.3085A>G r.(?) p.(Met1029Val)
?/. - c.3149T>C r.(?) p.(Leu1050Pro)
?/. - c.3247T>G r.(?) p.(Ser1083Ala)
?/. - c.3313C>G r.(?) p.(Leu1105Val)
-?/. - c.3313C>G r.(?) p.(Leu1105Val)
-/. - c.3317T>C r.(?) p.(Val1106Ala)
-?/. - c.3355G>A r.(?) p.(Ala1119Thr)
-?/. - c.3363C>G r.(?) p.(Leu1121=)
-?/. - c.3422A>G r.(?) p.(His1141Arg)
-/. - c.3466+8G>C r.(=) p.(=)
-/. - c.3466+8G>C r.(=) p.(=)
?/. - c.3537G>C r.(?) p.(Lys1179Asn)
?/. 23 c.3676_3678del r.(?) p.(Asn1226del)
+/. - c.3712C>G r.(?) p.(Leu1238Val)
-?/. - c.3729A>G r.(?) p.(Pro1243=)
-?/. - c.3732-3del r.spl? p.?
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