Transcript #00004961 (NM_016343.3, CENPF gene)

Transcript name centromere protein F, 350/400kDa (mitosin)
Gene name CENPF (centromere protein F, 350/400kDa)
Chromosome 1
Transcript - NCBI ID NM_016343.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_057427.3
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. 3 c.171_199del r.(?) p.(Asn57Lysfs*11)
-?/. - c.330A>G r.(?) p.(Gln110=)
-?/. - c.426C>T r.(?) p.(=)
+/. 5i c.574-2A>C r.spl? p.?
?/. - c.635C>A r.(?) p.(Ala212Asp)
?/. - c.767G>A r.(?) p.(Arg256Gln)
-?/. - c.866-4C>T r.spl? p.?
?/. - c.965T>C r.(?) p.(Leu322Pro)
?/. - c.965T>C r.(?) p.(Leu322Pro)
?/. - c.1070A>G r.(?) p.(Tyr357Cys)
?/. - c.1259G>T r.(?) p.(Arg420Ile)
-?/. - c.1451T>C r.(?) p.(Met484Thr)
?/. - c.1457A>G r.(?) p.(Lys486Arg)
+/. 12 c.1744G>T r.(?) p.(Glu582*)
+/. 12 c.1744G>T r.(?) p.(Glu582*)
+/. 12 c.1744G>T r.(?) p.(Glu582*)
+/. - c.1744G>T r.(?) p.(Glu582*)
+/. - c.1774_1777del r.(?) p.(Glu592Lysfs*7)
-?/. - c.2053G>A r.(?) p.(Val685Met)
-?/. - c.2111A>G r.(?) p.(Gln704Arg)
?/. - c.2251C>T r.(?) p.(Arg751Trp)
+?/. 12 c.2734G>T r.(?) p.(Glu912*)
-?/. - c.2951C>T r.(?) p.(Ala984Val)
-?/. - c.3013G>C r.(?) p.(Asp1005His)
?/. - c.3143A>G r.(?) p.(Glu1048Gly)
+?/. - c.3296del r.(?) p.(Leu1099Argfs*3)
-/. - c.3307T>C r.(?) p.(Leu1103=)
-?/. - c.3369C>T r.(?) p.(Ser1123=)
+/. - c.3577C>T r.(?) p.(Gln1193Ter)
-?/. - c.3617A>G r.(?) p.(Tyr1206Cys)
-/. - c.3623C>T r.(?) p.(Ala1208Val)
-/. - c.3623C>T r.(?) p.(Ala1208Val)
+/. - c.3774del r.(?) p.(Ser1259Valfs*8)
-?/. - c.3811A>G r.(?) p.(Lys1271Glu)
?/. - c.3811A>G r.(?) p.(Lys1271Glu)
?/. - c.3928C>G r.(?) p.(Leu1310Val)
-?/. - c.3974G>A r.(?) p.(Arg1325Lys)
-?/. - c.4182A>G r.(?) p.(Thr1394=)
-?/. - c.4182A>G r.(?) p.(Thr1394=)
?/. - c.4348T>A r.(?) p.(Ser1450Thr)
+?/. 12 c.4582T>C r.(?) p.(Cys1528Arg)
-?/. - c.4582T>C r.(?) p.(Cys1528Arg)
-?/. - c.4690G>A r.(?) p.(Glu1564Lys)
?/. - c.4719A>C r.(?) p.(Gln1573His)
+/. - c.4999C>T r.(?) p.(Arg1667Ter)
-?/. - c.5378G>A r.(?) p.(Arg1793His)
+?/. 13 c.5378G>A r.(?) p.(Arg1793His)
?/. - c.5520dup r.(?) p.(Asp1841Argfs*4)
?/. - c.5704A>C r.(?) p.(Asn1902His)
?/. - c.5814C>A r.(?) p.(Asp1938Glu)
?/. - c.5814C>A r.(?) p.(Asp1938Glu)
?/. - c.5814C>A r.(?) p.(Asp1938Glu)
?/. - c.5999A>G r.(?) p.(His2000Arg)
?/. - c.6391G>A r.(?) p.(Asp2131Asn)
?/. - c.6440G>A r.(?) p.(Arg2147Gln)
?/. - c.6532G>A r.(?) p.(Glu2178Lys)
?/. - c.6926G>A r.(?) p.(Arg2309His)
+?/. 13 c.6926G>A r.(?) p.(Arg2309His)
-?/. - c.6926G>A r.(?) p.(Arg2309His)
-?/. - c.6969A>G r.(?) p.(Gln2323=)
-?/. - c.7217A>G r.(?) p.(Glu2406Gly)
?/. - c.7314_7316dup r.(?) p.(Ala2439dup)
?/. - c.7326G>A r.(?) p.(Met2442Ile)
-?/. - c.7506A>G r.(?) p.(Ser2502=)
?/. - c.7524A>G r.(?) p.(Gln2508=)
+?/. 14 c.7904T>C r.(?) p.(Leu2635Pro)
?/. - c.8083G>A r.(?) p.(Glu2695Lys)
?/. - c.8322+1G>T r.spl? p.?
?/. - c.8322+1G>T r.spl? p.?
?/. - c.8391G>C r.(?) p.(Leu2797Phe)
+/. 18 c.8692C>T r.(?) p.(Arg2898*)
-?/. - c.8736A>C r.(?) p.(Pro2912=)
-?/. - c.8736A>C r.(?) p.(Pro2912=)
-?/. - c.8802A>G r.(?) p.(=)
-?/. - c.8963-9dup r.(=) p.(=)
?/. - c.8978C>T r.(?) p.(Pro2993Leu)
-/. - c.9081C>T r.(?) p.(Leu3027=)
?/. - c.9187C>T r.(?) p.(Arg3063*)
+/. 20 c.9280C>T r.(?) p.(Arg3094*)
+/. - c.9280C>T r.(?) p.(Arg3094*)
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