Transcript #00005040 (NM_000204.3, CFI gene)

Transcript name complement factor I
Gene name CFI (complement factor I)
Chromosome 4
Transcript - NCBI ID NM_000204.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000195.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-13G>A r.(=) p.(=)
-/. - c.-13G>A r.(?) p.(=)
-/. - c.-13G>A r.(?) p.(=)
-?/. - c.-13G>C r.(?) p.(=)
+?/. - c.1A>G r.(?) p.(Met1?)
-/. - c.57+54A>G r.(=) p.(=)
?/. - c.148C>G r.(?) p.(Pro50Ala)
-?/. - c.192G>A r.(?) p.(Pro64=)
-/. - c.192G>A r.(?) p.(Pro64=)
?/. - c.196C>A r.(?) p.(Gln66Lys)
+?/. - c.257G>A r.(?) p.(Cys86Tyr)
-?/. - c.315A>T r.(?) p.(Thr105=)
-/. - c.315A>T r.(?) p.(Thr105=)
+?/. - c.328+1G>A r.spl? p.?
+/. - c.329-1G>A r.spl? p.?
+?/. - c.355G>A r.(?) p.(Gly119Arg)
+?/. - c.355G>A r.(?) p.(Gly119Arg)
?/. - c.355G>A r.(?) p.(Gly119Arg)
+?/. - c.355G>A r.(?) p.(Gly119Arg)
+?/. - c.453del r.(?) p.(Asn151Lysfs*26)
+?/. - c.453del r.(?) p.(Asn151Lysfs*26)
+?/. - c.454G>A r.(?) p.(Val152Met)
-?/. - c.482+6C>A r.(=) p.(=)
-?/. - c.482+6C>A r.(=) p.(=)
-/. - c.482+6C>T r.(=) p.(=)
-/. - c.482+6C>T r.(=) p.(=)
-?/. - c.482+7G>A r.(=) p.(=)
-?/. - c.482+14T>A r.(=) p.(=)
-/. - c.482+14T>A r.(=) p.(=)
-?/. - c.548A>G r.(?) p.(His183Arg)
+?/. - c.563G>C r.(?) p.(Gly188Ala)
?/. - c.586T>C r.(?) p.(Cys196Arg)
-?/. - c.608C>T r.(?) p.(Thr203Ile)
-?/. - c.645T>C r.(?) p.(=)
+?/. - c.719C>G r.(?) p.(Ala240Gly)
-?/. - c.747C>T r.(?) p.(Asp249=)
+?/. - c.772G>A r.(?) p.(Ala258Thr)
?/. - c.781G>A r.(?) p.(Gly261Ser)
-?/. - c.781G>A r.(?) p.(Gly261Ser)
-/. - c.804G>A r.(?) p.(Ser268=)
-/. - c.804G>A r.(?) p.(Ser268=)
-/. - c.804G>A r.(?) p.(Ser268=)
+?/. - c.816_817del r.(?) p.(Pro273LysfsTer8)
+/. - c.816_817del r.(?) p.(Pro273LysfsTer8)
-/. - c.883+290A>C r.(=) p.(=)
-/. - c.883+330_883+333dup r.(=) p.(=)
-/. - c.884-7T>C r.(=) p.(=)
-/. - c.898= r.(=) p.(Ala300=)
-/. - c.898= r.(=) p.(Ala300=)
-?/. - c.905-3T>C r.spl? p.?
-?/. - c.905-3T>C r.spl? p.?
-?/. - c.916A>G r.(?) p.(Ile306Val)
-?/. - c.940+6C>A r.(=) p.(=)
-/. - c.941-49C>G r.(=) p.(=)
?/. - c.949C>T r.(?) p.(Arg317Trp)
?/. - c.949C>T r.(?) p.(Arg317Trp)
+?/. - c.1006C>T r.(?) p.(Arg336*)
+?/. - c.1019T>C r.(?) p.(Ile340Thr)
+/. - c.1019T>C r.(?) p.(Ile340Thr)
-?/. - c.1044+8C>T r.(=) p.(=)
-?/. - c.1044+9G>A r.(=) p.(=)
-?/. - c.1044+17A>G r.(=) p.(=)
-/. - c.1044+39A>G r.(=) p.(=)
?/. - c.1195T>C r.(?) p.(Trp399Arg)
-?/. - c.1206C>T r.(?) p.(Pro402=)
-?/. - c.1206C>T r.(?) p.(Pro402=)
-?/. - c.1217G>A r.(?) p.(Arg406His)
-?/. - c.1217G>A r.(?) p.(Arg406His)
-?/. - c.1224A>G r.(?) p.(=)
+/. - c.1234G>A r.(?) p.(Val412Met)
+/. - c.1234G>A r.(?) p.(Val412Met)
+?/. - c.1246A>C r.(?) p.(Ile416Leu)
?/. - c.1268C>A r.(?) p.(Ala423Glu)
-?/. - c.1322A>G r.(?) p.(Lys441Arg)
-?/. - c.1322A>G r.(?) p.(Lys441Arg)
-?/. - c.1322A>G r.(?) p.(Lys441Arg)
-/. - c.1322A>G r.(?) p.(Lys441Arg)
?/. - c.1333G>A r.(?) p.(Glu445Lys)
-?/. - c.1342C>T r.(?) p.(Arg448Cys)
-?/. - c.1347C>T r.(?) p.(Ser449=)
?/. - c.1354G>T r.(?) p.(Ala452Ser)
+/. - c.1376A>C r.(?) p.(Tyr459Ser)
+?/. 11 c.1399T>C r.(?) p.(Cys467Arg)
-?/. - c.1434C>T r.(?) p.(Asn478=)
-?/. - c.1443C>T r.(?) p.(Val481=)
-?/. - c.1443C>T r.(?) p.(Val481=)
-?/. - c.1443C>T r.(?) p.(Val481=)
-?/. - c.1534+5G>T r.spl? p.?
-?/. - c.1534+5G>T r.spl? p.?
-?/. - c.1581C>T r.(?) p.(Gly527=)
+?/. 13 c.1583C>T r.(?) p.(Pro528Leu)
?/. - c.1623G>T r.(?) p.(Trp541Cys)
?/. - c.1642G>C r.(?) p.(Glu548Gln)
-?/. - c.1642G>C r.(?) p.(Glu548Gln)
?/. - c.1642G>C r.(?) p.(Glu548Gln)
?/. - c.1642G>C r.(?) p.(Glu548Gln)
+/. - c.1650_1651del r.(?) p.(Cys550TrpfsTer17)
-?/. - c.1657C>T r.(?) p.(Pro553Ser)
-?/. - c.1657C>T r.(?) p.(Pro553Ser)
?/. - c.1657C>T r.(?) p.(Pro553Ser)
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