Transcript #00011907 (NM_003906.3, MCM3AP gene)

Transcript name minichromosome maintenance complex component 3 associated protein
Gene name MCM3AP (minichromosome maintenance complex component 3 associated protein)
Chromosome 21
Transcript - NCBI ID NM_003906.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003897.2
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

73 entries on 1 page. Showing entries 1 - 73.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-37A>G r.(?) p.(=)
-?/. - c.132C>T r.(?) p.(Thr44=)
-?/. - c.137C>T r.(?) p.(Ser46Phe)
?/. - c.200C>T r.(?) p.(Ser67Phe)
-?/. - c.248C>A r.(?) p.(Pro83His)
-/. - c.305C>T r.(?) p.(Ser102Leu)
-?/. - c.346A>G r.(?) p.(Thr116Ala)
-?/. - c.506G>A r.(?) p.(Ser169Asn)
-/. - c.948C>G r.(?) p.(Ser316=)
?/. - c.977C>T r.(?) p.(Pro326Leu)
-?/. - c.998G>T r.(?) p.(Arg333Leu)
+?/? 1 c.1110_1119del r.(?) p.(Glu371Thrfs*20)
?/. - c.1186G>A r.(?) p.(Glu396Lys)
-?/. - c.1238C>T r.(?) p.(Pro413Leu)
-?/. - c.1267A>G r.(?) p.(Thr423Ala)
-/. - c.1323C>T r.(?) p.(Asn441=)
?/. 2 c.1327C>T r.(?) p.(Pro443Ser)
-?/. - c.1523-20T>C r.(=) p.(=)
-?/. - c.1630G>A r.(?) p.(Ala544Thr)
+?/. - c.1933del r.(?) p.(Glu645Argfs*11)
?/. - c.2345G>A r.(?) p.(Cys782Tyr)
-/. - c.2409A>G r.(?) p.(Glu803=)
?/? 8 c.2411C>T r.(?) p.(Ala804Val)
?/. - c.2466-2A>G r.spl? p.?
+/. 9 c.2609T>C r.(?) p.(Leu870Ser)
+?/. 9 c.2615G>A r.(?) p.(Cys872Tyr)
+?/. - c.2633G>A r.(?) p.(Arg878His)
+/. 10 c.2633G>A r.(?) p.(Arg878His)
+?/. - c.2743G>A r.(?) p.(Glu915Lys)
+?/. - c.2743G>A r.(?) p.(Glu915Lys)
-/. - c.2833T>G r.(?) p.(Leu945Val)
+?/. - c.2861T>C r.(?) p.(Ile954Thr)
-/. - c.2931T>C r.(?) p.(His977=)
-/. - c.2931T>C r.(?) p.(His977=)
-?/. - c.3033C>T r.(?) p.(Gly1011=)
-?/. - c.3034G>A r.(?) p.(Gly1012Arg)
-?/. - c.3065C>T r.(?) p.(Pro1022Leu)
-/. - c.3152C>T r.(?) p.(Pro1051Leu)
-?/. - c.3152C>T r.(?) p.(Pro1051Leu)
-?/. - c.3169C>T r.(?) p.(Leu1057Phe)
-?/. - c.3336-7C>T r.(=) p.(=)
-?/. - c.3452G>A r.(?) p.(Arg1151Gln)
?/. - c.3476_3477del r.(?) p.(Gln1159ArgfsTer8)
?/. - c.3772C>T r.(?) p.(Arg1258Cys)
+?/. - c.3814G>A r.(?) p.(Val1272Met)
-/. - c.3924C>T r.(?) p.(Ser1308=)
?/. - c.3933-1G>T r.spl? p.?
-?/. - c.3940C>T r.(?) p.(Arg1314Trp)
+?/. - c.3949_3950insG r.(?) p.(Asn1317Argfs*19)
?/. - c.4290+3G>T r.spl? p.?
-/. - c.4347C>A r.(?) p.(Asp1449Glu)
?/. - c.4391T>C r.(?) p.(Met1464Thr)
-/. - c.5013G>A r.(?) p.(Pro1671=)
-?/. - c.5013G>A r.(?) p.(Pro1671=)
?/. - c.5042C>G r.(?) p.(Pro1681Arg)
-?/. - c.5049C>T r.(?) p.(Leu1683=)
?/. - c.5111C>G r.(?) p.(Pro1704Arg)
?/. - c.5197G>T r.(?) p.(Gly1733Cys)
-?/. - c.5205G>A r.(?) p.(Ser1735=)
+?/. - c.5278dup r.(?) p.(Arg1760Profs*11)
?/? 25 c.5300C>T r.(?) p.(Ala1767Val)
?/. - c.5383G>A r.(?) p.(Ala1795Thr)
-?/. - c.5426+6G>A r.(=) p.(=)
-/. - c.5426+6G>A r.(=) p.(=)
-/. - c.5491C>T r.(?) p.(Arg1831Cys)
+/. 26i c.5634-1G>T r.5634_5718del p.Phe1879Leufs*2
?/. - c.5785-2dup r.spl? p.?
-?/. - c.5823G>C r.(?) p.(=)
-?/. - c.5827G>C r.(?) p.(Gly1943Arg)
+/. - c.*6695A>G r.(=) p.(=)
?/. - c.*6695A>G r.(=) p.(=)
?/. - c.*6703G>A r.(=) p.(=)
?/. - c.*6764C>G r.(=) p.(=)
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