Transcript #00007724 (NM_021922.2, FANCE gene)

Transcript name Fanconi anemia, complementation group E
Gene name FANCE (Fanconi anemia, complementation group E)
Chromosome 6
Transcript - NCBI ID NM_021922.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_068741.1
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

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     
?/. - c.-105C>T r.(?) p.(=) -
?/. 1 c.9A>C r.(?) p.(Thr3=) FA
-?/. - c.52C>T r.(?) p.(Pro18Ser) -
-?/. - c.53C>T r.(?) p.(Pro18Leu) -
?/. - c.59C>T r.(?) p.(Ala20Val) -
-?/. - c.59C>T r.(?) p.(Ala20Val) -
+/. 1 c.91C>T r.(?) p.(Gln31*) FA
+/. 1 c.91C>T r.(?) p.(Gln31*) FA
+?/. - c.100C>T r.(?) p.(Gln34*) -
?/. - c.199C>A r.(?) p.(Leu67Met) -
?/. - c.229C>A r.(?) p.(Pro77Thr) -
+/. 1i c.248+1G>A r.spl p.? FA
+/. 1i c.248+1G>A r.spl p.? FA
+?/. In1 c.248+5G>A r.spl? p.? -
-?/. - c.248+7C>A r.(=) p.(=) -
?/. 1i c.248+58A>C r.(?) p.(=) FA
?/. 1i c.248+111C>T r.(?) p.(=) -
-/. - c.266G>T r.(?) p.(Arg89Leu) -
-?/. - c.313G>A r.(?) p.(Val105Ile) -
+/. 2 c.355C>T r.(?) p.(Gln119*) FA
+/. 2 c.355C>T r.(?) p.(Gln119*) FA
?/. 2 c.387A>C r.(?) p.(Pro129=) -
-/. - c.387A>C r.(?) p.(Pro129=) -
-?/. - c.400C>T r.(?) p.(Arg134Cys) -
+/. 2 c.421C>T r.(?) p.(Arg141*) FA
+/. 2 c.421C>T r.(?) p.(Arg141*) FA
+/. 2 c.436del r.(?) p.(Val146Trpfs*33) FA
+/. 2 c.436del r.(?) p.(Val146Trpfs*33) FA
-?/. - c.466C>T r.(?) p.(Leu156=) -
?/. 2 c.551C>A r.(?) p.(Pro184Gln) FA
+?/. - c.583C>T r.(?) p.(Gln195*) -
?/. 2 c.611C>T r.(?) p.(Ser204Leu) -
-?/. - c.611C>T r.(?) p.(Ser204Leu) -
-/. - c.611C>T r.(?) p.(Ser204Leu) -
-?/. - c.696G>A r.(?) p.(Glu232=) -
?/. 2i c.855+58A>G r.(?) p.(=) -
?/. 2i c.856-70G>A r.(?) p.(=) -
?/. 3i c.900+39A>G r.(?) p.(=) -
-?/. - c.901-5C>A r.spl? p.? -
?/. - c.926C>T r.(?) p.(Pro309Leu) -
-?/. - c.928C>G r.(?) p.(Pro310Ala) -
+/. 4 c.929dup r.(?) p.(Val311SerfsTer2) -
./. - c.929dup r.(?) p.(Val311Serfs*2) -
-?/. - c.951C>T r.(?) p.(His317=) -
?/. 4i c.970-84T>C r.(?) p.(=) -
?/. 5 c.1018G>C r.(?) p.(Gly340Arg) -
-?/. - c.1018G>C r.(?) p.(Gly340Arg) -
?/. - c.1018G>C r.(?) p.(Gly340Arg) -
+?/. 5 c.1041G>A r.(?) p.(Trp347*) -
?/. 5 c.1066A>G r.(?) p.(Ser356Gly) FA
?/. 5 c.1071C>T r.(?) p.(Leu357=) -
-?/. - c.1071C>T r.(?) p.(Leu357=) -
?/. 5 c.1094G>A r.(?) p.(Arg365Lys) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+?/. - c.1111C>T r.(?) p.(Arg371Trp) -
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
+/. 5 c.1111C>T r.(?) p.(Arg371Trp) FA
?/. - c.1113+6T>C r.(=) p.(=) -
?/. 5i c.1114-8G>A r.(?) p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
?/. 5i c.1114-8G>A r.spl? p.(Ile372Leufs*) FA
-?/. - c.1114-4G>A r.spl? p.? -
?/. 7i c.1316+19G>A r.(spl?) p.(=) -
?/. 7i c.1316+19G>A r.(spl?) p.(=) -
?/. - c.1402_1404del r.(?) p.(Lys468del) -
-?/. - c.1428C>T r.(?) p.(Leu476=) -
?/. 9 c.1463C>G r.(spl?) p.(Ala488Gly) -
?/. 9 c.1504G>A r.(spl?) p.(Ala502Thr) FA
-?/. - c.1510-11C>T r.(=) p.(=) -
+/. 9i c.1510-1G>A r.spl? p.? FA
+/. 9i c.1510-1G>A r.spl? p.? FA
+/. 9i c.1510-1G>A r.spl? p.? FA
+/. 9i c.1510-1G>A r.spl? p.? FA
?/. - c.1556A>C r.(?) p.(Asn519Thr) -
-?/. - c.1572G>A r.(?) p.(Arg524=) -
-?/. - c.1572G>A r.(?) p.(Arg524=) -
?/. - c.1588G>A r.(?) p.(Ala530Thr) -
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