Transcript #00023965 (NM_001113378.1, FANCI gene)

Transcript name transcript variant 1
Gene name FANCI (Fanconi anemia, complementation group I)
Chromosome 15
Transcript - NCBI ID NM_001113378.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001106849.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2014-10-05 12:34:28 +02:00 (CEST)
Date last edited N/A


Variants

484 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     
+/. 2 c.2T>C r.(?) p.0? FA
+/. 2 c.2T>C r.(?) p.0? FA
+/. 2 c.2T>C r.(?) p.0? FA
+/. 2 c.2T>C r.(?) p.0? FA
?/. - c.96_98del r.(?) p.(Leu33del) -
?/. - c.121A>G r.(?) p.(Lys41Glu) -
+/+ 3i c.157+78G>A r.(?) p.(Gly53Valfs*2) FA
+?/. - c.286G>A r.(?) p.(Glu96Lys) -
-/. - c.286G>A r.(?) p.(Glu96Lys) -
-?/. - c.446-6T>G r.(=) p.(=) -
-?/. - c.543C>T r.(?) p.(Phe181=) -
+?/. - c.545+1G>T r.spl? p.? -
-?/. - c.753C>T r.(?) p.(Asp251=) -
-?/. - c.753C>T r.(?) p.(Asp251=) -
-?/. - c.753C>T r.(?) p.(Asp251=) -
+/. 9i c.756-25_756-19delCATAACT r.756_882del p.fs*) FA
?/. - c.756-9A>G r.(=) p.(=) -
-?/. - c.814A>T r.(?) p.(Ile272Phe) -
-?/. - c.824T>C r.(?) p.(Ile275Thr) -
?/. - c.824T>C r.(?) p.(Ile275Thr) -
+/. 10 c.866T>C r.(?) p.(Leu289Prp) FA
-/. - c.868G>A r.(?) p.(Val290Met) -
+/. - c.967C>T r.(?) p.(Gln323Ter) -
?/. - c.975G>C r.(?) p.(Gln325His) -
-?/. - c.975+10dup r.(=) p.(=) -
-?/. - c.975+10dup r.(=) p.(=) -
-/. - c.1114G>A r.(?) p.(Val372Ile) -
?/. 12 c.1264G>A r.(?) p.(Gly422Arg) FA
+?/. - c.1264G>A r.(?) p.(Gly422Arg) -
+/. 13 c.1264G>C r.(?) p.(Gly422Arg) FA
?/. - c.1274T>C r.(?) p.(Ile425Thr) -
?/. - c.1316A>C r.(?) p.(Glu439Ala) -
-?/. - c.1329G>A r.(?) p.(Gln443=) -
-?/. - c.1382-11_1382-10del r.(=) p.(=) -
-?/. - c.1399G>A r.(?) p.(Val467Ile) -
-?/. - c.1441G>A r.(?) p.(Val481Ile) -
+/+ 15 c.1461T>A r.(?) p.(Tyr487*) FA
-?/. - c.1491A>G r.(?) p.(Gln497=) -
-?/. - c.1491A>G r.(?) p.(Gln497=) -
?/. - c.1517T>G r.(?) p.(Leu506Arg) -
?/. - c.1573A>G r.(?) p.(Met525Val) -
-?/. - c.1573A>G r.(?) p.(Met525Val) -
?/. - c.1573A>G r.(?) p.(Met525Val) -
-?/. - c.1573A>G r.(?) p.(Met525Val) -
?/. 16i c.1583+142C>T r.(?) p.(=) FA
-/. - c.1584-15C>G r.(=) p.(=) -
+/. - c.1597C>T r.(?) p.(Arg533*) -
+/. - c.1635del r.(?) p.(Asn546Thrfs*5) -
-/. - c.1698+15C>T r.(=) p.(=) -
-?/. - c.1698+16G>A r.(=) p.(=) -
-?/. - c.1734C>T r.(?) p.(Val578=) -
./. - c.1804C>T r.(?) p.(Arg602*) -
?/. - c.1810A>G r.(?) p.(Met604Val) -
-/. - c.1813C>T r.(?) p.(Leu605Phe) -
-?/. - c.1813C>T r.(?) p.(Leu605Phe) -
-?/. - c.1813C>T r.(?) p.(Leu605Phe) -
-?/. - c.1813C>T r.(?) p.(Leu605Phe) -
-?/. - c.1821+8C>T r.(=) p.(=) -
+/. - c.1822-1G>A r.spl p.? -
?/. - c.1837C>T r.(?) p.(Leu613Phe) -
+/. 19 c.1840C>T r.(?) p.(Arg614*) FA
-?/. - c.1890+5A>C r.spl? p.? -
-?/. - c.1893A>C r.(?) p.(Leu631Phe) -
?/. - c.1904A>G r.(?) p.(Tyr635Cys) -
?/. - c.2017C>T r.(?) p.(His673Tyr) -
-?/. - c.2098G>A r.(?) p.(Glu700Lys) -
+/. 22 c.2248T>C r.(?) p.(Cys750Gly) FA
?/. - c.2291+5G>A r.spl? p.? -
-?/. - c.2291+20C>G r.(=) p.(=) -
?/. - c.2341C>A r.(?) p.(Leu781Ile) -
-/. - c.2367G>T r.(?) p.(Ala789=) -
?/. - c.2419A>G r.(?) p.(Met807Val) -
-?/. - c.2487T>G r.(?) p.(Leu829=) -
-?/. - c.2487T>G r.(?) p.(Leu829=) -
-?/. - c.2487T>G r.(?) p.(Leu829=) -
+/. 24 c.2509G>T r.(?) p.(Glu837*) FA
+/. 24 c.2509G>T r.(?) p.(Glu837*) FA
+/. 24 c.2509G>T r.(?) p.(Glu837*) FA
-/. - c.2547= r.(=) p.(Lys849=) -
+/. 24 c.2572C>T r.(?) p.(His858Tyr) FA
+/. 24 c.2572C>T r.(?) p.(His858_Arg879del) FA
-?/. - c.2604A>C r.(?) p.(Glu868Asp) -
-?/. - c.2646A>G r.(?) p.(=) -
?/. - c.2660C>T r.(?) p.(Ser887Leu) -
-?/. - c.2803+16T>G r.(=) p.(=) -
+?/. - c.2833C>T r.(?) p.(Glu945Ter) -
?/. - c.2855C>T r.(?) p.(Thr952Ile) -
-?/. - c.2883A>G r.(?) p.(=) -
-?/. - c.2997C>T r.(?) p.(Ser999=) -
-?/. - c.2997C>T r.(?) p.(Ser999=) -
+/. 27i c.3006+3A>G r.(?) p.(Arg964_Gln1002del) FA
-/. - c.3006+15A>C r.(=) p.(=) -
+/. - c.3058+1G>A r.spl? p.? -
+/. 28i c.3058+1G>A r.3007_3058del p.fs* FA
+/+ 28i c.3058+4A>G r.(spl?) p.? FA
-?/. - c.3114G>A r.(?) p.(Ser1038=) -
+/. - c.3146T>A r.(?) p.(Leu1049*) -
-?/. - c.3206C>G r.(?) p.(Thr1069Arg) -
-?/. - c.3236C>T r.(?) p.(Thr1079Met) -
-?/. - c.3273G>A r.(?) p.(Gln1091=) -
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