Transcript #00007719 (NM_014967.4, FAN1 gene)

Transcript name transcript variant 1
Gene name FAN1 (FANCD2/FANCI-associated nuclease 1)
Chromosome 15
Transcript - NCBI ID NM_014967.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_055782.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

98 entries on 1 page. Showing entries 1 - 98.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-812163_*1688114del r.? p.?
./. - c.-531222_*1688114del r.? p.?
./. - c.-282801_*1480224del r.? p.?
-?/. - c.5T>C r.(?) p.(Met2Thr)
-?/. - c.107A>G r.(?) p.(Asn36Ser)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.149T>G r.(?) p.(Met50Arg)
?/. - c.150G>T r.(?) p.(Met50Ile)
-?/. - c.326T>C r.(?) p.(Leu109Ser)
-?/. - c.375C>T r.(?) p.(Ile125=)
?/. - c.400G>A r.(?) p.(Val134Met)
-?/. - c.434G>A r.(?) p.(Arg145His)
-?/. - c.434G>A r.(?) p.(Arg145His)
?/. - c.496G>C r.(?) p.(Ala166Pro)
?/. - c.541C>A r.(?) p.(Pro181Thr)
-?/. - c.602A>G r.(?) p.(Asp201Gly)
-/. - c.698G>A r.(?) p.(Gly233Glu)
-?/. - c.718G>A r.(?) p.(Glu240Lys)
-?/. - c.718G>A r.(?) p.(Glu240Lys)
-?/. - c.783G>A r.(?) p.(=)
+?/. - c.840del r.(?) p.(Asp281ThrfsTer4)
+?/. - c.844dup r.(?) p.(Ser282LysfsTer13)
-?/. - c.907G>C r.(?) p.(Glu303Gln)
?/. - c.922_923del r.(?) p.(Val308Cysfs*5)
+?/. - c.922_923del r.(?) p.(Val308Cysfs*5)
+?/. - c.929C>G r.(?) p.(Ser310*)
+/. - c.1075C>T r.(?) p.(Gln359*)
-?/. - c.1087T>C r.(?) p.(Cys363Arg)
-/. - c.1110C>T r.(?) p.(Thr370=)
?/. - c.1129C>T r.(?) p.(Arg377Trp)
-?/. - c.1129C>T r.(?) p.(Arg377Trp)
-/. - c.1177A>G r.(?) p.(Met393Val)
-/. - c.1177A>G r.(?) p.(Met393Val)
?/. - c.1184T>C r.(?) p.(Leu395Pro)
-?/. - c.1194G>A r.(?) p.(Glu398=)
-?/. - c.1194G>A r.(?) p.(Glu398=)
-?/. - c.1235-27dup r.(=) p.(=)
-?/. - c.1235-11C>T r.(=) p.(=)
-/. - c.1310A>G r.(?) p.(Glu437Gly)
-?/. - c.1520G>A r.(?) p.(Arg507His)
+/. - c.1571del r.(?) p.(Leu524*)
-?/. - c.1578-14T>G r.(=) p.(=)
?/. - c.1641_1644del r.(?) p.(Ile548CysfsTer6)
-?/. - c.1851C>T r.(?) p.(Ser617=)
-/. - c.1851C>T r.(?) p.(Ser617=)
?/. - c.1872G>C r.(?) p.(Trp624Cys)
?/. - c.1930C>T r.(?) p.(His644Tyr)
-?/. - c.1944-4T>C r.spl? p.?
-?/. - c.1944-4T>C r.spl? p.?
-/. - c.1944-4T>C r.spl? p.?
-?/. - c.1961C>T r.(?) p.(Pro654Leu)
?/. - c.1972C>T r.(?) p.(Arg658Trp)
?/. - c.1972C>T r.(?) p.(Arg658Trp)
-?/. - c.2052+16C>G r.(=) p.(=)
-?/. - c.2053-13_2053-11del r.(=) p.(=)
-/. - c.2053-13_2053-11del r.(=) p.(=)
-?/. - c.2058C>T r.(?) p.(Ala686=)
+/. - c.2128C>T r.(?) p.(Arg710*)
?/. - c.2155T>G r.(?) p.(Leu719Val)
?/. - c.2206C>G r.(?) p.(Pro736Ala)
-/. - c.2271G>C r.(?) p.(Pro757=)
+/. - c.2337+1G>A r.spl? p.?
?/. - c.2381A>G r.(?) p.(Lys794Arg)
?/. - c.2381A>G r.(?) p.(Lys794Arg)
-?/. - c.2403C>T r.(?) p.(Ala801=)
?/. - c.2404G>A r.(?) p.(Gly802Arg)
-/. - c.2413G>A r.(?) p.(Ala805Thr)
-?/. - c.2413G>A r.(?) p.(Ala805Thr)
-?/. - c.2418C>T r.(?) p.(Asp806=)
-?/. - c.2418C>T r.(?) p.(Asp806=)
-?/. - c.2418C>T r.(?) p.(Asp806=)
-?/. - c.2418C>T r.(?) p.(Asp806=)
-?/. - c.2427G>A r.(?) p.(Thr809=)
-?/. - c.2471G>A r.(?) p.(Arg824His)
-/. - c.2489-18_2489-13dup r.(=) p.(=)
-?/. - c.2583C>T r.(?) p.(Asn861=)
-?/. - c.2583C>T r.(?) p.(Asn861=)
+?/. - c.2592+2T>C r.spl? p.?
+/. - c.2616del r.(?) p.(Asp873ThrfsTer17)
?/. - c.2671C>G r.(?) p.(His891Asp)
-/. - c.2680C>T r.(?) p.(Pro894Ser)
-/. - c.2680C>T r.(?) p.(Pro894Ser)
-/. - c.2680C>T r.(?) p.(Pro894Ser)
-?/. - c.2696G>A r.(?) p.(Arg899Gln)
-?/. - c.2862T>C r.(?) p.(Cys954=)
./. - c.*3+1G>A r.spl? p.?
-?/. - c.*3+1G>A r.spl? p.?
-?/. - c.*3+15A>G r.(=) p.(=)
-?/. - c.*323T>C r.(=) p.(=)
-?/. - c.*1486G>C r.(=) p.(=)
-?/. - c.*5680G>A r.(=) p.(=)
-?/. - c.*49902G>A r.(=) p.(=)
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