Transcript #00000415 (NM_005334.2, HCFC1 gene)

Transcript name host cell factor C1 (VP16-accessory protein)
Gene name HCFC1 (host cell factor C1 (VP16-accessory protein))
Chromosome X
Transcript - NCBI ID NM_005334.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_005325.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-373615_*503992dup r.0? p.0?
-?/. - c.126G>A r.(?) p.(Lys42=)
+/. - c.218C>T r.(?) p.(Ala73Val)
-?/. - c.297G>C r.(?) p.(Gly99=)
-?/. - c.366A>G r.(?) p.(Arg122=)
?/. - c.367C>T r.(?) p.(Leu123Phe)
?/. - c.420C>G r.(?) p.(His140Gln)
?/. - c.439A>G r.(?) p.(Asn147Asp)
-?/. - c.474T>C r.(?) p.(Asp158=)
-?/. - c.503+14C>G r.(=) p.(=)
-?/. - c.648C>G r.(?) p.(Ser216=)
./. - c.674G>A r.(?) p.(Ser225Asn)
-/. - c.713-13C>T r.(=) p.(=)
-?/. - c.713-3C>T r.spl? p.?
-?/. - c.713-3C>T r.spl? p.?
-?/. - c.753G>T r.(?) p.(Ala251=)
-?/. - c.1113A>G r.(?) p.(Gln371=)
?/. - c.1120C>T r.(?) p.(Arg374Cys)
-?/. - c.1162G>A r.(?) p.(Ala388Thr)
-?/. - c.1200T>C r.(?) p.(Tyr400=)
-?/. - c.1233C>T r.(?) p.(Ser411=)
-?/. - c.1407C>T r.(?) p.(Gly469=)
?/. - c.1472G>T r.(?) p.(Gly491Val)
?/. - c.1616G>A r.(?) p.(Ser539Asn)
?/. - c.1885A>G r.(?) p.(Thr629Ala)
-?/. - c.1980C>T r.(?) p.(Thr660=)
?/. - c.2033C>T r.(?) p.(Ser678Phe)
?/. - c.2036A>G r.(?) p.(Asn679Ser)
-?/. - c.2109G>A r.(?) p.(Thr703=)
-/. - c.2283C>G r.(?) p.(Thr761=)
-?/. - c.2289C>T r.(?) p.(Pro763=)
-?/. - c.2289C>T r.(?) p.(Pro763=)
?/. - c.2299A>G r.(?) p.(Thr767Ala)
-?/. - c.2325G>A r.(?) p.(Ser775=)
-?/. - c.2463T>A r.(?) p.(Ile821=)
./. - c.2492C>T r.(?) p.(Thr831Ile)
-?/. - c.2589C>T r.(?) p.(Ser863=)
-?/. - c.2590G>A r.(?) p.(Ala864Thr)
-?/. - c.2590G>A r.(?) p.(Ala864Thr)
-/. - c.2590G>A r.(?) p.(Ala864Thr)
-?/. - c.2604C>T r.(?) p.(Ala868=)
-?/. - c.2626G>A r.(?) p.(Gly876Ser)
?/. - c.2626G>A r.(?) p.(Gly876Ser)
-?/. - c.2667C>T r.(?) p.(Thr889=)
?/. - c.2723C>T r.(?) p.(Thr908Met)
+?/. - c.2777C>T r.(?) p.(Pro926Leu)
-?/. - c.2787C>T r.(?) p.(Ile929=)
-?/. - c.2787C>T r.(?) p.(Ile929=)
?/. - c.2797G>A r.(?) p.(Ala933Thr)
-?/. - c.2817A>T r.(?) p.(Thr939=)
-/. - c.2841A>G r.(?) p.(Pro947=)
?/. - c.2860G>A r.(?) p.(Val954Met)
-?/. - c.2872A>G r.(?) p.(Thr958Ala)
-/. - c.2872A>G r.(?) p.(Thr958Ala)
-/. - c.2872A>G r.(?) p.(Thr958Ala)
-?/. - c.2974G>A r.(?) p.(Ala992Thr)
-?/. - c.3018T>C r.(?) p.(Pro1006=)
-?/. - c.3211G>A r.(?) p.(Val1071Met)
-?/. - c.3270C>T r.(?) p.(Thr1090=)
?/. - c.3270_3356del r.(?) p.(Thr1095_Ala1123del)
-?/. - c.3290A>C r.(?) p.(Asn1097Thr)
-?/. - c.3290A>C r.(?) p.(Asn1097Thr)
-?/. - c.3290A>C r.(?) p.(Asn1097Thr)
?/. - c.3292A>G r.(?) p.(Met1098Val)
?/. - c.3338A>C r.(?) p.(Glu1113Ala)
-?/. - c.3353A>G r.(?) p.(Asn1118Ser)
-?/. - c.3393C>T r.(?) p.(His1131=)
-/. - c.3490T>C r.(?) p.(Ser1164Pro)
-/. - c.3492C>T r.(?) p.(Ser1164=)
-?/. - c.3492C>T r.(?) p.(Ser1164=)
-?/. - c.3555C>T r.(?) p.(Ala1185=)
-?/. - c.3615C>T r.(?) p.(Ser1205=)
?/. - c.3644G>A r.(?) p.(Ser1215Asn)
-?/. - c.3690G>A r.(?) p.(Ala1230=)
-?/. - c.3757C>T r.(?) p.(Arg1253Cys)
-?/. - c.3775G>A r.(?) p.(Glu1259Lys)
?/. - c.3892G>A r.(?) p.(Glu1298Lys)
?/. - c.3894G>A r.(=) p.(=)
-?/. - c.3903C>T r.(?) p.(Thr1301=)
-?/. - c.3907A>C r.(?) p.(Asn1303His)
-?/. - c.3930A>T r.(?) p.(Ala1310=)
-?/. - c.3987C>T r.(?) p.(Thr1329=)
?/. - c.4006G>A r.(?) p.(Ala1336Thr)
-?/. - c.4025C>T r.(?) p.(Thr1342Met)
-?/. - c.4025C>T r.(?) p.(Thr1342Met)
?/. - c.4028G>A r.(?) p.(Gly1343Asp)
-/. - c.4068C>T r.(?) p.(Pro1356=)
-/. - c.4068C>T r.(?) p.(Pro1356=)
-?/. - c.4077A>G r.(?) p.(Thr1359=)
?/. - c.4109C>T r.(?) p.(Ser1370Leu)
-?/. - c.4125C>T r.(?) p.(Ala1375=)
-?/. - c.4135G>A r.(?) p.(Asp1379Asn)
-?/. - c.4158C>G r.(?) p.(Thr1386=)
-?/. - c.4158C>T r.(?) p.(Thr1386=)
-?/. - c.4159G>A r.(?) p.(Val1387Met)
-?/. - c.4159G>A r.(?) p.(Val1387Met)
-/. - c.4185G>A r.(?) p.(Ala1395=)
-?/. - c.4194C>T r.(?) p.(Ser1398=)
-?/. - c.4194C>T r.(?) p.(Ser1398=)
?/. - c.4195G>A r.(?) p.(Val1399Ile)
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