Transcript #00009418 (NM_006734.3, HIVEP2 gene)

Transcript name human immunodeficiency virus type I enhancer binding protein 2
Gene name HIVEP2 (human immunodeficiency virus type I enhancer binding protein 2)
Chromosome 6
Transcript - NCBI ID NM_006734.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006725.3
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

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-527-1516G>A r.(=) p.(=)
-?/. - c.2T>C r.(?) p.?
?/. - c.105G>C r.(?) p.(Lys35Asn)
-?/. - c.166G>A r.(?) p.(Gly56Arg)
-?/. - c.166G>A r.(?) p.(Gly56Arg)
-?/. - c.194G>T r.(?) p.(Gly65Val)
-?/. - c.212C>T r.(?) p.(Ser71Phe)
-?/. - c.258G>A r.(?) p.(Pro86=)
-?/. - c.260A>T r.(?) p.(His87Leu)
-?/. - c.312A>G r.(?) p.(Ser104=)
-?/. - c.404C>G r.(?) p.(Ser135Cys)
?/. - c.406G>A r.(?) p.(Glu136Lys)
+/. - c.618dup r.(?) p.(His207Thrfs*38)
?/. - c.776A>G r.(?) p.(Asp259Gly)
?/. - c.967A>G r.(?) p.(Met323Val)
-?/. - c.1033A>G r.(?) p.(Ile345Val)
-?/. - c.1085C>T r.(?) p.(Ser362Leu)
-?/. - c.1170G>A r.(?) p.(Pro390=)
-?/. - c.1171C>T r.(?) p.(His391Tyr)
+?/. - c.1195G>C r.(?) p.(Gly399Arg)
+?/. - c.1213G>A r.(?) p.(Glu405Lys)
-?/. - c.1308T>C r.(?) p.(Asn436=)
-?/. - c.1340G>A r.(?) p.(Arg447His)
-?/. - c.1456G>A r.(?) p.(Asp486Asn)
-?/. - c.1603G>A r.(?) p.(Val535Ile)
?/. - c.1733A>T r.(?) p.(Tyr578Phe)
+?/. - c.1762C>T r.(1762C>T) p.(Arg588Cys)
?/. - c.2099A>T r.(?) p.(Glu700Val)
?/. - c.2156C>T r.(?) p.(Thr719Ile)
-?/. - c.2179G>A r.(?) p.(Asp727Asn)
-?/. - c.2306G>T r.(?) p.(Ser769Ile)
?/. - c.2447G>A r.(?) p.(Arg816Lys)
-?/. - c.2533C>T r.(?) p.(Pro845Ser)
-?/. - c.2605G>A r.(?) p.(Val869Met)
?/. - c.2683G>A r.(?) p.(Glu895Lys)
-?/. - c.2724C>T r.(?) p.(Ser908=)
-?/. - c.2784C>G r.(?) p.(Ser928=)
+?/. - c.2827C>T r.(?) p.(Arg943*)
+/. - c.2827C>T r.? p.(Arg943*)
+/. - c.2968_2971del r.(?) p.(Lys990PhefsTer17)
?/. - c.3002G>A r.(?) p.(Gly1001Glu)
+?/. - c.3067C>T r.(?) p.(His1023Tyr)
-?/. 5 c.3193G>A r.(?) p.(Ala1065Thr)
?/. - c.3193G>A r.(?) p.(Ala1065Thr)
-?/. - c.3194C>T r.(?) p.(Ala1065Val)
?/. - c.3368C>T r.(?) p.(Pro1123Leu)
-?/. - c.3383C>T r.(?) p.(Pro1128Leu)
+?/. - c.3412C>T r.(?) p.(Gln1138Ter)
+?/. - c.3434del r.(?) p.(Pro1145ArgfsTer2)
-/. - c.3444G>C r.(?) p.(Ser1148=)
+?/. - c.3556C>T r.(?) p.(Gln1186*)
-?/. - c.3659C>T r.(?) p.(Ala1220Val)
-?/. - c.3957C>G r.(?) p.(Ala1319=)
?/. - c.4023C>G r.(?) p.(His1341Gln)
?/. - c.4079del r.(?) p.(Asn1360Ilefs*14)
-/. - c.4107C>T r.(?) p.(Val1369=)
-/. - c.4140C>T r.(?) p.(Thr1380=)
-?/. - c.4254A>C r.(?) p.(Glu1418Asp)
-?/. - c.4485G>A r.(?) p.(Leu1495=)
?/. - c.4487T>A r.(?) p.(Val1496Asp)
-/. - c.4613T>C r.(?) p.(Leu1538Pro)
-?/. - c.4636G>A r.(?) p.(Gly1546Ser)
-?/. - c.4654C>T r.(?) p.(Pro1552Ser)
?/. - c.4697C>T r.(?) p.(Ser1566Leu)
?/. - c.4721C>G r.(?) p.(Thr1574Arg)
-?/. - c.4829G>A r.(?) p.(Arg1610His)
?/. - c.4850G>C r.(?) p.(Gly1617Ala)
?/. - c.4939G>A r.(?) p.(Val1647Met)
?/. - c.4943G>A r.(?) p.(Ser1648Asn)
?/. - c.5089A>C r.(?) p.(Lys1697Gln)
-/. - c.5142A>G r.(?) p.(Gly1714=)
?/. - c.5225T>G r.(?) p.(Leu1742Arg)
-?/. - c.5225T>G r.(?) p.(Leu1742Arg)
-/. - c.5397C>T r.(?) p.(Tyr1799=)
-?/. - c.5460C>A r.(?) p.(Thr1820=)
+/. - c.5582C>A r.(?) p.(Ser1861Ter)
+?/. - c.5737del r.(?) p.(Asp1913Metfs*15)
?/. - c.5834C>T r.(?) p.(Ser1945Phe)
-?/. - c.5853C>T r.(?) p.(Gly1951=)
-?/. - c.5857G>A r.(?) p.(Val1953Ile)
-?/. - c.5857G>C r.(?) p.(Val1953Leu)
?/. - c.5866G>A r.(?) p.(Gly1956Arg)
-?/. - c.5892A>G r.(?) p.(Gly1964=)
?/. - c.5959A>T r.(?) p.(Ser1987Cys)
+/. - c.5989G>T r.(?) p.(Glu1997*)
?/. - c.5997G>C r.(?) p.(Gln1999His)
-?/. - c.6024C>G r.(?) p.(Asp2008Glu)
?/. - c.6421A>G r.(?) p.(Ile2141Val)
?/. - c.6478C>G r.(?) p.(Gln2160Glu)
?/. - c.6482_6484del r.(?) p.(Tyr2161del)
?/. - c.6517-5C>G r.spl? p.?
+/. - c.6609_6616del r.(?) p.(Glu2204*)
-?/. - c.6758T>C r.(?) p.(Leu2253Ser)
+/. - c.6871C>T - -
-/. - c.6885A>G r.(?) p.(Pro2295=)
-?/. - c.6989C>A r.(?) p.(Thr2330Lys)
-?/. - c.7036C>T r.(?) p.(Leu2346Phe)
?/. - c.7156C>T r.(?) p.(His2386Tyr)
-?/. - c.7223C>T r.(?) p.(Thr2408Met)
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