Transcript #00007167 (NM_004444.4, EPHB4 gene)

Transcript name EPH receptor B4
Gene name EPHB4 (EPH receptor B4)
Chromosome 7
Transcript - NCBI ID NM_004444.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004435.3
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.3G>A r.? p.?
+/. - c.33del r.(?) p.(Leu12TrpfsTer10)
-/. - c.52+14C>G r.(=) p.(=)
-/. - c.52+14del r.(=) p.(=)
-/. - c.52+14_52+15del r.(=) p.(=)
?/. - c.118G>A r.(?) p.(Gly40Arg)
+/. - c.123+3G>C r.123_411del p.Trp18Valfs*16
+?/. - c.175G>A r.(?) p.(Glu59Lys)
?/. - c.208G>A r.(?) p.(Ala70Thr)
+?/. - c.221G>C r.(?) p.(Arg74Pro)
?/. - c.239G>A r.(?) p.(Arg80Gln)
-?/. - c.267G>A r.(?) p.(Thr89=)
?/. - c.286G>A r.(?) p.(Glu96Lys)
-?/. - c.337G>A r.(?) p.(Val113Ile)
-?/. - c.337G>A r.(?) p.(Val113Ile)
+?/. - c.345_347del r.(?) p.(Tyr116del)
-?/. - c.360G>A r.(?) p.(Ala120=)
+/. - c.389G>A r.(?) p.(Trp130Ter)
?/. - c.399C>A r.(?) p.(Asn133Lys)
-?/. - c.412-9del r.(=) p.(=)
+/. - c.412-1G>T r.spl p.?
+/. - c.444_447dup r.(?) p.(Arg150GlufsTer74)
-?/. - c.469G>A r.(?) p.(Gly157Arg)
+?/. - c.481_485delinsTT r.(?) p.(Val161_Lys162delinsLeu)
-/. - c.489G>A r.(?) p.(Thr163=)
?/. - c.494G>A r.(?) p.(Arg165His)
-/. - c.546T>C r.(?) p.(Gly182=)
+?/. - c.560T>C r.(?) p.(Leu187Pro)
-?/. - c.623C>A r.(?) p.(Pro208Gln)
+/. - c.632_633del r.(?) p.(Val211AlafsTer11)
-?/. - c.691C>T r.(?) p.(Pro231Ser)
+/. - c.730C>T r.(?) p.(Gln244Ter)
?/. - c.770C>T r.(?) p.(Pro257Leu)
?/. - c.794A>G r.(?) p.(Asn265Ser)
+?/. - c.802T>C r.(?) p.(Cys268Arg)
?/. - c.830A>G r.(?) p.(Lys277Arg)
-?/. - c.901G>A r.(?) p.(Val301Ile)
?/. - c.928C>T r.(?) p.(Arg310Trp)
-?/. - c.981G>A r.(?) p.(Pro327=)
-?/. - c.1017G>T r.(?) p.(Leu339=)
+/. - c.1054C>T r.(?) p.(Arg352Ter)
+/. - c.1054C>T r.(?) p.(Arg352Ter)
-?/. - c.1067C>G r.(?) p.(Thr356Ser)
-?/. - c.1067C>G r.(?) p.(Thr356Ser)
+/. - c.1077_1081del r.(?) p.(Arg360ProfsTer19)
-?/. - c.1079G>A r.(?) p.(Arg360His)
-?/. - c.1099G>A r.(?) p.(Gly367Arg)
+/. - c.1123G>T r.(?) p.(Gly375Ter)
+/. - c.1177del r.(?) p.(Val393PhefsTer17)
?/. - c.1195G>A r.(?) p.(Asp399Asn)
+/. - c.1291C>T r.(?) p.(Arg431Ter)
-/. - c.1314T>C r.(?) p.(Ser438=)
-?/. - c.1384G>A r.(?) p.(Gly462Arg)
+?/. - c.1406T>G r.(?) p.(Val469Gly)
-/. - c.1422+3A>G r.spl? p.?
-/. - c.1423-15A>G r.(=) p.(=)
+/. - c.1423-6G>A r.1422 1423insacag p.Gly475Thrfs*39
?/. - c.1429G>A r.(?) p.(Glu477Lys)
?/. - c.1528C>A r.(?) p.(Arg510Ser)
+?/. - c.1546G>A r.(?) p.(Gly516Arg)
+?/. - c.1546G>A r.(?) p.(Gly516Arg)
+?/. - c.1546G>A r.(?) p.(Gly516Arg)
?/. - c.1546G>A r.(?) p.(Gly516Arg)
+/. - c.1558C>T r.(?) p.(Gln520Ter)
+/. - c.1558C>T r.(?) p.(Gln520Ter)
+?/. - c.1588+5G>C r.spl p.?
?/. - c.1603C>T r.(?) p.(Arg535Trp)
+/. - c.1615del r.(?) p.(Ala539ProfsTer2)
-?/. - c.1692-6C>A r.(=) p.(=)
+?/. - c.1692-1G>A r.spl p.?
+/. - c.1733dup r.(?) p.(His578GlnfsTer11)
?/. - c.1736G>T r.(?) p.(Gly579Val)
-/. - c.1743T>C r.(?) p.(Tyr581=)
-?/. - c.1749C>T r.(?) p.(Ile583=)
-/. - c.1752A>G r.(?) p.(Gly584=)
+/. - c.1788T>G r.(?) p.(Tyr596Ter)
+?/. - c.1870+2T>C r.spl p.?
?/. - c.1870+7G>A r.(=) p.(=)
-/. - c.1890C>T r.(?) p.(Cys630=)
?/. - c.1951G>C r.(?) p.(Gly651Arg)
-?/. - c.1961C>T r.(?) p.(Thr654Met)
+?/. - c.1966C>T r.(?) p.(Arg656Trp)
+?/. - c.1990G>A r.(?) p.(Glu664Lys)
?/. - c.2009A>C r.(?) p.(Gln670Pro)
?/. - c.2013C>G r.(?) p.(Phe671Leu)
+/. - c.2037_2038insT r.(?) p.(Glu680Ter)
?/. - c.2069T>C r.(?) p.(Met690Thr)
?/. - c.2172_2183dup r.(?) p.(Ile724_Gly727dup)
+?/. - c.2173G>A r.(?) p.(Ala725Thr)
?/. - c.2210T>G r.(?) p.(Val737Gly)
+/. - c.2215C>T r.(?) p.(Arg739Ter)
+/. - c.2215C>T r.(?) p.(Arg739Ter)
+/. 13 c.2216G>A r.(?) p.(Arg739Gln)
+?/. - c.2221C>G r.(?) p.(Leu741Val)
+?/. - c.2231G>A r.(?) p.(Arg744His)
+?/. - c.2233A>G r.(?) p.(Asn745Asp)
+?/. - c.2233A>G r.(?) p.(Asn745Asp)
+/. 14 c.2345T>G r.(?) p.(Ile782Ser)
+/. - c.2353C>T r.(?) p.(Arg785*)
+/. - c.2354G>A r.(?) p.(Arg785Gln)
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