Transcript #00011961 (NM_005121.2, MED13 gene)

Transcript name mediator complex subunit 13
Gene name MED13 (mediator complex subunit 13)
Chromosome 17
Transcript - NCBI ID NM_005121.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_005112.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

82 entries on 1 page. Showing entries 1 - 82.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-79G>C r.(?) p.(=)
-?/. - c.50G>T r.(?) p.(Cys17Phe)
?/. - c.50G>T r.(?) p.(Cys17Phe)
-?/. - c.98A>T r.(?) p.(Tyr33Phe)
-?/. - c.115A>G r.(?) p.(Thr39Ala)
-?/. - c.115A>G r.(?) p.(Thr39Ala)
?/. - c.127A>C r.(?) p.(Ile43Leu)
?/. - c.147dup r.(?) p.(Glu50ArgfsTer9)
?/. - c.163A>G r.(?) p.(Ser55Gly)
?/. - c.183_185dup r.(?) p.(Leu61_Lys62insAsn)
-?/. - c.563T>C r.(?) p.(Leu188Pro)
?/. - c.719A>G r.(?) p.(Tyr240Cys)
?/. - c.817G>T r.(?) p.(Gly273Cys)
-?/. - c.975T>A r.(?) p.(Leu325=)
?/. - c.977C>T r.(?) p.(Thr326Ile)
?/. - c.980C>A r.(?) p.(Pro327Gln)
?/. - c.1007C>G r.(?) p.(Thr336Arg)
+?/. - c.1009+1G>C r.spl? p.?
?/. - c.1048T>A r.(?) p.(Ser350Thr)
+?/. - c.1052dup r.(?) p.(Ser352Ilefs*2)
?/. - c.1303A>G r.(?) p.(Arg435Gly)
-?/. - c.1325A>C r.(?) p.(Gln442Pro)
+?/. - c.1352_1365del r.(?) p.(Gln451ProfsTer5)
-?/. - c.1388A>G r.(?) p.(Glu463Gly)
?/. - c.1462A>G r.(?) p.(Met488Val)
+?/. - c.1486A>T r.(?) p.(Arg496*)
-?/. - c.1496T>C r.(?) p.(Ile499Thr)
-?/. - c.1597C>T r.(?) p.(Pro533Ser)
-?/. - c.1751A>G r.(?) p.(Gln584Arg)
?/. - c.1790C>T r.(?) p.(Thr597Ile)
-?/. - c.1792G>T r.(?) p.(Val598Leu)
-?/. - c.1870A>G r.(?) p.(Lys624Glu)
+?/. - c.1880A>G r.(?) p.(Glu627Gly)
?/. - c.2069A>T r.(?) p.(Glu690Val)
-?/. - c.2186A>G r.(?) p.(Glu729Gly)
-?/. - c.2291G>A r.(?) p.(Arg764His)
-?/. - c.2590C>T r.(?) p.(Pro864Ser)
-?/. - c.2784G>A r.(?) p.(Leu928=)
?/. - c.2851C>A r.(?) p.(Leu951Ile)
-?/. - c.2869A>G r.(?) p.(Met957Val)
?/. - c.3217G>A r.(?) p.(Val1073Ile)
-?/. - c.3389T>C r.(?) p.(Met1130Thr)
-?/. - c.3451C>T r.(?) p.(Arg1151Cys)
-?/. - c.3625G>A r.(?) p.(Asp1209Asn)
?/. - c.3676C>G r.(?) p.(Arg1226Gly)
?/. - c.3676C>G r.(?) p.(Arg1226Gly)
-?/. - c.3676C>G r.(?) p.(Arg1226Gly)
?/. - c.3765del r.(?) p.(Val1256*)
-?/. - c.4003A>T r.(?) p.(Thr1335Ser)
-?/. - c.4019A>G r.(?) p.(Tyr1340Cys)
-?/. - c.4108G>A r.(?) p.(Ala1370Thr)
+?/. - c.4202del r.(?) p.(Leu1401*)
?/. - c.4436T>C r.(?) p.(Leu1479Ser)
-?/. - c.4447A>G r.(?) p.(Thr1483Ala)
-?/. - c.4450A>C r.(?) p.(Ser1484Arg)
-?/. - c.4450A>C r.(?) p.(Ser1484Arg)
?/. - c.4487C>T r.(?) p.(Thr1496Ile)
-?/. - c.4642A>G r.(?) p.(Ser1548Gly)
?/. - c.4654T>C r.(?) p.(Ser1552Pro)
?/. - c.4675C>G r.(?) p.(Pro1559Ala)
-?/. - c.4765A>G r.(?) p.(Thr1589Ala)
-?/. - c.4902G>A r.(?) p.(Thr1634=)
-?/. - c.5403G>T r.(?) p.(Arg1801Ser)
?/. - c.5443T>G r.(?) p.(Leu1815Val)
+?/. - c.5522_5523insTTTTGGGAGTGGT r.(?) p.(Gln1841Hisfs*54)
?/. - c.5530T>C r.(?) p.(Trp1844Arg)
?/. - c.5611G>A r.(?) p.(Gly1871Arg)
+?/. - c.5758C>T r.(?) p.(Gln1920*)
-?/. - c.5782+8A>G r.(=) p.(=)
?/. - c.5866T>G r.(?) p.(Ser1956Ala)
?/. - c.5870G>T r.(?) p.(Cys1957Phe)
?/. - c.6134G>A r.(?) p.(Arg2045Gln)
?/. - c.6137T>C r.(?) p.(Leu2046Pro)
?/. 28 c.6269A>G r.6269A>G p.Tyr2090Cys
?/. - c.6358C>T r.(?) p.(Pro2120Ser)
?/. - c.6407A>G r.(?) p.(Gln2136Arg)
?/. - c.6410A>G r.(?) p.(Tyr2137Cys)
?/. - c.6422C>T r.(?) p.(Ser2141Phe)
-?/. - c.6446C>G r.(?) p.(Thr2149Ser)
-?/. - c.6469C>T r.(?) p.(Pro2157Ser)
-?/. - c.6500A>G r.(?) p.(Tyr2167Cys)
?/. - c.6525A>G r.(?) p.(Ter2175TrpextTer29)
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