Transcript #00002649

Transcript name coiled-coil domain containing 15
Gene name CCDC15 (coiled-coil domain containing 15)
Chromosome 11
Transcript - NCBI ID NM_025004.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_079280.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-9-6A>C r.(=) p.(=)
?/? c.19C>T r.(?) p.(Arg7*)
?/? c.30T>C r.(=) p.(=)
?/? c.39C>T r.(=) p.(=)
?/? c.66C>G r.(=) p.(=)
?/? c.69G>A r.(=) p.(=)
?/? c.99T>C r.(=) p.(=)
?/? c.127G>A r.(?) p.(Gly43Arg)
?/? c.176A>T r.(?) p.(Tyr59Phe)
?/? c.177+4A>G r.spl? p.?
?/? c.177+8T>C r.(=) p.(=)
?/? c.177+34T>C r.(=) p.(=)
?/? c.177+52T>C r.(=) p.(=)
?/? c.178-42C>T r.(=) p.(=)
?/? c.202G>T r.(?) p.(Glu68*)
?/? c.327+41A>G r.(=) p.(=)
?/? c.328-43A>C r.(=) p.(=)
?/? c.341G>C r.(?) p.(Gly114Ala)
?/? c.362C>T r.(?) p.(Ser121Leu)
?/? c.382del r.(?) p.(Arg129Glyfs*9)
?/? c.395del r.(?) p.(Pro134Glnfs*4)
?/? c.443C>G r.(?) p.(Pro148Arg)
?/? c.490G>A r.(?) p.(Glu164Lys)
?/? c.516+15T>A r.(=) p.(=)
?/? c.517-28T>C r.(=) p.(=)
?/? c.517-27T>G r.(=) p.(=)
?/? c.535C>T r.(?) p.(Gln179*)
?/? c.541C>T r.(?) p.(Arg181Cys)
?/? c.542G>A r.(?) p.(Arg181His)
?/? c.556T>C r.(?) p.(Ser186Pro)
?/? c.624C>T r.(=) p.(=)
?/? c.630+19C>T r.(=) p.(=)
?/? c.631-12del r.(=) p.(=)
?/? c.650C>T r.(?) p.(Pro217Leu)
?/? c.684A>C r.(=) p.(=)
?/? c.699G>C r.(?) p.(Lys233Asn)
?/? c.743T>C r.(?) p.(Met248Thr)
?/? c.753+34T>C r.(=) p.(=)
?/? c.753+37G>T r.(=) p.(=)
?/? c.754-40C>T r.(=) p.(=)
?/? c.754-38C>T r.(=) p.(=)
?/? c.754-37G>A r.(=) p.(=)
?/? c.754-37_754-28del r.(=) p.(=)
?/? c.754-35G>A r.(=) p.(=)
?/? c.754-35_754-28del r.(=) p.(=)
?/? c.754-23G>A r.(=) p.(=)
?/? c.768G>A r.(=) p.(=)
?/? c.815G>T r.(?) p.(Gly272Val)
?/? c.818A>T r.(?) p.(Lys273Ile)
?/? c.900+18A>G r.(=) p.(=)
?/? c.901-49T>G r.(=) p.(=)
?/? c.946G>A r.(?) p.(Glu316Lys)
?/? c.1129A>G r.(?) p.(Ile377Val)
?/? c.1158A>G r.(=) p.(=)
?/? c.1162A>G r.(?) p.(Thr388Ala)
?/? c.1179G>A r.(=) p.(=)
?/? c.1218G>T r.(=) p.(=)
?/? c.1231G>A r.(?) p.(Asp411Asn)
?/? c.1262C>T r.(?) p.(Thr421Met)
?/? c.1268A>T r.(?) p.(Asn423Ile)
?/? c.1273G>A r.(?) p.(Asp425Asn)
?/? c.1276G>A r.(?) p.(Val426Ile)
?/? c.1286A>C r.(?) p.(Lys429Thr)
?/? c.1342G>A r.(?) p.(Asp448Asn)
?/? c.1342_1356del r.(?) p.(Phe449_Asp453del)
?/? c.1373A>C r.(?) p.(His458Pro)
?/? c.1391del r.(?) p.(Leu464Argfs*184)
?/? c.1392G>A r.(=) p.(=)
?/? c.1492C>G r.(?) p.(Gln498Glu)
?/? c.1586G>A r.(?) p.(Gly529Asp)
?/? c.1619T>A r.(?) p.(Leu540*)
?/? c.1635T>C r.(=) p.(=)
?/? c.1702G>A r.(?) p.(Gly568Ser)
?/? c.1710T>A r.(=) p.(=)
?/? c.1718A>T r.(?) p.(Asp573Val)
?/? c.1738T>G r.(?) p.(Cys580Gly)
?/? c.1760C>A r.(?) p.(Pro587His)
?/? c.1803C>T r.(=) p.(=)
?/? c.1867C>G r.(?) p.(Leu623Val)
?/? c.1884C>T r.(=) p.(=)
?/? c.1901A>G r.(?) p.(Lys634Arg)
?/? c.1908+45C>T r.(=) p.(=)
?/? c.1909-17A>G r.(=) p.(=)
?/? c.1909-7C>A r.(=) p.(=)
?/? c.1929A>G r.(=) p.(=)
?/? c.1932C>G r.(?) p.(Tyr644*)
?/? c.1945G>T r.(?) p.(Asp649Tyr)
?/? c.1963del r.(?) p.(Asp655Thrfs*29)
?/? c.1973T>C r.(?) p.(Leu658Pro)
?/? c.2021T>C r.(?) p.(Ile674Thr)
?/? c.2031+9G>A r.(=) p.(=)
?/? c.2032-44del r.(=) p.(=)
?/? c.2039C>T r.(?) p.(Ala680Val)
?/? c.2047A>G r.(?) p.(Met683Val)
?/? c.2070A>G r.(=) p.(=)
?/? c.2075T>C r.(?) p.(Leu692Ser)
?/? c.2135A>T r.(?) p.(Glu712Val)
?/? c.2139+9G>A r.(=) p.(=)
?/? c.2140-35T>G r.(=) p.(=)
?/? c.2140-32A>G r.(=) p.(=)
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