Transcript #00001861

Transcript name chromosome 2 open reading frame 16
Gene name C2orf16 (chromosome 2 open reading frame 16)
Chromosome 2
Transcript - NCBI ID NM_032266.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_115642.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-46A>G r.(=) p.(=)
?/? c.-29C>T r.(=) p.(=)
?/? c.-19C>T r.(=) p.(=)
?/? c.6_7insCTGA r.(?) p.(Pro5Aspfs*32)
?/? c.26A>G r.(?) p.(Gln9Arg)
?/? c.29A>G r.(?) p.(Gln10Arg)
?/? c.50T>C r.(?) p.(Leu17Ser)
?/? c.130A>C r.(?) p.(Thr44Pro)
?/? c.153G>A r.(=) p.(=)
?/? c.168G>A r.(=) p.(=)
?/? c.219C>T r.(=) p.(=)
?/? c.220G>A r.(?) p.(Val74Ile)
?/? c.329G>C r.(?) p.(Arg110Thr)
?/? c.334A>C r.(?) p.(Asn112His)
?/? c.468C>T r.(=) p.(=)
?/? c.497G>T r.(?) p.(Gly166Val)
?/? c.634A>G r.(?) p.(Met212Val)
?/? c.641G>A r.(?) p.(Arg214Lys)
?/? c.724C>T r.(?) p.(Arg242Trp)
?/? c.725G>A r.(?) p.(Arg242Gln)
?/? c.730C>T r.(?) p.(Arg244*)
?/? c.840C>T r.(=) p.(=)
?/? c.856C>G r.(?) p.(Gln286Glu)
?/? c.1001T>G r.(?) p.(Val334Gly)
?/? c.1054C>T r.(?) p.(Pro352Ser)
?/? c.1056T>C r.(=) p.(=)
?/? c.1070G>A r.(?) p.(Arg357Gln)
?/? c.1075C>T r.(?) p.(Pro359Ser)
?/? c.1085T>A r.(?) p.(Val362Glu)
?/? c.1090T>C r.(=) p.(=)
?/? c.1092G>C r.(?) p.(Leu364Phe)
?/? c.1116_1120del r.(?) p.(Glu373Asnfs*34)
?/? c.1220G>C r.(?) p.(Cys407Ser)
?/? c.1258C>G r.(?) p.(Pro420Ala)
?/? c.1300G>C r.(?) p.(Val434Leu)
?/? c.1331G>C r.(?) p.(Arg444Thr)
?/? c.1408C>T r.(?) p.(Arg470*)
?/? c.1450C>G r.(?) p.(Gln484Glu)
?/? c.1491A>G r.(=) p.(=)
?/? c.1514A>T r.(?) p.(Asp505Val)
?/? c.1535C>T r.(?) p.(Ser512Phe)
?/? c.1593G>A r.(=) p.(=)
?/? c.1601C>G r.(?) p.(Pro534Arg)
?/? c.1609G>A r.(?) p.(Val537Ile)
?/? c.1655C>G r.(?) p.(Ser552*)
?/? c.1676G>A r.(?) p.(Cys559Tyr)
?/? c.1679T>G r.(?) p.(Leu560Trp)
?/? c.1688T>C r.(?) p.(Val563Ala)
?/? c.1738_1740del r.(?) p.(Val580del)
?/? c.1762G>C r.(?) p.(Val588Leu)
?/? c.1842T>C r.(=) p.(=)
?/? c.1887A>G r.(?) p.(Ile629Met)
?/? c.1917T>A r.(?) p.(His639Gln)
?/? c.1964C>G r.(?) p.(Thr655Ser)
?/? c.1979C>A r.(?) p.(Ala660Glu)
?/? c.1995G>A r.(=) p.(=)
?/? c.2054T>C r.(?) p.(Val685Ala)
?/? c.2121C>T r.(=) p.(=)
?/? c.2132A>G r.(?) p.(Asn711Ser)
?/? c.2137G>C r.(?) p.(Asp713His)
?/? c.2215C>T r.(?) p.(Leu739Phe)
?/? c.2238A>G r.(=) p.(=)
?/? c.2300T>C r.(?) p.(Ile767Thr)
?/? c.2320A>G r.(?) p.(Ile774Val)
?/? c.2345T>C r.(?) p.(Ile782Thr)
?/? c.2362C>T r.(?) p.(Gln788*)
?/? c.2383G>A r.(?) p.(Ala795Thr)
?/? c.2393A>G r.(?) p.(Asn798Ser)
?/? c.2419A>T r.(?) p.(Ile807Phe)
?/? c.2420T>C r.(?) p.(Ile807Thr)
?/? c.2462T>C r.(?) p.(Ile821Thr)
?/? c.2466T>A r.(=) p.(=)
?/? c.2503G>A r.(?) p.(Glu835Lys)
?/? c.2526A>G r.(=) p.(=)
?/? c.2546G>A r.(?) p.(Arg849Gln)
?/? c.2607C>A r.(=) p.(=)
?/? c.2648G>A r.(?) p.(Arg883Gln)
?/? c.2674A>G r.(?) p.(Met892Val)
?/? c.2706T>C r.(=) p.(=)
?/? c.2758G>C r.(?) p.(Asp920His)
?/? c.2767C>G r.(?) p.(Gln923Glu)
?/? c.2826G>C r.(=) p.(=)
?/? c.2827C>T r.(?) p.(Pro943Ser)
?/? c.2839C>A r.(?) p.(Pro947Thr)
?/? c.2875T>G r.(?) p.(Tyr959Asp)
?/? c.2885G>A r.(?) p.(Arg962Lys)
?/? c.2970C>T r.(=) p.(=)
?/? c.2981G>C r.(?) p.(Arg994Thr)
?/? c.3009G>A r.(=) p.(=)
?/? c.3018T>C r.(=) p.(=)
?/? c.3040C>T r.(?) p.(His1014Tyr)
?/? c.3066C>T r.(=) p.(=)
?/? c.3082G>C r.(?) p.(Val1028Leu)
?/? c.3090A>G r.(=) p.(=)
?/? c.3188C>A r.(?) p.(Ser1063Tyr)
?/? c.3192A>T r.(?) p.(Gln1064His)
?/? c.3231T>G r.(=) p.(=)
?/? c.3299G>A r.(?) p.(Ser1100Asn)
?/? c.3312C>T r.(=) p.(=)
?/? c.3313G>A r.(?) p.(Asp1105Asn)
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