Transcript #00014561 (NM_182946.1, NIN gene)

Transcript name transcript variant 5
Gene name NIN (ninein (GSK3B interacting protein))
Chromosome 14
Transcript - NCBI ID NM_182946.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_891991.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.65C>T r.(?) p.(Thr22Met)
?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.436-5T>C r.spl? p.?
-?/. - c.475+9C>T r.(=) p.(=)
-?/. - c.612G>A r.(?) p.(Arg204=)
-?/. - c.667-5T>C r.spl? p.?
?/. - c.813+1G>C r.spl? p.?
-?/. - c.926G>C r.(?) p.(Arg309Thr)
-/. - c.933G>C r.(?) p.(Leu311=)
?/. - c.1002T>A r.(?) p.(Asp334Glu)
-?/. - c.1074C>T r.(?) p.(His358=)
+?/. - c.1381A>T r.(?) p.(Lys461*)
-?/. - c.1434+4A>C r.spl? p.?
?/. - c.1595G>T r.(?) p.(Arg532Ile)
?/. - c.1736_1738del r.(?) p.(Glu579del)
?/. - c.1737A>C r.(?) p.(Glu579Asp)
?/. - c.1737A>C r.(?) p.(Glu579Asp)
-?/. - c.1827G>C r.(?) p.(Leu609=)
-?/. - c.1900C>T r.(?) p.(Arg634Cys)
-?/. - c.1930G>A r.(?) p.(Val644Met)
?/. - c.2041G>A r.(?) p.(Gly681Arg)
-/. - c.2072A>G r.(?) p.(His691Arg)
-?/. - c.2476A>G r.(?) p.(Thr826Ala)
-?/. - c.2476A>G r.(?) p.(Thr826Ala)
-?/. - c.2609C>T r.(?) p.(Ala870Val)
?/. - c.2647_2650del r.(?) p.(Glu883Lysfs*7)
-?/. - c.2651A>G r.(?) p.(Lys884Arg)
?/. - c.2785C>A r.(?) p.(Gln929Lys)
?/. - c.2899C>T r.(?) p.(Gln967*)
-?/. - c.2987C>T r.(?) p.(Ala996Val)
-/. - c.2988G>A r.(?) p.(Ala996=)
?/. - c.3083_3085del r.(?) p.(Pro1028del)
?/. - c.3196G>A r.(?) p.(Val1066Ile)
-?/. - c.3197T>A r.(?) p.(Val1066Asp)
?/. - c.3197T>A r.(?) p.(Val1066Asp)
?/. - c.3317_3319del r.(?) p.(Ser1106del)
-/. - c.3331C>G r.(?) p.(Pro1111Ala)
-/. - c.3374= r.(=) p.(Pro1125=)
-?/. - c.3392G>A r.(?) p.(Arg1131Gln)
-/. - c.3454G>T r.(?) p.(Val1152Phe)
-?/. - c.3487G>C r.(?) p.(Val1163Leu)
-?/. - c.3487G>C r.(?) p.(Val1163Leu)
-?/. - c.3499G>A r.(?) p.(Glu1167Lys)
?/. - c.3532G>A r.(?) p.(Glu1178Lys)
-?/. - c.3611A>G r.(?) p.(Gln1204Arg)
-?/. - c.3647G>A r.(?) p.(Arg1216Gln)
-?/. - c.3647G>A r.(?) p.(Arg1216Gln)
-/. - c.3959= r.(=) p.(Glu1320=)
-?/. - c.4014C>T r.(?) p.(Ser1338=)
-?/. - c.4144C>G r.(?) p.(His1382Asp)
-?/. - c.4288A>T r.(?) p.(Ile1430Leu)
-?/. - c.4356A>G r.(?) p.(Ala1452=)
-/. - c.4395T>C r.(?) p.(Thr1465=)
?/. - c.4581A>T r.(?) p.(Arg1527Ser)
?/. - c.4628A>T r.(?) p.(Lys1543Ile)
?/. - c.4664+4A>G r.spl? p.?
?/. - c.4763A>T r.(?) p.(Gln1588Leu)
-?/. - c.4837C>T r.(?) p.(Arg1613Cys)
-?/. - c.4837C>T r.(?) p.(Arg1613Cys)
-?/. - c.4838G>A r.(?) p.(Arg1613His)
-?/. - c.4936C>T r.(?) p.(Arg1646Cys)
-?/. - c.4937G>A r.(?) p.(Arg1646His)
-?/. - c.4937G>A r.(?) p.(Arg1646His)
-?/. - c.4980G>A r.(?) p.(Ala1660=)
?/. - c.4990G>A r.(?) p.(Glu1664Lys)
-/. - c.5011A>G r.(?) p.(Ile1671Val)
-?/. - c.5188T>C r.(?) p.(Leu1730=)
?/. - c.5302G>T r.(?) p.(Val1768Phe)
-?/. - c.5351G>A r.(?) p.(Arg1784Gln)
-?/. - c.5509T>A r.(?) p.(Ser1837Thr)
-?/. - c.5584A>G r.(?) p.(Met1862Val)
-?/. - c.5584A>G r.(?) p.(Met1862Val)
-?/. - c.5586G>A r.(?) p.(Met1862Ile)
-?/. - c.5605G>A r.(?) p.(Glu1869Lys)
-/. - c.5628+5T>C r.spl? p.?
-?/. - c.5629-5G>A r.spl? p.?
-/. - c.5637G>A r.(?) p.(Gln1879=)
-?/. - c.5877+3A>G r.spl? p.?
-?/. - c.5903C>T r.(?) p.(Thr1968Met)
?/. - c.5912C>T r.(?) p.(Pro1971Leu)
-?/. - c.5913G>A r.(?) p.(Pro1971=)
?/. - c.5941C>T r.(?) p.(Leu1981Phe)
-?/. - c.5996G>A r.(?) p.(Arg1999His)
-?/. - c.6068A>G r.(?) p.(Asn2023Ser)
-?/. - c.6079-1679C>G r.(=) p.(=)
-/. - c.6204C>T r.(?) p.(Pro2068=)
?/. - c.*2282C>T r.(=) p.(=)
-?/. - c.*2350A>C r.(=) p.(=)
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