Transcript #00008960

Transcript name keratin 10
Gene name KRT10 (keratin 10)
Chromosome 17
Transcript - NCBI ID NM_000421.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000412.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-2C>T r.(=) p.(=)
?/? c.11G>A r.(?) p.(Arg4Gln)
?/? c.44G>A r.(?) p.(Arg15His)
?/? c.47G>A r.(?) p.(Ser16Asn)
?/? c.70_72del r.(?) p.(Gly24del)
?/? c.70_72dup r.(?) p.(Gly24dup)
?/? c.89_91del r.(?) p.(Gly30del)
?/? c.97T>A r.(?) p.(Ser33Thr)
?/? c.98C>T r.(?) p.(Ser33Phe)
?/? c.125C>T r.(?) p.(Ser42Phe)
?/? c.129T>C r.(=) p.(=)
?/? c.130G>C r.(?) p.(Gly44Arg)
?/? c.135A>G r.(=) p.(=)
?/? c.153G>T r.(=) p.(=)
?/? c.158G>A r.(?) p.(Ser53Asn)
?/? c.176G>A r.(?) p.(Arg59His)
?/? c.257G>A r.(?) p.(Arg86His)
?/? c.302T>G N/A N/A
?/? c.305T>C r.(?) p.(Phe102Ser)
?/? c.312G>A r.(=) p.(=)
?/? c.315C>A r.(=) p.(=)
?/? c.338G>A r.(?) p.(Gly113Asp)
?/? c.339T>C r.(=) p.(=)
?/? c.371G>T r.(?) p.(Gly124Val)
?/? c.375C>T r.(=) p.(=)
?/? c.376G>A r.(?) p.(Gly126Ser)
?/? c.430G>A r.(?) p.(Gly144Arg)
?/? c.514T>C r.(?) p.(Tyr172His)
?/? c.574G>A r.(?) p.(Glu192Lys)
?/? c.581G>A r.(?) p.(Arg194His)
?/? c.627+33T>A r.(=) p.(=)
?/? c.627+38T>C r.(=) p.(=)
?/? c.628-60C>A r.(=) p.(=)
?/? c.651T>C r.(=) p.(=)
?/? c.685C>T r.(=) p.(=)
?/? c.693T>G r.(=) p.(=)
?/? c.710+6T>C r.(=) p.(=)
?/? c.710+10G>A r.(=) p.(=)
?/? c.710+12G>C r.(=) p.(=)
?/? c.710+15C>T r.(=) p.(=)
?/? c.710+17T>C r.(=) p.(=)
?/? c.710+36C>T r.(=) p.(=)
?/? c.710+37G>T r.(=) p.(=)
?/? c.711-49A>G r.(=) p.(=)
?/? c.711-6T>C r.(=) p.(=)
?/? c.734G>A r.(?) p.(Arg245His)
?/? c.738G>A r.(=) p.(=)
?/? c.742G>A r.(?) p.(Val248Met)
?/? c.756C>T r.(=) p.(=)
?/? c.789C>T r.(=) p.(=)
?/? c.808G>A r.(?) p.(Glu270Lys)
?/? c.859C>T r.(?) p.(His287Tyr)
?/? c.867+16T>C r.(=) p.(=)
?/? c.867+38G>A r.(=) p.(=)
?/? c.867+39T>C r.(=) p.(=)
?/? c.868-41G>A r.(=) p.(=)
?/? c.906G>T r.(=) p.(=)
?/? c.1000A>C r.(?) p.(Lys334Gln)
?/? c.1006G>A r.(?) p.(Ala336Thr)
?/? c.1029+5_1029+9del r.spl? p.?
?/? c.1029+25_1029+26del r.(=) p.(=)
?/? c.1080C>T r.(=) p.(=)
?/? c.1095T>G r.(?) p.(Ile365Met)
?/? c.1140G>C r.(?) p.(Gln380His)
?/? c.1152C>G r.(=) p.(=)
?/? c.1155+35T>C r.(=) p.(=)
?/? c.1155+37A>G r.(=) p.(=)
?/? c.1155+50T>C r.(=) p.(=)
?/? c.1156-11del r.(=) p.(=)
?/? c.1156-11dup r.(=) p.(=)
?/? c.1196G>A r.(?) p.(Arg399His)
?/? c.1203T>C r.(=) p.(=)
?/? c.1228C>G r.(?) p.(Gln410Glu)
?/? c.1245A>G r.(=) p.(=)
?/? c.1327G>A r.(?) p.(Glu443Lys)
?/? c.1348C>T r.(?) p.(Arg450Cys)
?/? c.1368G>C r.(?) p.(Glu456Asp)
?/? c.1374-45T>C r.(=) p.(=)
?/? c.1374-38A>G r.(=) p.(=)
?/? c.1428_1430del r.(?) p.(Ser478del)
?/? c.1443_1445del r.(?) p.(Ser483del)
?/? c.1443_1457del r.(?) p.(Ser482_Gly486del)
?/? c.1456_1457insGAA r.(?) p.(Gly486_His487insSer)
?/? c.1468_1479del r.(?) p.(Gly490_Gly493del)
?/? c.1520_1521insC r.(?) p.(Ser508Lysfs*73)
?/? c.1521_1522insGC r.(?) p.(Ser508Alafs*112)
?/? c.1629G>C r.(=) p.(=)
?/? c.1632C>A r.(=) p.(=)
?/? c.1615_1635del r.(?) p.(Gly539_Gly545del)
?/? c.1629_1643del r.(?) p.(Gly548_Ser552del)
?/? c.1656_1657insAGC r.(?) p.(Ser553dup)
?/? c.1724G>T r.(?) p.(Gly575Val)
?/? c.1749-31G>C r.(=) p.(=)
?/? c.1749-11C>T r.(=) p.(=)
?/? c.1749-10A>G r.(=) p.(=)
?/? c.1749-2A>C r.spl? p.?
?/? c.1750T>C r.(?) p.(Tyr584His)
?/? c.*7C>T r.(=) p.(=)
?/? c.*40G>A r.(=) p.(=)
?/? c.*42C>T r.(=) p.(=)
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