Transcript #00000282

Transcript name ADAM metallopeptidase with thrombospondin type 1 motif, 4
Gene name ADAMTS4 (ADAM metallopeptidase with thrombospondin type 1 motif, 4)
Chromosome 1
Transcript - NCBI ID NM_005099.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005090.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-35C>T r.(=) p.(=)
?/? c.25G>A r.(?) p.(Gly9Arg)
?/? c.89C>T r.(?) p.(Pro30Leu)
?/? c.148C>T r.(?) p.(Arg50Trp)
?/? c.157_158insA r.(?) p.(Ser53Lysfs*65)
?/? c.227G>A r.(?) p.(Gly76Asp)
?/? c.229G>A r.(?) p.(Ala77Thr)
?/? c.230C>T r.(?) p.(Ala77Val)
?/? c.250C>T r.(?) p.(Arg84Cys)
?/? c.251G>A r.(?) p.(Arg84His)
?/? c.271A>G r.(?) p.(Thr91Ala)
?/? c.283G>A r.(?) p.(Glu95Lys)
?/? c.298T>C r.(?) p.(Ser100Pro)
?/? c.313G>A r.(?) p.(Glu105Lys)
?/? c.316G>A r.(?) p.(Gly106Arg)
?/? c.390C>A r.(=) p.(=)
?/? c.414G>A r.(=) p.(=)
?/? c.429C>T r.(=) p.(=)
?/? c.437G>A r.(?) p.(Gly146Glu)
?/? c.506C>T r.(?) p.(Thr169Ile)
?/? c.545G>A r.(?) p.(Arg182His)
?/? c.547C>T r.(?) p.(Arg183Trp)
?/? c.574C>T r.(?) p.(Pro192Ser)
?/? c.586G>A r.(?) p.(Val196Ile)
?/? c.633+28C>T r.(=) p.(=)
?/? c.633+29G>A r.(=) p.(=)
?/? c.633+37C>T r.(=) p.(=)
?/? c.633+39C>T r.(=) p.(=)
?/? c.694G>A r.(?) p.(Ala232Thr)
?/? c.708G>A r.(=) p.(=)
?/? c.718C>T r.(?) p.(Arg240Cys)
?/? c.719G>C r.(?) p.(Arg240Pro)
?/? c.783T>C r.(=) p.(=)
?/? c.855T>C r.(=) p.(=)
?/? c.889C>T r.(?) p.(Arg297Trp)
?/? c.915G>A r.(=) p.(=)
?/? c.922G>C r.(?) p.(Asp308His)
?/? c.957+9C>G r.(=) p.(=)
?/? c.957+14C>G r.(=) p.(=)
?/? c.957+31C>T r.(=) p.(=)
?/? c.957+32A>G r.(=) p.(=)
?/? c.958-12C>T r.(=) p.(=)
?/? c.1005G>A r.(=) p.(=)
?/? c.1011C>T r.(=) p.(=)
?/? c.1012G>A r.(?) p.(Val338Ile)
?/? c.1022C>T r.(?) p.(Pro341Leu)
?/? c.1028G>A r.(?) p.(Arg343Gln)
?/? c.1047G>A r.(=) p.(=)
?/? c.1090+38G>T r.(=) p.(=)
?/? c.1091-15C>T r.(=) p.(=)
?/? c.1092T>C r.(=) p.(=)
?/? c.1162C>T r.(?) p.(Arg388Cys)
?/? c.1163G>A r.(?) p.(Arg388His)
?/? c.1198C>G r.(?) p.(Pro400Ala)
?/? c.1217C>T r.(?) p.(Pro406Leu)
?/? c.1253A>G r.(?) p.(Asn418Ser)
?/? c.1261+10T>C r.(=) p.(=)
?/? c.1262-4C>T r.spl? p.?
?/? c.1340G>T r.(?) p.(Arg447Leu)
?/? c.1366G>A r.(?) p.(Asp456Asn)
?/? c.1372C>T r.(?) p.(Arg458Cys)
?/? c.1382C>T r.(?) p.(Pro461Leu)
?/? c.1383A>G r.(=) p.(=)
?/? c.1392G>A r.(=) p.(=)
?/? c.1395G>A r.(=) p.(=)
?/? c.1485C>T r.(=) p.(=)
?/? c.1487G>C r.(?) p.(Gly496Ala)
?/? c.1492G>A r.(?) p.(Ala498Thr)
?/? c.1519C>T r.(?) p.(Leu507Phe)
?/? c.1548+36G>A r.(=) p.(=)
?/? c.1548+40G>T r.(=) p.(=)
?/? c.1549-25C>T r.(=) p.(=)
?/? c.1549-17G>A r.(=) p.(=)
?/? c.1684C>T r.(?) p.(Arg562Cys)
?/? c.1688G>A r.(?) p.(Arg563His)
?/? c.1699C>T r.(?) p.(Arg567Cys)
?/? c.1700G>A r.(?) p.(Arg567His)
?/? c.1709A>G r.(?) p.(Asn570Ser)
?/? c.1726A>G r.(?) p.(Thr576Ala)
?/? c.1735+16G>A r.(=) p.(=)
?/? c.1735+20G>A r.(=) p.(=)
?/? c.1736-41T>A r.(=) p.(=)
?/? c.1736-25G>A r.(=) p.(=)
?/? c.1743C>T r.(=) p.(=)
?/? c.1749C>G r.(=) p.(=)
?/? c.1756C>T r.(?) p.(Gln586*)
?/? c.1770C>T r.(=) p.(=)
?/? c.1802C>T r.(?) p.(Pro601Leu)
?/? c.1806G>A r.(=) p.(=)
?/? c.1826G>A r.(?) p.(Arg609His)
?/? c.1846C>T r.(?) p.(Gln616*)
?/? c.1868G>T r.(?) p.(Cys623Phe)
?/? c.1876C>T r.(?) p.(Gln626*)
?/? c.1877A>G r.(?) p.(Gln626Arg)
?/? c.1910G>A r.(?) p.(Arg637Gln)
?/? c.1911+6G>T r.(=) p.(=)
?/? c.1912-52C>T r.(=) p.(=)
?/? c.1912-23A>G r.(=) p.(=)
?/? c.1938G>A r.(=) p.(=)
?/? c.1967G>A r.(?) p.(Arg656Gln)
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