Transcript #00002104 (NM_139057.2, ADAMTS17 gene)

Transcript name ADAM metallopeptidase with thrombospondin type 1 motif, 17
Gene name ADAMTS17 (ADAM metallopeptidase with thrombospondin type 1 motif, 17)
Chromosome 15
Transcript - NCBI ID NM_139057.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_620688.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_3i c.-80880_616+15062del r.0? p.0?
-?/. - c.32T>C r.(?) p.(Val11Ala)
-/. - c.79+31C>G r.(=) p.(=)
-/. - c.80-105G>C r.(=) p.(=)
?/. - c.80-29G>A r.(=) p.(=)
?/. - c.161C>T r.(?) p.(Pro54Leu)
-?/. - c.172G>T r.(?) p.(Gly58Trp)
-?/. - c.214C>A r.(?) p.(Pro72Thr)
?/. - c.292C>G r.(?) p.(Arg98Gly)
-/. - c.450+30C>A r.(=) p.(=)
?/. - c.526C>G r.(?) p.(Arg176Gly)
-?/. - c.542G>A r.(?) p.(Arg181Lys)
?/. - c.544C>G r.(?) p.(Arg182Gly)
-?/. - c.548A>G r.(?) p.(Lys183Arg)
-?/. - c.548A>G r.(?) p.(Lys183Arg)
-?/. - c.590C>T r.(?) p.(Pro197Leu)
?/. - c.607G>T r.(?) p.(Val203Phe)
-/. - c.617-41A>G r.(=) p.(=)
-/. - c.647C>T r.(?) p.(Ser216Leu)
-/. - c.647C>T r.(?) p.(Ser216Leu)
-/. - c.647C>T r.(?) p.(Ser216Leu)
+/. - c.650del r.(?) p.(Asp218Thrfs*41)
?/. - c.659G>A r.(?) p.(Arg220Gln)
?/. - c.664C>T r.(?) p.(Arg222Trp)
?/. - c.665G>A r.(?) p.(Arg222Gln)
-?/. - c.680G>A r.(?) p.(Arg227Gln)
-?/. - c.744C>T r.(?) p.(His248=)
-?/. - c.744C>T r.(?) p.(His248=)
-/. - c.756C>T r.(?) p.(Ala252=)
-/. - c.756C>T r.(?) p.(Ala252=)
-/. - c.756C>T r.(=) p.(=)
-?/. - c.771C>T r.(?) p.(Ile257=)
?/. - c.778G>A r.(?) p.(Val260Ile)
-/. - c.789+8C>T r.(=) p.(=)
-/. - c.789+8C>T r.(=) p.(=)
-/. - c.789+8C>T r.(=) p.(=)
-/. - c.790-126G>A r.(=) p.(=)
+?/. - c.862C>T r.(?) p.(Arg288Ter)
-/. - c.873+58T>C r.(=) p.(=)
-/. - c.873+62C>T r.(=) p.(=)
-?/. - c.903G>A r.(?) p.(Glu301=)
-?/. - c.905G>A r.(?) p.(Arg302Gln)
?/. - c.953C>A r.(?) p.(Ala318Glu)
-?/. - c.956G>A r.(?) p.(Arg319Gln)
-/. - c.1017C>T r.(?) p.(Ala339=)
-/. - c.1017C>T r.(?) p.(Ala339=)
-/. - c.1017C>T r.(=) p.(=)
-?/. - c.1031+6A>T r.(=) p.(=)
-/. - c.1053G>A r.(?) p.(Lys351=)
-/. - c.1053G>A r.(?) p.(Lys351=)
-/. - c.1053G>A r.(=) p.(=)
?/. - c.1054G>T r.(?) p.(Asp352Tyr)
-?/. - c.1062G>A r.(?) p.(Pro354=)
+/. - c.1075+1G>T r.spl? p.?
+/. - c.1075+1G>T r.spl? p.?
-?/. - c.1075+8T>G r.(=) p.(=)
-?/. - c.1288T>C r.(?) p.(Ser430Pro)
?/. - c.1288T>C r.(?) p.(Ser430Pro)
?/. - c.1317C>A r.(?) p.(Phe439Leu)
?/. - c.1317C>A r.(?) p.(Phe439Leu)
-/. - c.1337C>T r.(?) p.(Thr446Ile)
-?/. - c.1419C>T r.(?) p.(Asn473=)
-/. - c.1445T>C r.(?) p.(Met482Thr)
-/. - c.1445T>C r.(?) p.(Met482Thr)
-?/. - c.1474-6C>T r.(=) p.(=)
+?/. - c.1555del r.(?) p.(Thr519Profs*15)
-?/. - c.1558G>A r.(?) p.(Glu520Lys)
?/. - c.1589G>A r.(?) p.(Gly530Glu)
?/. - c.1630G>A r.(?) p.(Gly544Arg)
-?/. - c.1644G>A r.(?) p.(Pro548=)
-?/. - c.1651G>A r.(?) p.(Ala551Thr)
-/. - c.1651G>A r.(?) p.(Ala551Thr)
?/. - c.1682C>T r.(?) p.(Thr561Met)
?/. - c.1690C>T r.(?) p.(Arg564Cys)
-/. - c.1696A>C r.(?) p.(Arg566=)
-/. - c.1696A>C r.(?) p.(Arg566=)
-/. - c.1696A>C r.(=) p.(=)
?/. - c.1720C>T r.(?) p.(Pro574Ser)
?/. - c.1721C>T r.(?) p.(Pro574Leu)
-?/. - c.1748C>T r.(?) p.(Pro583Leu)
-?/. - c.1767T>C r.(?) p.(His589=)
?/. - c.1814G>A r.(?) p.(Arg605Gln)
-?/. - c.1840C>T r.(?) p.(Arg614Trp)
?/. - c.1868T>C r.(?) p.(Leu623Pro)
?/. - c.1873G>T r.(?) p.(Ala625Ser)
-/. - c.1875C>T r.(?) p.(Ala625=)
?/. - c.1876G>A r.(?) p.(Val626Met)
-?/. - c.1914G>T r.(?) p.(Ser638=)
+/. 14 c.1924A>T r.(?) p.(Lys642Ter)
-/. - c.1962C>T r.(?) p.(Asp654=)
-/. - c.1962C>T r.(=) p.(=)
-?/. - c.2017-5T>C r.spl? p.?
?/. - c.2017A>G r.(?) p.(Lys673Glu)
-?/. - c.2047G>A r.(?) p.(Ala683Thr)
?/. - c.2111G>A r.(?) p.(Gly704Asp)
-/. - c.2112C>T r.(?) p.(Gly704=)
-/. - c.2112C>T r.(?) p.(Gly704=)
-?/. - c.2137+3G>T r.spl? p.?
?/. - c.2137+3G>T r.spl? p.?
-/. - c.2138-12C>T r.(=) p.(=)
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