Transcript #00020189 (NM_001127698.1, SPINK5 gene)

Transcript name transcript variant 1
Gene name SPINK5 (serine peptidase inhibitor, Kazal type 5)
Chromosome 5
Transcript - NCBI ID NM_001127698.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001121170.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-19G>A r.(?) p.(=)
?/. - c.13A>C r.(?) p.(Thr5Pro)
?/. - c.13A>C r.(?) p.(Thr5Pro)
-?/. - c.17T>C r.(?) p.(Val6Ala)
?/. - c.56-3C>A r.spl? p.?
-?/. - c.119G>C r.(?) p.(Gly40Ala)
-/. - c.119G>C r.(?) p.(Gly40Ala)
?/. - c.211G>A r.(?) p.(Glu71Lys)
-/. - c.316G>A r.(?) p.(Asp106Asn)
+/. - c.377_378del r.(?) p.(Tyr126*)
+?/. - c.394_395del r.(?) p.(Leu132Valfs*3)
./. - c.394_395del r.(?) p.(Leu132Valfs*3)
-?/. - c.418G>A r.(?) p.(Gly140Arg)
?/. - c.452G>A r.(?) p.(Cys151Tyr)
?/. - c.452G>A r.(?) p.(Cys151Tyr)
-/. - c.475-443A>G r.(=) p.(=)
?/. - c.475-243T>G r.(=) p.(=)
-?/. - c.622G>A r.(?) p.(Ala208Thr)
-?/. - c.622G>A r.(?) p.(Ala208Thr)
+/. - c.649C>T r.(?) p.(Arg217Ter)
+/. - c.649C>T r.(?) p.(Arg217Ter)
?/. - c.666G>T r.(?) p.(Lys222Asn)
-?/. - c.677A>G r.(?) p.(Lys226Arg)
?/. - c.721C>T r.(?) p.(Arg241Trp)
+/. - c.724G>T r.(?) p.(Glu242Ter)
-/. - c.738C>T r.(?) p.(Val246=)
-?/. - c.750C>T r.(?) p.(=)
?/. - c.753C>T r.(?) p.(Gly251=)
+?/. - c.794+1del r.spl? p.?
+/. - c.794+6T>C r.(=) p.(=)
-?/. - c.799C>A r.(?) p.(Gln267Lys)
-/. - c.800A>G r.(?) p.(Gln267Arg)
-/. - c.802C>T r.(?) p.(Arg268Cys)
-?/. - c.802C>T r.(?) p.(Arg268Cys)
-?/. - c.802C>T r.(?) p.(Arg268Cys)
-?/. - c.802C>T r.(?) p.(Arg268Cys)
+?/. - c.882+2T>C r.(?) p.(?)
-/. - c.882+20A>G r.(=) p.(=)
+/. - c.891C>T r.(?) p.(Cys297=)
?/. - c.891C>T r.(?) p.(Cys297=)
+/. - c.891C>T r.(?) p.(Cys297=)
?/. - c.891C>T r.(?) p.(Cys297=)
?/. - c.896A>G r.(?) p.(Gln299Arg)
+?/. - c.957_960dup r.(?) p.(Pro321Trpfs*23)
-/. - c.1004C>T r.(?) p.(Ala335Val)
-/. - c.1011-12C>T r.(=) p.(=)
?/. - c.1011-5T>G r.spl? p.?
?/. - c.1092+5G>A r.spl? p.?
-/. - c.1093-10A>G r.(=) p.(=)
-?/. - c.1093-6C>T r.(=) p.(=)
-/. - c.1103G>A r.(?) p.(Ser368Asn)
-?/. - c.1132A>C r.(?) p.(Lys378Gln)
-?/. - c.1132A>C r.(?) p.(Lys378Gln)
-/. - c.1156G>A r.(?) p.(Asp386Asn)
-/. - c.1188T>C r.(?) p.(His396=)
?/. - c.1237G>A r.(?) p.(Glu413Lys)
-/. - c.1258A>G r.(?) p.(Lys420Glu)
+/. - c.1302+4A>T r.spl? p.?
-/. - c.1302+19G>A r.(=) p.(=)
-/. - c.1322G>A r.(?) p.(Arg441His)
-?/. - c.1322G>A r.(?) p.(Arg441His)
-?/. - c.1322G>A r.(?) p.(Arg441His)
?/. - c.1339G>A r.(?) p.(Gly447Arg)
?/. - c.1339G>A r.(?) p.(Gly447Arg)
?/. - c.1379G>T r.(?) p.(Gly460Val)
-/. - c.1389A>G r.(?) p.(Gly463=)
?/. - c.1401C>T r.(?) p.(Gly467=)
+?/. - c.1431-12G>A r.(=) p.(=)
+/. - c.1431-12G>A r.(=) p.(=)
-?/. - c.1431-12G>T r.(=) p.(=)
-?/. - c.1431-10T>G r.(=) p.(=)
+/. - c.1432C>T r.(?) p.(Gln478Ter)
-?/. - c.1451G>A r.(?) p.(Arg484Lys)
-?/. - c.1451G>A r.(?) p.(Arg484Lys)
-?/. - c.1480-10C>A r.(=) p.(=)
-?/. - c.1480-3C>T r.spl? p.?
-?/. - c.1552C>T r.(?) p.(Arg518Cys)
?/. - c.1553G>A r.(?) p.(Arg518His)
-/. - c.1557C>A r.(?) p.(Gly519=)
-?/. - c.1605G>T r.(?) p.(Val535=)
-?/. - c.1605G>T r.(?) p.(Val535=)
-?/. - c.1605G>T r.(?) p.(Val535=)
?/. - c.1658T>C r.(?) p.(Val553Ala)
-/. - c.1659C>T r.(?) p.(Val553=)
-?/. - c.1693-20G>A r.(=) p.(=)
-?/. - c.1693-19C>T r.(=) p.(=)
-?/. - c.1693-7T>C r.(=) p.(=)
+/. - c.1732C>T r.(?) p.(Arg578*)
+/. - c.1732C>T r.(?) p.(Arg578*)
-/. - c.1764T>G r.(?) p.(Ile588Met)
-?/. - c.1764T>G r.(?) p.(Ile588Met)
?/. - c.1774G>C r.(?) p.(Asp592His)
+/. - c.1820+53G>A r.(=) p.(=)
+?/. - c.1845_1848del r.(?) p.(Arg616LeufsTer98)
+?/. - c.1887+3A>T r.spl? p.?
+/. - c.1888-3T>C r.spl? p.?
-?/. - c.1896C>T r.(?) p.(Cys632=)
-?/. - c.1915T>C r.(?) p.(Leu639=)
?/. - c.1960C>T r.(?) p.(Arg654Cys)
-?/. - c.1964G>A r.(?) p.(Gly655Asp)
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