Transcript #00015973 (NM_000285.3, PEPD gene)

Transcript name transcript variant 1
Gene name PEPD (peptidase D)
Chromosome 19
Transcript - NCBI ID NM_000285.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000276.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.34G>A r.(?) p.(Gly12Arg)
?/. - c.34G>A r.(?) p.(Gly12Arg)
?/. - c.34G>A r.(?) p.(Gly12Arg)
-?/. - c.57G>A r.(?) p.(Pro19=)
-?/. - c.62C>T r.(?) p.(Ala21Val)
+?/. - c.76_79dup r.(?) p.(Arg27Glnfs*7)
-?/. - c.100C>T r.(?) p.(Leu34=)
-?/. - c.100C>T r.(?) p.(Leu34=)
-?/. - c.100C>T r.(?) p.(Leu34=)
?/. - c.103C>T r.(?) p.(Arg35Trp)
?/. - c.103C>T r.(?) p.(Arg35Trp)
-?/. - c.104G>A r.(?) p.(Arg35Gln)
-?/. - c.126C>T r.(?) p.(Ala42=)
?/. - c.152G>A r.(?) p.(Gly51Glu)
?/. - c.178G>A r.(?) p.(Asp60Asn)
-?/. - c.183C>T r.(?) p.(Thr61=)
-?/. - c.183C>T r.(?) p.(Thr61=)
-?/. - c.259G>A r.(?) p.(Asp87Asn)
-?/. - c.385G>A r.(?) p.(Val129Ile)
+/. - c.418A>T r.(?) p.(Lys140Ter)
?/. - c.425C>T r.(?) p.(Ser142Phe)
-?/. - c.442-7_442-6del r.(=) p.(=)
-/. - c.442C>T r.(?) p.(Arg148Cys)
-?/. - c.442C>T r.(?) p.(Arg148Cys)
-/. - c.442C>T r.(?) p.(Arg148Cys)
-?/. - c.447C>T r.(?) p.(=)
-?/. - c.456G>A r.(?) p.(Thr152=)
-?/. - c.456G>A r.(?) p.(Thr152=)
-?/. - c.492C>T r.(?) p.(Asp164=)
-/. - c.509A>T r.(?) p.(Glu170Val)
-?/. - c.509A>T r.(?) p.(Glu170Val)
-/. - c.509A>T r.(?) p.(Glu170Val)
-?/. - c.511G>C r.(?) p.(Val171Leu)
+/. - c.549-1G>A r.(?) p.(?)
?/. - c.610G>A r.(?) p.(Glu204Lys)
+/. - c.611_623dup r.(?) p.(Val209Glyfs*4)
-?/. - c.624+16G>A r.(=) p.(=)
-?/. - c.624+16G>A r.(=) p.(=)
-?/. - c.625-9G>A r.(=) p.(=)
-/. - c.660T>C r.(?) p.(Tyr220=)
-?/. - c.660T>C r.(=) p.(=)
-?/. - c.660T>C r.(=) p.(=)
+?/. - c.692_694del r.(?) p.(Tyr231del)
?/. - c.710G>A r.(?) p.(Arg237His)
?/. - c.710G>A r.(?) p.(Arg237His)
?/. - c.710G>A r.(?) p.(Arg237His)
-?/. - c.726C>G r.(?) p.(Thr242=)
-/. - c.741-17C>A r.(=) p.(=)
-?/. - c.741-17C>A r.(=) p.(=)
-/. - c.744T>C r.(?) p.(Gly248=)
-?/. - c.744T>C r.(=) p.(=)
-?/. - c.751T>A r.(?) p.(Ser251Thr)
?/. - c.768C>G r.(?) p.(Tyr256Ter)
+/. - c.768C>G r.(?) p.(Tyr256Ter)
?/. - c.789C>A r.(?) p.(Asn263Lys)
-?/. - c.796A>G r.(?) p.(Thr266Ala)
-?/. - c.807T>A r.(?) p.(Asn269Lys)
-?/. - c.807T>A r.(?) p.(Asn269Lys)
?/. - c.818+5G>C r.spl? p.?
-?/. - c.823T>C r.(?) p.(Phe275Leu)
?/. - c.841T>A r.(?) p.(Tyr281Asn)
-/. - c.863T>C r.(?) p.(Ile288Thr)
-/. - c.863T>C r.(?) p.(Ile288Thr)
?/. - c.886G>A r.(?) p.(Gly296Ser)
?/. - c.886G>A r.(?) p.(Gly296Ser)
-?/. - c.913G>A r.(?) p.(Val305Ile)
?/. - c.946G>A r.(?) p.(Val316Ile)
-?/. - c.967+20G>C r.(=) p.(=)
-/. - c.967+20G>C r.(=) p.(=)
?/. - c.968-3C>G r.spl? p.?
-?/. - c.1016A>C r.(?) p.(Glu339Ala)
+?/. - c.1051del r.(?) p.(Val351TrpfsTer107)
?/. - c.1051G>A r.(?) p.(Val351Met)
-?/. - c.1098C>T r.(?) p.(His366=)
-?/. - c.1098C>T r.(?) p.(His366=)
-?/. - c.1125C>T r.(?) p.(Asp375=)
-?/. - c.1125C>T r.(?) p.(Asp375=)
-/. - c.1131C>T r.(?) p.(His377=)
-/. - c.1131C>T r.(?) p.(His377=)
-?/. - c.1134C>T r.(?) p.(Asp378=)
-/. - c.1163G>A r.(?) p.(Arg388His)
-?/. - c.1163G>A r.(?) p.(Arg388His)
-?/. - c.1163G>A r.(?) p.(Arg388His)
-?/. - c.1173G>A r.(?) p.(Glu391=)
-?/. - c.1184G>A r.(?) p.(Arg395Gln)
-?/. - c.1195A>G r.(?) p.(Thr399Ala)
-/. - c.1256A>G r.(?) p.(Asp419Gly)
-?/. - c.1281G>A r.(?) p.(Ala427=)
-/. - c.1294G>A r.(?) p.(Ala432Thr)
-?/. - c.1294G>A r.(?) p.(Ala432Thr)
-?/. - c.1294G>A r.(?) p.(Ala432Thr)
?/. - c.1301T>C r.(?) p.(Phe434Ser)
-/. - c.1303C>T r.(?) p.(Leu435Phe)
-?/. - c.1317C>T r.(?) p.(Val439=)
-?/. - c.1317C>T r.(?) p.(Val439=)
?/. - c.1325G>A r.(?) p.(Arg442His)
?/. - c.1325G>A r.(?) p.(Arg442His)
-?/. - c.1329T>C r.(?) p.(Phe443=)
?/. - c.1330C>T r.(?) p.(Arg444Cys)
-?/. - c.1333G>T r.(?) p.(Gly445Cys)
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