Transcript #00015840 (NM_000439.4, PCSK1 gene)

Transcript name transcript variant 1
Gene name PCSK1 (proprotein convertase subtilisin/kexin type 1)
Chromosome 5
Transcript - NCBI ID NM_000439.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000430.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-101T>C r.(?) p.(=)
-/. - c.-96C>T r.(?) p.(=)
+/. - c.18G>A r.(?) p.(Trp6Ter)
-/. - c.159G>A r.(?) p.(Leu53=)
+?/. - c.164del r.(?) p.(Tyr55Leufs*42)
-/. - c.180+647A>G r.(=) p.(=)
-?/. - c.180+757A>G r.(=) p.(=)
-/. - c.180+769T>C r.(=) p.(=)
-?/. - c.183T>C r.(?) p.(Ile61=)
?/. - c.190C>G r.(?) p.(Leu64Val)
-?/. - c.258C>T r.(?) p.(=)
-?/. - c.334G>A r.(?) p.(Ala112Thr)
-?/. - c.334G>A r.(?) p.(Ala112Thr)
+?/. - c.375G>A r.(?) p.(Met125Ile)
+/. - c.395T>A r.(?) p.(Leu132Ter)
-?/. - c.397-10T>C r.(=) p.(=)
-/. - c.397-10T>C r.(=) p.(=)
-?/. - c.397-10T>C r.(=) p.(=)
?/. - c.540C>A r.(?) p.(Asn180Lys)
?/. - c.541T>C r.(?) p.(Tyr181His)
?/. - c.541T>C r.(?) p.(Tyr181His)
?/. - c.599A>G r.(?) p.(Tyr200Cys)
-/. - c.612C>T r.(?) p.(Asn204=)
-/. - c.612C>T r.(?) p.(Asn204=)
-?/. - c.624C>T r.(?) p.(His208=)
-/. - c.661A>G r.(?) p.(Asn221Asp)
-/. - c.661A>G r.(?) p.(Asn221Asp)
?/. - c.710-4_714del r.spl? p.?
?/. - c.710-4_714del r.spl? p.?
-?/. - c.781G>A r.(?) p.(Val261Met)
?/. - c.801C>T r.(?) p.(Ser267=)
-/. - c.909C>T r.(?) p.(Phe303=)
-/. - c.927C>T r.(?) p.(Asn309=)
-?/. - c.945T>C r.(?) p.(=)
-?/. - c.1029C>T r.(?) p.(Tyr343=)
-/. - c.1095+123A>C r.(=) p.(=)
-/. - c.1096-10C>T r.(=) p.(=)
-/. - c.1146G>A r.(?) p.(Ser382=)
-?/. - c.1179T>C r.(?) p.(Ala393=)
-/. - c.1179T>G r.(?) p.(Ala393=)
-?/. - c.1196+19C>G r.(=) p.(=)
-/. - c.1196+219G>A r.(=) p.(=)
-/. - c.1197-305C>T r.(=) p.(=)
-?/. - c.1197-9C>T r.(=) p.(=)
-/. - c.1197-9C>T r.(=) p.(=)
-?/. - c.1430+7A>G r.(=) p.(=)
-?/. - c.1497T>C r.(?) p.(Asn499=)
-?/. - c.1518T>C r.(?) p.(His506=)
+?/. - c.1549C>T r.(?) p.(Arg517*)
?/. - c.1585G>A r.(?) p.(Ala529Thr)
-/. - c.1650T>C r.(?) p.(Asn550=)
-/. - c.1650T>C r.(?) p.(Asn550=)
-/. - c.1650T>C r.(?) p.(Asn550=)
-/. - c.1722+54A>G r.(=) p.(=)
-?/. - c.1764G>A r.(?) p.(Lys588=)
-/. - c.1764G>A r.(?) p.(Lys588=)
+?/. - c.1777G>A r.(?) p.(Gly593Arg)
+?/. - c.1777G>A r.(?) p.(Gly593Arg)
-?/. - c.1824G>A r.(?) p.(Thr608=)
?/. - c.1870G>A r.(?) p.(Val624Met)
-?/. - c.1884+13C>G r.(=) p.(=)
-?/. - c.1918A>G r.(?) p.(Thr640Ala)
-/. - c.1918A>G r.(?) p.(Thr640Ala)
-?/. - c.1918A>G r.(?) p.(Thr640Ala)
-?/. - c.1918A>G r.(?) p.(Thr640Ala)
-/. - c.1923G>A r.(?) p.(Leu641=)
-?/. - c.1950C>T r.(?) p.(=)
-?/. - c.1991C>T r.(?) p.(Ser664Phe)
-/. - c.1993C>G r.(?) p.(Gln665Glu)
-/. - c.1993C>G r.(?) p.(Gln665Glu)
-/. - c.2069G>C r.(?) p.(Ser690Thr)
-/. - c.2069G>C r.(?) p.(Ser690Thr)
-/. - c.2097C>T r.(?) p.(Asn699=)
-?/. - c.2214C>T r.(?) p.(Asp738=)
-?/. - c.2257A>C r.(?) p.(Asn753His)
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