Transcript #00025505 (NM_182943.2, PLOD2 gene)

Transcript name transcript variant 1
Gene name PLOD2 (procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2)
Chromosome 3
Transcript - NCBI ID NM_182943.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_891988.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-04-30 17:14:36 +02:00 (CEST)
Date last edited N/A


Variants

91 entries on 1 page. Showing entries 1 - 91.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.201+100C>T r.(=) p.(=)
?/. - c.205C>T r.(?) p.(Leu69Phe)
-?/. - c.247A>G r.(?) p.(Ser83Gly)
-?/. - c.306T>A r.(?) p.(Asp102Glu)
-?/. - c.306T>A r.(?) p.(Asp102Glu)
?/. - c.335A>G r.(?) p.(Glu112Gly)
-/. - c.338+4G>A r.spl? p.?
-/. - c.338+4G>A r.spl? p.?
?/. - c.382A>G r.(?) p.(Lys128Glu)
?/. - c.382A>G r.(?) p.(Lys128Glu)
+?/. - c.392_411del r.(?) p.(Lys131IlefsTer11)
?/. - c.464C>A r.(?) p.(Pro155His)
-?/. - c.475A>T r.(?) p.(Ile159Phe)
+?/. - c.497C>G r.(?) p.(Ser166*)
+/. - c.497C>G r.(?) p.(Ser166*)
+/. - c.497C>G r.(?) p.(Ser166*)
+/. - c.503-2A>G r.spl p.?
+/. 4i c.503-2A>G r.spl p.?
+?/. - c.517G>C r.(?) p.(Ala173Pro)
?/. - c.587C>T r.(?) p.(Thr196Ile)
-?/. - c.587C>T r.(?) p.(Thr196Ile)
+?/. - c.615+5G>T r.(?) p.(?)
-?/. - c.615+221T>C r.(=) p.(=)
-/. - c.652A>G r.(?) p.(Ile218Val)
-?/. - c.652A>G r.(?) p.(Ile218Val)
+?/. - c.797G>T r.(?) p.(Gly266Val)
+?/. - c.797G>T r.(?) p.(Gly266Val)
?/. - c.803A>C r.(?) p.(Tyr268Ser)
-?/. - c.805G>A r.(?) p.(Val269Ile)
?/. - c.808C>T r.(?) p.(Pro270Ser)
-?/. - c.880-286T>C r.(=) p.(=)
?/. - c.892G>A r.(?) p.(Val298Ile)
-?/. - c.918A>G r.(?) p.(=)
-?/. - c.1005+10del r.(=) p.(=)
-?/. - c.1006-9_1006-8del r.(=) p.(=)
?/. - c.1076T>G r.(?) p.(Ile359Arg)
-?/. - c.1108G>A r.(?) p.(Glu370Lys)
-/. - c.1128-82A>T r.(=) p.(=)
-/. - c.1128-78A>G r.(=) p.(=)
-?/. - c.1128G>A r.(?) p.(Met376Ile)
+/. - c.1138C>T r.(?) p.(Arg380Cys)
+/. - c.1138C>T r.(?) p.(Arg380Cys)
+/. 11 c.1138C>T r.(?) p.(Arg380Cys)
+/. - c.1153T>C r.(?) p.(Cys385Arg)
?/. - c.1259G>A r.(?) p.(Arg420His)
+?/. - c.1280A>G r.(?) p.(Asn427Ser)
+/. - c.1358+5G>A r.spl p.?
+/. - c.1358+5G>A r.spl p.?
+?/. - c.1418G>A r.(?) p.(Arg473Gln)
?/. - c.1418G>A r.(?) p.(Arg473Gln)
-/. - c.1500+12A>G r.(=) p.(=)
-/. - c.1500+12A>G r.(=) p.(=)
?/. - c.1523C>T r.(?) p.(Ser508Phe)
+/. - c.1559dup r.(?) p.(Val523Cysfs*7)
+/. - c.1559dup r.(?) p.(Val523Cysfs*7)
-?/. - c.1564-19G>A r.(=) p.(=)
+/. - c.1624del r.(?) p.(Tyr542Thrfs*25)
-?/. - c.1639T>C r.(?) p.(Tyr547His)
-?/. - c.1644C>T r.(?) p.(Asn548=)
-?/. - c.1678-12T>C r.(=) p.(=)
+/. - c.1682G>A r.(?) p.(Trp561*)
-?/. - c.1744-20C>T r.(=) p.(=)
+/. - c.1754A>T r.(?) p.(Asp585Val)
+/. - c.1754A>T r.(?) p.(Asp585Val)
+/. - c.1764G>T r.(?) p.(Trp588Cys)
?/. - c.1772T>A r.(?) p.(Ile591Lys)
+/. - c.1828T>C r.(?) p.(Trp610Arg)
-?/. - c.1848+143C>T r.(=) p.(=)
+/+ 17 c.1856G>A r.? p.(Arg619His)
+/. - c.1856G>A r.(?) p.(Arg619His)
+/. - c.1856G>A r.(?) p.(Arg619His)
+/. - c.1856G>A r.(?) p.(Arg619His)
+/. - c.1864G>T r.(?) p.(Gly622Cys)
+/. - c.1864G>T r.(?) p.(Gly622Cys)
+/. - c.1865G>T r.(?) p.(Gly622Val)
+/. - c.1880T>C r.(?) p.(Val627Ala)
+/. - c.1886C>T r.(?) p.(Thr629Ile)
?/. - c.1942C>T r.(?) p.(Arg648Trp)
+/. - c.1982G>A r.(?) p.(Gly661Asp)
+?/. - c.1991C>T r.(?) p.(Thr664Met)
?/. - c.1995+3A>C r.spl? p.?
+/. - c.2038C>T r.(?) p.(Arg680*)
+/. - c.2060A>G r.(?) p.(His687Arg)
+/. - c.2060A>G r.(?) p.(His687Arg)
-?/. - c.2121+14T>C r.(=) p.(=)
?/. - c.2122-4T>A r.spl? p.?
+/. - c.2122-2A>G r.spl p.?
+/. - c.2122-2A>G r.spl p.?
-?/. - c.2184C>G r.(?) p.(Ser728Arg)
-/. - c.2229T>C r.(?) p.(Pro743=)
?/. - c.2273C>G r.(?) p.(Pro758Arg)
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