Transcript #00005493 (NM_030582.3, COL18A1 gene)

Transcript name transcript variant 1
Gene name COL18A1 (collagen, type XVIII, alpha 1)
Chromosome 21
Transcript - NCBI ID NM_030582.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_085059.2
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

461 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-50305del r.(?) p.(=)
?/. - c.? r.(?) p.?
-?/. - c.56C>T r.(?) p.(Ala19Val)
-?/. - c.65G>A r.(?) p.(Arg22Gln)
+/. - c.73del r.(?) p.(Leu25CysfsTer2)
-?/. - c.111C>T r.(?) p.(Asp37=)
-/. - c.120T>C r.(?) p.(His40=)
-/. - c.120T>C r.(?) p.(His40=)
-?/. - c.121G>A r.(?) p.(Ala41Thr)
-?/. - c.142C>G r.(?) p.(Pro48Ala)
-?/. - c.171A>G r.(?) p.(Thr57=)
?/. - c.179C>T r.(?) p.(Thr60Ile)
-?/. - c.199del r.(?) p.(Arg67Glyfs*49)
?/. - c.199dup r.(?) p.(Arg67Profs*15)
-?/. - c.200G>A r.(?) p.(Arg67Gln)
-?/. - c.200G>A r.(?) p.(Arg67Gln)
-?/. - c.300G>A r.(?) p.(Pro100=)
-?/. - c.312G>A r.(?) p.(Glu104=)
?/. - c.325G>A r.(?) p.(Gly109Ser)
-/. - c.330C>T r.(?) p.(Val110=)
-?/. - c.349G>A r.(?) p.(Val117Met)
-?/. - c.358G>A r.(?) p.(Gly120Ser)
?/. - c.359G>A r.(?) p.(Gly120Asp)
-?/. - c.430G>A r.(?) p.(Val144Ile)
?/. - c.450C>G r.(?) p.(Gly150=)
+?/. - c.484del r.(?) p.(Gln162ArgfsTer142)
?/. - c.514C>T r.(?) p.(Arg172Cys)
-?/. - c.515G>A r.(?) p.(Arg172His)
-?/. - c.515G>A r.(?) p.(Arg172His)
-?/. - c.517G>A r.(?) p.(Gly173Ser)
-?/. - c.517G>A r.(?) p.(Gly173Ser)
-?/. - c.534G>T r.(?) p.(Pro178=)
-/. - c.538G>A r.(?) p.(Ala180Thr)
-?/. - c.538G>A r.(?) p.(Ala180Thr)
-?/. - c.549C>T r.(?) p.(Thr183=)
-/. - c.560C>T r.(?) p.(Thr187Ile)
-?/. - c.600G>T r.(?) p.(Arg200Ser)
-?/. - c.601C>T r.(?) p.(Pro201Ser)
-/. - c.639A>G r.(?) p.(Pro213=)
?/. - c.646+16C>T r.(=) p.(=)
-?/. - c.646+33G>A r.(=) p.(=)
-/. - c.646+66A>C r.(=) p.(=)
-/. - c.646+83C>T r.(=) p.(=)
?/. - c.646+126C>T r.(=) p.(=)
-?/. - c.646+184C>A r.(=) p.(=)
-?/. - c.646+191C>T r.(=) p.(=)
-/. - c.646+216G>A r.(=) p.(=)
-?/. - c.646+231G>A r.(=) p.(=)
-/. - c.646+347C>T r.(=) p.(=)
?/. - c.646+399_646+415dup r.(=) p.(=)
-?/. - c.646+440C>T r.(=) p.(=)
-?/. - c.646+470G>A r.(=) p.(=)
-?/. - c.646+478dup r.(=) p.(=)
?/. - c.646+480del r.(=) p.(=)
-?/. - c.646+490C>G r.(=) p.(=)
-/. - c.646+490C>T r.(=) p.(=)
?/. - c.646+564G>A r.(=) p.(=)
-?/. - c.646+564G>A r.(=) p.(=)
-?/. - c.646+568C>T r.(=) p.(=)
?/. - c.646+587C>A r.(=) p.(=)
?/. - c.646+587C>A r.(=) p.(=)
-?/. - c.646+623G>C r.(=) p.(=)
-?/. - c.646+644C>T r.(=) p.(=)
?/. - c.658G>A r.(?) p.(Glu220Lys)
-?/. - c.666G>A r.(?) p.(Val222=)
-?/. - c.690C>T r.(?) p.(Asp230=)
?/. - c.738G>C r.(?) p.(Leu246=)
-?/. - c.801C>G r.(?) p.(Leu267=)
-?/. - c.828C>T r.(?) p.(Phe276=)
?/. - c.836G>A r.(?) p.(Arg279Gln)
?/. - c.884C>T r.(?) p.(Ala295Val)
?/. - c.908T>A r.(?) p.(Val303Glu)
-/. - c.960A>G r.(?) p.(Thr320=)
+/. - c.969dup r.(?) p.(Ala324Cysfs*38)
-?/. - c.990C>T r.(?) p.(Ala330=)
-?/. - c.1008C>T r.(?) p.(Pro336=)
-?/. - c.1036G>A r.(?) p.(Ala346Thr)
-/. - c.1050A>G r.(?) p.(Ala350=)
?/. - c.1070A>G r.(?) p.(Tyr357Cys)
-?/. - c.1087T>C r.(?) p.(Phe363Leu)
?/. - c.1117C>T r.(?) p.(Arg373Trp)
-/. - c.1143C>T r.(?) p.(Ala381=)
?/. - c.1144G>A r.(?) p.(Gly382Arg)
-?/. - c.1152C>T r.(?) p.(Phe384=)
-/. - c.1152C>T r.(?) p.(Phe384=)
?/. - c.1153G>A r.(?) p.(Val385Met)
-/. - c.1164G>A r.(?) p.(Ala388=)
?/. - c.1165G>A r.(?) p.(Gly389Arg)
-?/. - c.1191+6C>G r.(=) p.(=)
-?/. - c.1207C>T r.(?) p.(Leu403=)
?/. - c.1216C>T r.(?) p.(Arg406Cys)
?/. - c.1228dup r.(?) p.(Gln410ProfsTer14)
?/. - c.1231G>A r.(?) p.(Val411Met)
-?/. - c.1231G>A r.(?) p.(Val411Met)
-?/. - c.1233G>A r.(?) p.(Val411=)
?/. - c.1233G>A r.(?) p.(Val411=)
-?/. - c.1278+19A>C r.(=) p.(=)
-/. - c.1278+20C>T r.(=) p.(=)
?/. - c.1283C>T r.(?) p.(Ser428Phe)
?/. - c.1300G>A r.(?) p.(Gly434Arg)
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