Transcript #00024025 (NM_080680.2, COL11A2 gene)

Transcript name transcript variant 1
Gene name COL11A2 (collagen, type XI, alpha 2)
Chromosome 6
Transcript - NCBI ID NM_080680.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_542411.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-03-13 12:33:23 +01:00 (CET)
Date last edited N/A


Variants

396 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-200G>A r.(?) p.(=)
-/. - c.-174C>A r.(?) p.(=)
?/. - c.5A>G r.(?) p.(Glu2Gly)
+/+ 2 c.109G>T r.(?) p.(Ala37Ser)
-?/. - c.150G>A r.(?) p.(Ala50=)
-?/. - c.230C>A r.(?) p.(Pro77Gln)
?/. - c.230C>A r.(?) p.(Pro77Gln)
-?/. - c.261G>C r.(?) p.(Leu87=)
?/. - c.278G>A r.(?) p.(Arg93His)
?/. - c.291A>G r.(?) p.(Gln97=)
-?/. - c.291A>G r.(?) p.(Gln97=)
-?/. - c.329G>A r.(?) p.(Arg110Gln)
?/. - c.353G>C r.(?) p.(Arg118Pro)
-?/. - c.353G>C r.(?) p.(Arg118Pro)
-?/. - c.353G>C r.(?) p.(Arg118Pro)
?/? 3 c.388C>T r.(?) p.(Arg130Trp)
?/. - c.388C>T r.(?) p.(Arg130Trp)
?/. - c.419G>A r.(?) p.(Arg140Gln)
?/. - c.434C>G r.(?) p.(Ala145Gly)
?/. - c.434C>G r.(?) p.(Ala145Gly)
-?/. - c.480T>G r.(?) p.(Ser160=)
?/. - c.484A>T r.(?) p.(Thr162Ser)
+/+ 4 c.529C>T r.(?) p.(Arg177*)
?/. - c.539G>A r.(?) p.(Arg180His)
?/. - c.539G>A r.(?) p.(Arg180His)
-?/. - c.544G>A r.(?) p.(Val182Ile)
-?/. - c.544G>A r.(?) p.(Val182Ile)
?/. - c.587T>C r.(?) p.(Leu196Pro)
?/. - c.587T>C r.(?) p.(Leu196Pro)
-?/. - c.622C>T r.(?) p.(Leu208=)
-?/. - c.622C>T r.(?) p.(Leu208=)
-?/. - c.622C>T r.(?) p.(Leu208=)
-?/. - c.628A>G r.(?) p.(Ile210Val)
+?/+? 5 c.654T>A r.(?) p.(Tyr218*)
?/. - c.688G>T r.(?) p.(Gly230Trp)
-?/. - c.706C>T r.(?) p.(Pro236Ser)
+/+ 5 c.733del r.(?) p.(Gln245Argfs*38)
?/. - c.743C>T r.(?) p.(Pro248Leu)
+/. - c.745C>T r.(?) p.(Gln249Ter)
-?/. - c.751C>A r.(?) p.(Gln251Lys)
+/. - c.798+23del r.(=) p.(=)
-?/. - c.798+38C>A r.(=) p.(=)
?/? 5i c.798+38C>A r.(=) p.(=)
-?/. - c.798+38C>A r.(=) p.(=)
?/. - c.798+56C>T r.(=) p.(=)
?/. - c.798+67C>T r.(=) p.(=)
-?/. - c.813C>T r.(?) p.(Leu271=)
+/. - c.813_814del r.(?) p.(Tyr272LeufsTer2)
-/. - c.826G>A r.(?) p.(Glu276Lys)
-/. - c.826G>A r.(?) p.(Glu276Lys)
-/. - c.877-4T>A r.spl? p.?
-/. - c.877-4T>A r.spl? p.?
-/. - c.877-4T>A r.spl? p.?
-?/. - c.882C>T r.(?) p.(Pro294=)
?/. - c.889G>A r.(?) p.(Gly297Ser)
?/. - c.889G>A r.(?) p.(Gly297Ser)
?/. - c.889G>A r.(?) p.(Gly297Ser)
?/. - c.910G>C r.(?) p.(Glu304Gln)
-?/. - c.914C>T r.(?) p.(Ser305Leu)
+/. - c.939+1G>A r.spl? p.?
+?/. - c.966dup r.(?) p.(Thr323HisfsTer19)
+/. - c.966dup r.(?) p.(Thr323HisfsTer19)
+/+ 8 c.966dup r.(?) p.(Thr323Hisfs*19)
-?/. - c.972C>T r.(?) p.(Ala324=)
?/. - c.973G>A r.(?) p.(Asp325Asn)
?/. - c.973G>A r.(?) p.(Asp325Asn)
+?/. - c.1032C>G r.(?) p.(Tyr344*)
?/. 8 c.1063C>T r.(?) p.(Arg355Cys)
?/. - c.1178C>T r.(?) p.(Pro393Leu)
-/. - c.1179+10G>A r.(=) p.(=)
-/. - c.1179+10G>A r.(=) p.(=)
-?/-? 10 c.1188C>T r.(=) p.(=)
-?/. - c.1197G>C r.(?) p.(Gly399=)
?/. - c.1198C>A r.(?) p.(Pro400Thr)
?/. - c.1220C>T r.(?) p.(Ala407Val)
?/. - c.1297C>G r.(?) p.(Arg433Gly)
?/. - c.1327C>G r.(?) p.(Pro443Ala)
?/. - c.1327C>T r.(?) p.(Pro443Ser)
?/. 12 c.1334C>T r.(?) p.(Pro445Leu)
-/. - c.1360-7A>C r.(=) p.(=)
-/. - c.1360-7A>C r.(=) p.(=)
-/. - c.1360-7A>C r.(=) p.(=)
-/. - c.1360-7A>C r.(=) p.(=)
?/. 13 c.1363C>T r.(?) p.(Arg455Trp)
+/+ 13 c.1363C>T r.(?) p.(Arg455Trp)
?/. - c.1363C>T r.(?) p.(Arg455Trp)
?/. - c.1363C>T r.(?) p.(Arg455Trp)
?/. - c.1380G>A r.(?) p.(Gly460=)
?/. - c.1382G>A r.(?) p.(Gly461Asp)
?/. - c.1382G>A r.(?) p.(Gly461Asp)
?/? 13 c.1427C>T r.(?) p.(Ala476Val)
+/. - c.1489C>T r.(?) p.(Arg497Cys)
?/. - c.1489C>T r.(?) p.(Arg497Cys)
-?/. - c.1504-9C>G r.(=) p.(=)
-?/. - c.1524C>T r.(?) p.(Gly508=)
?/. - c.1559G>A r.(?) p.(Gly520Asp)
-?/. - c.1581C>T r.(?) p.(Leu527=)
+?/+? 16 c.1607G>A r.(?) p.(Arg536Gln)
?/. - c.1607G>A r.(?) p.(Arg536Gln)
?/. - c.1607G>A r.(?) p.(Arg536Gln)
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