Transcript #00025673 (NM_001854.3, COL11A1 gene)

Transcript name transcript variant A
Gene name COL11A1 (collagen, type XI, alpha 1)
Chromosome 1
Transcript - NCBI ID NM_001854.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001845.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2021-12-27 10:47:17 +01:00 (CET)
Date last edited N/A


Variants

589 entries on 6 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.52A>T r.(?) p.(Thr18Ser)
-?/. - c.70T>C r.(?) p.(Leu24=)
-?/. - c.81C>T r.(?) p.(Leu27=)
-?/. - c.97G>A r.(?) p.(Val33Ile)
-?/. - c.97G>A r.(?) p.(Val33Ile)
?/. - c.97G>A r.(?) p.(Val33Ile)
-?/. - c.106+6A>G r.(=) p.(=)
-?/. - c.129A>G r.(?) p.(Lys43=)
-/. - c.130G>A r.(?) p.(Ala44Thr)
-/. - c.130G>A r.(?) p.(Ala44Thr)
-/. - c.138T>G r.(?) p.(Asp46Glu)
-/. - c.138T>G r.(?) p.(Asp46Glu)
-/. - c.138T>G r.(?) p.(Asp46Glu)
-/. - c.138T>G r.(?) p.(Asp46Glu)
?/. 2 c.146A>G r.(?) p.(Asn49Ser)
+/. - c.158G>A r.(?) p.(Gly53Glu)
?/. 2 c.185C>G r.(?) p.(Thr62Arg)
?/. - c.202A>G r.(?) p.(Lys68Glu)
?/? - c.215C>G r.(?) p.(Thr72Ser)
?/. - c.226G>C r.(?) p.(Val76Leu)
+/. - c.274+1G>A r.spl? p.?
-/. - c.275-17del r.(=) p.(=)
-/. - c.275-7T>C r.(=) p.(=)
-/. - c.275-7T>C r.(=) p.(=)
-?/. - c.318A>G r.(?) p.(Lys106=)
-?/. - c.318A>G r.(?) p.(Lys106=)
-?/. - c.323A>G r.(?) p.(Lys108Arg)
?/. - c.328G>C r.(?) p.(Gly110Arg)
?/. - c.328G>C r.(?) p.(Gly110Arg)
-?/. - c.328G>C r.(?) p.(Gly110Arg)
-?/. - c.328G>C r.(?) p.(Gly110Arg)
-?/. - c.328G>C r.(?) p.(Gly110Arg)
?/. - c.344T>G r.(?) p.(Leu115Arg)
?/. - c.365A>C r.(?) p.(His122Pro)
?/. - c.419A>G r.(?) p.(Glu140Gly)
-?/. - c.426C>T r.(?) p.(=)
-?/. - c.439G>A r.(?) p.(Ala147Thr)
?/. - c.442C>G r.(?) p.(Pro148Ala)
?/. - c.442C>G r.(?) p.(Pro148Ala)
?/. - c.478G>A r.(?) p.(Ala160Thr)
?/. - c.478G>A r.(?) p.(Ala160Thr)
+/. - c.484G>A r.(?) p.(Gly162Arg)
+?/. - c.484G>A r.(?) p.(Gly162Arg)
-?/. - c.489-4T>A r.spl? p.?
?/. - c.497G>T r.(?) p.(Arg166Leu)
?/. - c.512T>C r.(?) p.(Val171Ala)
?/. - c.545G>T r.(?) p.(Cys182Phe)
+?/. - c.560C>T r.(?) p.(Thr187Met)
?/. - c.560C>T r.(?) p.(Thr187Met)
+/+ - c.560C>T r.(?) p.(Thr187Met)
?/. - c.565C>A r.(?) p.(Pro189Thr)
-?/. - c.612G>T r.(?) p.(Thr204=)
-?/. - c.612G>T r.(?) p.(Thr204=)
-/. - c.651+16A>G r.(=) p.(=)
-?/. - c.652-14_652-13insGTTT r.(=) p.(=)
-/. - c.652-13T>G r.(=) p.(=)
-?/. - c.652-9_652-6dup r.(=) p.(=)
-?/. - c.652-8_652-6dup r.(=) p.(=)
-/. - c.652-8_652-6dup r.(=) p.(=)
-?/. - c.652-8_652-6dup r.(=) p.(=)
-/. - c.652-8_652-6dup r.(=) p.(=)
-/. - c.652-8_652-6dup r.(=) p.(=)
-/. - c.652-7T>C r.(=) p.(=)
-/. - c.652-7_652-6del r.(=) p.(=)
-/. - c.652-7_652-6del r.(=) p.(=)
-/. - c.652-7_652-6dup r.(=) p.(=)
-?/. - c.652-7_652-6dup r.(=) p.(=)
-/. - c.652-7_652-6dup r.(=) p.(=)
-?/. - c.652-6del r.(=) p.(=)
-/. - c.652-6del r.(=) p.(=)
-?/. - c.652-6del r.(=) p.(=)
-?/. - c.652-6del r.(=) p.(=)
-/. - c.652-6del r.(=) p.(=)
-/. - c.652-6del r.(=) p.(=)
-?/. - c.652-6dup r.(=) p.(=)
-?/. - c.652-6dup r.(=) p.(=)
-/. - c.652-6dup r.(=) p.(=)
-?/. - c.652-6dup r.(=) p.(=)
-/. - c.652-6dup r.(=) p.(=)
-?/. - c.652-6_652-5insTTC r.spl? p.?
+?/. - c.652-1G>C r.[652_663del,652_666del] p.[Gly218_Gln221del,Gly218_Gln222del]
+?/. - c.652-1G>C r.[652_663del,652_666del] p.[Gly218_Gln221del,Gly218_Gln222del]
?/. - c.652G>A r.(?) p.(Gly218Arg)
-/. - c.660T>C r.(?) p.(Ile220=)
-/. - c.660T>C r.(?) p.(Ile220=)
-/. - c.660T>C r.(?) p.(Ile220=)
-?/. - c.682G>A r.(?) p.(Asp228Asn)
-?/. - c.698A>G r.(?) p.(Tyr233Cys)
?/. - c.725A>G r.(?) p.(Asp242Gly)
-?/. - c.747G>A r.(?) p.(Lys249=)
+?/. - c.767del r.(?) p.(Pro256LeufsTer3)
-?/. - c.780+30C>T r.(=) p.(=)
-/. - c.780+52C>A r.(=) p.(=)
+/+ - c.781-70T>G r.(=) p.?
-?/. - c.828A>T r.(?) p.(Ala276=)
?/. 6 c.833A>G r.(?) p.(Tyr278Cys)
?/? - c.893C>T r.(=) p.(Thr298Met)
?/. - c.893C>T r.(?) p.(Thr298Met)
?/. - c.897+285A>T r.(=) p.(=)
-/. - c.898-292A>C r.(=) p.(=)
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