Transcript #00005456 (NM_000089.3, COL1A2 gene)

Transcript name collagen, type I, alpha 2
Gene name COL1A2 (collagen type I alpha 2 chain)
Chromosome 7
Transcript - NCBI ID NM_000089.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000080.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

1640 entries on 17 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predicted     

Legacy protein change     
+/. 17 [NM_181678.2:c.-48-58227]::c.869del r.? p.? - -
+/+ _1_18i c.-471_(936+1_937-1){0} r.0? p.0? deletion, multi exon -
+/+ 1i c.70+717A>G r.(?) p.? other/complex -
-?/. 1i c.71-17C>T r.(=) p.(=) - -
-/. 1i c.71-8_71-7dup r.(=) p.(=) - -
-/. 1i c.71-7dup r.(=) p.(=) - -
-?/. 2i c.81+10A>G r.(=) p.(=) - -
-?/. 2i c.81+11del r.(=) p.(=) - -
-?/. 2i c.81+15T>C r.(=) p.(=) - -
-?/. 2i c.81+15T>C r.(=) p.(=) - -
-/. 2i c.82-12A>G r.(=) p.(=) - -
-/. 3 c.87T>C r.(?) p.(Thr29=) - -
-/- 3 c.87T>C r.(?) p.(=) silent -
-?/-? 4 c.118C>A r.(?) p.(Pro40Thr) missense -
-/. - c.132+31G>A r.(=) p.(=) - -
-?/. 4i c.133-304G>A r.(=) p.(=) - -
+/+ 5 c.133G>T r.(?) p.(Gly45Cys) missense -
+?/. - c.152_157dup r.(?) p.(Gly51_Arg52dup) - -
-?/. 5 c.180C>A r.(?) p.(Gly60=) - -
+?/. 5 c.197G>A r.(?) p.(Gly66Asp) - -
+?/. 5 c.197G>A r.(?) p.(Gly66Asp) - -
+?/. 5 c.197G>A r.(?) p.(Gly66Asp) - -
+/+? 5 c.214G>A r.(?) p.(Gly72Ser) missense -
+/+ 5i c.226-22_226-11del r.spl p.? splicing affected? -
+/+ 5i_6i c.226-17_279+12del r.spl p.(Asn76_Met93del) deletion, exon -
-/. 5i c.226-11del r.(=) p.(=) - -
-/. 5i c.226-11dup r.(=) p.(=) - -
-/. - c.226-11dup r.(=) p.(=) - -
-?/. 5i c.226-10A>T r.(=) p.(=) - -
-?/. 5i c.226-9C>T r.(=) p.(=) - -
-?/. 5i c.226-6C>T r.(=) p.(=) - -
+/+ 5i c.226-2A>G r.spl p.? splicing affected? -
+/+ 5i c.226-2A>G r.spl p.? splicing affected? -
+/+ 5i c.226-2A>G r.spl p.? splicing affected? -
+/. - c.226-2A>G r.spl? p.? - -
+/+ 5i c.226-1G>A r.spl p.? splicing affected? -
+/+ 5i c.226-1G>C r.spl p.? splicing affected? -
-/. 6 c.246T>C r.(?) p.(Asp82=) - -
-/- 6 c.246T>C r.(?) p.(=) silent -
+/+ 6 c.279G>A r.(?) p.(Met93Ile) splicing affected? Met3Ile
+/+ 6 c.279G>A r.(?) p.(Met93Ile) splicing affected? Met3Ile
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>A r.spl p.? splicing affected? -
+/+ 6i c.279+1G>C r.spl p.? splicing affected? -
+/+ 6i c.279+1G>T r.spl p.? splicing affected? -
+/+ 6i c.279+1G>T r.spl p.? splicing affected? -
+/+ 6i c.279+1G>T r.spl p.? splicing affected? -
+/+ 6i c.279+1G>T r.spl p.? splicing affected? -
+/+ 6i c.279+1G>T r.spl p.? splicing affected? -
+?/. 6i c.279+1_279+5del r.spl p.? - -
+/+ 6i c.279+2T>C r.spl p.? splicing affected? -
+/+ 6i c.279+2T>C r.spl p.? splicing affected? -
+/+ 6i c.279+2T>C r.spl p.? splicing affected? -
+/+ 6i c.279+2T>C r.spl p.? splicing affected? -
+/+ 6i c.279+2T>G r.spl p.? splicing affected? -
+/. 6i c.279+2T>G r.spl p.? - -
+/+ 6i_11i c.280-1149_540+63del r.? p.(Gly94_Arg180del) deletion, multi exon -
?/- 7 c.287T>A r.(?) p.(Met96Lys) missense -
+/+ 7 c.293dup r.(?) p.(Arg99*) frameshift -
+/. 7 c.299G>A r.(?) p.(Gly100Asp) missense -
-?/. 7 c.304C>T r.(?) p.(Pro102Ser) - -
?/-? 7 c.304C>T r.(?) p.(Pro102Ser) missense Pro12Ser
-/-? 7 c.304C>T r.(?) p.(Pro102Ser) missense Pro12Ser
-?/. 7 c.304C>T r.(?) p.(Pro102Ser) - -
+/+ 7 c.316G>A r.(?) p.(Gly106Arg) missense -
+/+ 7i c.324+4del r.spl? p.? splicing affected? -
+/+ 8 c.326G>A r.(?) p.(Gly109Asp) missense Gly19Asp
+/+ 8 c.326G>A r.(?) p.(Gly109Asp) missense Gly19Asp
+?/+ 8 c.326G>T r.(?) p.(Gly109Val) missense -
?/. 8 c.329C>T r.(?) p.(Pro110Leu) - -
+/+ 8 c.335G>A r.(?) p.(Gly112Asp) missense Gly22Asp
+?/. 8 c.335G>T r.(?) p.(Gly112Val) - -
+/+ 8 c.335G>T r.(?) p.(Gly112Val) missense Gly22Val
+/+ 8 c.335G>T r.(?) p.(Gly112Val) missense Gly22Val
+/+ 8 c.335G>T r.(?) p.(Gly112Val) missense Gly22Val
+/+ 8 c.335G>T r.(?) p.(Gly112Val) missense Gly22Val
+/+ 8 c.343G>A r.(?) p.(Gly115Arg) missense Gly25Arg
+?/. 8 c.353G>A r.(?) p.(Gly118Asp) - -
+/+ 8 c.353G>A r.(?) p.(Gly118Asp) missense Gly28Asp
+/+ 8 c.353G>T r.(?) p.(Gly118Val) missense -
+/+ 8 c.362G>A r.(?) p.(Gly121Asp) missense Gly31Asp
+/+ 8 c.371G>A r.(?) p.(Gly124Asp) missense Gly34Asp
+/+ 8 c.371G>A r.(?) p.(Gly124Asp) missense Gly34Asp
+/+ 8 c.371G>A r.(?) p.(Gly124Asp) missense Gly34Asp
+/+ 9 c.380G>A r.(?) p.(Gly127Asp) missense Gly37Asp
+/+ 9 c.380G>A r.(?) p.(Gly127Asp) missense Gly37Asp
+/+ 9 c.389G>A r.(?) p.(Gly130Asp) missense Gly40Asp
-?/. 9 c.390T>A r.(?) p.(Gly130=) - -
+/. - c.395G>A r.(?) p.(Arg132His) missense -
+/+ 9 c.397G>A r.(?) p.(Gly133Ser) missense Gly43Ser
+?/. 9 c.406G>A r.(?) p.(Gly136Ser) - -
+?/+ 9 c.407G>A r.(?) p.(Gly136Asp) missense Gly46Asp
+/+ 9 c.416G>T r.(?) p.(Gly139Val) missense Gly49Val
+?/. 9 c.425G>A r.(?) p.(Gly142Asp) - -
+/+ 9i c.432+1G>A r.spl p.? splicing affected -
+/+ 9i c.432+1G>A r.spl p.? splicing affected? -
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