Transcript #00023997 (NM_006129.4, BMP1 gene)

Transcript name transcript variant 3
Gene name BMP1 (bone morphogenetic protein 1)
Chromosome 8
Transcript - NCBI ID NM_006129.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_006120.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2014-12-23 21:56:59 +01:00 (CET)
Date last edited N/A


Variants

136 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3539G>A r.(?) p.(=)
+/. - c.-2310T>C r.(?) p.(=)
-?/. - c.-2240C>T r.(?) p.(=)
-/. - c.-1882C>A r.(?) p.(=)
?/. - c.-1848_-1847dup r.(?) p.(=)
?/. - c.-1472C>T r.(?) p.(=)
?/. - c.-1418C>G r.(?) p.(=)
-/. - c.-1402G>A r.(?) p.(=)
-?/. - c.-1389C>T r.(?) p.(=)
-/. - c.-1036G>A r.(?) p.(=)
-/. - c.-985G>A r.(?) p.(=)
-?/. - c.6C>A r.(?) p.(Pro2=)
+/. - c.34G>C r.(?) p.(Gly12Arg)
+/+ 1 c.34G>C r.(?) p.(Gly12Arg)
+/+ 1 c.34G>C r.(?) p.(Gly12Arg)
+/+ 1 c.34G>C r.(?) p.(Gly12Arg)
+/+ 1 c.34G>C r.(?) p.(Gly12Arg)
+/+ 1 c.34G>C r.(?) p.(Gly12Arg)
?/. - c.118C>G r.(?) p.(Pro40Ala)
+/+ 1i c.148+1G>A r.spl p.spl?
-?/. - c.149-98T>G r.(=) p.(=)
?/. - c.161G>C r.(?) p.(Gly54Ala)
-?/. - c.239G>A r.(?) p.(Arg80His)
-?/. - c.239G>A r.(?) p.(Arg80His)
?/. - c.304G>T r.(?) p.(Gly102Trp)
-?/. - c.310C>T r.(?) p.(Pro104Ser)
-?/. - c.317G>A r.(?) p.(Arg106Lys)
?/. - c.413T>C r.(?) p.(Val138Ala)
?/. - c.416T>C r.(?) p.(Ile139Thr)
?/. - c.449T>A r.(?) p.(Val150Asp)
?/. - c.549C>T r.(?) p.(=)
-?/. - c.551+20C>T r.(=) p.(=)
-?/. - c.551+132C>T r.(=) p.(=)
-?/. - c.564C>T r.(?) p.(=)
+/. - c.584dup r.(?) p.(Gln197Profs*10)
?/? 5 c.688C>G r.(?) p.(Arg230Gly)
+/? 5 c.691G>T r.(?) p.(Asp231Tyr)
-/. - c.731-112dup r.(=) p.(=)
+/+ 6 c.747C>G r.(?) p.(Phe249Leu)
+/? 6 c.796_797del r.(?) p.(Phe266Argfs*25)
+/+ 6 c.808A>G r.(?) p.(Met270Val)
?/? 6 c.818C>T r.(?) p.(Ala273Val)
?/. - c.910C>T r.(?) p.(Arg304Trp)
+/+ 7 c.925del r.(?) p.(Asp309Thrfs*54)
?/. - c.925G>A r.(?) p.(Asp309Asn)
-?/. - c.941G>A r.(?) p.(Arg314His)
+/. 7 c.941G>A r.(941g>a) p.(Arg314His)
+/. - c.965G>A r.(?) p.(Cys322Tyr)
?/. - c.1094C>T r.(?) p.(Thr365Met)
-?/. - c.1112G>A r.(?) p.(Arg371His)
-/. - c.1112G>A r.(?) p.(Arg371His)
-?/. - c.1112G>A r.(?) p.(Arg371His)
?/. - c.1117C>T r.(?) p.(Arg373Cys)
?/. - c.1121T>C r.(?) p.(Leu374Pro)
+/? 9 c.1148G>A r.(?) p.(Arg383Gln)
-?/. - c.1180+6G>A r.(=) p.(=)
?/. - c.1250G>T r.(?) p.(Arg417Leu)
+/? 10 c.1293C>G r.(?) p.(Tyr431*)
+/+ 10 c.1297G>T r.(1181_1297del) p.?
-?/. - c.1297+14C>T r.(=) p.(=)
+?/+ 11 c.1324G>T r.(?) p.Asp441Tyr
?/. - c.1413C>G r.(?) p.(Phe471Leu)
?/. - c.1443+6T>C r.(=) p.(=)
?/. - c.1471G>A r.(?) p.(Asp491Asn)
+/+ 12 c.1492G>A r.(?) p.(Gly498Arg)
+/+ 12 c.1530T>G r.(?) p.(Cys510Trp)
?/. - c.1597G>C r.(?) p.(Gly533Arg)
?/. - c.1597G>C r.(?) p.(Gly533Arg)
-?/. - c.1639+10_1639+11del r.(=) p.(=)
-?/. - c.1639+10_1639+11del r.(=) p.(=)
-?/. - c.1639+12G>C r.(=) p.(=)
-?/. - c.1728C>T r.(?) p.(Pro576=)
./. 13i c.1766-492T>G r.(=) p.(=)
-?/. - c.1766-10G>A r.(=) p.(=)
-?/. - c.1766-5C>T r.spl? p.?
-/. - c.1766-5C>T r.spl? p.?
-/. - c.1770T>C r.(?) p.(Ala590=)
-?/. - c.1797C>T r.(?) p.(Asn599=)
?/. - c.1804A>G r.(?) p.(Ile602Val)
+/+ 14 c.1839del r.(?) p.(Asn614Thrfs*138)
?/. - c.1839dup r.(?) p.(Asn614Glnfs*21)
-?/. - c.1883G>A r.(?) p.(Arg628His)
-?/. - c.1926+81del r.(=) p.(=)
?/. - c.2044C>T r.(?) p.(Arg682Cys)
?/. - c.2075C>T r.(?) p.(Ser692Phe)
?/. - c.2093C>T r.(?) p.(Ala698Val)
+/+ 15 c.2107G>C r.(?) p.spl?
+/. - c.2108-683_2108-682del r.? p.?
?/. - c.2108-647C>G r.(=) p.(=)
+?/+ 20 c.2108-602T>C r.spl? p.(Ter731ArgextTer81)
+/? 15i c.2108-2A>G r.spl p.?
-/. - c.2115C>T r.(?) p.(Asp705=)
-?/. - c.2115C>T r.(=) p.(=)
-?/. - c.2115C>T r.(?) p.(Asp705=)
?/. - c.2134G>A r.(?) p.(Gly712Ser)
-?/. - c.2154C>T r.(?) p.(Cys718=)
-/. - c.2155G>A r.(?) p.(Val719Ile)
-?/. - c.2187C>T r.(?) p.(=)
+/+ 16 c.2188dup r.(?) p.(Gln730Profs*?)
+/? 16 c.2188dup r.(?) p.(Gln730Profs*?)
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