Transcript #00003426 (NM_001202.3, BMP4 gene)

Transcript name transcript variant 1
Gene name BMP4 (bone morphogenetic protein 4)
Chromosome 14
Transcript - NCBI ID NM_001202.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001193.2
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

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.-2411514_*658706del r.0? p.0?
?/. - c.-347A>T r.(?) p.(=)
+/. - c.-132-1G>A r.spl p.?
./. - c.-132-1G>A r.spl? p.?
?/. - c.-115C>T r.(?) p.(=)
-/. - c.-7-39A>G r.(=) p.(=)
?/. - c.16C>G r.(?) p.(Arg6Gly)
+?/. - c.16C>T r.(?) p.(Arg6Ter)
-?/. - c.30C>G r.(?) p.(Val10=)
-?/. - c.76T>C r.(?) p.(Leu26=)
-?/. - c.76T>C r.(?) p.(Leu26=)
-?/. - c.76T>C r.(?) p.(Leu26=)
-/. - c.76T>C r.(?) p.(Leu26=)
-?/. - c.76T>C r.(?) p.(Leu26=)
-?/. - c.118G>A r.(?) p.(Gly40Ser)
?/. - c.124G>C r.(?) p.(Ala42Pro)
./. - c.124G>C r.(?) p.(Ala42Pro)
+/. 3 c.130G>T r.(130g>u) p.(Gly44*)
+/. 3 c.130G>T r.(130g>u) p.(Gly44*)
+/. 3 c.130G>T r.(130g>u) p.(Gly44*)
+/. 3 c.130G>T r.(130g>u) p.(Gly44*)
+/. 3 c.130G>T r.(130g>u) p.(Gly44*)
-?/. - c.228T>A r.(?) p.(Ser76Arg)
./. - c.228T>A r.(?) p.(Ser76Arg)
./. - c.250C>G r.(?) p.(Arg84Gly)
./. - c.272C>G r.(?) p.(Ser91Cys)
?/. 3 c.278A>G r.(?) p.(Glu93Gly)
-?/. - c.345C>T r.(?) p.(Asn115=)
-?/. - c.345C>T r.(?) p.(Asn115=)
-/. - c.345C>T r.(?) p.(Asn115=)
-/. - c.348C>T r.(?) p.(Thr116=)
-?/. - c.348C>T r.(?) p.(Thr116=)
-?/. - c.362A>G r.(?) p.(His121Arg)
./. - c.362A>G r.(?) p.(His121Arg)
+/. - c.367G>T r.(?) p.(Glu123*)
-?/. - c.370+28G>A r.(=) p.(=)
?/. - c.416G>A r.(?) p.(Arg139His)
+?/. - c.450C>G r.(?) p.(Asn150Lys)
-/. - c.455T>C r.(?) p.(Val152Ala)
-/. - c.455T>C r.(?) p.(Val152Ala)
-/- 4 c.455T>C r.(?) p.(Val152Ala)
-/- 4 c.455T>C r.(?) p.(Val152Ala)
-/. - c.455T>C r.(?) p.(Val152Ala)
-/. - c.455T>C r.(?) p.(Val152Ala)
?/. 4 c.461C>T r.(?) p.(Ser154Phe)
./. - c.464C>T r.(?) p.(Ser155Phe)
-?/. - c.502G>C r.(?) p.(Gly168Arg)
+?/. - c.502G>C r.(?) p.(Gly168Arg)
./. - c.566A>T r.(?) p.(Glu189Val)
?/. - c.608del r.(?) p.(Arg203AsnfsTer7)
+?/. - c.619C>G r.(?) p.(His207Asp)
-?/. - c.673A>G r.(?) p.(Thr225Ala)
?/. 4 c.673A>G r.(?) p.(Thr225Ala)
?/. - c.676C>T r.(?) p.(Arg226Trp)
?/. 4 c.676C>T r.(?) p.(Arg226Trp)
?/. 4 c.676C>T r.(?) p.(Arg226Trp)
./. - c.676C>T r.(?) p.(Arg226Trp)
?/. - c.722T>A r.(?) p.(Leu241His)
?/. - c.731C>T r.(?) p.(Thr244Ile)
?/. 4 c.751C>T r.(?) p.(His251Tyr)
?/. 4 c.751C>T r.(?) p.(His251Tyr)
+/. - c.751C>T r.(?) p.(His251Tyr)
-?/. 4 c.751C>T r.(?) p.(His251Tyr)
./. - c.751C>T r.(?) p.(His251Tyr)
+/. - c.766C>T r.(?) p.(Arg256*)
+/. 4 c.794G>A r.(?) p.(Trp265*)
./. - c.806G>A r.(?) p.(Arg269Gln)
?/. - c.839G>A r.(?) p.(Arg280Gln)
+/. - c.856C>T r.(?) p.(Arg286Ter)
+/. 4 c.856C>T r.(?) p.(Arg286*)
?/. - c.857G>C r.(?) p.(Arg286Pro)
./. - c.857G>T r.(?) p.(Arg286Leu)
-?/. - c.860G>A r.(?) p.(Arg287His)
?/. 4 c.860G>A r.(?) p.(Arg287His)
-?/. - c.860G>A r.(?) p.(Arg287His)
./. - c.860G>A r.(?) p.(Arg287His)
./. - c.898C>T r.(?) p.(Arg300Trp)
-?/. - c.926G>A r.(?) p.(Arg309Gln)
?/. - c.928C>T r.(?) p.(Arg310Cys)
+/. 4 c.975G>T r.(?) p.(Trp325Cys)
?/. - c.987A>G r.(?) p.(Pro329=)
?/. - c.988C>A r.(?) p.(Pro330Thr)
?/. - c.1001C>A r.(?) p.(Ala334Asp)
?/. - c.1001C>A r.(?) p.(Ala334Asp)
+?/. 4 c.1052C>G r.(?) p.(Ser351*)
+/. 4 c.1118G>C r.(?) p.(Cys373Ser)
?/. 4 c.1141A>G r.(?) p.(Ile381Val)
?/. - c.1149G>H r.(?) p.(Met383Ile)
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