Transcript #00000945 (NM_004115.3, FGF14 gene)

Transcript name transcript variant 1
Gene name FGF14 (fibroblast growth factor 14)
Chromosome 13
Transcript - NCBI ID NM_004115.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004106.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:00:36 +02:00 (CEST)
Date last edited N/A


Variants

85 entries on 1 page. Showing entries 1 - 85.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     
-?/. - c.-485009A>G - r.(?) p.(=)
-?/. - c.-485007G>C - r.(?) p.(=)
?/. - c.-485007G>C - r.(?) p.(=)
-?/. - c.-449974del - r.(?) p.(=)
+/. _1 - - r.? p.?
+?/. - - - r.? p.?
+?/. _1 - - r.(=) p.(=)
+/. 1i_5_ c.(193+1_194-1)_*1976{0} - r.? p.?
+/. 1i_5_ c.(193+1_194-1)_*1976{0} - r.? p.?
+/. 1i_5_ c.(193+1_194-1)_*1976{0} - r.? p.?
+/. 1i_5_ c.(208+99318_208+108913)_*1976{1} - r.? p.?
+/. _1_1i c.-1_(208+99318_208+108913){1} - r.0? p.0?
+/. _1_1i c.-1_208+171206{1} - r.0? p.0?
+/. _1_1i c.-1_208+171206{1} - r.0? p.0?
+/. 1i_5_ c.208+171206_*1976{1} - r.? p.?
+/. 1i_5_ c.208+171206_*1976{1} - r.? p.?
-?/. - c.78C>T - r.(?) p.(Ala26=)
-?/. - c.78C>T - r.(?) p.(Ala26=)
-?/. - c.88C>T - r.(?) p.(Arg30Trp)
-?/. - c.123C>T - r.(?) p.(Asn41=)
-?/. - c.123C>T - r.(?) p.(Asn41=)
-?/. - c.123C>T - r.(?) p.(Asn41=)
-?/. - c.124G>T - r.(?) p.(Gly42Cys)
-?/. - c.124G>T - r.(?) p.(Gly42Cys)
?/. - c.153G>A - r.(?) p.(Val51=)
?/. - c.197C>A - r.(?) p.(Pro66His)
+/. - c.211dup - r.(?) p.(Ile71Asnfs*27)
+/. - c.211dup - r.(?) p.(Ile71Asnfs*27)
+/. - c.211dup - r.(?) p.(Ile71Asnfs*27)
?/. - c.278G>A - r.(?) p.(Gly93Glu)
+/. - c.304+2T>C - r.spl? p.?
?/. - c.335G>A - r.(?) p.(Arg112His)
?/. - c.380T>A - r.(?) p.(Met127Lys)
?/. - c.380T>A - r.(?) p.(Met127Lys)
-?/. - c.384T>C - r.(?) p.(Asn128=)
?/. - c.408+40827A>G - r.(=) p.(=)
?/. - c.408+65468G>T - r.(=) p.(=)
?/. - c.408+65597del - r.(=) p.(=)
?/. - c.408+65769T>G - r.(=) p.(=)
?/. - c.408+66192G>A - r.(=) p.(=)
?/. - c.408+66192G>A - r.(=) p.(=)
?/. - c.408+66283C>G - r.(=) p.(=)
?/. - c.408+66283C>T - r.(=) p.(=)
?/. - c.408+66283C>T - r.(=) p.(=)
?/. - c.408+66417A>C - r.(=) p.(=)
?/. - c.408+66417A>C - r.(=) p.(=)
?/. - c.408+66608C>T - r.(=) p.(=)
?/. - c.408+66608C>T - r.(=) p.(=)
?/. - c.408+66952C>A - r.(=) p.(=)
?/. - c.408+66952C>A - r.(=) p.(=)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.434T>C - r.(?) p.(Phe145Ser)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
+/. - c.439G>T - r.(?) p.(Glu147Ter)
-/. - c.481T>C - r.(?) p.(Leu161=)
+/. - c.486_487del - r.(?) p.(Tyr162*)
+/. - c.487delA - r.(?) p.(Arg163AspfsTer13)
+/. - c.529A>T - r.(?) p.(Lys177*)
-?/. - c.543T>C - r.(?) p.(Ala181=)
-?/. - c.636T>C - r.(?) p.(His212=)
-?/. - c.636T>C - r.(?) p.(His212=)
?/. - c.671C>T - r.(?) p.(Thr224Met)
-/. - c.693G>A - r.(?) p.(Ala231=)
-/. - c.693G>A - r.(?) p.(Ala231=)
-?/. - c.693G>T - r.(?) p.(Ala231=)
-?/. - c.*31G>A - r.(?) p.(=)
-?/. - c.*31G>A - r.(?) p.(=)
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