Transcript #00000283 (NM_000177.4, GSN gene)

Transcript name transcript variant 1
Gene name GSN (gelsolin)
Chromosome 9
Transcript - NCBI ID NM_000177.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000168.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-08-30 17:19:51 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-17406A>G r.(?) p.(=)
?/. - c.-17392C>T r.(?) p.(=)
-?/. - c.-17392C>T r.(?) p.(=)
?/. - c.-17391G>A r.(?) p.(=)
-?/. - c.-17346C>T r.(?) p.(=)
-?/. - c.-13690A>G r.(?) p.(=)
?/. - c.-13676G>T r.(?) p.(=)
-?/. - c.-13668C>T r.(?) p.(=)
?/. - c.7C>T r.(?) p.(Pro3Ser)
+?/. - c.11_38del r.(?) p.(His4Argfs*86)
-?/. - c.63G>C r.(?) p.(Leu21=)
?/. - c.76C>T r.(?) p.(Arg26Cys)
-?/. - c.81G>A r.(?) p.(Ala27=)
-?/. - c.101C>T r.(?) p.(Ala34Val)
-?/. - c.102G>T r.(?) p.(Ala34=)
-?/. - c.111G>A r.(?) p.(Ala37=)
-?/. - c.119C>T r.(?) p.(Pro40Leu)
?/. - c.144+43_144+49dup r.(=) p.(=)
-?/. - c.144+62dup r.(=) p.(=)
?/. - c.144+122G>T r.(=) p.(=)
?/. - c.144+122G>T r.(=) p.(=)
?/. - c.173A>C r.(?) p.(Glu58Ala)
-?/. - c.182A>G r.(?) p.(Lys61Arg)
-/. - c.228C>G r.(?) p.(Phe76Leu)
?/. - c.312del r.(?) p.(Asn105Thrfs*35)
-?/. - c.339C>T r.(?) p.(=)
-?/. - c.349+7C>T r.(=) p.(=)
-?/. - c.349+7C>T r.(=) p.(=)
-?/. - c.380C>T r.(?) p.(Ala127Val)
-?/. - c.380C>T r.(?) p.(Ala127Val)
-?/. - c.396C>T r.(?) p.(Thr132=)
-?/. - c.396C>T r.(?) p.(Thr132=)
-?/. - c.396C>T r.(?) p.(Thr132=)
-?/. - c.424C>T r.(?) p.(Arg142Trp)
-?/. - c.425G>A r.(?) p.(Arg142Gln)
+?/. - c.444G>T r.(?) p.(Glu148Asp)
-?/. - c.456C>T r.(?) p.(Phe152=)
-?/. - c.475G>A r.(?) p.(Gly159Ser)
?/. - c.475G>A r.(?) p.(Gly159Ser)
?/. - c.512G>T r.(?) p.(Gly171Val)
-?/. - c.535G>A r.(?) p.(Val179Met)
+/. 4 c.580G>A r.(?) p.(Gly194Arg)
?/. - c.584G>A r.(?) p.(Arg195Gln)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.Asp214Asn
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.640g>a p.Asp214Asn
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. - c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>A r.(?) p.(Asp214Asn)
+/+ 4 c.640G>A r.(640g>a) p.(Asp214Asn)
+/. - c.640G>A r.(?) p.(Asp214Asn)
+/. 4 c.640G>T r.(?) p.(Asp214Tyr)
+/. 4 c.640G>T r.(?) p.(Asp214Tyr)
+/. 4 c.640G>T r.(?) p.(Asp214Tyr)
+/. 4 c.640G>T r.(?) p.(Asp214Tyr)
+/+ 4 c.640G>T r.(640g>u) p.(Asp214Tyr)
-?/. - c.666C>T r.(?) p.(=)
?/. - c.666+1G>A r.spl? p.?
-?/. - c.666+19T>C r.(=) p.(=)
-?/. - c.666+19T>C r.(=) p.(=)
-/. - c.691A>G r.(?) p.(Asn231Asp)
-/. - c.691A>G r.(?) p.(Asn231Asp)
?/. - c.700C>T r.(?) p.(Arg234Trp)
-?/. - c.700C>T r.(?) p.(Arg234Trp)
?/. - c.727G>C r.(?) p.(Val243Leu)
-?/. - c.750C>T r.(?) p.(Asn250=)
-?/. - c.750C>T r.(?) p.(Asn250=)
-?/. - c.750C>T r.(?) p.(Asn250=)
-?/. - c.763C>A r.(?) p.(Arg255=)
?/. - c.764G>A r.(?) p.(Arg255Gln)
-?/. - c.817-4A>G r.spl? p.?
-?/. - c.817-4A>G r.spl? p.?
-?/. - c.834G>A r.(?) p.(Pro278=)
?/. - c.856G>A r.(?) p.(Asp286Asn)
-?/. - c.939C>T r.(?) p.(Ser313=)
?/. - c.987_989del r.(?) p.(Glu329del)
-?/. - c.1039+19G>T r.(=) p.(=)
-?/. - c.1100C>A r.(?) p.(Thr367Asn)
?/. - c.1149C>T r.(?) p.(Gly383=)
-?/. - c.1162C>T r.(?) p.(Leu388=)
-?/. - c.1236C>T r.(?) p.(=)
-?/. - c.1251G>A r.(?) p.(Val417=)
-?/. - c.1251G>A r.(?) p.(Val417=)
-?/. - c.1272C>T r.(?) p.(Ala424=)
-?/. - c.1302C>T r.(?) p.(Ala434=)
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