Transcript #00000711 (NM_001615.3, ACTG2 gene)

Transcript name transcript variant 1
Gene name ACTG2 (actin, gamma 2, smooth muscle, enteric)
Chromosome 2
Transcript - NCBI ID NM_001615.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001606.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:49:04 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-37+3A>G r.spl? p.?
-/. - c.-36-12G>C r.(=) p.(=)
-/. - c.-6C>T r.(?) p.(=)
+/. - c.805+1_806-1)_(*78_?)del r.? p.?
?/. - c.10G>C r.(?) p.(Glu4Gln)
+/. - c.113G>A r.(?) p.(Arg38His)
+/. - c.116C>G r.(?) p.(Pro39Arg)
+/. - c.116C>G r.(?) p.(Pro39Arg)
+/. - c.118C>T r.(?) p.(Arg40Cys)
+/. - c.118C>T r.(?) p.(Arg40Cys)
+/. - c.118C>T r.(?) p.(Arg40Cys)
+/. - c.119G>A r.(?) p.(Arg40His)
+/. - c.119G>A r.(?) p.(Arg40His)
+/. - c.119G>A r.(?) p.(Arg40His)
+/. - c.119G>A r.(?) p.(Arg40His)
+/. - c.119G>A r.(?) p.(Arg40His)
+/. - c.119G>A r.(?) p.(Arg40His)
?/. - c.124dup r.(?) p.(Gln42Profs*17)
-/. - c.127-13T>C r.(=) p.(=)
+/. - c.134T>C r.(?) p.(Met45Thr)
+/. - c.187C>G r.(?) p.(Arg63Gly)
+/. - c.187C>G r.(?) p.(Arg63Gly)
?/. - c.187C>T r.(?) p.(Arg63*)
+/. - c.188G>A r.(?) p.(Arg63Gln)
+?/. - c.188G>T r.(?) p.(Arg63Leu)
-?/. - c.255+190A>G r.(?) p.(=)
-?/. - c.255+210C>A r.(=) p.(=)
+/. - c.255+210C>A r.(=) p.(=)
-/. - c.256-3T>C r.spl? p.?
+?/. 4 c.337C>G r.(?) p.(Pro113Ala)
-/. - c.354A>G r.(?) p.(Glu118=)
?/. - c.398T>C r.(?) p.(Met133Thr)
-?/. - c.398T>C r.(?) p.(Met133Thr)
+/. - c.400T>A r.(?) p.(Tyr134Asn)
+/. - c.439G>T r.(?) p.(Gly147Cys)
+/. - c.442C>A r.(?) p.(Arg148Ser)
+/. - c.442C>A r.(?) p.(Arg148Ser)
+/. - c.442C>A r.(?) p.(Arg148Ser)
+/. - c.443G>T r.(?) p.(Arg148Leu)
+/. - c.532C>A r.(?) p.(Arg178Ser)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.532C>T r.(?) p.(Arg178Cys)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>A r.(?) p.(Arg178His)
+/. - c.533G>T r.(?) p.(Arg178Leu)
+/. - c.533G>T r.(?) p.(Arg178Leu)
+/. - c.533G>T r.(?) p.(Arg178Leu)
+/. - c.533G>T r.(?) p.(Arg178Leu)
+?/. - c.577A>T r.(?) p.(Ile193Phe)
+/. - c.584C>T r.(?) p.(Thr195Ile)
+/. - c.593G>A r.(?) p.(Gly198Asp)
-?/. - c.606G>A r.(?) p.(Val202=)
-/. - c.613+16T>C r.(=) p.(=)
+/. - c.632G>A r.(?) p.(Arg211Gln)
+/. - c.632G>A r.(?) p.(Arg211Gln)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.769C>T r.(?) p.(Arg257Cys)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
+/. - c.770G>A r.(?) p.(Arg257His)
-?/. - c.789C>G r.(?) p.(Phe263Leu)
?/. - c.805+166del r.(=) p.(=)
?/. - c.805+166del r.(=) p.(=)
+/. - c.806_807delinsAA r.(?) p.(Gly269Glu)
?/. - c.865G>T r.(?) p.(Asp289Tyr)
?/. - c.958G>A r.(?) p.(Ala320Thr)
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