Transcript #00008123 (NM_001112808.2, FPGT-TNNI3K gene)

Transcript name transcript variant 1
Gene name FPGT-TNNI3K (FPGT-TNNI3K readthrough)
Chromosome 1
Transcript - NCBI ID NM_001112808.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001106279.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

251 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.10G>A r.(?) p.(Val4Met)
-/. - c.267G>A r.(?) p.(Val89=)
-?/. - c.382+3265C>T r.(=) p.(=)
-?/. - c.382+4189A>G r.(=) p.(=)
-?/. - c.383-604A>G r.(=) p.(=)
?/. - c.384T>A r.(?) p.(Asp128Glu)
?/. - c.404G>A r.(?) p.(Ser135Asn)
?/. - c.463G>A r.(?) p.(Glu155Lys)
?/. - c.491+1G>A r.spl? p.?
-/. - c.491+3790G>C r.(=) p.(=)
?/. - c.518A>T r.(?) p.(Asn173Ile)
-/. - c.531C>T r.(?) p.(Arg177=)
?/. - c.535G>T r.(?) p.(Glu179Ter)
-?/. - c.535G>T r.(?) p.(Glu179Ter)
?/. - c.535G>T r.(?) p.(Glu179Ter)
-?/. - c.535G>T r.(?) p.(Glu179Ter)
?/. - c.577+5G>C r.spl? p.?
-/. - c.578-18T>C r.(=) p.(=)
-/. - c.578-4T>G r.spl? p.?
?/. - c.578-2A>G r.spl? p.?
?/. - c.579C>T r.(?) p.(Gly193=)
?/. - c.596G>A r.(?) p.(Arg199Gln)
?/. - c.613G>A r.(?) p.(Gly205Arg)
?/. - c.652G>A r.(?) p.(Ala218Thr)
-/. - c.665C>T r.(?) p.(Ala222Val)
?/. - c.675+3A>C r.spl? p.?
-?/. - c.676-13T>C r.(=) p.(=)
-/. - c.676-8C>T r.(=) p.(=)
-/. - c.676-8C>T r.(=) p.(=)
-?/. - c.677A>T r.(?) p.(Asp226Val)
-/. - c.687A>G r.(?) p.(=)
?/. - c.728A>G r.(?) p.(Gln243Arg)
-?/. - c.739G>A r.(?) p.(Gly247Ser)
?/. - c.740G>T r.(?) p.(Gly247Val)
-/. - c.768A>G r.(?) p.(Thr256=)
?/. - c.773C>T r.(?) p.(Ala258Val)
?/. - c.773C>T r.(?) p.(Ala258Val)
-?/. - c.793G>C r.(?) p.(Asp265His)
-/. - c.793G>C r.(?) p.(Asp265His)
-?/. - c.807A>G r.(?) p.(Gln269=)
-/. - c.807A>G r.(?) p.(Gln269=)
-?/. - c.807A>G r.(?) p.(Gln269=)
?/. - c.824A>G r.(?) p.(Asn275Ser)
-/. - c.854T>C r.(?) p.(Leu285Ser)
-/. - c.854T>C r.(?) p.(Leu285Ser)
-/. - c.854T>C r.(?) p.(Leu285Ser)
-/. - c.867G>A r.(?) p.(=)
?/. - c.868T>C r.(?) p.(Tyr290His)
?/. - c.885+5G>T r.spl? p.?
?/. - c.885+5G>T r.spl? p.?
?/. - c.885+6T>A r.(=) p.(=)
?/. - c.885+6T>A r.(=) p.(=)
-/. - c.886-6C>A r.(=) p.(=)
-?/. - c.893G>A r.(?) p.(Arg298His)
-?/. - c.922A>G r.(?) p.(Asn308Asp)
-/. - c.933T>C r.(?) p.(Gly311=)
-/. - c.998T>C r.(?) p.(Leu333Ser)
-?/. - c.998T>C r.(?) p.(Leu333Ser)
-/. - c.1025-18C>G r.(=) p.(=)
?/. - c.1025-1G>A r.spl? p.?
-/. - c.1041T>C r.(?) p.(=)
-/. - c.1104G>T r.(?) p.(Leu368=)
-?/. - c.1119G>C r.(?) p.(Leu373Phe)
-/. - c.1119G>C r.(?) p.(Leu373Phe)
-?/. - c.1119G>C r.(?) p.(Leu373Phe)
-?/. - c.1119G>C r.(?) p.(Leu373Phe)
-/. - c.1130C>T r.(?) p.(Pro377Leu)
?/. - c.1130C>T r.(?) p.(Pro377Leu)
-?/. - c.1130C>T r.(?) p.(Pro377Leu)
-/. - c.1130C>T r.(?) p.(Pro377Leu)
?/. - c.1139T>C r.(?) p.(Val380Ala)
?/. - c.1144A>T r.(?) p.(Ile382Phe)
?/. - c.1169+4A>C r.spl? p.?
?/. - c.1169+4A>C r.spl? p.?
-?/. - c.1169+4A>C r.spl? p.?
-/. - c.1169+11T>C r.(=) p.(=)
-/. - c.1170-19A>C r.(=) p.(=)
?/. - c.1203G>T r.(?) p.(Lys401Asn)
?/. - c.1203G>T r.(?) p.(Lys401Asn)
?/. - c.1203G>T r.(?) p.(Lys401Asn)
?/. - c.1207A>G r.(?) p.(Ile403Val)
-/. - c.1216A>G r.(?) p.(Ile406Val)
-?/. - c.1216A>G r.(?) p.(Ile406Val)
?/. - c.1225del r.(?) p.(Thr409Glnfs*4)
?/. - c.1259A>G r.(?) p.(Glu420Gly)
?/. - c.1259A>G r.(?) p.(Glu420Gly)
-/. - c.1275-14G>T r.(=) p.(=)
-/. - c.1275-4dup r.spl? p.?
-?/. - c.1275-4T>C r.spl? p.?
-/. - c.1275-3dup r.spl? p.?
?/. - c.1275-2A>T r.spl? p.?
?/. - c.1275-2A>T r.spl? p.?
?/. - c.1275-1G>A r.spl? p.?
?/. - c.1275-1G>T r.spl? p.?
?/. - c.1276G>A r.(?) p.(Ala426Thr)
?/. - c.1277C>G r.(?) p.(Ala426Gly)
?/. - c.1285T>C r.(?) p.(Tyr429His)
-?/. - c.1311A>G r.(?) p.(Lys437=)
-/. - c.1311A>G r.(?) p.(Lys437=)
-?/. - c.1311A>G r.(?) p.(Lys437=)
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