Transcript #00016159 (NM_015937.5, PIGT gene)

Transcript name transcript variant 1
Gene name PIGT (phosphatidylinositol glycan anchor biosynthesis, class T)
Chromosome 20
Transcript - NCBI ID NM_015937.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_057021.2
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

82 entries on 1 page. Showing entries 1 - 82.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_11_ c.0 r.0 p.0
-?/. - c.14T>C r.(?) p.(Met5Thr)
-?/. - c.14T>C r.(?) p.(Met5Thr)
+?/. - c.250G>T r.(?) p.(Glu84*)
+?/. - c.250G>T r.(?) p.(Glu84*)
?/. - c.277T>A r.(?) p.(Phe93Ile)
-?/. - c.356C>T r.(?) p.(Thr119Ile)
?/. - c.366-8C>G r.(=) p.(=)
-?/. - c.367G>T r.(?) p.(Val123Leu)
-?/. - c.367G>T r.(?) p.(Val123Leu)
-?/. - c.494-3C>T r.spl? p.?
-?/. - c.494-3C>T r.spl? p.?
+?/+? - c.494-2A>G r.spl? p.?
-/. - c.533G>A r.(?) p.(Arg178Gln)
-/. - c.533G>A r.(?) p.(Arg178Gln)
-/. - c.533G>A r.(?) p.(Arg178Gln)
+/. 4 c.547A>C r.(?) p.(Thr183Pro)
+/. - c.547A>C r.(?) p.(Thr183Pro)
+/. 4 c.550G>A r.(?) p.(Glu184Lys)
+/. 4 c.550G>A r.(?) p.(Glu184Lys)
+?/. - c.594+1G>A r.spl? p.?
-/. - c.594+36dup r.(=) p.(=)
?/. - c.596C>T r.(?) p.(Ala199Val)
+?/. - c.659T>C r.(?) p.(Val220Ala)
?/. - c.667C>T r.(?) p.(Arg223Cys)
-?/. - c.667C>T r.(?) p.(Arg223Cys)
-?/. - c.675T>C r.(?) p.(Val225=)
-?/. - c.675T>C r.(?) p.(Val225=)
-?/. - c.689G>A r.(?) p.(Arg230His)
+?/. - c.709G>C r.(?) p.(Glu237Gln)
+?/. - c.709G>C r.(?) p.(Glu237Gln)
?/. - c.758A>G r.(?) p.(Gln253Arg)
-?/. - c.770-14G>A r.(=) p.(=)
-/. - c.770A>C r.(?) p.(Asp257Ala)
-/. - c.770A>C r.(?) p.(Asp257Ala)
-/. - c.770A>C r.(?) p.(Asp257Ala)
?/. - c.784C>T r.(?) p.(Arg262Trp)
+/. - c.784dup r.(?) p.(Arg262Profs*58)
?/. - c.806C>T r.(?) p.(Thr269Met)
?/. - c.806C>T r.(?) p.(Thr269Met)
+/. - c.917_929del r.(?) p.(Asp306AlafsTer16)
+?/. - c.918dup r.(?) p.(Val307Argfs*13)
+?/. - c.918dup r.(?) p.(Val307Argfs*13)
-?/. - c.925C>G r.(?) p.(Leu309Val)
-?/. - c.969C>T r.(?) p.(Thr323=)
+/. - c.988C>T r.(?) p.(Arg330*)
-?/. - c.1034-103dup r.(=) p.(=)
?/. - c.1058A>G r.(?) p.(His353Arg)
-?/. - c.1061C>T r.(?) p.(Ala354Val)
-?/. - c.1061C>T r.(?) p.(Ala354Val)
-?/. - c.1067G>A r.(?) p.(Arg356Gln)
+?/. - c.1079G>T r.(?) p.(Gly360Val)
+?/. - c.1079G>T r.(?) p.(Gly360Val)
+?/. - c.1096G>T r.(?) p.(Gly366Trp)
?/. - c.1130C>T r.(?) p.(Pro377Leu)
-?/. - c.1138G>A r.(?) p.(Ala380Thr)
?/. - c.1144C>G r.(?) p.(Pro382Ala)
?/. - c.1145C>T r.(?) p.(Pro382Leu)
-?/. - c.1145C>T r.(?) p.(Pro382Leu)
?/. - c.1165G>A r.(?) p.(Val389Ile)
+?/. - c.1342C>T r.(?) p.(Arg448Trp)
+?/. - c.1342C>T r.(?) p.(Arg448Trp)
+?/. - c.1342C>T r.(?) p.(Arg448Trp)
?/. - c.1343G>A r.(?) p.(Arg448Gln)
?/. - c.1363G>C r.(?) p.(Glu455Gln)
-/. - c.1371G>A r.(?) p.(Thr457=)
+/. 10i c.1401-2A>G r.1401_1484del p.Ser467_Leu495delinsArg
-?/. - c.1416C>T r.(?) p.(Ser472=)
-?/. - c.1417G>A r.(?) p.(Ala473Thr)
+?/+? - c.1472T>A r.(?) p.(Leu491His)
+?/+? - c.1484+2T>A r.spl? p.?
-?/. - c.1530G>A r.(?) p.(Thr510=)
?/. - c.1553C>T r.(?) p.(Pro518Leu)
?/. - c.1579A>C r.(?) p.(Asn527His)
+?/. - c.1582G>A r.(?) p.(Val528Met)
-/. - c.1620T>C r.(?) p.(Tyr540=)
?/. - c.1634A>G r.(?) p.(Asn545Ser)
-?/. - c.1692G>T r.(?) p.(Arg564=)
-?/. - c.1707C>T r.(?) p.(Ile569=)
?/. - c.1708C>T r.(?) p.(Arg570Trp)
+?/. - c.1730del r.(?) p.(Pro577Hisfs*67)
+?/. - c.1730dup r.(?) p.(Leu578Thrfs*35)
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