Transcript #00025360 (NM_000155.3, GALT gene)

Transcript name transcript variant 1
Gene name GALT (galactose-1-phosphate uridylyltransferase)
Chromosome 9
Transcript - NCBI ID NM_000155.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000146.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2019-01-09 15:23:34 +01:00 (CET)
Date last edited N/A


Variants

79 entries on 1 page. Showing entries 1 - 79.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-119_-116del r.(?) p.(=)
?/. - c.13G>A r.(?) p.(Gly5Arg)
-?/. - c.83-5C>T r.spl? p.?
?/. - c.196C>T r.(?) p.(Pro66Ser)
+/. - c.199C>T r.(?) p.(Arg67Cys)
+/. - c.200G>A r.(?) p.(Arg67His)
+?/. - c.292G>C r.(?) p.(Asp98His)
+/. 4 c.347T>C r.(?) p.Leu116Pro
-/. - c.378-27G>C r.(=) p.(=)
+/. - c.379A>G r.(?) p.(Lys127Glu)
+?/. - c.404C>G r.(?) p.(Ser135Trp)
+?/. - c.404C>G r.(?) p.(Ser135Trp)
+/. - c.404C>T r.(?) p.(Ser135Leu)
+/. - c.404C>T r.(?) p.(Ser135Leu)
+?/. - c.404C>T r.(?) p.(Ser135Leu)
+/. - c.413C>T r.(?) p.(Thr138Met)
+/. - c.502G>T r.(?) p.Val168Leu
+/. 5 c.502G>T r.(?) p.(Val168Leu)
+/. - c.502G>T r.(?) p.(Val168Leu)
-/. - c.507+62G>A r.(=) p.(=)
-/. - c.508-24G>A r.(=) p.(=)
-/. - c.508-24G>A r.(=) p.(=)
-/. - c.510C>A r.(?) p.(Ile170=)
-/. - c.510C>A r.(?) p.(Ile170=)
+/. - c.533T>G r.(?) p.Met178Arg
+/. - c.553C>T r.(?) p.(Pro185Ser)
?/. - c.563A>G r.(?) p.(Gln188Arg)
+/. - c.563A>G r.(?) p.(Gln188Arg)
+/. - c.563A>G r.(?) p.(Gln188Arg)
+?/. - c.563A>G r.(?) p.(Gln188Arg)
+?/. - c.563A>G r.(?) p.(Gln188Arg)
+/. - c.563A>G r.(?) p.(Gln188Arg)
?/. - c.563A>G r.(?) p.(Gln188Arg)
+/. - c.563A>G r.(?) p.(Gln188Arg)
+?/. - c.563A>G r.(?) p.(Gln188Arg)
+/. - c.563A>G r.(?) p.(Gln188Arg)
-?/. - c.567A>G r.(?) p.(Val189=)
+/. - c.584T>C r.(?) p.(Leu195Pro)
+/. - c.584T>C r.(?) p.(Leu195Pro)
+?/. - c.602G>A r.(?) p.(Arg201His)
?/. - c.611G>A r.(?) p.(Arg204Gln)
+?/. - c.626A>G r.(?) p.(Tyr209Cys)
?/. - c.632G>C r.(?) p.(Ser211Thr)
-/. - c.652C>T r.(?) p.(Leu218=)
-/. - c.652C>T r.(?) p.(Leu218=)
+/. - c.687G>T r.(?) p.(Lys229Asn)
-?/. - c.688-4C>T r.spl? p.?
?/. - c.772C>T r.(?) p.(Arg258Cys)
?/. - c.788G>A r.(?) p.(Arg263Gln)
+?/. - c.821-23T>G r.[821_904del,855-904del,820_821ins[820+1_821-24;g;821-22_821-1],[820_821ins[820+1_821-24;g;821-22_821-1];855_904del]] p.[Asp274_His301del,Ala303Serfs*49,Arp274Glyfs*6,Arp274Glyfs*6]
?/. - c.821-7A>G r.(=) p.(=)
-?/. - c.821-3C>T r.spl? p.?
?/. - c.855G>T r.(?) p.(Lys285Asn)
+/. - c.855G>T r.(?) p.(Lys285Asn)
+/. - c.855G>T r.(?) p.(Lys285Asn)
+/. - c.855G>T r.(?) p.(Lys285Asn)
+/. - c.855G>T r.(?) p.(Lys285Asn)
-/. - c.879C>T r.(?) p.(Ser293=)
?/. - c.940A>G r.(?) p.(Asn314Asp)
?/. - c.940A>G r.(?) p.(Asn314Asp)
?/. - c.940A>G r.(?) p.(Asn314Asp)
?/. - c.940A>G r.(?) p.(Asn314Asp)
+?/. - c.947G>A r.(?) p.(Trp316*)
+?/. - c.947G>A r.(?) p.(Trp316*)
?/. - c.957C>T r.(?) p.(=)
?/. - c.982C>T r.(?) p.(Arg328Cys)
+?/. - c.983G>A r.(?) p.(Arg328His)
?/. - c.998G>A r.(?) p.(Arg333Gln)
+/. - c.1018G>T r.(?) p.(Glu340*)
+?/. 10 c.1034C>A r.(?) p.(Ala345Asp)
+/. - c.1034C>A r.(?) p.(Ala345Asp)
+?/. - c.1042G>A r.(?) p.(Asp348Asn)
-/. - c.1060-79_1060-71dup r.(=) p.(=)
-/. - c.1060-78_1060-71dup r.(=) p.(=)
-?/. - c.1060-10C>T r.(=) p.(=)
+?/. - c.1132A>G r.(?) p.(Ile378Val)
+/. - c.1140A>C r.(?) p.(*380Cysext*49)
+?/. - c.1140A>C r.(?) p.(*380Cysext*49)
-?/. - c.*4782G>T r.(=) p.(=)
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