Transcript #00024218 (NM_002863.4, PYGL gene)

Transcript name transcript variant 1
Gene name PYGL (phosphorylase, glycogen, liver)
Chromosome 14
Transcript - NCBI ID NM_002863.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_002854.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-01-13 15:49:03 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/? 1 c.2T>A r.(?) p.0?
+?/? 1 c.2T>A r.(?) p.0?
+/. - c.38A>C r.(?) p.(Gln13Pro)
+?/. 1 c.43A>T r.(?) p.(Ser15Cys)
?/. - c.52G>A r.(?) p.(Gly18Ser)
?/. 1 c.93T>C r.(?) p.(Ser31=)
?/. 1 c.131G>T r.(?) p.(Arg44Leu)
+/. 1 c.148dup r.(?) p.(Arg50Profs*61)
+?/. 1 c.152A>T r.(?) p.(Asp51Val)
-?/. - c.153C>T r.(=) p.(=)
-?/. 1 c.153C>T r.(?) p.(Asp51=)
-?/. - c.153C>T r.(?) p.(=)
-?/. - c.153C>T r.(=) p.(=)
-/. - c.244-34G>A r.(=) p.(=)
-/. - c.244-34G>A r.(=) p.(=)
?/. - c.271T>C r.(?) p.(Tyr91His)
+/. - c.280C>T r.(?) p.(Arg94Ter)
+/. 2 c.280C>T r.(?) p.(Arg94*)
+/. 2 c.280C>T r.(?) p.(Arg94*)
+/. 2 c.280C>T r.(?) p.(Arg94*)
?/. 2 c.298A>G r.(?) p.(Met100Val)
+/. 2 c.320dup r.(?) p.(Asn107Lysfs*4)
?/. - c.346C>T r.(?) p.(Leu116Phe)
+?/. 3 c.350G>T r.(?) p.(Gly117Val)
+?/. 3 c.394C>G r.(?) p.(Leu132Val)
?/. 4 c.482G>C r.(?) p.(Arg161Pro)
+/. 4 c.501_502ins(361) r.? p.(Asn168Glufs*15)
+/. 41 c.528+2T>C r.spl p.?
+/. - c.529-1G>C r.529_660del p.?
?/. 5 c.547T>G r.(?) p.(Trp183Gly)
+?/. 5 c.564C>A r.(?) p.(Asn188Lys)
+?/. 5 c.580C>T r.(?) p.(Arg194Cys)
+?/. 5 c.580C>T r.(?) p.(Arg194Cys)
?/. - c.611A>G r.(?) p.(Tyr204Cys)
?/. - c.661G>A r.(?) p.(Val221Met)
+?/. 6 c.682G>T r.(?) p.(Asp228Tyr)
+?/. 6 c.697G>A r.(?) p.(Gly233Ser)
+?/. 6 c.697G>A r.(?) p.(Gly233Ser)
+/. - c.698G>A r.(?) p.(Gly233Asp)
+/. - c.698G>A r.(?) p.(Gly233Asp)
+/. 6 c.698G>A r.(?) p.(Gly233Asp)
+/. 6 c.698G>A r.(?) p.(Gly233Asp)
+/. 6 c.698G>A r.(?) p.(Gly233Asp)
+/. 6 c.698G>A r.(?) p.(Gly233Asp)
+/. 6 c.698G>A r.(?) p.(Gly233Asp)
+?/. 6 c.728G>A r.(?) p.(Arg243His)
+?/. 6 c.728G>A r.(?) p.(Arg243His)
+/. 6 c.730C>T r.(?) p.(Leu244Phe)
+/. 6 c.730C>T r.(?) p.(Leu244Phe)
+/. 6 c.730C>T r.(?) p.(Leu244Phe)
+?/. 6 c.730C>T r.(?) p.(Leu244Phe)
+/. 6 c.730C>T r.(?) p.(Leu244Phe)
+?/. 6 c.736T>C r.(?) p.(Ser246Pro)
+?/. 6 c.736T>C r.(?) p.(Ser246Pro)
+/. 6i c.772+1G>A r.spl p.?
+?/. 6i c.772+5G>A r.spl? p.?
+/. 6i_12i c.856-29_1518+614del r.spl p.?
+?/. 8 c.889G>A r.(?) p.(Glu297Lys)
+?/. 8 c.896T>C r.(?) p.(Phe299Ser)
+/? 8 c.911_914dup r.(?) p.(Leu305Phefs*25)
+?/. 8 c.928C>T r.(?) p.(Arg310Cys)
+?/. - c.928C>T r.(?) p.(Arg310Cys)
-/. - c.928C>T r.(?) p.(Arg310Cys)
-/. 8 c.962G>A r.(?) p.(Arg321His)
+/. 8i c.1000-1G>A r.spl p.?
+/. 8i c.1000-1G>A r.spl p.?
+/. 9 c.1007T>C r.(?) p.(Ile336Thr)
+/. - c.1016A>G r.(?) p.(Asn339Ser)
-/. - c.1020C>T r.(?) p.(Asp340=)
?/. 9 c.1020C>T r.(?) p.(Asp340=)
?/. 9 c.1079T>C r.(?) p.(Leu360Pro)
+/. - c.1099G>T r.(?) p.(Glu367Ter)
+/. - c.1131C>G r.(?) p.(Asn377Lys)
+?/. 10 c.1131C>G r.(?) p.(Asn377Lys)
-?/. - c.1137A>G r.(?) p.(Thr379=)
+?/. 10 c.1145C>T r.(?) p.(Pro382Leu)
?/. - c.1145C>T r.(?) p.(Pro382Leu)
?/. 10 c.1149A>C r.(?) p.(Glu383Asp)
+/. - c.1195C>T r.(?) p.(Arg399*)
+/. 10 c.1195C>T r.(?) p.(Arg399*)
+?/? 10 c.1208T>A r.(?) p.(Ile403Asn)
+?/. 10 c.1219A>G r.(?) p.(Ile407Val)
+/. 10i c.1239+1G>A r.spl? p.?
?/. - c.1274G>A r.(?) p.(Arg425His)
+/. 11 c.1279A>T r.(?) p.(Arg427*)
+/. - c.1366G>A r.(?) p.(Val456Met)
+/. - c.1366G>A r.(?) p.(Val456Met)
+?/. 11 c.1366G>A r.(?) p.(Val456Met)
+/. 11 c.1366G>A r.(?) p.(Val456Met)
+/. 11 c.1366G>A r.(?) p.(Val456Met)
+?/. 11 c.1379A>C r.(?) p.(His460Pro)
?/. 11 c.1390G>A r.(?) p.(Val464Met)
+/. 11 c.1392_1393insT r.(?) p.(Lys465*)
+/. 11i c.1403+2T>A r.spl p.?
+/. - c.1471C>T r.(?) p.(Arg491Cys)
+?/. 12 c.1472G>A r.(?) p.(Arg491His)
+/. 12 c.1475G>A r.(?) p.(Trp492*)
+/. 12 c.1475G>A r.(?) p.(Trp492*)
+/. 12 c.1475G>A r.(?) p.(Trp492*)
+?/. 12 c.1499T>G r.(?) p.(Leu500Arg)
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