Transcript #00025497 (NM_003900.4, SQSTM1 gene)

Transcript name transcript variant 1
Gene name SQSTM1 (sequestosome 1)
Chromosome 5
Transcript - NCBI ID NM_003900.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_003891.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-03-01 10:52:44 +01:00 (CET)
Date last edited N/A


Variants

96 entries on 1 page. Showing entries 1 - 96.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.87C>G r.(?) p.(Pro29=)
-?/. - c.98C>T r.(?) p.(Ala33Val)
?/. - c.139C>G r.(?) p.(Leu47Val)
?/. - c.139C>G r.(?) p.(Leu47Val)
-?/. - c.154G>T r.(?) p.(Ala52Ser)
?/. - c.154G>T r.(?) p.(Ala52Ser)
-?/. - c.183C>T r.(?) p.(Gly61=)
-?/. - c.183C>T r.(?) p.(Gly61=)
?/. - c.185G>T r.(?) p.(Gly62Val)
+?/. - c.241G>A r.(?) p.(Glu81Lys)
?/. - c.328C>T r.(?) p.(Arg110Cys)
-?/. - c.350C>T r.(?) p.(Ala117Val)
-?/. - c.350C>T r.(?) p.(Ala117Val)
-?/. - c.350C>T r.(?) p.(Ala117Val)
?/. - c.365T>G r.(?) p.(Val122Gly)
?/. - c.374A>G r.(?) p.(Asn125Ser)
?/. - c.431T>A r.(?) p.(Val144Asp)
?/. - c.457G>A r.(?) p.(Val153Ile)
-?/. - c.457G>A r.(?) p.(Val153Ile)
-?/. - c.457G>A r.(?) p.(Val153Ile)
?/. - c.530A>C r.(?) p.(Glu177Ala)
-?/. - c.530A>C r.(?) p.(Glu177Ala)
?/. - c.547C>T r.(?) p.(Arg183Cys)
?/. - c.547C>T r.(?) p.(Arg183Cys)
-?/. - c.555C>G r.(?) p.(Leu185=)
-?/. - c.663G>A r.(?) p.(Thr221=)
+/. - c.673+1G>T r.spl? p.?
-?/. - c.674-7dup r.(=) p.(=)
-?/. - c.712A>G r.(?) p.(Lys238Glu)
-?/. - c.712A>G r.(?) p.(Lys238Glu)
-/. - c.712A>G r.(?) p.(Lys238Glu)
-/. - c.712A>G r.(?) p.(Lys238Glu)
+?/. 5 c.712_713insTCCTCCGAGTGTGAATTTCCTGA r.(?) p.(Lys238IlefsTer5)
+?/. - c.717C>A r.(?) p.(Asn239Lys)
?/. - c.719T>C r.(?) p.(Val240Ala)
-/. - c.755-23G>A r.(=) p.(=)
-?/. - c.811G>A r.(?) p.(Val271Ile)
-/. - c.822G>C r.(?) p.(Glu274Asp)
-/. - c.822G>C r.(?) p.(Glu274Asp)
+/. - c.822G>Y r.(?) p.(Glu274Asp)
+/. 6 c.823_824del r.(?) p.(Ser275PhefsTer17)
+/. - c.823_824del r.(?) p.(Ser275Phefs*17)
-/. - c.876C>T r.(?) p.(Asp292=)
-/. - c.876C>T r.(?) p.(Asp292=)
-/. - c.876C>T r.(?) p.(Asp292=)
-/. - c.876C>T r.(?) p.(Asp292=)
-/. - c.876C>T r.(?) p.(Asp292=)
+?/. - c.889G>A r.(?) p.(Gly297Ser)
-?/. - c.906C>T r.(?) p.(Gly302=)
-?/. - c.924G>A r.(?) p.(Ala308=)
-?/. - c.924G>A r.(?) p.(Ala308=)
-?/. - c.924G>A r.(?) p.(Ala308=)
-?/. - c.924G>A r.(?) p.(Ala308=)
-/. - c.936G>A r.(?) p.(Arg312=)
-/. - c.936G>A r.(?) p.(Arg312=)
-/. - c.936G>A r.(?) p.(Arg312=)
-/. - c.936G>A r.(?) p.(Arg312=)
-/. - c.936G>A r.(?) p.(Arg312=)
-/. - c.954C>T r.(?) p.(Ser318=)
-/. - c.954C>T r.(?) p.(Ser318=)
-?/. - c.955G>A r.(?) p.(Glu319Lys)
-?/. - c.961C>T r.(?) p.(Arg321Cys)
?/. - c.962G>A r.(?) p.(Arg321His)
-?/. - c.970-8T>C r.(=) p.(=)
-/. - c.984G>A r.(?) p.(Ser328=)
-?/. - c.984G>A r.(?) p.(Ser328=)
-?/. - c.984G>A r.(?) p.(Ser328=)
-?/. - c.996A>G r.(?) p.(Ser332=)
-?/. - c.996A>G r.(?) p.(Ser332=)
-?/. - c.1032A>G r.(?) p.(Lys344=)
-?/. - c.1038G>A r.(?) p.(Val346=)
-?/. - c.1044G>A r.(?) p.(Pro348=)
-?/. - c.1108T>C r.(?) p.(Ser370Pro)
-?/. - c.1108T>C r.(?) p.(Ser370Pro)
+?/. - c.1116G>C r.(?) p.(Glu372Asp)
-?/. - c.1141G>A r.(?) p.(Ala381Thr)
?/. - c.1156C>G r.(?) p.(Leu386Val)
+?/. - c.1162C>T r.(?) p.(Pro388Ser)
+?/. 7i c.1165+1G>A r.spl p.?
-?/. - c.1165+9A>G r.(=) p.(=)
+?/. 8 c.1175C>T r.(?) p.(Pro392Leu)
+?/. - c.1175C>T r.(?) p.(Pro392Leu)
-?/. - c.1175C>T r.(?) p.(Pro392Leu)
?/. - c.1175C>T r.(?) p.(Pro392Leu)
?/. - c.1175C>T r.(?) p.(Pro392Leu)
-?/. - c.1176G>A r.(?) p.(Pro392=)
?/. - c.1178G>A r.(?) p.(Arg393Gln)
?/. - c.1207T>A r.(?) p.(Ser403Thr)
-?/. - c.1245G>A r.(?) p.(Arg415=)
?/. - c.1277C>T r.(?) p.(Ala426Val)
-?/. - c.1278G>A r.(?) p.(Ala426=)
-?/. - c.1278G>A r.(?) p.(Ala426=)
-?/. - c.1284G>T r.(?) p.(Leu428=)
?/. - c.1295A>G r.(?) p.(Gln432Arg)
-?/. - c.1316C>T r.(?) p.(Pro439Leu)
-?/. - c.*11462T>C r.(=) p.(=)
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