Transcript #00011446 (NM_005573.3, LMNB1 gene)

Transcript name transcript variant 1
Gene name LMNB1 (lamin B1)
Chromosome 5
Transcript - NCBI ID NM_005573.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_005564.1
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

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-2284677_*19545329dup - -
./. - c.-109916_*172112dup r.0? p.0?
./. - c.-16323_*94376dup r.0? p.0?
./. - c.-16323_*94376dup r.0? p.0?
+/? 1_11 c.(?_-886)_(*756_?)dup r.? p.?
+/? 1_11 c.(?_-886)_(*756_?)dup r.? p.?
+/? 1_11 c.(?_-886)_(*756_?)dup r.= p.=
-?/. - c.29G>T r.(?) p.(Arg10Leu)
-?/. - c.60G>A r.(?) p.(Thr20=)
-?/. - c.60G>A r.(?) p.(Thr20=)
+/. 1 c.97A>G r.(?) p.(Lys33Glu)
+/. 1 c.124C>T r.(?) p.(Arg42Trp)
+?/. - c.125G>C r.(?) p.(Arg42Pro)
?/. - c.154A>G r.(?) p.(Ser52Gly)
-?/. - c.157C>T r.(?) p.(=)
?/. - c.164C>T r.(?) p.(Thr55Met)
-/. - c.165G>A r.(?) p.(Thr55=)
-?/. - c.279C>T r.(?) p.(Leu93=)
+?/. - c.311_319del r.(311_319del) p.(Gln104_Glu106del)
-?/. - c.359+8256_359+8257insGT r.(=) p.(=)
-/. - c.360-19C>T r.(=) p.(=)
-?/. - c.360-19C>T r.(=) p.(=)
-?/. - c.360-8T>C r.(=) p.(=)
-?/. - c.360-3C>T r.spl? p.?
-/. - c.414T>C r.(?) p.(Tyr138=)
-/. - c.414T>C r.(?) p.(Tyr138=)
-?/. - c.432G>A r.(?) p.(Ser144=)
-/. - c.432G>A r.(?) p.(Ser144=)
-/. - c.432G>A r.(?) p.(Ser144=)
+/. 2 c.455C>G r.(?) p.(Ala152Gly)
?/. - c.457C>G r.(?) p.(Leu153Val)
?/. - c.478G>C r.(?) p.(Glu160Gln)
?/. - c.622C>T r.(?) p.(Arg208Cys)
-?/. - c.642+4_642+7dup r.spl? p.?
?/. - c.652G>A r.(?) p.(Glu218Lys)
?/. - c.676C>T r.(?) p.(Arg226Cys)
?/. - c.676C>T r.(?) p.(Arg226Cys)
?/. - c.734C>T r.(?) p.(Ala245Val)
-?/. - c.805C>T r.(?) p.(His269Tyr)
-?/. - c.852T>C r.(?) p.(Ser284=)
?/. - c.896G>T r.(?) p.(Arg299Ile)
+/. - c.939+1G>A r.spl? p.?
+/. 5i c.939+1G>A r.spl p.?
+/. 5i c.939+1G>A r.spl p.?
+/. 5i c.939+1G>A r.spl p.?
+?/. - c.939+1G>T r.spl? p.?
+/. 5i_8i c.(939+1_939+2362)_(1491+560_1492-1)del r.(940_1491del) p.(Ser314_Thr497del)
?/. - c.946G>C r.(?) p.(Ala316Pro)
-?/. - c.1031G>A r.(?) p.(Arg344Lys)
?/. - c.1079A>G r.(?) p.(Tyr360Cys)
-?/. - c.1161-4A>G r.spl? p.?
?/. - c.1190G>A r.(?) p.(Arg397His)
-?/. - c.1197A>C r.(?) p.(Thr399=)
-?/. - c.1221T>C r.(?) p.(Arg407=)
-?/. - c.1323T>C r.(?) p.(Asn441=)
-?/. - c.1332C>T r.(?) p.(=)
+?/. - c.1365C>T r.(?) p.(Arg455=)
?/. - c.1379C>T r.(?) p.(Ser460Phe)
?/. - c.1387-18C>G r.(=) p.(=)
?/. - c.1424T>C r.(?) p.(Ile475Thr)
?/. - c.1462_1464del r.(?) p.(Tyr488del)
?/. - c.1462_1464del r.(?) p.(Tyr488del)
?/. - c.1490C>A r.(?) p.(Thr497Lys)
-?/. - c.1502C>T r.(?) p.(Ala501Val)
-?/. - c.1502C>T r.(?) p.(Ala501Val)
-/. - c.1502C>T r.(?) p.(Ala501Val)
-?/. - c.1502C>T r.(?) p.(Ala501Val)
-/. - c.1502C>T r.(?) p.(Ala501Val)
-?/. - c.1503A>G r.(?) p.(Ala501=)
-?/. - c.1506C>T r.(?) p.(=)
?/. - c.1529dup r.(?) p.(Thr511Asnfs*2)
?/. - c.1559C>T r.(?) p.(Ser520Leu)
-/. - c.1560G>A r.(?) p.(Ser520=)
-?/. - c.1560G>A r.(?) p.(Ser520=)
?/. - c.1671_1673del r.(?) p.(Glu559del)
?/. - c.1671_1673dup r.(?) p.(Glu559dup)
?/. - c.1671_1673dup r.(?) p.(Glu559dup)
-/. - c.*18C>T r.(=) p.(=)
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