Transcript #00010986 (NM_002296.3, LBR gene)

Transcript name transcript variant 1
Gene name LBR (lamin B receptor)
Chromosome 1
Transcript - NCBI ID NM_002296.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002287.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
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     
-/? 1i c.-15+90C>G r.(=) p.(=)
?/? 1i c.-15+90C>G r.(=) p.(=)
?/. - c.-14-9A>G r.(=) p.(=)
-/? - c.? r.(=) p.(=)
-?/. - c.44G>A r.(?) p.(Arg15Gln)
-/? 2 c.90C>T r.(?) p.(=)
?/? 2 c.90C>T r.(?) p.(=)
-/? 2 c.117G>A r.(?) p.(=)
-/. - c.117G>A r.(?) p.(Val39=)
?/? 2 c.117G>A r.(?) p.(=)
-?/? 2i c.165+74C>T r.(=) p.(=)
-/? 2i c.166-261A>G r.(=) p.(=)
?/. - c.208A>T r.(?) p.(Ser70Cys)
?/. - c.236G>A r.(?) p.(Arg79Gln)
-/? 3 c.261T>C r.(?) p.(=)
?/? 3 c.261T>C r.(?) p.(=)
-/. - c.261T>C r.(?) p.(Pro87=)
-?/. - c.312C>T r.(?) p.(Ala104=)
?/. - c.326C>T r.(?) p.(Ala109Val)
?/. - c.356C>T r.(?) p.(Pro119Leu)
+?/. - c.366+1G>T r.spl? p.?
-/. - c.366+16C>T r.(=) p.(=)
-/? 3i c.366+16G>A r.(=) p.(=)
?/? 3i c.366+16G>A r.(=) p.(=)
+/. - c.367-2A>C r.spl? p.?
?/. - c.398A>T r.(?) p.(Asn133Ile)
-/. - c.461G>A r.(?) p.(Ser154Asn)
-/? 5 c.461G>A r.(?) p.(Ser154Asn)
?/? 5 c.461G>A r.(?) p.(Ser154Asn)
?/. - c.512G>A r.(?) p.(Arg171Lys)
-?/. - c.562G>A r.(?) p.(Val188Ile)
?/. - c.607C>T r.(?) p.(Arg203Trp)
-?/. - c.640+233C>G r.(=) p.(=)
?/. - c.655A>G r.(?) p.(Met219Val)
?/. - c.715A>T r.(?) p.(Ser239Cys)
?/. - c.724A>G r.(?) p.(Asn242Asp)
?/. - c.743C>T r.(?) p.(Pro248Leu)
?/. - c.743C>T r.(?) p.(Pro248Leu)
-?/. - c.837+4C>T r.spl? p.?
-/? 7i c.838-69G>A r.(=) p.(=)
?/? 7i c.838-69G>A r.(=) p.(=)
-/. - c.893-5del r.spl? p.?
-?/. - c.893-5del r.spl? p.?
-/. - c.893-5del r.spl? p.?
-?/. - c.893-5dup r.spl? p.?
?/. - c.899A>G r.(?) p.(Tyr300Cys)
-?/. - c.899A>G r.(?) p.(Tyr300Cys)
-?/. - c.959A>G r.(?) p.(His320Arg)
?/. - c.991C>T r.(?) p.(Leu331Phe)
?/. - c.1027T>C r.(?) p.(Tyr343His)
?/. - c.1040G>A r.(?) p.(Arg347His)
-?/. - c.1057C>T r.(?) p.(Arg353Trp)
-/? 8 c.1071G>A r.(?) p.(=)
?/. - c.1114C>T r.(?) p.(Arg372Cys)
+?/. - c.1114C>T r.(?) p.(Arg372Cys)
?/. - c.1115G>A r.(?) p.(Arg372His)
+/. 9 c.1174G>A r.(?) p.(Gly392Arg)
-?/. - c.1188+4T>C r.spl? p.?
?/. - c.1384G>T r.(?) p.(Val462Leu)
-?/. - c.1399A>T r.(?) p.(Ile467Phe)
+?/. - c.1432C>G r.(?) p.(His478Asp)
-?/. - c.1483C>T r.(?) p.(Leu495Phe)
+/. - c.1483+1G>A r.spl? p.?
-/. - c.1528G>A r.(?) p.(Ala510Thr)
+/. - c.1534C>T r.(?) p.(Arg512Trp)
+/. 12 c.1535G>A r.(?) p.(Arg512Gln)
?/. - c.1561G>T r.(?) p.(Ala521Ser)
?/. - c.1631G>A r.(?) p.(Arg544His)
+?/. - c.1639A>G r.(?) p.(Asn547Asp)
+/. - c.1672T>C r.(?) p.(Trp558Arg)
?/. - c.1771T>C r.(?) p.(Cys591Arg)
-?/. - c.1801A>G r.(?) p.(Lys601Glu)
?/. - c.1828A>C r.(?) p.(Ile610Leu)
+?/. - c.1834C>A r.(?) p.(Pro612Thr)
-?/? 14 c.*22A>C r.(?) p.(=)
-?/. - c.*4034T>A r.(=) p.(=)
-?/. - c.*4104G>T r.(=) p.(=)
-?/. - c.*4198C>T r.(=) p.(=)
-?/. - c.*4267dup r.(?) p.(=)
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