Transcript #00011065 (NM_002303.5, LEPR gene)

Transcript name transcript variant 1
Gene name LEPR (leptin receptor)
Chromosome 1
Transcript - NCBI ID NM_002303.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_002294.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-92C>T - p.(=)
-/. - c.-20-166G>A r.(=) p.(=)
-/. - c.-20-15A>T r.(=) p.(=)
-?/. - c.36T>C r.(?) p.(His12=)
-/. - c.129C>T r.(?) p.(Thr43=)
?/. - c.165G>C r.(?) p.(Lys55Asn)
?/. - c.200C>A r.(?) p.(Ala67Asp)
?/. - c.221C>T r.(?) p.(Ser74Leu)
-?/. - c.280G>A r.(?) p.(Glu94Lys)
?/. - c.323G>A r.(?) p.(Gly108Glu)
-/. - c.326A>G r.(?) p.(Lys109Arg)
-/. - c.326A>G r.(?) p.(Lys109Arg)
-/. - c.370+16G>T r.(=) p.(=)
-/. - c.370+16G>T r.(=) p.(=)
-/. - c.370+16G>T r.(=) p.(=)
-/. - c.371-342_371-337dup r.(=) p.(=)
-/. - c.371-16T>G r.(=) p.(=)
?/. - c.371-14_371-9dup r.(=) p.(=)
?/. - c.371-13_371-9dup r.(=) p.(=)
-?/. - c.371A>G r.(?) p.(Asp124Gly)
+/. - c.416T>G r.(?) p.(Leu139*)
-?/. - c.430G>T r.(?) p.(Val144Leu)
?/. - c.430G>T r.(?) p.(Val144Leu)
-?/. 5i c.495-5182_495-3861del r.(?) p.(=)
+/. 5i_20_ c.495-2107_*12391delinsGTGTGTATATGGGGGT r.? p.?
-/. - c.495-125dup r.(=) p.(=)
-/. - c.536G>A r.(?) p.(Gly179Asp)
-/. - c.594G>A r.(?) p.(Val198=)
-?/. - c.611A>G r.(?) p.(Lys204Arg)
-?/. - c.621C>T r.(?) p.(Asp207=)
-/. - c.668A>G r.(?) p.(Gln223Arg)
-/. - c.668A>G r.(?) p.(Gln223Arg)
-?/. - c.678A>G r.(?) p.(Leu226=)
-/. - c.703+304_703+305insATTA r.(=) p.(=)
+/. - c.808C>T r.(?) p.(Gln270*)
-?/. - c.850-6del r.(=) p.(=)
?/. - c.921G>C r.(?) p.(Gln307His)
?/. - c.966G>T r.(?) p.(Trp322Cys)
-?/. - c.977G>A r.(?) p.(Arg326His)
-/. - c.1029T>C r.(?) p.(Ser343=)
-/. - c.1029T>C r.(?) p.(Ser343=)
?/. - c.1030G>A r.(?) p.(Val344Ile)
-?/. - c.1209A>G r.(?) p.(=)
+/. - c.1226C>A r.(?) p.(Ala409Glu)
-?/. - c.1246C>T r.(?) p.(His416Tyr)
-?/. - c.1246C>T r.(?) p.(His416Tyr)
-/. - c.1284T>C r.(?) p.(Ile428=)
+?/. - c.1285+1G>A r.spl? p.?
-/. - c.1285+20G>A r.(=) p.(=)
-/. - c.1285+20G>A r.(=) p.(=)
+/. - c.1603+5G>T r.spl? p.?
-?/. - c.1604-16T>C r.(=) p.(=)
-?/. - c.1604-8A>G r.(=) p.(=)
+/. 12 c.1675G>A r.(?) p.(Trp558*)
?/. - c.1713G>T r.(?) p.(Gln571His)
?/. - c.1717C>A r.(?) p.(Arg573Ser)
+?/. - c.1752+2T>C r.spl? p.?
-?/. - c.1770T>C r.(?) p.(=)
+/. - c.1790del r.(?) p.(Ser597Ilefs*20)
+/. 13 c.1810T>A r.(?) p.(Cys604Ser)
+?/. - c.1835G>A r.(?) p.(Arg612His)
?/. - c.1867A>C r.(?) p.(Ser623Arg)
-/. - c.1968G>C r.(?) p.(Lys656Asn)
-/. - c.1968G>C r.(?) p.(Lys656Asn)
-/. - c.1968G>C r.(?) p.(Lys656Asn)
+?/. - c.1985T>C r.(?) p.(Leu662Ser)
-?/. - c.1995+10A>T r.(=) p.(=)
+/. - c.2051A>C r.(?) p.(His684Pro)
+/. - c.2051A>C r.(?) p.(His684Pro)
+/. - c.2051A>C r.(?) p.(His684Pro)
-/. - c.2096C>T r.(?) p.(Thr699Met)
+?/. - c.2168C>T r.(?) p.(Ser723Phe)
-?/. - c.2220C>T r.(?) p.(Ile740=)
-?/. - c.2260G>A r.(?) p.(Val754Met)
+/. 16i c.2396-1G>T r.spl p.?
+/. 16i c.2396-1G>T r.spl p.?
+/. 16i c.2396-1G>T r.spl p.?
-/. - c.2597+15G>C r.(=) p.(=)
-/. - c.2597+15G>C r.(=) p.(=)
+?/. - c.2627C>A r.(?) p.(Pro876Gln)
-/. - c.2674-5912A>C r.(=) p.(=)
-/. - c.2674-5912A>C r.(=) p.(=)
?/. - c.2674-5885A>T r.(=) p.(=)
-/. - c.2674-5843T>A r.(=) p.(=)
-?/. - c.2674-5771_2674-5769dup r.(=) p.(=)
-/. - c.2674-5770_2674-5769dup r.(=) p.(=)
-/. - c.2674-5769dup r.(=) p.(=)
-/. - c.2674-5768del r.(=) p.(=)
-/. - c.2674-5768G>A r.(=) p.(=)
-?/. - c.2698A>G r.(?) p.(Ile900Val)
-?/. - c.2918C>A r.(?) p.(Thr973Asn)
-?/. - c.2928C>T r.(?) p.(Asp976=)
+?/. - c.2958C>G r.(?) p.(Tyr986*)
?/. - c.2963C>T r.(?) p.(Thr988Met)
?/. - c.2977T>C r.(?) p.(Ser993Pro)
-/. - c.2987G>A r.(?) p.(Ser996Asn)
-/. - c.3019A>T r.(?) p.(Ser1007Cys)
-?/. - c.3019A>T r.(?) p.(Ser1007Cys)
-/. - c.3024A>G r.(?) p.(Ser1008=)
-?/. - c.3027C>T r.(?) p.(=)
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