Transcript #00007247 (NM_031475.2, ESPN gene)

Transcript name espin
Gene name ESPN (espin)
Chromosome 1
Transcript - NCBI ID NM_031475.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_113663.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.84G>T r.(?) p.(Gly28=)
-?/. - c.195C>G r.(?) p.(Ala65=)
?/. - c.277G>A r.(?) p.(Gly93Ser)
-?/. - c.290T>A r.(?) p.(Val97Glu)
?/. - c.337C>T r.(?) p.(Arg113Cys)
?/. - c.337C>T r.(?) p.(Arg113Cys)
?/? 2 c.382G>T r.(?) p.(Gly128Cys)
-?/. - c.390C>T r.(?) p.(Asp130=)
?/? 2 c.439G>A r.(?) p.(Ala147Thr)
-?/. - c.588C>T r.(?) p.(=)
+?/. - c.684C>A r.(?) p.(Cys228*)
?/. - c.688G>A r.(?) p.(Asp230Asn)
?/. - c.743C>T r.(?) p.(Ala248Val)
-?/. - c.826C>T r.(?) p.(Leu276=)
?/. - c.858+4A>C r.spl? p.?
-/. - c.858+11G>T r.(=) p.(=)
-?/. - c.898G>A r.(?) p.(Val300Ile)
-/. - c.909C>G r.(?) p.(Arg303=)
-/. - c.909C>G r.(?) p.(Arg303=)
?/. - c.980T>A r.(?) p.(Val327Glu)
?/. - c.990+5G>A r.spl? p.?
?/? 6 c.1016G>A r.(?) p.(Arg339Gln)
?/? 6 c.1048C>T r.(?) p.(Pro350Ser)
-?/. - c.1049C>G r.(?) p.(Pro350Arg)
-/. - c.1069C>T r.(?) p.(Pro357Ser)
-?/. - c.1092G>A r.(?) p.(Gln364=)
?/? 6 c.1094C>T r.(?) p.(Pro365Leu)
-/. - c.1104T>G r.(?) p.(Phe368Leu)
?/. - c.1141G>C r.(?) p.(Asp381His)
-?/. - c.1193-3C>T r.spl? p.?
-/. - c.1286C>T r.(?) p.(Thr429Ile)
-?/. - c.1286C>T r.(?) p.(Thr429Ile)
-/. - c.1286C>T r.(?) p.(Thr429Ile)
-?/. - c.1293A>C r.(?) p.(=)
-/. - c.1302A>C r.(?) p.(Pro434=)
?/. - c.1306_1310del r.(?) p.(Ser436Profs*31)
?/. - c.1317_1321del r.(?) p.(Pro441Alafs*26)
-?/. - c.1386A>G r.(?) p.(Val462=)
-?/. - c.1426A>C r.(?) p.(Lys476Gln)
?/. - c.1432C>T r.(?) p.(Arg478Cys)
?/. - c.1432C>T r.(?) p.(Arg478Cys)
-/. - c.1464+18C>A r.(=) p.(=)
-/. - c.1476T>C r.(?) p.(Cys492=)
-?/. - c.1631G>A r.(?) p.(Arg544His)
+?/. 8 c.1720del r.(?) p.(Ala574Argfs*72)
+/+ 9 c.1756dup r.(?) p.(Ala586Glyfs*52)
?/. - c.1797_1808del r.(?) p.(Pro602_Pro605del)
-?/. - c.1916-6G>A r.(=) p.(=)
+/+ 11 c.1988_1991del r.(?) p.(Ala664Serfs*72)
?/. - c.2006C>T r.(?) p.(Pro669Leu)
-?/. - c.2007C>A r.(?) p.(Pro669=)
+/. - c.2019dup r.(?) p.(Leu674AlafsTer72)
?/? 12 c.2026A>G r.(?) p.(Thr676Ala)
-?/. - c.2053G>A r.(?) p.(Ala685Thr)
-?/. - c.2064C>T r.(?) p.(Pro688=)
-/. - c.2070G>A r.(?) p.(Ser690=)
?/. - c.2101C>T r.(?) p.(Pro701Ser)
?/. - c.2150A>G r.(?) p.(Asn717Ser)
?/. - c.2150A>G r.(?) p.(Asn717Ser)
+/+ 12 c.2155A>C r.(?) p.(Ile719Leu)
?/. - c.2186C>A r.(?) p.(Ala729Glu)
+?/+? 12 c.2227C>T r.(=) p.(=)
+/+ 12 c.2230G>A r.(?) p.(Asp744Asn)
?/. - c.2239G>A r.(?) p.(Gly747Ser)
?/. - c.2239G>A r.(?) p.(Gly747Ser)
+?/. 10 c.2254G>T r.(?) p.(Glu752*)
-?/. - c.2256G>A r.(?) p.(Glu752=)
?/. - c.2264G>A r.(?) p.(Arg755His)
-?/. - c.2284A>T r.(?) p.(Met762Leu)
-?/. - c.2320C>T r.(?) p.(Arg774Trp)
+/+ 13 c.2321G>A r.(?) p.(Arg774Gln)
?/. - c.2321G>A r.(?) p.(Arg774Gln)
-/. - c.2326-1949A>G r.(=) p.(=)
-/. - c.2326-1947G>A r.(=) p.(=)
+?/. 15 c.2369_2386del r.(?) p.(Arg790_Glu795del)
+?/. 15 c.2369_2386del r.(?) p.(Arg790_Glu795del)
-?/. - c.2418-20C>T r.(=) p.(=)
+/+ 15 c.2440C>T r.(?) p.(Gln814*)
+/+ 15 c.2470_2473del r.(?) p.(Ile824*)
?/. - c.2472del r.(?) p.(Glu825Argfs*22)
?/. - c.2485_2487dup r.(?) p.(Thr829dup)
+/. - c.2496del r.(?) p.(Tyr832Ter)
?/. - c.2498A>G r.(?) p.(Asp833Gly)
?/? 15 c.2504G>A r.(=) p.(=)
+?/. - c.2515C>A r.(?) p.(Pro839Thr)
+/+ 15 c.2542_2544del r.(=) p.(=)
-/. - c.*6259C>G r.(=) p.(=)
-/. - c.*6720G>A r.(=) p.(=)
-/. - c.*7127A>G r.(=) p.(=)
-/. - c.*7505G>A r.(=) p.(=)
-/. - c.*7539C>T r.(=) p.(=)
-/. - c.*7863C>G r.(=) p.(=)
?/. - c.*7901C>T r.(=) p.(=)
?/. - c.*7944T>G r.(=) p.(=)
?/. - c.*7953C>G r.(=) p.(=)
?/. - c.*7953C>G r.(=) p.(=)
-?/. - c.*8056G>A r.(=) p.(=)
?/. - c.*8112G>A r.(=) p.(=)
-/. - c.*8114C>T r.(=) p.(=)
?/. - c.*8121G>A r.(=) p.(=)
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