Transcript #00009249 (NM_020760.1, HECW2 gene)

Transcript name HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2
Gene name HECW2 (HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2)
Chromosome 2
Transcript - NCBI ID NM_020760.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_065811.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-36+3C>G r.spl? p.?
-?/. - c.44G>A r.(?) p.(Arg15Gln)
-?/. - c.116A>C r.(?) p.(Glu39Ala)
?/. - c.205A>G r.(?) p.(Thr69Ala)
-?/. - c.207G>A r.(?) p.(Thr69=)
+?/. - c.412A>G r.(?) p.(Ile138Val)
-?/. - c.429C>T r.(?) p.(Tyr143=)
?/. - c.433G>A r.(?) p.(Gly145Ser)
-?/. - c.495+8C>T r.(=) p.(=)
-/. - c.533A>G r.(?) p.(Asn178Ser)
?/. - c.737G>A r.(?) p.(Arg246Gln)
?/. - c.812G>A r.(?) p.(Arg271His)
-?/. - c.872G>A r.(?) p.(Arg291Gln)
-?/. - c.1112C>G r.(?) p.(Pro371Arg)
+?/. - c.1160G>C r.(?) p.(Arg387Thr)
?/. - c.1207T>G r.(?) p.(Ser403Ala)
-?/. - c.1250A>G r.(?) p.(Asn417Ser)
?/. - c.1325G>A r.(?) p.(Gly442Asp)
?/. - c.1344_1346del r.(?) p.(Arg448del)
?/. - c.1564G>A r.(?) p.(Glu522Lys)
-?/. - c.1738G>A r.(?) p.(Ala580Thr)
-?/. - c.1745C>A r.(?) p.(Thr582Lys)
-?/. - c.1756G>A r.(?) p.(Asp586Asn)
-?/. - c.1820C>A r.(?) p.(Pro607His)
?/. - c.1878C>T r.(?) p.(Ser626=)
-?/. - c.2097A>C r.(?) p.(Glu699Asp)
-?/. - c.2097A>C r.(?) p.(Glu699Asp)
-?/. - c.2142T>G r.(?) p.(Ser714Arg)
?/. - c.2242G>C r.(?) p.(Ala748Pro)
?/. - c.2448_2450del r.(?) p.(Ile817del)
-?/. - c.2475C>T r.(?) p.(Tyr825=)
-?/. - c.2586-343C>T r.(=) p.(=)
+?/. - c.2587T>C r.spl p.(Tyr863His)
-?/. - c.2689+5G>C r.spl? p.?
-?/. - c.2689+7G>T r.(=) p.(=)
?/. - c.2818G>A r.(?) p.(Ala940Thr)
?/. - c.2843C>T r.(?) p.(Thr948Met)
?/. - c.2942C>T r.(?) p.(Ala981Val)
?/. - c.2963C>T r.(?) p.(Pro988Leu)
-?/. - c.3000+7C>T r.(=) p.(=)
?/. - c.3038T>G r.(?) p.(Phe1013Cys)
-?/. - c.3084G>A r.(?) p.(Ala1028=)
?/. - c.3110G>A r.(?) p.(Arg1037Lys)
?/. - c.3175C>T r.(?) p.(Pro1059Ser)
?/. - c.3272A>T r.(?) p.(Gln1091Leu)
-?/. - c.3318C>T r.(?) p.(Thr1106=)
-?/. - c.3335+440dup r.(=) p.(=)
-?/. - c.3380T>C r.(?) p.(Val1127Ala)
?/. - c.3382C>T r.(?) p.(Arg1128Cys)
+/. 20 c.3542C>G r.(?) p.(Ala1181Gly)
?/. - c.3545A>G r.(?) p.(Asn1182Ser)
+/. 20 c.3572G>A r.(?) p.(Arg1191Gln)
+/. 20 c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. - c.3572G>A r.(?) p.(Arg1191Gln)
+/. 20 c.3577T>G r.(?) p.(Phe1193Val)
+/. 20 c.3577T>G r.(?) p.(Phe1193Val)
+?/. - c.3583G>C r.(?) p.(Ala1195Pro)
+/. 20 c.3587A>G r.(?) p.(Lys1196Arg)
+?/. - c.3597C>A r.(?) p.(Asn1199Lys)
+?/. - c.3597C>A r.(?) p.(Asn1199Lys)
?/. - c.3629G>C r.(?) p.(Gly1210Ala)
+/. 22 c.3917+2_3917+12delinsG r.3765_3917del p.Leu1256_Trp1306del
+?/. - c.3980T>C r.(?) p.(Phe1327Ser)
+?/. - c.3980T>C r.(?) p.(Phe1327Ser)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+/. 23 c.3988C>T r.(?) p.(Arg1330Trp)
+/. 23 c.3988C>T r.(?) p.(Arg1330Trp)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+?/. - c.3988C>T r.(?) p.(Arg1330Trp)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+/. - c.3988C>T r.(?) p.(Arg1330Trp)
+?/. - c.3988C>T r.(?) p.(Arg1330Trp)
-?/. - c.4017T>G r.(?) p.(Ile1339Met)
-?/. - c.4096C>A r.(?) p.(His1366Asn)
-?/. - c.4181A>G r.(?) p.(Asn1394Ser)
-?/. - c.4223G>C r.(?) p.(Arg1408Thr)
?/. - c.4321T>A r.(?) p.(Phe1441Ile)
+?/. - c.4323T>G r.(?) p.(Phe1441Leu)
+/. - c.4333G>C r.(?) p.(Glu1445Gln)
+/. 26 c.4334A>G r.(?) p.(Glu1445Gly)
?/. - c.4341A>T r.(?) p.(Glu1447Asp)
+?/. - c.4351G>A r.(?) p.(Ala1451Thr)
+?/. - c.4355G>T r.(?) p.(Gly1452Val)
-?/. - c.4476A>C r.(?) p.(Gln1492His)
?/. - c.4478G>A r.(?) p.(Arg1493Gln)
+/. - c.4484G>A r.(?) p.(Arg1495Lys)
+/. - c.4485G>T r.(?) p.(Arg1495Ser)
+?/. - c.4507A>G r.(?) p.(Thr1503Ala)
+?/. - c.4511C>A r.(?) p.(Ser1504Tyr)
+?/. - c.4514G>C r.(?) p.(Ser1505Thr)
?/. - c.4556G>T r.(?) p.(Gly1519Val)
-?/. - c.4610C>T r.(?) p.(Ala1537Val)
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