Transcript #00014698 (NM_017617.3, NOTCH1 gene)

Transcript name notch 1
Gene name NOTCH1 (notch 1)
Chromosome 9
Transcript - NCBI ID NM_017617.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_060087.3
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

816 entries on 9 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_34_ c.-1*1627{2} r.? p.?
-?/. - c.17C>T r.(?) p.(Ala6Val)
-?/. - c.18G>T r.(?) p.(Ala6=)
?/. - c.25del r.(?) p.(Leu9Serfs*24)
+/. - c.36dup r.(?) p.(Leu13Alafs*17)
-?/. - c.62-9C>G r.(=) p.(=)
-?/. - c.64C>T r.(?) p.(Pro22Ser)
-/. - c.64C>T r.(?) p.(Pro22Ser)
-?/. - c.64C>T r.(?) p.(Pro22Ser)
-?/. - c.78G>A r.(?) p.(Gln26=)
-?/. - c.79C>A r.(?) p.(Pro27Thr)
-?/. - c.94C>T r.(?) p.(Leu32=)
+/. 2i c.140+3G>C r.[62_140del,=] p.[Gly21AlafsTer53,=]
+/. - c.140+3G>C r.spl? p.?
-?/. - c.141-293G>T r.(=) p.(=)
-?/. - c.147C>T r.(?) p.(Gly49=)
-?/. - c.156C>T r.(?) p.(Phe52=)
-?/. - c.165G>A r.(?) p.(Pro55=)
-?/. - c.165G>A r.(?) p.(Pro55=)
?/. - c.178C>T r.(?) p.(Pro60Ser)
-/. - c.186G>C r.(?) p.(Pro62=)
?/. - c.211G>C r.(?) p.(Ala71Pro)
?/. - c.214G>A r.(?) p.(Gly72Arg)
-?/. - c.230T>G r.(?) p.(Val77Gly)
?/. - c.253T>C r.(?) p.(Tyr85His)
-?/. - c.263G>A r.(?) p.(Ser88Asn)
-?/. - c.304C>A r.(?) p.(Leu102Met)
?/. - c.311A>G r.(?) p.(Asn104Ser)
-/. - c.312T>C r.(?) p.(Asn104=)
-?/. - c.312T>C r.(?) p.(Asn104=)
-/. - c.312T>C r.(?) p.(Asn104=)
-/. - c.312T>C r.(?) p.(Asn104=)
-/. - c.312T>C r.(?) p.(Asn104=)
?/. - c.313G>A r.(?) p.(Ala105Thr)
-?/. - c.368C>T r.(?) p.(Thr123Met)
-?/. - c.368C>T r.(?) p.(Thr123Met)
-?/. - c.368C>T r.(?) p.(Thr123Met)
-?/. - c.383G>A r.(?) p.(Arg128His)
-?/. - c.390G>A r.(?) p.(Pro130=)
-?/. - c.393C>T r.(?) p.(Pro131=)
-?/. - c.403+40G>C r.(=) p.(=)
-?/. - c.432C>T r.(?) p.(Cys144=)
-?/. - c.432C>T r.(?) p.(Cys144=)
-?/. - c.453C>T r.(?) p.(Asn151=)
-?/. - c.505A>G r.(?) p.(Ser169Gly)
?/. - c.518C>T r.(?) p.(Pro173Leu)
+?/. - c.568C>T r.(?) p.(Arg190Cys)
?/. - c.574G>A r.(?) p.(Gly192Arg)
-?/. - c.597C>T r.(?) p.(Val199=)
-?/. - c.621C>T r.(?) p.(Arg207=)
-?/. - c.621C>T r.(?) p.(Arg207=)
?/. - c.631A>G r.(?) p.(Thr211Ala)
?/. - c.631A>G r.(?) p.(Thr211Ala)
./. - c.646G>A r.(?) p.(Glu216Lys)
-?/. - c.663C>T r.(?) p.(Pro221=)
?/. - c.707C>T r.(?) p.(Thr236Met)
-/. - c.711C>T r.(?) p.(Gly237=)
?/. - c.724G>A r.(?) p.(Glu242Lys)
?/. - c.724G>C r.(?) p.(Glu242Gln)
-?/. - c.742+19C>T r.(=) p.(=)
-?/. - c.742+40C>T r.(=) p.(=)
-?/. - c.742+139C>T r.(=) p.(=)
-?/. - c.750C>A r.(?) p.(Thr250=)
-?/. - c.750C>T r.(?) p.(Thr250=)
?/. - c.775G>A r.(?) p.(Asp259Asn)
?/. - c.823G>A r.(?) p.(Gly275Ser)
-?/. - c.839A>G r.(?) p.(Asn280Ser)
?/. - c.839A>G r.(?) p.(Asn280Ser)
-/. - c.852G>A r.(?) p.(Pro284=)
-/. - c.852G>A r.(?) p.(Pro284=)
-/. - c.852G>A r.(?) p.(Pro284=)
-/. - c.852G>A r.(?) p.(Pro284=)
+/. - c.865+2C>A r.spl? p.?
-?/. - c.865+18C>T r.(=) p.(=)
-?/. - c.865+18C>T r.(=) p.(=)
-?/. - c.866-157G>A r.(=) p.(=)
-/. - c.873C>T r.(?) p.(Tyr291=)
-?/. - c.879C>T r.(?) p.(Thr293=)
-?/. - c.879C>T r.(?) p.(Thr293=)
+?/. - c.971T>A r.(?) p.(Val324Asp)
?/. - c.1007T>C r.(?) p.(Ile336Thr)
?/. - c.1016G>A r.(?) p.(Cys339Tyr)
+/. - c.1017_1018del r.(?) p.(Ala340GlnfsTer12)
?/. - c.1039G>A r.(?) p.(Gly347Ser)
?/. - c.1045A>C r.(?) p.(Thr349Pro)
-/. - c.1100-140G>A r.(=) p.(=)
-/. - c.1100-16G>C r.(=) p.(=)
-?/. - c.1100-14C>T r.(=) p.(=)
-?/. - c.1119C>T r.(?) p.(Asn373=)
-?/. - c.1146C>T r.(?) p.(Asn382=)
-?/. - c.1147G>A r.(?) p.(Glu383Lys)
?/. - c.1205C>T r.(?) p.(Ser402Leu)
?/. - c.1205C>T r.(?) p.(Ser402Leu)
-?/. - c.1205C>T r.(?) p.(Ser402Leu)
?/. - c.1205C>T r.(?) p.(Ser402Leu)
-?/. - c.1214C>T r.(?) p.(Thr405Met)
-?/. - c.1245G>A r.(?) p.(Glu415=)
-?/. - c.1245G>A r.(?) p.(Glu415=)
-?/. - c.1245G>A r.(?) p.(Glu415=)
-?/. - c.1256-6C>T r.(=) p.(=)
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