Transcript #00024069 (NM_016434.3, RTEL1 gene)

Transcript name transcript variant 1
Gene name RTEL1 (regulator of telomere elongation helicase 1)
Chromosome 20
Transcript - NCBI ID NM_016434.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_057518.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-10-26 21:42:29 +01:00 (CET)
Date last edited N/A


Variants

280 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-376G>C r.(?) p.(=)
-/. - c.-93C>T r.(?) p.(=)
-/. - c.-93C>T r.(?) p.(=)
-?/. - c.-59A>C r.(?) p.(=)
?/. - c.29C>T r.(?) p.(Thr10Ile)
?/. - c.62A>T r.(?) p.(Gln21Leu)
-?/. - c.108G>C r.(?) p.(Val36=)
?/. - c.152G>C r.(?) p.(Cys51Ser)
?/. - c.173C>G r.(?) p.(Ala58Gly)
-?/. - c.183A>T r.(?) p.(Glu61Asp)
?/. - c.190C>T r.(?) p.(Arg64*)
+/. 3 c.190C>T r.(?) p.(Arg64Ter)
?/. - c.208C>T r.(?) p.(Arg70Cys)
-?/. - c.245C>T r.(?) p.(Pro82Leu)
?/. - c.287_289dup r.(?) p.(Ala96dup)
-?/. - c.293A>C r.(?) p.(Asp98Ala)
-?/. - c.301+7C>T r.(=) p.(=)
?/. - c.334G>A r.(?) p.(Ala112Thr)
?/. - c.350C>T r.(?) p.(Ser117Leu)
-/. - c.371A>G r.(?) p.(Asn124Ser)
-?/. - c.372C>T r.(?) p.(Asn124=)
-?/. - c.372C>T r.(?) p.(Asn124=)
-?/. - c.395+12G>A r.(=) p.(=)
-?/. - c.395+12G>A r.(=) p.(=)
-?/. - c.396-37C>T r.(=) p.(=)
?/. - c.396-10C>T r.(=) p.(=)
-?/. - c.411G>T r.(?) p.(Val137=)
+?/. - c.416G>A r.(?) p.(Gly139Asp)
-/. - c.477+82G>A r.(=) p.(=)
-/. - c.478-88T>C r.(=) p.(=)
-?/. - c.489C>T r.(?) p.(Cys163=)
?/. - c.518A>G r.(?) p.(His173Arg)
?/. - c.522C>A r.(?) p.(Phe174Leu)
?/. - c.527A>G r.(?) p.(Asn176Ser)
?/. - c.538+3A>G r.spl? p.?
-?/. - c.540A>T r.(?) p.(Glu180Asp)
-?/. - c.542A>G r.(?) p.(Lys181Arg)
-?/. - c.549G>A r.(?) p.(Leu183=)
?/. - c.554A>G r.(?) p.(Gln185Arg)
-/. - c.582T>C r.(?) p.(Ile194=)
?/. - c.600C>A r.(?) p.(Ser200Arg)
?/. - c.600C>A r.(?) p.(Ser200Arg)
-?/. - c.615-4C>T r.spl? p.?
?/. - c.638G>A r.(?) p.(Arg213Gln)
?/. - c.703C>T r.(?) p.(Arg235Cys)
-?/. - c.744C>T r.(?) p.(Ile248=)
-/. - c.766-19G>A r.(=) p.(=)
-/. - c.786G>A r.(?) p.(Ser262=)
?/. - c.802A>G r.(?) p.(Thr268Ala)
-?/. - c.860C>T r.(?) p.(Thr287Ile)
-/. - c.879T>C r.(?) p.(Gly293=)
?/. - c.904G>T r.(?) p.(Asp302Tyr)
-?/. - c.905A>G r.(?) p.(Asp302Gly)
-?/. - c.919+5G>A r.spl? p.?
-/. - c.936G>A r.(=) p.(=)
-?/. - c.947C>T r.(?) p.(Ala316Val)
-/. - c.958+18C>T r.(=) p.(=)
-/. - c.958+18C>T r.(=) p.(=)
-?/. - c.959-10C>T r.(=) p.(=)
-?/. - c.959-10C>T r.(=) p.(=)
-?/. - c.959T>C r.(?) p.(Met320Thr)
?/. - c.959T>C r.(?) p.(Met320Thr)
-?/. - c.959T>C r.(?) p.(Met320Thr)
-?/. - c.959T>C r.(?) p.(Met320Thr)
-/. - c.978G>A r.(?) p.(Glu326=)
-/. - c.978G>A r.(?) p.(Glu326=)
-/. - c.978G>A r.(=) p.(=)
-?/. - c.1011C>T r.(?) p.(Asp337=)
-/. - c.1017C>T r.(?) p.(Ser339=)
-?/. - c.1017C>T r.(?) p.(Ser339=)
-?/. - c.1038-15T>C r.(=) p.(=)
?/. - c.1073C>T r.(?) p.(Thr358Met)
-?/. - c.1104G>A r.(?) p.(Ser368=)
-?/. - c.1179G>A r.(?) p.(Ala393=)
-?/. - c.1189C>G r.(?) p.(Gln397Glu)
-?/. - c.1189C>G r.(?) p.(Gln397Glu)
-?/. - c.1192-13C>T r.(=) p.(=)
-/. - c.1192-9del r.(=) p.(=)
-/. - c.1260C>T r.(?) p.(Ser420=)
?/. - c.1262A>G r.(?) p.(Tyr421Cys)
+?/. - c.1266+3_1266+80del r.spl? p.?
-?/. - c.1348+6G>A r.(=) p.(=)
-?/. - c.1348+6G>A r.(=) p.(=)
-?/. - c.1349-14C>T r.(=) p.(=)
-?/. - c.1349-13C>T r.(=) p.(=)
?/. - c.1374C>G r.(?) p.(Phe458Leu)
-?/. - c.1405C>T r.(?) p.(Arg469Cys)
-?/. - c.1437C>T r.(?) p.(Ser479=)
-?/. - c.1443G>A r.(?) p.(Thr481=)
?/. - c.1474A>T r.(?) p.(Met492Leu)
-?/. - c.1481+6G>A r.(=) p.(=)
-?/. - c.1482-13T>C r.(=) p.(=)
-?/. - c.1482-7C>T r.(=) p.(=)
-/. - c.1482-6G>A r.(=) p.(=)
-/. - c.1482-6G>A r.(=) p.(=)
-?/. - c.1548C>T r.(?) p.(Val516=)
-/. - c.1548C>T r.(?) p.(Val516=)
-?/. - c.1581C>T r.(?) p.(Ser527=)
-?/. - c.1582G>A r.(?) p.(Ala528Thr)
-?/. - c.1584G>A r.(?) p.(Ala528=)
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