All transcript variants in gene TNFRSF10C

Information The variants shown are described using the NM_003841.3 transcript reference sequence.

48 entries on 1 page. Showing entries 1 - 48.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-62G>T r.(=) p.(=) g.22960573G>T Copied from the Exome Variant Server TNFRSF10C_000001 31/4566 0/3182 31/1384
?/? c.-41G>A r.(=) p.(=) g.22960594G>A Copied from the Exome Variant Server TNFRSF10C_000002 1/12986 1/8596 0/4390
?/? c.-4T>C r.(=) p.(=) g.22960631T>C Copied from the Exome Variant Server TNFRSF10C_000003 1/13000 0/8596 1/4404
?/? c.20C>T r.(?) p.(Thr7Ile) g.22960654C>T Copied from the Exome Variant Server TNFRSF10C_000006 455/13000 12/8596 443/4404
?/? c.21C>T r.(=) p.(=) g.22960655C>T Copied from the Exome Variant Server TNFRSF10C_000008 450/13002 12/8598 438/4404
?/? c.24A>G r.(=) p.(=) g.22960658A>G Copied from the Exome Variant Server TNFRSF10C_000010 1/13002 0/8598 1/4404
?/? c.43G>T r.(?) p.(Val15Phe) g.22960677G>T Copied from the Exome Variant Server TNFRSF10C_000012 28/13002 0/8596 28/4406
?/? c.60+10G>C r.(=) p.(=) g.22960704G>C Copied from the Exome Variant Server TNFRSF10C_000004 10528/13006 6669/8600 3859/4406
?/? c.60+16G>A r.(=) p.(=) g.22960710G>A Copied from the Exome Variant Server TNFRSF10C_000005 1/13002 1/8598 0/4404
?/? c.60+17G>T r.(=) p.(=) g.22960711G>T Copied from the Exome Variant Server TNFRSF10C_000007 230/13002 200/8598 30/4404
?/? c.61-50G>T r.(=) p.(=) g.22969183G>T Copied from the Exome Variant Server TNFRSF10C_000009 1/12998 0/8598 1/4400
?/? c.61-32C>T r.(=) p.(=) g.22969201C>T Copied from the Exome Variant Server TNFRSF10C_000011 1/13004 1/8598 0/4406
?/? c.68C>T r.(?) p.(Ala23Val) g.22969240C>T Copied from the Exome Variant Server TNFRSF10C_000013 1/13006 1/8600 0/4406
?/? c.135G>A r.(=) p.(=) g.22969307G>A Copied from the Exome Variant Server TNFRSF10C_000014 1/13006 1/8600 0/4406
?/? c.166+31T>G r.(=) p.(=) g.22969369T>G Copied from the Exome Variant Server TNFRSF10C_000015 1/13004 1/8598 0/4406
?/? c.172C>G r.(?) p.(His58Asp) g.22972175C>G Copied from the Exome Variant Server TNFRSF10C_000016 4/13006 0/8600 4/4406
?/? c.204G>A r.(=) p.(=) g.22972207G>A Copied from the Exome Variant Server TNFRSF10C_000017 41/13006 39/8600 2/4406
?/? c.213_214del r.(?) p.(Gly72Cysfs*10) g.22972216_22972217del Copied from the Exome Variant Server TNFRSF10C_000018 1/12518 1/8254 0/4264
?/? c.217G>A r.(?) p.(Val73Met) g.22972220G>A Copied from the Exome Variant Server TNFRSF10C_000019 12/13006 0/8600 12/4406
?/? c.224A>G r.(?) p.(Tyr75Cys) g.22972227A>G Copied from the Exome Variant Server TNFRSF10C_000020 1/13006 1/8600 0/4406
?/? c.225C>T r.(=) p.(=) g.22972228C>T Copied from the Exome Variant Server TNFRSF10C_000021 134/13006 119/8600 15/4406
?/? c.269del r.(?) p.(Cys91Valfs*13) g.22972272del Copied from the Exome Variant Server TNFRSF10C_000022 48/12516 43/8252 5/4264
?/? c.272G>A r.(?) p.(Cys91Tyr) g.22972275G>A Copied from the Exome Variant Server TNFRSF10C_000023 2/13006 2/8600 0/4406
?/? c.280+36_280+37del r.(=) p.(=) g.22972319_22972320del Copied from the Exome Variant Server TNFRSF10C_000024 46/12516 1/8252 45/4264
?/? c.280+38G>A r.(=) p.(=) g.22972321G>A Copied from the Exome Variant Server TNFRSF10C_000025 1091/13006 593/8600 498/4406
?/? c.280+43G>A r.(=) p.(=) g.22972326G>A Copied from the Exome Variant Server TNFRSF10C_000026 1/13006 1/8600 0/4406
?/? c.280+44del r.(=) p.(=) g.22972327del Copied from the Exome Variant Server TNFRSF10C_000027 44/12516 1/8252 43/4264
?/? c.280+45A>C r.(=) p.(=) g.22972328A>C Copied from the Exome Variant Server TNFRSF10C_000028 2/13006 0/8600 2/4406
?/? c.281-51G>A r.(=) p.(=) g.22972970G>A Copied from the Exome Variant Server TNFRSF10C_000029 1/13006 1/8600 0/4406
?/? c.293A>G r.(?) p.(Lys98Arg) g.22973033A>G Copied from the Exome Variant Server TNFRSF10C_000030 1/13006 0/8600 1/4406
?/? c.342C>T r.(=) p.(=) g.22973082C>T Copied from the Exome Variant Server TNFRSF10C_000031 1/13006 0/8600 1/4406
?/? c.350G>A r.(?) p.(Arg117Gln) g.22973090G>A Copied from the Exome Variant Server TNFRSF10C_000032 2/13006 0/8600 2/4406
?/? c.389+10C>T r.(=) p.(=) g.22973139C>T Copied from the Exome Variant Server TNFRSF10C_000033 1/13006 0/8600 1/4406
?/? c.389+46A>T r.(=) p.(=) g.22973175A>T Copied from the Exome Variant Server TNFRSF10C_000034 1/13006 1/8600 0/4406
?/? c.389+48G>A r.(=) p.(=) g.22973177G>A Copied from the Exome Variant Server TNFRSF10C_000035 1/13006 1/8600 0/4406
?/? c.420T>C r.(=) p.(=) g.22974184T>C Copied from the Exome Variant Server TNFRSF10C_000036 1/13006 1/8600 0/4406
?/? c.426G>A r.(=) p.(=) g.22974190G>A Copied from the Exome Variant Server TNFRSF10C_000037 1/13006 1/8600 0/4406
?/? c.467A>G r.(?) p.(Asn156Ser) g.22974231A>G Copied from the Exome Variant Server TNFRSF10C_000038 1/13006 1/8600 0/4406
?/? c.514C>T r.(?) p.(Pro172Ser) g.22974278C>T Copied from the Exome Variant Server TNFRSF10C_000039 117/13006 104/8600 13/4406
?/? c.547A>G r.(?) p.(Met183Val) g.22974311A>G Copied from the Exome Variant Server TNFRSF10C_000040 1/13000 0/8594 1/4406
?/? c.552C>T r.(=) p.(=) g.22974316C>T Copied from the Exome Variant Server TNFRSF10C_000041 1/13000 0/8594 1/4406
?/? c.627T>C r.(=) p.(=) g.22974391T>C Copied from the Exome Variant Server TNFRSF10C_000042 1/13002 0/8596 1/4406
?/? c.686T>C N/A N/A g.22974450T>C Copied from the Exome Variant Server TNFRSF10C_000043 9818/13004 6994/8598 2824/4406
?/? c.695C>T r.(?) p.(Pro232Leu) g.22974459C>T Copied from the Exome Variant Server TNFRSF10C_000044 2/13006 1/8600 1/4406
?/? c.696G>A r.(=) p.(=) g.22974460G>A Copied from the Exome Variant Server TNFRSF10C_000045 18/13006 0/8600 18/4406
?/? c.735C>T r.(=) p.(=) g.22974499C>T Copied from the Exome Variant Server TNFRSF10C_000046 1/13006 1/8600 0/4406
?/? c.736G>A r.(?) p.(Val246Ile) g.22974500G>A Copied from the Exome Variant Server TNFRSF10C_000047 2/13006 2/8600 0/4406
?/? c.*10C>T r.(=) p.(=) g.22974554C>T Copied from the Exome Variant Server TNFRSF10C_000048 1/13006 1/8600 0/4406
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