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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.23191779_23191780del | CA645551268 | TNFRSF10A | c.1326_1327del (p.Lys443AspfsTer?) c.852_853del (p.Lys285AspfsTer?) | COSMIC |
| 8 | g.23191778_23191779delinsTC | CA1770754058 | TNFRSF10A | c.1322_1323delinsGA (p.Arg441=) c.848_849delinsGA (p.Arg283=) | |
| 8 | g.23191779del | CA1770754061 | TNFRSF10A | c.1322del (p.Arg441LysfsTer17) c.848del (p.Arg283LysfsTer17) | dbSNP gnomAD v4 |
| 8 | g.23191779C>A | CA370568400 | TNFRSF10A | c.1322G>T (p.Arg441Ile) c.848G>T (p.Arg283Ile) | |
| 8 | g.23191779C= | CA1770754063 | TNFRSF10A | c.1322G= (p.Arg441=) c.848G= (p.Arg283=) | |
| 8 | g.23191779C>G | CA370568402 | TNFRSF10A | c.1322G>C (p.Arg441Thr) c.848G>C (p.Arg283Thr) | dbSNP |
| 8 | g.23191779C>T | CA4674550 | TNFRSF10A | c.1322G>A (p.Arg441Lys) c.848G>A (p.Arg283Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191780T>A | CA370568408 | TNFRSF10A | c.1321A>T (p.Arg441Ter) c.847A>T (p.Arg283Ter) | |
| 8 | g.23191780T>C | CA370568411 | TNFRSF10A | c.1321A>G (p.Arg441Gly) c.847A>G (p.Arg283Gly) | |
| 8 | g.23191780T>G | CA460179327 | TNFRSF10A | c.1321A>C (p.Arg441=) c.847A>C (p.Arg283=) | |
| 8 | g.23191781T>A | CA460179328 | TNFRSF10A | c.1320A>T (p.Ala440=) c.846A>T (p.Ala282=) | |
| 8 | g.23191781T>C | CA460179329 | TNFRSF10A | c.1320A>G (p.Ala440=) c.846A>G (p.Ala282=) | |
| 8 | g.23191781T>G | CA4674551 | TNFRSF10A | c.1320A>C (p.Ala440=) c.846A>C (p.Ala282=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191781T= | CA1770754067 | TNFRSF10A | c.1320A= (p.Ala440=) c.846A= (p.Ala282=) | |
| 8 | g.23191782G>A | CA370568414 | TNFRSF10A | c.1319C>T (p.Ala440Val) c.845C>T (p.Ala282Val) | |
| 8 | g.23191782G>C | CA370568419 | TNFRSF10A | c.1319C>G (p.Ala440Gly) c.845C>G (p.Ala282Gly) | |
| 8 | g.23191782G= | CA1770754071 | TNFRSF10A | c.1319C= (p.Ala440=) c.845C= (p.Ala282=) | |
| 8 | g.23191782G>T | CA4674552 | TNFRSF10A | c.1319C>A (p.Ala440Glu) c.845C>A (p.Ala282Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191783C>A | CA370568429 | TNFRSF10A | c.1318G>T (p.Ala440Ser) c.844G>T (p.Ala282Ser) | |
| 8 | g.23191783C>G | CA370568434 | TNFRSF10A | c.1318G>C (p.Ala440Pro) c.844G>C (p.Ala282Pro) | |
| 8 | g.23191783C>T | CA370568436 | TNFRSF10A | c.1318G>A (p.Ala440Thr) c.844G>A (p.Ala282Thr) | gnomAD v4 |
| 8 | g.23191784A= | CA1770754075 | TNFRSF10A | c.1317T= (p.His439=) c.843T= (p.His281=) | |
| 8 | g.23191784A>C | CA173931884 | TNFRSF10A | c.1317T>G (p.His439Gln) c.843T>G (p.His281Gln) | dbSNP gnomAD v4 |
| 8 | g.23191784A>G | CA460179332 | TNFRSF10A | c.1317T>C (p.His439=) c.843T>C (p.His281=) | |
| 8 | g.23191784A>T | CA370568437 | TNFRSF10A | c.1317T>A (p.His439Gln) c.843T>A (p.His281Gln) | |
| 8 | g.23191785T>A | CA370568440 | TNFRSF10A | c.1316A>T (p.His439Leu) c.842A>T (p.His281Leu) | |
| 8 | g.23191785T>C | CA370568444 | TNFRSF10A | c.1316A>G (p.His439Arg) c.842A>G (p.His281Arg) | gnomAD v4 |
| 8 | g.23191785T>G | CA370568446 | TNFRSF10A | c.1316A>C (p.His439Pro) c.842A>C (p.His281Pro) | |
| 8 | g.23191786G>A | CA370568450 | TNFRSF10A | c.1315C>T (p.His439Tyr) c.841C>T (p.His281Tyr) | gnomAD v4 |
| 8 | g.23191786G>C | CA173931885 | TNFRSF10A | c.1315C>G (p.His439Asp) c.841C>G (p.His281Asp) | dbSNP gnomAD v4 |
| 8 | g.23191786G= | CA1770754083 | TNFRSF10A | c.1315C= (p.His439=) c.841C= (p.His281=) | |
| 8 | g.23191786G>T | CA370568451 | TNFRSF10A | c.1315C>A (p.His439Asn) c.841C>A (p.His281Asn) | dbSNP |
| 8 | g.23191787T>A | CA370568456 | TNFRSF10A | c.1314A>T (p.Arg438Ser) c.840A>T (p.Arg280Ser) | |
| 8 | g.23191787T>C | CA460179336 | TNFRSF10A | c.1314A>G (p.Arg438=) c.840A>G (p.Arg280=) | |
| 8 | g.23191787T>G | CA370568458 | TNFRSF10A | c.1314A>C (p.Arg438Ser) c.840A>C (p.Arg280Ser) | |
| 8 | g.23191788C>A | CA370568463 | TNFRSF10A | c.1313G>T (p.Arg438Ile) c.839G>T (p.Arg280Ile) | |
| 8 | g.23191788C= | CA1770754088 | TNFRSF10A | c.1313G= (p.Arg438=) c.839G= (p.Arg280=) | |
| 8 | g.23191788C>G | CA370568466 | TNFRSF10A | c.1313G>C (p.Arg438Thr) c.839G>C (p.Arg280Thr) | |
| 8 | g.23191788C>T | CA370568468 | TNFRSF10A | c.1313G>A (p.Arg438Lys) c.839G>A (p.Arg280Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191789T>A | CA370568473 | TNFRSF10A | c.1312A>T (p.Arg438Ter) c.838A>T (p.Arg280Ter) | |
| 8 | g.23191789T>C | CA370568478 | TNFRSF10A | c.1312A>G (p.Arg438Gly) c.838A>G (p.Arg280Gly) | |
| 8 | g.23191789T>G | CA460179341 | TNFRSF10A | c.1312A>C (p.Arg438=) c.838A>C (p.Arg280=) | |
| 8 | g.23191790C>A | CA370568479 | TNFRSF10A | c.1311G>T (p.Glu437Asp) c.837G>T (p.Glu279Asp) | |
| 8 | g.23191790C= | CA1770754095 | TNFRSF10A | c.1311G= (p.Glu437=) c.837G= (p.Glu279=) | |
| 8 | g.23191790C>G | CA4674553 | TNFRSF10A | c.1311G>C (p.Glu437Asp) c.837G>C (p.Glu279Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191790C>T | CA460179342 | TNFRSF10A | c.1311G>A (p.Glu437=) c.837G>A (p.Glu279=) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191791T>A | CA370568487 | TNFRSF10A | c.1310A>T (p.Glu437Val) c.836A>T (p.Glu279Val) | |
| 8 | g.23191791T>C | CA4674554 | TNFRSF10A | c.1310A>G (p.Glu437Gly) c.836A>G (p.Glu279Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191791T>G | CA370568492 | TNFRSF10A | c.1310A>C (p.Glu437Ala) c.836A>C (p.Glu279Ala) | |
| 8 | g.23191791T= | CA1770754099 | TNFRSF10A | c.1310A= (p.Glu437=) c.836A= (p.Glu279=) | |
| 8 | g.23191792C>A | CA370568493 | TNFRSF10A | c.1309G>T (p.Glu437Ter) c.835G>T (p.Glu279Ter) | |
| 8 | g.23191792C= | CA1770754104 | TNFRSF10A | c.1309G= (p.Glu437=) c.835G= (p.Glu279=) | |
| 8 | g.23191792C>G | CA370568494 | TNFRSF10A | c.1309G>C (p.Glu437Gln) c.835G>C (p.Glu279Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191792C>T | CA370568496 | TNFRSF10A | c.1309G>A (p.Glu437Lys) c.835G>A (p.Glu279Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191793T>A | CA370568499 | TNFRSF10A | c.1308A>T (p.Glu436Asp) c.834A>T (p.Glu278Asp) | |
| 8 | g.23191793T>C | CA460179348 | TNFRSF10A | c.1308A>G (p.Glu436=) c.834A>G (p.Glu278=) | |
| 8 | g.23191793T>G | CA370568498 | TNFRSF10A | c.1308A>C (p.Glu436Asp) c.834A>C (p.Glu278Asp) | |
| 8 | g.23191794T>A | CA370568500 | TNFRSF10A | c.1307A>T (p.Glu436Val) c.833A>T (p.Glu278Val) | |
| 8 | g.23191794T>C | CA370568502 | TNFRSF10A | c.1307A>G (p.Glu436Gly) c.833A>G (p.Glu278Gly) | |
| 8 | g.23191794T>G | CA370568505 | TNFRSF10A | c.1307A>C (p.Glu436Ala) c.833A>C (p.Glu278Ala) | |
| 8 | g.23191795C>A | CA370568508 | TNFRSF10A | c.1306G>T (p.Glu436Ter) c.832G>T (p.Glu278Ter) | |
| 8 | g.23191795C= | CA1770754111 | TNFRSF10A | c.1306G= (p.Glu436=) c.832G= (p.Glu278=) | |
| 8 | g.23191795C>G | CA173931890 | TNFRSF10A | c.1306G>C (p.Glu436Gln) c.832G>C (p.Glu278Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191795C>T | CA370568513 | TNFRSF10A | c.1306G>A (p.Glu436Lys) c.832G>A (p.Glu278Lys) | COSMIC |
| 8 | g.23191796C>A | CA370568517 | TNFRSF10A | c.1305G>T (p.Met435Ile) c.831G>T (p.Met277Ile) | gnomAD v4 |
| 8 | g.23191796C>G | CA370568520 | TNFRSF10A | c.1305G>C (p.Met435Ile) c.831G>C (p.Met277Ile) | |
| 8 | g.23191796C>T | CA370568524 | TNFRSF10A | c.1305G>A (p.Met435Ile) c.831G>A (p.Met277Ile) | |
| 8 | g.23191797A= | CA1770754116 | TNFRSF10A | c.1304T= (p.Met435=) c.830T= (p.Met277=) | |
| 8 | g.23191797A>C | CA370568527 | TNFRSF10A | c.1304T>G (p.Met435Arg) c.830T>G (p.Met277Arg) | gnomAD v4 |
| 8 | g.23191797A>G | CA370568544 | TNFRSF10A | c.1304T>C (p.Met435Thr) c.830T>C (p.Met277Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191797A>T | CA370568549 | TNFRSF10A | c.1304T>A (p.Met435Lys) c.830T>A (p.Met277Lys) | |
| 8 | g.23191798T>A | CA370568555 | TNFRSF10A | c.1303A>T (p.Met435Leu) c.829A>T (p.Met277Leu) | gnomAD v4 |
| 8 | g.23191798T>C | CA370568559 | TNFRSF10A | c.1303A>G (p.Met435Val) c.829A>G (p.Met277Val) | |
| 8 | g.23191798T>G | CA370568557 | TNFRSF10A | c.1303A>C (p.Met435Leu) c.829A>C (p.Met277Leu) | |
| 8 | g.23191799C>A | CA370568563 | TNFRSF10A | c.1302G>T (p.Arg434Ser) c.828G>T (p.Arg276Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191799C= | CA1770754121 | TNFRSF10A | c.1302G= (p.Arg434=) c.828G= (p.Arg276=) | |
| 8 | g.23191799C>G | CA370568566 | TNFRSF10A | c.1302G>C (p.Arg434Ser) c.828G>C (p.Arg276Ser) | |
| 8 | g.23191799C>T | CA4674555 | TNFRSF10A | c.1302G>A (p.Arg434=) c.828G>A (p.Arg276=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.23191800C>A | CA370568570 | TNFRSF10A | c.1301G>T (p.Arg434Met) c.827G>T (p.Arg276Met) | |
| 8 | g.23191800C= | CA1770754131 | TNFRSF10A | c.1301G= (p.Arg434=) c.827G= (p.Arg276=) | |
| 8 | g.23191800C>G | CA370568580 | TNFRSF10A | c.1301G>C (p.Arg434Thr) c.827G>C (p.Arg276Thr) | ClinVar gnomAD v4 |
| 8 | g.23191800C>T | CA370568576 | TNFRSF10A | c.1301G>A (p.Arg434Lys) c.827G>A (p.Arg276Lys) | dbSNP gnomAD v4 |
| 8 | g.23191801T>A | CA370568582 | TNFRSF10A | c.1300A>T (p.Arg434Trp) c.826A>T (p.Arg276Trp) | gnomAD v4 |
| 8 | g.23191801T>C | CA370568589 | TNFRSF10A | c.1300A>G (p.Arg434Gly) c.826A>G (p.Arg276Gly) | |
| 8 | g.23191801T>G | CA4674556 | TNFRSF10A | c.1300A>C (p.Arg434=) c.826A>C (p.Arg276=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191801T= | CA1770754137 | TNFRSF10A | c.1300A= (p.Arg434=) c.826A= (p.Arg276=) | |
| 8 | g.23191802C>A | CA370568593 | TNFRSF10A | c.1299G>T (p.Glu433Asp) c.825G>T (p.Glu275Asp) | |
| 8 | g.23191802C= | CA1770754142 | TNFRSF10A | c.1299G= (p.Glu433=) c.825G= (p.Glu275=) | |
| 8 | g.23191802C>G | CA370568595 | TNFRSF10A | c.1299G>C (p.Glu433Asp) c.825G>C (p.Glu275Asp) | gnomAD v4 |
| 8 | g.23191802C>T | CA460179360 | TNFRSF10A | c.1299G>A (p.Glu433=) c.825G>A (p.Glu275=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191803T>A | CA370568600 | TNFRSF10A | c.1298A>T (p.Glu433Val) c.824A>T (p.Glu275Val) | |
| 8 | g.23191803T>C | CA370568602 | TNFRSF10A | c.1298A>G (p.Glu433Gly) c.824A>G (p.Glu275Gly) | |
| 8 | g.23191803T>G | CA370568604 | TNFRSF10A | c.1298A>C (p.Glu433Ala) c.824A>C (p.Glu275Ala) | |
| 8 | g.23191804C>A | CA370568608 | TNFRSF10A | c.1297G>T (p.Glu433Ter) c.823G>T (p.Glu275Ter) | |
| 8 | g.23191804C>G | CA370568610 | TNFRSF10A | c.1297G>C (p.Glu433Gln) c.823G>C (p.Glu275Gln) | |
| 8 | g.23191804C>T | CA370568612 | TNFRSF10A | c.1297G>A (p.Glu433Lys) c.823G>A (p.Glu275Lys) | COSMIC |
| 8 | g.23191805C>A | CA370568618 | TNFRSF10A | c.1296G>T (p.Leu432Phe) c.822G>T (p.Leu274Phe) | |
| 8 | g.23191805C= | CA1770754148 | TNFRSF10A | c.1296G= (p.Leu432=) c.822G= (p.Leu274=) | |
| 8 | g.23191805C>G | CA370568619 | TNFRSF10A | c.1296G>C (p.Leu432Phe) c.822G>C (p.Leu274Phe) | |
| 8 | g.23191805C>T | CA4674557 | TNFRSF10A | c.1296G>A (p.Leu432=) c.822G>A (p.Leu274=) | dbSNP ExAC gnomAD v2 |
| 8 | g.23191806A= | CA1770754153 | TNFRSF10A | c.1295T= (p.Leu432=) c.821T= (p.Leu274=) | |
| 8 | g.23191806A>C | CA173931895 | TNFRSF10A | c.1295T>G (p.Leu432Trp) c.821T>G (p.Leu274Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191806A>G | CA370568625 | TNFRSF10A | c.1295T>C (p.Leu432Ser) c.821T>C (p.Leu274Ser) | |
| 8 | g.23191806A>T | CA370568629 | TNFRSF10A | c.1295T>A (p.Leu432Ter) c.821T>A (p.Leu274Ter) | |
| 8 | g.23191807A>C | CA370568636 | TNFRSF10A | c.1294T>G (p.Leu432Val) c.820T>G (p.Leu274Val) | |
| 8 | g.23191807A>G | CA460179365 | TNFRSF10A | c.1294T>C (p.Leu432=) c.820T>C (p.Leu274=) | |
| 8 | g.23191807A>T | CA370568638 | TNFRSF10A | c.1294T>A (p.Leu432Met) c.820T>A (p.Leu274Met) | |
| 8 | g.23191808G>A | CA460179366 | TNFRSF10A | c.1293C>T (p.Ala431=) c.819C>T (p.Ala273=) | |
| 8 | g.23191808G>C | CA460179369 | TNFRSF10A | c.1293C>G (p.Ala431=) c.819C>G (p.Ala273=) | |
| 8 | g.23191808G>T | CA460179367 | TNFRSF10A | c.1293C>A (p.Ala431=) c.819C>A (p.Ala273=) | |
| 8 | g.23191809G>A | CA370568641 | TNFRSF10A | c.1292C>T (p.Ala431Val) c.818C>T (p.Ala273Val) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191809G>C | CA370568643 | TNFRSF10A | c.1292C>G (p.Ala431Gly) c.818C>G (p.Ala273Gly) | |
| 8 | g.23191809G= | CA1770754158 | TNFRSF10A | c.1292C= (p.Ala431=) c.818C= (p.Ala273=) | |
| 8 | g.23191809G>T | CA370568644 | TNFRSF10A | c.1292C>A (p.Ala431Asp) c.818C>A (p.Ala273Asp) | |
| 8 | g.23191810C>A | CA370568646 | TNFRSF10A | c.1291G>T (p.Ala431Ser) c.817G>T (p.Ala273Ser) | |
| 8 | g.23191810C>G | CA370568647 | TNFRSF10A | c.1291G>C (p.Ala431Pro) c.817G>C (p.Ala273Pro) | |
| 8 | g.23191810C>T | CA370568648 | TNFRSF10A | c.1291G>A (p.Ala431Thr) c.817G>A (p.Ala273Thr) | |
| 8 | g.23191811A>C | CA370568649 | TNFRSF10A | c.1290T>G (p.Asp430Glu) c.816T>G (p.Asp272Glu) | |
| 8 | g.23191811A>G | CA460179372 | TNFRSF10A | c.1290T>C (p.Asp430=) c.816T>C (p.Asp272=) | |
| 8 | g.23191811A>T | CA370568650 | TNFRSF10A | c.1290T>A (p.Asp430Glu) c.816T>A (p.Asp272Glu) | gnomAD v4 |
| 8 | g.23191812T>A | CA370568655 | TNFRSF10A | c.1289A>T (p.Asp430Val) c.815A>T (p.Asp272Val) | |
| 8 | g.23191812T>C | CA370568657 | TNFRSF10A | c.1289A>G (p.Asp430Gly) c.815A>G (p.Asp272Gly) | |
| 8 | g.23191812T>G | CA370568653 | TNFRSF10A | c.1289A>C (p.Asp430Ala) c.815A>C (p.Asp272Ala) | |
| 8 | g.23191813C>A | CA370568660 | TNFRSF10A | c.1288G>T (p.Asp430Tyr) c.814G>T (p.Asp272Tyr) | |
| 8 | g.23191813C= | CA1770754162 | TNFRSF10A | c.1288G= (p.Asp430=) c.814G= (p.Asp272=) | |
| 8 | g.23191813C>G | CA370568665 | TNFRSF10A | c.1288G>C (p.Asp430His) c.814G>C (p.Asp272His) | gnomAD v4 |
| 8 | g.23191813C>T | CA4674558 | TNFRSF10A | c.1288G>A (p.Asp430Asn) c.814G>A (p.Asp272Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191814C>A | CA460179384 | TNFRSF10A | c.1287G>T (p.Leu429=) n.342G>T c.813G>T (p.Leu271=) | |
| 8 | g.23191814C= | CA1770754164 | TNFRSF10A | c.1287G= (p.Leu429=) n.342G= c.813G= (p.Leu271=) | |
| 8 | g.23191814C>G | CA460179385 | TNFRSF10A | c.1287G>C (p.Leu429=) n.342G>C c.813G>C (p.Leu271=) | |
| 8 | g.23191814C>T | CA460179386 | TNFRSF10A | c.1287G>A (p.Leu429=) n.342G>A c.813G>A (p.Leu271=) | |
| 8 | g.23191815A>C | CA370568670 | TNFRSF10A | c.1286T>G (p.Leu429Arg) n.341T>G c.812T>G (p.Leu271Arg) | |
| 8 | g.23191815A>G | CA370568671 | TNFRSF10A | c.1286T>C (p.Leu429Pro) n.341T>C c.812T>C (p.Leu271Pro) | |
| 8 | g.23191815A>T | CA370568675 | TNFRSF10A | c.1286T>A (p.Leu429Gln) n.341T>A c.812T>A (p.Leu271Gln) | |
| 8 | g.23191815dup | CA1111807653 | TNFRSF10A | c.1286dup (p.Asp430GlyfsTer?) n.341dup c.812dup (p.Asp272GlyfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191816G>A | CA460179388 | TNFRSF10A | c.1285C>T (p.Leu429=) n.340C>T c.811C>T (p.Leu271=) | gnomAD v3 gnomAD v4 |
| 8 | g.23191816G>C | CA370568681 | TNFRSF10A | c.1285C>G (p.Leu429Val) n.340C>G c.811C>G (p.Leu271Val) | gnomAD v4 |
| 8 | g.23191816G>T | CA370568683 | TNFRSF10A | c.1285C>A (p.Leu429Met) n.340C>A c.811C>A (p.Leu271Met) | gnomAD v3 gnomAD v4 |
| 8 | g.23191817C>A | CA460179391 | TNFRSF10A | c.1284G>T (p.Leu428=) n.339G>T c.810G>T (p.Leu270=) | |
| 8 | g.23191817C>G | CA460179393 | TNFRSF10A | c.1284G>C (p.Leu428=) n.339G>C c.810G>C (p.Leu270=) | |
| 8 | g.23191817C>T | CA460179394 | TNFRSF10A | c.1284G>A (p.Leu428=) n.339G>A c.810G>A (p.Leu270=) | |
| 8 | g.23191818A= | CA1770754175 | TNFRSF10A | c.1283T= (p.Leu428=) n.338T= c.809T= (p.Leu270=) | |
| 8 | g.23191818A>C | CA370568686 | TNFRSF10A | c.1283T>G (p.Leu428Arg) n.338T>G c.809T>G (p.Leu270Arg) | |
| 8 | g.23191818A>G | CA4674559 | TNFRSF10A | c.1283T>C (p.Leu428Pro) n.338T>C c.809T>C (p.Leu270Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191818A>T | CA370568692 | TNFRSF10A | c.1283T>A (p.Leu428Gln) n.338T>A c.809T>A (p.Leu270Gln) | gnomAD v4 |
| 8 | g.23191819G>A | CA460179395 | TNFRSF10A | c.1282C>T (p.Leu428=) n.337C>T c.808C>T (p.Leu270=) | gnomAD v4 |
| 8 | g.23191819G>C | CA370568696 | TNFRSF10A | c.1282C>G (p.Leu428Val) n.337C>G c.808C>G (p.Leu270Val) | dbSNP |
| 8 | g.23191819G= | CA1770754182 | TNFRSF10A | c.1282C= (p.Leu428=) n.337C= c.808C= (p.Leu270=) | |
| 8 | g.23191819G>T | CA370568699 | TNFRSF10A | c.1282C>A (p.Leu428Met) n.337C>A c.808C>A (p.Leu270Met) | |
| 8 | g.23191820G>A | CA460179401 | TNFRSF10A | c.1281C>T (p.Thr427=) n.336C>T c.807C>T (p.Thr269=) | |
| 8 | g.23191820G>C | CA4674560 | TNFRSF10A | c.1281C>G (p.Thr427=) n.336C>G c.807C>G (p.Thr269=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.23191820G= | CA1770754187 | TNFRSF10A | c.1281C= (p.Thr427=) n.336C= c.807C= (p.Thr269=) | |
| 8 | g.23191820G>T | CA460179402 | TNFRSF10A | c.1281C>A (p.Thr427=) n.336C>A c.807C>A (p.Thr269=) | |
| 8 | g.23191821G>A | CA370568708 | TNFRSF10A | c.1280C>T (p.Thr427Ile) n.335C>T c.806C>T (p.Thr269Ile) | |
| 8 | g.23191821G>C | CA370568711 | TNFRSF10A | c.1280C>G (p.Thr427Ser) n.335C>G c.806C>G (p.Thr269Ser) | gnomAD v4 |
| 8 | g.23191821G>T | CA370568712 | TNFRSF10A | c.1280C>A (p.Thr427Asn) n.335C>A c.806C>A (p.Thr269Asn) | |
| 8 | g.23191822T>A | CA370568715 | TNFRSF10A | c.1279A>T (p.Thr427Ser) n.334A>T c.805A>T (p.Thr269Ser) | |
| 8 | g.23191822T>C | CA370568716 | TNFRSF10A | c.1279A>G (p.Thr427Ala) n.334A>G c.805A>G (p.Thr269Ala) | |
| 8 | g.23191822T>G | CA370568718 | TNFRSF10A | c.1279A>C (p.Thr427Pro) n.334A>C c.805A>C (p.Thr269Pro) | |
| 8 | g.23191823G>A | CA460179407 | TNFRSF10A | c.1278C>T (p.His426=) n.333C>T c.804C>T (p.His268=) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191823G>C | CA370568722 | TNFRSF10A | c.1278C>G (p.His426Gln) n.333C>G c.804C>G (p.His268Gln) | |
| 8 | g.23191823G= | CA1770754189 | TNFRSF10A | c.1278C= (p.His426=) n.333C= c.804C= (p.His268=) | |
| 8 | g.23191823G>T | CA370568724 | TNFRSF10A | c.1278C>A (p.His426Gln) n.333C>A c.804C>A (p.His268Gln) | |
| 8 | g.23191824T>A | CA370568729 | TNFRSF10A | c.1277A>T (p.His426Leu) n.332A>T c.803A>T (p.His268Leu) | |
| 8 | g.23191824T>C | CA370568732 | TNFRSF10A | c.1277A>G (p.His426Arg) n.332A>G c.803A>G (p.His268Arg) | gnomAD v4 |
| 8 | g.23191824T>G | CA370568738 | TNFRSF10A | c.1277A>C (p.His426Pro) n.332A>C c.803A>C (p.His268Pro) | |
| 8 | g.23191825G>A | CA370568741 | TNFRSF10A | c.1276C>T (p.His426Tyr) n.331C>T c.802C>T (p.His268Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191825G>C | CA370568742 | TNFRSF10A | c.1276C>G (p.His426Asp) n.331C>G c.802C>G (p.His268Asp) | |
| 8 | g.23191825G= | CA1770754193 | TNFRSF10A | c.1276C= (p.His426=) n.331C= c.802C= (p.His268=) | |
| 8 | g.23191825G>T | CA370568745 | TNFRSF10A | c.1276C>A (p.His426Asn) n.331C>A c.802C>A (p.His268Asn) | |
| 8 | g.23191826G>A | CA460179416 | TNFRSF10A | c.1275C>T (p.Ile425=) n.330C>T c.801C>T (p.Ile267=) | |
| 8 | g.23191826G>C | CA370568750 | TNFRSF10A | c.1275C>G (p.Ile425Met) n.330C>G c.801C>G (p.Ile267Met) | |
| 8 | g.23191826G>T | CA460179417 | TNFRSF10A | c.1275C>A (p.Ile425=) n.330C>A c.801C>A (p.Ile267=) | |
| 8 | g.23191827A>C | CA370568764 | TNFRSF10A | c.1274T>G (p.Ile425Ser) n.329T>G c.800T>G (p.Ile267Ser) | |
| 8 | g.23191827A>G | CA370568751 | TNFRSF10A | c.1274T>C (p.Ile425Thr) n.329T>C c.800T>C (p.Ile267Thr) | |
| 8 | g.23191827A>T | CA370568765 | TNFRSF10A | c.1274T>A (p.Ile425Asn) n.329T>A c.800T>A (p.Ile267Asn) | |
| 8 | g.23191828T>A | CA370568770 | TNFRSF10A | c.1273A>T (p.Ile425Phe) n.328A>T c.799A>T (p.Ile267Phe) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191828T>C | CA370568775 | TNFRSF10A | c.1273A>G (p.Ile425Val) n.328A>G c.799A>G (p.Ile267Val) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191828T>G | CA370568779 | TNFRSF10A | c.1273A>C (p.Ile425Leu) n.328A>C c.799A>C (p.Ile267Leu) | dbSNP |
| 8 | g.23191828T= | CA1770754198 | TNFRSF10A | c.1273A= (p.Ile425=) n.328A= c.799A= (p.Ile267=) | |
| 8 | g.23191829C>A | CA460179420 | TNFRSF10A | c.1272G>T (p.Ser424=) n.327G>T c.798G>T (p.Ser266=) | gnomAD v4 |
| 8 | g.23191829C= | CA1770754205 | TNFRSF10A | c.1272G= (p.Ser424=) n.327G= c.798G= (p.Ser266=) | |
| 8 | g.23191829C>G | CA460179419 | TNFRSF10A | c.1272G>C (p.Ser424=) n.327G>C c.798G>C (p.Ser266=) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191829C>T | CA4674561 | TNFRSF10A | c.1272G>A (p.Ser424=) n.327G>A c.798G>A (p.Ser266=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191829_23191830insTCG | CA580952716 | TNFRSF10A | c.1271_1272insCGA (p.Ser424_Ile425insGlu) n.326_327insCGA c.797_798insCGA (p.Ser266_Ile267insGlu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191830G>A | CA4674562 | TNFRSF10A | c.1271C>T (p.Ser424Leu) n.326C>T c.797C>T (p.Ser266Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191830G>C | CA173931898 | TNFRSF10A | c.1271C>G (p.Ser424Trp) n.326C>G c.797C>G (p.Ser266Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191830G= | CA1770754214 | TNFRSF10A | c.1271C= (p.Ser424=) n.326C= c.797C= (p.Ser266=) | |
| 8 | g.23191830G>T | CA4674563 | TNFRSF10A | c.1271C>A (p.Ser424Ter) n.326C>A c.797C>A (p.Ser266Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191831A= | CA1770754222 | TNFRSF10A | c.1270T= (p.Ser424=) n.325T= c.796T= (p.Ser266=) | |
| 8 | g.23191831A>C | CA370568801 | TNFRSF10A | c.1270T>G (p.Ser424Ala) n.325T>G c.796T>G (p.Ser266Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191831A>G | CA370568805 | TNFRSF10A | c.1270T>C (p.Ser424Pro) n.325T>C c.796T>C (p.Ser266Pro) | |
| 8 | g.23191831A>T | CA370568810 | TNFRSF10A | c.1270T>A (p.Ser424Thr) n.325T>A c.796T>A (p.Ser266Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191832G>A | CA460179425 | TNFRSF10A | c.1269C>T (p.Ala423=) n.324C>T c.795C>T (p.Ala265=) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191832G>C | CA460179426 | TNFRSF10A | c.1269C>G (p.Ala423=) n.324C>G c.795C>G (p.Ala265=) | |
| 8 | g.23191832G= | CA1770754229 | TNFRSF10A | c.1269C= (p.Ala423=) n.324C= c.795C= (p.Ala265=) | |
| 8 | g.23191832G>T | CA460179427 | TNFRSF10A | c.1269C>A (p.Ala423=) n.324C>A c.795C>A (p.Ala265=) | |
| 8 | g.23191833G>A | CA370568821 | TNFRSF10A | c.1268C>T (p.Ala423Val) n.323C>T c.794C>T (p.Ala265Val) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191833G>C | CA370568818 | TNFRSF10A | c.1268C>G (p.Ala423Gly) n.323C>G c.794C>G (p.Ala265Gly) | |
| 8 | g.23191833G= | CA1770754237 | TNFRSF10A | c.1268C= (p.Ala423=) n.323C= c.794C= (p.Ala265=) | |
| 8 | g.23191833G>T | CA370568814 | TNFRSF10A | c.1268C>A (p.Ala423Asp) n.323C>A c.794C>A (p.Ala265Asp) | |
| 8 | g.23191833_23191834insT | CA580952718 | TNFRSF10A | c.1267_1268insA (p.Ala423AspfsTer?) n.322_323insA c.793_794insA (p.Ala265AspfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191833_23191834insTCGC | CA580952719 | TNFRSF10A | c.1267_1268insGCGA (p.Ala423GlyfsTer?) n.322_323insGCGA c.793_794insGCGA (p.Ala265GlyfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191834C>A | CA370568826 | TNFRSF10A | c.1267G>T (p.Ala423Ser) n.322G>T c.793G>T (p.Ala265Ser) | |
| 8 | g.23191834C= | CA1770754252 | TNFRSF10A | c.1267G= (p.Ala423=) n.322G= c.793G= (p.Ala265=) | |
| 8 | g.23191834C>G | CA173931901 | TNFRSF10A | c.1267G>C (p.Ala423Pro) n.322G>C c.793G>C (p.Ala265Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.23191834C>T | CA370568830 | TNFRSF10A | c.1267G>A (p.Ala423Thr) n.322G>A c.793G>A (p.Ala265Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191835G>A | CA4674564 | TNFRSF10A | c.1266C>T (p.Asn422=) n.321C>T c.792C>T (p.Asn264=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.23191835G>C | CA370568835 | TNFRSF10A | c.1266C>G (p.Asn422Lys) n.321C>G c.792C>G (p.Asn264Lys) | |
| 8 | g.23191835G= | CA1770754261 | TNFRSF10A | c.1266C= (p.Asn422=) n.321C= c.792C= (p.Asn264=) | |
| 8 | g.23191835G>T | CA370568837 | TNFRSF10A | c.1266C>A (p.Asn422Lys) n.321C>A c.792C>A (p.Asn264Lys) | gnomAD v4 |
| 8 | g.23191835_23191837delinsGTT | CA1770754260 | TNFRSF10A | c.1264_1266delinsAAC (p.Asn422=) n.319_321delinsAAC c.790_792delinsAAC (p.Asn264=) | |
| 8 | g.23191835_23191839delinsGTTCC | CA1770754259 | TNFRSF10A | c.1262_1266delinsGGAAC (p.Arg421=) n.317_321delinsGGAAC c.788_792delinsGGAAC (p.Arg263=) | |
| 8 | g.23191835_23191836insCCGTATCA | CA1111807670 | TNFRSF10A | c.1265_1266insTGATACGG (p.Ala423AspfsTer?) n.320_321insTGATACGG c.791_792insTGATACGG (p.Ala265AspfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191835_23191836insCCGTATCATTAAAAAACCAT | CA1111807672 | TNFRSF10A | c.1265_1266insATGGTTTTTTAATGATACGG (p.Asn422LysfsTer?) n.320_321insATGGTTTTTTAATGATACGG c.791_792insATGGTTTTTTAATGATACGG (p.Asn264LysfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191836T>A | CA370568842 | TNFRSF10A | c.1265A>T (p.Asn422Ile) n.320A>T c.791A>T (p.Asn264Ile) | |
| 8 | g.23191836T>C | CA370568844 | TNFRSF10A | c.1265A>G (p.Asn422Ser) n.320A>G c.791A>G (p.Asn264Ser) | |
| 8 | g.23191836T>G | CA370568846 | TNFRSF10A | c.1265A>C (p.Asn422Thr) n.320A>C c.791A>C (p.Asn264Thr) | gnomAD v3 gnomAD v4 |
| 8 | g.23191836_23191837del | CA580952720 | TNFRSF10A | c.1264_1265del (p.Asn422ArgfsTer?) n.319_320del c.790_791del (p.Asn264ArgfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191836_23191839del | CA580952721 | TNFRSF10A | c.1262_1265del (p.Arg421ProfsTer?) n.317_320del c.788_791del (p.Arg263ProfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191836_23191837insA | CA1111807675 | TNFRSF10A | c.1264_1265insT (p.Asn422IlefsTer?) n.319_320insT c.790_791insT (p.Asn264IlefsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191837T>A | CA370568849 | TNFRSF10A | c.1264A>T (p.Asn422Tyr) n.319A>T c.790A>T (p.Asn264Tyr) | |
| 8 | g.23191837T>C | CA4674565 | TNFRSF10A | c.1264A>G (p.Asn422Asp) n.319A>G c.790A>G (p.Asn264Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191837T>G | CA370568855 | TNFRSF10A | c.1264A>C (p.Asn422His) n.319A>C c.790A>C (p.Asn264His) | |
| 8 | g.23191837T= | CA1770754279 | TNFRSF10A | c.1264A= (p.Asn422=) n.319A= c.790A= (p.Asn264=) | |
| 8 | g.23191838C>A | CA460179431 | TNFRSF10A | c.1263G>T (p.Arg421=) n.318G>T c.789G>T (p.Arg263=) | |
| 8 | g.23191838C= | CA1770754287 | TNFRSF10A | c.1263G= (p.Arg421=) n.318G= c.789G= (p.Arg263=) | |
| 8 | g.23191838C>G | CA460179432 | TNFRSF10A | c.1263G>C (p.Arg421=) n.318G>C c.789G>C (p.Arg263=) | |
| 8 | g.23191838C>T | CA460179433 | TNFRSF10A | c.1263G>A (p.Arg421=) n.318G>A c.789G>A (p.Arg263=) | dbSNP COSMIC |
| 8 | g.23191838_23191839insGC | CA1111807678 | TNFRSF10A | c.1263_1264insCG (p.Asn422ArgfsTer?) n.318_319insCG c.789_790insCG (p.Asn264ArgfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191838_23191839insATTAAAAAA | CA1111807680 | TNFRSF10A | c.1262_1263insTTTTTTAAT (p.Arg421_Asn422insPheLeuMet) n.317_318insTTTTTTAAT c.788_789insTTTTTTAAT (p.Arg263_Asn264insPheLeuMet) | gnomAD v3 gnomAD v4 |
| 8 | g.23191839C>A | CA370568862 | TNFRSF10A | c.1262G>T (p.Arg421Leu) n.317G>T c.788G>T (p.Arg263Leu) | |
| 8 | g.23191839C= | CA1770754294 | TNFRSF10A | c.1262G= (p.Arg421=) n.317G= c.788G= (p.Arg263=) | |
| 8 | g.23191839C>G | CA370568865 | TNFRSF10A | c.1262G>C (p.Arg421Pro) n.317G>C c.788G>C (p.Arg263Pro) | |
| 8 | g.23191839C>T | CA4674566 | TNFRSF10A | c.1262G>A (p.Arg421Gln) n.317G>A c.788G>A (p.Arg263Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 8 | g.23191840G>A | CA4674567 | TNFRSF10A | c.1261C>T (p.Arg421Trp) n.316C>T c.787C>T (p.Arg263Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191840G>C | CA370568872 | TNFRSF10A | c.1261C>G (p.Arg421Gly) n.316C>G c.787C>G (p.Arg263Gly) | gnomAD v3 gnomAD v4 |
| 8 | g.23191840G= | CA1770754303 | TNFRSF10A | c.1261C= (p.Arg421=) n.316C= c.787C= (p.Arg263=) | |
| 8 | g.23191840G>T | CA460179434 | TNFRSF10A | c.1261C>A (p.Arg421=) n.316C>A c.787C>A (p.Arg263=) | |
| 8 | g.23191840_23191841del | CA1111807683 | TNFRSF10A | c.1260_1261del (p.Arg421GlufsTer?) n.315_316del c.786_787del (p.Arg263GlufsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191841del | CA2594689405 | TNFRSF10A | c.1260del (p.Arg421GlyfsTer?) n.315del c.786del (p.Arg263GlyfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191841T>A | CA460179435 | TNFRSF10A | c.1260A>T (p.Gly420=) n.315A>T c.786A>T (p.Gly262=) | |
| 8 | g.23191841T>C | CA460179436 | TNFRSF10A | c.1260A>G (p.Gly420=) n.315A>G c.786A>G (p.Gly262=) | |
| 8 | g.23191841T>G | CA460179437 | TNFRSF10A | c.1260A>C (p.Gly420=) n.315A>C c.786A>C (p.Gly262=) | |
| 8 | g.23191841T= | CA1770754308 | TNFRSF10A | c.1260A= (p.Gly420=) n.315A= c.786A= (p.Gly262=) | |
| 8 | g.23191841_23191842insA | CA580952722 | TNFRSF10A | c.1259_1260insT (p.Arg421ThrfsTer?) n.314_315insT c.785_786insT (p.Arg263ThrfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191842C>A | CA370568879 | TNFRSF10A | c.1259G>T (p.Gly420Val) n.314G>T c.785G>T (p.Gly262Val) | |
| 8 | g.23191842C= | CA1770754314 | TNFRSF10A | c.1259G= (p.Gly420=) n.314G= c.785G= (p.Gly262=) | |
| 8 | g.23191842C>G | CA370568881 | TNFRSF10A | c.1259G>C (p.Gly420Ala) n.314G>C c.785G>C (p.Gly262Ala) | |
| 8 | g.23191842C>T | CA370568885 | TNFRSF10A | c.1259G>A (p.Gly420Glu) n.314G>A c.785G>A (p.Gly262Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191842_23191843del | CA1111807684 | TNFRSF10A | c.1258_1259del (p.Gly420ThrfsTer?) n.313_314del c.784_785del (p.Gly262ThrfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191842_23191843insG | CA580952723 | TNFRSF10A | c.1258_1259insC (p.Gly420AlafsTer?) n.313_314insC c.784_785insC (p.Gly262AlafsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191842_23191843insAT | CA1111807689 | TNFRSF10A | c.1258_1259insAT (p.Gly420AspfsTer?) n.313_314insAT c.784_785insAT (p.Gly262AspfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191843C>A | CA370568889 | TNFRSF10A | c.1258G>T (p.Gly420Ter) n.313G>T c.784G>T (p.Gly262Ter) | |
| 8 | g.23191843C>G | CA370568897 | TNFRSF10A | c.1258G>C (p.Gly420Arg) n.313G>C c.784G>C (p.Gly262Arg) | |
| 8 | g.23191843C>T | CA370568900 | TNFRSF10A | c.1258G>A (p.Gly420Arg) n.313G>A c.784G>A (p.Gly262Arg) | gnomAD v4 COSMIC |
| 8 | g.23191844del | CA1111807691 | TNFRSF10A | c.1257del (p.Gly420AspfsTer?) n.312del c.783del (p.Gly262AspfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191844A= | CA1770754321 | TNFRSF10A | c.1257T= (p.Thr419=) n.312T= c.783T= (p.Thr261=) | |
| 8 | g.23191844A>C | CA173931906 | TNFRSF10A | c.1257T>G (p.Thr419=) n.312T>G c.783T>G (p.Thr261=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191844A>G | CA460179439 | TNFRSF10A | c.1257T>C (p.Thr419=) n.312T>C c.783T>C (p.Thr261=) | |
| 8 | g.23191844A>T | CA460179440 | TNFRSF10A | c.1257T>A (p.Thr419=) n.312T>A c.783T>A (p.Thr261=) | |
| 8 | g.23191844_23191850delinsAGTTTTG | CA1770754320 | TNFRSF10A | c.1251_1257delinsCAAAACT (p.Asn417=) n.306_312delinsCAAAACT c.777_783delinsCAAAACT (p.Asn259=) | |
| 8 | g.23191845del | CA1111807693 | TNFRSF10A | c.1256del (p.Thr419MetfsTer?) n.311del c.782del (p.Thr261MetfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191845G>A | CA370568903 | TNFRSF10A | c.1256C>T (p.Thr419Ile) n.311C>T c.782C>T (p.Thr261Ile) | |
| 8 | g.23191845G>C | CA370568907 | TNFRSF10A | c.1256C>G (p.Thr419Ser) n.311C>G c.782C>G (p.Thr261Ser) | |
| 8 | g.23191845G>T | CA370568910 | TNFRSF10A | c.1256C>A (p.Thr419Asn) n.311C>A c.782C>A (p.Thr261Asn) | |
| 8 | g.23191845_23191850del | CA580952724 | TNFRSF10A | c.1251_1256del (p.Lys418_Thr419del) n.306_311del c.777_782del (p.Lys260_Thr261del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191845_23191846insCA | CA1111807696 | TNFRSF10A | c.1255_1256insTG (p.Thr419MetfsTer?) n.310_311insTG c.781_782insTG (p.Thr261MetfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191846T>A | CA370568915 | TNFRSF10A | c.1255A>T (p.Thr419Ser) n.310A>T c.781A>T (p.Thr261Ser) | |
| 8 | g.23191846T>C | CA370568924 | TNFRSF10A | c.1255A>G (p.Thr419Ala) n.310A>G c.781A>G (p.Thr261Ala) | gnomAD v3 gnomAD v4 |
| 8 | g.23191846T>G | CA370568927 | TNFRSF10A | c.1255A>C (p.Thr419Pro) n.310A>C c.781A>C (p.Thr261Pro) | dbSNP gnomAD v4 |
| 8 | g.23191849dup | CA2579117645 | TNFRSF10A | c.1255dup (p.Thr419AsnfsTer?) n.310dup c.781dup (p.Thr261AsnfsTer?) | |
| 8 | g.23191847T>A | CA370568936 | TNFRSF10A | c.1254A>T (p.Lys418Asn) n.309A>T c.780A>T (p.Lys260Asn) | gnomAD v3 gnomAD v4 |
| 8 | g.23191847T>C | CA460179441 | TNFRSF10A | c.1254A>G (p.Lys418=) n.309A>G c.780A>G (p.Lys260=) | |
| 8 | g.23191847T>G | CA4674568 | TNFRSF10A | c.1254A>C (p.Lys418Asn) n.309A>C c.780A>C (p.Lys260Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191847T= | CA1770754329 | TNFRSF10A | c.1254A= (p.Lys418=) n.309A= c.780A= (p.Lys260=) | |
| 8 | g.23191848T>A | CA370568940 | TNFRSF10A | c.1253A>T (p.Lys418Ile) n.308A>T c.779A>T (p.Lys260Ile) | |
| 8 | g.23191848T>C | CA370568943 | TNFRSF10A | c.1253A>G (p.Lys418Arg) n.308A>G c.779A>G (p.Lys260Arg) | |
| 8 | g.23191848T>G | CA370568945 | TNFRSF10A | c.1253A>C (p.Lys418Thr) n.308A>C c.779A>C (p.Lys260Thr) | |
| 8 | g.23191848_23191853del | CA1111807700 | TNFRSF10A | c.1248_1253del (p.Asn417_Lys418del) n.303_308del c.774_779del (p.Asn259_Lys260del) | gnomAD v3 gnomAD v4 |
| 8 | g.23191849T>A | CA370568950 | TNFRSF10A | c.1252A>T (p.Lys418Ter) n.307A>T c.778A>T (p.Lys260Ter) | |
| 8 | g.23191849T>C | CA370568952 | TNFRSF10A | c.1252A>G (p.Lys418Glu) n.307A>G c.778A>G (p.Lys260Glu) | gnomAD v3 gnomAD v4 |
| 8 | g.23191849T>G | CA370568955 | TNFRSF10A | c.1252A>C (p.Lys418Gln) n.307A>C c.778A>C (p.Lys260Gln) | |
| 8 | g.23191849_23191850delinsTG | CA1770754332 | TNFRSF10A | c.1251_1252delinsCA (p.Asn417=) n.306_307delinsCA c.777_778delinsCA (p.Asn259=) | |
| 8 | g.23191849_23191856del | CA1111807702 | TNFRSF10A | c.1245_1252del (p.Trp415Ter) n.300_307del c.771_778del (p.Trp257Ter) | gnomAD v3 gnomAD v4 |
| 8 | g.23191850del | CA1770754334 | TNFRSF10A | c.1251del (p.Asn417LysfsTer?) n.306del c.777del (p.Asn259LysfsTer?) | dbSNP |
| 8 | g.23191850G>A | CA4674569 | TNFRSF10A | c.1251C>T (p.Asn417=) n.306C>T c.777C>T (p.Asn259=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191850G>C | CA370568960 | TNFRSF10A | c.1251C>G (p.Asn417Lys) n.306C>G c.777C>G (p.Asn259Lys) | |
| 8 | g.23191850G= | CA1770754335 | TNFRSF10A | c.1251C= (p.Asn417=) n.306C= c.777C= (p.Asn259=) | |
| 8 | g.23191850G>T | CA370568963 | TNFRSF10A | c.1251C>A (p.Asn417Lys) n.306C>A c.777C>A (p.Asn259Lys) | |
| 8 | g.23191851T>A | CA370568965 | TNFRSF10A | c.1250A>T (p.Asn417Ile) n.305A>T c.776A>T (p.Asn259Ile) | |
| 8 | g.23191851T>C | CA370568968 | TNFRSF10A | c.1250A>G (p.Asn417Ser) n.305A>G c.776A>G (p.Asn259Ser) | |
| 8 | g.23191851T>G | CA370568970 | TNFRSF10A | c.1250A>C (p.Asn417Thr) n.305A>C c.776A>C (p.Asn259Thr) | |
| 8 | g.23191852T>A | CA370568982 | TNFRSF10A | c.1249A>T (p.Asn417Tyr) n.304A>T c.775A>T (p.Asn259Tyr) | |
| 8 | g.23191852T>C | CA370568979 | TNFRSF10A | c.1249A>G (p.Asn417Asp) n.304A>G c.775A>G (p.Asn259Asp) | gnomAD v4 |
| 8 | g.23191852T>G | CA370568975 | TNFRSF10A | c.1249A>C (p.Asn417His) n.304A>C c.775A>C (p.Asn259His) | gnomAD v4 |
| 8 | g.23191852T= | CA1770754339 | TNFRSF10A | c.1249A= (p.Asn417=) n.304A= c.775A= (p.Asn259=) | |
| 8 | g.23191852_23191853insAAA | CA580952725 | TNFRSF10A | c.1248_1249insTTT (p.Val416_Asn417insPhe) n.303_304insTTT c.774_775insTTT (p.Val258_Asn259insPhe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191852_23191853insAAAA | CA2686537747 | TNFRSF10A | c.1248_1249insTTTT (p.Asn417PhefsTer2) n.303_304insTTTT c.774_775insTTTT (p.Asn259PhefsTer2) | gnomAD v4 |
| 8 | g.23191853G>A | CA460179444 | TNFRSF10A | c.1248C>T (p.Val416=) n.303C>T c.774C>T (p.Val258=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191853G>C | CA460179445 | TNFRSF10A | c.1248C>G (p.Val416=) n.303C>G c.774C>G (p.Val258=) | |
| 8 | g.23191853G= | CA1770754343 | TNFRSF10A | c.1248C= (p.Val416=) n.303C= c.774C= (p.Val258=) | |
| 8 | g.23191853G>T | CA460179446 | TNFRSF10A | c.1248C>A (p.Val416=) n.303C>A c.774C>A (p.Val258=) | |
| 8 | g.23191854A>C | CA370568988 | TNFRSF10A | c.1247T>G (p.Val416Gly) n.302T>G c.773T>G (p.Val258Gly) | gnomAD v4 |
| 8 | g.23191854A>G | CA370568996 | TNFRSF10A | c.1247T>C (p.Val416Ala) n.302T>C c.773T>C (p.Val258Ala) | |
| 8 | g.23191854A>T | CA370568989 | TNFRSF10A | c.1247T>A (p.Val416Asp) n.302T>A c.773T>A (p.Val258Asp) | |
| 8 | g.23191854_23191855insAAAA | CA1111807707 | TNFRSF10A | c.1247_1248insTTTT (p.Asn417PhefsTer?) n.302_303insTTTT c.773_774insTTTT (p.Asn259PhefsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191855C>A | CA370569003 | TNFRSF10A | c.1246G>T (p.Val416Phe) n.301G>T c.772G>T (p.Val258Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191855C= | CA1770754348 | TNFRSF10A | c.1246G= (p.Val416=) n.301G= c.772G= (p.Val258=) | |
| 8 | g.23191855C>G | CA370569006 | TNFRSF10A | c.1246G>C (p.Val416Leu) n.301G>C c.772G>C (p.Val258Leu) | |
| 8 | g.23191855C>T | CA370569007 | TNFRSF10A | c.1246G>A (p.Val416Ile) n.301G>A c.772G>A (p.Val258Ile) | |
| 8 | g.23191856_23191857del | CA2686537748 | TNFRSF10A | c.1245_1246del (p.Trp415CysfsTer?) n.300_301del c.771_772del (p.Trp257CysfsTer?) | gnomAD v4 |
| 8 | g.23191856C>A | CA4674570 | TNFRSF10A | c.1245G>T (p.Trp415Cys) n.300G>T c.771G>T (p.Trp257Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191856C= | CA1770754353 | TNFRSF10A | c.1245G= (p.Trp415=) n.300G= c.771G= (p.Trp257=) | |
| 8 | g.23191856C>G | CA370569012 | TNFRSF10A | c.1245G>C (p.Trp415Cys) n.300G>C c.771G>C (p.Trp257Cys) | |
| 8 | g.23191856C>T | CA370569014 | TNFRSF10A | c.1245G>A (p.Trp415Ter) n.300G>A c.771G>A (p.Trp257Ter) | dbSNP |
| 8 | g.23191857C>A | CA370569018 | TNFRSF10A | c.1244G>T (p.Trp415Leu) n.299G>T c.770G>T (p.Trp257Leu) | gnomAD v4 |
| 8 | g.23191857C= | CA1770754357 | TNFRSF10A | c.1244G= (p.Trp415=) n.299G= c.770G= (p.Trp257=) | |
| 8 | g.23191857C>G | CA370569020 | TNFRSF10A | c.1244G>C (p.Trp415Ser) n.299G>C c.770G>C (p.Trp257Ser) | |
| 8 | g.23191857C>T | CA370569024 | TNFRSF10A | c.1244G>A (p.Trp415Ter) n.299G>A c.770G>A (p.Trp257Ter) | dbSNP |
| 8 | g.23191858A= | CA1770754359 | TNFRSF10A | c.1243T= (p.Trp415=) n.298T= c.769T= (p.Trp257=) | |
| 8 | g.23191858A>C | CA370569026 | TNFRSF10A | c.1243T>G (p.Trp415Gly) n.298T>G c.769T>G (p.Trp257Gly) | |
| 8 | g.23191858A>G | CA370569029 | TNFRSF10A | c.1243T>C (p.Trp415Arg) n.298T>C c.769T>C (p.Trp257Arg) | dbSNP |
| 8 | g.23191858A>T | CA370569032 | TNFRSF10A | c.1243T>A (p.Trp415Arg) n.298T>A c.769T>A (p.Trp257Arg) | |
| 8 | g.23191859T>A | CA370569039 | TNFRSF10A | c.1242A>T (p.Lys414Asn) n.297A>T c.768A>T (p.Lys256Asn) | |
| 8 | g.23191859T>C | CA460179449 | TNFRSF10A | c.1242A>G (p.Lys414=) n.297A>G c.768A>G (p.Lys256=) | |
| 8 | g.23191859T>G | CA173931911 | TNFRSF10A | c.1242A>C (p.Lys414Asn) n.297A>C c.768A>C (p.Lys256Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191859T= | CA1770754361 | TNFRSF10A | c.1242A= (p.Lys414=) n.297A= c.768A= (p.Lys256=) | |
| 8 | g.23191860T>A | CA370569043 | TNFRSF10A | c.1241A>T (p.Lys414Ile) n.296A>T c.767A>T (p.Lys256Ile) | |
| 8 | g.23191860T>C | CA370569045 | TNFRSF10A | c.1241A>G (p.Lys414Arg) n.296A>G c.767A>G (p.Lys256Arg) | dbSNP |
| 8 | g.23191860T>G | CA370569049 | TNFRSF10A | c.1241A>C (p.Lys414Thr) n.296A>C c.767A>C (p.Lys256Thr) | gnomAD v3 gnomAD v4 |
| 8 | g.23191860_23191861insAAAAAAAAAAT | CA1111807713 | TNFRSF10A | c.1241_1242insTTTTTTTTTTA (p.Lys414AsnfsTer?) n.296_297insTTTTTTTTTTA c.767_768insTTTTTTTTTTA (p.Lys256AsnfsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191860_23191861insAAAAAAAAAAA | CA1111807715 | TNFRSF10A | c.1240_1241insTTTTTTTTTTT (p.Lys414IlefsTer?) n.295_296insTTTTTTTTTTT c.766_767insTTTTTTTTTTT (p.Lys256IlefsTer?) | gnomAD v3 gnomAD v4 |
| 8 | g.23191861T>A | CA370569053 | TNFRSF10A | c.1240A>T (p.Lys414Ter) n.295A>T c.766A>T (p.Lys256Ter) | gnomAD v4 |
| 8 | g.23191861T>C | CA370569056 | TNFRSF10A | c.1240A>G (p.Lys414Glu) n.295A>G c.766A>G (p.Lys256Glu) | gnomAD v3 gnomAD v4 |
| 8 | g.23191861T>G | CA370569059 | TNFRSF10A | c.1240A>C (p.Lys414Gln) n.295A>C c.766A>C (p.Lys256Gln) | gnomAD v3 gnomAD v4 |
| 8 | g.23191862C>A | CA370569063 | TNFRSF10A | c.1239G>T (p.Met413Ile) n.294G>T c.765G>T (p.Met255Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.23191862C= | CA1770754363 | TNFRSF10A | c.1239G= (p.Met413=) n.294G= c.765G= (p.Met255=) | |
| 8 | g.23191862C>G | CA370569067 | TNFRSF10A | c.1239G>C (p.Met413Ile) n.294G>C c.765G>C (p.Met255Ile) | |
| 8 | g.23191862C>T | CA370569070 | TNFRSF10A | c.1239G>A (p.Met413Ile) n.294G>A c.765G>A (p.Met255Ile) | |
| 8 | g.23191863A>C | CA370569073 | TNFRSF10A | c.1238T>G (p.Met413Arg) n.293T>G c.764T>G (p.Met255Arg) | |
| 8 | g.23191863A>G | CA370569074 | TNFRSF10A | c.1238T>C (p.Met413Thr) n.293T>C c.764T>C (p.Met255Thr) | |
| 8 | g.23191863A>T | CA370569077 | TNFRSF10A | c.1238T>A (p.Met413Lys) n.293T>A c.764T>A (p.Met255Lys) | |
| 8 | g.23191864T>A | CA370569089 | TNFRSF10A | c.1237A>T (p.Met413Leu) n.292A>T c.763A>T (p.Met255Leu) | |
| 8 | g.23191864T>C | CA370569085 | TNFRSF10A | c.1237A>G (p.Met413Val) n.292A>G c.763A>G (p.Met255Val) | |
| 8 | g.23191864T>G | CA370569082 | TNFRSF10A | c.1237A>C (p.Met413Leu) n.292A>C c.763A>C (p.Met255Leu) | |
| 8 | g.23191865C>A | CA460179453 | TNFRSF10A | c.1236G>T (p.Leu412=) n.291G>T c.762G>T (p.Leu254=) | |
| 8 | g.23191865C>G | CA460179454 | TNFRSF10A | c.1236G>C (p.Leu412=) n.291G>C c.762G>C (p.Leu254=) | |
| 8 | g.23191865C>T | CA460179455 | TNFRSF10A | c.1236G>A (p.Leu412=) n.291G>A c.762G>A (p.Leu254=) | COSMIC |
| 8 | g.23191866A>C | CA370569100 | TNFRSF10A | c.1235T>G (p.Leu412Arg) n.290T>G c.761T>G (p.Leu254Arg) | |
| 8 | g.23191866A>G | CA370569093 | TNFRSF10A | c.1235T>C (p.Leu412Pro) n.290T>C c.761T>C (p.Leu254Pro) | |
| 8 | g.23191866A>T | CA370569096 | TNFRSF10A | c.1235T>A (p.Leu412Gln) n.290T>A c.761T>A (p.Leu254Gln) | |
| 8 | g.23191867G>A | CA460179457 | TNFRSF10A | c.1234C>T (p.Leu412=) n.289C>T c.760C>T (p.Leu254=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191867G>C | CA370569104 | TNFRSF10A | c.1234C>G (p.Leu412Val) n.289C>G c.760C>G (p.Leu254Val) | |
| 8 | g.23191867G= | CA1770754365 | TNFRSF10A | c.1234C= (p.Leu412=) n.289C= c.760C= (p.Leu254=) | |
| 8 | g.23191867G>T | CA370569107 | TNFRSF10A | c.1234C>A (p.Leu412Met) n.289C>A c.760C>A (p.Leu254Met) | |
| 8 | g.23191868C>A | CA370569110 | TNFRSF10A | c.1233G>T (p.Met411Ile) n.288G>T c.759G>T (p.Met253Ile) | |
| 8 | g.23191868C= | CA1770754369 | TNFRSF10A | c.1233G= (p.Met411=) n.288G= c.759G= (p.Met253=) | |
| 8 | g.23191868C>G | CA370569113 | TNFRSF10A | c.1233G>C (p.Met411Ile) n.288G>C c.759G>C (p.Met253Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191868C>T | CA370569115 | TNFRSF10A | c.1233G>A (p.Met411Ile) n.288G>A c.759G>A (p.Met253Ile) | dbSNP |
| 8 | g.23191869A= | CA1770754376 | TNFRSF10A | c.1232T= (p.Met411=) n.287T= c.758T= (p.Met253=) | |
| 8 | g.23191869A>C | CA370569117 | TNFRSF10A | c.1232T>G (p.Met411Arg) n.287T>G c.758T>G (p.Met253Arg) | |
| 8 | g.23191869A>G | CA4674571 | TNFRSF10A | c.1232T>C (p.Met411Thr) n.287T>C c.758T>C (p.Met253Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.23191869A>T | CA370569126 | TNFRSF10A | c.1232T>A (p.Met411Lys) n.287T>A c.758T>A (p.Met253Lys) | |
| 8 | g.23191870T>A | CA370569131 | TNFRSF10A | c.1231A>T (p.Met411Leu) n.286A>T c.757A>T (p.Met253Leu) | |
| 8 | g.23191870T>C | CA4674572 | TNFRSF10A | c.1231A>G (p.Met411Val) n.286A>G c.757A>G (p.Met253Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.23191870T>G | CA370569135 | TNFRSF10A | c.1231A>C (p.Met411Leu) n.286A>C c.757A>C (p.Met253Leu) | |
| 8 | g.23191870T= | CA1770754381 | TNFRSF10A | c.1231A= (p.Met411=) n.286A= c.757A= (p.Met253=) | |
| 8 | g.23191871T>A | CA460179506 | TNFRSF10A | c.1230A>T (p.Ala410=) n.285A>T c.756A>T (p.Ala252=) | |
| 8 | g.23191871T>C | CA460179507 | TNFRSF10A | c.1230A>G (p.Ala410=) n.285A>G c.756A>G (p.Ala252=) | gnomAD v4 |
| 8 | g.23191871T>G | CA460179508 | TNFRSF10A | c.1230A>C (p.Ala410=) n.285A>C c.756A>C (p.Ala252=) | |
| 8 | g.23191872G>A | CA370569145 | TNFRSF10A | c.1229C>T (p.Ala410Val) n.284C>T c.755C>T (p.Ala252Val) | |
| 8 | g.23191872G>C | CA370569140 | TNFRSF10A | c.1229C>G (p.Ala410Gly) n.284C>G c.755C>G (p.Ala252Gly) | |
| 8 | g.23191872G>T | CA370569142 | TNFRSF10A | c.1229C>A (p.Ala410Glu) n.284C>A c.755C>A (p.Ala252Glu) | |
| 8 | g.23191873C>A | CA370569149 | TNFRSF10A | c.1228G>T (p.Ala410Ser) n.283G>T c.754G>T (p.Ala252Ser) | |
| 8 | g.23191873C>G | CA370569153 | TNFRSF10A | c.1228G>C (p.Ala410Pro) n.283G>C c.754G>C (p.Ala252Pro) | |
| 8 | g.23191873C>T | CA370569154 | TNFRSF10A | c.1228G>A (p.Ala410Thr) n.283G>A c.754G>A (p.Ala252Thr) | |
| 8 | g.23191874A>C | CA370569155 | TNFRSF10A | c.1227T>G (p.Tyr409Ter) n.282T>G c.753T>G (p.Tyr251Ter) | gnomAD v4 |
| 8 | g.23191874A>G | CA460179510 | TNFRSF10A | c.1227T>C (p.Tyr409=) n.282T>C c.753T>C (p.Tyr251=) | |
| 8 | g.23191874A>T | CA370569156 | TNFRSF10A | c.1227T>A (p.Tyr409Ter) n.282T>A c.753T>A (p.Tyr251Ter) | |
| 8 | g.23191875T>A | CA370569160 | TNFRSF10A | c.1226A>T (p.Tyr409Phe) n.281A>T c.752A>T (p.Tyr251Phe) | |
| 8 | g.23191875T>C | CA370569163 | TNFRSF10A | c.1226A>G (p.Tyr409Cys) n.281A>G c.752A>G (p.Tyr251Cys) | |
| 8 | g.23191875T>G | CA370569165 | TNFRSF10A | c.1226A>C (p.Tyr409Ser) n.281A>C c.752A>C (p.Tyr251Ser) | |
| 8 | g.23191876A>C | CA370569170 | TNFRSF10A | c.1225T>G (p.Tyr409Asp) n.280T>G c.751T>G (p.Tyr251Asp) | |
| 8 | g.23191876A>G | CA370569173 | TNFRSF10A | c.1225T>C (p.Tyr409His) n.280T>C c.751T>C (p.Tyr251His) | |
| 8 | g.23191876A>T | CA370569175 | TNFRSF10A | c.1225T>A (p.Tyr409Asn) n.280T>A c.751T>A (p.Tyr251Asn) | |
| 8 | g.23191877C>A | CA370569178 | TNFRSF10A | c.1224G>T (p.Leu408Phe) n.279G>T c.750G>T (p.Leu250Phe) | gnomAD v4 |
| 8 | g.23191877C>G | CA370569182 | TNFRSF10A | c.1224G>C (p.Leu408Phe) n.279G>C c.750G>C (p.Leu250Phe) | |
| 8 | g.23191877C>T | CA460179511 | TNFRSF10A | c.1224G>A (p.Leu408=) n.279G>A c.750G>A (p.Leu250=) | |
| 8 | g.23191878A>C | CA370569190 | TNFRSF10A | c.1223T>G (p.Leu408Trp) n.278T>G c.749T>G (p.Leu250Trp) | |
| 8 | g.23191878A>G | CA370569192 | TNFRSF10A | c.1223T>C (p.Leu408Ser) n.278T>C c.749T>C (p.Leu250Ser) | gnomAD v4 |
| 8 | g.23191878A>T | CA370569187 | TNFRSF10A | c.1223T>A (p.Leu408Ter) n.278T>A c.749T>A (p.Leu250Ter) | |
| 8 | g.23191879A>C | CA370569196 | TNFRSF10A | c.1222T>G (p.Leu408Val) n.277T>G c.748T>G (p.Leu250Val) | |
| 8 | g.23191879A>G | CA460179514 | TNFRSF10A | c.1222T>C (p.Leu408=) n.277T>C c.748T>C (p.Leu250=) | |
| 8 | g.23191879A>T | CA370569199 | TNFRSF10A | c.1222T>A (p.Leu408Met) n.277T>A c.748T>A (p.Leu250Met) | |
| 8 | g.23191879_23191880delinsAG | CA1770754383 | TNFRSF10A | c.1221_1222delinsCT (p.Ala407=) n.276_277delinsCT c.747_748delinsCT (p.Ala249=) |