All transcript variants in gene TMEM119

Information The variants shown are described using the NM_181724.2 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.-9G>A r.(=) p.(=) g.108986168C>T Copied from the Exome Variant Server TMEM119_000048 1/12222 1/8060 0/4162
?/? c.2del r.? p.? g.108986158del Copied from the Exome Variant Server TMEM119_000047 2/11724 0/7706 2/4018
?/? c.9G>A r.(=) p.(=) g.108986151C>T Copied from the Exome Variant Server TMEM119_000046 552/12144 12/8022 540/4122
?/? c.11C>T r.(?) p.(Ala4Val) g.108986149G>A Copied from the Exome Variant Server TMEM119_000045 2/12124 0/8002 2/4122
?/? c.48C>G r.(=) p.(=) g.108986112G>C Copied from the Exome Variant Server TMEM119_000044 1936/12600 1365/8302 571/4298
?/? c.76C>T r.(?) p.(Arg26Cys) g.108986084G>A Copied from the Exome Variant Server TMEM119_000043 1/12798 1/8444 0/4354
?/? c.99G>A r.(=) p.(=) g.108986061C>T Copied from the Exome Variant Server TMEM119_000042 2/12776 2/8430 0/4346
?/? c.116C>T r.(?) p.(Ala39Val) g.108986044G>A Copied from the Exome Variant Server TMEM119_000041 9/12724 8/8404 1/4320
?/? c.129G>A r.(=) p.(=) g.108986031C>T Copied from the Exome Variant Server TMEM119_000040 1555/12904 1399/8534 156/4370
?/? c.143C>T r.(?) p.(Ser48Leu) g.108986017G>A Copied from the Exome Variant Server TMEM119_000039 261/12966 4/8576 257/4390
?/? c.179C>T r.(?) p.(Pro60Leu) g.108985981G>A Copied from the Exome Variant Server TMEM119_000038 4/13002 2/8598 2/4404
?/? c.184C>T r.(?) p.(Leu62Phe) g.108985976G>A Copied from the Exome Variant Server TMEM119_000037 262/13004 242/8598 20/4406
?/? c.195A>G r.(=) p.(=) g.108985965T>C Copied from the Exome Variant Server TMEM119_000036 1/13006 1/8600 0/4406
?/? c.197C>T r.(?) p.(Ser66Leu) g.108985963G>A Copied from the Exome Variant Server TMEM119_000035 1/13006 1/8600 0/4406
?/? c.215T>C r.(?) p.(Ile72Thr) g.108985945A>G Copied from the Exome Variant Server TMEM119_000034 7044/13006 3865/8600 3179/4406
?/? c.218C>A r.(?) p.(Thr73Asn) g.108985942G>T Copied from the Exome Variant Server TMEM119_000033 1/13006 0/8600 1/4406
?/? c.243C>G r.(=) p.(=) g.108985917G>C Copied from the Exome Variant Server TMEM119_000032 1/13006 0/8600 1/4406
?/? c.274C>T r.(?) p.(Arg92Cys) g.108985886G>A Copied from the Exome Variant Server TMEM119_000031 1/13006 0/8600 1/4406
?/? c.275G>A r.(?) p.(Arg92His) g.108985885C>T Copied from the Exome Variant Server TMEM119_000030 1/13006 1/8600 0/4406
?/? c.327G>A r.(?) p.(Met109Ile) g.108985833C>T Copied from the Exome Variant Server TMEM119_000029 1/13006 0/8600 1/4406
?/? c.344C>T r.(?) p.(Ala115Val) g.108985816G>A Copied from the Exome Variant Server TMEM119_000028 4/13006 2/8600 2/4406
?/? c.375G>A r.(=) p.(=) g.108985785C>T Copied from the Exome Variant Server TMEM119_000027 582/13006 536/8600 46/4406
?/? c.381T>C r.(=) p.(=) g.108985779A>G Copied from the Exome Variant Server TMEM119_000026 16/13006 0/8600 16/4406
?/? c.406A>C r.(?) p.(Lys136Gln) g.108985754T>G Copied from the Exome Variant Server TMEM119_000025 1/13000 0/8598 1/4402
?/? c.408_409insAAG r.(?) p.(Lys136dup) g.108985751_108985752insCTT Copied from the Exome Variant Server TMEM119_000024 1/12512 1/8252 0/4260
?/? c.411C>T r.(=) p.(=) g.108985749G>A Copied from the Exome Variant Server TMEM119_000023 2/13002 1/8600 1/4402
?/? c.427C>T r.(?) p.(Arg143Trp) g.108985733G>A Copied from the Exome Variant Server TMEM119_000022 1/12988 1/8592 0/4396
?/? c.453T>C r.(=) p.(=) g.108985707A>G Copied from the Exome Variant Server TMEM119_000021 394/12892 0/8544 394/4348
?/? c.494C>A r.(?) p.(Ala165Asp) g.108985666G>T Copied from the Exome Variant Server TMEM119_000020 1/12958 0/8560 1/4398
?/? c.511C>T r.(?) p.(Gln171*) g.108985649G>A Copied from the Exome Variant Server TMEM119_000019 11/12974 9/8578 2/4396
?/? c.514C>T r.(?) p.(Leu172Phe) g.108985646G>A Copied from the Exome Variant Server TMEM119_000018 1/12978 1/8580 0/4398
?/? c.532G>T r.(?) p.(Ala178Ser) g.108985628C>A Copied from the Exome Variant Server TMEM119_000017 1/12976 0/8580 1/4396
?/? c.535G>A r.(?) p.(Ala179Thr) g.108985625C>T Copied from the Exome Variant Server TMEM119_000016 1/12978 0/8582 1/4396
?/? c.565G>T r.(?) p.(Ala189Ser) g.108985595C>A Copied from the Exome Variant Server TMEM119_000015 1/12994 1/8596 0/4398
?/? c.576C>T r.(=) p.(=) g.108985584G>A Copied from the Exome Variant Server TMEM119_000014 1/13002 0/8600 1/4402
?/? c.589G>A r.(?) p.(Ala197Thr) g.108985571C>T Copied from the Exome Variant Server TMEM119_000013 1/13006 0/8600 1/4406
?/? c.611G>T r.(?) p.(Gly204Val) g.108985549C>A Copied from the Exome Variant Server TMEM119_000012 1/13006 0/8600 1/4406
?/? c.636C>A r.(?) p.(Ser212Arg) g.108985524G>T Copied from the Exome Variant Server TMEM119_000011 2/13006 2/8600 0/4406
?/? c.681G>A r.(=) p.(=) g.108985479C>T Copied from the Exome Variant Server TMEM119_000010 784/13006 160/8600 624/4406
?/? c.692C>T r.(?) p.(Ala231Val) g.108985468G>A Copied from the Exome Variant Server TMEM119_000009 2/13006 0/8600 2/4406
?/? c.705G>A r.(=) p.(=) g.108985455C>T Copied from the Exome Variant Server TMEM119_000008 1/13006 0/8600 1/4406
?/? c.738C>T r.(=) p.(=) g.108985422G>A Copied from the Exome Variant Server TMEM119_000007 2/13006 0/8600 2/4406
?/? c.781C>T r.(?) p.(Gln261*) g.108985379G>A Copied from the Exome Variant Server TMEM119_000006 3/13006 0/8600 3/4406
?/? c.806C>T r.(?) p.(Pro269Leu) g.108985354G>A Copied from the Exome Variant Server TMEM119_000004 2/13004 2/8600 0/4404
?/? c.*10C>T r.(=) p.(=) g.108985298G>A Copied from the Exome Variant Server TMEM119_000005 1/12996 0/8590 1/4406
?/? c.*11G>A r.(=) p.(=) g.108985297C>T Copied from the Exome Variant Server TMEM119_000003 1/12992 1/8588 0/4404
?/? c.*33G>A r.(=) p.(=) g.108985275C>T Copied from the Exome Variant Server TMEM119_000002 1/12920 1/8550 0/4370
?/? c.*41A>G r.(=) p.(=) g.108985267T>C Copied from the Exome Variant Server TMEM119_000001 3/12916 3/8544 0/4372
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