All transcript variants in gene PTGER2

Information The variants shown are described using the NM_000956.3 transcript reference sequence.

43 entries on 1 page. Showing entries 1 - 43.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-1C>T r.(=) p.(=) g.52781266C>T Copied from the Exome Variant Server PTGER2_000001 1/12980 1/8592 0/4388
?/? c.1A>G r.? p.? g.52781267A>G Copied from the Exome Variant Server PTGER2_000002 1/12988 1/8594 0/4394
?/? c.27G>A r.(=) p.(=) g.52781293G>A Copied from the Exome Variant Server PTGER2_000003 1/12990 0/8586 1/4404
?/? c.32A>G r.(?) p.(Glu11Gly) g.52781298A>G Copied from the Exome Variant Server PTGER2_000004 1/12990 0/8586 1/4404
?/? c.33G>A r.(=) p.(=) g.52781299G>A Copied from the Exome Variant Server PTGER2_000005 1/12992 1/8588 0/4404
?/? c.75A>T r.(=) p.(=) g.52781341A>T Copied from the Exome Variant Server PTGER2_000006 897/12994 309/8594 588/4400
?/? c.120C>T r.(=) p.(=) g.52781386C>T Copied from the Exome Variant Server PTGER2_000007 11/13000 10/8600 1/4400
?/? c.134T>C r.(?) p.(Leu45Pro) g.52781400T>C Copied from the Exome Variant Server PTGER2_000008 1/12988 1/8588 0/4400
?/? c.152G>T r.(?) p.(Arg51Leu) g.52781418G>T Copied from the Exome Variant Server PTGER2_000009 3/12912 0/8546 3/4366
?/? c.179G>A r.(?) p.(Arg60His) g.52781445G>A Copied from the Exome Variant Server PTGER2_000010 1/12950 0/8558 1/4392
?/? c.183G>C r.(?) p.(Arg61Ser) g.52781449G>C Copied from the Exome Variant Server PTGER2_000011 1/12964 0/8572 1/4392
?/? c.207G>T r.(=) p.(=) g.52781473G>T Copied from the Exome Variant Server PTGER2_000012 1/12964 0/8576 1/4388
?/? c.216C>T r.(=) p.(=) g.52781482C>T Copied from the Exome Variant Server PTGER2_000013 1/12956 1/8570 0/4386
?/? c.217G>A r.(?) p.(Glu73Lys) g.52781483G>A Copied from the Exome Variant Server PTGER2_000014 2/12960 1/8572 1/4388
?/? c.240C>T r.(=) p.(=) g.52781506C>T Copied from the Exome Variant Server PTGER2_000015 1/12858 1/8490 0/4368
?/? c.247T>G r.(?) p.(Cys83Gly) g.52781513T>G Copied from the Exome Variant Server PTGER2_000016 77/12844 74/8482 3/4362
?/? c.312C>T r.(=) p.(=) g.52781578C>T Copied from the Exome Variant Server PTGER2_000017 10/12932 0/8552 10/4380
?/? c.336C>T r.(=) p.(=) g.52781602C>T Copied from the Exome Variant Server PTGER2_000018 3/12966 1/8574 2/4392
?/? c.406C>G r.(?) p.(Leu136Val) g.52781672C>G Copied from the Exome Variant Server PTGER2_000019 1/13004 1/8600 0/4404
?/? c.493C>A r.(?) p.(Leu165Met) g.52781759C>A Copied from the Exome Variant Server PTGER2_000020 3/13006 3/8600 0/4406
?/? c.537C>G r.(=) p.(=) g.52781803C>G Copied from the Exome Variant Server PTGER2_000021 1/13006 1/8600 0/4406
?/? c.546C>T r.(=) p.(=) g.52781812C>T Copied from the Exome Variant Server PTGER2_000022 3/13004 3/8600 0/4404
?/? c.548C>T r.(?) p.(Pro183Leu) g.52781814C>T Copied from the Exome Variant Server PTGER2_000023 1/13004 0/8600 1/4404
?/? c.613C>T r.(=) p.(=) g.52781879C>T Copied from the Exome Variant Server PTGER2_000024 5/13006 4/8600 1/4406
?/? c.628T>C r.(?) p.(Ser210Pro) g.52781894T>C Copied from the Exome Variant Server PTGER2_000025 1/13006 1/8600 0/4406
?/? c.666C>T r.(=) p.(=) g.52781932C>T Copied from the Exome Variant Server PTGER2_000026 8/13006 0/8600 8/4406
?/? c.667A>C r.(?) p.(Ile223Leu) g.52781933A>C Copied from the Exome Variant Server PTGER2_000027 1/13006 0/8600 1/4406
?/? c.724C>T r.(?) p.(Arg242Trp) g.52781990C>T Copied from the Exome Variant Server PTGER2_000028 1/13000 0/8594 1/4406
?/? c.771G>A r.(=) p.(=) g.52782037G>A Copied from the Exome Variant Server PTGER2_000029 3/13006 3/8600 0/4406
?/? c.786C>G r.(?) p.(His262Gln) g.52782052C>G Copied from the Exome Variant Server PTGER2_000030 1/13004 1/8598 0/4406
?/? c.810C>T r.(=) p.(=) g.52782076C>T Copied from the Exome Variant Server PTGER2_000031 42/13000 0/8596 42/4404
?/? c.843+16C>T r.(=) p.(=) g.52782125C>T Copied from the Exome Variant Server PTGER2_000032 3/12982 3/8586 0/4396
?/? c.843+30G>T r.(=) p.(=) g.52782139G>T Copied from the Exome Variant Server PTGER2_000033 2/12958 2/8574 0/4384
?/? c.844-46G>C r.(=) p.(=) g.52793893G>C Copied from the Exome Variant Server PTGER2_000034 1/12994 0/8596 1/4398
?/? c.844-41G>A r.(=) p.(=) g.52793898G>A Copied from the Exome Variant Server PTGER2_000035 1/12992 0/8596 1/4396
?/? c.854A>G r.(?) p.(Tyr285Cys) g.52793949A>G Copied from the Exome Variant Server PTGER2_000036 34/13006 33/8600 1/4406
?/? c.867C>G r.(=) p.(=) g.52793962C>G Copied from the Exome Variant Server PTGER2_000037 9/13006 0/8600 9/4406
?/? c.891C>T r.(=) p.(=) g.52793986C>T Copied from the Exome Variant Server PTGER2_000038 2/13006 0/8600 2/4406
?/? c.912A>G r.(=) p.(=) g.52794007A>G Copied from the Exome Variant Server PTGER2_000039 418/13006 384/8600 34/4406
?/? c.951C>T r.(=) p.(=) g.52794046C>T Copied from the Exome Variant Server PTGER2_000040 1/13006 1/8600 0/4406
?/? c.954T>C r.(=) p.(=) g.52794049T>C Copied from the Exome Variant Server PTGER2_000041 2/13006 2/8600 0/4406
?/? c.1025C>T r.(?) p.(Thr342Ile) g.52794120C>T Copied from the Exome Variant Server PTGER2_000042 1/13006 1/8600 0/4406
?/? c.*12T>G r.(=) p.(=) g.52794184T>G Copied from the Exome Variant Server PTGER2_000043 4/13004 0/8598 4/4406
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