| 11087749 | CV227744 | single nucleotide variant | NM_000959.3(PTGFR):c.-562T>C | latanoprost response - Efficacy [RCV000211367] | drug response | 1 | 78490747 | 78490747 | Human | | name |
| 15110607 | CV719090 | single nucleotide variant | NM_000959.4(PTGFR):c.23A>T (p.Gln8Leu) | not provided [RCV000894100] | benign | 1 | 78492766 | 78492766 | Human | | name |
| 155927036 | CV2345326 | single nucleotide variant | NM_000959.4(PTGFR):c.29T>C (p.Val10Ala) | not specified [RCV004198106] | uncertain significance | 1 | 78492772 | 78492772 | Human | | name |
| 405673227 | CV3377775 | single nucleotide variant | NM_000959.4(PTGFR):c.68A>G (p.Gln23Arg) | not specified [RCV004515635] | uncertain significance | 1 | 78492811 | 78492811 | Human | | name |
| 597751538 | CV3588729 | single nucleotide variant | NM_000959.4(PTGFR):c.41C>T (p.Ala14Val) | not specified [RCV004846703] | uncertain significance | 1 | 78492784 | 78492784 | Human | | name |
| 8625054 | CV80173 | single nucleotide variant | NM_000959.3(PTGFR):c.86C>T (p.Ser29Phe) | Malignant melanoma [RCV000060249] | not provided | 1 | 78492829 | 78492829 | Human | | name |
| 405673216 | CV3377772 | single nucleotide variant | NM_000959.4(PTGFR):c.135C>G (p.Ser45Arg) | not specified [RCV004515632] | uncertain significance | 1 | 78492878 | 78492878 | Human | | name |
| 407472127 | CV3468285 | single nucleotide variant | NM_000959.4(PTGFR):c.277G>A (p.Ala93Thr) | not specified [RCV004662446] | uncertain significance | 1 | 78493020 | 78493020 | Human | | name |
| 598172620 | CV3904657 | single nucleotide variant | NM_000959.4(PTGFR):c.263C>T (p.Ala88Val) | not specified [RCV005263572] | uncertain significance | 1 | 78493006 | 78493006 | Human | | name |
| 155795212 | CV1858998 | single nucleotide variant | NM_000959.4(PTGFR):c.449A>T (p.Lys150Ile) | Myoepithelial tumor [RCV002463963] | uncertain significance | 1 | 78493192 | 78493192 | Human | 1 | name |
| 155989907 | CV2285184 | single nucleotide variant | NM_000959.4(PTGFR):c.611T>A (p.Leu204His) | not specified [RCV004145394] | uncertain significance | 1 | 78493354 | 78493354 | Human | | name |
| 156144148 | CV2358639 | single nucleotide variant | NM_000959.4(PTGFR):c.442A>G (p.Thr148Ala) | not specified [RCV004207512] | uncertain significance | 1 | 78493185 | 78493185 | Human | | name |
| 401725402 | CV2697397 | single nucleotide variant | NM_000959.4(PTGFR):c.299G>A (p.Arg100His) | not specified [RCV004304147] | uncertain significance | 1 | 78493042 | 78493042 | Human | | name |
| 401867476 | CV2792522 | single nucleotide variant | NM_000959.4(PTGFR):c.504G>T (p.Leu168Phe) | not specified [RCV004363565] | uncertain significance | 1 | 78493247 | 78493247 | Human | | name |
| 405673220 | CV3377773 | single nucleotide variant | NM_000959.4(PTGFR):c.397C>T (p.Arg133Trp) | not specified [RCV004515633] | uncertain significance | 1 | 78493140 | 78493140 | Human | | name |
| 405673223 | CV3377774 | single nucleotide variant | NM_000959.4(PTGFR):c.677C>G (p.Thr226Arg) | not specified [RCV004515634] | uncertain significance | 1 | 78493420 | 78493420 | Human | | name |
| 407472121 | CV3468284 | single nucleotide variant | NM_000959.4(PTGFR):c.718G>A (p.Gly240Ser) | not specified [RCV004662445] | uncertain significance | 1 | 78493461 | 78493461 | Human | | name |
| 597751533 | CV3588728 | single nucleotide variant | NM_000959.4(PTGFR):c.914T>C (p.Ile305Thr) | not specified [RCV004846702] | uncertain significance | 1 | 78536521 | 78536521 | Human | | name |
| 597751550 | CV3588731 | single nucleotide variant | NM_000959.4(PTGFR):c.815T>A (p.Ile272Asn) | not specified [RCV004846705] | uncertain significance | 1 | 78536422 | 78536422 | Human | | name |
| 597751555 | CV3588732 | single nucleotide variant | NM_000959.4(PTGFR):c.398G>A (p.Arg133Gln) | not specified [RCV004846706] | uncertain significance | 1 | 78493141 | 78493141 | Human | | name |
| 597751560 | CV3588733 | single nucleotide variant | NM_000959.4(PTGFR):c.316G>A (p.Val106Ile) | not specified [RCV004846707] | likely benign | 1 | 78493059 | 78493059 | Human | | name |
| 598172612 | CV3904656 | single nucleotide variant | NM_000959.4(PTGFR):c.535A>G (p.Ile179Val) | not specified [RCV005263571] | uncertain significance | 1 | 78493278 | 78493278 | Human | | name |
| 598172627 | CV3904658 | single nucleotide variant | NM_000959.4(PTGFR):c.902C>T (p.Pro301Leu) | not specified [RCV005263573] | uncertain significance | 1 | 78536509 | 78536509 | Human | | name |
| 15171056 | CV719091 | single nucleotide variant | NM_000959.4(PTGFR):c.653T>C (p.Leu218Ser) | not provided [RCV000883584] | benign | 1 | 78493396 | 78493396 | Human | | name |
| 8629680 | CV84827 | single nucleotide variant | NM_000959.3(PTGFR):c.817G>A (p.Gly273Arg) | Malignant melanoma [RCV000064909] | not provided | 1 | 78536424 | 78536424 | Human | | name |
| 8576115 | CV110470 | single nucleotide variant | NM_000959.3(PTGFR):c.1064A>C (p.Lys355Thr) | Lung cancer [RCV000090993] | uncertain significance | 1 | 78536671 | 78536671 | Human | | name |
| 401927870 | CV2808972 | single nucleotide variant | NM_000959.4(PTGFR):c.1012A>G (p.Ile338Val) | not provided [RCV003406570] | likely benign | 1 | 78536619 | 78536619 | Human | | name |
| 597751529 | CV3588727 | single nucleotide variant | NM_000959.4(PTGFR):c.1027A>C (p.Lys343Gln) | not specified [RCV004846701] | uncertain significance | 1 | 78536634 | 78536634 | Human | | name |
| 8629681 | CV84828 | single nucleotide variant | NM_000959.3(PTGFR):c.1022C>T (p.Ser341Phe) | Malignant melanoma [RCV000064910] | not provided | 1 | 78536629 | 78536629 | Human | | name |
| 8574875 | CV109213 | single nucleotide variant | NM_020440.3(PTGFRN):c.50-3715A>G | Lung cancer [RCV000089738] | uncertain significance | 1 | 116938000 | 116938000 | Human | | name |
| 597751714 | CV3588741 | single nucleotide variant | NM_020440.4(PTGFRN):c.22C>T (p.Pro8Ser) | not specified [RCV004846715] | uncertain significance | 1 | 116910225 | 116910225 | Human | | name |
| 15187680 | CV731613 | single nucleotide variant | NM_020440.4(PTGFRN):c.294C>T (p.Ala98=) | not provided [RCV000909155] | benign | 1 | 116941959 | 116941959 | Human | | name |
| 405673296 | CV3377793 | single nucleotide variant | NM_020440.4(PTGFRN):c.38T>C (p.Leu13Pro) | not specified [RCV004515653] | uncertain significance | 1 | 116910241 | 116910241 | Human | | name |
| 407472136 | CV3468287 | single nucleotide variant | NM_020440.4(PTGFRN):c.64C>T (p.Arg22Cys) | not specified [RCV004662448] | uncertain significance | 1 | 116941729 | 116941729 | Human | | name |
| 15194872 | CV696009 | single nucleotide variant | NM_020440.4(PTGFRN):c.462G>A (p.Pro154=) | not provided [RCV000955764] | benign | 1 | 116944722 | 116944722 | Human | | name |
| 156092884 | CV2300175 | single nucleotide variant | NM_020440.4(PTGFRN):c.243G>T (p.Gln81His) | not specified [RCV004151364] | uncertain significance | 1 | 116941908 | 116941908 | Human | | name |
| 329387494 | CV2470759 | single nucleotide variant | NM_020440.4(PTGFRN):c.104T>C (p.Val35Ala) | not specified [RCV004275991] | uncertain significance | 1 | 116941769 | 116941769 | Human | | name |
| 405673253 | CV3377782 | single nucleotide variant | NM_020440.4(PTGFRN):c.143A>T (p.Tyr48Phe) | not specified [RCV004515642] | uncertain significance | 1 | 116941808 | 116941808 | Human | | name |
| 598172671 | CV3904664 | single nucleotide variant | NM_020440.4(PTGFRN):c.1332G>A (p.Thr444=) | not specified [RCV005263579] | likely benign | 1 | 116961361 | 116961361 | Human | | name |
| 15194876 | CV696010 | single nucleotide variant | NM_020440.4(PTGFRN):c.1542C>T (p.Tyr514=) | not provided [RCV000955765] | benign | 1 | 116961571 | 116961571 | Human | | name |
| 15187684 | CV731615 | single nucleotide variant | NM_020440.4(PTGFRN):c.2310C>T (p.Arg770=) | not provided [RCV000909156] | benign | 1 | 116984822 | 116984822 | Human | | name |
| 15099465 | CV745598 | single nucleotide variant | NM_020440.4(PTGFRN):c.1839G>T (p.Val613=) | not provided [RCV000914458] | likely benign | 1 | 116967110 | 116967110 | Human | | name |
| 15099473 | CV745599 | single nucleotide variant | NM_020440.4(PTGFRN):c.2040G>A (p.Glu680=) | not provided [RCV000914459] | likely benign | 1 | 116967311 | 116967311 | Human | | name |
| 156089229 | CV2202047 | single nucleotide variant | NM_020440.4(PTGFRN):c.701T>C (p.Val234Ala) | not specified [RCV004075965] | uncertain significance | 1 | 116944961 | 116944961 | Human | | name |
| 156248385 | CV2203109 | single nucleotide variant | NM_020440.4(PTGFRN):c.871G>A (p.Glu291Lys) | not specified [RCV004069351] | uncertain significance | 1 | 116949230 | 116949230 | Human | | name |
| 156235571 | CV2224053 | single nucleotide variant | NM_020440.4(PTGFRN):c.496G>A (p.Glu166Lys) | not specified [RCV004095927] | uncertain significance | 1 | 116944756 | 116944756 | Human | | name |
| 156226100 | CV2226342 | single nucleotide variant | NM_020440.4(PTGFRN):c.760G>A (p.Ala254Thr) | not specified [RCV004099574] | uncertain significance | 1 | 116945020 | 116945020 | Human | | name |
| 156119328 | CV2228883 | single nucleotide variant | NM_020440.4(PTGFRN):c.655G>T (p.Asp219Tyr) | not specified [RCV004095114] | uncertain significance | 1 | 116944915 | 116944915 | Human | | name |
| 156137968 | CV2236558 | single nucleotide variant | NM_020440.4(PTGFRN):c.574G>C (p.Ala192Pro) | not specified [RCV004110552] | uncertain significance | 1 | 116944834 | 116944834 | Human | | name |
| 155997388 | CV2250549 | single nucleotide variant | NM_020440.4(PTGFRN):c.650G>A (p.Ser217Asn) | not specified [RCV004127407] | uncertain significance | 1 | 116944910 | 116944910 | Human | | name |
| 156052977 | CV2269463 | single nucleotide variant | NM_020440.4(PTGFRN):c.988G>A (p.Val330Met) | not specified [RCV004124578] | uncertain significance | 1 | 116949347 | 116949347 | Human | | name |
| 156088680 | CV2344253 | single nucleotide variant | NM_020440.4(PTGFRN):c.397G>C (p.Glu133Gln) | not specified [RCV004195022] | uncertain significance | 1 | 116942062 | 116942062 | Human | | name |
| 155935111 | CV2372608 | single nucleotide variant | NM_020440.4(PTGFRN):c.514G>A (p.Ala172Thr) | not specified [RCV004219398] | uncertain significance | 1 | 116944774 | 116944774 | Human | | name |
| 156042502 | CV2381461 | single nucleotide variant | NM_020440.4(PTGFRN):c.797C>T (p.Ala266Val) | not specified [RCV004229944] | uncertain significance | 1 | 116945057 | 116945057 | Human | | name |
| 329355884 | CV2430522 | single nucleotide variant | NM_020440.4(PTGFRN):c.731C>T (p.Ser244Phe) | not specified [RCV004252108] | uncertain significance | 1 | 116944991 | 116944991 | Human | | name |
| 329368769 | CV2450410 | single nucleotide variant | NM_020440.4(PTGFRN):c.841G>T (p.Ala281Ser) | not specified [RCV004265339] | uncertain significance | 1 | 116949200 | 116949200 | Human | | name |
| 329396494 | CV2462611 | single nucleotide variant | NM_020440.4(PTGFRN):c.646C>G (p.His216Asp) | not specified [RCV004278555] | uncertain significance | 1 | 116944906 | 116944906 | Human | | name |
| 329362092 | CV2465997 | single nucleotide variant | NM_020440.4(PTGFRN):c.937G>T (p.Val313Leu) | not specified [RCV004277898] | uncertain significance | 1 | 116949296 | 116949296 | Human | | name |
| 329380494 | CV2466653 | single nucleotide variant | NM_020440.4(PTGFRN):c.607G>A (p.Gly203Ser) | not specified [RCV004274171] | uncertain significance | 1 | 116944867 | 116944867 | Human | | name |
| 401731039 | CV2674240 | single nucleotide variant | NM_020440.4(PTGFRN):c.461C>G (p.Pro154Arg) | not specified [RCV004289128] | uncertain significance | 1 | 116944721 | 116944721 | Human | | name |
| 401875001 | CV2756167 | single nucleotide variant | NM_020440.4(PTGFRN):c.941C>T (p.Thr314Met) | not specified [RCV004338273] | uncertain significance | 1 | 116949300 | 116949300 | Human | | name |
| 405673293 | CV3377792 | single nucleotide variant | NM_020440.4(PTGFRN):c.325G>T (p.Val109Phe) | not specified [RCV004515652] | uncertain significance | 1 | 116941990 | 116941990 | Human | | name |
| 405673299 | CV3377794 | single nucleotide variant | NM_020440.4(PTGFRN):c.412G>T (p.Val138Phe) | not specified [RCV004515654] | uncertain significance | 1 | 116942077 | 116942077 | Human | | name |
| 405673303 | CV3377795 | single nucleotide variant | NM_020440.4(PTGFRN):c.859G>A (p.Val287Met) | not specified [RCV004515655] | uncertain significance | 1 | 116949218 | 116949218 | Human | | name |
| 405673306 | CV3377796 | single nucleotide variant | NM_020440.4(PTGFRN):c.929G>A (p.Arg310Gln) | not specified [RCV004515656] | uncertain significance | 1 | 116949288 | 116949288 | Human | | name |
| 407472142 | CV3468288 | single nucleotide variant | NM_020440.4(PTGFRN):c.452C>T (p.Ala151Val) | not specified [RCV004662449] | uncertain significance | 1 | 116944712 | 116944712 | Human | | name |
| 597751593 | CV3588739 | single nucleotide variant | NM_020440.4(PTGFRN):c.487G>A (p.Glu163Lys) | not specified [RCV004846713] | uncertain significance | 1 | 116944747 | 116944747 | Human | | name |
| 597751598 | CV3588740 | single nucleotide variant | NM_020440.4(PTGFRN):c.455G>C (p.Arg152Pro) | not specified [RCV004846714] | uncertain significance | 1 | 116944715 | 116944715 | Human | | name |
| 597751717 | CV3588742 | single nucleotide variant | NM_020440.4(PTGFRN):c.998G>A (p.Arg333Gln) | not specified [RCV004846716] | uncertain significance | 1 | 116949357 | 116949357 | Human | | name |
| 597751722 | CV3588743 | single nucleotide variant | NM_020440.4(PTGFRN):c.880G>A (p.Glu294Lys) | not specified [RCV004846717] | uncertain significance | 1 | 116949239 | 116949239 | Human | | name |
| 597751731 | CV3588745 | single nucleotide variant | NM_020440.4(PTGFRN):c.803A>G (p.Glu268Gly) | not specified [RCV004846719] | uncertain significance | 1 | 116945063 | 116945063 | Human | | name |
| 597751744 | CV3588748 | single nucleotide variant | NM_020440.4(PTGFRN):c.634G>A (p.Glu212Lys) | not specified [RCV004846722] | uncertain significance | 1 | 116944894 | 116944894 | Human | | name |
| 598172634 | CV3904659 | single nucleotide variant | NM_020440.4(PTGFRN):c.767A>G (p.Gln256Arg) | not specified [RCV005263574] | uncertain significance | 1 | 116945027 | 116945027 | Human | | name |
| 598172649 | CV3904661 | single nucleotide variant | NM_020440.4(PTGFRN):c.691C>T (p.Arg231Cys) | not specified [RCV005263576] | uncertain significance | 1 | 116944951 | 116944951 | Human | | name |
| 15163947 | CV718123 | single nucleotide variant | NM_020440.4(PTGFRN):c.725A>G (p.Gln242Arg) | not provided [RCV000882086] | likely benign | 1 | 116944985 | 116944985 | Human | | name |
| 15145501 | CV731614 | single nucleotide variant | NM_020440.4(PTGFRN):c.685G>A (p.Ala229Thr) | not provided [RCV000900171] | likely benign | 1 | 116944945 | 116944945 | Human | | name |
| 156401322 | CV2210908 | single nucleotide variant | NM_020440.4(PTGFRN):c.2084A>G (p.His695Arg) | not specified [RCV004085986] | uncertain significance | 1 | 116974240 | 116974240 | Human | | name |
| 156135089 | CV2213291 | single nucleotide variant | NM_020440.4(PTGFRN):c.1151G>T (p.Arg384Met) | not specified [RCV004085505] | uncertain significance | 1 | 116949510 | 116949510 | Human | | name |
| 155982924 | CV2233242 | single nucleotide variant | NM_020440.4(PTGFRN):c.1393G>A (p.Ala465Thr) | not specified [RCV004105633] | uncertain significance | 1 | 116961422 | 116961422 | Human | | name |
| 156209483 | CV2250217 | single nucleotide variant | NM_020440.4(PTGFRN):c.1370A>G (p.Asn457Ser) | not specified [RCV004117007] | uncertain significance | 1 | 116961399 | 116961399 | Human | | name |
| 155988150 | CV2251193 | single nucleotide variant | NM_020440.4(PTGFRN):c.1822C>A (p.Leu608Met) | not specified [RCV004115420] | uncertain significance | 1 | 116967093 | 116967093 | Human | | name |
| 156341391 | CV2268257 | single nucleotide variant | NM_020440.4(PTGFRN):c.1384G>A (p.Glu462Lys) | not specified [RCV004138556] | uncertain significance | 1 | 116961413 | 116961413 | Human | | name |
| 156360128 | CV2268985 | single nucleotide variant | NM_020440.4(PTGFRN):c.1055A>G (p.Asp352Gly) | not specified [RCV004128384] | uncertain significance | 1 | 116949414 | 116949414 | Human | | name |
| 156025152 | CV2273944 | single nucleotide variant | NM_020440.4(PTGFRN):c.1177G>A (p.Val393Met) | not specified [RCV004134347] | likely benign | 1 | 116949536 | 116949536 | Human | | name |
| 155929388 | CV2278091 | single nucleotide variant | NM_020440.4(PTGFRN):c.1124T>C (p.Val375Ala) | not specified [RCV004141308] | uncertain significance | 1 | 116949483 | 116949483 | Human | | name |
| 156067744 | CV2345825 | single nucleotide variant | NM_020440.4(PTGFRN):c.1645G>A (p.Val549Met) | not specified [RCV004198871] | uncertain significance | 1 | 116966916 | 116966916 | Human | | name |
| 155904217 | CV2353792 | single nucleotide variant | NM_020440.4(PTGFRN):c.1057G>A (p.Ala353Thr) | not specified [RCV004201797] | uncertain significance | 1 | 116949416 | 116949416 | Human | | name |
| 156191318 | CV2356847 | single nucleotide variant | NM_020440.4(PTGFRN):c.2611C>T (p.Arg871Cys) | not specified [RCV004202181] | uncertain significance | 1 | 116986938 | 116986938 | Human | | name |
| 155927134 | CV2365878 | single nucleotide variant | NM_020440.4(PTGFRN):c.1570C>T (p.Arg524Trp) | not specified [RCV004214407] | uncertain significance | 1 | 116961599 | 116961599 | Human | | name |
| 156000719 | CV2391791 | single nucleotide variant | NM_020440.4(PTGFRN):c.2273C>T (p.Ser758Phe) | not specified [RCV004235672] | uncertain significance | 1 | 116984785 | 116984785 | Human | | name |
| 329383538 | CV2425018 | single nucleotide variant | NM_020440.4(PTGFRN):c.1992G>C (p.Arg664Ser) | not specified [RCV004250675] | uncertain significance | 1 | 116967263 | 116967263 | Human | | name |
| 329356068 | CV2445633 | single nucleotide variant | NM_020440.4(PTGFRN):c.1358G>A (p.Arg453Gln) | not specified [RCV004259716] | uncertain significance | 1 | 116961387 | 116961387 | Human | | name |
| 401733185 | CV2691228 | single nucleotide variant | NM_020440.4(PTGFRN):c.2101G>C (p.Val701Leu) | not specified [RCV004302996] | uncertain significance | 1 | 116974257 | 116974257 | Human | | name |
| 401775095 | CV2696216 | single nucleotide variant | NM_020440.4(PTGFRN):c.2588T>C (p.Val863Ala) | not specified [RCV004310258] | uncertain significance | 1 | 116986915 | 116986915 | Human | | name |
| 401739098 | CV2708318 | single nucleotide variant | NM_020440.4(PTGFRN):c.1549G>T (p.Val517Leu) | not specified [RCV004311652] | uncertain significance | 1 | 116961578 | 116961578 | Human | | name |
| 401725217 | CV2726025 | single nucleotide variant | NM_020440.4(PTGFRN):c.2206T>A (p.Ser736Thr) | not specified [RCV004324386] | uncertain significance | 1 | 116984718 | 116984718 | Human | | name |
| 401870443 | CV2762728 | single nucleotide variant | NM_020440.4(PTGFRN):c.2389C>T (p.Pro797Ser) | not specified [RCV004340285] | uncertain significance | 1 | 116984901 | 116984901 | Human | | name |
| 401895761 | CV2778694 | single nucleotide variant | NM_020440.4(PTGFRN):c.1502G>A (p.Arg501Gln) | not specified [RCV004346611] | uncertain significance | 1 | 116961531 | 116961531 | Human | | name |
| 401882979 | CV2788698 | single nucleotide variant | NM_020440.4(PTGFRN):c.2599C>T (p.Arg867Trp) | not specified [RCV004361177] | uncertain significance | 1 | 116986926 | 116986926 | Human | | name |
| 405673232 | CV3377776 | single nucleotide variant | NM_020440.4(PTGFRN):c.1007G>A (p.Arg336His) | not specified [RCV004515636] | uncertain significance | 1 | 116949366 | 116949366 | Human | | name |
| 405673235 | CV3377777 | single nucleotide variant | NM_020440.4(PTGFRN):c.1121A>T (p.His374Leu) | not specified [RCV004515637] | uncertain significance | 1 | 116949480 | 116949480 | Human | | name |
| 405673242 | CV3377779 | single nucleotide variant | NM_020440.4(PTGFRN):c.1255G>A (p.Gly419Arg) | not specified [RCV004515639] | uncertain significance | 1 | 116961284 | 116961284 | Human | | name |
| 405673246 | CV3377780 | single nucleotide variant | NM_020440.4(PTGFRN):c.1325G>A (p.Arg442Gln) | not specified [RCV004515640] | uncertain significance | 1 | 116961354 | 116961354 | Human | | name |
| 405673249 | CV3377781 | single nucleotide variant | NM_020440.4(PTGFRN):c.1405G>A (p.Gly469Arg) | not specified [RCV004515641] | uncertain significance | 1 | 116961434 | 116961434 | Human | | name |
| 405673257 | CV3377783 | single nucleotide variant | NM_020440.4(PTGFRN):c.1456G>A (p.Gly486Arg) | not specified [RCV004515643] | uncertain significance | 1 | 116961485 | 116961485 | Human | | name |
| 405673260 | CV3377784 | single nucleotide variant | NM_020440.4(PTGFRN):c.2177C>T (p.Ala726Val) | not specified [RCV004515644] | uncertain significance | 1 | 116984689 | 116984689 | Human | | name |
| 405673263 | CV3377785 | single nucleotide variant | NM_020440.4(PTGFRN):c.2246T>G (p.Leu749Arg) | not specified [RCV004515645] | uncertain significance | 1 | 116984758 | 116984758 | Human | | name |
| 405673269 | CV3377786 | single nucleotide variant | NM_020440.4(PTGFRN):c.2296C>T (p.Leu766Phe) | not specified [RCV004515646] | uncertain significance | 1 | 116984808 | 116984808 | Human | | name |
| 405673273 | CV3377787 | single nucleotide variant | NM_020440.4(PTGFRN):c.2356C>G (p.Gln786Glu) | not specified [RCV004515647] | uncertain significance | 1 | 116984868 | 116984868 | Human | | name |
| 405673277 | CV3377788 | single nucleotide variant | NM_020440.4(PTGFRN):c.2574T>G (p.Cys858Trp) | not specified [RCV004515648] | uncertain significance | 1 | 116986901 | 116986901 | Human | | name |
| 405673281 | CV3377789 | single nucleotide variant | NM_020440.4(PTGFRN):c.2599C>G (p.Arg867Gly) | not specified [RCV004515649] | uncertain significance | 1 | 116986926 | 116986926 | Human | | name |
| 405673284 | CV3377790 | single nucleotide variant | NM_020440.4(PTGFRN):c.2612G>A (p.Arg871His) | not specified [RCV004515650] | uncertain significance | 1 | 116986939 | 116986939 | Human | | name |
| 405673289 | CV3377791 | single nucleotide variant | NM_020440.4(PTGFRN):c.2634G>T (p.Met878Ile) | not specified [RCV004515651] | uncertain significance | 1 | 116986961 | 116986961 | Human | | name |
| 407472132 | CV3468286 | single nucleotide variant | NM_020440.4(PTGFRN):c.1301C>T (p.Thr434Met) | not specified [RCV004662447] | likely benign | 1 | 116961330 | 116961330 | Human | | name |
| 407472147 | CV3468289 | single nucleotide variant | NM_020440.4(PTGFRN):c.1408G>T (p.Asp470Tyr) | not specified [RCV004662450] | uncertain significance | 1 | 116961437 | 116961437 | Human | | name |
| 407491305 | CV3468290 | single nucleotide variant | NM_020440.4(PTGFRN):c.1031C>T (p.Pro344Leu) | not specified [RCV004666863] | uncertain significance | 1 | 116949390 | 116949390 | Human | | name |
| 407472152 | CV3468291 | single nucleotide variant | NM_020440.4(PTGFRN):c.1926G>A (p.Met642Ile) | not specified [RCV004662451] | uncertain significance | 1 | 116967197 | 116967197 | Human | | name |
| 407491310 | CV3468292 | single nucleotide variant | NM_020440.4(PTGFRN):c.1615G>T (p.Val539Phe) | not specified [RCV004666864] | uncertain significance | 1 | 116961644 | 116961644 | Human | | name |
| 597751565 | CV3588734 | single nucleotide variant | NM_020440.4(PTGFRN):c.1690G>A (p.Gly564Arg) | not specified [RCV004846708] | uncertain significance | 1 | 116966961 | 116966961 | Human | | name |
| 597751573 | CV3588735 | single nucleotide variant | NM_020440.4(PTGFRN):c.2234T>C (p.Leu745Pro) | not specified [RCV004846709] | uncertain significance | 1 | 116984746 | 116984746 | Human | | name |
| 597751578 | CV3588736 | single nucleotide variant | NM_020440.4(PTGFRN):c.1490C>T (p.Thr497Met) | not specified [RCV004846710] | uncertain significance | 1 | 116961519 | 116961519 | Human | | name |
| 597751582 | CV3588737 | single nucleotide variant | NM_020440.4(PTGFRN):c.2407A>G (p.Thr803Ala) | not specified [RCV004846711] | uncertain significance | 1 | 116984919 | 116984919 | Human | | name |
| 597751727 | CV3588744 | single nucleotide variant | NM_020440.4(PTGFRN):c.1349G>A (p.Arg450Lys) | not specified [RCV004846718] | uncertain significance | 1 | 116961378 | 116961378 | Human | | name |
| 597751736 | CV3588746 | single nucleotide variant | NM_020440.4(PTGFRN):c.2126T>C (p.Leu709Ser) | not specified [RCV004846720] | uncertain significance | 1 | 116974282 | 116974282 | Human | | name |
| 597751749 | CV3588749 | single nucleotide variant | NM_020440.4(PTGFRN):c.1624T>C (p.Phe542Leu) | not specified [RCV004846723] | uncertain significance | 1 | 116961653 | 116961653 | Human | | name |
| 597751753 | CV3588750 | single nucleotide variant | NM_020440.4(PTGFRN):c.2165C>T (p.Pro722Leu) | not specified [RCV004846724] | uncertain significance | 1 | 116974321 | 116974321 | Human | | name |
| 598172641 | CV3904660 | single nucleotide variant | NM_020440.4(PTGFRN):c.1028C>T (p.Ser343Leu) | not specified [RCV005263575] | uncertain significance | 1 | 116949387 | 116949387 | Human | | name |
| 598172656 | CV3904662 | single nucleotide variant | NM_020440.4(PTGFRN):c.1235T>C (p.Leu412Pro) | not specified [RCV005263577] | uncertain significance | 1 | 116961264 | 116961264 | Human | | name |
| 598172663 | CV3904663 | single nucleotide variant | NM_020440.4(PTGFRN):c.2158C>G (p.Leu720Val) | not specified [RCV005263578] | uncertain significance | 1 | 116974314 | 116974314 | Human | | name |
| 598172678 | CV3904665 | single nucleotide variant | NM_020440.4(PTGFRN):c.2503A>T (p.Ile835Phe) | not specified [RCV005263580] | uncertain significance | 1 | 116986830 | 116986830 | Human | | name |
| 598172685 | CV3904666 | single nucleotide variant | NM_020440.4(PTGFRN):c.1234C>A (p.Leu412Met) | not specified [RCV005263581] | uncertain significance | 1 | 116961263 | 116961263 | Human | | name |
| 8628818 | CV83962 | single nucleotide variant | NM_020440.3(PTGFRN):c.2381C>T (p.Ser794Phe) | Malignant melanoma [RCV000064043] | not provided | 1 | 116984893 | 116984893 | Human | | name |
