| 15201264 | CV777459 | single nucleotide variant | NM_001083.4(PDE5A):c.2190-4G>A | not provided [RCV000957571] | benign | 4 | 119505936 | 119505936 | Human | | name |
| 15120490 | CV744119 | duplication | NM_001083.4(PDE5A):c.2490+3_2490+5dup | not provided [RCV000895903] | benign | 4 | 119501164 | 119501165 | Human | | name |
| 155935481 | CV2225609 | single nucleotide variant | NM_001083.4(PDE5A):c.97T>C (p.Trp33Arg) | not specified [RCV004100982] | uncertain significance | 4 | 119628575 | 119628575 | Human | | name |
| 15169586 | CV748696 | single nucleotide variant | NM_001083.4(PDE5A):c.822T>C (p.His274=) | not provided [RCV000927528] | likely benign | 4 | 119596532 | 119596532 | Human | | name |
| 155970943 | CV2241629 | single nucleotide variant | NM_001083.4(PDE5A):c.232T>A (p.Ser78Thr) | not specified [RCV004104510] | uncertain significance | 4 | 119607218 | 119607218 | Human | | name |
| 401854334 | CV2766645 | single nucleotide variant | NM_001083.4(PDE5A):c.268G>A (p.Asp90Asn) | not specified [RCV004347255] | uncertain significance | 4 | 119607182 | 119607182 | Human | | name |
| 401923477 | CV2820138 | single nucleotide variant | NM_001083.4(PDE5A):c.2010T>C (p.His670=) | not provided [RCV003435142] | likely benign | 4 | 119511125 | 119511125 | Human | | name |
| 401928442 | CV2820139 | single nucleotide variant | NM_001083.4(PDE5A):c.1071T>A (p.Thr357=) | not provided [RCV003439482] | likely benign | 4 | 119562893 | 119562893 | Human | | name |
| 405776251 | CV3375281 | single nucleotide variant | NM_001083.4(PDE5A):c.263G>A (p.Arg88His) | not specified [RCV004503157] | uncertain significance | 4 | 119607187 | 119607187 | Human | | name |
| 405776257 | CV3375282 | single nucleotide variant | NM_001083.4(PDE5A):c.274A>G (p.Ser92Gly) | not specified [RCV004503158] | uncertain significance | 4 | 119607176 | 119607176 | Human | | name |
| 15150965 | CV709146 | single nucleotide variant | NM_001083.4(PDE5A):c.2424G>A (p.Glu808=) | not provided [RCV000968043] | benign | 4 | 119501236 | 119501236 | Human | | name |
| 15172449 | CV709148 | single nucleotide variant | NM_001083.4(PDE5A):c.2013A>C (p.Pro671=) | not provided [RCV000972406] | benign | 4 | 119511122 | 119511122 | Human | | name |
| 15107239 | CV709149 | single nucleotide variant | NM_001083.4(PDE5A):c.1425G>A (p.Glu475=) | not provided [RCV000960250] | benign|likely benign | 4 | 119542606 | 119542606 | Human | | name |
| 15103266 | CV720733 | single nucleotide variant | NM_001083.4(PDE5A):c.2380A>C (p.Arg794=) | not provided [RCV000892638] | benign | 4 | 119502607 | 119502607 | Human | | name |
| 15108897 | CV764282 | single nucleotide variant | NM_001083.4(PDE5A):c.1962T>C (p.Asp654=) | not provided [RCV000938238] | likely benign | 4 | 119519083 | 119519083 | Human | | name |
| 156389179 | CV2373617 | single nucleotide variant | NM_001083.4(PDE5A):c.410C>A (p.Thr137Asn) | not specified [RCV004222708] | uncertain significance | 4 | 119607040 | 119607040 | Human | | name |
| 329381942 | CV2424273 | single nucleotide variant | NM_001083.4(PDE5A):c.665G>A (p.Arg222His) | not specified [RCV004252184] | uncertain significance | 4 | 119606785 | 119606785 | Human | | name |
| 405776263 | CV3375283 | single nucleotide variant | NM_001083.4(PDE5A):c.382T>C (p.Ser128Pro) | not specified [RCV004503159] | uncertain significance | 4 | 119607068 | 119607068 | Human | | name |
| 405776268 | CV3375284 | single nucleotide variant | NM_001083.4(PDE5A):c.638T>C (p.Leu213Pro) | not specified [RCV004503160] | uncertain significance | 4 | 119606812 | 119606812 | Human | | name |
| 405776275 | CV3375285 | single nucleotide variant | NM_001083.4(PDE5A):c.845C>T (p.Ala282Val) | not specified [RCV004503161] | uncertain significance | 4 | 119567131 | 119567131 | Human | | name |
| 405776282 | CV3375286 | single nucleotide variant | NM_001083.4(PDE5A):c.874G>A (p.Gly292Ser) | not specified [RCV004503162] | uncertain significance | 4 | 119567102 | 119567102 | Human | | name |
| 405776287 | CV3375287 | single nucleotide variant | NM_001083.4(PDE5A):c.961G>A (p.Glu321Lys) | not specified [RCV004503163] | uncertain significance | 4 | 119565353 | 119565353 | Human | | name |
| 407463359 | CV3460205 | single nucleotide variant | NM_001083.4(PDE5A):c.704C>T (p.Ala235Val) | not specified [RCV004659667] | uncertain significance | 4 | 119606746 | 119606746 | Human | | name |
| 597699260 | CV3568834 | single nucleotide variant | NM_001083.4(PDE5A):c.664C>T (p.Arg222Cys) | not specified [RCV004839563] | uncertain significance | 4 | 119606786 | 119606786 | Human | | name |
| 597699285 | CV3568837 | single nucleotide variant | NM_001083.4(PDE5A):c.437G>C (p.Gly146Ala) | not specified [RCV004839566] | uncertain significance | 4 | 119607013 | 119607013 | Human | | name |
| 15195525 | CV720735 | single nucleotide variant | NM_001083.4(PDE5A):c.356A>T (p.Glu119Val) | not provided [RCV000889527] | benign | 4 | 119607094 | 119607094 | Human | | name |
| 156388010 | CV2221686 | single nucleotide variant | NM_001083.4(PDE5A):c.1010C>G (p.Ala337Gly) | not specified [RCV004098455] | uncertain significance | 4 | 119562954 | 119562954 | Human | | name |
| 156202249 | CV2234474 | single nucleotide variant | NM_001083.4(PDE5A):c.2377G>A (p.Glu793Lys) | not specified [RCV004100679] | uncertain significance | 4 | 119502610 | 119502610 | Human | | name |
| 155903227 | CV2274841 | single nucleotide variant | NM_001083.4(PDE5A):c.1408C>A (p.Leu470Ile) | not specified [RCV004133042] | uncertain significance | 4 | 119542623 | 119542623 | Human | | name |
| 156000650 | CV2287410 | single nucleotide variant | NM_001083.4(PDE5A):c.1757A>G (p.Gln586Arg) | not specified [RCV004147015] | uncertain significance | 4 | 119525571 | 119525571 | Human | | name |
| 156157440 | CV2314450 | single nucleotide variant | NM_001083.4(PDE5A):c.1790G>A (p.Arg597Lys) | not specified [RCV004168559] | uncertain significance | 4 | 119521050 | 119521050 | Human | | name |
| 156288450 | CV2327412 | single nucleotide variant | NM_001083.4(PDE5A):c.1333C>G (p.Gln445Glu) | not specified [RCV004174836] | uncertain significance | 4 | 119552613 | 119552613 | Human | | name |
| 155963950 | CV2330386 | single nucleotide variant | NM_001083.4(PDE5A):c.1271T>G (p.Ile424Ser) | not specified [RCV004180960] | uncertain significance | 4 | 119553675 | 119553675 | Human | | name |
| 156084691 | CV2343307 | single nucleotide variant | NM_001083.4(PDE5A):c.1067C>T (p.Ala356Val) | not specified [RCV004194925] | uncertain significance | 4 | 119562897 | 119562897 | Human | | name |
| 156282648 | CV2363144 | single nucleotide variant | NM_001083.4(PDE5A):c.2351C>G (p.Thr784Ser) | not specified [RCV004211267] | likely benign | 4 | 119502636 | 119502636 | Human | | name |
| 156214256 | CV2385905 | single nucleotide variant | NM_001083.4(PDE5A):c.2320A>G (p.Ile774Val) | not specified [RCV004226943] | uncertain significance | 4 | 119504547 | 119504547 | Human | | name |
| 401720498 | CV2673349 | single nucleotide variant | NM_001083.4(PDE5A):c.2596A>G (p.Asn866Asp) | not specified [RCV004288332] | uncertain significance | 4 | 119498633 | 119498633 | Human | | name |
| 401879745 | CV2788498 | single nucleotide variant | NM_001083.4(PDE5A):c.1361C>T (p.Thr454Ile) | not specified [RCV004359480] | uncertain significance | 4 | 119552585 | 119552585 | Human | | name |
| 405776206 | CV3375273 | single nucleotide variant | NM_001083.4(PDE5A):c.1019T>C (p.Ile340Thr) | not specified [RCV004503149] | uncertain significance | 4 | 119562945 | 119562945 | Human | | name |
| 405776211 | CV3375274 | single nucleotide variant | NM_001083.4(PDE5A):c.1196C>T (p.Thr399Ile) | not specified [RCV004503150] | uncertain significance | 4 | 119560299 | 119560299 | Human | | name |
| 405776216 | CV3375275 | single nucleotide variant | NM_001083.4(PDE5A):c.1303T>C (p.Trp435Arg) | not specified [RCV004503151] | uncertain significance | 4 | 119553643 | 119553643 | Human | | name |
| 405776221 | CV3375276 | single nucleotide variant | NM_001083.4(PDE5A):c.1324A>G (p.Asn442Asp) | not specified [RCV004503152] | uncertain significance | 4 | 119552622 | 119552622 | Human | | name |
| 405776232 | CV3375278 | single nucleotide variant | NM_001083.4(PDE5A):c.1455C>A (p.Asn485Lys) | not specified [RCV004503154] | uncertain significance | 4 | 119542576 | 119542576 | Human | | name |
| 405776240 | CV3375279 | single nucleotide variant | NM_001083.4(PDE5A):c.1943T>C (p.Ile648Thr) | not specified [RCV004503155] | uncertain significance | 4 | 119519102 | 119519102 | Human | | name |
| 405776246 | CV3375280 | single nucleotide variant | NM_001083.4(PDE5A):c.2404A>T (p.Thr802Ser) | not specified [RCV004503156] | uncertain significance | 4 | 119502583 | 119502583 | Human | | name |
| 407524055 | CV3460204 | single nucleotide variant | NM_001083.4(PDE5A):c.1634C>T (p.Ala545Val) | not specified [RCV004653520] | uncertain significance | 4 | 119525694 | 119525694 | Human | | name |
| 407528522 | CV3460206 | single nucleotide variant | NM_001083.4(PDE5A):c.1111A>G (p.Ile371Val) | not specified [RCV004655496] | uncertain significance | 4 | 119562853 | 119562853 | Human | | name |
| 597699269 | CV3568835 | single nucleotide variant | NM_001083.4(PDE5A):c.2455G>C (p.Gly819Arg) | not specified [RCV004839564] | uncertain significance | 4 | 119501205 | 119501205 | Human | | name |
| 597699279 | CV3568836 | single nucleotide variant | NM_001083.4(PDE5A):c.1327G>A (p.Val443Ile) | not specified [RCV004839565] | uncertain significance | 4 | 119552619 | 119552619 | Human | | name |
| 597699296 | CV3568838 | single nucleotide variant | NM_001083.4(PDE5A):c.2422G>A (p.Glu808Lys) | not specified [RCV004839567] | uncertain significance | 4 | 119501238 | 119501238 | Human | | name |
| 597699305 | CV3568839 | single nucleotide variant | NM_001083.4(PDE5A):c.2385A>T (p.Lys795Asn) | not specified [RCV004839568] | uncertain significance | 4 | 119502602 | 119502602 | Human | | name |
| 597756800 | CV3568840 | single nucleotide variant | NM_001083.4(PDE5A):c.1232A>C (p.Tyr411Ser) | not specified [RCV004848197] | uncertain significance | 4 | 119553714 | 119553714 | Human | | name |
| 597699517 | CV3568841 | single nucleotide variant | NM_001083.4(PDE5A):c.1210G>A (p.Ala404Thr) | not specified [RCV004839569] | uncertain significance | 4 | 119553736 | 119553736 | Human | | name |
| 598166468 | CV4006268 | single nucleotide variant | NM_001083.4(PDE5A):c.2488G>C (p.Glu830Gln) | not specified [RCV005391479] | uncertain significance | 4 | 119501172 | 119501172 | Human | | name |
| 598166462 | CV4006269 | single nucleotide variant | NM_001083.4(PDE5A):c.1874T>C (p.Met625Thr) | not specified [RCV005391480] | uncertain significance | 4 | 119520966 | 119520966 | Human | | name |
| 598166456 | CV4006270 | single nucleotide variant | NM_001083.4(PDE5A):c.1195A>G (p.Thr399Ala) | not specified [RCV005391481] | uncertain significance | 4 | 119560300 | 119560300 | Human | | name |
| 598166449 | CV4006271 | single nucleotide variant | NM_001083.4(PDE5A):c.2193G>T (p.Arg731Ser) | not specified [RCV005391482] | uncertain significance | 4 | 119505929 | 119505929 | Human | | name |
| 598166445 | CV4006272 | single nucleotide variant | NM_001083.4(PDE5A):c.1742A>T (p.Asp581Val) | not specified [RCV005391483] | uncertain significance | 4 | 119525586 | 119525586 | Human | | name |
| 15107234 | CV709147 | single nucleotide variant | NM_001083.4(PDE5A):c.2333T>C (p.Ile778Thr) | not provided [RCV000960249] | likely benign | 4 | 119502654 | 119502654 | Human | 1 | name |
| 15107234 | CV709147 | single nucleotide variant | NM_001083.4(PDE5A):c.2333T>C (p.Ile778Thr) | not provided [RCV000960249] | likely benign | 4 | 119502654 | 119502655 | Human | 1 | name |
| 15153317 | CV720734 | single nucleotide variant | NM_001083.4(PDE5A):c.2219G>A (p.Arg740Lys) | not provided [RCV000879985] | likely benign | 4 | 119505903 | 119505903 | Human | | name |
| 15162829 | CV734422 | single nucleotide variant | NM_001083.4(PDE5A):c.1922T>C (p.Leu641Pro) | not provided [RCV000903640] | benign | 4 | 119519123 | 119519123 | Human | | name |
| 15134996 | CV734423 | single nucleotide variant | NM_001083.4(PDE5A):c.1438A>C (p.Lys480Gln) | not provided [RCV000898383] | benign | 4 | 119542593 | 119542593 | Human | | name |
