| 597644233 | CV3667454 | single nucleotide variant | NM_014674.3(EDEM1):c.13G>T (p.Ala5Ser) | not specified [RCV004909639] | uncertain significance | 3 | 5187818 | 5187818 | Human | | name |
| 156380138 | CV2211813 | single nucleotide variant | NM_014674.3(EDEM1):c.31G>A (p.Val11Met) | not specified [RCV004086640] | uncertain significance | 3 | 5187836 | 5187836 | Human | | name |
| 401869182 | CV2766927 | single nucleotide variant | NM_014674.3(EDEM1):c.34C>T (p.Leu12Phe) | not specified [RCV004343314] | uncertain significance | 3 | 5187839 | 5187839 | Human | | name |
| 597644641 | CV3667458 | single nucleotide variant | NM_014674.3(EDEM1):c.86C>G (p.Pro29Arg) | not specified [RCV004909642] | uncertain significance | 3 | 5187891 | 5187891 | Human | | name |
| 156379456 | CV2214794 | single nucleotide variant | NM_014674.3(EDEM1):c.172G>T (p.Gly58Trp) | not specified [RCV004090598] | uncertain significance | 3 | 5187977 | 5187977 | Human | | name |
| 156245057 | CV2231649 | single nucleotide variant | NM_014674.3(EDEM1):c.176C>T (p.Pro59Leu) | not specified [RCV004098218] | uncertain significance | 3 | 5187981 | 5187981 | Human | | name |
| 156063336 | CV2321067 | single nucleotide variant | NM_014674.3(EDEM1):c.173G>A (p.Gly58Glu) | not specified [RCV004174895] | uncertain significance | 3 | 5187978 | 5187978 | Human | | name |
| 155933051 | CV2372211 | single nucleotide variant | NM_014674.3(EDEM1):c.209C>T (p.Ser70Leu) | not specified [RCV004216990] | uncertain significance | 3 | 5188014 | 5188014 | Human | | name |
| 329367613 | CV2427469 | single nucleotide variant | NM_014674.3(EDEM1):c.197T>C (p.Val66Ala) | not specified [RCV004250109] | uncertain significance | 3 | 5188002 | 5188002 | Human | | name |
| 401729721 | CV2690476 | single nucleotide variant | NM_014674.3(EDEM1):c.178G>T (p.Val60Leu) | not specified [RCV004304243] | uncertain significance | 3 | 5187983 | 5187983 | Human | | name |
| 401856492 | CV2764820 | single nucleotide variant | NM_014674.3(EDEM1):c.223C>T (p.Pro75Ser) | not specified [RCV004334923] | uncertain significance | 3 | 5188028 | 5188028 | Human | | name |
| 405767315 | CV3248225 | single nucleotide variant | NM_014674.3(EDEM1):c.190G>C (p.Gly64Arg) | not specified [RCV004384518] | uncertain significance | 3 | 5187995 | 5187995 | Human | | name |
| 405767318 | CV3248226 | single nucleotide variant | NM_014674.3(EDEM1):c.193G>C (p.Gly65Arg) | not specified [RCV004384519] | uncertain significance | 3 | 5187998 | 5187998 | Human | | name |
| 405767323 | CV3248227 | single nucleotide variant | NM_014674.3(EDEM1):c.256G>C (p.Ala86Pro) | not specified [RCV004384520] | uncertain significance | 3 | 5188061 | 5188061 | Human | | name |
| 407478770 | CV3441557 | single nucleotide variant | NM_014674.3(EDEM1):c.238G>T (p.Ala80Ser) | not specified [RCV004617604] | uncertain significance | 3 | 5188043 | 5188043 | Human | | name |
| 407478783 | CV3441560 | single nucleotide variant | NM_014674.3(EDEM1):c.293C>G (p.Ala98Gly) | not specified [RCV004617607] | uncertain significance | 3 | 5188098 | 5188098 | Human | | name |
| 407478804 | CV3441563 | single nucleotide variant | NM_014674.3(EDEM1):c.221C>T (p.Pro74Leu) | not specified [RCV004617610] | uncertain significance | 3 | 5188026 | 5188026 | Human | | name |
| 597644222 | CV3667452 | single nucleotide variant | NM_014674.3(EDEM1):c.125G>C (p.Gly42Ala) | not specified [RCV004909637] | uncertain significance | 3 | 5187930 | 5187930 | Human | | name |
| 598165919 | CV3954082 | single nucleotide variant | NM_014674.3(EDEM1):c.133C>A (p.Arg45Ser) | not specified [RCV005329781] | uncertain significance | 3 | 5187938 | 5187938 | Human | | name |
| 598165925 | CV3954083 | single nucleotide variant | NM_014674.3(EDEM1):c.190G>A (p.Gly64Arg) | not specified [RCV005329782] | uncertain significance | 3 | 5187995 | 5187995 | Human | | name |
| 598165931 | CV3954084 | single nucleotide variant | NM_014674.3(EDEM1):c.191G>T (p.Gly64Val) | not specified [RCV005329783] | uncertain significance | 3 | 5187996 | 5187996 | Human | | name |
| 156400776 | CV2217160 | single nucleotide variant | NM_014674.3(EDEM1):c.313G>A (p.Gly105Ser) | not specified [RCV004087619] | uncertain significance | 3 | 5188118 | 5188118 | Human | | name |
| 156219661 | CV2225973 | single nucleotide variant | NM_014674.3(EDEM1):c.911C>T (p.Ala304Val) | not specified [RCV004105137] | uncertain significance | 3 | 5203018 | 5203018 | Human | | name |
| 156234607 | CV2271204 | single nucleotide variant | NM_014674.3(EDEM1):c.358G>T (p.Gly120Cys) | not specified [RCV004134565] | uncertain significance | 3 | 5188163 | 5188163 | Human | | name |
| 155990229 | CV2285222 | single nucleotide variant | NM_014674.3(EDEM1):c.358G>A (p.Gly120Ser) | not specified [RCV004145423] | uncertain significance | 3 | 5188163 | 5188163 | Human | | name |
| 156118669 | CV2353963 | single nucleotide variant | NM_014674.3(EDEM1):c.808C>T (p.Arg270Trp) | not specified [RCV004204400] | uncertain significance | 3 | 5201874 | 5201874 | Human | | name |
| 155930134 | CV2354118 | single nucleotide variant | NM_014674.3(EDEM1):c.680C>T (p.Thr227Met) | not specified [RCV004206555] | uncertain significance | 3 | 5199689 | 5199689 | Human | | name |
| 156014314 | CV2368697 | single nucleotide variant | NM_014674.3(EDEM1):c.820G>A (p.Ala274Thr) | not specified [RCV004214588] | uncertain significance | 3 | 5201886 | 5201886 | Human | | name |
| 156051710 | CV2386415 | single nucleotide variant | NM_014674.3(EDEM1):c.856C>T (p.Arg286Trp) | not specified [RCV004228743] | uncertain significance | 3 | 5201922 | 5201922 | Human | | name |
| 329386957 | CV2452727 | single nucleotide variant | NM_014674.3(EDEM1):c.729C>G (p.Asp243Glu) | not specified [RCV004275275] | uncertain significance | 3 | 5201795 | 5201795 | Human | | name |
| 401749086 | CV2692940 | single nucleotide variant | NM_014674.3(EDEM1):c.734A>G (p.Lys245Arg) | not specified [RCV004306459] | uncertain significance | 3 | 5201800 | 5201800 | Human | | name |
| 405767329 | CV3248228 | single nucleotide variant | NM_014674.3(EDEM1):c.373C>A (p.Gln125Lys) | not specified [RCV004384521] | uncertain significance | 3 | 5188178 | 5188178 | Human | | name |
| 405767335 | CV3248229 | single nucleotide variant | NM_014674.3(EDEM1):c.496G>T (p.Asp166Tyr) | not specified [RCV004384522] | uncertain significance | 3 | 5188301 | 5188301 | Human | | name |
| 405767341 | CV3248230 | single nucleotide variant | NM_014674.3(EDEM1):c.739C>A (p.Pro247Thr) | not specified [RCV004384523] | uncertain significance | 3 | 5201805 | 5201805 | Human | | name |
| 405767349 | CV3248231 | single nucleotide variant | NM_014674.3(EDEM1):c.784T>C (p.Tyr262His) | not specified [RCV004384524] | likely benign | 3 | 5201850 | 5201850 | Human | | name |
| 405767363 | CV3248233 | single nucleotide variant | NM_014674.3(EDEM1):c.837G>C (p.Lys279Asn) | not specified [RCV004384526] | uncertain significance | 3 | 5201903 | 5201903 | Human | | name |
| 405767372 | CV3248234 | single nucleotide variant | NM_014674.3(EDEM1):c.893A>G (p.Asn298Ser) | not specified [RCV004384527] | uncertain significance | 3 | 5203000 | 5203000 | Human | | name |
| 405767378 | CV3248235 | single nucleotide variant | NM_014674.3(EDEM1):c.935A>C (p.Glu312Ala) | not specified [RCV004384528] | uncertain significance | 3 | 5203042 | 5203042 | Human | | name |
| 407478778 | CV3441559 | single nucleotide variant | NM_014674.3(EDEM1):c.401C>T (p.Ala134Val) | not specified [RCV004617606] | uncertain significance | 3 | 5188206 | 5188206 | Human | | name |
| 407478795 | CV3441562 | single nucleotide variant | NM_014674.3(EDEM1):c.332C>G (p.Pro111Arg) | not specified [RCV004617609] | uncertain significance | 3 | 5188137 | 5188137 | Human | | name |
| 407478811 | CV3441564 | single nucleotide variant | NM_014674.3(EDEM1):c.467A>G (p.Asn156Ser) | not specified [RCV004617611] | uncertain significance | 3 | 5188272 | 5188272 | Human | | name |
| 407478817 | CV3441565 | single nucleotide variant | NM_014674.3(EDEM1):c.752T>C (p.Met251Thr) | not specified [RCV004617612] | uncertain significance | 3 | 5201818 | 5201818 | Human | | name |
| 597644240 | CV3667456 | single nucleotide variant | NM_014674.3(EDEM1):c.815T>C (p.Leu272Pro) | not specified [RCV004909640] | uncertain significance | 3 | 5201881 | 5201881 | Human | | name |
| 597644261 | CV3667459 | single nucleotide variant | NM_014674.3(EDEM1):c.481C>T (p.Arg161Cys) | not specified [RCV004909643] | uncertain significance | 3 | 5188286 | 5188286 | Human | | name |
| 597644275 | CV3667461 | single nucleotide variant | NM_014674.3(EDEM1):c.788T>G (p.Met263Arg) | not specified [RCV004909645] | uncertain significance | 3 | 5201854 | 5201854 | Human | | name |
| 598165935 | CV3954085 | single nucleotide variant | NM_014674.3(EDEM1):c.667G>A (p.Val223Ile) | not specified [RCV005329784] | uncertain significance | 3 | 5199676 | 5199676 | Human | | name |
| 598165939 | CV3954086 | single nucleotide variant | NM_014674.3(EDEM1):c.832A>C (p.Thr278Pro) | not specified [RCV005329785] | uncertain significance | 3 | 5201898 | 5201898 | Human | | name |
| 156001511 | CV2284489 | single nucleotide variant | NM_014674.3(EDEM1):c.1520A>G (p.Asn507Ser) | not specified [RCV004140671] | uncertain significance | 3 | 5210185 | 5210185 | Human | | name |
| 401720073 | CV2675766 | single nucleotide variant | NM_014674.3(EDEM1):c.1837C>T (p.His613Tyr) | not specified [RCV004288008] | uncertain significance | 3 | 5213475 | 5213475 | Human | | name |
| 401761101 | CV2689024 | single nucleotide variant | NM_014674.3(EDEM1):c.1810G>A (p.Gly604Arg) | not specified [RCV004305803] | uncertain significance | 3 | 5213448 | 5213448 | Human | | name |
| 401775857 | CV2692514 | single nucleotide variant | NM_014674.3(EDEM1):c.1466C>A (p.Pro489Gln) | not specified [RCV004312264] | uncertain significance | 3 | 5208220 | 5208220 | Human | | name |
| 401771928 | CV2711979 | single nucleotide variant | NM_014674.3(EDEM1):c.1192A>T (p.Ser398Cys) | not specified [RCV004311408] | uncertain significance | 3 | 5205216 | 5205216 | Human | | name |
| 401881047 | CV2763223 | single nucleotide variant | NM_014674.3(EDEM1):c.1766A>G (p.His589Arg) | not specified [RCV004336258] | uncertain significance | 3 | 5213404 | 5213404 | Human | | name |
| 405767298 | CV3248222 | single nucleotide variant | NM_014674.3(EDEM1):c.1570T>C (p.Tyr524His) | not specified [RCV004384515] | uncertain significance | 3 | 5210235 | 5210235 | Human | | name |
| 405767305 | CV3248223 | single nucleotide variant | NM_014674.3(EDEM1):c.1612A>G (p.Ile538Val) | not specified [RCV004384516] | uncertain significance | 3 | 5211148 | 5211148 | Human | | name |
| 405767310 | CV3248224 | single nucleotide variant | NM_014674.3(EDEM1):c.1853A>G (p.His618Arg) | not specified [RCV004384517] | uncertain significance | 3 | 5213491 | 5213491 | Human | | name |
| 407478758 | CV3441555 | single nucleotide variant | NM_014674.3(EDEM1):c.1617C>G (p.Asp539Glu) | not specified [RCV004617602] | uncertain significance | 3 | 5211153 | 5211153 | Human | | name |
| 407478764 | CV3441556 | single nucleotide variant | NM_014674.3(EDEM1):c.1906A>G (p.Arg636Gly) | not specified [RCV004617603] | uncertain significance | 3 | 5215850 | 5215850 | Human | | name |
| 407478772 | CV3441558 | single nucleotide variant | NM_014674.3(EDEM1):c.1609G>A (p.Val537Ile) | not specified [RCV004617605] | uncertain significance | 3 | 5211145 | 5211145 | Human | | name |
| 407478824 | CV3441566 | single nucleotide variant | NM_014674.3(EDEM1):c.1298C>G (p.Thr433Ser) | not specified [RCV004617613] | uncertain significance | 3 | 5207233 | 5207233 | Human | | name |
| 597644229 | CV3667453 | single nucleotide variant | NM_014674.3(EDEM1):c.1273A>G (p.Met425Val) | not specified [RCV004909638] | uncertain significance | 3 | 5207208 | 5207208 | Human | | name |
| 597644247 | CV3667457 | single nucleotide variant | NM_014674.3(EDEM1):c.1535A>G (p.His512Arg) | not specified [RCV004909641] | uncertain significance | 3 | 5210200 | 5210200 | Human | | name |
| 597644268 | CV3667460 | single nucleotide variant | NM_014674.3(EDEM1):c.1633C>T (p.Arg545Trp) | not specified [RCV004909644] | uncertain significance | 3 | 5211169 | 5211169 | Human | | name |
