| 15172223 | CV778837 | single nucleotide variant | NM_003790.3(TNFRSF25):c.745-10T>C | TNFRSF25-related disorder [RCV003906039]|not provided [RCV000972358] | likely benign | 1 | 6462184 | 6462184 | Human | | name , trait , alternate_id |
| 405279216 | CV3217421 | single nucleotide variant | NM_003790.3(TNFRSF25):c.72C>T (p.Ala24=) | TNFRSF25-related disorder [RCV003976841] | likely benign | 1 | 6465528 | 6465528 | Human | | name , trait , alternate_id |
| 329350442 | CV2471424 | single nucleotide variant | NM_003790.3(TNFRSF25):c.11G>C (p.Arg4Pro) | not specified [RCV004280425] | uncertain significance | 1 | 6466097 | 6466097 | Human | | name |
| 405285595 | CV3209664 | single nucleotide variant | NM_003790.3(TNFRSF25):c.108C>T (p.Ala36=) | TNFRSF25-related disorder [RCV003959241] | likely benign | 1 | 6465492 | 6465492 | Human | | name , trait , alternate_id |
| 156322553 | CV2205126 | single nucleotide variant | NM_003790.3(TNFRSF25):c.95G>A (p.Arg32Lys) | not specified [RCV004077724] | uncertain significance | 1 | 6465505 | 6465505 | Human | | name |
| 156079914 | CV2258117 | single nucleotide variant | NM_003790.3(TNFRSF25):c.64G>A (p.Ala22Thr) | not specified [RCV004121508] | uncertain significance | 1 | 6465536 | 6465536 | Human | | name |
| 401935300 | CV2805599 | single nucleotide variant | NM_003790.3(TNFRSF25):c.624T>A (p.Ala208=) | not provided [RCV003412724] | likely benign | 1 | 6462945 | 6462945 | Human | | name |
| 405280761 | CV3195730 | single nucleotide variant | NM_003790.3(TNFRSF25):c.696C>T (p.Pro232=) | TNFRSF25-related disorder [RCV003906962] | likely benign | 1 | 6462873 | 6462873 | Human | | name , trait , alternate_id |
| 405258526 | CV3203836 | single nucleotide variant | NM_003790.3(TNFRSF25):c.372G>A (p.Glu124=) | TNFRSF25-related disorder [RCV003942003] | benign | 1 | 6464643 | 6464643 | Human | | name , trait , alternate_id |
| 405286984 | CV3205569 | single nucleotide variant | NM_003790.3(TNFRSF25):c.816C>T (p.Cys272=) | TNFRSF25-related disorder [RCV003959712] | likely benign | 1 | 6462103 | 6462103 | Human | | name , trait , alternate_id |
| 405278849 | CV3220488 | single nucleotide variant | NM_003790.3(TNFRSF25):c.387A>G (p.Gln129=) | TNFRSF25-related disorder [RCV003976679] | benign | 1 | 6464628 | 6464628 | Human | | name , trait , alternate_id |
| 597674191 | CV3620802 | single nucleotide variant | NM_003790.3(TNFRSF25):c.79G>A (p.Gly27Ser) | not specified [RCV004882841] | likely benign | 1 | 6465521 | 6465521 | Human | | name |
| 598253297 | CV3935163 | single nucleotide variant | NM_003790.3(TNFRSF25):c.576C>T (p.Ala192=) | not specified [RCV005278225] | likely benign | 1 | 6463094 | 6463094 | Human | | name |
| 15097828 | CV696836 | single nucleotide variant | NM_003790.3(TNFRSF25):c.426A>G (p.Leu142=) | not provided [RCV000958403] | benign | 1 | 6464589 | 6464589 | Human | | name |
| 15101702 | CV719053 | single nucleotide variant | NM_003790.3(TNFRSF25):c.771C>T (p.Ser257=) | not provided [RCV000892331] | benign | 1 | 6462148 | 6462148 | Human | | name |
| 156060881 | CV2280292 | single nucleotide variant | NM_003790.3(TNFRSF25):c.285T>G (p.Cys95Trp) | not specified [RCV004140493] | uncertain significance | 1 | 6465098 | 6465098 | Human | | name |
| 401866401 | CV2782830 | single nucleotide variant | NM_003790.3(TNFRSF25):c.113A>G (p.Asp38Gly) | not specified [RCV004361642] | uncertain significance | 1 | 6465487 | 6465487 | Human | | name |
| 405278556 | CV3216715 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1047G>A (p.Glu349=) | TNFRSF25-related disorder [RCV003954601] | likely benign | 1 | 6461641 | 6461641 | Human | | name , trait , alternate_id |
| 155974868 | CV2211213 | single nucleotide variant | NM_003790.3(TNFRSF25):c.854A>G (p.Tyr285Cys) | not specified [RCV004088364] | uncertain significance | 1 | 6462065 | 6462065 | Human | | name |
| 156282172 | CV2295176 | single nucleotide variant | NM_003790.3(TNFRSF25):c.886G>T (p.Val296Leu) | not specified [RCV004158271] | uncertain significance | 1 | 6462033 | 6462033 | Human | | name |
| 156096204 | CV2310165 | single nucleotide variant | NM_003790.3(TNFRSF25):c.584G>A (p.Cys195Tyr) | not specified [RCV004163275] | uncertain significance | 1 | 6463086 | 6463086 | Human | | name |
| 156091246 | CV2384656 | single nucleotide variant | NM_003790.3(TNFRSF25):c.523G>A (p.Gly175Ser) | not specified [RCV004232434] | likely benign | 1 | 6464394 | 6464394 | Human | | name |
| 156226034 | CV2390730 | single nucleotide variant | NM_003790.3(TNFRSF25):c.599T>C (p.Met200Thr) | not specified [RCV004241024] | uncertain significance | 1 | 6462970 | 6462970 | Human | | name |
| 156001797 | CV2391972 | single nucleotide variant | NM_003790.3(TNFRSF25):c.955G>C (p.Glu319Gln) | not specified [RCV004235833] | uncertain significance | 1 | 6461733 | 6461733 | Human | | name |
| 401722259 | CV2680876 | single nucleotide variant | NM_003790.3(TNFRSF25):c.743C>T (p.Pro248Leu) | not specified [RCV004293521] | uncertain significance | 1 | 6462630 | 6462630 | Human | | name |
| 401859659 | CV2771782 | single nucleotide variant | NM_003790.3(TNFRSF25):c.779C>A (p.Thr260Asn) | not specified [RCV004350557] | uncertain significance | 1 | 6462140 | 6462140 | Human | | name |
| 401897136 | CV2789856 | single nucleotide variant | NM_003790.3(TNFRSF25):c.664T>C (p.Tyr222His) | not specified [RCV004362243] | uncertain significance | 1 | 6462905 | 6462905 | Human | | name |
| 405283471 | CV3217168 | single nucleotide variant | NM_003790.3(TNFRSF25):c.476A>G (p.Asp159Gly) | TNFRSF25-related disorder [RCV003979268] | benign | 1 | 6464441 | 6464441 | Human | | name , trait , alternate_id |
| 405787693 | CV3339950 | single nucleotide variant | NM_003790.3(TNFRSF25):c.377A>G (p.Gln126Arg) | not specified [RCV004473186] | uncertain significance | 1 | 6464638 | 6464638 | Human | | name |
| 405787698 | CV3339951 | single nucleotide variant | NM_003790.3(TNFRSF25):c.446G>A (p.Arg149His) | not specified [RCV004473187] | uncertain significance | 1 | 6464569 | 6464569 | Human | | name |
| 405787703 | CV3339952 | single nucleotide variant | NM_003790.3(TNFRSF25):c.668C>T (p.Thr223Ile) | not specified [RCV004473188] | uncertain significance | 1 | 6462901 | 6462901 | Human | | name |
| 405787707 | CV3339953 | single nucleotide variant | NM_003790.3(TNFRSF25):c.886G>A (p.Val296Met) | not specified [RCV004473189] | likely benign | 1 | 6462033 | 6462033 | Human | | name |
| 407530874 | CV3479229 | single nucleotide variant | NM_003790.3(TNFRSF25):c.569G>A (p.Arg190His) | not specified [RCV004682132] | uncertain significance | 1 | 6463101 | 6463101 | Human | | name |
| 597674149 | CV3620799 | single nucleotide variant | NM_003790.3(TNFRSF25):c.872C>T (p.Ala291Val) | not specified [RCV004882838] | uncertain significance | 1 | 6462047 | 6462047 | Human | | name |
| 597674162 | CV3620800 | single nucleotide variant | NM_003790.3(TNFRSF25):c.934G>A (p.Ala312Thr) | not specified [RCV004882839] | uncertain significance | 1 | 6461754 | 6461754 | Human | | name |
| 597674201 | CV3620803 | single nucleotide variant | NM_003790.3(TNFRSF25):c.982A>C (p.Met328Leu) | not specified [RCV004882842] | uncertain significance | 1 | 6461706 | 6461706 | Human | | name |
| 597674217 | CV3620805 | single nucleotide variant | NM_003790.3(TNFRSF25):c.593G>A (p.Arg198Lys) | not specified [RCV004882844] | uncertain significance | 1 | 6463077 | 6463077 | Human | | name |
| 597674226 | CV3620806 | single nucleotide variant | NM_003790.3(TNFRSF25):c.334G>A (p.Asp112Asn) | not specified [RCV004882845] | uncertain significance | 1 | 6464681 | 6464681 | Human | | name |
| 597674235 | CV3620807 | single nucleotide variant | NM_003790.3(TNFRSF25):c.337A>C (p.Thr113Pro) | not specified [RCV004882846] | uncertain significance | 1 | 6464678 | 6464678 | Human | | name |
| 597674244 | CV3620808 | single nucleotide variant | NM_003790.3(TNFRSF25):c.338C>A (p.Thr113Asn) | not specified [RCV004882847] | uncertain significance | 1 | 6464677 | 6464677 | Human | | name |
| 598229463 | CV3935161 | single nucleotide variant | NM_003790.3(TNFRSF25):c.634G>T (p.Val212Phe) | not specified [RCV005294892] | uncertain significance | 1 | 6462935 | 6462935 | Human | | name |
| 598253291 | CV3935162 | single nucleotide variant | NM_003790.3(TNFRSF25):c.398G>T (p.Ser133Ile) | not specified [RCV005278224] | uncertain significance | 1 | 6464617 | 6464617 | Human | | name |
| 156136169 | CV2257058 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1037G>C (p.Arg346Pro) | not specified [RCV004123025] | uncertain significance | 1 | 6461651 | 6461651 | Human | | name |
| 401723629 | CV2724972 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1066C>G (p.Leu356Val) | not specified [RCV004319735] | uncertain significance | 1 | 6461622 | 6461622 | Human | | name |
| 405787674 | CV3339946 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1075G>A (p.Ala359Thr) | not specified [RCV004473182] | uncertain significance | 1 | 6461613 | 6461613 | Human | | name |
| 405787678 | CV3339947 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1139A>C (p.Lys380Thr) | not specified [RCV004473183] | uncertain significance | 1 | 6461549 | 6461549 | Human | | name |
| 405787683 | CV3339948 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1195C>T (p.Arg399Cys) | not specified [RCV004473184] | uncertain significance | 1 | 6461493 | 6461493 | Human | | name |
| 405787688 | CV3339949 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1231A>G (p.Ser411Gly) | not specified [RCV004473185] | uncertain significance | 1 | 6461457 | 6461457 | Human | | name |
| 407530872 | CV3479228 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1201G>C (p.Gly401Arg) | not specified [RCV004682131] | uncertain significance | 1 | 6461487 | 6461487 | Human | | name |
| 407530876 | CV3479230 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1184C>A (p.Ala395Glu) | not specified [RCV004682133] | uncertain significance | 1 | 6461504 | 6461504 | Human | | name |
| 597674206 | CV3620804 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1228C>A (p.Arg410Ser) | not specified [RCV004882843] | uncertain significance | 1 | 6461460 | 6461460 | Human | | name |
| 597674254 | CV3620809 | single nucleotide variant | NM_003790.3(TNFRSF25):c.1148G>A (p.Arg383His) | not specified [RCV004882848] | uncertain significance | 1 | 6461540 | 6461540 | Human | | name |
