| 405277422 | CV3195769 | single nucleotide variant | NM_003059.3(SLC22A4):c.*5A>G | SLC22A4-related disorder [RCV003904302] | likely benign | 5 | 132343840 | 132343840 | Human | | name , trait , alternate_id |
| 405292931 | CV3207043 | single nucleotide variant | NM_003059.3(SLC22A4):c.-10A>T | SLC22A4-related disorder [RCV003931459] | likely benign | 5 | 132294607 | 132294607 | Human | | name , trait , alternate_id |
| 150477528 | CV1240043 | single nucleotide variant | NM_003059.3(SLC22A4):c.824+37= | not provided [RCV001652221] | benign | 5 | 132322392 | 132322392 | Human | | name |
| 152119845 | CV1579218 | single nucleotide variant | NM_003059.3(SLC22A4):c.498-7T>C | SLC22A4-related disorder [RCV003951158]|not provided [RCV002081402] | benign | 5 | 132313607 | 132313607 | Human | 1 | name , trait , alternate_id |
| 156054768 | CV1935076 | single nucleotide variant | NM_003059.3(SLC22A4):c.393+1G>A | SLC22A4-related disorder [RCV003418543]|not specified [RCV002510363] | uncertain significance | 5 | 132295010 | 132295010 | Human | 1 | name , trait , alternate_id |
| 597961059 | CV3840401 | single nucleotide variant | NM_003059.3(SLC22A4):c.825-4A>G | not provided [RCV005192885] | likely benign | 5 | 132327273 | 132327273 | Human | | name |
| 150438016 | CV1237966 | single nucleotide variant | NM_003059.3(SLC22A4):c.952-96A>G | not provided [RCV001644464] | benign | 5 | 132331660 | 132331660 | Human | 4 | name |
| 150472225 | CV1270220 | single nucleotide variant | NM_003059.3(SLC22A4):c.498-85G>A | not provided [RCV001695508] | benign | 5 | 132313529 | 132313529 | Human | | name |
| 150495983 | CV1272768 | single nucleotide variant | NM_003059.3(SLC22A4):c.653-93G>C | not provided [RCV001688691] | benign | 5 | 132322091 | 132322091 | Human | | name |
| 150439937 | CV1287114 | single nucleotide variant | NM_003059.3(SLC22A4):c.1046+5G>A | not provided [RCV001725029] | benign | 5 | 132331855 | 132331855 | Human | | name |
| 152128126 | CV1530730 | single nucleotide variant | NM_003059.3(SLC22A4):c.498-20T>C | not provided [RCV002082497] | benign | 5 | 132313594 | 132313594 | Human | | name |
| 152093198 | CV1584710 | single nucleotide variant | NM_003059.3(SLC22A4):c.1445-8C>T | SLC22A4-related disorder [RCV003958839]|not provided [RCV002114356] | likely benign | 5 | 132340557 | 132340557 | Human | 1 | name , trait , alternate_id |
| 156415161 | CV1961835 | single nucleotide variant | NM_003059.3(SLC22A4):c.498-15T>C | not provided [RCV002589009] | likely benign | 5 | 132313599 | 132313599 | Human | | name |
| 156414734 | CV1982964 | single nucleotide variant | NM_003059.3(SLC22A4):c.1445-9G>A | not provided [RCV002609339] | likely benign | 5 | 132340556 | 132340556 | Human | | name |
| 156113551 | CV1993757 | single nucleotide variant | NM_003059.3(SLC22A4):c.952-16A>G | not provided [RCV002662582] | likely benign | 5 | 132331740 | 132331740 | Human | | name |
| 405078174 | CV3004419 | single nucleotide variant | NM_003059.3(SLC22A4):c.652+18G>A | not provided [RCV003716926] | likely benign | 5 | 132313786 | 132313786 | Human | | name |
| 405079084 | CV3137073 | single nucleotide variant | NM_003059.3(SLC22A4):c.824+19C>T | not provided [RCV003833972] | likely benign | 5 | 132322374 | 132322374 | Human | | name |
| 405196686 | CV3168178 | single nucleotide variant | NM_003059.3(SLC22A4):c.825-16T>A | not provided [RCV003860310] | likely benign | 5 | 132327261 | 132327261 | Human | | name |
| 597848216 | CV3736776 | single nucleotide variant | NM_003059.3(SLC22A4):c.653-14C>T | not provided [RCV005065935] | likely benign | 5 | 132322170 | 132322170 | Human | | name |
| 597852377 | CV3737633 | single nucleotide variant | NM_003059.3(SLC22A4):c.1445-3C>T | not provided [RCV005066406] | uncertain significance | 5 | 132340562 | 132340562 | Human | | name |
| 150502760 | CV1212313 | single nucleotide variant | NM_003059.3(SLC22A4):c.498-121A>G | not provided [RCV001595187] | benign | 5 | 132313493 | 132313493 | Human | | name |
| 150513059 | CV1228885 | single nucleotide variant | NM_003059.3(SLC22A4):c.393+150A>C | not provided [RCV001637727] | benign | 5 | 132295159 | 132295159 | Human | 2 | name |
| 150513059 | CV1228885 | single nucleotide variant | NM_003059.3(SLC22A4):c.393+150A>C | not provided [RCV001637727] | benign | 5 | 132295159 | 132295160 | Human | 2 | name |
| 150440247 | CV1265082 | single nucleotide variant | NM_003059.3(SLC22A4):c.1444+76T>C | not provided [RCV001679075] | benign | 5 | 132336076 | 132336076 | Human | | name |
| 152037900 | CV1524986 | single nucleotide variant | NM_003059.3(SLC22A4):c.1046+11A>C | not provided [RCV002165248] | likely benign | 5 | 132331861 | 132331861 | Human | | name |
| 152040753 | CV1561866 | single nucleotide variant | NM_003059.3(SLC22A4):c.1261+19T>C | not provided [RCV002188223] | benign | 5 | 132334951 | 132334951 | Human | | name |
| 156316062 | CV1869827 | single nucleotide variant | NM_003059.3(SLC22A4):c.1262-10T>C | not provided [RCV003062751] | likely benign | 5 | 132335808 | 132335808 | Human | | name |
| 405049214 | CV3137946 | single nucleotide variant | NM_003059.3(SLC22A4):c.1445-12C>T | not provided [RCV003831984] | likely benign | 5 | 132340553 | 132340553 | Human | | name |
| 597959556 | CV3752342 | single nucleotide variant | NM_003059.3(SLC22A4):c.1444+12C>T | not provided [RCV005081292] | benign | 5 | 132336012 | 132336012 | Human | | name |
| 597847655 | CV3762069 | single nucleotide variant | NM_003059.3(SLC22A4):c.1445-11G>A | not provided [RCV005087487] | uncertain significance | 5 | 132340554 | 132340554 | Human | | name |
| 150483715 | CV1263036 | single nucleotide variant | NM_003059.3(SLC22A4):c.1047-196G>A | not provided [RCV001686436] | benign | 5 | 132334522 | 132334522 | Human | | name |
| 152130552 | CV1523445 | single nucleotide variant | NM_003059.3(SLC22A4):c.394-7318A>G | not provided [RCV002136867] | benign | 5 | 132304843 | 132304843 | Human | 11 | name |
| 8558898 | CV20788 | single nucleotide variant | NM_003059.3(SLC22A4):c.393+6607C>T | Rheumatoid arthritis [RCV000006105] | risk factor | 5 | 132301616 | 132301616 | Human | 2 | name |
| 152123153 | CV1570540 | single nucleotide variant | NM_003059.3(SLC22A4):c.78C>T (p.Ser26=) | SLC22A4-related disorder [RCV004752148]|not provided [RCV002217053] | likely benign | 5 | 132294694 | 132294694 | Human | 1 | name , trait , alternate_id |
| 156194320 | CV2146548 | single nucleotide variant | NM_003059.3(SLC22A4):c.31C>T (p.Leu11=) | not provided [RCV003006105] | likely benign | 5 | 132294647 | 132294647 | Human | | name |
| 151797858 | CV1352662 | single nucleotide variant | NM_003059.3(SLC22A4):c.225C>T (p.Arg75=) | not provided [RCV001877107] | likely benign|uncertain significance | 5 | 132294841 | 132294841 | Human | | name |
| 152048813 | CV1615045 | single nucleotide variant | NM_003059.3(SLC22A4):c.267C>T (p.Ile89=) | not provided [RCV002088881] | likely benign | 5 | 132294883 | 132294883 | Human | | name |
| 155932175 | CV2096140 | single nucleotide variant | NM_003059.3(SLC22A4):c.264C>T (p.Thr88=) | not provided [RCV002903890] | likely benign | 5 | 132294880 | 132294880 | Human | | name |
| 156280996 | CV2186846 | single nucleotide variant | NM_003059.3(SLC22A4):c.159G>C (p.Pro53=) | not provided [RCV003044778] | likely benign | 5 | 132294775 | 132294775 | Human | | name |
| 402484510 | CV2857440 | single nucleotide variant | NM_003059.3(SLC22A4):c.285C>T (p.Leu95=) | not provided [RCV003544265] | likely benign | 5 | 132294901 | 132294901 | Human | | name |
| 405078226 | CV3136947 | single nucleotide variant | NM_003059.3(SLC22A4):c.216G>C (p.Arg72=) | not provided [RCV003833845] | likely benign | 5 | 132294832 | 132294832 | Human | | name |
| 597888392 | CV3805589 | single nucleotide variant | NM_003059.3(SLC22A4):c.180C>T (p.Ser60=) | not provided [RCV005150931] | likely benign | 5 | 132294796 | 132294796 | Human | | name |
| 15174712 | CV764817 | single nucleotide variant | NM_003059.3(SLC22A4):c.162C>T (p.Asp54=) | not provided [RCV000928498] | likely benign | 5 | 132294778 | 132294778 | Human | | name |
| 21067611 | CV793069 | single nucleotide variant | NM_003059.3(SLC22A4):c.138G>A (p.Pro46=) | not provided [RCV000992766] | likely benign | 5 | 132294754 | 132294754 | Human | | name |
| 151873291 | CV1429712 | deletion | NM_003059.3(SLC22A4):c.294del (p.Glu98fs) | not provided [RCV001998625] | uncertain significance | 5 | 132294910 | 132294910 | Human | | name |
| 151814295 | CV1444360 | single nucleotide variant | NM_003059.3(SLC22A4):c.456C>T (p.Gly152=) | SLC22A4-related disorder [RCV003892968]|not provided [RCV001933511] | likely benign|uncertain significance | 5 | 132312223 | 132312223 | Human | 1 | name , trait , alternate_id |
| 152126567 | CV1582365 | single nucleotide variant | NM_003059.3(SLC22A4):c.339C>T (p.Cys113=) | not provided [RCV002198754] | benign|likely benign | 5 | 132294955 | 132294955 | Human | | name |
| 152145010 | CV1582603 | single nucleotide variant | NM_003059.3(SLC22A4):c.606C>T (p.Ile202=) | not provided [RCV002201104] | benign | 5 | 132313722 | 132313722 | Human | | name |
| 152046590 | CV1600380 | single nucleotide variant | NM_003059.3(SLC22A4):c.441C>A (p.Ser147=) | not provided [RCV002088618] | benign | 5 | 132312208 | 132312208 | Human | | name |
| 152149340 | CV1616782 | single nucleotide variant | NM_003059.3(SLC22A4):c.747T>C (p.Phe249=) | not provided [RCV002201726] | likely benign | 5 | 132322278 | 132322278 | Human | | name |
| 156307642 | CV2079898 | single nucleotide variant | NM_003059.3(SLC22A4):c.558G>C (p.Leu186=) | not provided [RCV002857487] | likely benign | 5 | 132313674 | 132313674 | Human | | name |
| 156123927 | CV2088228 | single nucleotide variant | NM_003059.3(SLC22A4):c.591T>A (p.Thr197=) | not provided [RCV002871375] | likely benign | 5 | 132313707 | 132313707 | Human | | name |
| 156228199 | CV2115471 | single nucleotide variant | NM_003059.3(SLC22A4):c.744G>C (p.Leu248=) | not provided [RCV002932723] | likely benign | 5 | 132322275 | 132322275 | Human | | name |
| 156317313 | CV2140418 | single nucleotide variant | NM_003059.3(SLC22A4):c.765C>T (p.Asp255=) | not provided [RCV003011467] | likely benign | 5 | 132322296 | 132322296 | Human | | name |
| 156016345 | CV2155034 | single nucleotide variant | NM_003059.3(SLC22A4):c.95A>G (p.Asn32Ser) | not provided [RCV003018011] | uncertain significance | 5 | 132294711 | 132294711 | Human | | name |
| 405080518 | CV2945600 | single nucleotide variant | NM_003059.3(SLC22A4):c.912C>T (p.Asn304=) | not provided [RCV003664556] | likely benign | 5 | 132327364 | 132327364 | Human | | name |
| 405128073 | CV3054306 | single nucleotide variant | NM_003059.3(SLC22A4):c.43G>A (p.Gly15Arg) | not provided [RCV003724566] | uncertain significance | 5 | 132294659 | 132294659 | Human | | name |
| 405177092 | CV3148580 | single nucleotide variant | NM_003059.3(SLC22A4):c.639A>G (p.Val213=) | not provided [RCV003858357] | likely benign | 5 | 132313755 | 132313755 | Human | | name |
| 405254043 | CV3174949 | single nucleotide variant | NM_003059.3(SLC22A4):c.417C>T (p.Asn139=) | not provided [RCV003871401] | likely benign | 5 | 132312184 | 132312184 | Human | | name |
| 405250378 | CV3180721 | single nucleotide variant | NM_003059.3(SLC22A4):c.786G>A (p.Ala262=) | not provided [RCV003869998] | likely benign | 5 | 132322317 | 132322317 | Human | | name |
| 402501384 | CV3180976 | single nucleotide variant | NM_003059.3(SLC22A4):c.990G>A (p.Leu330=) | not provided [RCV003877993] | likely benign | 5 | 132331794 | 132331794 | Human | | name |
| 405260189 | CV3190260 | single nucleotide variant | NM_003059.3(SLC22A4):c.792G>A (p.Thr264=) | SLC22A4-related disorder [RCV003894659]|not provided [RCV005101631] | likely benign | 5 | 132322323 | 132322323 | Human | 1 | name , trait , alternate_id |
| 405285263 | CV3212286 | single nucleotide variant | NM_003059.3(SLC22A4):c.769C>A (p.Arg257=) | SLC22A4-related disorder [RCV003958910] | likely benign | 5 | 132322300 | 132322300 | Human | | name , trait , alternate_id |
| 597839134 | CV3736976 | single nucleotide variant | NM_003059.3(SLC22A4):c.333G>A (p.Glu111=) | not provided [RCV005064456] | likely benign | 5 | 132294949 | 132294949 | Human | | name |
| 597902749 | CV3741535 | single nucleotide variant | NM_003059.3(SLC22A4):c.642C>A (p.Ala214=) | not provided [RCV005072506] | likely benign | 5 | 132313758 | 132313758 | Human | | name |
| 597956302 | CV3792370 | single nucleotide variant | NM_003059.3(SLC22A4):c.735G>A (p.Leu245=) | not provided [RCV005137258] | likely benign | 5 | 132322266 | 132322266 | Human | | name |
| 597972425 | CV3812968 | single nucleotide variant | NM_003059.3(SLC22A4):c.37G>A (p.Glu13Lys) | not provided [RCV005167421] | uncertain significance | 5 | 132294653 | 132294653 | Human | | name |
| 597921294 | CV3852138 | single nucleotide variant | NM_003059.3(SLC22A4):c.975G>A (p.Gln325=) | not provided [RCV005205118] | likely benign | 5 | 132331779 | 132331779 | Human | | name |
| 15149408 | CV709614 | single nucleotide variant | NM_003059.3(SLC22A4):c.465C>T (p.Leu155=) | SLC22A4-related disorder [RCV003905937]|not provided [RCV000967748]|not specified [RCV001288366] | benign | 5 | 132312232 | 132312232 | Human | 1 | name , trait , alternate_id |
| 150449040 | CV1275620 | single nucleotide variant | NM_003059.3(SLC22A4):c.1182C>G (p.Thr394=) | not provided [RCV001708075] | benign | 5 | 132334853 | 132334853 | Human | | name |
| 151718409 | CV1458686 | single nucleotide variant | NM_003059.3(SLC22A4):c.209G>C (p.Arg70Pro) | not provided [RCV002003283]|not specified [RCV004043232] | uncertain significance | 5 | 132294825 | 132294825 | Human | | name |
| 152171568 | CV1544253 | single nucleotide variant | NM_003059.3(SLC22A4):c.1239C>T (p.Leu413=) | not provided [RCV002162159] | likely benign | 5 | 132334910 | 132334910 | Human | | name |
| 152089215 | CV1580610 | single nucleotide variant | NM_003059.3(SLC22A4):c.1236T>C (p.Leu412=) | not provided [RCV002093937] | likely benign | 5 | 132334907 | 132334907 | Human | | name |
| 156413048 | CV1904705 | single nucleotide variant | NM_003059.3(SLC22A4):c.286G>C (p.Gly96Arg) | not provided [RCV002588033]|not specified [RCV004073401] | uncertain significance | 5 | 132294902 | 132294902 | Human | | name |
| 156404550 | CV1916616 | single nucleotide variant | NM_003059.3(SLC22A4):c.134C>T (p.Thr45Ile) | not provided [RCV002606122] | uncertain significance | 5 | 132294750 | 132294750 | Human | | name |
| 156397118 | CV1985298 | single nucleotide variant | NM_003059.3(SLC22A4):c.1044A>G (p.Leu348=) | not provided [RCV002635601] | likely benign | 5 | 132331848 | 132331848 | Human | | name |
| 156040003 | CV2094073 | single nucleotide variant | NM_003059.3(SLC22A4):c.1647T>C (p.Thr549=) | SLC22A4-related disorder [RCV003926455]|not provided [RCV002885775] | likely benign | 5 | 132343826 | 132343826 | Human | 1 | name , trait , alternate_id |
| 155977334 | CV2100158 | single nucleotide variant | NM_003059.3(SLC22A4):c.1551A>G (p.Glu517=) | not provided [RCV002881765] | likely benign | 5 | 132340671 | 132340671 | Human | | name |
| 156094873 | CV2106396 | single nucleotide variant | NM_003059.3(SLC22A4):c.1380G>A (p.Ala460=) | not provided [RCV002952506] | likely benign | 5 | 132335936 | 132335936 | Human | | name |
| 156286348 | CV2360902 | single nucleotide variant | NM_003059.3(SLC22A4):c.181G>A (p.Ala61Thr) | not provided [RCV003720733]|not specified [RCV004215719] | uncertain significance | 5 | 132294797 | 132294797 | Human | | name |
| 401899984 | CV2780146 | single nucleotide variant | NM_003059.3(SLC22A4):c.218A>G (p.Asp73Gly) | not specified [RCV004355802] | uncertain significance | 5 | 132294834 | 132294834 | Human | | name |
| 405218967 | CV2873739 | single nucleotide variant | NM_003059.3(SLC22A4):c.1473C>T (p.Ile491=) | not provided [RCV003553537] | likely benign | 5 | 132340593 | 132340593 | Human | | name |
| 405253629 | CV3048320 | single nucleotide variant | NM_003059.3(SLC22A4):c.1174T>C (p.Leu392=) | not provided [RCV003722619] | likely benign | 5 | 132334845 | 132334845 | Human | | name |
| 405109228 | CV3136798 | single nucleotide variant | NM_003059.3(SLC22A4):c.1569G>A (p.Gln523=) | not provided [RCV003835952] | likely benign | 5 | 132340689 | 132340689 | Human | | name |
| 405233400 | CV3145053 | single nucleotide variant | NM_003059.3(SLC22A4):c.209G>T (p.Arg70Leu) | not provided [RCV003853310] | uncertain significance | 5 | 132294825 | 132294825 | Human | | name |
| 405044889 | CV3150340 | single nucleotide variant | NM_003059.3(SLC22A4):c.1002G>A (p.Arg334=) | not provided [RCV003849134] | likely benign | 5 | 132331806 | 132331806 | Human | | name |
| 405733505 | CV3325311 | single nucleotide variant | NM_003059.3(SLC22A4):c.158C>G (p.Pro53Arg) | not specified [RCV004451335] | uncertain significance | 5 | 132294774 | 132294774 | Human | | name |
| 597944283 | CV3776553 | single nucleotide variant | NM_003059.3(SLC22A4):c.1506C>A (p.Ile502=) | not provided [RCV005119409] | likely benign | 5 | 132340626 | 132340626 | Human | | name |
| 598200237 | CV3921926 | single nucleotide variant | NM_003059.3(SLC22A4):c.193A>G (p.Asn65Asp) | not specified [RCV005268511] | uncertain significance | 5 | 132294809 | 132294809 | Human | | name |
| 15183025 | CV721209 | single nucleotide variant | NM_003059.3(SLC22A4):c.1350G>A (p.Glu450=) | not provided [RCV000886132] | benign | 5 | 132335906 | 132335906 | Human | | name |
| 15186849 | CV734836 | single nucleotide variant | NM_003059.3(SLC22A4):c.1500T>C (p.Ile500=) | SLC22A4-related disorder [RCV003932943]|not provided [RCV000908921] | benign|likely benign | 5 | 132340620 | 132340620 | Human | 1 | name , trait , alternate_id |
| 21067612 | CV793070 | single nucleotide variant | NM_003059.3(SLC22A4):c.1413C>G (p.Gly471=) | not provided [RCV000992767] | benign | 5 | 132335969 | 132335969 | Human | 3 | name |
| 150470664 | CV1258632 | single nucleotide variant | NM_003059.3(SLC22A4):c.917T>C (p.Ile306Thr) | not provided [RCV001684177] | benign | 5 | 132327369 | 132327369 | Human | | name |
| 151859733 | CV1403819 | single nucleotide variant | NM_003059.3(SLC22A4):c.710C>A (p.Thr237Lys) | not provided [RCV001996983] | uncertain significance | 5 | 132322241 | 132322241 | Human | | name |
| 151734528 | CV1409655 | single nucleotide variant | NM_003059.3(SLC22A4):c.475G>A (p.Val159Met) | not provided [RCV001911228] | uncertain significance | 5 | 132312242 | 132312242 | Human | | name |
| 151828610 | CV1479986 | single nucleotide variant | NM_003059.3(SLC22A4):c.680G>A (p.Arg227His) | not provided [RCV001901576] | uncertain significance | 5 | 132322211 | 132322211 | Human | | name |
| 155983804 | CV1883807 | single nucleotide variant | NM_003059.3(SLC22A4):c.797C>T (p.Pro266Leu) | not provided [RCV003075791] | uncertain significance | 5 | 132322328 | 132322328 | Human | | name |
| 156342765 | CV1897023 | single nucleotide variant | NM_003059.3(SLC22A4):c.451G>A (p.Val151Ile) | not provided [RCV003090458] | uncertain significance | 5 | 132312218 | 132312218 | Human | | name |
| 156435770 | CV1937132 | single nucleotide variant | NM_003059.3(SLC22A4):c.874G>A (p.Glu292Lys) | not provided [RCV003105001] | uncertain significance | 5 | 132327326 | 132327326 | Human | | name |
| 156415765 | CV1966236 | single nucleotide variant | NM_003059.3(SLC22A4):c.466G>A (p.Gly156Ser) | not provided [RCV002589353] | uncertain significance | 5 | 132312233 | 132312233 | Human | | name |
| 156303830 | CV2079661 | single nucleotide variant | NM_003059.3(SLC22A4):c.497G>C (p.Arg166Thr) | not provided [RCV002857308] | uncertain significance | 5 | 132312264 | 132312264 | Human | | name |
| 156118144 | CV2111280 | single nucleotide variant | NM_003059.3(SLC22A4):c.872G>C (p.Arg291Thr) | not provided [RCV002914051] | uncertain significance | 5 | 132327324 | 132327324 | Human | | name |
| 156093359 | CV2114038 | single nucleotide variant | NM_003059.3(SLC22A4):c.937T>C (p.Phe313Leu) | not provided [RCV002926764]|not specified [RCV005266429] | uncertain significance | 5 | 132327389 | 132327389 | Human | | name |
| 156131793 | CV2121628 | single nucleotide variant | NM_003059.3(SLC22A4):c.699A>T (p.Leu233Phe) | SLC22A4-related disorder [RCV003418664]|not provided [RCV002953906] | uncertain significance | 5 | 132322230 | 132322230 | Human | 1 | name , trait , alternate_id |
| 156325132 | CV2195193 | single nucleotide variant | NM_003059.3(SLC22A4):c.496A>G (p.Arg166Gly) | not specified [RCV004080135] | uncertain significance | 5 | 132312263 | 132312263 | Human | | name |
| 156082290 | CV2301153 | single nucleotide variant | NM_003059.3(SLC22A4):c.313C>G (p.Leu105Val) | not specified [RCV004160065] | uncertain significance | 5 | 132294929 | 132294929 | Human | | name |
| 156305373 | CV2305097 | single nucleotide variant | NM_003059.3(SLC22A4):c.629A>G (p.Asn210Ser) | not specified [RCV004168971] | uncertain significance | 5 | 132313745 | 132313745 | Human | | name |
| 156288261 | CV2336322 | single nucleotide variant | NM_003059.3(SLC22A4):c.584T>C (p.Met195Thr) | not specified [RCV004192071] | uncertain significance | 5 | 132313700 | 132313700 | Human | | name |
| 156217140 | CV2386124 | single nucleotide variant | NM_003059.3(SLC22A4):c.892C>A (p.Gln298Lys) | not specified [RCV004229176] | uncertain significance | 5 | 132327344 | 132327344 | Human | | name |
| 156191689 | CV2388534 | single nucleotide variant | NM_003059.3(SLC22A4):c.523G>A (p.Ala175Thr) | not specified [RCV004237385] | uncertain significance | 5 | 132313639 | 132313639 | Human | | name |
| 401748079 | CV2699998 | single nucleotide variant | NM_003059.3(SLC22A4):c.886A>G (p.Ile296Val) | not specified [RCV004310428] | uncertain significance | 5 | 132327338 | 132327338 | Human | | name |
| 401750172 | CV2715532 | single nucleotide variant | NM_003059.3(SLC22A4):c.857C>G (p.Ser286Cys) | not specified [RCV004326933] | uncertain significance | 5 | 132327309 | 132327309 | Human | | name |
| 401961611 | CV2843933 | single nucleotide variant | NM_003059.3(SLC22A4):c.514G>A (p.Val172Ile) | not provided [RCV003481772] | uncertain significance | 5 | 132313630 | 132313630 | Human | | name |
| 405121234 | CV2888086 | single nucleotide variant | NM_003059.3(SLC22A4):c.630C>G (p.Asn210Lys) | not provided [RCV003559114] | uncertain significance | 5 | 132313746 | 132313746 | Human | | name |
| 405217954 | CV2968609 | single nucleotide variant | NM_003059.3(SLC22A4):c.613A>G (p.Met205Val) | not provided [RCV003680273] | uncertain significance | 5 | 132313729 | 132313729 | Human | | name |
| 402484443 | CV2998173 | single nucleotide variant | NM_003059.3(SLC22A4):c.431T>C (p.Leu144Pro) | not provided [RCV003686874] | uncertain significance | 5 | 132312198 | 132312198 | Human | | name |
| 405218606 | CV3034920 | single nucleotide variant | NM_003059.3(SLC22A4):c.445T>C (p.Phe149Leu) | not provided [RCV003709647] | uncertain significance | 5 | 132312212 | 132312212 | Human | | name |
| 405184421 | CV3155940 | single nucleotide variant | NM_003059.3(SLC22A4):c.634G>A (p.Val212Met) | not provided [RCV003859014]|not specified [RCV004673993] | uncertain significance | 5 | 132313750 | 132313750 | Human | | name |
| 405209230 | CV3162578 | single nucleotide variant | NM_003059.3(SLC22A4):c.545G>A (p.Gly182Asp) | not provided [RCV003861877] | uncertain significance | 5 | 132313661 | 132313661 | Human | | name |
| 405733514 | CV3325312 | single nucleotide variant | NM_003059.3(SLC22A4):c.985A>G (p.Ile329Val) | not specified [RCV004451336] | uncertain significance | 5 | 132331789 | 132331789 | Human | | name |
| 407509092 | CV3473889 | single nucleotide variant | NM_003059.3(SLC22A4):c.768G>C (p.Trp256Cys) | not specified [RCV004672251] | uncertain significance | 5 | 132322299 | 132322299 | Human | | name |
| 407509100 | CV3473891 | single nucleotide variant | NM_003059.3(SLC22A4):c.721G>A (p.Val241Ile) | not specified [RCV004672253] | uncertain significance | 5 | 132322252 | 132322252 | Human | | name |
| 597678883 | CV3596594 | single nucleotide variant | NM_003059.3(SLC22A4):c.646A>G (p.Ile216Val) | not specified [RCV004857218] | uncertain significance | 5 | 132313762 | 132313762 | Human | | name |
| 597699022 | CV3596596 | single nucleotide variant | NM_003059.3(SLC22A4):c.760A>G (p.Arg254Gly) | not specified [RCV004859700] | uncertain significance | 5 | 132322291 | 132322291 | Human | | name |
| 597699031 | CV3596597 | single nucleotide variant | NM_003059.3(SLC22A4):c.470C>T (p.Ser157Phe) | not specified [RCV004859701] | uncertain significance | 5 | 132312237 | 132312237 | Human | | name |
| 597957625 | CV3755124 | single nucleotide variant | NM_003059.3(SLC22A4):c.575G>T (p.Ser192Ile) | not provided [RCV005080794] | uncertain significance | 5 | 132313691 | 132313691 | Human | | name |
| 597890398 | CV3784845 | single nucleotide variant | NM_003059.3(SLC22A4):c.841C>A (p.Pro281Thr) | not provided [RCV005125624] | uncertain significance | 5 | 132327293 | 132327293 | Human | | name |
| 597876386 | CV3813220 | single nucleotide variant | NM_003059.3(SLC22A4):c.437C>T (p.Thr146Ile) | not provided [RCV005149156] | uncertain significance | 5 | 132312204 | 132312204 | Human | | name |
| 127323036 | CV976812 | single nucleotide variant | NM_003059.3(SLC22A4):c.338G>A (p.Cys113Tyr) | Hereditary hearing loss and deafness [RCV001523786]|not provided [RCV001880208] | likely pathogenic|uncertain significance | 5 | 132294954 | 132294954 | Human | 1 | name |
| 151740614 | CV1402205 | single nucleotide variant | NM_003059.3(SLC22A4):c.1390A>G (p.Thr464Ala) | not provided [RCV001911895] | uncertain significance | 5 | 132335946 | 132335946 | Human | | name |
| 151864962 | CV1405918 | single nucleotide variant | NM_003059.3(SLC22A4):c.1007G>A (p.Arg336Gln) | not provided [RCV001959713]|not specified [RCV004042026] | likely benign|uncertain significance | 5 | 132331811 | 132331811 | Human | | name |
| 151840855 | CV1415446 | single nucleotide variant | NM_003059.3(SLC22A4):c.1543C>T (p.Leu515Phe) | not provided [RCV001921518] | uncertain significance | 5 | 132340663 | 132340663 | Human | | name |
| 151864131 | CV1445665 | single nucleotide variant | NM_003059.3(SLC22A4):c.1474G>A (p.Val492Ile) | not provided [RCV002018129] | uncertain significance | 5 | 132340594 | 132340594 | Human | | name |
| 151712756 | CV1479558 | single nucleotide variant | NM_003059.3(SLC22A4):c.1174T>A (p.Leu392Met) | not provided [RCV001889714] | uncertain significance | 5 | 132334845 | 132334845 | Human | | name |
| 156093870 | CV1895772 | single nucleotide variant | NM_003059.3(SLC22A4):c.1363C>G (p.Leu455Val) | not provided [RCV003080328]|not specified [RCV004073182] | uncertain significance | 5 | 132335919 | 132335919 | Human | | name |
| 156127010 | CV2012477 | single nucleotide variant | NM_003059.3(SLC22A4):c.1511C>T (p.Thr504Ile) | not provided [RCV002696259] | uncertain significance | 5 | 132340631 | 132340631 | Human | | name |
| 8558899 | CV20789 | single nucleotide variant | NM_003059.3(SLC22A4):c.1507C>T (p.Leu503Phe) | SLC22A4 POLYMORPHISM [RCV000006106]|not provided [RCV001682707] | benign | 5 | 132340627 | 132340627 | Human | 2 | name , trait |
| 8558899 | CV20789 | single nucleotide variant | NM_003059.3(SLC22A4):c.1507C>T (p.Leu503Phe) | SLC22A4 POLYMORPHISM [RCV000006106]|not provided [RCV001682707] | benign | 5 | 132340627 | 132340628 | Human | 2 | name , trait |
| 156123967 | CV2088229 | single nucleotide variant | NM_003059.3(SLC22A4):c.1004C>T (p.Thr335Ile) | not provided [RCV002871376] | uncertain significance | 5 | 132331808 | 132331808 | Human | | name |
| 156101940 | CV2132327 | single nucleotide variant | NM_003059.3(SLC22A4):c.1460T>C (p.Met487Thr) | not provided [RCV003002246] | benign | 5 | 132340580 | 132340580 | Human | | name |
| 156251469 | CV2232305 | single nucleotide variant | NM_003059.3(SLC22A4):c.1391C>T (p.Thr464Ile) | not specified [RCV004105080] | uncertain significance | 5 | 132335947 | 132335947 | Human | | name |
| 11525932 | CV246973 | single nucleotide variant | NM_003059.3(SLC22A4):c.1291A>G (p.Met431Val) | not specified [RCV000239084] | uncertain significance | 5 | 132335847 | 132335847 | Human | | name |
| 401936148 | CV2802714 | single nucleotide variant | NM_003059.3(SLC22A4):c.1471A>G (p.Ile491Val) | SLC22A4-related disorder [RCV003414119] | uncertain significance | 5 | 132340591 | 132340591 | Human | | name , trait , alternate_id |
| 401934720 | CV2802782 | single nucleotide variant | NM_003059.3(SLC22A4):c.1071T>A (p.Phe357Leu) | SLC22A4-related disorder [RCV003412146]|not specified [RCV004857965] | uncertain significance | 5 | 132334742 | 132334742 | Human | 1 | name , trait , alternate_id |
| 401903004 | CV2804782 | single nucleotide variant | NM_003059.3(SLC22A4):c.1205C>T (p.Ala402Val) | SLC22A4-related disorder [RCV003394320] | uncertain significance | 5 | 132334876 | 132334876 | Human | | name , trait , alternate_id |
| 405065003 | CV2937160 | single nucleotide variant | NM_003059.3(SLC22A4):c.1336G>A (p.Val446Ile) | not provided [RCV003663628] | uncertain significance | 5 | 132335892 | 132335892 | Human | | name |
| 405075269 | CV2940588 | single nucleotide variant | NM_003059.3(SLC22A4):c.1513C>A (p.Leu505Ile) | not provided [RCV003659576] | uncertain significance | 5 | 132340633 | 132340633 | Human | | name |
| 405207088 | CV3064465 | single nucleotide variant | NM_003059.3(SLC22A4):c.1444G>A (p.Gly482Ser) | not provided [RCV003731449] | uncertain significance | 5 | 132336000 | 132336000 | Human | | name |
| 405207645 | CV3145588 | single nucleotide variant | NM_003059.3(SLC22A4):c.1231G>A (p.Val411Met) | not provided [RCV003845318] | uncertain significance | 5 | 132334902 | 132334902 | Human | | name |
| 405733471 | CV3325307 | single nucleotide variant | NM_003059.3(SLC22A4):c.1103G>A (p.Gly368Glu) | not provided [RCV005104697]|not specified [RCV004451331] | uncertain significance | 5 | 132334774 | 132334774 | Human | | name |
| 405733478 | CV3325308 | single nucleotide variant | NM_003059.3(SLC22A4):c.1181C>T (p.Thr394Ile) | not specified [RCV004451332] | uncertain significance | 5 | 132334852 | 132334852 | Human | | name |
| 405733487 | CV3325309 | single nucleotide variant | NM_003059.3(SLC22A4):c.1301A>C (p.Lys434Thr) | SLC22A4-related disorder [RCV004750963]|not specified [RCV004451333] | likely benign|uncertain significance | 5 | 132335857 | 132335857 | Human | 1 | name , trait , alternate_id |
| 407509097 | CV3473890 | single nucleotide variant | NM_003059.3(SLC22A4):c.1027A>G (p.Ile343Val) | not specified [RCV004672252] | uncertain significance | 5 | 132331831 | 132331831 | Human | | name |
| 597678874 | CV3596593 | single nucleotide variant | NM_003059.3(SLC22A4):c.1033T>A (p.Ser345Thr) | not specified [RCV004857217] | uncertain significance | 5 | 132331837 | 132331837 | Human | | name |
| 597919805 | CV3738003 | single nucleotide variant | NM_003059.3(SLC22A4):c.1193G>A (p.Arg398His) | not provided [RCV005074602] | uncertain significance | 5 | 132334864 | 132334864 | Human | | name |
| 597852474 | CV3743400 | single nucleotide variant | NM_003059.3(SLC22A4):c.1379C>T (p.Ala460Val) | not provided [RCV005060750] | uncertain significance | 5 | 132335935 | 132335935 | Human | | name |
| 597922111 | CV3775021 | single nucleotide variant | NM_003059.3(SLC22A4):c.1031T>A (p.Met344Lys) | not provided [RCV005115367] | benign | 5 | 132331835 | 132331835 | Human | | name |
| 597838477 | CV3824817 | single nucleotide variant | NM_003059.3(SLC22A4):c.1371G>T (p.Arg457Ser) | not provided [RCV005171681] | uncertain significance | 5 | 132335927 | 132335927 | Human | | name |
| 597841429 | CV3825518 | single nucleotide variant | NM_003059.3(SLC22A4):c.1603A>G (p.Arg535Gly) | not provided [RCV005172201] | uncertain significance | 5 | 132343782 | 132343782 | Human | | name |
| 405077425 | CV3136946 | deletion | NM_003059.3(SLC22A4):c.200_215del (p.Val67fs) | not provided [RCV003833844] | uncertain significance | 5 | 132294815 | 132294830 | Human | | name |
| 151794479 | CV1348259 | microsatellite | NM_003059.3(SLC22A4):c.1263TTA[1] (p.Tyr423del) | not provided [RCV001876813] | uncertain significance | 5 | 132335818 | 132335820 | Human | | name |
| 151768211 | CV1450764 | indel | NM_003059.3(SLC22A4):c.1181_1182delinsTG (p.Thr394Met) | not provided [RCV001929261] | uncertain significance | 5 | 132334852 | 132334853 | Human | | name |
