| 405712974 | CV3325208 | single nucleotide variant | NM_018420.3(SLC22A15):c.26C>A (p.Ala9Glu) | not specified [RCV004448755] | uncertain significance | 1 | 115976653 | 115976653 | Human | | name |
| 156258022 | CV2277703 | single nucleotide variant | NM_018420.3(SLC22A15):c.43A>G (p.Ile15Val) | not specified [RCV004147149] | uncertain significance | 1 | 115976670 | 115976670 | Human | | name |
| 401897520 | CV2787126 | single nucleotide variant | NM_018420.3(SLC22A15):c.49C>G (p.Gln17Glu) | not specified [RCV004360560] | uncertain significance | 1 | 115976676 | 115976676 | Human | | name |
| 405712987 | CV3325210 | single nucleotide variant | NM_018420.3(SLC22A15):c.47A>C (p.Tyr16Ser) | not specified [RCV004448757] | uncertain significance | 1 | 115976674 | 115976674 | Human | | name |
| 156382081 | CV2227179 | single nucleotide variant | NM_018420.3(SLC22A15):c.223T>G (p.Trp75Gly) | not provided [RCV004691511]|not specified [RCV004091788] | uncertain significance | 1 | 115992166 | 115992166 | Human | | name |
| 156289395 | CV2229911 | single nucleotide variant | NM_018420.3(SLC22A15):c.216T>A (p.Phe72Leu) | not specified [RCV004105457] | likely benign | 1 | 115992159 | 115992159 | Human | | name |
| 401759658 | CV2701658 | single nucleotide variant | NM_018420.3(SLC22A15):c.134C>G (p.Thr45Arg) | not specified [RCV004314072] | uncertain significance | 1 | 115992077 | 115992077 | Human | | name |
| 597677930 | CV3596493 | single nucleotide variant | NM_018420.3(SLC22A15):c.280T>G (p.Phe94Val) | not specified [RCV004857117] | uncertain significance | 1 | 115992223 | 115992223 | Human | | name |
| 598269490 | CV3921852 | single nucleotide variant | NM_018420.3(SLC22A15):c.292G>A (p.Ala98Thr) | not specified [RCV005281969] | uncertain significance | 1 | 115992235 | 115992235 | Human | | name |
| 156236823 | CV2193510 | single nucleotide variant | NM_018420.3(SLC22A15):c.817C>T (p.Arg273Cys) | not specified [RCV004072991] | uncertain significance | 1 | 116031454 | 116031454 | Human | | name |
| 156335941 | CV2228465 | single nucleotide variant | NM_018420.3(SLC22A15):c.870G>C (p.Arg290Ser) | not specified [RCV004098432] | uncertain significance | 1 | 116031507 | 116031507 | Human | | name |
| 156291945 | CV2246547 | single nucleotide variant | NM_018420.3(SLC22A15):c.443T>C (p.Leu148Pro) | not specified [RCV004110300] | uncertain significance | 1 | 116020730 | 116020730 | Human | | name |
| 156277533 | CV2277064 | single nucleotide variant | NM_018420.3(SLC22A15):c.970G>A (p.Gly324Ser) | not specified [RCV004140383] | uncertain significance | 1 | 116035212 | 116035212 | Human | | name |
| 156186464 | CV2292392 | single nucleotide variant | NM_018420.3(SLC22A15):c.334A>C (p.Ser112Arg) | not specified [RCV004150196] | uncertain significance | 1 | 116019615 | 116019615 | Human | | name |
| 156151588 | CV2307567 | single nucleotide variant | NM_018420.3(SLC22A15):c.574G>A (p.Gly192Ser) | not specified [RCV004167996] | uncertain significance | 1 | 116020861 | 116020861 | Human | | name |
| 156151611 | CV2307568 | single nucleotide variant | NM_018420.3(SLC22A15):c.580G>T (p.Ala194Ser) | not specified [RCV004167997] | uncertain significance | 1 | 116020867 | 116020867 | Human | | name |
| 155937331 | CV2379999 | single nucleotide variant | NM_018420.3(SLC22A15):c.827A>G (p.Lys276Arg) | not provided [RCV004691548]|not specified [RCV004222139] | uncertain significance | 1 | 116031464 | 116031464 | Human | | name |
| 401734250 | CV2690526 | single nucleotide variant | NM_018420.3(SLC22A15):c.560T>C (p.Leu187Pro) | not specified [RCV004304640] | uncertain significance | 1 | 116020847 | 116020847 | Human | | name |
| 401744537 | CV2697022 | single nucleotide variant | NM_018420.3(SLC22A15):c.986C>T (p.Ala329Val) | not specified [RCV004293012] | uncertain significance | 1 | 116035228 | 116035228 | Human | | name |
| 401750163 | CV2701037 | single nucleotide variant | NM_018420.3(SLC22A15):c.466A>G (p.Asn156Asp) | not specified [RCV004309642] | uncertain significance | 1 | 116020753 | 116020753 | Human | | name |
| 401738703 | CV2708114 | single nucleotide variant | NM_018420.3(SLC22A15):c.550T>C (p.Phe184Leu) | not specified [RCV004311490] | uncertain significance | 1 | 116020837 | 116020837 | Human | | name |
| 401739242 | CV2708385 | single nucleotide variant | NM_018420.3(SLC22A15):c.562A>C (p.Asn188His) | not specified [RCV004313500] | uncertain significance | 1 | 116020849 | 116020849 | Human | | name |
| 401758204 | CV2729587 | single nucleotide variant | NM_018420.3(SLC22A15):c.664C>T (p.Arg222Cys) | not specified [RCV004331853] | uncertain significance | 1 | 116026958 | 116026958 | Human | | name |
| 401781577 | CV2731697 | single nucleotide variant | NM_018420.3(SLC22A15):c.665G>A (p.Arg222His) | not specified [RCV004331800] | uncertain significance | 1 | 116026959 | 116026959 | Human | | name |
| 405712980 | CV3325209 | single nucleotide variant | NM_018420.3(SLC22A15):c.473T>A (p.Phe158Tyr) | not specified [RCV004448756] | uncertain significance | 1 | 116020760 | 116020760 | Human | | name |
| 405713001 | CV3325212 | single nucleotide variant | NM_018420.3(SLC22A15):c.592C>T (p.Leu198Phe) | not specified [RCV004448759] | uncertain significance | 1 | 116020879 | 116020879 | Human | | name |
| 407508992 | CV3473843 | single nucleotide variant | NM_018420.3(SLC22A15):c.404G>A (p.Arg135His) | not specified [RCV004672222] | uncertain significance | 1 | 116019685 | 116019685 | Human | | name |
| 597677852 | CV3596486 | single nucleotide variant | NM_018420.3(SLC22A15):c.890A>C (p.Asp297Ala) | not specified [RCV004857110] | uncertain significance | 1 | 116031527 | 116031527 | Human | | name |
| 597677891 | CV3596490 | single nucleotide variant | NM_018420.3(SLC22A15):c.799C>T (p.Leu267Phe) | not specified [RCV004857114] | uncertain significance | 1 | 116031436 | 116031436 | Human | | name |
| 597677908 | CV3596491 | single nucleotide variant | NM_018420.3(SLC22A15):c.482C>T (p.Ser161Leu) | not specified [RCV004857115] | uncertain significance | 1 | 116020769 | 116020769 | Human | | name |
| 597677948 | CV3596495 | single nucleotide variant | NM_018420.3(SLC22A15):c.961G>T (p.Val321Leu) | not specified [RCV004857119] | uncertain significance | 1 | 116035203 | 116035203 | Human | | name |
| 598269483 | CV3921851 | single nucleotide variant | NM_018420.3(SLC22A15):c.904C>T (p.Arg302Trp) | not specified [RCV005281968] | uncertain significance | 1 | 116031541 | 116031541 | Human | | name |
| 156388477 | CV2231845 | single nucleotide variant | NM_018420.3(SLC22A15):c.1336G>A (p.Gly446Arg) | not specified [RCV004098647] | uncertain significance | 1 | 116064479 | 116064479 | Human | | name |
| 329399542 | CV2470146 | single nucleotide variant | NM_018420.3(SLC22A15):c.1484A>T (p.Asp495Val) | not specified [RCV004287395] | uncertain significance | 1 | 116066638 | 116066638 | Human | | name |
| 401738947 | CV2673192 | single nucleotide variant | NM_018420.3(SLC22A15):c.1556G>T (p.Cys519Phe) | not specified [RCV004286003] | uncertain significance | 1 | 116067020 | 116067020 | Human | | name |
| 401731521 | CV2693845 | single nucleotide variant | NM_018420.3(SLC22A15):c.1504C>T (p.Arg502Cys) | not specified [RCV004300151] | uncertain significance | 1 | 116066658 | 116066658 | Human | | name |
| 401885448 | CV2783299 | single nucleotide variant | NM_018420.3(SLC22A15):c.1006A>C (p.Ile336Leu) | not specified [RCV004363903] | uncertain significance | 1 | 116035248 | 116035248 | Human | | name |
| 405712961 | CV3325206 | single nucleotide variant | NM_018420.3(SLC22A15):c.1418C>T (p.Thr473Ile) | not specified [RCV004448753] | likely benign | 1 | 116066572 | 116066572 | Human | | name |
| 405712967 | CV3325207 | single nucleotide variant | NM_018420.3(SLC22A15):c.1628C>T (p.Thr543Ile) | not specified [RCV004448754] | uncertain significance | 1 | 116067092 | 116067092 | Human | | name |
| 597677842 | CV3596485 | single nucleotide variant | NM_018420.3(SLC22A15):c.1202A>G (p.His401Arg) | not specified [RCV004857109] | likely benign | 1 | 116062792 | 116062792 | Human | | name |
| 597677861 | CV3596487 | single nucleotide variant | NM_018420.3(SLC22A15):c.1288A>T (p.Ile430Phe) | not specified [RCV004857111] | uncertain significance | 1 | 116062878 | 116062878 | Human | | name |
| 597677872 | CV3596488 | single nucleotide variant | NM_018420.3(SLC22A15):c.1409C>T (p.Thr470Met) | not specified [RCV004857112] | uncertain significance | 1 | 116066563 | 116066563 | Human | | name |
| 597677918 | CV3596492 | single nucleotide variant | NM_018420.3(SLC22A15):c.1492G>A (p.Val498Met) | not specified [RCV004857116] | uncertain significance | 1 | 116066646 | 116066646 | Human | | name |
| 597677941 | CV3596494 | single nucleotide variant | NM_018420.3(SLC22A15):c.1046C>T (p.Pro349Leu) | not specified [RCV004857118] | uncertain significance | 1 | 116035288 | 116035288 | Human | | name |
| 598269496 | CV3921853 | single nucleotide variant | NM_018420.3(SLC22A15):c.1393A>G (p.Ile465Val) | not specified [RCV005281970] | uncertain significance | 1 | 116066547 | 116066547 | Human | | name |
| 8628815 | CV83959 | single nucleotide variant | NM_018420.2(SLC22A15):c.1201C>T (p.His401Tyr) | Malignant melanoma [RCV000064040] | not provided | 1 | 116062791 | 116062791 | Human | | name |
