| 401935323 | CV2805622 | single nucleotide variant | NM_006786.4(UTS2):c.72T>C (p.Leu24=) | not provided [RCV003412747] | likely benign | 1 | 7852932 | 7852932 | Human | | name |
| 156287004 | CV2334983 | single nucleotide variant | NM_021995.2(UTS2):c.34G>A (p.Val12Ile) | not specified [RCV004182079] | uncertain significance | 1 | 7853398 | 7853398 | Human | | name |
| 329349588 | CV2435643 | single nucleotide variant | NM_021995.2(UTS2):c.86A>C (p.Asn29Thr) | not specified [RCV004254886] | uncertain significance | 1 | 7853346 | 7853346 | Human | | name |
| 401747786 | CV2709678 | single nucleotide variant | NM_021995.2(UTS2):c.37A>G (p.Thr13Ala) | not specified [RCV004320678] | uncertain significance | 1 | 7853395 | 7853395 | Human | | name |
| 401856853 | CV2772484 | single nucleotide variant | NM_021995.2(UTS2):c.92A>G (p.Tyr31Cys) | not specified [RCV004355263] | likely benign | 1 | 7853340 | 7853340 | Human | | name |
| 405867171 | CV2842684 | single nucleotide variant | NM_006786.4(UTS2):c.49C>T (p.Pro17Ser) | EBV-positive nodal T- and NK-cell lymphoma [RCV004558041] | likely benign | 1 | 7852955 | 7852955 | Human | | name |
| 597691287 | CV3633038 | single nucleotide variant | NM_021995.2(UTS2):c.82T>G (p.Phe28Val) | not specified [RCV004881781] | uncertain significance | 1 | 7853350 | 7853350 | Human | | name |
| 15156021 | CV719092 | single nucleotide variant | NM_006786.4(UTS2):c.89C>T (p.Ser30Phe) | not provided [RCV000880537] | benign | 1 | 7852915 | 7852915 | Human | | name |
| 156179462 | CV2225679 | single nucleotide variant | NM_006786.4(UTS2):c.151T>G (p.Ser51Ala) | not specified [RCV004103102] | uncertain significance | 1 | 7850875 | 7850875 | Human | | name |
| 156066993 | CV2270810 | single nucleotide variant | NM_006786.4(UTS2):c.208A>G (p.Lys70Glu) | not specified [RCV004131860] | likely benign | 1 | 7850818 | 7850818 | Human | | name |
| 156116021 | CV2349346 | single nucleotide variant | NM_006786.4(UTS2):c.283C>A (p.Pro95Thr) | not specified [RCV004199285] | uncertain significance | 1 | 7847858 | 7847858 | Human | | name |
| 401864509 | CV2760938 | single nucleotide variant | NM_006786.4(UTS2):c.272C>T (p.Ser91Phe) | not specified [RCV004336570] | uncertain significance | 1 | 7847869 | 7847869 | Human | | name |
| 407529294 | CV3493257 | single nucleotide variant | NM_006786.4(UTS2):c.220A>G (p.Ser74Gly) | not specified [RCV004680824] | uncertain significance | 1 | 7849678 | 7849678 | Human | | name |
| 407464732 | CV3493258 | single nucleotide variant | NM_006786.4(UTS2):c.119C>T (p.Ala40Val) | not specified [RCV004688583] | uncertain significance | 1 | 7850907 | 7850907 | Human | | name |
| 407451724 | CV3493259 | single nucleotide variant | NM_021995.2(UTS2):c.112C>T (p.His38Tyr) | not specified [RCV004680825] | uncertain significance | 1 | 7853320 | 7853320 | Human | | name |
| 598239726 | CV3929295 | single nucleotide variant | NM_006786.4(UTS2):c.193G>A (p.Gly65Arg) | not specified [RCV005296642] | uncertain significance | 1 | 7850833 | 7850833 | Human | | name |
| 598205145 | CV3929297 | single nucleotide variant | NM_006786.4(UTS2):c.143A>G (p.Glu48Gly) | not specified [RCV005290804] | uncertain significance | 1 | 7850883 | 7850883 | Human | | name |
| 15157897 | CV707526 | single nucleotide variant | NM_006786.4(UTS2):c.270C>A (p.Phe90Leu) | not provided [RCV000969396] | likely benign | 1 | 7847871 | 7847871 | Human | | name |
| 156056342 | CV2343465 | single nucleotide variant | NM_006786.4(UTS2):c.316A>G (p.Ile106Val) | not specified [RCV004197535] | uncertain significance | 1 | 7847825 | 7847825 | Human | | name |
| 598239733 | CV3929296 | single nucleotide variant | NM_006786.4(UTS2):c.308T>C (p.Leu103Ser) | not specified [RCV005296643] | uncertain significance | 1 | 7847833 | 7847833 | Human | | name |
| 8578494 | CV112877 | single nucleotide variant | NM_198152.3(UTS2B):c.-125+1630C>A | Lung cancer [RCV000093400] | uncertain significance | 3 | 191302862 | 191302862 | Human | | name |
| 15201694 | CV704514 | single nucleotide variant | NM_018949.3(UTS2R):c.96C>T (p.Leu32=) | not provided [RCV000957698] | benign | 17 | 82374420 | 82374420 | Human | | name |
| 156255892 | CV2397700 | single nucleotide variant | NM_198152.5(UTS2B):c.80A>G (p.His27Arg) | not specified [RCV004237140] | likely benign | 3 | 191282110 | 191282110 | Human | | name |
| 405805999 | CV3348652 | single nucleotide variant | NM_198152.5(UTS2B):c.53C>A (p.Ser18Tyr) | not specified [RCV004479984] | uncertain significance | 3 | 191282137 | 191282137 | Human | | name |
| 15113718 | CV715854 | single nucleotide variant | NM_018949.3(UTS2R):c.543G>A (p.Thr181=) | not provided [RCV000961541] | benign | 17 | 82374867 | 82374867 | Human | | name |
| 329378753 | CV2447102 | single nucleotide variant | NM_198152.5(UTS2B):c.140G>A (p.Arg47His) | not specified [RCV004259975] | likely benign | 3 | 191278134 | 191278134 | Human | | name |
| 401747714 | CV2691665 | single nucleotide variant | NM_198152.5(UTS2B):c.217A>G (p.Asn73Asp) | not specified [RCV004305476] | uncertain significance | 3 | 191276830 | 191276830 | Human | | name |
| 405805995 | CV3348650 | single nucleotide variant | NM_198152.5(UTS2B):c.122A>C (p.Asp41Ala) | not specified [RCV004479982] | uncertain significance | 3 | 191278152 | 191278152 | Human | | name |
| 401907952 | CV2818131 | single nucleotide variant | NM_018949.3(UTS2R):c.734C>T (p.Ser245Phe) | not provided [RCV003422997] | likely benign | 17 | 82375058 | 82375058 | Human | | name |
| 597697644 | CV3633039 | single nucleotide variant | NM_198152.5(UTS2B):c.305G>T (p.Gly102Val) | not specified [RCV004885290] | uncertain significance | 3 | 191275281 | 191275281 | Human | | name |
| 597697652 | CV3633040 | single nucleotide variant | NM_198152.5(UTS2B):c.311T>G (p.Phe104Cys) | not specified [RCV004885291] | uncertain significance | 3 | 191275275 | 191275275 | Human | | name |
| 15119865 | CV715853 | single nucleotide variant | NM_018949.3(UTS2R):c.361G>T (p.Val121Leu) | not provided [RCV000962622] | benign | 17 | 82374685 | 82374685 | Human | | name |
