| 156192775 | CV2350433 | single nucleotide variant | NM_001013641.3(TMEM82):c.19C>G (p.Leu7Val) | not specified [RCV004204807] | uncertain significance | 1 | 15742578 | 15742578 | Human | | name |
| 598252752 | CV3914061 | single nucleotide variant | NM_001013641.3(TMEM82):c.14C>T (p.Pro5Leu) | not specified [RCV005278136] | likely benign | 1 | 15742573 | 15742573 | Human | | name |
| 401876949 | CV2764237 | single nucleotide variant | NM_001013641.3(TMEM82):c.50T>G (p.Leu17Arg) | not specified [RCV004336775] | uncertain significance | 1 | 15742609 | 15742609 | Human | | name |
| 401900096 | CV2780407 | single nucleotide variant | NM_001013641.3(TMEM82):c.34C>T (p.Pro12Ser) | not specified [RCV004357801] | uncertain significance | 1 | 15742593 | 15742593 | Human | | name |
| 401907434 | CV2805772 | single nucleotide variant | NM_001013641.3(TMEM82):c.450G>A (p.Thr150=) | not provided [RCV003422637] | likely benign | 1 | 15744273 | 15744273 | Human | | name |
| 401907435 | CV2805773 | single nucleotide variant | NM_001013641.3(TMEM82):c.922C>T (p.Leu308=) | not provided [RCV003422638] | likely benign | 1 | 15747031 | 15747031 | Human | | name |
| 405772332 | CV3343279 | single nucleotide variant | NM_001013641.3(TMEM82):c.62C>T (p.Ser21Phe) | not specified [RCV004470506] | uncertain significance | 1 | 15742621 | 15742621 | Human | | name |
| 407526951 | CV3482838 | single nucleotide variant | NM_001013641.3(TMEM82):c.97G>A (p.Gly33Arg) | not specified [RCV004679828] | uncertain significance | 1 | 15742843 | 15742843 | Human | | name |
| 597800687 | CV3610698 | single nucleotide variant | NM_001013641.3(TMEM82):c.52G>A (p.Glu18Lys) | not specified [RCV004880345] | uncertain significance | 1 | 15742611 | 15742611 | Human | | name |
| 155932831 | CV2372174 | single nucleotide variant | NM_001013641.3(TMEM82):c.292G>A (p.Glu98Lys) | not specified [RCV004216956] | uncertain significance | 1 | 15743150 | 15743150 | Human | | name |
| 329355853 | CV2442361 | single nucleotide variant | NM_001013641.3(TMEM82):c.232G>A (p.Ala78Thr) | not specified [RCV004266620] | uncertain significance | 1 | 15743090 | 15743090 | Human | | name |
| 401741281 | CV2680585 | single nucleotide variant | NM_001013641.3(TMEM82):c.131T>A (p.Leu44Gln) | not specified [RCV004291211] | uncertain significance | 1 | 15742877 | 15742877 | Human | | name |
| 401774504 | CV2691760 | single nucleotide variant | NM_001013641.3(TMEM82):c.126C>G (p.Ser42Arg) | not specified [RCV004299215] | uncertain significance | 1 | 15742872 | 15742872 | Human | | name |
| 401864773 | CV2761040 | single nucleotide variant | NM_001013641.3(TMEM82):c.173G>A (p.Arg58Gln) | not specified [RCV004338707] | uncertain significance | 1 | 15743031 | 15743031 | Human | | name |
| 405772298 | CV3346729 | single nucleotide variant | NM_001013641.3(TMEM82):c.181G>A (p.Glu61Lys) | not specified [RCV004470500] | uncertain significance | 1 | 15743039 | 15743039 | Human | | name |
| 405772304 | CV3346730 | single nucleotide variant | NM_001013641.3(TMEM82):c.253A>T (p.Thr85Ser) | not specified [RCV004470501] | uncertain significance | 1 | 15743111 | 15743111 | Human | | name |
| 598252765 | CV3914064 | single nucleotide variant | NM_001013641.3(TMEM82):c.107G>A (p.Gly36Glu) | not specified [RCV005278138] | uncertain significance | 1 | 15742853 | 15742853 | Human | | name |
| 156072547 | CV2201348 | single nucleotide variant | NM_001013641.3(TMEM82):c.640G>A (p.Val214Met) | not specified [RCV004077474] | uncertain significance | 1 | 15744463 | 15744463 | Human | | name |
| 156252166 | CV2232377 | single nucleotide variant | NM_001013641.3(TMEM82):c.338G>A (p.Gly113Asp) | not specified [RCV004099009] | uncertain significance | 1 | 15744161 | 15744161 | Human | | name |
| 155986391 | CV2233989 | single nucleotide variant | NM_001013641.3(TMEM82):c.503G>A (p.Arg168Gln) | not specified [RCV004106113] | uncertain significance | 1 | 15744326 | 15744326 | Human | | name |
| 156000681 | CV2296336 | single nucleotide variant | NM_001013641.3(TMEM82):c.821G>T (p.Gly274Val) | not specified [RCV004148094] | uncertain significance | 1 | 15746930 | 15746930 | Human | | name |
| 156253445 | CV2311456 | single nucleotide variant | NM_001013641.3(TMEM82):c.734C>T (p.Thr245Met) | not specified [RCV004168300] | uncertain significance | 1 | 15744557 | 15744557 | Human | | name |
| 155925677 | CV2348474 | single nucleotide variant | NM_001013641.3(TMEM82):c.850C>T (p.Arg284Cys) | not specified [RCV004193662] | uncertain significance | 1 | 15746959 | 15746959 | Human | | name |
| 156389852 | CV2380883 | single nucleotide variant | NM_001013641.3(TMEM82):c.355G>A (p.Glu119Lys) | not specified [RCV004218431] | uncertain significance | 1 | 15744178 | 15744178 | Human | | name |
| 156151664 | CV2394771 | single nucleotide variant | NM_001013641.3(TMEM82):c.304C>T (p.Arg102Trp) | not specified [RCV004234441] | uncertain significance | 1 | 15743162 | 15743162 | Human | | name |
| 329383143 | CV2424618 | single nucleotide variant | NM_001013641.3(TMEM82):c.449C>T (p.Thr150Met) | not specified [RCV004254114] | uncertain significance | 1 | 15744272 | 15744272 | Human | | name |
| 329384959 | CV2435111 | single nucleotide variant | NM_001013641.3(TMEM82):c.527G>A (p.Arg176His) | not specified [RCV004252756] | uncertain significance | 1 | 15744350 | 15744350 | Human | | name |
| 329375239 | CV2440861 | single nucleotide variant | NM_001013641.3(TMEM82):c.716C>T (p.Pro239Leu) | not specified [RCV004261257] | uncertain significance | 1 | 15744539 | 15744539 | Human | | name |
| 329402439 | CV2454260 | single nucleotide variant | NM_001013641.3(TMEM82):c.538C>A (p.Leu180Met) | not specified [RCV004265733] | uncertain significance | 1 | 15744361 | 15744361 | Human | | name |
| 329397962 | CV2467112 | single nucleotide variant | NM_001013641.3(TMEM82):c.595G>T (p.Gly199Cys) | not specified [RCV004282842] | uncertain significance | 1 | 15744418 | 15744418 | Human | | name |
| 401732651 | CV2685291 | single nucleotide variant | NM_001013641.3(TMEM82):c.400G>A (p.Gly134Arg) | not specified [RCV004292291] | uncertain significance | 1 | 15744223 | 15744223 | Human | | name |
| 401888504 | CV2761571 | single nucleotide variant | NM_001013641.3(TMEM82):c.377T>C (p.Leu126Pro) | not specified [RCV004334738] | uncertain significance | 1 | 15744200 | 15744200 | Human | | name |
| 405772327 | CV3343278 | single nucleotide variant | NM_001013641.3(TMEM82):c.554G>A (p.Arg185His) | not specified [RCV004470505] | likely benign | 1 | 15744377 | 15744377 | Human | | name |
| 405772309 | CV3346731 | single nucleotide variant | NM_001013641.3(TMEM82):c.482C>T (p.Thr161Met) | not specified [RCV004470502] | uncertain significance | 1 | 15744305 | 15744305 | Human | | name |
| 405772315 | CV3346732 | single nucleotide variant | NM_001013641.3(TMEM82):c.514C>T (p.Arg172Cys) | not specified [RCV004470503] | uncertain significance | 1 | 15744337 | 15744337 | Human | | name |
| 407526954 | CV3482839 | single nucleotide variant | NM_001013641.3(TMEM82):c.357G>C (p.Glu119Asp) | not specified [RCV004679829] | uncertain significance | 1 | 15744180 | 15744180 | Human | | name |
| 407526957 | CV3482840 | single nucleotide variant | NM_001013641.3(TMEM82):c.698C>G (p.Ala233Gly) | not specified [RCV004679830] | uncertain significance | 1 | 15744521 | 15744521 | Human | | name |
| 597800685 | CV3610697 | single nucleotide variant | NM_001013641.3(TMEM82):c.617G>A (p.Arg206His) | not specified [RCV004880344] | uncertain significance | 1 | 15744440 | 15744440 | Human | | name |
| 597800691 | CV3610700 | single nucleotide variant | NM_001013641.3(TMEM82):c.851G>A (p.Arg284His) | not specified [RCV004880347] | uncertain significance | 1 | 15746960 | 15746960 | Human | | name |
| 597800694 | CV3610701 | single nucleotide variant | NM_001013641.3(TMEM82):c.299C>T (p.Ser100Phe) | not specified [RCV004880348] | uncertain significance | 1 | 15743157 | 15743157 | Human | | name |
| 597800696 | CV3610702 | single nucleotide variant | NM_001013641.3(TMEM82):c.352G>A (p.Ala118Thr) | not specified [RCV004880349] | likely benign | 1 | 15744175 | 15744175 | Human | | name |
| 597800698 | CV3610703 | single nucleotide variant | NM_001013641.3(TMEM82):c.310G>A (p.Val104Met) | not specified [RCV004880350] | uncertain significance | 1 | 15743168 | 15743168 | Human | | name |
| 597800700 | CV3610704 | single nucleotide variant | NM_001013641.3(TMEM82):c.420C>G (p.Ser140Arg) | not specified [RCV004880351] | uncertain significance | 1 | 15744243 | 15744243 | Human | | name |
| 598227636 | CV3914062 | single nucleotide variant | NM_001013641.3(TMEM82):c.577C>A (p.Leu193Met) | not specified [RCV005294617] | uncertain significance | 1 | 15744400 | 15744400 | Human | | name |
| 598252758 | CV3914063 | single nucleotide variant | NM_001013641.3(TMEM82):c.346G>T (p.Gly116Cys) | not specified [RCV005278137] | uncertain significance | 1 | 15744169 | 15744169 | Human | | name |
| 598252771 | CV3914065 | single nucleotide variant | NM_001013641.3(TMEM82):c.703C>T (p.Arg235Trp) | not specified [RCV005278139] | uncertain significance | 1 | 15744526 | 15744526 | Human | | name |
| 401743810 | CV2726170 | single nucleotide variant | NM_001013641.3(TMEM82):c.1006C>A (p.Gln336Lys) | not specified [RCV004326647] | uncertain significance | 1 | 15747606 | 15747606 | Human | | name |
