| 405294989 | CV3215037 | single nucleotide variant | NM_002923.4(RGS2):c.-3A>G | RGS2-related disorder [RCV003936886] | benign | 1 | 192809069 | 192809069 | Human | | name , trait , alternate_id |
| 12742121 | CV359224 | single nucleotide variant | NM_002923.4(RGS2):c.274+1G>T | not provided [RCV000412916] | likely pathogenic | 1 | 192810432 | 192810432 | Human | | name |
| 401753775 | CV2722582 | single nucleotide variant | NM_002923.4(RGS2):c.32A>G (p.His11Arg) | not specified [RCV004322955] | uncertain significance | 1 | 192809103 | 192809103 | Human | | name |
| 405715686 | CV3309219 | single nucleotide variant | NM_002923.4(RGS2):c.49G>A (p.Asp17Asn) | not specified [RCV004449158] | uncertain significance | 1 | 192809120 | 192809120 | Human | | name |
| 597788081 | CV3586346 | single nucleotide variant | NM_002923.4(RGS2):c.29A>T (p.Gln10Leu) | not specified [RCV004855403] | uncertain significance | 1 | 192809100 | 192809100 | Human | | name |
| 12896699 | CV389327 | single nucleotide variant | NM_002923.4(RGS2):c.68G>A (p.Gly23Asp) | not provided [RCV004691232]|not specified [RCV000455699] | uncertain significance | 1 | 192809139 | 192809139 | Human | | name |
| 155939706 | CV2293957 | single nucleotide variant | NM_002923.4(RGS2):c.255C>A (p.Asp85Glu) | not specified [RCV004155496] | uncertain significance | 1 | 192810412 | 192810412 | Human | | name |
| 405715669 | CV3309216 | single nucleotide variant | NM_002923.4(RGS2):c.203C>T (p.Ala68Val) | not specified [RCV004449155] | uncertain significance | 1 | 192810258 | 192810258 | Human | | name |
| 597775785 | CV3586345 | single nucleotide variant | NM_002923.4(RGS2):c.217T>G (p.Ser73Ala) | not specified [RCV004852341] | uncertain significance | 1 | 192810374 | 192810374 | Human | | name |
| 15173082 | CV718467 | single nucleotide variant | NM_002923.4(RGS2):c.148C>A (p.Gln50Lys) | not provided [RCV000883967] | likely benign | 1 | 192810203 | 192810203 | Human | | name |
| 401753640 | CV2722536 | single nucleotide variant | NM_002923.4(RGS2):c.517G>A (p.Ala173Thr) | not specified [RCV004322918] | uncertain significance | 1 | 192811477 | 192811477 | Human | | name |
| 405715682 | CV3309218 | single nucleotide variant | NM_002923.4(RGS2):c.429A>C (p.Glu143Asp) | not specified [RCV004449157] | uncertain significance | 1 | 192811135 | 192811135 | Human | | name |
| 407474265 | CV3472819 | single nucleotide variant | NM_002923.4(RGS2):c.419T>C (p.Ile140Thr) | not specified [RCV004662954] | uncertain significance | 1 | 192811125 | 192811125 | Human | | name |
| 597775788 | CV3586347 | single nucleotide variant | NM_002923.4(RGS2):c.532T>C (p.Tyr178His) | not specified [RCV004852342] | uncertain significance | 1 | 192811492 | 192811492 | Human | | name |
| 598188970 | CV3902557 | single nucleotide variant | NM_002923.4(RGS2):c.397A>G (p.Arg133Gly) | not specified [RCV005266651] | uncertain significance | 1 | 192811103 | 192811103 | Human | | name |
| 8575380 | CV109727 | single nucleotide variant | NM_001039152.3(RGS21):c.255+827A>G | Lung cancer [RCV000090252] | uncertain significance | 1 | 192353040 | 192353040 | Human | | name |
| 8575379 | CV109726 | single nucleotide variant | NM_001039152.3(RGS21):c.-61+7455T>A | Lung cancer [RCV000090251] | uncertain significance | 1 | 192324560 | 192324560 | Human | | name |
| 8575381 | CV109728 | single nucleotide variant | NM_001039152.3(RGS21):c.255+2528T>A | Lung cancer [RCV000090253] | uncertain significance | 1 | 192354741 | 192354741 | Human | | name |
| 401909217 | CV2821086 | single nucleotide variant | NM_003702.5(RGS20):c.9G>C (p.Thr3=) | not provided [RCV003423924] | likely benign | 8 | 53881024 | 53881024 | Human | | name |
| 15198103 | CV700326 | single nucleotide variant | NM_015668.5(RGS22):c.63T>C (p.Ser21=) | not provided [RCV000956653] | benign | 8 | 100093501 | 100093501 | Human | | name |
| 401889672 | CV2758371 | single nucleotide variant | NM_015668.5(RGS22):c.22G>T (p.Ala8Ser) | not specified [RCV004341719] | uncertain significance | 8 | 100105900 | 100105900 | Human | | name |
| 156304406 | CV2359627 | single nucleotide variant | NM_015668.5(RGS22):c.43G>A (p.Glu15Lys) | not specified [RCV004214922] | uncertain significance | 8 | 100105385 | 100105385 | Human | | name |
| 15101149 | CV700615 | single nucleotide variant | NM_170587.4(RGS20):c.336G>A (p.Pro112=) | not provided [RCV000959029] | benign | 8 | 53879428 | 53879428 | Human | | name |
| 15197977 | CV700616 | single nucleotide variant | NM_003702.5(RGS20):c.324A>G (p.Glu108=) | not provided [RCV000956617] | benign | 8 | 53954097 | 53954097 | Human | | name |
| 15160306 | CV722778 | single nucleotide variant | NM_015668.5(RGS22):c.744T>C (p.Asp248=) | not provided [RCV000881357] | benign | 8 | 100064024 | 100064024 | Human | | name |
| 15116065 | CV750869 | single nucleotide variant | NM_015668.5(RGS22):c.300C>T (p.Pro100=) | not provided [RCV000917559] | likely benign | 8 | 100080173 | 100080173 | Human | | name |
| 8632740 | CV87955 | single nucleotide variant | NM_015668.4(RGS22):c.507C>T (p.Ile169=) | Malignant melanoma [RCV000068047] | not provided | 8 | 100071456 | 100071456 | Human | | name |
| 156381956 | CV2212505 | single nucleotide variant | NM_003702.5(RGS20):c.133G>A (p.Gly45Ser) | not specified [RCV004091389] | uncertain significance | 8 | 53939639 | 53939639 | Human | | name |
| 156033825 | CV2275165 | single nucleotide variant | NM_003702.5(RGS20):c.122A>G (p.Gln41Arg) | not specified [RCV004136963] | uncertain significance | 8 | 53939628 | 53939628 | Human | | name |
| 156279819 | CV2285121 | single nucleotide variant | NM_003702.5(RGS20):c.231A>C (p.Arg77Ser) | not specified [RCV004145345] | uncertain significance | 8 | 53946677 | 53946677 | Human | | name |
| 156179244 | CV2331376 | single nucleotide variant | NM_003702.5(RGS20):c.166C>T (p.Arg56Cys) | not specified [RCV004184015] | uncertain significance | 8 | 53939672 | 53939672 | Human | | name |
| 156385443 | CV2379636 | single nucleotide variant | NM_003702.5(RGS20):c.119C>T (p.Ala40Val) | not specified [RCV004217333] | uncertain significance | 8 | 53939625 | 53939625 | Human | | name |
| 156104909 | CV2400328 | single nucleotide variant | NM_170587.4(RGS20):c.100T>C (p.Tyr34His) | not specified [RCV004244387] | uncertain significance | 8 | 53851999 | 53851999 | Human | | name |
| 329390080 | CV2441277 | single nucleotide variant | NM_170587.4(RGS20):c.289G>A (p.Ala97Thr) | not specified [RCV004264006] | uncertain significance | 8 | 53879381 | 53879381 | Human | | name |
| 329392157 | CV2441278 | single nucleotide variant | NM_170587.4(RGS20):c.290C>A (p.Ala97Asp) | not specified [RCV004264007] | uncertain significance | 8 | 53879382 | 53879382 | Human | | name |
| 401722937 | CV2677142 | single nucleotide variant | NM_003702.5(RGS20):c.104G>A (p.Arg35Gln) | not specified [RCV004295776] | uncertain significance | 8 | 53939610 | 53939610 | Human | | name |
| 401730615 | CV2677238 | single nucleotide variant | NM_003702.5(RGS20):c.154G>A (p.Gly52Arg) | not specified [RCV004295861] | uncertain significance | 8 | 53939660 | 53939660 | Human | | name |
| 401761971 | CV2699476 | single nucleotide variant | NM_015668.5(RGS22):c.233G>A (p.Arg78Gln) | not specified [RCV004299693] | uncertain significance | 8 | 100080240 | 100080240 | Human | | name |
| 401856727 | CV2756425 | single nucleotide variant | NM_170587.4(RGS20):c.172C>A (p.Pro58Thr) | not specified [RCV004342962] | uncertain significance | 8 | 53879264 | 53879264 | Human | | name |
| 401924081 | CV2821195 | single nucleotide variant | NM_015668.5(RGS22):c.1728C>A (p.Pro576=) | not provided [RCV003435569] | likely benign | 8 | 100047558 | 100047558 | Human | | name |
| 405715703 | CV3309221 | single nucleotide variant | NM_003702.5(RGS20):c.175A>C (p.Asn59His) | not specified [RCV004449160] | uncertain significance | 8 | 53939681 | 53939681 | Human | | name |
| 407450662 | CV3472820 | single nucleotide variant | NM_170587.4(RGS20):c.203C>T (p.Ala68Val) | not specified [RCV004662955] | uncertain significance | 8 | 53879295 | 53879295 | Human | | name |
| 407450665 | CV3472821 | single nucleotide variant | NM_170587.4(RGS20):c.243C>A (p.Ser81Arg) | not specified [RCV004662956] | uncertain significance | 8 | 53879335 | 53879335 | Human | | name |
| 597686762 | CV3586349 | single nucleotide variant | NM_170587.4(RGS20):c.242G>A (p.Ser81Asn) | not specified [RCV004855404] | uncertain significance | 8 | 53879334 | 53879334 | Human | | name |
| 597788085 | CV3586350 | single nucleotide variant | NM_003702.5(RGS20):c.143C>T (p.Pro48Leu) | not specified [RCV004855405] | uncertain significance | 8 | 53939649 | 53939649 | Human | | name |
| 597686430 | CV3586352 | single nucleotide variant | NM_170587.4(RGS20):c.166T>C (p.Ser56Pro) | not specified [RCV004852345] | likely benign | 8 | 53879258 | 53879258 | Human | | name |
| 597788090 | CV3586355 | single nucleotide variant | NM_003702.5(RGS20):c.111G>A (p.Met37Ile) | not specified [RCV004855406] | uncertain significance | 8 | 53939617 | 53939617 | Human | | name |
| 597775800 | CV3586356 | single nucleotide variant | NM_003702.5(RGS20):c.256A>G (p.Ile86Val) | not specified [RCV004852348] | uncertain significance | 8 | 53946702 | 53946702 | Human | | name |
| 598189008 | CV3902562 | single nucleotide variant | NM_003702.5(RGS20):c.118G>T (p.Ala40Ser) | not specified [RCV005266656] | uncertain significance | 8 | 53939624 | 53939624 | Human | | name |
| 598189016 | CV3902563 | single nucleotide variant | NM_170587.4(RGS20):c.286G>A (p.Glu96Lys) | not specified [RCV005266657] | uncertain significance | 8 | 53879378 | 53879378 | Human | | name |
| 598189025 | CV3902564 | single nucleotide variant | NM_003702.5(RGS20):c.111G>T (p.Met37Ile) | not specified [RCV005266658] | uncertain significance | 8 | 53939617 | 53939617 | Human | | name |
| 15187773 | CV766861 | single nucleotide variant | NM_003702.5(RGS20):c.161G>A (p.Gly54Glu) | not provided [RCV000931756] | likely benign | 8 | 53939667 | 53939667 | Human | | name |
| 155916691 | CV2197552 | single nucleotide variant | NM_015668.5(RGS22):c.726G>T (p.Glu242Asp) | not specified [RCV004081273] | uncertain significance | 8 | 100064042 | 100064042 | Human | | name |
| 156378917 | CV2207838 | single nucleotide variant | NM_003702.5(RGS20):c.553C>T (p.Arg185Trp) | not specified [RCV004084270] | uncertain significance | 8 | 53958285 | 53958285 | Human | | name |
| 156092493 | CV2300142 | single nucleotide variant | NM_003702.5(RGS20):c.662T>G (p.Phe221Cys) | not specified [RCV004151332] | uncertain significance | 8 | 53958394 | 53958394 | Human | | name |
| 156056869 | CV2320651 | single nucleotide variant | NM_015668.5(RGS22):c.911G>A (p.Ser304Asn) | not specified [RCV004172261] | uncertain significance | 8 | 100063857 | 100063857 | Human | | name |
| 155917499 | CV2332828 | single nucleotide variant | NM_170587.4(RGS20):c.394G>C (p.Gly132Arg) | not specified [RCV004192092] | uncertain significance | 8 | 53879486 | 53879486 | Human | | name |
| 156166547 | CV2398942 | single nucleotide variant | NM_015668.5(RGS22):c.812A>G (p.Glu271Gly) | not specified [RCV004245254] | uncertain significance | 8 | 100063956 | 100063956 | Human | | name |
| 329384543 | CV2435128 | single nucleotide variant | NM_015668.5(RGS22):c.508G>A (p.Val170Met) | not specified [RCV004252770] | uncertain significance | 8 | 100071455 | 100071455 | Human | | name |
| 329402675 | CV2451217 | single nucleotide variant | NM_015668.5(RGS22):c.601T>C (p.Tyr201His) | not specified [RCV004270131] | uncertain significance | 8 | 100066290 | 100066290 | Human | | name |
| 401729060 | CV2694006 | single nucleotide variant | NM_003702.5(RGS20):c.722C>T (p.Ala241Val) | not specified [RCV004300292] | uncertain significance | 8 | 53958454 | 53958454 | Human | | name |
| 401861597 | CV2756366 | single nucleotide variant | NM_003702.5(RGS20):c.554G>A (p.Arg185Gln) | not specified [RCV004342910] | uncertain significance | 8 | 53958286 | 53958286 | Human | | name |
| 401855830 | CV2757517 | single nucleotide variant | NM_015668.5(RGS22):c.583T>A (p.Ser195Thr) | not specified [RCV004340896] | uncertain significance | 8 | 100071380 | 100071380 | Human | | name |
| 401871556 | CV2783539 | single nucleotide variant | NM_015668.5(RGS22):c.539C>T (p.Ala180Val) | not specified [RCV004365869] | uncertain significance | 8 | 100071424 | 100071424 | Human | | name |
| 401881535 | CV2784583 | single nucleotide variant | NM_015668.5(RGS22):c.848A>G (p.Gln283Arg) | not specified [RCV004358733] | uncertain significance | 8 | 100063920 | 100063920 | Human | | name |
| 405715714 | CV3309222 | single nucleotide variant | NM_003702.5(RGS20):c.446A>G (p.Glu149Gly) | not specified [RCV004449161] | uncertain significance | 8 | 53954219 | 53954219 | Human | | name |
| 405715824 | CV3309238 | single nucleotide variant | NM_015668.5(RGS22):c.359G>A (p.Gly120Asp) | not specified [RCV004449177] | uncertain significance | 8 | 100072211 | 100072211 | Human | | name |
| 405715841 | CV3309240 | single nucleotide variant | NM_015668.5(RGS22):c.361A>G (p.Ile121Val) | not specified [RCV004449179] | uncertain significance | 8 | 100072209 | 100072209 | Human | | name |
| 405715853 | CV3309242 | single nucleotide variant | NM_015668.5(RGS22):c.466G>A (p.Gly156Ser) | not specified [RCV004449181] | uncertain significance | 8 | 100071497 | 100071497 | Human | | name |
| 405715866 | CV3309244 | single nucleotide variant | NM_015668.5(RGS22):c.664T>G (p.Ser222Ala) | not specified [RCV004449183] | uncertain significance | 8 | 100066227 | 100066227 | Human | | name |
| 405715877 | CV3309245 | single nucleotide variant | NM_015668.5(RGS22):c.678T>G (p.Cys226Trp) | not specified [RCV004449184] | uncertain significance | 8 | 100066213 | 100066213 | Human | | name |
| 597686420 | CV3586348 | single nucleotide variant | NM_170587.4(RGS20):c.335C>A (p.Pro112Gln) | not specified [RCV004852343] | uncertain significance | 8 | 53879427 | 53879427 | Human | | name |
| 597686438 | CV3586353 | single nucleotide variant | NM_170587.4(RGS20):c.413C>G (p.Pro138Arg) | not specified [RCV004852346] | uncertain significance | 8 | 53879505 | 53879505 | Human | | name |
| 597775797 | CV3586354 | single nucleotide variant | NM_003702.5(RGS20):c.324A>C (p.Glu108Asp) | not specified [RCV004852347] | uncertain significance | 8 | 53954097 | 53954097 | Human | | name |
| 597686449 | CV3586357 | single nucleotide variant | NM_170587.4(RGS20):c.416G>C (p.Gly139Ala) | not specified [RCV004852349] | uncertain significance | 8 | 53879508 | 53879508 | Human | | name |
| 597686458 | CV3586358 | single nucleotide variant | NM_170587.4(RGS20):c.467C>T (p.Pro156Leu) | not specified [RCV004852350] | uncertain significance | 8 | 53879559 | 53879559 | Human | | name |
| 597775805 | CV3586359 | single nucleotide variant | NM_003702.5(RGS20):c.490G>A (p.Ala164Thr) | not specified [RCV004852351] | uncertain significance | 8 | 53954263 | 53954263 | Human | | name |
| 597788099 | CV3586365 | single nucleotide variant | NM_015668.5(RGS22):c.880T>C (p.Tyr294His) | not specified [RCV004855409] | uncertain significance | 8 | 100063888 | 100063888 | Human | | name |
| 597788104 | CV3586368 | single nucleotide variant | NM_015668.5(RGS22):c.592G>C (p.Glu198Gln) | not specified [RCV004855410] | uncertain significance | 8 | 100071371 | 100071371 | Human | | name |
| 597788107 | CV3586371 | single nucleotide variant | NM_015668.5(RGS22):c.937G>C (p.Glu313Gln) | not specified [RCV004855411] | uncertain significance | 8 | 100063831 | 100063831 | Human | | name |
| 597788120 | CV3586380 | single nucleotide variant | NM_015668.5(RGS22):c.788A>C (p.Lys263Thr) | not specified [RCV004855414] | uncertain significance | 8 | 100063980 | 100063980 | Human | | name |
| 598188977 | CV3902558 | single nucleotide variant | NM_003702.5(RGS20):c.648C>A (p.Asp216Glu) | not specified [RCV005266652] | uncertain significance | 8 | 53958380 | 53958380 | Human | | name |
| 598189000 | CV3902561 | single nucleotide variant | NM_003702.5(RGS20):c.586G>C (p.Glu196Gln) | not specified [RCV005266655] | uncertain significance | 8 | 53958318 | 53958318 | Human | | name |
| 598189067 | CV3902569 | single nucleotide variant | NM_015668.5(RGS22):c.936T>G (p.Cys312Trp) | not specified [RCV005266663] | uncertain significance | 8 | 100063832 | 100063832 | Human | | name |
| 598189111 | CV3902575 | single nucleotide variant | NM_015668.5(RGS22):c.823G>A (p.Glu275Lys) | not specified [RCV005266669] | uncertain significance | 8 | 100063945 | 100063945 | Human | | name |
| 598189152 | CV3902580 | single nucleotide variant | NM_015668.5(RGS22):c.317T>G (p.Ile106Ser) | not specified [RCV005266674] | uncertain significance | 8 | 100080156 | 100080156 | Human | | name |
| 598189161 | CV3902581 | single nucleotide variant | NM_015668.5(RGS22):c.318T>G (p.Ile106Met) | not specified [RCV005266675] | uncertain significance | 8 | 100080155 | 100080155 | Human | | name |
| 15198099 | CV700705 | single nucleotide variant | NM_015668.5(RGS22):c.3651A>G (p.Leu1217=) | not provided [RCV000956652] | benign | 8 | 99962943 | 99962943 | Human | | name |
| 8624832 | CV79947 | single nucleotide variant | NM_001039152.3(RGS21):c.150C>T (p.Phe50=) | Malignant melanoma [RCV000060023] | not provided | 1 | 192352108 | 192352108 | Human | | name |
| 8626494 | CV81638 | single nucleotide variant | NM_015668.4(RGS22):c.379G>A (p.Glu127Lys) | Malignant melanoma [RCV000061716] | not provided | 8 | 100072191 | 100072191 | Human | | name |
| 156136383 | CV2196169 | single nucleotide variant | NM_015668.5(RGS22):c.2935C>T (p.Arg979Cys) | not specified [RCV004073528] | uncertain significance | 8 | 99999276 | 99999276 | Human | | name |
| 155947158 | CV2262573 | single nucleotide variant | NM_015668.5(RGS22):c.2105C>T (p.Ala702Val) | not specified [RCV004130781] | uncertain significance | 8 | 100038992 | 100038992 | Human | | name |
| 156337803 | CV2271182 | single nucleotide variant | NM_015668.5(RGS22):c.1805A>T (p.Asp602Val) | not specified [RCV004134545] | uncertain significance | 8 | 100047481 | 100047481 | Human | | name |
| 156019675 | CV2272664 | single nucleotide variant | NM_015668.5(RGS22):c.1669C>T (p.Pro557Ser) | not specified [RCV004133541] | uncertain significance | 8 | 100052822 | 100052822 | Human | | name |
| 155983307 | CV2273065 | single nucleotide variant | NM_015668.5(RGS22):c.2185G>A (p.Val729Ile) | not specified [RCV004137713] | likely benign | 8 | 100008551 | 100008551 | Human | | name |
| 156077003 | CV2331851 | single nucleotide variant | NM_015668.5(RGS22):c.2288A>G (p.Glu763Gly) | not specified [RCV004186509] | uncertain significance | 8 | 100008448 | 100008448 | Human | | name |
| 155985866 | CV2343960 | single nucleotide variant | NM_015668.5(RGS22):c.2489C>T (p.Ser830Leu) | not provided [RCV004695626]|not specified [RCV004195579] | uncertain significance | 8 | 100004064 | 100004064 | Human | | name |
| 156386145 | CV2364661 | single nucleotide variant | NM_015668.5(RGS22):c.2154C>G (p.Cys718Trp) | not specified [RCV004219550] | uncertain significance | 8 | 100038943 | 100038943 | Human | | name |
| 155933679 | CV2372322 | single nucleotide variant | NM_015668.5(RGS22):c.2210T>C (p.Ile737Thr) | not specified [RCV004217093] | uncertain significance | 8 | 100008526 | 100008526 | Human | | name |
| 156222347 | CV2394642 | single nucleotide variant | NM_015668.5(RGS22):c.1894A>C (p.Lys632Gln) | not specified [RCV004240982] | uncertain significance | 8 | 100041846 | 100041846 | Human | | name |
| 329372958 | CV2428725 | single nucleotide variant | NM_015668.5(RGS22):c.1080T>G (p.Ile360Met) | not specified [RCV004255515] | uncertain significance | 8 | 100063688 | 100063688 | Human | | name |
| 329391197 | CV2452143 | single nucleotide variant | NM_015668.5(RGS22):c.2555A>G (p.Lys852Arg) | not specified [RCV004278859] | uncertain significance | 8 | 100003998 | 100003998 | Human | | name |
| 401756417 | CV2687138 | single nucleotide variant | NM_015668.5(RGS22):c.1253T>G (p.Phe418Cys) | not specified [RCV004304441] | uncertain significance | 8 | 100063515 | 100063515 | Human | | name |
| 401876720 | CV2767692 | single nucleotide variant | NM_015668.5(RGS22):c.2471T>C (p.Ile824Thr) | not specified [RCV004345826] | uncertain significance | 8 | 100004082 | 100004082 | Human | | name |
| 401893937 | CV2770131 | single nucleotide variant | NM_015668.5(RGS22):c.1241A>G (p.Glu414Gly) | not specified [RCV004356032] | uncertain significance | 8 | 100063527 | 100063527 | Human | | name |
| 401890450 | CV2778735 | single nucleotide variant | NM_015668.5(RGS22):c.2779C>G (p.Gln927Glu) | not specified [RCV004346646] | uncertain significance | 8 | 100002213 | 100002213 | Human | | name |
| 401864560 | CV2781851 | single nucleotide variant | NM_015668.5(RGS22):c.2444A>G (p.Lys815Arg) | not specified [RCV004356799] | uncertain significance | 8 | 100006027 | 100006027 | Human | | name |
| 401881766 | CV2783950 | single nucleotide variant | NM_015668.5(RGS22):c.1679C>G (p.Pro560Arg) | not specified [RCV004362370] | uncertain significance | 8 | 100052812 | 100052812 | Human | | name |
| 401866038 | CV2786238 | single nucleotide variant | NM_015668.5(RGS22):c.1618C>A (p.Pro540Thr) | not specified [RCV004360026] | uncertain significance | 8 | 100052873 | 100052873 | Human | | name |
| 405715736 | CV3309225 | single nucleotide variant | NM_001039152.3(RGS21):c.38C>T (p.Ala13Val) | not specified [RCV004449164] | uncertain significance | 1 | 192347339 | 192347339 | Human | | name |
| 405715746 | CV3309226 | single nucleotide variant | NM_015668.5(RGS22):c.1075T>C (p.Ser359Pro) | not specified [RCV004449165] | likely benign | 8 | 100063693 | 100063693 | Human | | name |
| 405715760 | CV3309228 | single nucleotide variant | NM_015668.5(RGS22):c.1274C>G (p.Thr425Arg) | not specified [RCV004449167] | uncertain significance | 8 | 100063494 | 100063494 | Human | | name |
| 405715766 | CV3309229 | single nucleotide variant | NM_015668.5(RGS22):c.1585C>A (p.Leu529Ile) | not specified [RCV004449168] | uncertain significance | 8 | 100052906 | 100052906 | Human | | name |
| 405715771 | CV3309230 | single nucleotide variant | NM_015668.5(RGS22):c.1589G>A (p.Arg530His) | not specified [RCV004449169] | uncertain significance | 8 | 100052902 | 100052902 | Human | | name |
| 405715776 | CV3309231 | single nucleotide variant | NM_015668.5(RGS22):c.1775G>A (p.Arg592Gln) | not specified [RCV004449170] | uncertain significance | 8 | 100047511 | 100047511 | Human | | name |
| 405715782 | CV3309232 | single nucleotide variant | NM_015668.5(RGS22):c.1834A>G (p.Met612Val) | not specified [RCV004449171] | likely benign | 8 | 100041906 | 100041906 | Human | | name |
| 405715788 | CV3309233 | single nucleotide variant | NM_015668.5(RGS22):c.2126A>G (p.Gln709Arg) | not specified [RCV004449172] | uncertain significance | 8 | 100038971 | 100038971 | Human | | name |
| 405715800 | CV3309235 | single nucleotide variant | NM_015668.5(RGS22):c.2640G>A (p.Met880Ile) | not specified [RCV004449174] | uncertain significance | 8 | 100002352 | 100002352 | Human | | name |
| 405715810 | CV3309236 | single nucleotide variant | NM_015668.5(RGS22):c.2668A>G (p.Arg890Gly) | not specified [RCV004449175] | uncertain significance | 8 | 100002324 | 100002324 | Human | | name |
| 407508110 | CV3472822 | single nucleotide variant | NM_015668.5(RGS22):c.1757C>T (p.Thr586Ile) | not specified [RCV004671938] | likely benign | 8 | 100047529 | 100047529 | Human | | name |
| 407474272 | CV3472823 | single nucleotide variant | NM_015668.5(RGS22):c.1379A>G (p.Tyr460Cys) | not specified [RCV004662957] | uncertain significance | 8 | 100062726 | 100062726 | Human | | name |
| 407508113 | CV3472825 | single nucleotide variant | NM_015668.5(RGS22):c.2794A>G (p.Met932Val) | not specified [RCV004671939] | uncertain significance | 8 | 99999417 | 99999417 | Human | | name |
| 407474282 | CV3472827 | single nucleotide variant | NM_015668.5(RGS22):c.2140C>T (p.Pro714Ser) | not specified [RCV004662959] | uncertain significance | 8 | 100038957 | 100038957 | Human | | name |
| 407508119 | CV3472828 | single nucleotide variant | NM_015668.5(RGS22):c.1793G>A (p.Gly598Asp) | not specified [RCV004671941] | likely benign | 8 | 100047493 | 100047493 | Human | | name |
| 597775821 | CV3586366 | single nucleotide variant | NM_015668.5(RGS22):c.2179A>G (p.Thr727Ala) | not specified [RCV004852355] | uncertain significance | 8 | 100008557 | 100008557 | Human | | name |
| 597775824 | CV3586367 | single nucleotide variant | NM_015668.5(RGS22):c.2947A>C (p.Lys983Gln) | not specified [RCV004852356] | uncertain significance | 8 | 99999264 | 99999264 | Human | | name |
| 597788112 | CV3586372 | single nucleotide variant | NM_015668.5(RGS22):c.2327A>G (p.Lys776Arg) | not specified [RCV004855412] | uncertain significance | 8 | 100008409 | 100008409 | Human | | name |
| 597775836 | CV3586373 | single nucleotide variant | NM_015668.5(RGS22):c.1630A>G (p.Met544Val) | not specified [RCV004852359] | uncertain significance | 8 | 100052861 | 100052861 | Human | | name |
| 597775840 | CV3586374 | single nucleotide variant | NM_015668.5(RGS22):c.1048A>G (p.Lys350Glu) | not specified [RCV004852360] | likely benign | 8 | 100063720 | 100063720 | Human | | name |
| 597775844 | CV3586375 | single nucleotide variant | NM_015668.5(RGS22):c.1609G>T (p.Asp537Tyr) | not specified [RCV004852361] | uncertain significance | 8 | 100052882 | 100052882 | Human | | name |
| 597775848 | CV3586376 | single nucleotide variant | NM_015668.5(RGS22):c.2215C>T (p.Leu739Phe) | not specified [RCV004852362] | uncertain significance | 8 | 100008521 | 100008521 | Human | | name |
| 597775851 | CV3586377 | single nucleotide variant | NM_015668.5(RGS22):c.2524G>C (p.Asp842His) | not specified [RCV004852363] | uncertain significance | 8 | 100004029 | 100004029 | Human | | name |
| 597788116 | CV3586378 | single nucleotide variant | NM_015668.5(RGS22):c.2504C>G (p.Ser835Cys) | not specified [RCV004855413] | uncertain significance | 8 | 100004049 | 100004049 | Human | | name |
| 597775859 | CV3586381 | single nucleotide variant | NM_015668.5(RGS22):c.2966T>C (p.Ile989Thr) | not specified [RCV004852365] | uncertain significance | 8 | 99996514 | 99996514 | Human | | name |
| 598189049 | CV3902567 | single nucleotide variant | NM_001039152.3(RGS21):c.44C>T (p.Thr15Ile) | not specified [RCV005266661] | uncertain significance | 1 | 192347345 | 192347345 | Human | | name |
| 598189058 | CV3902568 | single nucleotide variant | NM_001039152.3(RGS21):c.34A>T (p.Thr12Ser) | not specified [RCV005266662] | uncertain significance | 1 | 192347335 | 192347335 | Human | | name |
| 598189071 | CV3902570 | single nucleotide variant | NM_015668.5(RGS22):c.1610A>G (p.Asp537Gly) | not specified [RCV005266664] | uncertain significance | 8 | 100052881 | 100052881 | Human | | name |
| 598189088 | CV3902572 | single nucleotide variant | NM_015668.5(RGS22):c.1252T>A (p.Phe418Ile) | not specified [RCV005266666] | uncertain significance | 8 | 100063516 | 100063516 | Human | | name |
| 598189103 | CV3902574 | single nucleotide variant | NM_015668.5(RGS22):c.1262T>G (p.Phe421Cys) | not specified [RCV005266668] | uncertain significance | 8 | 100063506 | 100063506 | Human | | name |
| 598189122 | CV3902576 | single nucleotide variant | NM_015668.5(RGS22):c.2508A>T (p.Lys836Asn) | not specified [RCV005266670] | uncertain significance | 8 | 100004045 | 100004045 | Human | | name |
| 598189129 | CV3902577 | single nucleotide variant | NM_015668.5(RGS22):c.1050A>C (p.Lys350Asn) | not specified [RCV005266671] | uncertain significance | 8 | 100063718 | 100063718 | Human | | name |
| 598189136 | CV3902578 | single nucleotide variant | NM_015668.5(RGS22):c.1051G>T (p.Val351Leu) | not specified [RCV005266672] | uncertain significance | 8 | 100063717 | 100063717 | Human | | name |
| 598189144 | CV3902579 | single nucleotide variant | NM_015668.5(RGS22):c.1618C>T (p.Pro540Ser) | not specified [RCV005266673] | uncertain significance | 8 | 100052873 | 100052873 | Human | | name |
| 598189176 | CV3902583 | single nucleotide variant | NM_015668.5(RGS22):c.1927G>A (p.Glu643Lys) | not specified [RCV005266677] | uncertain significance | 8 | 100041813 | 100041813 | Human | | name |
| 598189184 | CV3902584 | single nucleotide variant | NM_015668.5(RGS22):c.2785A>C (p.Asn929His) | not specified [RCV005266678] | uncertain significance | 8 | 100002207 | 100002207 | Human | | name |
| 598189193 | CV3902585 | single nucleotide variant | NM_015668.5(RGS22):c.2714A>T (p.Tyr905Phe) | not specified [RCV005266679] | uncertain significance | 8 | 100002278 | 100002278 | Human | | name |
| 598189208 | CV3902587 | single nucleotide variant | NM_015668.5(RGS22):c.2501T>C (p.Val834Ala) | not specified [RCV005266681] | uncertain significance | 8 | 100004052 | 100004052 | Human | | name |
| 598189217 | CV3902588 | single nucleotide variant | NM_015668.5(RGS22):c.2777A>G (p.Tyr926Cys) | not specified [RCV005266682] | uncertain significance | 8 | 100002215 | 100002215 | Human | | name |
| 598189232 | CV3902590 | single nucleotide variant | NM_015668.5(RGS22):c.2854G>A (p.Val952Ile) | not specified [RCV005266684] | likely benign | 8 | 99999357 | 99999357 | Human | | name |
| 8626493 | CV81637 | single nucleotide variant | NM_015668.4(RGS22):c.2344C>T (p.Gln782Ter) | Malignant melanoma [RCV000061715] | not provided | 8 | 100008392 | 100008392 | Human | | name |
| 8632739 | CV87954 | single nucleotide variant | NM_015668.4(RGS22):c.1187G>A (p.Ser396Asn) | Malignant melanoma [RCV000068046] | not provided | 8 | 100063581 | 100063581 | Human | | name |
| 156180219 | CV2225876 | single nucleotide variant | NM_015668.5(RGS22):c.3485A>T (p.Lys1162Ile) | not specified [RCV004103269] | uncertain significance | 8 | 99977951 | 99977951 | Human | | name |
| 156057181 | CV2266674 | single nucleotide variant | NM_015668.5(RGS22):c.3509A>T (p.Lys1170Ile) | not provided [RCV004695472]|not specified [RCV004131207] | uncertain significance | 8 | 99977927 | 99977927 | Human | | name |
| 156084938 | CV2343371 | single nucleotide variant | NM_015668.5(RGS22):c.3323G>A (p.Arg1108Gln) | not specified [RCV004194985] | uncertain significance | 8 | 99981974 | 99981974 | Human | | name |
| 156284307 | CV2349012 | single nucleotide variant | NM_001039152.3(RGS21):c.148T>C (p.Phe50Leu) | not specified [RCV004203438] | uncertain significance | 1 | 192352106 | 192352106 | Human | | name |
| 156172732 | CV2355101 | single nucleotide variant | NM_015668.5(RGS22):c.3151C>G (p.Leu1051Val) | not specified [RCV004198493] | uncertain significance | 8 | 99987487 | 99987487 | Human | | name |
| 155906644 | CV2379085 | single nucleotide variant | NM_015668.5(RGS22):c.3505G>A (p.Glu1169Lys) | not specified [RCV004233839] | uncertain significance | 8 | 99977931 | 99977931 | Human | | name |
| 156188639 | CV2395482 | single nucleotide variant | NM_015668.5(RGS22):c.3523G>A (p.Gly1175Arg) | not specified [RCV004241348] | uncertain significance | 8 | 99965427 | 99965427 | Human | | name |
| 329381323 | CV2440786 | single nucleotide variant | NM_015668.5(RGS22):c.3236T>C (p.Ile1079Thr) | not specified [RCV004258729] | uncertain significance | 8 | 99982061 | 99982061 | Human | | name |
| 401779004 | CV2702012 | single nucleotide variant | NM_001039152.3(RGS21):c.140A>G (p.Asn47Ser) | not specified [RCV004320600] | uncertain significance | 1 | 192352098 | 192352098 | Human | | name |
| 405715729 | CV3309224 | single nucleotide variant | NM_001039152.3(RGS21):c.146A>C (p.Glu49Ala) | not specified [RCV004449163] | uncertain significance | 1 | 192352104 | 192352104 | Human | | name |
| 405715832 | CV3309239 | single nucleotide variant | NM_015668.5(RGS22):c.3611G>A (p.Arg1204Gln) | not specified [RCV004449178] | uncertain significance | 8 | 99965339 | 99965339 | Human | | name |
| 405715847 | CV3309241 | single nucleotide variant | NM_015668.5(RGS22):c.3628T>C (p.Tyr1210His) | not specified [RCV004449180] | uncertain significance | 8 | 99962966 | 99962966 | Human | | name |
| 407508116 | CV3472826 | single nucleotide variant | NM_015668.5(RGS22):c.3355G>A (p.Ala1119Thr) | not specified [RCV004671940] | uncertain significance | 8 | 99981942 | 99981942 | Human | | name |
| 597775809 | CV3586360 | single nucleotide variant | NM_001039152.3(RGS21):c.219T>G (p.Ile73Met) | not specified [RCV004852352] | uncertain significance | 1 | 192352177 | 192352177 | Human | | name |
| 597775813 | CV3586361 | single nucleotide variant | NM_001039152.3(RGS21):c.166G>T (p.Asp56Tyr) | not specified [RCV004852353] | uncertain significance | 1 | 192352124 | 192352124 | Human | | name |
| 597788092 | CV3586363 | single nucleotide variant | NM_001039152.3(RGS21):c.171T>A (p.Phe57Leu) | not specified [RCV004855407] | uncertain significance | 1 | 192352129 | 192352129 | Human | | name |
| 597788096 | CV3586364 | single nucleotide variant | NM_001039152.3(RGS21):c.248C>G (p.Pro83Arg) | not specified [RCV004855408] | uncertain significance | 1 | 192352206 | 192352206 | Human | | name |
| 597775828 | CV3586369 | single nucleotide variant | NM_015668.5(RGS22):c.3469A>C (p.Asn1157His) | not specified [RCV004852357] | uncertain significance | 8 | 99977967 | 99977967 | Human | | name |
| 598189034 | CV3902565 | single nucleotide variant | NM_001039152.3(RGS21):c.161G>A (p.Cys54Tyr) | not specified [RCV005266659] | uncertain significance | 1 | 192352119 | 192352119 | Human | | name |
| 598189041 | CV3902566 | single nucleotide variant | NM_001039152.3(RGS21):c.248C>T (p.Pro83Leu) | not specified [RCV005266660] | uncertain significance | 1 | 192352206 | 192352206 | Human | | name |
| 598189095 | CV3902573 | single nucleotide variant | NM_015668.5(RGS22):c.3152T>C (p.Leu1051Pro) | not specified [RCV005266667] | uncertain significance | 8 | 99987486 | 99987486 | Human | | name |
| 598189200 | CV3902586 | single nucleotide variant | NM_015668.5(RGS22):c.3647C>G (p.Ala1216Gly) | not specified [RCV005266680] | uncertain significance | 8 | 99962947 | 99962947 | Human | | name |
| 598189225 | CV3902589 | single nucleotide variant | NM_015668.5(RGS22):c.3707C>A (p.Ala1236Glu) | not specified [RCV005266683] | uncertain significance | 8 | 99962887 | 99962887 | Human | | name |
| 15168836 | CV723228 | single nucleotide variant | NM_015668.5(RGS22):c.3793T>C (p.Ter1265Arg) | not provided [RCV000889201] | benign | 8 | 99962441 | 99962441 | Human | | name |
| 156240564 | CV2213663 | single nucleotide variant | NM_001039152.3(RGS21):c.410T>C (p.Val137Ala) | not specified [RCV004089740] | uncertain significance | 1 | 192366075 | 192366075 | Human | | name |
