| 405272839 | CV3190662 | single nucleotide variant | NM_006995.5(BTN2A2):c.932-3C>T | BTN2A2-related disorder [RCV003907099] | likely benign | 6 | 26390684 | 26390684 | Human | | name , trait , alternate_id |
| 405272810 | CV3195744 | single nucleotide variant | NM_006995.5(BTN2A2):c.443-8C>G | BTN2A2-related disorder [RCV003906975] | likely benign | 6 | 26388005 | 26388005 | Human | | name , trait , alternate_id |
| 405280006 | CV3197025 | single nucleotide variant | NM_006995.5(BTN2A2):c.980-88G>C | BTN2A2-related disorder [RCV003979866] | benign | 6 | 26392287 | 26392287 | Human | | name , trait , alternate_id |
| 405279344 | CV3200046 | single nucleotide variant | NM_006995.5(BTN2A2):c.57G>A (p.Leu19=) | BTN2A2-related disorder [RCV003974045] | benign | 6 | 26383878 | 26383878 | Human | 1 | name , trait , alternate_id |
| 405279344 | CV3200046 | single nucleotide variant | NM_006995.5(BTN2A2):c.57G>A (p.Leu19=) | BTN2A2-related disorder [RCV003974045] | benign | 6 | 26383878 | 26383879 | Human | 1 | name , trait , alternate_id |
| 329350129 | CV2466257 | single nucleotide variant | NM_006995.5(BTN2A2):c.13G>A (p.Ala5Thr) | not specified [RCV004279882] | uncertain significance | 6 | 26383834 | 26383834 | Human | | name |
| 15174590 | CV710367 | single nucleotide variant | NM_006995.5(BTN2A2):c.11C>T (p.Ala4Val) | not provided [RCV000972749] | benign | 6 | 26383832 | 26383832 | Human | | name |
| 156069554 | CV2203800 | single nucleotide variant | NM_006995.5(BTN2A2):c.47T>C (p.Leu16Pro) | not specified [RCV004074440] | uncertain significance | 6 | 26383868 | 26383868 | Human | | name |
| 401745394 | CV2711819 | single nucleotide variant | NM_006995.5(BTN2A2):c.43C>T (p.Leu15Phe) | not specified [RCV004309458] | uncertain significance | 6 | 26383864 | 26383864 | Human | | name |
| 405280121 | CV3192969 | single nucleotide variant | NM_006995.5(BTN2A2):c.411C>T (p.Tyr137=) | BTN2A2-related disorder [RCV003981655] | likely benign | 6 | 26385331 | 26385331 | Human | | name , trait , alternate_id |
| 405276358 | CV3209851 | single nucleotide variant | NM_006995.5(BTN2A2):c.354C>T (p.Asn118=) | BTN2A2-related disorder [RCV003944499] | likely benign | 6 | 26385274 | 26385274 | Human | | name , trait , alternate_id |
| 405277737 | CV3216237 | single nucleotide variant | NM_006995.5(BTN2A2):c.780C>T (p.Thr260=) | BTN2A2-related disorder [RCV003956755] | likely benign | 6 | 26390060 | 26390060 | Human | | name , trait , alternate_id |
| 405278684 | CV3220788 | single nucleotide variant | NM_006995.5(BTN2A2):c.627A>G (p.Thr209=) | BTN2A2-related disorder [RCV003968969] | likely benign | 6 | 26388197 | 26388197 | Human | | name , trait , alternate_id |
| 597785007 | CV3647163 | single nucleotide variant | NM_006995.5(BTN2A2):c.79T>C (p.Cys27Arg) | not specified [RCV004900628] | uncertain significance | 6 | 26383900 | 26383900 | Human | | name |
| 598186804 | CV3949840 | single nucleotide variant | NM_006995.5(BTN2A2):c.89T>G (p.Val30Gly) | not specified [RCV005311916] | uncertain significance | 6 | 26383910 | 26383910 | Human | | name |
| 155993418 | CV2286298 | single nucleotide variant | NM_006995.5(BTN2A2):c.143G>T (p.Gly48Val) | not specified [RCV004146250] | uncertain significance | 6 | 26385063 | 26385063 | Human | | name |
| 156298276 | CV2310602 | single nucleotide variant | NM_006995.5(BTN2A2):c.206G>A (p.Arg69Gln) | not specified [RCV004157269] | uncertain significance | 6 | 26385126 | 26385126 | Human | | name |
| 156281917 | CV2321964 | single nucleotide variant | NM_006995.5(BTN2A2):c.232G>A (p.Ala78Thr) | not specified [RCV004173420] | uncertain significance | 6 | 26385152 | 26385152 | Human | | name |
| 405279440 | CV3193528 | single nucleotide variant | NM_006995.5(BTN2A2):c.1398G>A (p.Ser466=) | BTN2A2-related disorder [RCV003974696] | benign | 6 | 26392793 | 26392793 | Human | 4 | name , trait , alternate_id |
| 405274809 | CV3210398 | single nucleotide variant | NM_006995.5(BTN2A2):c.1095C>T (p.Phe365=) | BTN2A2-related disorder [RCV003931370] | likely benign | 6 | 26392490 | 26392490 | Human | | name , trait , alternate_id |
| 405711154 | CV3298662 | single nucleotide variant | NM_006995.5(BTN2A2):c.112G>T (p.Gly38Trp) | not specified [RCV004426832] | uncertain significance | 6 | 26385032 | 26385032 | Human | | name |
| 405711172 | CV3298665 | single nucleotide variant | NM_006995.5(BTN2A2):c.115C>A (p.Pro39Thr) | not specified [RCV004426835] | uncertain significance | 6 | 26385035 | 26385035 | Human | | name |
| 405711185 | CV3298667 | single nucleotide variant | NM_006995.5(BTN2A2):c.178G>A (p.Glu60Lys) | not specified [RCV004426837] | uncertain significance | 6 | 26385098 | 26385098 | Human | | name |
| 405711192 | CV3298668 | single nucleotide variant | NM_006995.5(BTN2A2):c.185A>C (p.Asn62Thr) | not specified [RCV004426838] | uncertain significance | 6 | 26385105 | 26385105 | Human | | name |
| 597749803 | CV3647164 | single nucleotide variant | NM_006995.5(BTN2A2):c.230C>G (p.Pro77Arg) | not specified [RCV004892431] | uncertain significance | 6 | 26385150 | 26385150 | Human | | name |
| 598186792 | CV3949838 | single nucleotide variant | NM_006995.5(BTN2A2):c.196A>G (p.Met66Val) | not specified [RCV005311914] | uncertain significance | 6 | 26385116 | 26385116 | Human | | name |
| 15174595 | CV710368 | single nucleotide variant | NM_006995.5(BTN2A2):c.115C>G (p.Pro39Ala) | not provided [RCV000972750] | benign | 6 | 26385035 | 26385035 | Human | | name |
| 155920943 | CV2240446 | single nucleotide variant | NM_006995.5(BTN2A2):c.397G>A (p.Glu133Lys) | not specified [RCV004117332] | uncertain significance | 6 | 26385317 | 26385317 | Human | | name |
| 156360828 | CV2329677 | single nucleotide variant | NM_006995.5(BTN2A2):c.382C>T (p.Arg128Cys) | not specified [RCV004180789] | uncertain significance | 6 | 26385302 | 26385302 | Human | | name |
| 156138697 | CV2374245 | single nucleotide variant | NM_006995.5(BTN2A2):c.980C>T (p.Ala327Val) | not specified [RCV004603392] | uncertain significance | 6 | 26392375 | 26392375 | Human | | name |
| 155993452 | CV2379416 | single nucleotide variant | NM_006995.5(BTN2A2):c.311G>T (p.Ser104Ile) | not specified [RCV004223867] | uncertain significance | 6 | 26385231 | 26385231 | Human | | name |
| 156042899 | CV2381498 | single nucleotide variant | NM_006995.5(BTN2A2):c.691G>A (p.Gly231Ser) | not specified [RCV004229976] | uncertain significance | 6 | 26388261 | 26388261 | Human | | name |
| 329349549 | CV2446025 | single nucleotide variant | NM_006995.5(BTN2A2):c.430C>A (p.Leu144Ile) | not specified [RCV004270602] | uncertain significance | 6 | 26385350 | 26385350 | Human | | name |
| 401746269 | CV2712155 | single nucleotide variant | NM_006995.5(BTN2A2):c.427C>T (p.Arg143Cys) | not specified [RCV004311878] | uncertain significance | 6 | 26385347 | 26385347 | Human | | name |
| 401857162 | CV2778479 | single nucleotide variant | NM_006995.5(BTN2A2):c.825C>A (p.Phe275Leu) | not specified [RCV004344142] | likely benign | 6 | 26390105 | 26390105 | Human | | name |
| 405279336 | CV3199985 | single nucleotide variant | NM_006995.5(BTN2A2):c.607G>A (p.Gly203Ser) | BTN2A2-related disorder [RCV003973997] | benign | 6 | 26388177 | 26388177 | Human | | name , trait , alternate_id |
| 405277944 | CV3205588 | single nucleotide variant | NM_006995.5(BTN2A2):c.574G>T (p.Ala192Ser) | BTN2A2-related disorder [RCV003959729] | likely benign | 6 | 26388144 | 26388144 | Human | | name , trait , alternate_id |
| 405711200 | CV3298669 | single nucleotide variant | NM_006995.5(BTN2A2):c.359C>T (p.Thr120Ile) | not specified [RCV004426839] | uncertain significance | 6 | 26385279 | 26385279 | Human | | name |
| 405711218 | CV3298671 | single nucleotide variant | NM_006995.5(BTN2A2):c.559G>A (p.Gly187Ser) | not specified [RCV004426841] | likely benign | 6 | 26388129 | 26388129 | Human | | name |
| 405711223 | CV3298672 | single nucleotide variant | NM_006995.5(BTN2A2):c.665C>A (p.Ser222Tyr) | not specified [RCV004426842] | uncertain significance | 6 | 26388235 | 26388235 | Human | | name |
| 405711228 | CV3298673 | single nucleotide variant | NM_006995.5(BTN2A2):c.760G>A (p.Ala254Thr) | not specified [RCV004426843] | uncertain significance | 6 | 26390040 | 26390040 | Human | | name |
| 405711236 | CV3298674 | single nucleotide variant | NM_006995.5(BTN2A2):c.845G>A (p.Ser282Asn) | not specified [RCV004426844] | uncertain significance | 6 | 26390125 | 26390125 | Human | | name |
| 407489140 | CV3417779 | single nucleotide variant | NM_006995.5(BTN2A2):c.733A>T (p.Met245Leu) | not specified [RCV004604126] | uncertain significance | 6 | 26390013 | 26390013 | Human | | name |
| 597784991 | CV3647158 | single nucleotide variant | NM_006995.5(BTN2A2):c.410A>T (p.Tyr137Phe) | not specified [RCV004900624] | uncertain significance | 6 | 26385330 | 26385330 | Human | | name |
| 597785000 | CV3647161 | single nucleotide variant | NM_006995.5(BTN2A2):c.913G>A (p.Glu305Lys) | not specified [RCV004900626] | uncertain significance | 6 | 26390193 | 26390193 | Human | | name |
| 597749808 | CV3647165 | single nucleotide variant | NM_006995.5(BTN2A2):c.749C>T (p.Pro250Leu) | not specified [RCV004892432] | uncertain significance | 6 | 26390029 | 26390029 | Human | | name |
| 598211301 | CV3949833 | single nucleotide variant | NM_006995.5(BTN2A2):c.657G>C (p.Arg219Ser) | not specified [RCV005315990] | uncertain significance | 6 | 26388227 | 26388227 | Human | | name |
| 598211309 | CV3949836 | single nucleotide variant | NM_006995.5(BTN2A2):c.583G>A (p.Glu195Lys) | not specified [RCV005315991] | uncertain significance | 6 | 26388153 | 26388153 | Human | | name |
| 598186798 | CV3949839 | single nucleotide variant | NM_006995.5(BTN2A2):c.683C>T (p.Thr228Ile) | not specified [RCV005311915] | uncertain significance | 6 | 26388253 | 26388253 | Human | | name |
| 598186811 | CV3949842 | single nucleotide variant | NM_006995.5(BTN2A2):c.832T>G (p.Phe278Val) | not specified [RCV005311917] | uncertain significance | 6 | 26390112 | 26390112 | Human | | name |
| 15108418 | CV721921 | single nucleotide variant | NM_006995.5(BTN2A2):c.799T>G (p.Ser267Ala) | not provided [RCV000893667] | benign | 6 | 26390079 | 26390079 | Human | | name |
| 156141555 | CV2208427 | single nucleotide variant | NM_006995.5(BTN2A2):c.1052G>A (p.Arg351Gln) | not specified [RCV004090971] | uncertain significance | 6 | 26392447 | 26392447 | Human | | name |
| 155934369 | CV2225275 | single nucleotide variant | NM_006995.5(BTN2A2):c.1288C>G (p.Leu430Val) | not specified [RCV004098920] | uncertain significance | 6 | 26392683 | 26392683 | Human | | name |
| 156274799 | CV2279847 | single nucleotide variant | NM_006995.5(BTN2A2):c.1144C>G (p.His382Asp) | not specified [RCV004144446] | uncertain significance | 6 | 26392539 | 26392539 | Human | | name |
| 155955580 | CV2303923 | single nucleotide variant | NM_006995.5(BTN2A2):c.1382A>T (p.Asn461Ile) | not specified [RCV004168201] | uncertain significance | 6 | 26392777 | 26392777 | Human | | name |
| 156297886 | CV2310565 | single nucleotide variant | NM_006995.5(BTN2A2):c.1152G>C (p.Trp384Cys) | not specified [RCV004163582] | uncertain significance | 6 | 26392547 | 26392547 | Human | | name |
| 156289730 | CV2333212 | single nucleotide variant | NM_006995.5(BTN2A2):c.1015G>A (p.Glu339Lys) | not specified [RCV004599584] | uncertain significance | 6 | 26392410 | 26392410 | Human | | name |
| 156129944 | CV2364788 | single nucleotide variant | NM_006995.5(BTN2A2):c.1178T>A (p.Val393Glu) | BTN2A2-related disorder [RCV003936684]|not specified [RCV004219656] | likely benign|uncertain significance | 6 | 26392573 | 26392573 | Human | | name , trait , alternate_id |
| 156386825 | CV2364858 | single nucleotide variant | NM_006995.5(BTN2A2):c.1176G>T (p.Met392Ile) | BTN2A2-related disorder [RCV003928929]|not specified [RCV004219718] | likely benign|uncertain significance | 6 | 26392571 | 26392571 | Human | | name , trait , alternate_id |
| 156101881 | CV2367706 | single nucleotide variant | NM_006995.5(BTN2A2):c.1361C>T (p.Ala454Val) | not specified [RCV004211620] | uncertain significance | 6 | 26392756 | 26392756 | Human | | name |
| 329349501 | CV2430499 | single nucleotide variant | NM_006995.5(BTN2A2):c.1525G>A (p.Glu509Lys) | not specified [RCV004252085] | uncertain significance | 6 | 26392920 | 26392920 | Human | | name |
| 329350536 | CV2470081 | single nucleotide variant | NM_006995.5(BTN2A2):c.1484T>C (p.Ile495Thr) | not specified [RCV004287343] | uncertain significance | 6 | 26392879 | 26392879 | Human | | name |
| 401858508 | CV2780789 | single nucleotide variant | NM_006995.5(BTN2A2):c.1334G>C (p.Arg445Pro) | not specified [RCV004352111] | uncertain significance | 6 | 26392729 | 26392729 | Human | | name |
| 405276321 | CV3204279 | single nucleotide variant | NM_006995.5(BTN2A2):c.1517T>C (p.Met506Thr) | BTN2A2-related disorder [RCV003944121] | likely benign | 6 | 26392912 | 26392912 | Human | | name , trait , alternate_id |
| 405272869 | CV3213687 | single nucleotide variant | NM_006995.5(BTN2A2):c.1379A>G (p.Tyr460Cys) | BTN2A2-related disorder [RCV003907371] | benign | 6 | 26392774 | 26392774 | Human | | name , trait , alternate_id |
| 405274436 | CV3213949 | single nucleotide variant | NM_006995.5(BTN2A2):c.1201C>G (p.His401Asp) | BTN2A2-related disorder [RCV003926802] | likely benign | 6 | 26392596 | 26392596 | Human | | name , trait , alternate_id |
| 405279899 | CV3217004 | single nucleotide variant | NM_006995.5(BTN2A2):c.1006G>A (p.Ala336Thr) | BTN2A2-related disorder [RCV003979150] | benign | 6 | 26392401 | 26392401 | Human | | name , trait , alternate_id |
| 405711146 | CV3298661 | single nucleotide variant | NM_006995.5(BTN2A2):c.1003A>G (p.Thr335Ala) | not specified [RCV004426831] | uncertain significance | 6 | 26392398 | 26392398 | Human | | name |
| 405711159 | CV3298663 | single nucleotide variant | NM_006995.5(BTN2A2):c.1132G>A (p.Ala378Thr) | not specified [RCV004426833] | uncertain significance | 6 | 26392527 | 26392527 | Human | | name |
| 405711178 | CV3298666 | single nucleotide variant | NM_006995.5(BTN2A2):c.1429A>T (p.Thr477Ser) | not specified [RCV004426836] | likely benign | 6 | 26392824 | 26392824 | Human | | name |
| 597784987 | CV3647157 | single nucleotide variant | NM_006995.5(BTN2A2):c.1011T>A (p.His337Gln) | not specified [RCV004900623] | uncertain significance | 6 | 26392406 | 26392406 | Human | | name |
| 597749798 | CV3647159 | single nucleotide variant | NM_006995.5(BTN2A2):c.1013C>A (p.Pro338His) | not specified [RCV004892430] | uncertain significance | 6 | 26392408 | 26392408 | Human | | name |
| 597784995 | CV3647160 | single nucleotide variant | NM_006995.5(BTN2A2):c.1418G>A (p.Arg473His) | not specified [RCV004900625] | uncertain significance | 6 | 26392813 | 26392813 | Human | | name |
| 597785003 | CV3647162 | single nucleotide variant | NM_006995.5(BTN2A2):c.1304G>A (p.Arg435Lys) | not specified [RCV004900627] | likely benign | 6 | 26392699 | 26392699 | Human | | name |
| 598186779 | CV3949834 | single nucleotide variant | NM_006995.5(BTN2A2):c.1017G>T (p.Glu339Asp) | not specified [RCV005311912] | uncertain significance | 6 | 26392412 | 26392412 | Human | | name |
| 598186786 | CV3949835 | single nucleotide variant | NM_006995.5(BTN2A2):c.1061A>G (p.Tyr354Cys) | not specified [RCV005311913] | uncertain significance | 6 | 26392456 | 26392456 | Human | | name |
| 598211316 | CV3949837 | single nucleotide variant | NM_006995.5(BTN2A2):c.1159G>A (p.Glu387Lys) | not specified [RCV005315992] | uncertain significance | 6 | 26392554 | 26392554 | Human | | name |
| 15099924 | CV699488 | single nucleotide variant | NM_006995.5(BTN2A2):c.1435C>T (p.Pro479Ser) | BTN2A2-related disorder [RCV003926089]|not provided [RCV000958835] | benign | 6 | 26392830 | 26392830 | Human | | name , trait , alternate_id |
| 15127229 | CV710369 | single nucleotide variant | NM_006995.5(BTN2A2):c.1282C>T (p.Arg428Trp) | BTN2A2-related disorder [RCV003905863]|not provided [RCV000963865] | benign | 6 | 26392677 | 26392677 | Human | | name , trait , alternate_id |
| 15174600 | CV710370 | single nucleotide variant | NM_006995.5(BTN2A2):c.1538A>C (p.Lys513Thr) | not provided [RCV000972751] | benign | 6 | 26392933 | 26392933 | Human | | name |
| 8631936 | CV87142 | single nucleotide variant | NM_001197237.1(BTN2A2):c.184A>T (p.Asn62Tyr) | Malignant melanoma [RCV000067233] | not provided | 6 | 26385104 | 26385104 | Human | | name |
