| 405282617 | CV3220627 | single nucleotide variant | NM_001783.4(CD79A):c.*4C>T | CD79A-related disorder [RCV003978943] | likely benign | 19 | 41880984 | 41880984 | Human | | name , trait , alternate_id |
| 156315591 | CV1910281 | single nucleotide variant | NM_001783.4(CD79A):c.79+6T>C | Agammaglobulinemia 3, autosomal recessive [RCV002599923] | uncertain significance | 19 | 41877389 | 41877389 | Human | 1 | name , alternate_id |
| 156021959 | CV2148233 | single nucleotide variant | NM_001783.4(CD79A):c.79+8G>A | Agammaglobulinemia 3, autosomal recessive [RCV003018274] | likely benign | 19 | 41877391 | 41877391 | Human | 1 | name , alternate_id |
| 597916614 | CV3811003 | single nucleotide variant | NM_001783.4(CD79A):c.80-8C>G | Agammaglobulinemia 3, autosomal recessive [RCV005155038] | likely benign | 19 | 41878982 | 41878982 | Human | 1 | name , alternate_id |
| 126743294 | CV998622 | single nucleotide variant | NM_001783.4(CD79A):c.80-3C>T | Agammaglobulinemia 3, autosomal recessive [RCV001296170] | uncertain significance | 19 | 41878987 | 41878987 | Human | 1 | name , alternate_id |
| 151817475 | CV1441172 | single nucleotide variant | NM_001783.4(CD79A):c.79+14G>A | Agammaglobulinemia 3, autosomal recessive [RCV001933816] | likely benign|uncertain significance | 19 | 41877397 | 41877397 | Human | 1 | name , alternate_id |
| 156446932 | CV1948617 | single nucleotide variant | NM_001783.4(CD79A):c.380-8C>T | Agammaglobulinemia 3, autosomal recessive [RCV003118453] | likely benign | 19 | 41879527 | 41879527 | Human | 1 | name , alternate_id |
| 155902554 | CV2007101 | single nucleotide variant | NM_001783.4(CD79A):c.80-12G>A | Agammaglobulinemia 3, autosomal recessive [RCV002681193] | likely benign | 19 | 41878978 | 41878978 | Human | 1 | name , alternate_id |
| 156303004 | CV2013561 | single nucleotide variant | NM_001783.4(CD79A):c.379+3G>A | Agammaglobulinemia 3, autosomal recessive [RCV002716146] | uncertain significance | 19 | 41879292 | 41879292 | Human | 1 | name , alternate_id |
| 156243704 | CV2086099 | single nucleotide variant | NM_001783.4(CD79A):c.568-6T>C | Agammaglobulinemia 3, autosomal recessive [RCV002876689] | likely benign | 19 | 41880861 | 41880861 | Human | 1 | name , alternate_id |
| 156167332 | CV2169700 | single nucleotide variant | NM_001783.4(CD79A):c.499-1G>A | Agammaglobulinemia 3, autosomal recessive [RCV003023406] | likely pathogenic | 19 | 41880669 | 41880669 | Human | 1 | name , alternate_id |
| 156170473 | CV2190296 | single nucleotide variant | NM_001783.4(CD79A):c.498+6C>A | Agammaglobulinemia 3, autosomal recessive [RCV003041016] | uncertain significance | 19 | 41879659 | 41879659 | Human | 1 | name , alternate_id |
| 405065093 | CV3036819 | single nucleotide variant | NM_001783.4(CD79A):c.499-8C>T | Agammaglobulinemia 3, autosomal recessive [RCV003632382] | likely benign | 19 | 41880662 | 41880662 | Human | 1 | name , alternate_id |
| 8566354 | CV32745 | single nucleotide variant | NM_001783.4(CD79A):c.380-2A>G | Agammaglobulinemia 3, autosomal recessive [RCV000019280] | pathogenic | 19 | 41879533 | 41879533 | Human | 1 | name , alternate_id |
| 8566355 | CV32746 | single nucleotide variant | NM_001783.4(CD79A):c.379+1G>A | Agammaglobulinemia 3, autosomal recessive [RCV000019281] | pathogenic|likely pathogenic | 19 | 41879290 | 41879290 | Human | 1 | name , alternate_id |
| 597914872 | CV3740661 | single nucleotide variant | NM_001783.4(CD79A):c.380-7C>T | Agammaglobulinemia 3, autosomal recessive [RCV005073998] | likely benign | 19 | 41879528 | 41879528 | Human | 1 | name , alternate_id |
| 597926736 | CV3778534 | single nucleotide variant | NM_001783.4(CD79A):c.80-13T>G | Agammaglobulinemia 3, autosomal recessive [RCV005131057] | likely benign | 19 | 41878977 | 41878977 | Human | 1 | name , alternate_id |
| 597893792 | CV3809991 | single nucleotide variant | NM_001783.4(CD79A):c.568-9C>G | Agammaglobulinemia 3, autosomal recessive [RCV005151712] | likely benign | 19 | 41880858 | 41880858 | Human | 1 | name , alternate_id |
| 597936147 | CV3845380 | single nucleotide variant | NM_001783.4(CD79A):c.79+15G>A | Agammaglobulinemia 3, autosomal recessive [RCV005186693] | likely benign | 19 | 41877398 | 41877398 | Human | 1 | name , alternate_id |
| 150484471 | CV1222502 | single nucleotide variant | NM_001783.4(CD79A):c.80-303G>A | not provided [RCV001617505] | benign | 19 | 41878687 | 41878687 | Human | | name |
| 151814940 | CV1507470 | single nucleotide variant | NM_001783.4(CD79A):c.499-17C>T | Agammaglobulinemia 3, autosomal recessive [RCV001954188] | likely benign | 19 | 41880653 | 41880653 | Human | 1 | name , alternate_id |
| 152171337 | CV1544102 | single nucleotide variant | NM_001783.4(CD79A):c.498+10C>A | Agammaglobulinemia 3, autosomal recessive [RCV002162076] | likely benign | 19 | 41879663 | 41879663 | Human | 1 | name , alternate_id |
| 152083273 | CV1554688 | single nucleotide variant | NM_001783.4(CD79A):c.567+12G>A | Agammaglobulinemia 3, autosomal recessive [RCV002211698] | likely benign | 19 | 41880750 | 41880750 | Human | 1 | name , alternate_id |
| 152107705 | CV1624090 | single nucleotide variant | NM_001783.4(CD79A):c.498+12C>T | Agammaglobulinemia 3, autosomal recessive [RCV002134074] | likely benign | 19 | 41879665 | 41879665 | Human | 1 | name , alternate_id |
| 152135099 | CV1638500 | single nucleotide variant | NM_001783.4(CD79A):c.498+13G>A | Agammaglobulinemia 3, autosomal recessive [RCV002083397] | likely benign | 19 | 41879666 | 41879666 | Human | 1 | name , alternate_id |
| 152032736 | CV1643169 | single nucleotide variant | NM_001783.4(CD79A):c.567+19T>G | Agammaglobulinemia 3, autosomal recessive [RCV002205036] | likely benign | 19 | 41880757 | 41880757 | Human | 1 | name , alternate_id |
| 152040669 | CV1649239 | single nucleotide variant | NM_001783.4(CD79A):c.499-15C>T | Agammaglobulinemia 3, autosomal recessive [RCV002206296] | likely benign | 19 | 41880655 | 41880655 | Human | 1 | name , alternate_id |
| 155945719 | CV1875475 | single nucleotide variant | NM_001783.4(CD79A):c.499-18C>A | Agammaglobulinemia 3, autosomal recessive [RCV003073833] | likely benign | 19 | 41880652 | 41880652 | Human | 1 | name , alternate_id |
| 405042151 | CV2870458 | duplication | NM_001783.4(CD79A):c.379+23dup | Agammaglobulinemia 3, autosomal recessive [RCV003518097] | benign | 19 | 41879308 | 41879309 | Human | 1 | name , alternate_id |
| 405029486 | CV2895785 | single nucleotide variant | NM_001783.4(CD79A):c.568-16C>T | Agammaglobulinemia 3, autosomal recessive [RCV003516657] | likely benign | 19 | 41880851 | 41880851 | Human | 1 | name , alternate_id |
| 405051710 | CV2942934 | single nucleotide variant | NM_001783.4(CD79A):c.499-18C>T | Agammaglobulinemia 3, autosomal recessive [RCV003631339] | likely benign | 19 | 41880652 | 41880652 | Human | 1 | name , alternate_id |
| 405061746 | CV3016698 | single nucleotide variant | NM_001783.4(CD79A):c.499-14A>C | Agammaglobulinemia 3, autosomal recessive [RCV003632119] | benign | 19 | 41880656 | 41880656 | Human | 1 | name , alternate_id |
| 405061711 | CV3016779 | single nucleotide variant | NM_001783.4(CD79A):c.499-10A>C | Agammaglobulinemia 3, autosomal recessive [RCV003632122]|CD79A-related disorder [RCV003966575] | benign|likely benign | 19 | 41880660 | 41880660 | Human | 1 | name , trait , alternate_id |
| 404978265 | CV3127310 | single nucleotide variant | NM_001783.4(CD79A):c.567+15G>C | Agammaglobulinemia 3, autosomal recessive [RCV003825534] | likely benign | 19 | 41880753 | 41880753 | Human | 1 | name , alternate_id |
| 404992068 | CV3132275 | single nucleotide variant | NM_001783.4(CD79A):c.379+19G>T | Agammaglobulinemia 3, autosomal recessive [RCV003827213] | likely benign | 19 | 41879308 | 41879308 | Human | 1 | name , alternate_id |
| 402470552 | CV3171094 | single nucleotide variant | NM_001783.4(CD79A):c.380-14C>A | Agammaglobulinemia 3, autosomal recessive [RCV003874057] | likely benign | 19 | 41879521 | 41879521 | Human | 1 | name , alternate_id |
| 597973663 | CV3801484 | single nucleotide variant | NM_001783.4(CD79A):c.380-13T>C | Agammaglobulinemia 3, autosomal recessive [RCV005143473] | likely benign | 19 | 41879522 | 41879522 | Human | 1 | name , alternate_id |
| 150490881 | CV1267686 | single nucleotide variant | NM_001783.4(CD79A):c.498+195G>T | not provided [RCV001687710] | benign | 19 | 41879848 | 41879848 | Human | 1 | name |
| 150490881 | CV1267686 | single nucleotide variant | NM_001783.4(CD79A):c.498+195G>T | not provided [RCV001687710] | benign | 19 | 41879848 | 41879849 | Human | 1 | name |
| 150490563 | CV1267634 | microsatellite | NM_001783.4(CD79A):c.499-218GGAA[14] | not provided [RCV001687658] | benign | 19 | 41880451 | 41880452 | Human | | name |
| 152030620 | CV1632237 | single nucleotide variant | NM_001783.4(CD79A):c.24C>T (p.Leu8=) | Agammaglobulinemia 3, autosomal recessive [RCV002124372] | likely benign | 19 | 41877328 | 41877328 | Human | 1 | name , alternate_id |
| 156408527 | CV1870115 | single nucleotide variant | NM_001783.4(CD79A):c.12T>G (p.Gly4=) | Agammaglobulinemia 3, autosomal recessive [RCV003071304] | likely benign | 19 | 41877316 | 41877316 | Human | 1 | name , alternate_id |
| 13506508 | CV468842 | single nucleotide variant | NM_001783.4(CD79A):c.21C>T (p.Val7=) | Agammaglobulinemia 3, autosomal recessive [RCV000576174] | likely benign | 19 | 41877325 | 41877325 | Human | 1 | name , alternate_id |
| 127277101 | CV1106551 | single nucleotide variant | NM_001783.4(CD79A):c.30T>C (p.Ala10=) | Agammaglobulinemia 3, autosomal recessive [RCV001444194] | likely benign | 19 | 41877334 | 41877334 | Human | 1 | name , alternate_id |
| 151849208 | CV1439981 | single nucleotide variant | NM_001783.4(CD79A):c.8G>C (p.Gly3Ala) | Agammaglobulinemia 3, autosomal recessive [RCV002016343] | uncertain significance | 19 | 41877312 | 41877312 | Human | 1 | name , alternate_id |
| 152032078 | CV1624680 | single nucleotide variant | NM_001783.4(CD79A):c.54C>A (p.Leu18=) | Agammaglobulinemia 3, autosomal recessive [RCV002186826] | likely benign | 19 | 41877358 | 41877358 | Human | 1 | name , alternate_id |
| 156384903 | CV2001733 | single nucleotide variant | NM_001783.4(CD79A):c.51C>A (p.Leu17=) | Agammaglobulinemia 3, autosomal recessive [RCV002653921] | likely benign | 19 | 41877355 | 41877355 | Human | 1 | name , alternate_id |
| 401937250 | CV2808726 | single nucleotide variant | NM_001783.4(CD79A):c.81C>G (p.Gly27=) | CD79A-related disorder [RCV003919151]|not provided [RCV003415258] | likely benign | 19 | 41878991 | 41878991 | Human | 1 | name , trait , alternate_id |
| 401910547 | CV2808727 | single nucleotide variant | NM_001783.4(CD79A):c.87G>C (p.Gly29=) | CD79A-related disorder [RCV003908916]|not provided [RCV003425191] | likely benign | 19 | 41878997 | 41878997 | Human | 1 | name , trait , alternate_id |
| 15179710 | CV716471 | single nucleotide variant | NM_001783.4(CD79A):c.61C>T (p.Leu21=) | Agammaglobulinemia 3, autosomal recessive [RCV001480000] | likely benign | 19 | 41877365 | 41877365 | Human | 1 | name , alternate_id |
| 127235530 | CV1084774 | single nucleotide variant | NM_001783.4(CD79A):c.183C>T (p.Asn61=) | Agammaglobulinemia 3, autosomal recessive [RCV001414484]|not provided [RCV001815548] | likely benign | 19 | 41879093 | 41879093 | Human | 1 | name , alternate_id |
| 127278948 | CV1084775 | single nucleotide variant | NM_001783.4(CD79A):c.225G>A (p.Thr75=) | Agammaglobulinemia 3, autosomal recessive [RCV001408818] | likely benign | 19 | 41879135 | 41879135 | Human | 1 | name , alternate_id |
| 127248412 | CV1084776 | single nucleotide variant | NM_001783.4(CD79A):c.270G>A (p.Thr90=) | Agammaglobulinemia 3, autosomal recessive [RCV001399374]|not specified [RCV005308441] | likely benign | 19 | 41879180 | 41879180 | Human | 1 | name , alternate_id |
| 127318738 | CV1127921 | single nucleotide variant | NM_001783.4(CD79A):c.165G>A (p.Pro55=) | Agammaglobulinemia 3, autosomal recessive [RCV001466341] | likely benign | 19 | 41879075 | 41879075 | Human | 1 | name , alternate_id |
| 127315043 | CV1148891 | single nucleotide variant | NM_001783.4(CD79A):c.210C>A (p.Leu70=) | Agammaglobulinemia 3, autosomal recessive [RCV001502616] | likely benign | 19 | 41879120 | 41879120 | Human | 1 | name , alternate_id |
| 152045304 | CV1590679 | single nucleotide variant | NM_001783.4(CD79A):c.204C>T (p.Arg68=) | Agammaglobulinemia 3, autosomal recessive [RCV002108275] | likely benign | 19 | 41879114 | 41879114 | Human | 1 | name , alternate_id |
| 156370276 | CV1923472 | single nucleotide variant | NM_001783.4(CD79A):c.189C>T (p.Asn63=) | Agammaglobulinemia 3, autosomal recessive [RCV002633329] | likely benign | 19 | 41879099 | 41879099 | Human | 1 | name , alternate_id |
| 156437256 | CV1937391 | single nucleotide variant | NM_001783.4(CD79A):c.108C>T (p.His36=) | Agammaglobulinemia 3, autosomal recessive [RCV003106787] | likely benign | 19 | 41879018 | 41879018 | Human | 1 | name , alternate_id |
| 156126422 | CV2088409 | single nucleotide variant | NM_001783.4(CD79A):c.150C>T (p.Ala50=) | Agammaglobulinemia 3, autosomal recessive [RCV002871468] | likely benign | 19 | 41879060 | 41879060 | Human | 1 | name , alternate_id |
| 155931392 | CV2370906 | single nucleotide variant | NM_001783.4(CD79A):c.13C>T (p.Pro5Ser) | not specified [RCV004218636] | uncertain significance | 19 | 41877317 | 41877317 | Human | | name |
| 405038784 | CV2929579 | single nucleotide variant | NM_001783.4(CD79A):c.120A>C (p.Ala40=) | Agammaglobulinemia 3, autosomal recessive [RCV003517757] | likely benign | 19 | 41879030 | 41879030 | Human | 1 | name , alternate_id |
| 597877512 | CV3776029 | single nucleotide variant | NM_001783.4(CD79A):c.159A>G (p.Gln53=) | Agammaglobulinemia 3, autosomal recessive [RCV005123556] | likely benign | 19 | 41879069 | 41879069 | Human | 1 | name , alternate_id |
| 15115723 | CV786207 | single nucleotide variant | NM_001783.4(CD79A):c.147C>T (p.Asp49=) | Agammaglobulinemia 3, autosomal recessive [RCV002066473] | likely benign | 19 | 41879057 | 41879057 | Human | 1 | name , alternate_id |
| 127232742 | CV1084777 | single nucleotide variant | NM_001783.4(CD79A):c.465C>T (p.Cys155=) | Agammaglobulinemia 3, autosomal recessive [RCV001413598] | likely benign | 19 | 41879620 | 41879620 | Human | 1 | name , alternate_id |
| 127262844 | CV1106552 | single nucleotide variant | NM_001783.4(CD79A):c.400C>T (p.Leu134=) | Agammaglobulinemia 3, autosomal recessive [RCV001439145] | likely benign | 19 | 41879555 | 41879555 | Human | 1 | name , alternate_id |
| 127271219 | CV1106553 | single nucleotide variant | NM_001783.4(CD79A):c.552T>C (p.Asp184=) | Agammaglobulinemia 3, autosomal recessive [RCV001441746] | likely benign | 19 | 41880723 | 41880723 | Human | 1 | name , alternate_id |
| 127298996 | CV1148892 | single nucleotide variant | NM_001783.4(CD79A):c.327G>A (p.Gln109=) | Agammaglobulinemia 3, autosomal recessive [RCV001498200] | likely benign | 19 | 41879237 | 41879237 | Human | 1 | name , alternate_id |
| 150442524 | CV1287738 | duplication | NM_001783.4(CD79A):c.499-212_499-210dup | not provided [RCV001725459] | benign | 19 | 41880456 | 41880457 | Human | | name |
| 8687137 | CV137570 | single nucleotide variant | NM_001783.4(CD79A):c.28G>A (p.Ala10Thr) | Agammaglobulinemia 3, autosomal recessive [RCV001401104]|not specified [RCV000120483] | likely benign|uncertain significance|not provided | 19 | 41877332 | 41877332 | Human | 1 | name , alternate_id |
| 151854350 | CV1455706 | single nucleotide variant | NM_001783.4(CD79A):c.624C>T (p.Gly208=) | Agammaglobulinemia 3, autosomal recessive [RCV002016991]|CD79A-related disorder [RCV003948871] | likely benign|uncertain significance | 19 | 41880923 | 41880923 | Human | 1 | name , trait , alternate_id |
| 151780812 | CV1458194 | single nucleotide variant | NM_001783.4(CD79A):c.309A>C (p.Ile103=) | Agammaglobulinemia 3, autosomal recessive [RCV001951056] | likely benign | 19 | 41879219 | 41879219 | Human | 1 | name , alternate_id |
| 152116959 | CV1555995 | single nucleotide variant | NM_001783.4(CD79A):c.453C>T (p.Ile151=) | Agammaglobulinemia 3, autosomal recessive [RCV002216268] | likely benign | 19 | 41879608 | 41879608 | Human | 1 | name , alternate_id |
| 152141306 | CV1571519 | single nucleotide variant | NM_001783.4(CD79A):c.372C>T (p.Arg124=) | Agammaglobulinemia 3, autosomal recessive [RCV002138212] | likely benign | 19 | 41879282 | 41879282 | Human | 1 | name , alternate_id |
| 152138584 | CV1572298 | single nucleotide variant | NM_001783.4(CD79A):c.678G>A (p.Pro226=) | Agammaglobulinemia 3, autosomal recessive [RCV002219065] | likely benign | 19 | 41880977 | 41880977 | Human | 1 | name , alternate_id |
| 152171501 | CV1628353 | single nucleotide variant | NM_001783.4(CD79A):c.387C>T (p.Pro129=) | Agammaglobulinemia 3, autosomal recessive [RCV002183520] | likely benign | 19 | 41879542 | 41879542 | Human | 1 | name , alternate_id |
| 152039685 | CV1649049 | single nucleotide variant | NM_001783.4(CD79A):c.483G>A (p.Thr161=) | Agammaglobulinemia 3, autosomal recessive [RCV002206156] | likely benign | 19 | 41879638 | 41879638 | Human | 1 | name , alternate_id |
| 156311259 | CV2000097 | single nucleotide variant | NM_001783.4(CD79A):c.384G>A (p.Pro128=) | Agammaglobulinemia 3, autosomal recessive [RCV002671649] | likely benign | 19 | 41879539 | 41879539 | Human | 1 | name , alternate_id |
| 156242790 | CV2043870 | single nucleotide variant | NM_001783.4(CD79A):c.357C>T (p.Cys119=) | Agammaglobulinemia 3, autosomal recessive [RCV002805736] | likely benign | 19 | 41879267 | 41879267 | Human | 1 | name , alternate_id |
| 156133922 | CV2097255 | single nucleotide variant | NM_001783.4(CD79A):c.427C>A (p.Arg143=) | Agammaglobulinemia 3, autosomal recessive [RCV002890052] | likely benign | 19 | 41879582 | 41879582 | Human | 1 | name , alternate_id |
| 405058151 | CV2976414 | single nucleotide variant | NM_001783.4(CD79A):c.519G>A (p.Lys173=) | Agammaglobulinemia 3, autosomal recessive [RCV003631683] | likely benign | 19 | 41880690 | 41880690 | Human | 1 | name , alternate_id |
| 405058114 | CV2993494 | single nucleotide variant | NM_001783.4(CD79A):c.561T>G (p.Leu187=) | Agammaglobulinemia 3, autosomal recessive [RCV003631985] | likely benign | 19 | 41880732 | 41880732 | Human | 1 | name , alternate_id |
| 405176393 | CV3152340 | single nucleotide variant | NM_001783.4(CD79A):c.525G>T (p.Gly175=) | Agammaglobulinemia 3, autosomal recessive [RCV003858295] | likely benign | 19 | 41880696 | 41880696 | Human | 1 | name , alternate_id |
| 597955577 | CV3754436 | single nucleotide variant | NM_001783.4(CD79A):c.490C>T (p.Leu164=) | Agammaglobulinemia 3, autosomal recessive [RCV005080286] | likely benign | 19 | 41879645 | 41879645 | Human | 1 | name , alternate_id |
| 13506541 | CV470263 | single nucleotide variant | NM_001783.4(CD79A):c.534C>T (p.Ala178=) | Agammaglobulinemia 3, autosomal recessive [RCV000576241] | likely benign | 19 | 41880705 | 41880705 | Human | 1 | name , alternate_id |
| 14742046 | CV648144 | single nucleotide variant | NM_001783.4(CD79A):c.64T>A (p.Ser22Thr) | Agammaglobulinemia 3, autosomal recessive [RCV000822533] | uncertain significance | 19 | 41877368 | 41877368 | Human | 1 | name , alternate_id |
| 15180051 | CV741923 | single nucleotide variant | NM_001783.4(CD79A):c.375G>A (p.Val125=) | Agammaglobulinemia 3, autosomal recessive [RCV001483772] | likely benign | 19 | 41879285 | 41879285 | Human | 1 | name , alternate_id |
| 15147258 | CV741924 | single nucleotide variant | NM_001783.4(CD79A):c.513C>T (p.Asn171=) | Agammaglobulinemia 3, autosomal recessive [RCV000900481] | likely benign | 19 | 41880684 | 41880684 | Human | 1 | name , alternate_id |
| 15127231 | CV757053 | single nucleotide variant | NM_001783.4(CD79A):c.459G>A (p.Leu153=) | not provided [RCV000919460] | likely benign | 19 | 41879614 | 41879614 | Human | | name |
| 15185233 | CV772715 | single nucleotide variant | NM_001783.4(CD79A):c.312C>T (p.Tyr104=) | Agammaglobulinemia 3, autosomal recessive [RCV002544432]|not provided [RCV000931002] | likely benign | 19 | 41879222 | 41879222 | Human | 1 | name , alternate_id |
| 15184523 | CV772716 | single nucleotide variant | NM_001783.4(CD79A):c.336C>T (p.Asn112=) | Agammaglobulinemia 3, autosomal recessive [RCV000930829] | likely benign | 19 | 41879246 | 41879246 | Human | 1 | name , alternate_id |
| 15146634 | CV772717 | single nucleotide variant | NM_001783.4(CD79A):c.582C>T (p.Asp194=) | Agammaglobulinemia 3, autosomal recessive [RCV001396288]|not provided [RCV004704357] | likely benign | 19 | 41880881 | 41880881 | Human | 1 | name , alternate_id |
| 126741704 | CV998623 | single nucleotide variant | NM_001783.4(CD79A):c.80G>T (p.Gly27Val) | Agammaglobulinemia 3, autosomal recessive [RCV001295939] | uncertain significance | 19 | 41878990 | 41878990 | Human | 1 | name , alternate_id |
| 126741024 | CV1013754 | single nucleotide variant | NM_001783.4(CD79A):c.137T>C (p.Leu46Pro) | Agammaglobulinemia 3, autosomal recessive [RCV001325286] | uncertain significance | 19 | 41879047 | 41879047 | Human | 1 | name , alternate_id |
| 126733768 | CV1013755 | single nucleotide variant | NM_001783.4(CD79A):c.182A>T (p.Asn61Ile) | Agammaglobulinemia 3, autosomal recessive [RCV001313454] | uncertain significance | 19 | 41879092 | 41879092 | Human | 1 | name , alternate_id |
| 126755556 | CV1034325 | single nucleotide variant | NM_001783.4(CD79A):c.128T>A (p.Met43Lys) | Agammaglobulinemia 3, autosomal recessive [RCV001339065] | uncertain significance | 19 | 41879038 | 41879038 | Human | 1 | name , alternate_id |
| 126759296 | CV1034326 | single nucleotide variant | NM_001783.4(CD79A):c.202C>T (p.Arg68Cys) | Agammaglobulinemia 3, autosomal recessive [RCV001340090] | uncertain significance | 19 | 41879112 | 41879112 | Human | 1 | name , alternate_id |
| 126922402 | CV1051334 | single nucleotide variant | NM_001783.4(CD79A):c.259C>T (p.Pro87Ser) | Agammaglobulinemia 3, autosomal recessive [RCV001364634] | uncertain significance | 19 | 41879169 | 41879169 | Human | 1 | name , alternate_id |
| 151810980 | CV1340864 | single nucleotide variant | NM_001783.4(CD79A):c.263A>G (p.Asn88Ser) | Agammaglobulinemia 3, autosomal recessive [RCV001974769] | uncertain significance | 19 | 41879173 | 41879173 | Human | 1 | name , alternate_id |
| 8687138 | CV137571 | single nucleotide variant | NM_001783.4(CD79A):c.258C>A (p.Asp86Glu) | Agammaglobulinemia 3, autosomal recessive [RCV000685379]|not specified [RCV000120484] | uncertain significance|not provided | 19 | 41879168 | 41879168 | Human | 1 | name , alternate_id |
| 151783732 | CV1474304 | single nucleotide variant | NM_001783.4(CD79A):c.164C>T (p.Pro55Leu) | Agammaglobulinemia 3, autosomal recessive [RCV001875606]|not specified [RCV004041428] | likely benign|uncertain significance | 19 | 41879074 | 41879074 | Human | 1 | name , alternate_id |
| 156013397 | CV1880688 | single nucleotide variant | NM_001783.4(CD79A):c.190G>A (p.Val64Ile) | Agammaglobulinemia 3, autosomal recessive [RCV003077222] | uncertain significance | 19 | 41879100 | 41879100 | Human | 1 | name , alternate_id |
| 156116346 | CV1993958 | single nucleotide variant | NM_001783.4(CD79A):c.188A>T (p.Asn63Ile) | Agammaglobulinemia 3, autosomal recessive [RCV002662680] | uncertain significance | 19 | 41879098 | 41879098 | Human | 1 | name , alternate_id |
| 156335759 | CV2109277 | single nucleotide variant | NM_001783.4(CD79A):c.253G>A (p.Glu85Lys) | Agammaglobulinemia 3, autosomal recessive [RCV002938625] | uncertain significance | 19 | 41879163 | 41879163 | Human | 1 | name , alternate_id |
| 156298436 | CV2159427 | single nucleotide variant | NM_001783.4(CD79A):c.242T>C (p.Leu81Ser) | Agammaglobulinemia 3, autosomal recessive [RCV003045436] | uncertain significance | 19 | 41879152 | 41879152 | Human | 1 | name , alternate_id |
| 598166671 | CV3950833 | single nucleotide variant | NM_001783.4(CD79A):c.257A>C (p.Asp86Ala) | not specified [RCV005307925] | uncertain significance | 19 | 41879167 | 41879167 | Human | | name |
| 13816982 | CV572530 | single nucleotide variant | NM_001783.4(CD79A):c.269C>T (p.Thr90Met) | Agammaglobulinemia 3, autosomal recessive [RCV000706721] | uncertain significance | 19 | 41879179 | 41879179 | Human | 1 | name , alternate_id |
| 13815605 | CV573150 | single nucleotide variant | NM_001783.4(CD79A):c.198G>A (p.Trp66Ter) | Agammaglobulinemia 3, autosomal recessive [RCV000691714] | pathogenic | 19 | 41879108 | 41879108 | Human | 1 | name , alternate_id |
| 13812879 | CV573151 | single nucleotide variant | NM_001783.4(CD79A):c.224C>A (p.Thr75Lys) | Agammaglobulinemia 3, autosomal recessive [RCV000689793] | uncertain significance | 19 | 41879134 | 41879134 | Human | 1 | name , alternate_id |
| 14730563 | CV648145 | single nucleotide variant | NM_001783.4(CD79A):c.188A>G (p.Asn63Ser) | Agammaglobulinemia 3, autosomal recessive [RCV000801006]|not specified [RCV004887660] | uncertain significance | 19 | 41879098 | 41879098 | Human | 1 | name , alternate_id |
| 26915052 | CV847730 | single nucleotide variant | NM_001783.4(CD79A):c.134G>C (p.Ser45Thr) | Agammaglobulinemia 3, autosomal recessive [RCV001041092] | uncertain significance | 19 | 41879044 | 41879044 | Human | 1 | name , alternate_id |
| 26903061 | CV847731 | single nucleotide variant | NM_001783.4(CD79A):c.184G>A (p.Ala62Thr) | Agammaglobulinemia 3, autosomal recessive [RCV001036083] | uncertain significance | 19 | 41879094 | 41879094 | Human | 1 | name , alternate_id |
| 26900282 | CV847732 | single nucleotide variant | NM_001783.4(CD79A):c.203G>A (p.Arg68His) | Agammaglobulinemia 3, autosomal recessive [RCV001035269]|not provided [RCV003413815] | likely benign|uncertain significance | 19 | 41879113 | 41879113 | Human | 1 | name , alternate_id |
| 26901911 | CV847733 | single nucleotide variant | NM_001783.4(CD79A):c.224C>T (p.Thr75Met) | Agammaglobulinemia 3, autosomal recessive [RCV001035807] | uncertain significance | 19 | 41879134 | 41879134 | Human | 1 | name , alternate_id |
| 126762391 | CV998624 | single nucleotide variant | NM_001783.4(CD79A):c.179A>G (p.Asn60Ser) | Agammaglobulinemia 3, autosomal recessive [RCV001300381]|not specified [RCV004897670] | uncertain significance | 19 | 41879089 | 41879089 | Human | 1 | name , alternate_id |
| 126766856 | CV1013756 | single nucleotide variant | NM_001783.4(CD79A):c.377G>A (p.Arg126His) | Agammaglobulinemia 3, autosomal recessive [RCV001320618] | uncertain significance | 19 | 41879287 | 41879287 | Human | 1 | name , alternate_id |
| 126752635 | CV1034327 | single nucleotide variant | NM_001783.4(CD79A):c.373G>A (p.Val125Met) | Agammaglobulinemia 3, autosomal recessive [RCV001338464]|not provided [RCV002261345] | uncertain significance | 19 | 41879283 | 41879283 | Human | 1 | name , alternate_id |
| 126909757 | CV1036911 | single nucleotide variant | NM_001783.4(CD79A):c.374T>G (p.Val125Gly) | Agammaglobulinemia 3, autosomal recessive [RCV001354050] | uncertain significance | 19 | 41879284 | 41879284 | Human | 1 | name , alternate_id |
| 126910810 | CV1051335 | single nucleotide variant | NM_001783.4(CD79A):c.523G>A (p.Gly175Arg) | Agammaglobulinemia 3, autosomal recessive [RCV001368933] | uncertain significance | 19 | 41880694 | 41880694 | Human | 1 | name , alternate_id |
| 126919834 | CV1051336 | single nucleotide variant | NM_001783.4(CD79A):c.653T>A (p.Ile218Lys) | Agammaglobulinemia 3, autosomal recessive [RCV001362520]|not specified [RCV004036839] | uncertain significance | 19 | 41880952 | 41880952 | Human | 1 | name , alternate_id |
| 126924130 | CV1051337 | single nucleotide variant | NM_001783.4(CD79A):c.677C>T (p.Pro226Leu) | Agammaglobulinemia 3, autosomal recessive [RCV001366670] | uncertain significance | 19 | 41880976 | 41880976 | Human | 1 | name , alternate_id |
| 151856680 | CV1372722 | single nucleotide variant | NM_001783.4(CD79A):c.395C>T (p.Pro132Leu) | Agammaglobulinemia 3, autosomal recessive [RCV002033859] | uncertain significance | 19 | 41879550 | 41879550 | Human | 1 | name , alternate_id |
| 8687139 | CV137572 | single nucleotide variant | NM_001783.4(CD79A):c.320G>A (p.Arg107Gln) | Agammaglobulinemia 3, autosomal recessive [RCV001854604]|not specified [RCV000120485] | uncertain significance|not provided | 19 | 41879230 | 41879230 | Human | 1 | name , alternate_id |
| 8687140 | CV137573 | single nucleotide variant | NM_001783.4(CD79A):c.371G>A (p.Arg124His) | Agammaglobulinemia 3, autosomal recessive [RCV000704625]|not provided [RCV002288609]|not specified [RCV000120486] | uncertain significance|not provided | 19 | 41879281 | 41879281 | Human | 1 | name , alternate_id |
| 8687141 | CV137574 | single nucleotide variant | NM_001783.4(CD79A):c.419C>A (p.Thr140Asn) | Agammaglobulinemia 3, autosomal recessive [RCV000576287]|not provided [RCV001528854]|not specified [RCV000120487] | likely benign|conflicting interpretations of pathogenicity|uncertain significance|not provided | 19 | 41879574 | 41879574 | Human | 1 | name , alternate_id |
| 8687142 | CV137575 | single nucleotide variant | NM_001783.4(CD79A):c.643A>G (p.Ser215Gly) | Agammaglobulinemia 3, autosomal recessive [RCV001854605]|not specified [RCV000120488] | uncertain significance|not provided | 19 | 41880942 | 41880942 | Human | 1 | name , alternate_id |
| 8687143 | CV137576 | single nucleotide variant | NM_001783.4(CD79A):c.593T>C (p.Met198Thr) | Agammaglobulinemia 3, autosomal recessive [RCV000648340]|not specified [RCV000120489] | uncertain significance|not provided | 19 | 41880892 | 41880892 | Human | 1 | name , alternate_id |
| 151801209 | CV1378737 | single nucleotide variant | NM_001783.4(CD79A):c.466G>A (p.Ala156Thr) | Agammaglobulinemia 3, autosomal recessive [RCV001877389] | uncertain significance | 19 | 41879621 | 41879621 | Human | 1 | name , alternate_id |
| 151777538 | CV1381975 | single nucleotide variant | NM_001783.4(CD79A):c.610C>G (p.Arg204Gly) | Agammaglobulinemia 3, autosomal recessive [RCV001950752] | uncertain significance | 19 | 41880909 | 41880909 | Human | 1 | name , alternate_id |
| 151751281 | CV1385321 | single nucleotide variant | NM_001783.4(CD79A):c.310T>C (p.Tyr104His) | Agammaglobulinemia 3, autosomal recessive [RCV001969212] | uncertain significance | 19 | 41879220 | 41879220 | Human | 1 | name , alternate_id |
| 151799621 | CV1403904 | single nucleotide variant | NM_001783.4(CD79A):c.498G>C (p.Arg166Ser) | Agammaglobulinemia 3, autosomal recessive [RCV001973786] | uncertain significance | 19 | 41879653 | 41879653 | Human | 1 | name , alternate_id |
| 151853267 | CV1406928 | single nucleotide variant | NM_001783.4(CD79A):c.611G>A (p.Arg204Gln) | Agammaglobulinemia 3, autosomal recessive [RCV002033452]|not specified [RCV004045216] | uncertain significance | 19 | 41880910 | 41880910 | Human | 1 | name , alternate_id |
| 151667487 | CV1414410 | single nucleotide variant | NM_001783.4(CD79A):c.469G>A (p.Val157Met) | Agammaglobulinemia 3, autosomal recessive [RCV001870604] | uncertain significance | 19 | 41879624 | 41879624 | Human | 1 | name , alternate_id |
| 151832995 | CV1456131 | single nucleotide variant | NM_001783.4(CD79A):c.650A>T (p.Asn217Ile) | Agammaglobulinemia 3, autosomal recessive [RCV002050907] | uncertain significance | 19 | 41880949 | 41880949 | Human | 1 | name , alternate_id |
| 151819676 | CV1488378 | single nucleotide variant | NM_001783.4(CD79A):c.358G>A (p.Gly120Ser) | Agammaglobulinemia 3, autosomal recessive [RCV001975606] | uncertain significance | 19 | 41879268 | 41879268 | Human | 1 | name , alternate_id |
| 156034857 | CV1890085 | single nucleotide variant | NM_001783.4(CD79A):c.394C>A (p.Pro132Thr) | Agammaglobulinemia 3, autosomal recessive [RCV003078272] | uncertain significance | 19 | 41879549 | 41879549 | Human | 1 | name , alternate_id |
| 156359418 | CV1908312 | single nucleotide variant | NM_001783.4(CD79A):c.428G>A (p.Arg143Gln) | Agammaglobulinemia 3, autosomal recessive [RCV002602391] | uncertain significance | 19 | 41879583 | 41879583 | Human | 1 | name , alternate_id |
| 156193638 | CV1994784 | single nucleotide variant | NM_001783.4(CD79A):c.416G>A (p.Gly139Asp) | Agammaglobulinemia 3, autosomal recessive [RCV002643390] | uncertain significance | 19 | 41879571 | 41879571 | Human | 1 | name , alternate_id |
| 156011644 | CV2011511 | single nucleotide variant | NM_001783.4(CD79A):c.335A>G (p.Asn112Ser) | Agammaglobulinemia 3, autosomal recessive [RCV002690546] | uncertain significance | 19 | 41879245 | 41879245 | Human | 1 | name , alternate_id |
| 156024155 | CV2043364 | single nucleotide variant | NM_001783.4(CD79A):c.664C>T (p.Gln222Ter) | Agammaglobulinemia 3, autosomal recessive [RCV002780806] | uncertain significance | 19 | 41880963 | 41880963 | Human | 1 | name , alternate_id |
| 156165147 | CV2137079 | single nucleotide variant | NM_001783.4(CD79A):c.493T>C (p.Phe165Leu) | Agammaglobulinemia 3, autosomal recessive [RCV003005210] | uncertain significance | 19 | 41879648 | 41879648 | Human | 1 | name , alternate_id |
| 156316233 | CV2169144 | single nucleotide variant | NM_001783.4(CD79A):c.514G>A (p.Glu172Lys) | Agammaglobulinemia 3, autosomal recessive [RCV003028877] | uncertain significance | 19 | 41880685 | 41880685 | Human | 1 | name , alternate_id |
| 156338323 | CV2178381 | single nucleotide variant | NM_001783.4(CD79A):c.338A>G (p.Glu113Gly) | Agammaglobulinemia 3, autosomal recessive [RCV003047602] | uncertain significance | 19 | 41879248 | 41879248 | Human | 1 | name , alternate_id |
| 156257578 | CV2322075 | single nucleotide variant | NM_001783.4(CD79A):c.613G>A (p.Gly205Ser) | not specified [RCV004173818] | uncertain significance | 19 | 41880912 | 41880912 | Human | | name |
| 401894584 | CV2788125 | single nucleotide variant | NM_001783.4(CD79A):c.641G>C (p.Gly214Ala) | not specified [RCV004352747] | uncertain significance | 19 | 41880940 | 41880940 | Human | | name |
| 405031508 | CV2915232 | single nucleotide variant | NM_001783.4(CD79A):c.503G>A (p.Arg168Gln) | Agammaglobulinemia 3, autosomal recessive [RCV003516875] | uncertain significance | 19 | 41880674 | 41880674 | Human | 1 | name , alternate_id |
| 405068874 | CV3081533 | single nucleotide variant | NM_001783.4(CD79A):c.576C>A (p.Asn192Lys) | Agammaglobulinemia 3, autosomal recessive [RCV003632978] | uncertain significance | 19 | 41880875 | 41880875 | Human | 1 | name , alternate_id |
| 13436105 | CV433403 | single nucleotide variant | NM_001783.4(CD79A):c.452T>C (p.Ile151Thr) | Agammaglobulinemia 3, autosomal recessive [RCV001065347]|not specified [RCV000506577] | uncertain significance | 19 | 41879607 | 41879607 | Human | 1 | name , alternate_id |
| 13488534 | CV446138 | single nucleotide variant | NM_001783.4(CD79A):c.370C>T (p.Arg124Cys) | Agammaglobulinemia 3, autosomal recessive [RCV000817060]|not provided [RCV000523593] | uncertain significance | 19 | 41879280 | 41879280 | Human | 1 | name , alternate_id |
| 13806772 | CV570810 | single nucleotide variant | NM_001783.4(CD79A):c.502C>G (p.Arg168Gly) | Agammaglobulinemia 3, autosomal recessive [RCV000700732] | uncertain significance | 19 | 41880673 | 41880673 | Human | 1 | name , alternate_id |
| 13827605 | CV578566 | single nucleotide variant | NM_001783.4(CD79A):c.419C>T (p.Thr140Ile) | Agammaglobulinemia 3, autosomal recessive [RCV001862005]|Autosomal recessive agammaglobulinemia 1 [RCV000714760] | uncertain significance | 19 | 41879574 | 41879574 | Human | 2 | name , alternate_id |
| 15136850 | CV757052 | single nucleotide variant | NM_001783.4(CD79A):c.301G>A (p.Gly101Arg) | Agammaglobulinemia 3, autosomal recessive [RCV001419356] | likely benign | 19 | 41879211 | 41879211 | Human | 1 | name , alternate_id |
| 25327502 | CV815938 | single nucleotide variant | NM_001783.4(CD79A):c.323T>G (p.Val108Gly) | Inherited Immunodeficiency Diseases [RCV001027560] | pathogenic | 19 | 41879233 | 41879233 | Human | 1 | name |
| 26887149 | CV847734 | single nucleotide variant | NM_001783.4(CD79A):c.309A>G (p.Ile103Met) | Agammaglobulinemia 3, autosomal recessive [RCV001044692]|not specified [RCV004887664] | likely benign|uncertain significance | 19 | 41879219 | 41879219 | Human | 1 | name , alternate_id |
| 26919421 | CV847735 | single nucleotide variant | NM_001783.4(CD79A):c.313G>A (p.Val105Met) | Agammaglobulinemia 3, autosomal recessive [RCV001058956]|not specified [RCV004031858] | uncertain significance | 19 | 41879223 | 41879223 | Human | 1 | name , alternate_id |
| 26902015 | CV847736 | single nucleotide variant | NM_001783.4(CD79A):c.442G>A (p.Glu148Lys) | Agammaglobulinemia 3, autosomal recessive [RCV001035847] | uncertain significance | 19 | 41879597 | 41879597 | Human | 1 | name , alternate_id |
| 26901770 | CV847737 | single nucleotide variant | NM_001783.4(CD79A):c.535G>A (p.Gly179Arg) | Agammaglobulinemia 3, autosomal recessive [RCV001035760] | uncertain significance | 19 | 41880706 | 41880706 | Human | 1 | name , alternate_id |
| 26887426 | CV847738 | single nucleotide variant | NM_001783.4(CD79A):c.677C>A (p.Pro226Gln) | Agammaglobulinemia 3, autosomal recessive [RCV001066667] | uncertain significance | 19 | 41880976 | 41880976 | Human | 1 | name , alternate_id |
| 38482004 | CV938705 | single nucleotide variant | NM_001783.4(CD79A):c.341C>T (p.Ser114Leu) | Agammaglobulinemia 3, autosomal recessive [RCV001207083] | uncertain significance | 19 | 41879251 | 41879251 | Human | 1 | name , alternate_id |
| 38467540 | CV938706 | single nucleotide variant | NM_001783.4(CD79A):c.467C>T (p.Ala156Val) | Agammaglobulinemia 3, autosomal recessive [RCV001212967] | uncertain significance | 19 | 41879622 | 41879622 | Human | 1 | name , alternate_id |
| 38496348 | CV950808 | single nucleotide variant | NM_001783.4(CD79A):c.583G>A (p.Asp195Asn) | Agammaglobulinemia 3, autosomal recessive [RCV001226334] | uncertain significance | 19 | 41880882 | 41880882 | Human | 1 | name , alternate_id |
| 156395746 | CV1980408 | indel | NM_001783.4(CD79A):c.567+20_567+21delinsAT | Agammaglobulinemia 3, autosomal recessive [RCV002605115] | likely benign | 19 | 41880758 | 41880759 | Human | | name , alternate_id |
| 155692984 | CV1775277 | indel | NM_001783.4(CD79A):c.466_467delinsTT (p.Ala156Leu) | Agammaglobulinemia 3, autosomal recessive [RCV002299415] | uncertain significance | 19 | 41879621 | 41879622 | Human | | name , alternate_id |
| 156109188 | CV1996902 | indel | NM_001783.4(CD79A):c.463_464delinsCT (p.Cys155Leu) | Agammaglobulinemia 3, autosomal recessive [RCV002662420] | uncertain significance | 19 | 41879618 | 41879619 | Human | | name , alternate_id |
| 156437925 | CV1939394 | duplication | NC_000019.9:g.(?_42363988)_(42385047_?)dup | Agammaglobulinemia 3, autosomal recessive [RCV003107468] | uncertain significance | | | | Human | 1 | alternate_id |
| 156132307 | CV2182218 | deletion | NC_000019.10:g.41878996_41879009del | Agammaglobulinemia 3, autosomal recessive [RCV003055884] | pathogenic | 19 | 41878987 | 41879000 | Human | 1 | alternate_id |
