| 598183302 | CV3917054 | single nucleotide variant | NM_022366.3(TFB2M):c.4T>A (p.Trp2Arg) | not specified [RCV005287084] | uncertain significance | 1 | 246566135 | 246566135 | Human | | name |
| 401890880 | CV2768768 | single nucleotide variant | NM_022366.3(TFB2M):c.25C>T (p.Pro9Ser) | not specified [RCV004346906] | uncertain significance | 1 | 246566114 | 246566114 | Human | | name |
| 156241779 | CV2231383 | single nucleotide variant | NM_022366.3(TFB2M):c.58G>A (p.Ala20Thr) | not specified [RCV004096470] | uncertain significance | 1 | 246566081 | 246566081 | Human | | name |
| 156353283 | CV2327506 | single nucleotide variant | NM_022366.3(TFB2M):c.67T>G (p.Phe23Val) | not specified [RCV004176817] | uncertain significance | 1 | 246566072 | 246566072 | Human | | name |
| 405783388 | CV3342679 | single nucleotide variant | NM_022366.3(TFB2M):c.53C>T (p.Ala18Val) | not specified [RCV004472355] | uncertain significance | 1 | 246566086 | 246566086 | Human | | name |
| 598183308 | CV3917055 | single nucleotide variant | NM_022366.3(TFB2M):c.62G>T (p.Gly21Val) | not specified [RCV005287085] | uncertain significance | 1 | 246566077 | 246566077 | Human | | name |
| 15199048 | CV718853 | single nucleotide variant | NM_022366.3(TFB2M):c.378C>T (p.Asp126=) | not provided [RCV000890526] | benign | 1 | 246564370 | 246564370 | Human | | name |
| 15113043 | CV746375 | single nucleotide variant | NM_022366.3(TFB2M):c.480A>G (p.Gly160=) | not provided [RCV000917021] | benign | 1 | 246557457 | 246557457 | Human | | name |
| 401746488 | CV2695581 | single nucleotide variant | NM_022366.3(TFB2M):c.221A>T (p.Tyr74Phe) | not specified [RCV004299405] | uncertain significance | 1 | 246565918 | 246565918 | Human | | name |
| 401937128 | CV2812926 | single nucleotide variant | NM_022366.3(TFB2M):c.1176C>T (p.Thr392=) | not provided [RCV003415106] | likely benign | 1 | 246541046 | 246541046 | Human | | name |
| 401937103 | CV2812927 | single nucleotide variant | NM_022366.3(TFB2M):c.190G>A (p.Ala64Thr) | not provided [RCV003415107] | likely benign | 1 | 246565949 | 246565949 | Human | | name |
| 401937088 | CV2812928 | single nucleotide variant | NM_022366.3(TFB2M):c.143C>T (p.Ser48Phe) | not provided [RCV003415108] | likely benign | 1 | 246565996 | 246565996 | Human | | name |
| 405783357 | CV3342674 | single nucleotide variant | NM_022366.3(TFB2M):c.187A>G (p.Lys63Glu) | not specified [RCV004472350] | uncertain significance | 1 | 246565952 | 246565952 | Human | | name |
| 405783362 | CV3342675 | single nucleotide variant | NM_022366.3(TFB2M):c.223G>A (p.Val75Ile) | not specified [RCV004472351] | likely benign | 1 | 246565916 | 246565916 | Human | | name |
| 405783370 | CV3342676 | single nucleotide variant | NM_022366.3(TFB2M):c.229G>T (p.Asp77Tyr) | not specified [RCV004472352] | uncertain significance | 1 | 246565910 | 246565910 | Human | | name |
| 405783375 | CV3342677 | single nucleotide variant | NM_022366.3(TFB2M):c.253G>T (p.Ala85Ser) | not specified [RCV004472353] | uncertain significance | 1 | 246565886 | 246565886 | Human | | name |
| 405783382 | CV3342678 | single nucleotide variant | NM_022366.3(TFB2M):c.293T>C (p.Leu98Pro) | not specified [RCV004472354] | uncertain significance | 1 | 246565846 | 246565846 | Human | | name |
| 597751440 | CV3619846 | single nucleotide variant | NM_022366.3(TFB2M):c.259A>G (p.Ile87Val) | not specified [RCV004866928] | uncertain significance | 1 | 246565880 | 246565880 | Human | | name |
| 597751445 | CV3619847 | single nucleotide variant | NM_022366.3(TFB2M):c.268G>A (p.Gly90Arg) | not specified [RCV004866929] | uncertain significance | 1 | 246565871 | 246565871 | Human | | name |
| 597751487 | CV3619857 | single nucleotide variant | NM_022366.3(TFB2M):c.218G>A (p.Arg73His) | not specified [RCV004866938] | uncertain significance | 1 | 246565921 | 246565921 | Human | | name |
| 156286296 | CV2334921 | single nucleotide variant | NM_022366.3(TFB2M):c.830A>C (p.Lys277Thr) | not specified [RCV004182025] | uncertain significance | 1 | 246548573 | 246548573 | Human | | name |
| 156040887 | CV2384398 | single nucleotide variant | NM_022366.3(TFB2M):c.992G>A (p.Arg331His) | not specified [RCV004229816] | uncertain significance | 1 | 246544548 | 246544548 | Human | | name |
| 401737880 | CV2700771 | single nucleotide variant | NM_022366.3(TFB2M):c.490C>T (p.Pro164Ser) | not specified [RCV004307056] | uncertain significance | 1 | 246557447 | 246557447 | Human | | name |
| 401759566 | CV2701613 | single nucleotide variant | NM_022366.3(TFB2M):c.334G>A (p.Ala112Thr) | not specified [RCV004314034] | uncertain significance | 1 | 246564414 | 246564414 | Human | | name |
| 401861754 | CV2756482 | single nucleotide variant | NM_022366.3(TFB2M):c.724G>A (p.Gly242Arg) | not specified [RCV004343013] | likely benign | 1 | 246551284 | 246551284 | Human | | name |
| 401871807 | CV2779405 | single nucleotide variant | NM_022366.3(TFB2M):c.824C>A (p.Thr275Asn) | not specified [RCV004351049] | uncertain significance | 1 | 246548579 | 246548579 | Human | | name |
| 401881854 | CV2783981 | single nucleotide variant | NM_022366.3(TFB2M):c.878A>C (p.Gln293Pro) | not specified [RCV004362396] | uncertain significance | 1 | 246544662 | 246544662 | Human | | name |
| 405783393 | CV3342680 | single nucleotide variant | NM_022366.3(TFB2M):c.827G>A (p.Arg276Gln) | not specified [RCV004472356] | likely benign | 1 | 246548576 | 246548576 | Human | | name |
| 407518677 | CV3482568 | single nucleotide variant | NM_022366.3(TFB2M):c.818T>C (p.Ile273Thr) | not specified [RCV004676072] | uncertain significance | 1 | 246548585 | 246548585 | Human | | name |
| 407518680 | CV3482569 | single nucleotide variant | NM_022366.3(TFB2M):c.509G>A (p.Arg170Gln) | not specified [RCV004676073] | likely benign | 1 | 246557428 | 246557428 | Human | | name |
| 407519948 | CV3482571 | single nucleotide variant | NM_022366.3(TFB2M):c.694A>G (p.Lys232Glu) | not specified [RCV004676769] | uncertain significance | 1 | 246556584 | 246556584 | Human | | name |
| 407518687 | CV3482572 | single nucleotide variant | NM_022366.3(TFB2M):c.652T>C (p.Tyr218His) | not specified [RCV004676075] | uncertain significance | 1 | 246556626 | 246556626 | Human | | name |
| 597751450 | CV3619848 | single nucleotide variant | NM_022366.3(TFB2M):c.361G>T (p.Val121Phe) | not specified [RCV004866930] | uncertain significance | 1 | 246564387 | 246564387 | Human | | name |
| 597751455 | CV3619849 | single nucleotide variant | NM_022366.3(TFB2M):c.509G>T (p.Arg170Leu) | not specified [RCV004866931] | uncertain significance | 1 | 246557428 | 246557428 | Human | | name |
| 597795065 | CV3619851 | single nucleotide variant | NM_022366.3(TFB2M):c.356A>G (p.Lys119Arg) | not specified [RCV004878063] | likely benign | 1 | 246564392 | 246564392 | Human | | name |
| 597751465 | CV3619852 | single nucleotide variant | NM_022366.3(TFB2M):c.443A>G (p.His148Arg) | not specified [RCV004866933] | uncertain significance | 1 | 246557494 | 246557494 | Human | | name |
| 597751470 | CV3619853 | single nucleotide variant | NM_022366.3(TFB2M):c.545C>G (p.Pro182Arg) | not specified [RCV004866934] | uncertain significance | 1 | 246557392 | 246557392 | Human | | name |
| 597751474 | CV3619854 | single nucleotide variant | NM_022366.3(TFB2M):c.563C>T (p.Pro188Leu) | not specified [RCV004866935] | uncertain significance | 1 | 246556715 | 246556715 | Human | | name |
| 597751479 | CV3619855 | single nucleotide variant | NM_022366.3(TFB2M):c.535G>A (p.Glu179Lys) | not specified [RCV004866936] | likely benign | 1 | 246557402 | 246557402 | Human | | name |
| 597751483 | CV3619856 | single nucleotide variant | NM_022366.3(TFB2M):c.925A>G (p.Thr309Ala) | not specified [RCV004866937] | likely benign | 1 | 246544615 | 246544615 | Human | | name |
| 598183269 | CV3917048 | single nucleotide variant | NM_022366.3(TFB2M):c.991C>T (p.Arg331Cys) | not specified [RCV005287079] | uncertain significance | 1 | 246544549 | 246544549 | Human | | name |
| 598183275 | CV3917049 | single nucleotide variant | NM_022366.3(TFB2M):c.651A>G (p.Ile217Met) | not specified [RCV005287080] | uncertain significance | 1 | 246556627 | 246556627 | Human | | name |
| 598183282 | CV3917050 | single nucleotide variant | NM_022366.3(TFB2M):c.911G>A (p.Arg304His) | not specified [RCV005287081] | uncertain significance | 1 | 246544629 | 246544629 | Human | | name |
| 598183287 | CV3917052 | single nucleotide variant | NM_022366.3(TFB2M):c.595G>A (p.Gly199Ser) | not specified [RCV005287082] | likely benign | 1 | 246556683 | 246556683 | Human | | name |
| 598165692 | CV3917056 | single nucleotide variant | NM_022366.3(TFB2M):c.874T>A (p.Leu292Ile) | not specified [RCV005283492] | likely benign | 1 | 246544666 | 246544666 | Human | | name |
| 156360641 | CV2269076 | single nucleotide variant | NM_022366.3(TFB2M):c.1000A>G (p.Thr334Ala) | not specified [RCV004130255] | uncertain significance | 1 | 246544540 | 246544540 | Human | | name |
| 156172201 | CV2326767 | single nucleotide variant | NM_022366.3(TFB2M):c.1006A>G (p.Ile336Val) | not specified [RCV004176610] | uncertain significance | 1 | 246544534 | 246544534 | Human | | name |
| 401758986 | CV2705305 | single nucleotide variant | NM_022366.3(TFB2M):c.1050A>G (p.Ile350Met) | not specified [RCV004311992] | uncertain significance | 1 | 246541172 | 246541172 | Human | | name |
| 401864284 | CV2760877 | single nucleotide variant | NM_022366.3(TFB2M):c.1018C>T (p.Arg340Cys) | not specified [RCV004336512] | uncertain significance | 1 | 246544522 | 246544522 | Human | | name |
| 404994821 | CV2851264 | single nucleotide variant | NM_022366.3(TFB2M):c.1161G>A (p.Trp387Ter) | not provided [RCV003491667] | uncertain significance | 1 | 246541061 | 246541061 | Human | | name |
| 405783345 | CV3342672 | single nucleotide variant | NM_022366.3(TFB2M):c.1135C>T (p.Arg379Cys) | not specified [RCV004472348] | likely benign | 1 | 246541087 | 246541087 | Human | | name |
| 405783351 | CV3342673 | single nucleotide variant | NM_022366.3(TFB2M):c.1157A>G (p.Lys386Arg) | not specified [RCV004472349] | uncertain significance | 1 | 246541065 | 246541065 | Human | | name |
| 598165686 | CV3917051 | single nucleotide variant | NM_022366.3(TFB2M):c.1102C>G (p.Gln368Glu) | not specified [RCV005283491] | likely benign | 1 | 246541120 | 246541120 | Human | | name |
