Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54812 |
| ensemblid | ENSG00000119844.17 |
| hgncid | 25951 |
| symbol | AFTPH |
| name | aftiphilin |
| refseq_nuc | NM_203437.4 |
| refseq_prot | NP_982261.2 |
| ensembl_nuc | ENST00000409933.6 |
| ensembl_prot | ENSP00000387071.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 64524328 |
| end | 64593005 |
| strand | + |
| ver | v1.2 |
| region | chr2:64524328-64593005 |
| region5000 | chr2:64519328-64598005 |
| regionname0 | AFTPH_chr2_64524328_64593005 |
| regionname5000 | AFTPH_chr2_64519328_64598005 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 936 | 267 | 41 | 57 | 125 | 11 | 31 | 104 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0002 | 0/0 | 936 | 85 | 36 | 0 | 45 | 1 | 3 | 35 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0003 | 0/0 | 936 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0004 | 0/0 | 936 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0005 | 0/0 | 936 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0006 | 0/0 | 936 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0007 | 0/0 | 936 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0008 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0009 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0010 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0011 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| a0012 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | MEPDI others(931): Show |
chr2 | 64519328 | 64598005 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2808 | 262 | 41 | 56 | 124 | 9 | 30 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0001c0005 | 0/0 | 2808 | 3 | 0 | 0 | 0 | 2 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0001c0012 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0001c0016 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0002c0002 | 0/0 | 2808 | 84 | 35 | 0 | 45 | 1 | 3 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0002c0010 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0003c0003 | 0/0 | 2808 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0004c0004 | 0/0 | 2808 | 4 | 0 | 0 | 4 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0005c0007 | 0/0 | 2808 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0005c0008 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0006c0006 | 0/0 | 2808 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0007c0015 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0008c0017 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0009c0009 | 0/0 | 2808 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0010c0013 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0011c0011 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 | ||
| a0012c0014 | 0/0 | 2808 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | ATGGA others(2803): Show |
chr2 | 64519328 | 64598005 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4098 | 129 | 15 | 33 | 59 | 6 | 14 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0002 | 0/0 | 4103 | 3 | 1 | 1 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0003 | 0/0 | 4104 | 19 | 1 | 3 | 13 | 1 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4099): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0004 | 0/0 | 4101 | 40 | 14 | 4 | 16 | 0 | 6 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4096): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0005 | 0/0 | 4101 | 37 | 2 | 12 | 14 | 2 | 7 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4096): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0006 | 0/0 | 4099 | 9 | 3 | 0 | 4 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4094): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0007 | 0/0 | 4097 | 8 | 1 | 2 | 5 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4092): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0009 | 0/0 | 4102 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4097): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0010 | 0/0 | 4105 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4100): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0011 | 0/0 | 4100 | 3 | 0 | 1 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4095): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0012 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0013 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0014 | 0/0 | 4100 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4095): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0015 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0018 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0001t0020 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0005t0001 | 0/0 | 4098 | 3 | 0 | 0 | 0 | 2 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0001c0012t0004 | 0/0 | 4101 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4096): Show |
chr2 | 64519328 | 64598005 |
| a0001c0016t0001 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0001 | 0/0 | 4098 | 9 | 9 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0002 | 0/0 | 4103 | 46 | 16 | 0 | 28 | 1 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0003 | 0/0 | 4104 | 25 | 6 | 0 | 17 | 0 | 2 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4099): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0009 | 0/0 | 4102 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4097): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0010 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4100): Show |
chr2 | 64519328 | 64598005 |
| a0002c0002t0019 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0002c0010t0016 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0003c0003t0008 | 0/0 | 4103 | 5 | 5 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0004c0004t0001 | 0/0 | 4098 | 4 | 0 | 0 | 4 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0005c0007t0002 | 0/0 | 4103 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0005c0007t0009 | 0/0 | 4102 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4097): Show |
chr2 | 64519328 | 64598005 |
| a0005c0008t0005 | 0/0 | 4101 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4096): Show |
chr2 | 64519328 | 64598005 |
| a0006c0006t0002 | 0/0 | 4103 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4098): Show |
chr2 | 64519328 | 64598005 |
| a0007c0015t0001 | 0/0 | 4098 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0008c0017t0003 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4099): Show |
chr2 | 64519328 | 64598005 |
| a0009c0009t0004 | 0/0 | 4101 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4096): Show |
chr2 | 64519328 | 64598005 |
| a0010c0013t0017 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4095): Show |
chr2 | 64519328 | 64598005 |
| a0011c0011t0001 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| a0012c0014t0001 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | GCTGC others(4093): Show |
chr2 | 64519328 | 64598005 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0018g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0001t0020g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0012t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0001c0016t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0002t0019g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0002c0010t0016g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0003c0003t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0007t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0007t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0005c0008t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0006c0006t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0006c0006t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0007c0015t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0008c0017t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0009c0009t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0010c0013t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0011c0011t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| a0012c0014t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0078 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0187 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0101 | EUR | GBR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0366 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0298 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00408 | hp2 | a0006 | c0006 | t0002 | g0343 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0305 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0363 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0291 | EAS | CHS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0099 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0197 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0324 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02004 | hp1 | a0007 | c0015 | t0001 | g0155 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02004 | hp2 | a0001 | c0012 | t0004 | g0073 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0345 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0365 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02080 | hp1 | a0001 | c0001 | t0018 | g0166 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0303 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0290 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02145 | hp2 | a0002 | c0002 | t0010 | g0323 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | CDX | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0307 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0218 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | PEL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0356 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | KHV | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0329 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0308 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0310 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02683 | hp1 | a0001 | c0005 | t0001 | g0122 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0121 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0285 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0286 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02723 | hp2 | a0002 | c0010 | t0016 | g0317 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0060 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0281 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0327 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02886 | hp2 | a0008 | c0017 | t0003 | g0326 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0284 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02896 | hp1 | a0003 | c0003 | t0008 | g0266 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02897 | hp2 | a0003 | c0003 | t0008 | g0263 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02970 | hp1 | a0003 | c0003 | t0008 | g0264 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02976 | hp2 | a0002 | c0002 | t0009 | g0325 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03017 | hp2 | a0009 | c0009 | t0004 | g0071 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03041 | hp1 | a0002 | c0002 | t0019 | g0360 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0283 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0320 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0309 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03195 | hp2 | a0010 | c0013 | t0017 | g0268 | AFR | ESN | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0043 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03225 | hp2 | a0003 | c0003 | t0008 | g0265 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03453 | hp2 | a0003 | c0003 | t0008 | g0232 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03486 | hp1 | a0011 | c0011 | t0001 | g0233 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03486 | hp2 | a0005 | c0008 | t0005 | g0279 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0322 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | GWD | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0361 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0246 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03688 | hp1 | a0012 | c0014 | t0001 | g0241 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0077 | SAS | PJL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0033 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0091 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0100 | SAS | BEB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0330 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0333 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0346 | EAS | CHB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0296 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0083 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0059 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18946 | hp2 | a0005 | c0007 | t0009 | g0331 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18950 | hp2 | a0001 | c0016 | t0001 | g0170 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0304 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18956 | hp1 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0294 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0353 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0347 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0300 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18967 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18968 | hp1 | a0002 | c0002 | t0003 | g0289 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0359 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0352 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0225 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0301 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0295 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0355 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0357 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19011 | hp1 | a0001 | c0001 | t0013 | g0235 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19011 | hp2 | a0006 | c0006 | t0002 | g0349 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19012 | hp1 | a0002 | c0002 | t0003 | g0299 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19043 | hp2 | a0002 | c0002 | t0009 | g0282 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0328 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19055 | hp2 | a0005 | c0007 | t0002 | g0354 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0342 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0269 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0351 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0362 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19077 | hp2 | a0004 | c0004 | t0001 | g0132 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19083 | hp1 | a0004 | c0004 | t0001 | g0221 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19085 | hp1 | a0001 | c0001 | t0020 | g0149 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19086 | hp2 | a0004 | c0004 | t0001 | g0223 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0321 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | YRI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0280 | AFR | ASW | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | ASW | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0141 | EUR | TSI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0311 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | USA | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0211 | REF | REF | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0186 | REF | REF | AFTPH_chr2_64519328_64598005 | AFTPH | chr2 | 64519328 | 64598005 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64552061 | G | A | 1 | a0009 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.587G>A | p.Gly196Glu | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 904/4098 | 587/2811 | 196/936 | chr2 | 64552061 | |||
| chr2:64552187 | C | T | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.713C>T | p.Ser238Phe | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1030/4098 | 713/2811 | 238/936 | chr2 | 64552187 | |||
| chr2:64552318 | G | A | 1 | a0004 | 4 | NA18981.hp2 NA19077.hp2 NA19083.hp1 others(1): Show |
missense_variant | MODERATE | c.844G>A | p.Gly282Ser | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1161/4098 | 844/2811 | 282/936 | chr2 | 64552318 | |||
| chr2:64552375 | G | A | 4 | a0002 a0005 a0006 others(1): Show |
91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
missense_variant | MODERATE | c.901G>A | p.Glu301Lys | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1218/4098 | 901/2811 | 301/936 | chr2 | 64552375 | |||
| chr2:64552492 | T | C | 1 | a0003 | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.1018T>C | p.Ser340Pro | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1335/4098 | 1018/2811 | 340/936 | chr2 | 64552492 | |||
| chr2:64552528 | T | C | 1 | a0011 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1054T>C | p.Cys352Arg | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1371/4098 | 1054/2811 | 352/936 | chr2 | 64552528 | |||
| chr2:64553123 | A | G | 1 | a0005 | 3 | HG03486.hp2 NA18946.hp2 NA19055.hp2 |
missense_variant | MODERATE | c.1649A>G | p.Asn550Ser | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1966/4098 | 1649/2811 | 550/936 | chr2 | 64553123 | |||
| chr2:64553225 | C | G | 1 | a0007 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1751C>G | p.Ser584Cys | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 2068/4098 | 1751/2811 | 584/936 | chr2 | 64553225 | |||
| chr2:64553337 | C | G | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1863C>G | p.His621Gln | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 2180/4098 | 1863/2811 | 621/936 | chr2 | 64553337 | |||
| chr2:64581253 | G | A | 1 | a0006 | 2 | HG00408.hp2 NA19011.hp2 |
missense_variant | MODERATE | c.2519G>A | p.Ser840Asn | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/10 | 2836/4098 | 2519/2811 | 840/936 | chr2 | 64581253 | |||
| chr2:64592009 | A | C | 1 | a0010 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2785A>C | p.Ser929Arg | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 3102/4098 | 2785/2811 | 929/936 | chr2 | 64592009 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64551852 | T | C | 1 | a0005c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.378T>C | p.Asp126Asp | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 695/4098 | 378/2811 | 126/936 | chr2 | 64551852 | |||
| chr2:64552248 | A | T | 1 | a0001c0016 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.774A>T | p.Ala258Ala | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1091/4098 | 774/2811 | 258/936 | chr2 | 64552248 | |||
| chr2:64553010 | A | G | 2 | a0001c0005 a0002c0010 |
4 | HG00099.hp2 HG02683.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1536A>G | p.Gln512Gln | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/10 | 1853/4098 | 1536/2811 | 512/936 | chr2 | 64553010 | |||
| chr2:64592029 | C | T | 1 | a0001c0012 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.2805C>T | p.Asp935Asp | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 3122/4098 | 2805/2811 | 935/936 | chr2 | 64592029 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64524355 | G | A | 1 | a0001c0001t0015 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-290G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27120 | chr2 | 64524355 | ||||||
| chr2:64524402 | G | A | 1 | a0002c0010t0016 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27073 | chr2 | 64524402 | ||||||
| chr2:64524404 | A | C | 1 | a0001c0001t0020 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-241A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 27071 | chr2 | 64524404 | ||||||
| chr2:64524485 | C | G | 1 | a0001c0001t0013 | 3 | NA18946.hp1 NA19011.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-160C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | 26990 | chr2 | 64524485 | ||||||
| chr2:64524601 | C | T | 1 | a0002c0002t0019 | 1 | HG03041.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/10 | chr2 | 64524601 | |||||||
| chr2:64592115 | T | TA | 7 | a0001c0001t0002 a0001c0001t0006 a0002c0002t0002 others(4): Show |
67 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*100dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | |||||
| chr2:64592115 | T | TAA | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(3): Show |
51 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*99_*100dupAA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | |||||
| chr2:64592115 | T | TAAA | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0010 others(4): Show |
83 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*100dupAAA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 101 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | |||||
| chr2:64592115 | TA | T | 1 | a0001c0001t0007 | 8 | HG01168.hp2 HG01169.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*100delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 100 | INFO_REALIGN_3_PRIME | chr2 | 64592115 | |||||
| chr2:64592246 | G | A | 4 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(1): Show |
44 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*211G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 211 | chr2 | 64592246 | ||||||
| chr2:64592381 | G | A | 1 | a0001c0001t0018 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 346 | chr2 | 64592381 | ||||||
| chr2:64592516 | G | A | 1 | a0003c0003t0008 | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*481G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 481 | chr2 | 64592516 | ||||||
| chr2:64592575 | G | A | 1 | a0010c0013t0017 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 540 | chr2 | 64592575 | ||||||
| chr2:64592605 | T | TAATC | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(11): Show |
110 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*573_*574insCAAT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 10/10 | 574 | INFO_REALIGN_3_PRIME | chr2 | 64592605 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:64524619 | G | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.-33+7G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524619 | |||||||
| chr2:64524881 | C | T | 90 | a0001c0001t0001g0332 a0001c0001t0004g0363 a0001c0001t0004g0364 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33+269C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524881 | |||||||
| chr2:64524926 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+314T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524926 | |||||||
| chr2:64524938 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+326G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524938 | |||||||
| chr2:64524952 | C | T | 1 | a0002c0002t0002g0366 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-33+340C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64524952 | |||||||
| chr2:64525009 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | NA18987.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-33+397C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525009 | |||||||
| chr2:64525088 | A | G | 1 | a0001c0001t0004g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-33+476A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525088 | |||||||
| chr2:64525160 | T | C | 201 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(198): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-33+548T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525160 | |||||||
| chr2:64525320 | G | A | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33+708G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525320 | |||||||
| chr2:64525320 | G | T | 1 | a0001c0001t0005g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-33+708G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525320 | |||||||
| chr2:64525346 | A | G | 1 | a0002c0002t0002g0365 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-33+734A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525346 | |||||||
| chr2:64525359 | A | G | 92 | a0001c0001t0001g0332 a0001c0001t0004g0363 a0001c0001t0004g0364 others(89): Show |
94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-33+747A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525359 | |||||||
| chr2:64525506 | A | G | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | NA18954.hp2 NA18957.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+894A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525506 | |||||||
| chr2:64525507 | A | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+895A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525507 | |||||||
| chr2:64525580 | C | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+968C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525580 | |||||||
| chr2:64525738 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-33+1126A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525738 | |||||||
| chr2:64525776 | A | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(86): Show |
91 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-33+1164A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525776 | |||||||
| chr2:64525807 | C | A | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-33+1195C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525807 | |||||||
| chr2:64525959 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1347T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64525959 | |||||||
| chr2:64526065 | T | G | 1 | a0011c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-33+1453T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526065 | |||||||
| chr2:64526129 | C | T | 90 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33+1517C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526129 | |||||||
| chr2:64526196 | T | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+1584T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526196 | |||||||
| chr2:64526315 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1703A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526315 | |||||||
| chr2:64526542 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0003g0007 a0001c0001t0003g0008 |
3 | HG00741.hp2 HG01496.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-33+1930T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526542 | |||||||
| chr2:64526595 | C | T | 1 | a0001c0001t0013g0269 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-33+1983C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526595 | |||||||
| chr2:64526600 | C | T | 108 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-33+1988C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526600 | |||||||
| chr2:64526645 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33+2033T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526645 | |||||||
| chr2:64526701 | A | T | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+2089A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526701 | |||||||
| chr2:64526714 | A | T | 35 | a0001c0001t0001g0332 a0002c0002t0002g0005 a0002c0002t0002g0333 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-33+2102A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526714 | |||||||
| chr2:64526721 | A | G | 2 | a0001c0001t0009g0267 a0010c0013t0017g0268 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-33+2109A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526721 | |||||||
| chr2:64526991 | T | G | 2 | a0001c0001t0001g0115 a0001c0001t0007g0116 |
2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-33+2379T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64526991 | |||||||
| chr2:64527212 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(30): Show |
34 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+2600T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527212 | |||||||
| chr2:64527242 | G | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+2630G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527242 | |||||||
| chr2:64527441 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-33+2829G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527441 | |||||||
| chr2:64527489 | G | A | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+2877G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527489 | |||||||
| chr2:64527495 | G | A | 34 | a0001c0001t0001g0332 a0002c0002t0002g0005 a0002c0002t0002g0333 others(31): Show |
35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+2883G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527495 | |||||||
| chr2:64527580 | C | CA | 243 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(240): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.-33+2981dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64527580 | ||||||
| chr2:64527627 | A | G | 6 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+3015A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527627 | |||||||
| chr2:64527825 | C | T | 1 | a0002c0002t0003g0329 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-33+3213C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527825 | |||||||
| chr2:64527829 | C | G | 1 | a0002c0002t0003g0328 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-33+3217C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527829 | |||||||
| chr2:64527863 | A | G | 2 | a0001c0001t0002g0109 a0001c0001t0005g0108 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-33+3251A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64527863 | |||||||
| chr2:64528162 | C | A | 88 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+3550C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528162 | |||||||
| chr2:64528381 | C | A | 88 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+3769C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528381 | |||||||
| chr2:64528657 | G | C | 1 | a0001c0001t0004g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33+4045G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528657 | |||||||
| chr2:64528750 | G | A | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+4138G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528750 | |||||||
| chr2:64528762 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-33+4150G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528762 | |||||||
| chr2:64528800 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33+4188G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528800 | |||||||
| chr2:64528842 | G | A | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+4230G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528842 | |||||||
| chr2:64528920 | T | C | 1 | a0002c0002t0003g0330 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-33+4308T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64528920 | |||||||
| chr2:64529111 | A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+4499A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529111 | |||||||
| chr2:64529150 | T | C | 1 | a0001c0001t0005g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-33+4538T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529150 | |||||||
| chr2:64529315 | G | GT | 88 | a0001c0001t0001g0231 a0001c0001t0001g0332 a0001c0001t0014g0006 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+4715dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529315 | ||||||
| chr2:64529315 | G | GTT | 111 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-33+4714_-33+4715d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529315 | ||||||
| chr2:64529347 | A | G | 1 | a0002c0002t0002g0361 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33+4735A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529347 | |||||||
| chr2:64529528 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-33+4916T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529528 | |||||||
| chr2:64529584 | G | A | 201 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(198): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-33+4972G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529584 | |||||||
| chr2:64529633 | CT | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(149): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-33+5035delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64529633 | ||||||
| chr2:64529758 | T | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5146T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529758 | |||||||
| chr2:64529775 | G | A | 2 | a0001c0001t0005g0035 a0001c0001t0011g0034 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-33+5163G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529775 | |||||||
| chr2:64529786 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(150): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-33+5174T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529786 | |||||||
| chr2:64529891 | C | T | 86 | a0001c0001t0001g0332 a0002c0002t0001g0004 a0002c0002t0001g0312 others(83): Show |
88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-33+5279C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529891 | |||||||
| chr2:64529892 | G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5280G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64529892 | |||||||
| chr2:64530087 | T | C | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-33+5475T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530087 | |||||||
| chr2:64530167 | A | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+5555A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530167 | |||||||
| chr2:64530362 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(150): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-33+5750T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530362 | |||||||
| chr2:64530693 | T | G | 1 | a0001c0001t0003g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-33+6081T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530693 | |||||||
| chr2:64530705 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-33+6093C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530705 | |||||||
| chr2:64530716 | C | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(29): Show |
33 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-33+6104C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530716 | |||||||
| chr2:64530780 | G | A | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+6168G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530780 | |||||||
| chr2:64530797 | C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+6185C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530797 | |||||||
| chr2:64530830 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33+6218G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530830 | |||||||
| chr2:64530832 | C | T | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-33+6220C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530832 | |||||||
| chr2:64530891 | G | A | 2 | a0002c0002t0002g0285 a0002c0002t0002g0365 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-33+6279G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530891 | |||||||
| chr2:64530936 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-33+6324C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530936 | |||||||
| chr2:64530946 | C | T | 1 | a0008c0017t0003g0326 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-33+6334C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530946 | |||||||
| chr2:64530987 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-33+6375G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530987 | |||||||
| chr2:64530989 | G | A | 3 | a0001c0001t0013g0235 a0001c0001t0013g0236 a0001c0001t0013g0269 |
3 | NA18946.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-33+6377G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64530989 | |||||||
| chr2:64531061 | C | CA | 34 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0001g0128 others(31): Show |
35 | HG01261.hp1 HG01261.hp2 HG01993.hp1 others(32): Show |
intron_variant | MODIFIER | c.-33+6469dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | ||||||
| chr2:64531061 | C | CAA | 105 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-33+6468_-33+6469d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | ||||||
| chr2:64531061 | C | CAAA | 8 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0004g0036 others(5): Show |
8 | HG00621.hp1 HG02135.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+6467_-33+6469d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | ||||||
| chr2:64531061 | CA | C | 29 | a0001c0001t0001g0262 a0001c0001t0014g0006 a0002c0002t0001g0004 others(26): Show |
30 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+6469delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531061 | ||||||
| chr2:64531079 | AAAC | A | 34 | a0001c0001t0001g0332 a0002c0002t0002g0005 a0002c0002t0002g0333 others(31): Show |
35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+6469_-33+6471d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64531079 | ||||||
| chr2:64531081 | AC | A | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+6470delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531081 | |||||||
| chr2:64531082 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+6470C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531082 | |||||||
| chr2:64531276 | G | A | 111 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-33+6664G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531276 | |||||||
| chr2:64531546 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+6934A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531546 | |||||||
| chr2:64531584 | A | G | 1 | a0002c0002t0019g0360 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-33+6972A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64531584 | |||||||
| chr2:64532011 | C | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+7399C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532011 | |||||||
| chr2:64532186 | CTGTAAGT others(12): Show |
C | 9 | a0002c0002t0002g0281 a0002c0002t0002g0285 a0002c0002t0002g0286 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+7577_-33+7595d others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64532186 | ||||||
| chr2:64532308 | G | T | 199 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(196): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-33+7696G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532308 | |||||||
| chr2:64532310 | G | A | 88 | a0001c0001t0001g0332 a0002c0002t0001g0004 a0002c0002t0001g0312 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-33+7698G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532310 | |||||||
| chr2:64532337 | T | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+7725T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532337 | |||||||
| chr2:64532344 | A | T | 2 | a0001c0001t0001g0120 a0001c0001t0004g0230 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-33+7732A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532344 | |||||||
| chr2:64532750 | G | C | 1 | a0001c0001t0006g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-33+8138G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532750 | |||||||
| chr2:64532892 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+8280C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532892 | |||||||
| chr2:64532914 | G | C | 1 | a0001c0001t0006g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-33+8302G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532914 | |||||||
| chr2:64532985 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(237): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.-33+8373G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64532985 | |||||||
| chr2:64533088 | T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+8476T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533088 | |||||||
| chr2:64533209 | G | A | 35 | a0001c0001t0001g0332 a0002c0002t0002g0005 a0002c0002t0002g0333 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-33+8597G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533209 | |||||||
| chr2:64533398 | G | C | 1 | a0001c0001t0004g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-33+8786G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533398 | |||||||
| chr2:64533487 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(146): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+8875T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533487 | |||||||
| chr2:64533607 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(146): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+8995G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533607 | |||||||
| chr2:64533611 | A | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+8999A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533611 | |||||||
| chr2:64533669 | A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+9057A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533669 | |||||||
| chr2:64533990 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+9378A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533990 | |||||||
| chr2:64533996 | T | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(146): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-33+9384T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64533996 | |||||||
| chr2:64534075 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0005g0108 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-33+9463T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534075 | |||||||
| chr2:64534107 | GT | G | 14 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0004g0030 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+9499delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534107 | ||||||
| chr2:64534337 | T | C | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+9725T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534337 | |||||||
| chr2:64534351 | AT | A | 91 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(88): Show |
93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+9745delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534351 | ||||||
| chr2:64534419 | C | T | 91 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(88): Show |
93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+9807C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534419 | |||||||
| chr2:64534580 | A | G | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-33+9968A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534580 | |||||||
| chr2:64534582 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-33+9970G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534582 | |||||||
| chr2:64534742 | GT | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.-33+10144delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64534742 | ||||||
| chr2:64534764 | T | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+10152T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534764 | |||||||
| chr2:64534906 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+10294C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534906 | |||||||
| chr2:64534996 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-33+10384C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64534996 | |||||||
| chr2:64535206 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-33+10594C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535206 | |||||||
| chr2:64535229 | A | G | 1 | a0002c0002t0002g0357 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-33+10617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535229 | |||||||
| chr2:64535284 | AGTATCAT others(5): Show |
A | 6 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+10673_-33+1068 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535284 | |||||||
| chr2:64535331 | C | T | 107 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-33+10719C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535331 | |||||||
| chr2:64535358 | C | T | 2 | a0001c0001t0005g0101 a0001c0001t0005g0102 |
2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-33+10746C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535358 | |||||||
| chr2:64535454 | C | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+10842C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535454 | |||||||
| chr2:64535568 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-33+10956G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535568 | |||||||
| chr2:64535589 | ATG | A | 91 | a0001c0001t0001g0332 a0001c0001t0014g0006 a0002c0002t0001g0004 others(88): Show |
93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+10979_-33+1098 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64535589 | ||||||
| chr2:64535771 | C | CAT | 199 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(196): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-33+11159_-33+1116 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64535771 | |||||||
| chr2:64536023 | G | T | 1 | a0001c0001t0005g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-33+11411G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536023 | |||||||
| chr2:64536102 | T | C | 1 | a0001c0001t0004g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-33+11490T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536102 | |||||||
| chr2:64536404 | T | TAAAAATA others(172): Show |
1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-33+11807_-33+1180 others(183): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536404 | ||||||
| chr2:64536532 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-33+11920A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536532 | |||||||
| chr2:64536537 | G | A | 1 | a0001c0001t0004g0011 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-33+11925G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536537 | |||||||
| chr2:64536566 | TA | T | 17 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0226 others(14): Show |
17 | HG01515.hp2 HG02027.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+11977delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536566 | TAA | T | 95 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(92): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-33+11976_-33+1197 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536566 | TAAA | T | 6 | a0001c0001t0002g0109 a0001c0001t0004g0052 a0001c0001t0004g0097 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+11975_-33+1197 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536566 | TAAAA | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-33+11974_-33+1197 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536566 | TAAAAAAA others(2): Show |
T | 85 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(82): Show |
87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-33+11969_-33+1197 others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536566 | TAAAAAAA others(3): Show |
T | 2 | a0002c0002t0003g0280 a0002c0002t0003g0305 |
2 | HG00558.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-33+11968_-33+1197 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536566 | ||||||
| chr2:64536640 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33+12028A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536640 | |||||||
| chr2:64536720 | A | G | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+12108A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536720 | |||||||
| chr2:64536856 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(35): Show |
39 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-33+12244A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64536856 | |||||||
| chr2:64536951 | C | CA | 6 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0271 others(3): Show |
6 | HG02683.hp2 HG02738.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+12363dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | ||||||
| chr2:64536951 | CA | C | 22 | a0001c0001t0001g0124 a0001c0001t0001g0135 a0001c0001t0001g0219 others(19): Show |
23 | HG01106.hp2 HG01496.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-33+12363delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | ||||||
| chr2:64536951 | CAA | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0238 others(93): Show |
98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-33+12362_-33+1236 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | ||||||
| chr2:64536951 | CAAA | C | 82 | a0001c0001t0001g0042 a0001c0001t0001g0107 a0001c0001t0001g0254 others(79): Show |
84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-33+12361_-33+1236 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | ||||||
| chr2:64536951 | CAAAA | C | 37 | a0001c0001t0001g0095 a0001c0001t0002g0021 a0001c0001t0002g0109 others(34): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-33+12360_-33+1236 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64536951 | ||||||
| chr2:64537078 | C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33+12466C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537078 | |||||||
| chr2:64537107 | T | C | 89 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(86): Show |
91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-33+12495T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537107 | |||||||
| chr2:64537111 | C | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(231): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-33+12499C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537111 | |||||||
| chr2:64537129 | T | TA | 235 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(232): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-33+12523dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64537129 | ||||||
| chr2:64537268 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0015g0218 |
3 | HG02280.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33+12656A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537268 | |||||||
| chr2:64537369 | C | T | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+12757C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537369 | |||||||
| chr2:64537798 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-33+13186T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64537798 | |||||||
| chr2:64538122 | A | T | 9 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0002c0002t0002g0283 others(6): Show |
9 | HG00558.hp2 HG02145.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-13321A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538122 | |||||||
| chr2:64538207 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-32-13236C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538207 | |||||||
| chr2:64538340 | T | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(235): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-32-13103T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538340 | |||||||
| chr2:64538363 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-32-13080A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538363 | |||||||
| chr2:64538418 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-32-13025G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538418 | |||||||
| chr2:64538425 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(140): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-32-13018C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538425 | |||||||
| chr2:64538457 | C | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-32-12986C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538457 | |||||||
| chr2:64538608 | G | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG00323.hp2 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-32-12835G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538608 | |||||||
| chr2:64538620 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG00323.hp2 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-32-12823C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538620 | |||||||
| chr2:64538644 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-12799T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538644 | |||||||
| chr2:64538831 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-32-12612T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64538831 | |||||||
| chr2:64538866 | GCTT | G | 38 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(35): Show |
39 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32-12573_-32-1257 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64538866 | ||||||
| chr2:64538984 | A | AT | 235 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(232): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-32-12453dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64538984 | ||||||
| chr2:64539124 | A | C | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-12319A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539124 | |||||||
| chr2:64539156 | G | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-12287G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539156 | |||||||
| chr2:64539168 | T | G | 1 | a0001c0001t0005g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-32-12275T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539168 | |||||||
| chr2:64539191 | G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-12252G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539191 | |||||||
| chr2:64539365 | A | G | 22 | a0001c0001t0002g0021 a0001c0001t0003g0007 a0001c0001t0003g0008 others(19): Show |
22 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-12078A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539365 | |||||||
| chr2:64539376 | G | GT | 9 | a0002c0002t0002g0281 a0002c0002t0002g0285 a0002c0002t0002g0286 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-12061dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64539376 | ||||||
| chr2:64539434 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-32-12009T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539434 | |||||||
| chr2:64539518 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-32-11925T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539518 | |||||||
| chr2:64539594 | T | C | 3 | a0002c0002t0001g0312 a0002c0002t0001g0313 a0002c0002t0001g0314 |
3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-11849T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539594 | |||||||
| chr2:64539676 | G | C | 5 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0306 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-11767G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539676 | |||||||
| chr2:64539702 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-11741A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539702 | |||||||
| chr2:64539779 | A | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-11664A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539779 | |||||||
| chr2:64539785 | G | T | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02080.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-11658G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539785 | |||||||
| chr2:64539844 | G | A | 35 | a0002c0002t0002g0005 a0002c0002t0002g0333 a0002c0002t0002g0334 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-11599G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64539844 | |||||||
| chr2:64539891 | TGAG | T | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-11545_-32-1154 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64539891 | ||||||
| chr2:64540003 | G | GTGATGGA others(2902): Show |
1 | a0002c0002t0003g0304 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-32-11425_-32-1142 others(2913): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64540003 | ||||||
| chr2:64540128 | C | T | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-11315C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540128 | |||||||
| chr2:64540163 | A | C | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-11280A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540163 | |||||||
| chr2:64540321 | A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-11122A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540321 | |||||||
| chr2:64540340 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-32-11103A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540340 | |||||||
| chr2:64540546 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0133 |
2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-32-10897G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540546 | |||||||
| chr2:64540629 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(237): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.-32-10814A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540629 | |||||||
| chr2:64540646 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-10797T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540646 | |||||||
| chr2:64540656 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-32-10787A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540656 | |||||||
| chr2:64540797 | C | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-32-10646C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540797 | |||||||
| chr2:64540815 | C | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-10628C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540815 | |||||||
| chr2:64540854 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(144): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-10589T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540854 | |||||||
| chr2:64540867 | G | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-10576G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540867 | |||||||
| chr2:64540940 | C | G | 2 | a0002c0002t0003g0324 a0002c0002t0010g0323 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-32-10503C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540940 | |||||||
| chr2:64540943 | A | G | 1 | a0001c0001t0005g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-32-10500A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540943 | |||||||
| chr2:64540957 | A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-10486A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540957 | |||||||
| chr2:64540992 | AC | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-10450delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540992 | |||||||
| chr2:64540993 | C | T | 21 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0001g0150 others(18): Show |
21 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-10450C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540993 | |||||||
| chr2:64540994 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-10449G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64540994 | |||||||
| chr2:64541061 | T | C | 108 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-10382T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541061 | |||||||
| chr2:64541103 | C | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(35): Show |
39 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.-32-10340C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541103 | |||||||
| chr2:64541133 | CAT | C | 14 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0004g0030 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-10307_-32-1030 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64541133 | ||||||
| chr2:64541254 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0226 a0001c0001t0004g0121 |
3 | HG01515.hp2 HG01928.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-32-10189C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541254 | |||||||
| chr2:64541424 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-32-10019C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541424 | |||||||
| chr2:64541440 | C | T | 1 | a0002c0002t0001g0319 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32-10003C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541440 | |||||||
| chr2:64541490 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32-9953A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541490 | |||||||
| chr2:64541576 | G | T | 1 | a0011c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-9867G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541576 | |||||||
| chr2:64541650 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-32-9793G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541650 | |||||||
| chr2:64541829 | A | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-9614A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64541829 | |||||||
| chr2:64542018 | C | T | 1 | a0002c0002t0003g0303 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32-9425C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542018 | |||||||
| chr2:64542020 | A | G | 2 | a0002c0002t0002g0285 a0002c0002t0002g0365 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-32-9423A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542020 | |||||||
| chr2:64542034 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-32-9409A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542034 | |||||||
| chr2:64542090 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-9353T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542090 | |||||||
| chr2:64542234 | G | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-9209G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542234 | |||||||
| chr2:64542250 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-32-9193C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542250 | |||||||
| chr2:64542301 | T | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(144): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-9142T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542301 | |||||||
| chr2:64542347 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(144): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-9096C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542347 | |||||||
| chr2:64542415 | A | G | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-32-9028A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542415 | |||||||
| chr2:64542525 | T | A | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-8918T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542525 | |||||||
| chr2:64542624 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0004g0090 |
2 | HG03669.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-32-8819C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542624 | |||||||
| chr2:64542805 | ATGTT | A | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-32-8634_-32-8631d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64542805 | ||||||
| chr2:64542892 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-8551A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542892 | |||||||
| chr2:64542957 | T | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-8486T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64542957 | |||||||
| chr2:64543133 | C | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-8310C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543133 | |||||||
| chr2:64543253 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-8190T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543253 | |||||||
| chr2:64543291 | C | T | 5 | a0001c0001t0006g0125 a0001c0001t0006g0200 a0002c0002t0002g0285 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-8152C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543291 | |||||||
| chr2:64543391 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(145): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-32-8052A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543391 | |||||||
| chr2:64543419 | T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-8024T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543419 | |||||||
| chr2:64543645 | A | G | 108 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-7798A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543645 | |||||||
| chr2:64543703 | G | A | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-32-7740G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543703 | |||||||
| chr2:64543747 | T | C | 108 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-32-7696T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543747 | |||||||
| chr2:64543773 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-32-7670T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543773 | |||||||
| chr2:64543847 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-7596C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543847 | |||||||
| chr2:64543865 | C | T | 6 | a0001c0001t0009g0267 a0003c0003t0008g0232 a0003c0003t0008g0263 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-7578C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543865 | |||||||
| chr2:64543952 | C | G | 2 | a0002c0002t0002g0281 a0002c0002t0002g0327 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-32-7491C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64543952 | |||||||
| chr2:64544006 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(144): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-7437T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544006 | |||||||
| chr2:64544137 | A | G | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-7306A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544137 | |||||||
| chr2:64544141 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(144): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-7302C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544141 | |||||||
| chr2:64544311 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-32-7132G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544311 | |||||||
| chr2:64544366 | C | T | 34 | a0002c0002t0002g0005 a0002c0002t0002g0333 a0002c0002t0002g0334 others(31): Show |
35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-7077C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544366 | |||||||
| chr2:64544468 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-6975T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544468 | |||||||
| chr2:64544505 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-32-6938G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544505 | |||||||
| chr2:64544594 | CCT | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(28): Show |
32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32-6848_-32-6847d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544594 | |||||||
| chr2:64544650 | T | TAGAAATG others(319): Show |
1 | a0001c0001t0001g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(328): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544650 | T | TAGAAATG others(318): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0237 a0001c0001t0001g0238 others(17): Show |
21 | HG01243.hp1 HG01993.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(327): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544650 | T | TAGAAATG others(317): Show |
11 | a0001c0001t0001g0234 a0001c0001t0001g0256 a0001c0001t0001g0257 others(8): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(326): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544650 | T | TAGAAATG others(315): Show |
5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-6777_-32-6776i others(324): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544650 | T | TAGAAATG others(314): Show |
1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(323): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544650 | T | TAGAAATG others(317): Show |
1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-6777_-32-6776i others(326): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64544650 | ||||||
| chr2:64544771 | C | T | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-6672C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544771 | |||||||
| chr2:64544809 | C | G | 7 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0089 others(4): Show |
7 | HG02027.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-6634C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544809 | |||||||
| chr2:64544874 | C | T | 79 | a0002c0002t0002g0005 a0002c0002t0002g0111 a0002c0002t0002g0112 others(76): Show |
80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-32-6569C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544874 | |||||||
| chr2:64544885 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(224): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-32-6558G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544885 | |||||||
| chr2:64544892 | A | G | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6551A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64544892 | |||||||
| chr2:64545012 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(37): Show |
41 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-32-6431C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545012 | |||||||
| chr2:64545089 | G | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-6354G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545089 | |||||||
| chr2:64545122 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-6321A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545122 | |||||||
| chr2:64545137 | A | T | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-6306A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545137 | |||||||
| chr2:64545319 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-32-6124C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545319 | |||||||
| chr2:64545475 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-5968T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545475 | |||||||
| chr2:64545570 | T | TA | 28 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0124 others(25): Show |
28 | HG00323.hp2 HG01071.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-5831dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAA | 19 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0137 others(16): Show |
19 | HG00597.hp1 HG00621.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.-32-5832_-32-5831d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAA | 10 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 others(7): Show |
10 | HG00280.hp1 HG00558.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-5833_-32-5831d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAA | 7 | a0001c0001t0001g0126 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5835_-32-5831d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAAAA | 9 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0145 others(6): Show |
9 | HG00140.hp1 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-5837_-32-5831d others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0114 a0001c0001t0001g0144 a0001c0001t0001g0270 others(4): Show |
7 | HG00741.hp2 HG03831.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5838_-32-5831d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-5840_-32-5831d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0143 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-5841_-32-5831d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-32-5844_-32-5831d others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAA | T | 17 | a0001c0001t0001g0189 a0002c0002t0002g0292 a0002c0002t0002g0327 others(14): Show |
17 | HG00673.hp2 HG01074.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-5833_-32-5831d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAA | T | 18 | a0001c0001t0004g0037 a0001c0001t0005g0087 a0001c0001t0009g0267 others(15): Show |
18 | HG00408.hp1 HG00558.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-5834_-32-5831d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAA | T | 10 | a0001c0001t0005g0088 a0001c0001t0005g0089 a0001c0001t0005g0100 others(7): Show |
10 | HG02132.hp1 HG02135.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-5835_-32-5831d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAA | T | 20 | a0001c0001t0001g0256 a0001c0001t0003g0012 a0001c0001t0005g0057 others(17): Show |
20 | HG00408.hp2 HG00642.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-5836_-32-5831d others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA | T | 38 | a0001c0001t0002g0109 a0001c0001t0004g0011 a0001c0001t0004g0036 others(35): Show |
38 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-32-5837_-32-5831d others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(1): Show |
T | 59 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(56): Show |
61 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-32-5838_-32-5831d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(2): Show |
T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(37): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-32-5839_-32-5831d others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(3): Show |
T | 6 | a0001c0001t0001g0191 a0001c0001t0001g0242 a0001c0001t0001g0254 others(3): Show |
6 | HG00673.hp1 HG01261.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-5840_-32-5831d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(4): Show |
T | 6 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-5841_-32-5831d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-32-5842_-32-5831d others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(9): Show |
T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0220 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-32-5846_-32-5831d others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(10): Show |
T | 4 | a0001c0001t0001g0193 a0001c0001t0003g0008 a0002c0002t0002g0309 others(1): Show |
4 | HG01496.hp1 HG02735.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5847_-32-5831d others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(11): Show |
T | 6 | a0001c0001t0001g0194 a0001c0001t0005g0098 a0002c0002t0002g0111 others(3): Show |
6 | HG01975.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-5848_-32-5831d others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0001g0196 a0001c0001t0007g0195 |
2 | HG01168.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-32-5849_-32-5831d others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(13): Show |
T | 3 | a0001c0001t0001g0252 a0001c0001t0007g0197 a0001c0001t0014g0006 |
3 | HG01169.hp1 HG01993.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-32-5850_-32-5831d others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(14): Show |
T | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-5851_-32-5831d others(23): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(15): Show |
T | 2 | a0001c0001t0001g0198 a0002c0002t0002g0005 |
3 | NA19009.hp1 NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-32-5852_-32-5831d others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(16): Show |
T | 1 | a0001c0001t0007g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-32-5853_-32-5831d others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545570 | TAAAAAAA others(17): Show |
T | 4 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 others(1): Show |
4 | HG01123.hp1 HG01167.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-5854_-32-5831d others(26): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545570 | ||||||
| chr2:64545709 | T | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5734T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545709 | |||||||
| chr2:64545710 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5733C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545710 | |||||||
| chr2:64545711 | CT | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5729delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64545711 | ||||||
| chr2:64545715 | C | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-32-5728C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545715 | |||||||
| chr2:64545835 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-32-5608G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545835 | |||||||
| chr2:64545847 | G | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-5596G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545847 | |||||||
| chr2:64545894 | C | T | 1 | a0001c0001t0006g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-32-5549C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545894 | |||||||
| chr2:64545955 | C | T | 4 | a0003c0003t0008g0263 a0003c0003t0008g0264 a0003c0003t0008g0265 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-5488C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545955 | |||||||
| chr2:64545956 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0005g0108 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-32-5487G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64545956 | |||||||
| chr2:64546081 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-5362T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546081 | |||||||
| chr2:64546117 | T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-5326T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546117 | |||||||
| chr2:64546133 | T | C | 1 | a0001c0001t0006g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-32-5310T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546133 | |||||||
| chr2:64546193 | C | CT | 145 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(142): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-32-5240dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64546193 | ||||||
| chr2:64546289 | A | G | 2 | a0001c0001t0001g0367 a0001c0001t0003g0027 |
2 | HG01891.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-32-5154A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546289 | |||||||
| chr2:64546439 | T | G | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-5004T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546439 | |||||||
| chr2:64546468 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32-4975A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546468 | |||||||
| chr2:64546526 | A | G | 1 | a0002c0002t0001g0314 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-32-4917A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546526 | |||||||
| chr2:64546550 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-32-4893C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546550 | |||||||
| chr2:64546573 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-32-4870T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546573 | |||||||
| chr2:64546645 | G | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(233): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-32-4798G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546645 | |||||||
| chr2:64546799 | C | T | 1 | a0001c0001t0005g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-32-4644C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546799 | |||||||
| chr2:64546870 | T | A | 1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-4573T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546870 | |||||||
| chr2:64546870 | TA | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(142): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-32-4562delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64546870 | ||||||
| chr2:64546884 | C | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4559C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546884 | |||||||
| chr2:64546887 | A | G | 1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-4556A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546887 | |||||||
| chr2:64546972 | C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4471C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546972 | |||||||
| chr2:64546973 | C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-32-4470C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64546973 | |||||||
| chr2:64547043 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-4400T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547043 | |||||||
| chr2:64547056 | T | C | 1 | a0001c0001t0005g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-32-4387T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547056 | |||||||
| chr2:64547242 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-32-4201C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547242 | |||||||
| chr2:64547247 | A | G | 2 | a0002c0002t0003g0294 a0002c0002t0003g0301 |
2 | NA18956.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-32-4196A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547247 | |||||||
| chr2:64547322 | G | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(235): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-32-4121G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547322 | |||||||
| chr2:64547324 | C | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(30): Show |
34 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32-4119C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547324 | |||||||
| chr2:64547372 | A | G | 32 | a0001c0001t0004g0276 a0002c0002t0002g0005 a0002c0002t0002g0334 others(29): Show |
33 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32-4071A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547372 | |||||||
| chr2:64547401 | C | T | 2 | a0002c0002t0003g0300 a0002c0002t0003g0303 |
2 | HG02083.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-32-4042C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547401 | |||||||
| chr2:64547412 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-4031T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547412 | |||||||
| chr2:64547450 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-32-3993A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547450 | |||||||
| chr2:64547671 | A | G | 1 | a0001c0001t0004g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-32-3772A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547671 | |||||||
| chr2:64547740 | T | C | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-3703T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547740 | |||||||
| chr2:64547740 | T | TGTATC | 227 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(224): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-32-3703_-32-3702i others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547740 | |||||||
| chr2:64547905 | C | T | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-32-3538C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547905 | |||||||
| chr2:64547907 | T | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-3536T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64547907 | |||||||
| chr2:64548070 | T | C | 1 | a0011c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-3373T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548070 | |||||||
| chr2:64548083 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-3360G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548083 | |||||||
| chr2:64548119 | C | T | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-3324C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548119 | |||||||
| chr2:64548310 | G | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3133G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548310 | |||||||
| chr2:64548322 | A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3121A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548322 | |||||||
| chr2:64548348 | G | CCGCCACT others(168): Show |
1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-3096_-32-3095i others(177): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548348 | |||||||
| chr2:64548363 | G | A | 2 | a0002c0002t0003g0324 a0002c0002t0010g0323 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-32-3080G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548363 | |||||||
| chr2:64548407 | G | GA | 28 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0140 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-3008dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | ||||||
| chr2:64548407 | GA | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0131 a0001c0001t0001g0134 others(92): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-32-3008delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | ||||||
| chr2:64548407 | GAAAAA | G | 8 | a0001c0001t0003g0010 a0001c0001t0003g0017 a0001c0001t0003g0022 others(5): Show |
8 | NA18954.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-3012_-32-3008d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | ||||||
| chr2:64548407 | GAAAAAAA others(8): Show |
G | 1 | a0002c0002t0002g0302 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-32-3022_-32-3008d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548407 | ||||||
| chr2:64548412 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-32-3031A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548412 | |||||||
| chr2:64548429 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-32-3014A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548429 | |||||||
| chr2:64548433 | A | AAAAAC | 23 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0003g0018 others(20): Show |
23 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-3008_-32-3007i others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548433 | ||||||
| chr2:64548433 | A | AAAAC | 69 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0002g0109 others(66): Show |
71 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-32-3008_-32-3007i others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64548433 | ||||||
| chr2:64548433 | A | C | 9 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(6): Show |
9 | NA18954.hp1 NA18957.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-3010A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548433 | |||||||
| chr2:64548615 | G | A | 20 | a0001c0001t0002g0021 a0001c0001t0003g0009 a0001c0001t0003g0010 others(17): Show |
20 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-2828G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548615 | |||||||
| chr2:64548656 | CAA | C | 3 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0310 |
3 | HG02630.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-32-2786_-32-2785d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548656 | |||||||
| chr2:64548682 | G | A | 34 | a0002c0002t0002g0005 a0002c0002t0002g0333 a0002c0002t0002g0334 others(31): Show |
35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-2761G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548682 | |||||||
| chr2:64548983 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0014g0043 |
4 | HG01243.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-2460G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64548983 | |||||||
| chr2:64549250 | G | A | 1 | a0001c0001t0006g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-32-2193G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549250 | |||||||
| chr2:64549308 | C | CTTTTTTT others(6): Show |
1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-2117_-32-2105d others(15): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CT | C | 127 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0114 others(124): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-2105delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTT | C | 75 | a0001c0001t0001g0107 a0001c0001t0001g0151 a0001c0001t0001g0160 others(72): Show |
76 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-32-2106_-32-2105d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTT | C | 35 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(32): Show |
36 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-2109_-32-2105d others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(2): Show |
C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(28): Show |
32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32-2113_-32-2105d others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0245 a0001c0001t0001g0367 a0001c0001t0007g0251 others(1): Show |
4 | HG01891.hp1 NA18948.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-2114_-32-2105d others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(4): Show |
C | 35 | a0001c0001t0014g0006 a0002c0002t0002g0005 a0002c0002t0002g0111 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG02135.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-2115_-32-2105d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(5): Show |
C | 6 | a0002c0002t0002g0334 a0002c0002t0002g0336 a0002c0002t0002g0338 others(3): Show |
6 | HG02040.hp2 NA18949.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-2116_-32-2105d others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-32-2118_-32-2105d others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549308 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-32-2119_-32-2105d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549308 | ||||||
| chr2:64549338 | T | G | 1 | a0002c0002t0003g0295 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-32-2105T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549338 | |||||||
| chr2:64549446 | A | C | 39 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(36): Show |
40 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-1997A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549446 | |||||||
| chr2:64549461 | C | CTTAGGAA others(28): Show |
1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-32-1982_-32-1981i others(37): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549461 | |||||||
| chr2:64549478 | G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32-1965G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549478 | |||||||
| chr2:64549482 | G | T | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-1961G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549482 | |||||||
| chr2:64549513 | G | T | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1930G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549513 | |||||||
| chr2:64549601 | G | A | 5 | a0002c0002t0002g0281 a0002c0002t0002g0285 a0002c0002t0002g0307 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1842G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549601 | |||||||
| chr2:64549632 | T | C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-32-1811T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549632 | |||||||
| chr2:64549639 | C | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-1804C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549639 | |||||||
| chr2:64549663 | A | G | 2 | a0002c0002t0002g0286 a0002c0002t0002g0306 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-32-1780A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549663 | |||||||
| chr2:64549720 | A | G | 49 | a0002c0002t0002g0005 a0002c0002t0002g0111 a0002c0002t0002g0112 others(46): Show |
50 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(47): Show |
intron_variant | MODIFIER | c.-32-1723A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549720 | |||||||
| chr2:64549781 | GA | G | 88 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-32-1652delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64549781 | ||||||
| chr2:64549959 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-1484C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64549959 | |||||||
| chr2:64550009 | C | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-1434C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550009 | |||||||
| chr2:64550020 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-1423C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550020 | |||||||
| chr2:64550047 | G | A | 3 | a0002c0002t0001g0312 a0002c0002t0001g0313 a0002c0002t0001g0314 |
3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-1396G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550047 | |||||||
| chr2:64550127 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-32-1316A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550127 | |||||||
| chr2:64550304 | G | T | 1 | a0012c0014t0001g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-32-1139G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550304 | |||||||
| chr2:64550380 | A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-1063A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550380 | |||||||
| chr2:64550470 | A | G | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32-973A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550470 | |||||||
| chr2:64550598 | T | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-32-845T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550598 | |||||||
| chr2:64550677 | G | GCA | 25 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0001t0001g0129 others(22): Show |
25 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-32-713_-32-712dup others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | G | GCACA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0134 others(28): Show |
32 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.-32-715_-32-712dup others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | G | GCACACA | 25 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0135 others(22): Show |
25 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-32-717_-32-712dup others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0142 a0001c0001t0001g0191 a0001c0001t0001g0227 others(4): Show |
7 | HG00673.hp1 HG01978.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-719_-32-712dup others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | G | GCACACAC others(3): Show |
3 | a0001c0001t0001g0150 a0001c0001t0001g0172 a0002c0002t0003g0293 |
3 | HG00642.hp1 HG04115.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-32-721_-32-712dup others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | G | GCACACAC others(7): Show |
1 | a0001c0001t0007g0136 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-32-725_-32-712dup others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCA | G | 40 | a0001c0001t0001g0118 a0001c0001t0001g0130 a0001c0001t0001g0139 others(37): Show |
41 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-32-713_-32-712del others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACA | G | 24 | a0001c0001t0001g0137 a0001c0001t0001g0177 a0001c0001t0001g0204 others(21): Show |
24 | HG01168.hp2 HG01169.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-32-715_-32-712del others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACA | G | 27 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0231 others(24): Show |
27 | HG01891.hp1 HG02129.hp1 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.-32-717_-32-712del others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(1): Show |
G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0256 a0001c0001t0006g0033 others(16): Show |
20 | HG00408.hp2 HG01109.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-719_-32-712del others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(3): Show |
G | 7 | a0001c0001t0001g0126 a0002c0002t0001g0316 a0002c0002t0002g0286 others(4): Show |
7 | HG00558.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-721_-32-712del others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(5): Show |
G | 6 | a0001c0001t0003g0028 a0001c0001t0004g0036 a0001c0001t0006g0246 others(3): Show |
6 | HG01433.hp1 HG02083.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-723_-32-712del others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(7): Show |
G | 22 | a0001c0001t0001g0042 a0001c0001t0001g0222 a0001c0001t0004g0001 others(19): Show |
23 | HG01243.hp2 HG01943.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-725_-32-712del others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(9): Show |
G | 77 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0120 others(74): Show |
78 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-32-727_-32-712del others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(11): Show |
G | 23 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(20): Show |
23 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-729_-32-712del others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550677 | GCACACAC others(15): Show |
G | 1 | a0001c0001t0003g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32-733_-32-712del others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550677 | ||||||
| chr2:64550679 | A | ACG | 3 | a0002c0002t0002g0347 a0005c0007t0009g0331 a0006c0006t0002g0349 |
3 | NA18946.hp2 NA18962.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-32-763_-32-762ins others(2): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 64550679 | ||||||
| chr2:64550681 | A | G | 1 | a0002c0002t0002g0348 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-32-762A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550681 | |||||||
| chr2:64550683 | A | G | 9 | a0002c0002t0002g0005 a0002c0002t0002g0336 a0002c0002t0002g0338 others(6): Show |
10 | HG00323.hp1 HG02040.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-760A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550683 | |||||||
| chr2:64550685 | A | G | 4 | a0002c0002t0002g0355 a0002c0002t0002g0357 a0002c0002t0002g0359 others(1): Show |
4 | NA18972.hp1 NA19009.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-758A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550685 | |||||||
| chr2:64550687 | A | G | 5 | a0001c0001t0001g0256 a0002c0002t0002g0335 a0002c0002t0002g0346 others(2): Show |
5 | HG01109.hp2 HG02135.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-756A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550687 | |||||||
| chr2:64550689 | A | G | 4 | a0001c0001t0001g0256 a0002c0002t0002g0358 a0002c0002t0019g0360 others(1): Show |
4 | HG00408.hp2 HG01109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-754A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550689 | |||||||
| chr2:64550691 | A | G | 1 | a0002c0002t0002g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32-752A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550691 | |||||||
| chr2:64550692 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-751C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550692 | |||||||
| chr2:64550697 | A | G | 9 | a0002c0002t0002g0337 a0002c0002t0002g0340 a0002c0002t0002g0341 others(6): Show |
9 | NA18961.hp1 NA18969.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-746A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550697 | |||||||
| chr2:64550783 | T | C | 1 | a0003c0003t0008g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-32-660T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550783 | |||||||
| chr2:64550984 | T | C | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-459T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64550984 | |||||||
| chr2:64551025 | T | C | 5 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0306 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-418T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551025 | |||||||
| chr2:64551308 | C | A | 88 | a0001c0001t0014g0006 a0002c0002t0001g0004 a0002c0002t0001g0312 others(85): Show |
90 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-32-135C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551308 | |||||||
| chr2:64551338 | A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-32-105A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551338 | |||||||
| chr2:64551388 | G | A | 1 | a0011c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-55G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 1/9 | chr2 | 64551388 | |||||||
| chr2:64553519 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1935+110C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553519 | |||||||
| chr2:64553641 | G | A | 5 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+232G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553641 | |||||||
| chr2:64553655 | A | T | 40 | a0002c0002t0002g0005 a0002c0002t0002g0111 a0002c0002t0002g0112 others(37): Show |
41 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(38): Show |
intron_variant | MODIFIER | c.1935+246A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553655 | |||||||
| chr2:64553702 | TA | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(208): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1935+310delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553702 | ||||||
| chr2:64553702 | TAA | T | 40 | a0001c0001t0001g0237 a0001c0001t0004g0011 a0001c0001t0010g0025 others(37): Show |
41 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1935+309_1935+310d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553702 | ||||||
| chr2:64553714 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1935+305A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64553714 | |||||||
| chr2:64553812 | C | CT | 111 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1935+414dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64553812 | ||||||
| chr2:64554264 | G | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+855G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554264 | |||||||
| chr2:64554266 | GGTGTAGC others(8): Show |
G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+858_1935+872d others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554266 | |||||||
| chr2:64554289 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+880T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554289 | |||||||
| chr2:64554291 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+882C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554291 | |||||||
| chr2:64554319 | A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+910A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554319 | |||||||
| chr2:64554324 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+915T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554324 | |||||||
| chr2:64554329 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+920T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554329 | |||||||
| chr2:64554330 | T | TGTCTAAA others(9): Show |
1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+921_1935+922i others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554330 | |||||||
| chr2:64554331 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+922T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554331 | |||||||
| chr2:64554334 | C | G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+925C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554334 | |||||||
| chr2:64554347 | G | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+938G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554347 | |||||||
| chr2:64554383 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+974T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554383 | |||||||
| chr2:64554394 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+985G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554394 | |||||||
| chr2:64554395 | A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+986A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554395 | |||||||
| chr2:64554396 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+987T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554396 | |||||||
| chr2:64554405 | C | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+996C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554405 | |||||||
| chr2:64554413 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1004T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554413 | |||||||
| chr2:64554416 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1007T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554416 | |||||||
| chr2:64554417 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1008C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554417 | |||||||
| chr2:64554443 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1034T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554443 | |||||||
| chr2:64554444 | A | G | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1035A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554444 | |||||||
| chr2:64554445 | A | C | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1036A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554445 | |||||||
| chr2:64554447 | A | T | 1 | a0001c0001t0005g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1935+1038A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554447 | |||||||
| chr2:64554450 | C | T | 5 | a0001c0001t0004g0061 a0001c0001t0004g0074 a0001c0001t0004g0080 others(2): Show |
5 | HG02735.hp2 NA18949.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+1041C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554450 | |||||||
| chr2:64554479 | T | G | 113 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(110): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1935+1070T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554479 | |||||||
| chr2:64554583 | A | G | 1 | a0001c0005t0001g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1935+1174A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554583 | |||||||
| chr2:64554650 | A | T | 198 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(195): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1935+1241A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554650 | |||||||
| chr2:64554678 | T | C | 1 | a0001c0001t0005g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935+1269T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554678 | |||||||
| chr2:64554829 | C | T | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1935+1420C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64554829 | |||||||
| chr2:64555289 | A | G | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG01123.hp1 HG01167.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1935+1880A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555289 | |||||||
| chr2:64555441 | A | G | 1 | a0002c0002t0002g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1935+2032A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555441 | |||||||
| chr2:64555509 | C | T | 1 | a0001c0001t0005g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1935+2100C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555509 | |||||||
| chr2:64555555 | T | TCA | 73 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0131 others(70): Show |
74 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1935+2189_1935+219 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | T | TCACA | 17 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0220 others(14): Show |
17 | HG01175.hp1 HG01175.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1935+2187_1935+219 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | T | TCACACA | 7 | a0001c0001t0001g0124 a0001c0001t0001g0169 a0001c0001t0001g0258 others(4): Show |
7 | HG01993.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+2185_1935+219 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | T | TCACACAC others(1): Show |
4 | a0001c0001t0001g0175 a0001c0001t0001g0192 a0001c0001t0001g0257 others(1): Show |
4 | HG02486.hp2 HG03486.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+2183_1935+219 others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | TCA | T | 75 | a0001c0001t0001g0042 a0001c0001t0001g0117 a0001c0001t0001g0126 others(72): Show |
78 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1935+2189_1935+219 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | TCACA | T | 33 | a0001c0001t0001g0118 a0001c0001t0001g0151 a0001c0001t0001g0178 others(30): Show |
33 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1935+2187_1935+219 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | TCACACA | T | 28 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0004g0066 others(25): Show |
28 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2185_1935+219 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555555 | TCACACAC others(3): Show |
T | 2 | a0002c0002t0002g0347 a0002c0002t0002g0366 |
2 | HG00323.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1935+2181_1935+219 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555555 | ||||||
| chr2:64555835 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1935+2426A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64555835 | |||||||
| chr2:64555989 | C | CTTTTTTT others(6): Show |
1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1935+2583_1935+259 others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(7): Show |
27 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(24): Show |
28 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2582_1935+259 others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(8): Show |
14 | a0002c0002t0001g0315 a0002c0002t0001g0319 a0002c0002t0002g0111 others(11): Show |
14 | HG00673.hp2 HG02129.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1935+2581_1935+259 others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(9): Show |
5 | a0002c0002t0002g0112 a0002c0002t0002g0310 a0002c0002t0002g0311 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(10): Show |
20 | a0001c0001t0004g0276 a0002c0002t0002g0005 a0002c0002t0002g0333 others(17): Show |
21 | HG00323.hp1 HG00408.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(11): Show |
11 | a0002c0002t0002g0334 a0002c0002t0002g0335 a0002c0002t0002g0336 others(8): Show |
11 | HG02040.hp2 HG02135.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0201 a0002c0002t0002g0339 a0002c0002t0002g0357 |
3 | NA18949.hp2 NA18993.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1935+2595_1935+259 others(23): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0002g0346 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1935+2595_1935+259 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64555989 | C | CTTTTTTT others(14): Show |
1 | a0002c0002t0002g0361 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1935+2595_1935+259 others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64555989 | ||||||
| chr2:64556068 | G | A | 28 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(25): Show |
28 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1935+2659G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556068 | |||||||
| chr2:64556435 | G | A | 1 | a0001c0001t0003g0012 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1935+3026G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556435 | |||||||
| chr2:64556468 | A | G | 90 | a0001c0001t0002g0201 a0002c0002t0001g0004 a0002c0002t0001g0312 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1935+3059A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556468 | |||||||
| chr2:64556736 | G | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(233): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1935+3327G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556736 | |||||||
| chr2:64556746 | A | G | 5 | a0001c0001t0004g0061 a0001c0001t0004g0074 a0001c0001t0004g0080 others(2): Show |
5 | HG02735.hp2 NA18949.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+3337A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556746 | |||||||
| chr2:64556751 | T | C | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+3342T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556751 | |||||||
| chr2:64556752 | G | A | 1 | a0001c0001t0003g0008 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1935+3343G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556752 | |||||||
| chr2:64556860 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1935+3451G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556860 | |||||||
| chr2:64556863 | G | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+3454G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64556863 | |||||||
| chr2:64557026 | A | G | 5 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+3617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557026 | |||||||
| chr2:64557081 | A | AT | 9 | a0002c0002t0002g0281 a0002c0002t0002g0285 a0002c0002t0002g0286 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935+3681dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64557081 | ||||||
| chr2:64557256 | T | C | 1 | a0001c0001t0005g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1935+3847T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557256 | |||||||
| chr2:64557639 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1935+4230T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557639 | |||||||
| chr2:64557662 | C | T | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1935+4253C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557662 | |||||||
| chr2:64557684 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+4275T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64557684 | |||||||
| chr2:64557977 | ACT | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+4571_1935+457 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64557977 | ||||||
| chr2:64558019 | T | C | 108 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1935+4610T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558019 | |||||||
| chr2:64558316 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1935+4907A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558316 | |||||||
| chr2:64558480 | C | T | 202 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(199): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1935+5071C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558480 | |||||||
| chr2:64558764 | A | G | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1935+5355A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64558764 | |||||||
| chr2:64559002 | A | G | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+5593A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559002 | |||||||
| chr2:64559010 | C | A | 105 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1935+5601C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559010 | |||||||
| chr2:64559025 | C | T | 1 | a0002c0002t0003g0288 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1935+5616C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559025 | |||||||
| chr2:64559087 | G | A | 1 | a0002c0002t0002g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1935+5678G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559087 | |||||||
| chr2:64559212 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1935+5803T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559212 | |||||||
| chr2:64559233 | A | ATTCG | 90 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0001g0004 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1935+5826_1935+582 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64559233 | ||||||
| chr2:64559277 | G | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.1935+5868G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559277 | |||||||
| chr2:64559332 | G | T | 2 | a0001c0001t0003g0017 a0001c0001t0005g0070 |
2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1935+5923G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559332 | |||||||
| chr2:64559333 | A | T | 2 | a0001c0001t0003g0017 a0001c0001t0005g0070 |
2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1935+5924A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559333 | |||||||
| chr2:64559404 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(35): Show |
39 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1935+5995G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559404 | |||||||
| chr2:64559468 | G | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(233): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1935+6059G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559468 | |||||||
| chr2:64559558 | C | A | 2 | a0001c0001t0004g0363 a0001c0001t0004g0364 |
2 | HG00597.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1935+6149C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559558 | |||||||
| chr2:64559705 | G | A | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+6296G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559705 | |||||||
| chr2:64559711 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1935+6302T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559711 | |||||||
| chr2:64559749 | G | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+6340G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64559749 | |||||||
| chr2:64560000 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1935+6591C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560000 | |||||||
| chr2:64560091 | T | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1935+6682T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560091 | |||||||
| chr2:64560093 | C | T | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1935+6684C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560093 | |||||||
| chr2:64560133 | C | G | 4 | a0001c0001t0005g0058 a0001c0001t0005g0060 a0001c0001t0005g0084 others(1): Show |
4 | HG01261.hp1 HG02559.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+6724C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560133 | |||||||
| chr2:64560301 | A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1935+6892A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560301 | |||||||
| chr2:64560305 | A | G | 1 | a0001c0001t0005g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1935+6896A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560305 | |||||||
| chr2:64560316 | C | T | 1 | a0001c0001t0009g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+6907C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560316 | |||||||
| chr2:64560643 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1936-6919C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560643 | |||||||
| chr2:64560646 | A | G | 1 | a0001c0001t0006g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1936-6916A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560646 | |||||||
| chr2:64560718 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0018g0166 |
2 | HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1936-6844C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560718 | |||||||
| chr2:64560778 | C | T | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1936-6784C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560778 | |||||||
| chr2:64560783 | G | T | 107 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1936-6779G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560783 | |||||||
| chr2:64560948 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-6614G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64560948 | |||||||
| chr2:64561004 | A | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0227 a0001c0001t0001g0234 others(112): Show |
118 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1936-6558A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561004 | |||||||
| chr2:64561049 | C | G | 1 | a0005c0007t0002g0354 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1936-6513C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561049 | |||||||
| chr2:64561202 | T | C | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-6360T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561202 | |||||||
| chr2:64561223 | G | A | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02080.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-6339G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561223 | |||||||
| chr2:64561274 | G | A | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-6288G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561274 | |||||||
| chr2:64561410 | C | T | 1 | a0002c0002t0003g0301 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1936-6152C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561410 | |||||||
| chr2:64561581 | T | C | 1 | a0001c0001t0004g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1936-5981T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561581 | |||||||
| chr2:64561712 | C | A | 191 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(188): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1936-5850C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561712 | |||||||
| chr2:64561902 | C | T | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-5660C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561902 | |||||||
| chr2:64561914 | C | T | 1 | a0001c0001t0006g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1936-5648C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64561914 | |||||||
| chr2:64562030 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1936-5532T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562030 | |||||||
| chr2:64562313 | T | C | 38 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(35): Show |
39 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1936-5249T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562313 | |||||||
| chr2:64562360 | G | A | 187 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(184): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1936-5202G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562360 | |||||||
| chr2:64562447 | A | G | 1 | a0003c0003t0008g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1936-5115A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562447 | |||||||
| chr2:64562742 | T | A | 188 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(185): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1936-4820T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562742 | |||||||
| chr2:64562866 | C | G | 2 | a0002c0002t0002g0285 a0002c0002t0002g0365 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1936-4696C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562866 | |||||||
| chr2:64562940 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-4622T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64562940 | |||||||
| chr2:64563037 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(223): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-4525G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563037 | |||||||
| chr2:64563108 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(29): Show |
33 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(30): Show |
intron_variant | MODIFIER | c.1936-4454C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563108 | |||||||
| chr2:64563190 | A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1936-4372A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563190 | |||||||
| chr2:64563300 | CAG | C | 6 | a0001c0001t0009g0267 a0003c0003t0008g0232 a0003c0003t0008g0263 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-4260_1936-425 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64563300 | ||||||
| chr2:64563305 | G | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(223): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-4257G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563305 | |||||||
| chr2:64563322 | C | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1936-4240C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563322 | |||||||
| chr2:64563332 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1936-4230T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563332 | |||||||
| chr2:64563880 | A | G | 81 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0111 others(78): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1936-3682A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563880 | |||||||
| chr2:64563898 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1936-3664G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64563898 | |||||||
| chr2:64564034 | T | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.1936-3528T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564034 | |||||||
| chr2:64564062 | A | G | 41 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(38): Show |
42 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.1936-3500A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564062 | |||||||
| chr2:64564104 | T | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-3458T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564104 | |||||||
| chr2:64564106 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-3456T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564106 | |||||||
| chr2:64564283 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0097 a0001c0001t0004g0276 |
3 | NA18962.hp2 NA18966.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1936-3279A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564283 | |||||||
| chr2:64564310 | C | A | 2 | a0002c0002t0002g0286 a0002c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1936-3252C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564310 | |||||||
| chr2:64564381 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1936-3181G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564381 | |||||||
| chr2:64564583 | C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2979C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564583 | |||||||
| chr2:64564589 | C | T | 29 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(26): Show |
29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1936-2973C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564589 | |||||||
| chr2:64564616 | AAAAATAA others(5): Show |
A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2941_1936-293 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564616 | ||||||
| chr2:64564633 | AAT | A | 77 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0111 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1936-2927_1936-292 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564633 | ||||||
| chr2:64564635 | T | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(146): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1936-2927T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564635 | |||||||
| chr2:64564637 | A | T | 110 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(107): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1936-2925A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564637 | |||||||
| chr2:64564638 | A | G | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1936-2924A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564638 | |||||||
| chr2:64564640 | T | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(223): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1936-2922T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564640 | |||||||
| chr2:64564700 | A | G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-2862A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564700 | |||||||
| chr2:64564734 | G | A | 24 | a0001c0001t0001g0120 a0001c0001t0002g0021 a0001c0001t0003g0007 others(21): Show |
24 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1936-2828G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564734 | |||||||
| chr2:64564855 | TA | T | 4 | a0001c0001t0001g0107 a0001c0001t0004g0074 a0001c0001t0005g0084 others(1): Show |
4 | HG02559.hp2 HG03195.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-2705delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64564855 | ||||||
| chr2:64564856 | A | T | 188 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0120 others(185): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1936-2706A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564856 | |||||||
| chr2:64564861 | C | A | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2701C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564861 | |||||||
| chr2:64564997 | C | A | 1 | a0001c0001t0004g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1936-2565C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64564997 | |||||||
| chr2:64565068 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1936-2494A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565068 | |||||||
| chr2:64565086 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1936-2476G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565086 | |||||||
| chr2:64565104 | G | T | 80 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0111 others(77): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1936-2458G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565104 | |||||||
| chr2:64565111 | T | C | 1 | a0001c0001t0004g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1936-2451T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565111 | |||||||
| chr2:64565119 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1936-2443G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565119 | |||||||
| chr2:64565180 | T | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0142 a0001c0001t0001g0150 others(37): Show |
41 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1936-2382T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565180 | |||||||
| chr2:64565335 | C | T | 5 | a0002c0002t0002g0281 a0002c0002t0002g0285 a0002c0002t0002g0307 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2227C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565335 | |||||||
| chr2:64565446 | A | G | 12 | a0001c0001t0005g0002 a0001c0001t0005g0035 a0001c0001t0005g0038 others(9): Show |
13 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1936-2116A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565446 | |||||||
| chr2:64565461 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1936-2101C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565461 | |||||||
| chr2:64565474 | C | CA | 49 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0129 others(46): Show |
50 | HG00673.hp1 HG00673.hp2 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.1936-2069dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | ||||||
| chr2:64565474 | C | CAA | 100 | a0001c0001t0001g0042 a0001c0001t0001g0107 a0001c0001t0001g0120 others(97): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1936-2070_1936-206 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | ||||||
| chr2:64565474 | C | CAAA | 6 | a0001c0001t0001g0095 a0001c0001t0003g0023 a0001c0001t0004g0090 others(3): Show |
6 | HG00642.hp2 HG03139.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-2071_1936-206 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | ||||||
| chr2:64565474 | CA | C | 49 | a0001c0001t0001g0275 a0001c0001t0004g0276 a0002c0002t0002g0005 others(46): Show |
50 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1936-2069delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64565474 | ||||||
| chr2:64565497 | T | C | 81 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(78): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1936-2065T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64565497 | |||||||
| chr2:64566168 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1936-1394G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566168 | |||||||
| chr2:64566278 | TC | T | 80 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0111 others(77): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1936-1283delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566278 | |||||||
| chr2:64566418 | AT | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0207 a0001c0001t0005g0075 others(4): Show |
7 | HG01069.hp1 HG02523.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1936-1133delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566418 | ||||||
| chr2:64566530 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-1032T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566530 | |||||||
| chr2:64566660 | ATAGT | A | 4 | a0002c0002t0002g0285 a0002c0002t0002g0307 a0002c0002t0002g0365 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-898_1936-895d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566660 | ||||||
| chr2:64566693 | G | T | 1 | a0002c0002t0003g0289 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1936-869G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64566693 | |||||||
| chr2:64566774 | T | TA | 90 | a0001c0001t0001g0239 a0001c0001t0002g0201 a0002c0002t0001g0004 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1936-777dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 64566774 | ||||||
| chr2:64567303 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG00323.hp2 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1936-259T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 2/9 | chr2 | 64567303 | |||||||
| chr2:64567806 | C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2087+93C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567806 | |||||||
| chr2:64567811 | G | A | 107 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2087+98G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567811 | |||||||
| chr2:64567897 | CA | C | 107 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2087+185delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64567897 | |||||||
| chr2:64568009 | C | A | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2087+296C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568009 | |||||||
| chr2:64568106 | T | C | 4 | a0001c0001t0005g0067 a0001c0001t0005g0069 a0001c0001t0005g0098 others(1): Show |
4 | NA18941.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.2087+393T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568106 | |||||||
| chr2:64568139 | A | C | 81 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(78): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2087+426A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568139 | |||||||
| chr2:64568143 | A | T | 109 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(106): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2087+430A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568143 | |||||||
| chr2:64568258 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2087+545T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568258 | |||||||
| chr2:64568286 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2087+573C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568286 | |||||||
| chr2:64568303 | C | CTT | 189 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(186): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2087+590_2087+591i others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568303 | |||||||
| chr2:64568444 | G | A | 1 | a0002c0002t0003g0305 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2088-648G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568444 | |||||||
| chr2:64568650 | C | T | 31 | a0001c0001t0005g0091 a0002c0002t0002g0292 a0002c0002t0002g0297 others(28): Show |
31 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2088-442C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568650 | |||||||
| chr2:64568792 | A | G | 2 | a0002c0002t0002g0281 a0002c0002t0002g0327 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2088-300A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568792 | |||||||
| chr2:64568798 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2088-294G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568798 | |||||||
| chr2:64568902 | G | A | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2088-190G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568902 | |||||||
| chr2:64568965 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2088-127T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568965 | |||||||
| chr2:64568977 | G | A | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2088-115G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568977 | |||||||
| chr2:64568978 | T | C | 1 | a0002c0002t0002g0286 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2088-114T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64568978 | |||||||
| chr2:64569015 | A | C | 1 | a0002c0002t0003g0328 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2088-77A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64569015 | |||||||
| chr2:64569069 | T | C | 1 | a0002c0002t0002g0366 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2088-23T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 3/9 | chr2 | 64569069 | |||||||
| chr2:64569345 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(224): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2214+127C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569345 | |||||||
| chr2:64569510 | A | G | 1 | a0002c0002t0002g0352 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2215-113A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569510 | |||||||
| chr2:64569593 | A | T | 5 | a0002c0002t0003g0308 a0002c0002t0003g0320 a0002c0002t0003g0321 others(2): Show |
5 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2215-30A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 4/9 | chr2 | 64569593 | |||||||
| chr2:64569683 | A | C | 29 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(26): Show |
29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2271+4A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569683 | |||||||
| chr2:64569713 | A | G | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+34A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569713 | |||||||
| chr2:64569754 | C | T | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2271+75C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569754 | |||||||
| chr2:64569766 | A | G | 1 | a0002c0002t0003g0287 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2271+87A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569766 | |||||||
| chr2:64569798 | G | A | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+119G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64569798 | |||||||
| chr2:64570019 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2271+340T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570019 | |||||||
| chr2:64570058 | G | A | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+379G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570058 | |||||||
| chr2:64570070 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2271+391A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570070 | |||||||
| chr2:64570071 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0237 a0001c0001t0001g0238 others(17): Show |
21 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.2271+392C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570071 | |||||||
| chr2:64570199 | C | T | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2271+520C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570199 | |||||||
| chr2:64570200 | G | A | 105 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2271+521G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570200 | |||||||
| chr2:64570293 | T | C | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2271+614T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570293 | |||||||
| chr2:64570381 | G | T | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2271+702G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570381 | |||||||
| chr2:64570915 | T | TC | 47 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0120 others(44): Show |
48 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2271+1249dupC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570915 | T | TCC | 49 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0123 others(46): Show |
49 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.2271+1248_2271+124 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570915 | T | TCCC | 16 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0001c0001t0001g0157 others(13): Show |
16 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+1247_2271+124 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570915 | TC | T | 28 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0111 others(25): Show |
28 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.2271+1249delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570915 | TCC | T | 63 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0245 others(60): Show |
64 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2271+1248_2271+124 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570915 | TCCC | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(121): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2271+1247_2271+124 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64570915 | ||||||
| chr2:64570923 | C | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2271+1244C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570923 | |||||||
| chr2:64570950 | A | G | 1 | a0001c0005t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2271+1271A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64570950 | |||||||
| chr2:64571155 | C | T | 185 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(182): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2271+1476C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571155 | |||||||
| chr2:64571243 | A | G | 6 | a0002c0002t0002g0327 a0002c0002t0003g0308 a0002c0002t0003g0320 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2271+1564A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571243 | |||||||
| chr2:64571267 | AC | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(28): Show |
32 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.2271+1594delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64571267 | ||||||
| chr2:64571272 | CCT | C | 81 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(78): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2271+1594_2271+159 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571272 | |||||||
| chr2:64571318 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2272-1628G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571318 | |||||||
| chr2:64571362 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2272-1584C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571362 | |||||||
| chr2:64571397 | A | C | 1 | a0002c0002t0003g0288 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2272-1549A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571397 | |||||||
| chr2:64571404 | C | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(222): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2272-1542C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571404 | |||||||
| chr2:64571480 | TA | T | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2272-1465delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571480 | |||||||
| chr2:64571483 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0244 |
2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2272-1463A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571483 | |||||||
| chr2:64571741 | G | A | 1 | a0002c0002t0002g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2272-1205G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571741 | |||||||
| chr2:64571889 | A | G | 2 | a0002c0002t0002g0333 a0002c0002t0019g0360 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2272-1057A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571889 | |||||||
| chr2:64571934 | G | A | 1 | a0002c0002t0003g0308 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2272-1012G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571934 | |||||||
| chr2:64571937 | C | T | 1 | a0005c0007t0002g0354 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2272-1009C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571937 | |||||||
| chr2:64571953 | C | T | 3 | a0001c0001t0001g0256 a0002c0002t0009g0325 a0010c0013t0017g0268 |
3 | HG01109.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2272-993C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571953 | |||||||
| chr2:64571987 | G | T | 7 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0286 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2272-959G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64571987 | |||||||
| chr2:64572121 | G | A | 3 | a0001c0001t0005g0068 a0001c0001t0005g0085 a0001c0001t0012g0081 |
3 | NA18967.hp2 NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2272-825G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572121 | |||||||
| chr2:64572123 | G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2272-823G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572123 | |||||||
| chr2:64572201 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0219 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2272-745C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572201 | |||||||
| chr2:64572220 | C | CA | 8 | a0001c0001t0001g0129 a0001c0001t0001g0174 a0001c0001t0001g0278 others(5): Show |
8 | HG00741.hp1 HG02135.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2272-710dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | ||||||
| chr2:64572220 | C | CAA | 84 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(81): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2272-711_2272-710d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | ||||||
| chr2:64572220 | C | CAAA | 21 | a0001c0001t0004g0031 a0001c0001t0004g0037 a0001c0001t0004g0039 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2272-712_2272-710d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | ||||||
| chr2:64572220 | CA | C | 25 | a0001c0001t0001g0173 a0001c0001t0007g0136 a0002c0002t0002g0284 others(22): Show |
25 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.2272-710delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572220 | ||||||
| chr2:64572292 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(36): Show |
40 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.2272-654A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572292 | |||||||
| chr2:64572316 | G | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0237 a0001c0001t0001g0238 others(17): Show |
21 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.2272-630G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572316 | |||||||
| chr2:64572394 | T | C | 1 | a0002c0002t0003g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2272-552T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | chr2 | 64572394 | |||||||
| chr2:64572522 | ATTG | A | 3 | a0001c0001t0001g0129 a0001c0001t0007g0195 a0001c0001t0007g0197 |
3 | HG01168.hp2 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2272-419_2272-417d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572522 | ||||||
| chr2:64572803 | T | TA | 11 | a0001c0001t0001g0222 a0001c0001t0007g0136 a0002c0002t0001g0004 others(8): Show |
12 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2272-130dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572803 | ||||||
| chr2:64572803 | TAA | T | 224 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(221): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2272-131_2272-130d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 64572803 | ||||||
| chr2:64573105 | G | A | 46 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0128 others(43): Show |
46 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.2394+37G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573105 | |||||||
| chr2:64573110 | T | C | 6 | a0001c0001t0009g0267 a0003c0003t0008g0232 a0003c0003t0008g0263 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2394+42T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573110 | |||||||
| chr2:64573318 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG00140.hp1 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+250C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573318 | |||||||
| chr2:64573432 | T | TA | 111 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2394+379dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64573432 | ||||||
| chr2:64573432 | TA | T | 11 | a0001c0001t0001g0143 a0001c0001t0001g0273 a0001c0001t0001g0332 others(8): Show |
11 | HG02040.hp2 HG02280.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2394+379delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64573432 | ||||||
| chr2:64573631 | C | G | 105 | a0001c0001t0001g0042 a0001c0001t0001g0120 a0001c0001t0002g0021 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+563C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573631 | |||||||
| chr2:64573812 | C | T | 4 | a0001c0001t0005g0058 a0001c0001t0005g0060 a0001c0001t0005g0084 others(1): Show |
4 | HG01261.hp1 HG02559.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+744C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573812 | |||||||
| chr2:64573850 | G | C | 81 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(78): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2394+782G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573850 | |||||||
| chr2:64573953 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0156 others(1): Show |
4 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+885C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64573953 | |||||||
| chr2:64574042 | C | T | 1 | a0002c0002t0003g0304 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2394+974C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574042 | |||||||
| chr2:64574282 | T | C | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2394+1214T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574282 | |||||||
| chr2:64574390 | TCACAA | T | 9 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(6): Show |
10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2394+1327_2394+133 others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64574390 | ||||||
| chr2:64574519 | G | A | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+1451G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574519 | |||||||
| chr2:64574621 | C | T | 4 | a0002c0002t0002g0337 a0002c0002t0002g0342 a0002c0002t0002g0352 others(1): Show |
4 | NA18979.hp2 NA18981.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+1553C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574621 | |||||||
| chr2:64574778 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2394+1710T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574778 | |||||||
| chr2:64574797 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2394+1729C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574797 | |||||||
| chr2:64574819 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0004g0030 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2394+1751C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574819 | |||||||
| chr2:64574902 | T | G | 7 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0286 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2394+1834T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574902 | |||||||
| chr2:64574928 | C | G | 29 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(26): Show |
29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2394+1860C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64574928 | |||||||
| chr2:64574964 | C | CTACTTGG others(8): Show |
2 | a0002c0002t0002g0285 a0002c0002t0002g0365 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2394+1912_2394+192 others(19): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64574964 | ||||||
| chr2:64575043 | T | TGCTTCCT others(13): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0133 |
2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+1976_2394+199 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575043 | ||||||
| chr2:64575064 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0133 |
2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+1996A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575064 | |||||||
| chr2:64575123 | AT | A | 103 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(100): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2394+2061delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575123 | ||||||
| chr2:64575313 | A | C | 6 | a0002c0002t0002g0327 a0002c0002t0003g0308 a0002c0002t0003g0320 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2394+2245A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575313 | |||||||
| chr2:64575344 | G | A | 1 | a0002c0002t0002g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2394+2276G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575344 | |||||||
| chr2:64575468 | T | C | 1 | a0002c0002t0003g0293 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2394+2400T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575468 | |||||||
| chr2:64575516 | C | G | 1 | a0001c0001t0004g0011 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2394+2448C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575516 | |||||||
| chr2:64575550 | G | C | 105 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+2482G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575550 | |||||||
| chr2:64575679 | T | A | 33 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(30): Show |
34 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.2394+2611T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575679 | |||||||
| chr2:64575679 | T | TTA | 3 | a0001c0001t0005g0057 a0001c0001t0005g0077 a0001c0001t0005g0086 |
3 | HG00642.hp2 HG00735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2394+2621_2394+262 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575679 | ||||||
| chr2:64575703 | ATG | A | 11 | a0001c0001t0001g0160 a0002c0002t0002g0281 a0002c0002t0002g0283 others(8): Show |
11 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2394+2673_2394+267 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTG | A | 37 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0167 others(34): Show |
37 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.2394+2671_2394+267 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTG | A | 107 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0114 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2394+2669_2394+267 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2394+2667_2394+267 others(12): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2394+2665_2394+267 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTGT others(5): Show |
A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(35): Show |
39 | HG01243.hp1 HG01261.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.2394+2663_2394+267 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0004g0076 a0001c0001t0004g0090 |
2 | HG01943.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2394+2657_2394+267 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575703 | ATGTGTGT others(13): Show |
A | 102 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(99): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2394+2655_2394+267 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575703 | ||||||
| chr2:64575705 | G | A | 52 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0001g0004 others(49): Show |
54 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(51): Show |
intron_variant | MODIFIER | c.2394+2637G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575705 | |||||||
| chr2:64575707 | G | A | 3 | a0002c0002t0002g0281 a0002c0002t0002g0283 a0002c0002t0002g0284 |
3 | HG02818.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2394+2639G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575707 | |||||||
| chr2:64575709 | G | A | 5 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2394+2641G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575709 | |||||||
| chr2:64575711 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2394+2643G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575711 | |||||||
| chr2:64575737 | G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2394+2669G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575737 | |||||||
| chr2:64575737 | GTGTGTA | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0176 others(1): Show |
4 | HG00621.hp2 HG01106.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2394+2671_2394+267 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575737 | ||||||
| chr2:64575739 | G | A | 52 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(49): Show |
53 | HG00408.hp1 HG00673.hp2 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.2394+2671G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575739 | |||||||
| chr2:64575741 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0169 others(212): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2394+2673G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575741 | |||||||
| chr2:64575746 | TA | T | 3 | a0002c0002t0002g0286 a0002c0002t0002g0306 a0004c0004t0001g0221 |
3 | HG02717.hp2 NA19083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2394+2679delA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575746 | |||||||
| chr2:64575747 | A | ATATT | 10 | a0001c0001t0004g0276 a0002c0002t0002g0337 a0002c0002t0002g0340 others(7): Show |
10 | NA18961.hp1 NA18966.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.2394+2680_2394+268 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575747 | ||||||
| chr2:64575747 | A | ATT | 24 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0334 others(21): Show |
25 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.2394+2686_2394+268 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64575747 | ||||||
| chr2:64575747 | A | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(49): Show |
53 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.2394+2679A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575747 | |||||||
| chr2:64575749 | T | A | 103 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(100): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2394+2681T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575749 | |||||||
| chr2:64575756 | G | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2394+2688G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575756 | |||||||
| chr2:64575792 | G | A | 1 | a0002c0002t0002g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2394+2724G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575792 | |||||||
| chr2:64575962 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2394+2894C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64575962 | |||||||
| chr2:64576018 | C | T | 1 | a0002c0002t0003g0287 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2394+2950C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576018 | |||||||
| chr2:64576033 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2394+2965C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576033 | |||||||
| chr2:64576074 | T | TAC | 20 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(17): Show |
20 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.2394+3049_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TAC | T | 24 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0135 others(21): Show |
24 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2394+3049_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACAC | T | 27 | a0001c0001t0001g0095 a0001c0001t0001g0115 a0001c0001t0001g0137 others(24): Show |
27 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2394+3047_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACAC | T | 30 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0134 others(27): Show |
30 | HG00323.hp2 HG01175.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.2394+3045_2394+305 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(3): Show |
T | 16 | a0001c0001t0001g0367 a0001c0001t0009g0267 a0002c0002t0001g0004 others(13): Show |
17 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2394+3041_2394+305 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0002c0002t0009g0282 |
3 | NA18998.hp2 NA19043.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2394+3039_2394+305 others(16): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(7): Show |
T | 2 | a0001c0001t0003g0008 a0001c0001t0004g0053 |
2 | HG01496.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2394+3037_2394+305 others(18): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(9): Show |
T | 11 | a0002c0002t0002g0283 a0002c0002t0002g0284 a0002c0002t0002g0327 others(8): Show |
11 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2394+3035_2394+305 others(20): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(11): Show |
T | 1 | a0002c0002t0003g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2394+3033_2394+305 others(22): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(13): Show |
T | 26 | a0001c0001t0001g0163 a0002c0002t0002g0111 a0002c0002t0002g0112 others(23): Show |
26 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2394+3031_2394+305 others(24): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2394+3029_2394+305 others(26): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(17): Show |
T | 42 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0002c0002t0002g0005 others(39): Show |
43 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(40): Show |
intron_variant | MODIFIER | c.2394+3027_2394+305 others(28): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576074 | TACACACA others(19): Show |
T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0142 a0001c0001t0001g0150 others(37): Show |
41 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.2394+3025_2394+305 others(30): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576074 | ||||||
| chr2:64576110 | CACACACA others(14): Show |
C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3044_2394+306 others(25): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576110 | ||||||
| chr2:64576115 | A | G | 9 | a0002c0002t0002g0327 a0002c0002t0003g0280 a0002c0002t0003g0287 others(6): Show |
9 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2394+3047A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576115 | |||||||
| chr2:64576116 | C | T | 9 | a0002c0002t0002g0327 a0002c0002t0003g0280 a0002c0002t0003g0287 others(6): Show |
9 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2394+3048C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576116 | |||||||
| chr2:64576117 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0001g0142 others(140): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2394+3049A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576117 | |||||||
| chr2:64576118 | C | CACACACA others(3): Show |
1 | a0001c0001t0005g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2394+3050_2394+305 others(14): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | |||||||
| chr2:64576118 | C | CACACGT | 4 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0004g0094 others(1): Show |
5 | HG01074.hp2 HG01243.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2394+3050_2394+305 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | |||||||
| chr2:64576118 | C | CACGT | 30 | a0001c0001t0002g0109 a0001c0001t0004g0011 a0001c0001t0004g0030 others(27): Show |
30 | HG00140.hp2 HG00621.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.2394+3050_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | |||||||
| chr2:64576118 | C | CGT | 37 | a0001c0001t0002g0021 a0001c0001t0003g0010 a0001c0001t0003g0019 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.2394+3055_2394+305 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576118 | ||||||
| chr2:64576118 | C | CGTGT | 26 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0292 others(23): Show |
26 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2394+3053_2394+305 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576118 | ||||||
| chr2:64576118 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0001g0142 others(140): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2394+3050C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576118 | |||||||
| chr2:64576135 | A | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3067A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576135 | |||||||
| chr2:64576140 | CGT | C | 105 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0001t0002g0021 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2394+3087_2394+308 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576140 | ||||||
| chr2:64576140 | CGTGT | C | 7 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2394+3085_2394+308 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576140 | ||||||
| chr2:64576157 | A | G | 23 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(20): Show |
23 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.2394+3089A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576157 | |||||||
| chr2:64576159 | GTATATAT others(34): Show |
G | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2394+3104_2394+314 others(45): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576159 | ||||||
| chr2:64576172 | G | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(220): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2394+3104G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576172 | |||||||
| chr2:64576184 | C | CAT | 4 | a0001c0001t0005g0075 a0001c0001t0009g0267 a0001c0001t0011g0059 others(1): Show |
4 | HG03041.hp2 NA18942.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+3128_2394+312 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576184 | ||||||
| chr2:64576216 | A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2394+3148A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576216 | |||||||
| chr2:64576496 | T | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2395-2990T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576496 | |||||||
| chr2:64576551 | T | C | 29 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(26): Show |
29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2395-2935T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576551 | |||||||
| chr2:64576640 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0142 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2395-2846G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576640 | |||||||
| chr2:64576661 | C | T | 1 | a0002c0002t0003g0294 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2395-2825C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576661 | |||||||
| chr2:64576671 | T | C | 103 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(100): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2395-2815T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576671 | |||||||
| chr2:64576815 | A | G | 1 | a0001c0001t0003g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2395-2671A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576815 | |||||||
| chr2:64576861 | C | T | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2395-2625C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576861 | |||||||
| chr2:64576902 | G | GCACCTGC | 89 | a0001c0001t0002g0201 a0002c0002t0001g0004 a0002c0002t0001g0312 others(86): Show |
91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2395-2579_2395-257 others(11): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64576902 | ||||||
| chr2:64576979 | A | C | 1 | a0001c0001t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2395-2507A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64576979 | |||||||
| chr2:64577042 | AGCCACCG others(6): Show |
A | 29 | a0002c0002t0002g0292 a0002c0002t0002g0297 a0002c0002t0002g0302 others(26): Show |
29 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2395-2437_2395-242 others(17): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577042 | ||||||
| chr2:64577051 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2395-2435G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577051 | |||||||
| chr2:64577051 | G | T | 1 | a0001c0001t0005g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2395-2435G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577051 | |||||||
| chr2:64577176 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2395-2310A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577176 | |||||||
| chr2:64577330 | C | T | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2395-2156C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577330 | |||||||
| chr2:64577332 | G | GTATCCTG others(10): Show |
5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2395-2152_2395-213 others(21): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577332 | ||||||
| chr2:64577361 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0126 others(240): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2395-2125G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577361 | |||||||
| chr2:64577376 | G | A | 3 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0052 |
3 | HG02257.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2395-2110G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577376 | |||||||
| chr2:64577463 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2395-2023A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577463 | |||||||
| chr2:64577690 | T | C | 2 | a0002c0002t0003g0287 a0002c0002t0003g0295 |
2 | NA18986.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2395-1796T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64577690 | |||||||
| chr2:64577946 | ACCACCAC others(24): Show |
A | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2395-1527_2395-149 others(35): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577946 | ||||||
| chr2:64577966 | T | TA | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG00140.hp1 HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2395-1519dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64577966 | ||||||
| chr2:64578203 | TAAC | T | 3 | a0002c0002t0002g0285 a0002c0002t0002g0307 a0002c0002t0002g0365 |
3 | HG02055.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2395-1282_2395-128 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578203 | |||||||
| chr2:64578271 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2395-1215T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578271 | |||||||
| chr2:64578316 | C | T | 115 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2395-1170C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578316 | |||||||
| chr2:64578353 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2395-1133A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578353 | |||||||
| chr2:64578385 | A | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0142 a0001c0001t0001g0150 others(38): Show |
42 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.2395-1101A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578385 | |||||||
| chr2:64578465 | A | C | 3 | a0001c0005t0001g0122 a0001c0005t0001g0141 a0001c0005t0001g0187 |
3 | HG00099.hp2 HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2395-1021A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578465 | |||||||
| chr2:64578485 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2395-1001T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578485 | |||||||
| chr2:64578516 | A | T | 1 | a0009c0009t0004g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2395-970A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578516 | |||||||
| chr2:64578558 | AT | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 others(142): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2395-911delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578558 | ||||||
| chr2:64578558 | ATTT | A | 89 | a0001c0001t0001g0042 a0001c0001t0002g0201 a0001c0001t0004g0001 others(86): Show |
91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2395-913_2395-911d others(5): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578558 | ||||||
| chr2:64578589 | C | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0204 others(4): Show |
7 | HG02080.hp2 HG02132.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2395-897C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578589 | |||||||
| chr2:64578611 | G | C | 6 | a0002c0002t0002g0327 a0002c0002t0003g0308 a0002c0002t0003g0320 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2395-875G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578611 | |||||||
| chr2:64578621 | G | A | 2 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2395-865G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578621 | |||||||
| chr2:64578724 | AT | A | 185 | a0001c0001t0001g0042 a0001c0001t0001g0117 a0001c0001t0001g0118 others(182): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2395-753delT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64578724 | ||||||
| chr2:64578752 | G | T | 1 | a0001c0001t0003g0017 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2395-734G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578752 | |||||||
| chr2:64578846 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2395-640C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578846 | |||||||
| chr2:64578867 | T | G | 1 | a0001c0001t0005g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2395-619T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578867 | |||||||
| chr2:64578897 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2395-589C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64578897 | |||||||
| chr2:64579060 | TATTAGCC others(1): Show |
T | 35 | a0001c0001t0002g0201 a0002c0002t0002g0005 a0002c0002t0002g0333 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.2395-423_2395-416d others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64579060 | ||||||
| chr2:64579091 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2395-395T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579091 | |||||||
| chr2:64579117 | C | T | 1 | a0001c0012t0004g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2395-369C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579117 | |||||||
| chr2:64579125 | C | A | 1 | a0001c0001t0005g0099 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2395-361C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | chr2 | 64579125 | |||||||
| chr2:64579410 | A | AT | 10 | a0001c0001t0009g0267 a0001c0005t0001g0122 a0001c0005t0001g0141 others(7): Show |
10 | HG00099.hp2 HG02622.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.2395-65dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 64579410 | ||||||
| chr2:64579652 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2455+106T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579652 | |||||||
| chr2:64579713 | G | A | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2455+167G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579713 | |||||||
| chr2:64579784 | A | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2455+238A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579784 | |||||||
| chr2:64579794 | T | G | 87 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2455+248T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64579794 | |||||||
| chr2:64579810 | ATATCTAG others(4): Show |
A | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2455+266_2455+276d others(13): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 64579810 | ||||||
| chr2:64579941 | CAATT | C | 5 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2455+397_2455+400d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 64579941 | ||||||
| chr2:64580160 | T | G | 86 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(83): Show |
88 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.2455+614T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580160 | |||||||
| chr2:64580191 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2455+645C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580191 | |||||||
| chr2:64580323 | T | G | 38 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(35): Show |
39 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.2455+777T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580323 | |||||||
| chr2:64580344 | C | G | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2455+798C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580344 | |||||||
| chr2:64580430 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2456-760C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580430 | |||||||
| chr2:64580443 | T | C | 1 | a0002c0002t0002g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2456-747T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580443 | |||||||
| chr2:64580700 | T | A | 7 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0089 others(4): Show |
7 | HG02027.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456-490T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580700 | |||||||
| chr2:64580706 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2456-484C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580706 | |||||||
| chr2:64580710 | G | T | 1 | a0001c0001t0004g0062 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2456-480G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580710 | |||||||
| chr2:64580725 | C | T | 1 | a0001c0001t0007g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2456-465C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580725 | |||||||
| chr2:64580990 | T | C | 17 | a0002c0002t0001g0004 a0002c0002t0001g0312 a0002c0002t0001g0313 others(14): Show |
18 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2456-200T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 7/9 | chr2 | 64580990 | |||||||
| chr2:64581526 | G | GTTAA | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2539+254_2539+257d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64581526 | ||||||
| chr2:64581638 | GAGAT | G | 93 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0002c0002t0001g0004 others(90): Show |
95 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2539+373_2539+376d others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64581638 | ||||||
| chr2:64581645 | A | G | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2539+372A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581645 | |||||||
| chr2:64581699 | T | G | 91 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0002c0002t0001g0004 others(88): Show |
93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2539+426T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581699 | |||||||
| chr2:64581884 | G | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0017 a0001c0001t0003g0022 others(5): Show |
8 | NA18954.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2539+611G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581884 | |||||||
| chr2:64581946 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG00323.hp2 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2539+673G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581946 | |||||||
| chr2:64581990 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2539+717A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64581990 | |||||||
| chr2:64582138 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2539+865G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582138 | |||||||
| chr2:64582144 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG00140.hp1 HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2539+871G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582144 | |||||||
| chr2:64582152 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2539+879G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582152 | |||||||
| chr2:64582262 | A | G | 1 | a0005c0008t0005g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2539+989A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582262 | |||||||
| chr2:64582297 | T | A | 11 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
11 | HG02083.hp1 NA18950.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.2539+1024T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582297 | |||||||
| chr2:64582404 | G | A | 80 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(77): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2539+1131G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582404 | |||||||
| chr2:64582507 | T | C | 1 | a0002c0002t0009g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2539+1234T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582507 | |||||||
| chr2:64582621 | C | CG | 34 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(31): Show |
35 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.2539+1355dupG | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64582621 | ||||||
| chr2:64582674 | C | A | 1 | a0002c0002t0003g0300 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2539+1401C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582674 | |||||||
| chr2:64582924 | G | C | 2 | a0002c0002t0002g0361 a0002c0002t0003g0330 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2539+1651G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582924 | |||||||
| chr2:64582987 | C | T | 1 | a0001c0001t0004g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2539+1714C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64582987 | |||||||
| chr2:64583316 | T | TA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(37): Show |
41 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.2539+2057dupA | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | ||||||
| chr2:64583316 | T | TAA | 6 | a0001c0001t0003g0012 a0001c0001t0004g0076 a0001c0001t0005g0075 others(3): Show |
6 | HG00099.hp1 HG01943.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2539+2056_2539+205 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | ||||||
| chr2:64583316 | T | TAAA | 106 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(103): Show |
108 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2539+2055_2539+205 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583316 | ||||||
| chr2:64583420 | GTGGTGGT others(81): Show |
G | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2540-2000_2540-191 others(92): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64583420 | ||||||
| chr2:64583633 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2540-1789G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583633 | |||||||
| chr2:64583638 | A | C | 1 | a0002c0002t0002g0286 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2540-1784A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583638 | |||||||
| chr2:64583901 | T | C | 87 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(84): Show |
88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2540-1521T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64583901 | |||||||
| chr2:64584308 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2540-1114G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584308 | |||||||
| chr2:64584438 | C | T | 88 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0093 others(85): Show |
89 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2540-984C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584438 | |||||||
| chr2:64584593 | A | AT | 216 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0120 others(213): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2540-808dupT | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584593 | ||||||
| chr2:64584593 | A | ATT | 20 | a0001c0001t0001g0042 a0001c0001t0001g0107 a0001c0001t0001g0249 others(17): Show |
20 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.2540-809_2540-808d others(4): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584593 | ||||||
| chr2:64584621 | C | G | 199 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(196): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2540-801C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584621 | |||||||
| chr2:64584659 | T | C | 1 | a0002c0002t0003g0293 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2540-763T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584659 | |||||||
| chr2:64584659 | T | G | 82 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0172 others(79): Show |
83 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2540-763T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584659 | |||||||
| chr2:64584662 | T | G | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2540-760T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584662 | |||||||
| chr2:64584687 | TC | T | 5 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0309 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2540-733delC | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584687 | ||||||
| chr2:64584697 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0189 others(1): Show |
4 | HG01074.hp1 HG03490.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540-725T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584697 | |||||||
| chr2:64584712 | C | T | 1 | a0002c0002t0003g0298 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2540-710C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584712 | |||||||
| chr2:64584721 | T | C | 2 | a0002c0002t0002g0281 a0002c0002t0002g0327 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2540-701T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584721 | |||||||
| chr2:64584756 | C | CCGGCTAA others(95): Show |
1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2540-645_2540-644i others(104): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 64584756 | ||||||
| chr2:64584812 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2540-610G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584812 | |||||||
| chr2:64584838 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2540-584T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584838 | |||||||
| chr2:64584843 | G | A | 6 | a0002c0002t0002g0297 a0002c0002t0003g0288 a0002c0002t0003g0291 others(3): Show |
6 | HG00673.hp2 HG02523.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.2540-579G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584843 | |||||||
| chr2:64584895 | C | T | 2 | a0001c0001t0006g0253 a0001c0001t0006g0255 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2540-527C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584895 | |||||||
| chr2:64584918 | C | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2540-504C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64584918 | |||||||
| chr2:64585068 | T | A | 5 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0306 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2540-354T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585068 | |||||||
| chr2:64585114 | T | C | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2540-308T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585114 | |||||||
| chr2:64585133 | C | G | 1 | a0001c0001t0003g0015 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2540-289C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585133 | |||||||
| chr2:64585139 | G | A | 80 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(77): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2540-283G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585139 | |||||||
| chr2:64585304 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2540-118T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 8/9 | chr2 | 64585304 | |||||||
| chr2:64585624 | C | T | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2663+79C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585624 | |||||||
| chr2:64585789 | T | C | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+244T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585789 | |||||||
| chr2:64585790 | G | T | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+245G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585790 | |||||||
| chr2:64585791 | C | G | 1 | a0004c0004t0001g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2663+246C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585791 | |||||||
| chr2:64585803 | A | T | 2 | a0002c0002t0002g0281 a0002c0002t0002g0327 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2663+258A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585803 | |||||||
| chr2:64585990 | C | T | 110 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0201 others(107): Show |
111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2663+445C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64585990 | |||||||
| chr2:64586023 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0183 others(227): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2663+478G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586023 | |||||||
| chr2:64586078 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2663+533C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586078 | |||||||
| chr2:64586162 | A | G | 4 | a0001c0001t0005g0087 a0001c0001t0005g0100 a0001c0001t0005g0106 others(1): Show |
4 | HG02027.hp2 HG02155.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663+617A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586162 | |||||||
| chr2:64586195 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2663+650A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586195 | |||||||
| chr2:64586201 | C | G | 1 | a0009c0009t0004g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2663+656C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586201 | |||||||
| chr2:64586346 | T | A | 3 | a0001c0001t0004g0093 a0002c0002t0002g0283 a0002c0002t0002g0284 |
3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2663+801T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586346 | |||||||
| chr2:64586357 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0095 others(229): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2663+812A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586357 | |||||||
| chr2:64586369 | A | T | 1 | a0002c0002t0002g0334 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2663+824A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586369 | |||||||
| chr2:64586718 | T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2663+1173T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586718 | |||||||
| chr2:64586774 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2663+1229A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586774 | |||||||
| chr2:64586788 | A | T | 187 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0107 others(184): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2663+1243A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64586788 | |||||||
| chr2:64587046 | G | T | 2 | a0002c0002t0002g0285 a0002c0002t0002g0365 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2663+1501G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587046 | |||||||
| chr2:64587109 | C | T | 4 | a0001c0001t0005g0067 a0001c0001t0005g0069 a0001c0001t0005g0098 others(1): Show |
4 | NA18941.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663+1564C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587109 | |||||||
| chr2:64587132 | C | G | 2 | a0006c0006t0002g0343 a0006c0006t0002g0349 |
2 | HG00408.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2663+1587C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587132 | |||||||
| chr2:64587182 | A | T | 1 | a0001c0001t0005g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2663+1637A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587182 | |||||||
| chr2:64587415 | C | A | 84 | a0001c0001t0001g0042 a0001c0001t0001g0189 a0001c0001t0004g0001 others(81): Show |
86 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2663+1870C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587415 | |||||||
| chr2:64587422 | T | A | 1 | a0001c0001t0014g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2663+1877T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587422 | |||||||
| chr2:64587433 | C | G | 84 | a0001c0001t0001g0042 a0001c0001t0001g0189 a0001c0001t0004g0001 others(81): Show |
86 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2663+1888C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587433 | |||||||
| chr2:64587570 | C | A | 121 | a0001c0001t0001g0120 a0001c0001t0002g0021 a0001c0001t0002g0109 others(118): Show |
123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2663+2025C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587570 | |||||||
| chr2:64587621 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0237 others(20): Show |
24 | HG01243.hp1 HG01261.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.2663+2076G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587621 | |||||||
| chr2:64587631 | A | G | 116 | a0001c0001t0001g0120 a0001c0001t0002g0021 a0001c0001t0002g0109 others(113): Show |
118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2663+2086A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587631 | |||||||
| chr2:64587703 | G | A | 205 | a0001c0001t0001g0042 a0001c0001t0001g0120 a0001c0001t0001g0189 others(202): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2663+2158G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587703 | |||||||
| chr2:64587799 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2663+2254G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587799 | |||||||
| chr2:64587800 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2255T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587800 | |||||||
| chr2:64587801 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2256T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587801 | |||||||
| chr2:64587802 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2257T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587802 | |||||||
| chr2:64587803 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2258T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587803 | |||||||
| chr2:64587806 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2261A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587806 | |||||||
| chr2:64587809 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2264A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587809 | |||||||
| chr2:64587811 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2266T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587811 | |||||||
| chr2:64587812 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2267T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587812 | |||||||
| chr2:64587814 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2269C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587814 | |||||||
| chr2:64587820 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2275C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587820 | |||||||
| chr2:64587821 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2276T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587821 | |||||||
| chr2:64587822 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2277T>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587822 | |||||||
| chr2:64587823 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2278G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587823 | |||||||
| chr2:64587824 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663+2279C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587824 | |||||||
| chr2:64587875 | A | C | 2 | a0001c0001t0004g0063 a0001c0001t0004g0097 |
2 | NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2663+2330A>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64587875 | |||||||
| chr2:64587942 | TTC | T | 38 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0001c0001t0004g0276 others(35): Show |
39 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.2663+2399_2663+240 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64587942 | ||||||
| chr2:64588038 | C | T | 1 | a0001c0001t0005g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2663+2493C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588038 | |||||||
| chr2:64588205 | A | G | 117 | a0001c0001t0001g0120 a0001c0001t0002g0021 a0001c0001t0002g0109 others(114): Show |
119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2663+2660A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588205 | |||||||
| chr2:64588385 | G | A | 205 | a0001c0001t0001g0042 a0001c0001t0001g0189 a0001c0001t0002g0021 others(202): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2663+2840G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588385 | |||||||
| chr2:64588730 | C | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0139 a0001c0001t0001g0227 others(1): Show |
4 | HG00438.hp2 HG01928.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2664-3158C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588730 | |||||||
| chr2:64588932 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2664-2956G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64588932 | |||||||
| chr2:64589124 | C | T | 1 | a0001c0001t0004g0001 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2664-2764C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589124 | |||||||
| chr2:64589226 | G | A | 117 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0201 others(114): Show |
119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2664-2662G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589226 | |||||||
| chr2:64589293 | T | C | 207 | a0001c0001t0001g0042 a0001c0001t0001g0189 a0001c0001t0002g0021 others(204): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2664-2595T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589293 | |||||||
| chr2:64589596 | C | CTTG | 202 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(199): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2664-2290_2664-228 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589596 | ||||||
| chr2:64589596 | C | G | 2 | a0001c0001t0003g0018 a0001c0001t0004g0031 |
2 | HG04228.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2664-2292C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589596 | |||||||
| chr2:64589718 | C | T | 1 | a0002c0002t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2664-2170C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589718 | |||||||
| chr2:64589926 | C | T | 8 | a0001c0001t0004g0093 a0002c0002t0002g0283 a0002c0002t0002g0284 others(5): Show |
8 | HG01167.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2664-1962C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589926 | |||||||
| chr2:64589944 | TG | T | 25 | a0001c0001t0001g0095 a0001c0001t0001g0127 a0001c0001t0001g0128 others(22): Show |
25 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.2664-1928delG | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589944 | TGG | T | 59 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(56): Show |
59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.2664-1929_2664-192 others(6): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589944 | TGGG | T | 26 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0158 others(23): Show |
26 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2664-1930_2664-192 others(7): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589944 | TGGGG | T | 40 | a0001c0001t0001g0129 a0001c0001t0001g0162 a0001c0001t0001g0205 others(37): Show |
41 | HG00280.hp2 HG01069.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2664-1931_2664-192 others(8): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589944 | TGGGGG | T | 147 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0001g0139 others(144): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2664-1932_2664-192 others(9): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589944 | TGGGGGG | T | 37 | a0001c0001t0002g0201 a0001c0001t0004g0276 a0001c0001t0005g0060 others(34): Show |
38 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.2664-1933_2664-192 others(10): Show |
AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 64589944 | ||||||
| chr2:64589949 | G | C | 12 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0157 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2664-1939G>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589949 | |||||||
| chr2:64589950 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2664-1938G>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64589950 | |||||||
| chr2:64590005 | C | T | 1 | a0010c0013t0017g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2664-1883C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590005 | |||||||
| chr2:64590041 | C | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0234 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.2664-1847C>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590041 | |||||||
| chr2:64590081 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2664-1807C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590081 | |||||||
| chr2:64590122 | G | A | 82 | a0001c0001t0001g0042 a0001c0001t0004g0001 a0001c0001t0004g0011 others(79): Show |
84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2664-1766G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590122 | |||||||
| chr2:64590129 | A | G | 1 | a0001c0001t0001g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2664-1759A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590129 | |||||||
| chr2:64590634 | A | G | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2664-1254A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590634 | |||||||
| chr2:64590748 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2664-1140C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64590748 | |||||||
| chr2:64591005 | T | G | 3 | a0002c0002t0002g0333 a0002c0002t0002g0358 a0002c0002t0019g0360 |
3 | HG03041.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2664-883T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591005 | |||||||
| chr2:64591038 | C | T | 5 | a0003c0003t0008g0232 a0003c0003t0008g0263 a0003c0003t0008g0264 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2664-850C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591038 | |||||||
| chr2:64591084 | A | G | 2 | a0002c0002t0002g0355 a0002c0002t0002g0359 |
2 | NA18972.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2664-804A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591084 | |||||||
| chr2:64591184 | C | T | 3 | a0001c0001t0004g0093 a0002c0002t0002g0283 a0002c0002t0002g0284 |
3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2664-704C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591184 | |||||||
| chr2:64591260 | A | T | 108 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0201 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-628A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591260 | |||||||
| chr2:64591485 | C | G | 108 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0201 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-403C>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591485 | |||||||
| chr2:64591526 | A | G | 1 | a0001c0001t0005g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2664-362A>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591526 | |||||||
| chr2:64591565 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2664-323T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591565 | |||||||
| chr2:64591600 | G | A | 1 | a0011c0011t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2664-288G>A | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591600 | |||||||
| chr2:64591650 | T | G | 1 | a0002c0002t0009g0325 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2664-238T>G | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591650 | |||||||
| chr2:64591675 | C | T | 3 | a0001c0001t0004g0093 a0002c0002t0002g0283 a0002c0002t0002g0284 |
3 | HG01167.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2664-213C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591675 | |||||||
| chr2:64591690 | C | T | 194 | a0001c0001t0001g0042 a0001c0001t0002g0021 a0001c0001t0002g0109 others(191): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2664-198C>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591690 | |||||||
| chr2:64591706 | A | T | 41 | a0001c0001t0002g0109 a0001c0001t0002g0201 a0002c0002t0002g0005 others(38): Show |
42 | HG00323.hp1 HG00408.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.2664-182A>T | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591706 | |||||||
| chr2:64591730 | T | C | 108 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0201 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2664-158T>C | AFTPH | ENSG00000119844.17 | transcript | ENST00000409933.6 | protein_coding | 9/9 | chr2 | 64591730 |