Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23431 |
| ensemblid | ENSG00000081014.11 |
| hgncid | 573 |
| symbol | AP4E1 |
| name | adaptor related protein complex 4 subunit epsilon 1 |
| refseq_nuc | NM_007347.5 |
| refseq_prot | NP_031373.2 |
| ensembl_nuc | ENST00000261842.10 |
| ensembl_prot | ENSP00000261842.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 50908683 |
| end | 51005895 |
| strand | + |
| ver | v1.2 |
| region | chr15:50908683-51005895 |
| region5000 | chr15:50903683-51010895 |
| regionname0 | AP4E1_chr15_50908683_51005895 |
| regionname5000 | AP4E1_chr15_50903683_51010895 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1137 | 192 | 59 | 41 | 62 | 6 | 22 | 49 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0002 | 0/0 | 1137 | 183 | 19 | 32 | 108 | 8 | 16 | 83 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0003 | 0/0 | 1137 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0004 | 0/0 | 1137 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0005 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0006 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0007 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0008 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0009 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0010 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| a0011 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | MSDIV others(1132): Show |
chr15 | 50903683 | 51010895 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3411 | 191 | 59 | 41 | 61 | 6 | 22 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0001c0010 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0002c0002 | 0/0 | 3411 | 95 | 2 | 14 | 67 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0002c0003 | 0/0 | 3411 | 86 | 15 | 18 | 41 | 4 | 8 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0002c0006 | 0/0 | 3411 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0003c0004 | 0/0 | 3411 | 6 | 6 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0004c0005 | 0/0 | 3411 | 3 | 0 | 0 | 3 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0005c0007 | 0/0 | 3411 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0006c0013 | 0/0 | 3411 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0007c0011 | 0/0 | 3411 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0008c0008 | 0/0 | 3411 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0009c0012 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0010c0014 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 | ||
| a0011c0009 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | ATGAG others(3406): Show |
chr15 | 50903683 | 51010895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6743 | 106 | 16 | 23 | 55 | 1 | 10 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0003 | 0/1 | 6743 | 14 | 2 | 3 | 1 | 2 | 5 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0004 | 0/0 | 6743 | 39 | 14 | 12 | 3 | 3 | 7 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0005 | 0/0 | 6743 | 17 | 16 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0008 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0009 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0019 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0025 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0026 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0027 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0028 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0001c0001t0029 | 0/0 | 6731 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6726): Show |
chr15 | 50903683 | 51010895 |
| a0001c0010t0002 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0002 | 0/0 | 6743 | 86 | 1 | 12 | 63 | 4 | 6 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0012 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0016 | 0/0 | 6743 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0017 | 0/0 | 6743 | 2 | 0 | 1 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0021 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0023 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0002t0024 | 0/0 | 6743 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0001 | 0/0 | 6743 | 3 | 0 | 1 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0002 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0003 | 0/0 | 6743 | 66 | 5 | 12 | 38 | 4 | 7 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0006 | 0/0 | 6743 | 7 | 6 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0010 | 0/0 | 6743 | 3 | 1 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0013 | 0/0 | 6743 | 2 | 0 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0014 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0020 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6756): Show |
chr15 | 50903683 | 51010895 |
| a0002c0003t0022 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0002c0006t0015 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0003c0004t0007 | 0/0 | 6743 | 4 | 4 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0003c0004t0018 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0004c0005t0001 | 0/0 | 6743 | 3 | 0 | 0 | 3 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0005c0007t0011 | 0/0 | 6743 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0006c0013t0005 | 0/0 | 6743 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0007c0011t0005 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0008c0008t0002 | 0/0 | 6743 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0009c0012t0001 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0010c0014t0001 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| a0011c0009t0003 | 0/0 | 6743 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | AGTGC others(6738): Show |
chr15 | 50903683 | 51010895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0004g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0019g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0025g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0027g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0028g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0001t0029g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0001c0010t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0016g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0017g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0017g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0023g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0002t0024g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0010g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0013g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0020g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0003t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0006t0015g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0002c0006t0015g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0003c0004t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0004c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0005c0007t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0005c0007t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0006c0013t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0007c0011t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0008c0008t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0009c0012t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0010c0014t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| a0011c0009t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0383 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00099 | hp2 | a0002 | c0003 | t0003 | g0157 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0058 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0346 | EUR | GBR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0386 | EUR | FIN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0061 | EUR | FIN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0175 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0133 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00621 | hp2 | a0002 | c0003 | t0003 | g0026 | EAS | CHS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0377 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0137 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0194 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00741 | hp1 | a0002 | c0002 | t0017 | g0056 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0147 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0369 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0370 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01074 | hp2 | a0002 | c0003 | t0013 | g0001 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01099 | hp1 | a0002 | c0003 | t0013 | g0001 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0384 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0334 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01109 | hp2 | a0002 | c0003 | t0003 | g0142 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01167 | hp1 | a0002 | c0003 | t0006 | g0186 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01167 | hp2 | a0002 | c0003 | t0010 | g0034 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0136 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0025 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01169 | hp1 | a0002 | c0003 | t0010 | g0032 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0156 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0380 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0151 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0193 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01255 | hp1 | a0006 | c0013 | t0005 | g0333 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0365 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0143 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01346 | hp2 | a0001 | c0001 | t0025 | g0372 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0076 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0382 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01496 | hp1 | a0001 | c0001 | t0029 | g0306 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0371 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0376 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01515 | hp2 | a0002 | c0003 | t0003 | g0141 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0311 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0013 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0130 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0069 | EUR | IBS | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0217 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0337 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01891 | hp1 | a0005 | c0007 | t0011 | g0185 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01891 | hp2 | a0002 | c0003 | t0022 | g0007 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01943 | hp1 | a0002 | c0002 | t0023 | g0042 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0030 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0373 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0374 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0375 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0029 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0176 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0155 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0166 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0165 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02145 | hp2 | a0003 | c0004 | t0018 | g0020 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | CDX | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02257 | hp1 | a0002 | c0006 | t0015 | g0347 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02280 | hp1 | a0002 | c0003 | t0003 | g0170 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0385 | AMR | PEL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0218 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0379 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02615 | hp1 | a0002 | c0003 | t0006 | g0187 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02615 | hp2 | a0003 | c0004 | t0007 | g0024 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0356 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0331 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0363 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02647 | hp2 | a0007 | c0011 | t0005 | g0340 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0357 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0341 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02809 | hp2 | a0008 | c0008 | t0002 | g0005 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02818 | hp1 | a0002 | c0003 | t0014 | g0017 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0318 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02895 | hp2 | a0002 | c0003 | t0003 | g0139 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0359 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02897 | hp2 | a0002 | c0003 | t0003 | g0128 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02922 | hp1 | a0002 | c0003 | t0014 | g0018 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02922 | hp2 | a0003 | c0004 | t0007 | g0021 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0349 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02976 | hp2 | a0001 | c0001 | t0028 | g0220 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03041 | hp1 | a0005 | c0007 | t0011 | g0184 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03041 | hp2 | a0002 | c0002 | t0021 | g0006 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0329 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03098 | hp2 | a0002 | c0003 | t0003 | g0132 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0320 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0352 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03195 | hp1 | a0003 | c0004 | t0018 | g0019 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0361 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03209 | hp2 | a0002 | c0006 | t0015 | g0348 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0381 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03239 | hp1 | a0002 | c0003 | t0003 | g0160 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0339 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0362 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0127 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0134 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03516 | hp2 | a0002 | c0003 | t0006 | g0192 | AFR | ESN | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0338 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | GWD | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0216 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | MSL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0387 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0342 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0378 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0183 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03710 | hp1 | a0002 | c0003 | t0020 | g0008 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03710 | hp2 | a0002 | c0002 | t0017 | g0055 | SAS | PJL | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0367 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03834 | hp2 | a0002 | c0003 | t0003 | g0138 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03927 | hp1 | a0002 | c0003 | t0003 | g0149 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0167 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0368 | SAS | BEB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04199 | hp1 | a0002 | c0002 | t0024 | g0047 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0366 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0388 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0351 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0153 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18747 | hp2 | a0002 | c0003 | t0003 | g0181 | EAS | CHB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0360 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18906 | hp2 | a0003 | c0004 | t0007 | g0022 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0158 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0358 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0180 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18944 | hp2 | a0004 | c0005 | t0001 | g0237 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0171 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18947 | hp2 | a0002 | c0003 | t0003 | g0152 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18948 | hp2 | a0002 | c0003 | t0003 | g0163 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18949 | hp2 | a0002 | c0002 | t0012 | g0111 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18956 | hp2 | a0002 | c0003 | t0003 | g0144 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0146 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0172 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18962 | hp1 | a0004 | c0005 | t0001 | g0238 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18964 | hp2 | a0002 | c0003 | t0003 | g0148 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18965 | hp1 | a0002 | c0003 | t0003 | g0159 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0174 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18974 | hp2 | a0009 | c0012 | t0001 | g0289 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18975 | hp1 | a0002 | c0003 | t0003 | g0182 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18975 | hp2 | a0004 | c0005 | t0001 | g0266 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18979 | hp1 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18981 | hp2 | a0002 | c0003 | t0003 | g0178 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18982 | hp1 | a0002 | c0003 | t0003 | g0162 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0154 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0126 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18986 | hp2 | a0001 | c0001 | t0019 | g0215 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18990 | hp2 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18992 | hp1 | a0002 | c0003 | t0003 | g0028 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18993 | hp1 | a0010 | c0014 | t0001 | g0231 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18993 | hp2 | a0002 | c0003 | t0003 | g0164 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19000 | hp2 | a0002 | c0003 | t0003 | g0179 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0161 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19012 | hp2 | a0002 | c0002 | t0016 | g0073 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0364 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0335 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0173 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19058 | hp1 | a0011 | c0009 | t0003 | g0145 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19060 | hp2 | a0001 | c0001 | t0019 | g0230 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19067 | hp1 | a0002 | c0003 | t0003 | g0140 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19072 | hp2 | a0002 | c0002 | t0016 | g0116 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19074 | hp2 | a0002 | c0003 | t0003 | g0129 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19079 | hp1 | a0002 | c0003 | t0003 | g0177 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19088 | hp1 | a0002 | c0003 | t0003 | g0150 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19088 | hp2 | a0002 | c0002 | t0012 | g0112 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19090 | hp2 | a0002 | c0003 | t0002 | g0123 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA19240 | hp2 | a0001 | c0001 | t0026 | g0294 | AFR | YRI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20129 | hp1 | a0002 | c0003 | t0006 | g0190 | AFR | ASW | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20129 | hp2 | a0003 | c0004 | t0007 | g0023 | AFR | ASW | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0312 | EUR | TSI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0168 | EUR | TSI | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02109 | hp1 | a0002 | c0003 | t0006 | g0189 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0224 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02486 | hp1 | a0002 | c0003 | t0006 | g0188 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0169 | AFR | ACB | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG06807 | hp1 | a0002 | c0003 | t0010 | g0033 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| HG06807 | hp2 | a0002 | c0003 | t0006 | g0191 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA18955 | hp2 | a0001 | c0010 | t0002 | g0355 | EAS | JPT | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0330 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0308 | REF | REF | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0038 | REF | REF | AP4E1_chr15_50903683_51010895 | AP4E1 | chr15 | 50903683 | 51010895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50925164 | T | C | 5 | a0002 a0003 a0005 others(2): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
missense_variant | MODERATE | c.487T>C | p.Cys163Arg | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/21 | 583/6743 | 487/3414 | 163/1137 | chr15 | 50925164 | |||
| chr15:50930893 | A | G | 1 | a0011 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.791A>G | p.Asn264Ser | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/21 | 887/6743 | 791/3414 | 264/1137 | chr15 | 50930893 | |||
| chr15:50941684 | A | G | 1 | a0008 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1085A>G | p.Tyr362Cys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/21 | 1181/6743 | 1085/3414 | 362/1137 | chr15 | 50941684 | |||
| chr15:50948126 | A | G | 1 | a0005 | 2 | HG01891.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.1283A>G | p.Asn428Ser | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/21 | 1379/6743 | 1283/3414 | 428/1137 | chr15 | 50948126 | |||
| chr15:50958529 | C | T | 1 | a0008 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1586C>T | p.Thr529Met | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/21 | 1682/6743 | 1586/3414 | 529/1137 | chr15 | 50958529 | |||
| chr15:50958637 | C | T | 1 | a0010 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1694C>T | p.Ala565Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/21 | 1790/6743 | 1694/3414 | 565/1137 | chr15 | 50958637 | |||
| chr15:50968362 | C | G | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1951C>G | p.Leu651Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/21 | 2047/6743 | 1951/3414 | 651/1137 | chr15 | 50968362 | |||
| chr15:50997359 | A | G | 1 | a0009 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2380A>G | p.Arg794Gly | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2476/6743 | 2380/3414 | 794/1137 | chr15 | 50997359 | |||
| chr15:50997408 | C | T | 1 | a0003 | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.2429C>T | p.Thr810Ile | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2525/6743 | 2429/3414 | 810/1137 | chr15 | 50997408 | |||
| chr15:50997597 | C | G | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2618C>G | p.Ser873Cys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2714/6743 | 2618/3414 | 873/1137 | chr15 | 50997597 | |||
| chr15:50997734 | A | G | 1 | a0005 | 2 | HG01891.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2755A>G | p.Met919Val | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/21 | 2851/6743 | 2755/3414 | 919/1137 | chr15 | 50997734 | |||
| chr15:51001147 | C | A | 1 | a0004 | 3 | NA18944.hp2 NA18962.hp1 NA18975.hp2 |
missense_variant | MODERATE | c.3217C>A | p.Gln1073Lys | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/21 | 3313/6743 | 3217/3414 | 1073/1137 | chr15 | 51001147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50912098 | G | A | 1 | a0002c0006 | 2 | HG02257.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.171G>A | p.Gln57Gln | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/21 | 267/6743 | 171/3414 | 57/1137 | chr15 | 50912098 | |||
| chr15:51002635 | G | A | 3 | a0001c0010 a0002c0002 a0008c0008 |
97 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
synonymous_variant | LOW | c.3387G>A | p.Gln1129Gln | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3483/6743 | 3387/3414 | 1129/1137 | chr15 | 51002635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50908702 | C | T | 1 | a0001c0001t0019 | 2 | NA18986.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 77 | chr15 | 50908702 | ||||||
| chr15:50908713 | GGCCGGGC others(5): Show |
G | 1 | a0001c0001t0029 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58_-47delATGAAGCC others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 47 | INFO_REALIGN_3_PRIME | chr15 | 50908713 | |||||
| chr15:50908741 | G | GATCGCGG others(11): Show |
1 | a0002c0003t0020 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19_-2dupATCGCGGGC others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/21 | 1 | INFO_REALIGN_3_PRIME | chr15 | 50908741 | |||||
| chr15:51002798 | G | A | 23 | a0001c0001t0003 a0001c0010t0002 a0002c0002t0002 others(20): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 136 | chr15 | 51002798 | ||||||
| chr15:51002821 | C | T | 1 | a0001c0001t0028 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 159 | chr15 | 51002821 | ||||||
| chr15:51003057 | A | G | 1 | a0003c0004t0018 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 395 | chr15 | 51003057 | ||||||
| chr15:51003215 | G | C | 1 | a0002c0002t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 553 | chr15 | 51003215 | ||||||
| chr15:51003284 | G | A | 1 | a0005c0007t0011 | 2 | HG01891.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*622G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 622 | chr15 | 51003284 | ||||||
| chr15:51003382 | T | A | 1 | a0002c0002t0012 | 2 | NA18949.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*720T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 720 | chr15 | 51003382 | ||||||
| chr15:51003451 | C | A | 1 | a0002c0003t0013 | 2 | HG01074.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*789C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 789 | chr15 | 51003451 | ||||||
| chr15:51003535 | C | T | 1 | a0001c0001t0009 | 4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*873C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 873 | chr15 | 51003535 | ||||||
| chr15:51003583 | C | T | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 921 | chr15 | 51003583 | ||||||
| chr15:51003736 | A | C | 2 | a0003c0004t0007 a0003c0004t0018 |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1074A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1074 | chr15 | 51003736 | ||||||
| chr15:51003737 | G | A | 10 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0010 others(7): Show |
95 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1075 | chr15 | 51003737 | ||||||
| chr15:51003818 | G | A | 2 | a0001c0001t0004 a0001c0001t0025 |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1156 | chr15 | 51003818 | ||||||
| chr15:51003990 | C | T | 1 | a0002c0003t0014 | 2 | HG02818.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1328C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1328 | chr15 | 51003990 | ||||||
| chr15:51004036 | T | C | 1 | a0001c0001t0026 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1374 | chr15 | 51004036 | ||||||
| chr15:51004045 | A | G | 1 | a0001c0001t0019 | 2 | NA18986.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1383A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1383 | chr15 | 51004045 | ||||||
| chr15:51004210 | T | C | 28 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(25): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1548T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1548 | chr15 | 51004210 | ||||||
| chr15:51004221 | G | T | 2 | a0002c0003t0010 a0002c0003t0014 |
5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1559G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1559 | chr15 | 51004221 | ||||||
| chr15:51004364 | A | G | 1 | a0002c0002t0017 | 2 | HG00741.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1702A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1702 | chr15 | 51004364 | ||||||
| chr15:51004572 | T | C | 1 | a0002c0006t0015 | 2 | HG02257.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1910T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 1910 | chr15 | 51004572 | ||||||
| chr15:51004765 | A | T | 5 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0029 others(2): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2103A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2103 | chr15 | 51004765 | ||||||
| chr15:51004842 | C | T | 1 | a0002c0002t0024 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2180C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2180 | chr15 | 51004842 | ||||||
| chr15:51004856 | T | A | 1 | a0002c0003t0006 | 7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2194T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2194 | chr15 | 51004856 | ||||||
| chr15:51005097 | G | A | 1 | a0002c0003t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2435G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2435 | chr15 | 51005097 | ||||||
| chr15:51005166 | G | A | 1 | a0001c0001t0008 | 4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2504G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2504 | chr15 | 51005166 | ||||||
| chr15:51005389 | G | A | 1 | a0001c0001t0025 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 2727 | chr15 | 51005389 | ||||||
| chr15:51005693 | T | G | 1 | a0002c0002t0016 | 2 | NA19012.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3031 | chr15 | 51005693 | ||||||
| chr15:51005694 | G | A | 1 | a0002c0002t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3032G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 21/21 | 3032 | chr15 | 51005694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50908961 | A | G | 40 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.150+33A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50908961 | |||||||
| chr15:50909084 | A | G | 24 | a0001c0001t0004g0365 a0001c0001t0004g0366 a0001c0001t0004g0367 others(21): Show |
24 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.150+156A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909084 | |||||||
| chr15:50909160 | G | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.150+232G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909160 | |||||||
| chr15:50909167 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+239C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909167 | |||||||
| chr15:50909187 | C | T | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.150+259C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909187 | |||||||
| chr15:50909204 | A | T | 1 | a0001c0001t0004g0364 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.150+276A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909204 | |||||||
| chr15:50909323 | C | T | 2 | a0002c0003t0003g0193 a0002c0003t0003g0194 |
2 | HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.150+395C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909323 | |||||||
| chr15:50909440 | C | T | 9 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(6): Show |
9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+512C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909440 | |||||||
| chr15:50909498 | G | T | 4 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(1): Show |
4 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+570G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909498 | |||||||
| chr15:50909583 | A | C | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.150+655A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909583 | |||||||
| chr15:50909585 | T | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+657T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909585 | |||||||
| chr15:50909710 | C | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.150+782C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909710 | |||||||
| chr15:50909804 | C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.150+876C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909804 | |||||||
| chr15:50909843 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
197 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.150+915G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909843 | |||||||
| chr15:50909869 | T | A | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.150+941T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909869 | |||||||
| chr15:50909888 | T | C | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150+960T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50909888 | |||||||
| chr15:50910032 | G | T | 1 | a0002c0003t0003g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.150+1104G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910032 | |||||||
| chr15:50910140 | C | G | 13 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0331 others(10): Show |
13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+1212C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910140 | |||||||
| chr15:50910338 | A | G | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.150+1410A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910338 | |||||||
| chr15:50910346 | A | G | 1 | a0002c0003t0003g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.150+1418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910346 | |||||||
| chr15:50910686 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
197 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.151-1392C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910686 | |||||||
| chr15:50910700 | G | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.151-1378G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910700 | |||||||
| chr15:50910704 | G | A | 1 | a0002c0003t0020g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151-1374G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910704 | |||||||
| chr15:50910974 | A | G | 40 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.151-1104A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50910974 | |||||||
| chr15:50911213 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.151-865G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911213 | |||||||
| chr15:50911264 | G | A | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG01993.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-814G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911264 | |||||||
| chr15:50911431 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.151-647T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911431 | |||||||
| chr15:50911479 | A | AT | 11 | a0002c0002t0002g0120 a0002c0002t0002g0121 a0002c0002t0002g0122 others(8): Show |
11 | HG01175.hp2 HG01192.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-577dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | ||||||
| chr15:50911479 | AT | A | 50 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(47): Show |
50 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.151-577delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | ||||||
| chr15:50911479 | ATT | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.151-578_151-577del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | ||||||
| chr15:50911479 | ATTT | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG00408.hp1 HG01257.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-579_151-577del others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911479 | ||||||
| chr15:50911629 | C | T | 1 | a0001c0001t0005g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.151-449C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911629 | |||||||
| chr15:50911666 | C | CG | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
197 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.151-408dupG | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr15 | 50911666 | ||||||
| chr15:50911773 | C | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.151-305C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911773 | |||||||
| chr15:50911936 | C | T | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.151-142C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 1/20 | chr15 | 50911936 | |||||||
| chr15:50912167 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
197 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.222+18G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912167 | |||||||
| chr15:50912197 | C | CT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.222+48_222+49insT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912197 | |||||||
| chr15:50912223 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.222+74A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912223 | |||||||
| chr15:50912303 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.222+154C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912303 | |||||||
| chr15:50912358 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.222+209G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912358 | |||||||
| chr15:50912364 | GTGA | G | 4 | a0001c0001t0005g0321 a0001c0001t0009g0318 a0001c0001t0009g0319 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+223_222+225del others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912364 | ||||||
| chr15:50912472 | A | T | 1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.222+323A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912472 | |||||||
| chr15:50912519 | A | G | 9 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(6): Show |
9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+370A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912519 | |||||||
| chr15:50912552 | C | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.222+403C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912552 | |||||||
| chr15:50912657 | A | AT | 9 | a0002c0002t0002g0119 a0002c0002t0002g0125 a0002c0003t0003g0173 others(6): Show |
9 | HG00408.hp2 HG00735.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+526dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | ||||||
| chr15:50912657 | ATTTT | A | 9 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0295 others(6): Show |
9 | HG01243.hp2 HG02148.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+523_222+526del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | ||||||
| chr15:50912657 | ATTTTT | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0195 others(140): Show |
145 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.222+522_222+526del others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | ||||||
| chr15:50912657 | ATTTTTT | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+521_222+526del others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50912657 | ||||||
| chr15:50912788 | G | A | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.222+639G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912788 | |||||||
| chr15:50912806 | G | T | 1 | a0001c0001t0004g0387 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.222+657G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912806 | |||||||
| chr15:50912811 | C | T | 2 | a0002c0003t0003g0171 a0002c0003t0003g0172 |
2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.222+662C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912811 | |||||||
| chr15:50912823 | T | C | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+674T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912823 | |||||||
| chr15:50912988 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.222+839A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50912988 | |||||||
| chr15:50913091 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.222+942A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913091 | |||||||
| chr15:50913126 | G | A | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.222+977G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913126 | |||||||
| chr15:50913913 | A | G | 13 | a0002c0002t0002g0107 a0002c0002t0002g0108 a0002c0002t0002g0109 others(10): Show |
13 | HG02071.hp2 HG02155.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.223-1535A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50913913 | |||||||
| chr15:50914107 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.223-1341A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914107 | |||||||
| chr15:50914170 | T | G | 1 | a0008c0008t0002g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.223-1278T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914170 | |||||||
| chr15:50914212 | T | C | 60 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.223-1236T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914212 | |||||||
| chr15:50914303 | T | C | 1 | a0001c0001t0004g0350 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223-1145T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914303 | |||||||
| chr15:50914381 | T | C | 1 | a0002c0002t0002g0037 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.223-1067T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914381 | |||||||
| chr15:50914448 | T | G | 1 | a0002c0003t0003g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1000T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914448 | |||||||
| chr15:50914512 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0004g0366 |
2 | HG04199.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.223-936G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914512 | |||||||
| chr15:50914637 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223-811C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914637 | |||||||
| chr15:50914638 | G | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-810G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914638 | |||||||
| chr15:50914650 | CA | C | 7 | a0001c0001t0001g0214 a0001c0001t0004g0367 a0001c0001t0019g0215 others(4): Show |
7 | HG01167.hp1 HG01256.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-777delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50914650 | ||||||
| chr15:50914650 | CAA | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.223-778_223-777del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr15 | 50914650 | ||||||
| chr15:50914885 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223-563C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914885 | |||||||
| chr15:50914946 | T | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-502T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50914946 | |||||||
| chr15:50915008 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.223-440A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915008 | |||||||
| chr15:50915070 | A | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0195 others(103): Show |
108 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.223-378A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915070 | |||||||
| chr15:50915367 | C | T | 1 | a0002c0003t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-81C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915367 | |||||||
| chr15:50915416 | T | C | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-32T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 2/20 | chr15 | 50915416 | |||||||
| chr15:50915621 | G | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.346+50G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915621 | |||||||
| chr15:50915752 | T | G | 1 | a0002c0003t0003g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.346+181T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915752 | |||||||
| chr15:50915786 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.346+215G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915786 | |||||||
| chr15:50915800 | G | A | 4 | a0001c0001t0005g0321 a0001c0001t0009g0318 a0001c0001t0009g0319 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+229G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915800 | |||||||
| chr15:50915807 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.346+236C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915807 | |||||||
| chr15:50915892 | C | G | 1 | a0002c0002t0002g0105 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.346+321C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50915892 | |||||||
| chr15:50916055 | T | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+484T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916055 | |||||||
| chr15:50916195 | G | T | 3 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.346+624G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916195 | |||||||
| chr15:50916237 | C | T | 1 | a0002c0003t0003g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.346+666C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916237 | |||||||
| chr15:50916276 | G | C | 1 | a0001c0001t0004g0368 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.346+705G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916276 | |||||||
| chr15:50916371 | G | T | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+800G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916371 | |||||||
| chr15:50916387 | A | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.346+816A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916387 | |||||||
| chr15:50916537 | G | T | 13 | a0002c0002t0002g0093 a0002c0002t0002g0094 a0002c0002t0002g0095 others(10): Show |
13 | HG00438.hp2 NA18747.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+966G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916537 | |||||||
| chr15:50916551 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+980C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916551 | |||||||
| chr15:50916611 | G | A | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1040G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916611 | |||||||
| chr15:50916648 | C | G | 13 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0331 others(10): Show |
13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+1077C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916648 | |||||||
| chr15:50916751 | A | G | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.346+1180A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916751 | |||||||
| chr15:50916861 | C | G | 1 | a0002c0003t0003g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.346+1290C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916861 | |||||||
| chr15:50916861 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+1290C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916861 | |||||||
| chr15:50916896 | C | G | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1325C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916896 | |||||||
| chr15:50916985 | A | G | 1 | a0009c0012t0001g0289 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.346+1414A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50916985 | |||||||
| chr15:50917071 | T | C | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1500T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917071 | |||||||
| chr15:50917073 | A | G | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.346+1502A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917073 | |||||||
| chr15:50917173 | C | A | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+1602C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917173 | |||||||
| chr15:50917238 | G | A | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+1667G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917238 | |||||||
| chr15:50917282 | T | A | 1 | a0002c0003t0003g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.346+1711T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917282 | |||||||
| chr15:50917374 | G | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.346+1803G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917374 | |||||||
| chr15:50917388 | G | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.346+1817G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917388 | |||||||
| chr15:50917442 | T | C | 23 | a0001c0001t0005g0302 a0001c0001t0005g0303 a0001c0001t0005g0304 others(20): Show |
23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.346+1871T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917442 | |||||||
| chr15:50917477 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.346+1906A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917477 | |||||||
| chr15:50917496 | C | A | 4 | a0001c0001t0005g0321 a0001c0001t0009g0318 a0001c0001t0009g0319 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1925C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917496 | |||||||
| chr15:50917536 | CAG | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+1967_346+1968d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50917536 | ||||||
| chr15:50917658 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.346+2087A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917658 | |||||||
| chr15:50917678 | A | G | 1 | a0002c0002t0002g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.346+2107A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917678 | |||||||
| chr15:50917718 | C | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0323 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+2147C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917718 | |||||||
| chr15:50917777 | G | A | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.346+2206G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917777 | |||||||
| chr15:50917795 | CAG | C | 6 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+2226_346+2227d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50917795 | ||||||
| chr15:50917851 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.346+2280G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917851 | |||||||
| chr15:50917957 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346+2386A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917957 | |||||||
| chr15:50917989 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.346+2418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50917989 | |||||||
| chr15:50918358 | C | T | 3 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.346+2787C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918358 | |||||||
| chr15:50918366 | T | G | 12 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(9): Show |
12 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2795T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918366 | |||||||
| chr15:50918388 | C | G | 2 | a0002c0002t0002g0015 a0002c0002t0002g0090 |
2 | HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.346+2817C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918388 | |||||||
| chr15:50918443 | AGTAG | A | 4 | a0001c0001t0008g0216 a0001c0001t0008g0217 a0001c0001t0008g0218 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2873_346+2876d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918443 | |||||||
| chr15:50918444 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.346+2873G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918444 | |||||||
| chr15:50918452 | T | A | 4 | a0001c0001t0008g0216 a0001c0001t0008g0217 a0001c0001t0008g0218 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+2881T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918452 | |||||||
| chr15:50918674 | T | G | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+3103T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918674 | |||||||
| chr15:50918830 | A | G | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.346+3259A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918830 | |||||||
| chr15:50918913 | T | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.346+3342T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918913 | |||||||
| chr15:50918934 | T | A | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.346+3363T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918934 | |||||||
| chr15:50918936 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.346+3365T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918936 | |||||||
| chr15:50918995 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.346+3424G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50918995 | |||||||
| chr15:50919150 | A | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.346+3579A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919150 | |||||||
| chr15:50919186 | C | A | 1 | a0001c0001t0001g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.346+3615C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919186 | |||||||
| chr15:50919301 | G | C | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.346+3730G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919301 | |||||||
| chr15:50919535 | A | AAAAT | 6 | a0002c0002t0002g0045 a0002c0002t0002g0046 a0002c0003t0003g0127 others(3): Show |
6 | HG00609.hp1 HG03098.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+4003_346+4006d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | ||||||
| chr15:50919535 | AAAAT | A | 91 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0003g0307 others(88): Show |
91 | HG00438.hp2 HG00639.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.346+4003_346+4006d others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | ||||||
| chr15:50919535 | AAAATAAA others(1): Show |
A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0195 others(103): Show |
108 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.346+3999_346+4006d others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | ||||||
| chr15:50919535 | AAAATAAA others(5): Show |
A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(11): Show |
15 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+3995_346+4006d others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | ||||||
| chr15:50919535 | AAAATAAA others(9): Show |
A | 7 | a0001c0001t0004g0380 a0001c0001t0004g0381 a0001c0001t0004g0382 others(4): Show |
7 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+3991_346+4006d others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919535 | ||||||
| chr15:50919570 | ATAAATAA others(1): Show |
A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0027g0224 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.346+4007_346+4014d others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50919570 | ||||||
| chr15:50919685 | C | G | 1 | a0002c0002t0002g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.346+4114C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919685 | |||||||
| chr15:50919719 | C | T | 8 | a0001c0001t0001g0286 a0002c0003t0006g0186 a0002c0003t0006g0187 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+4148C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919719 | |||||||
| chr15:50919812 | A | G | 1 | a0002c0002t0002g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.347-4119A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919812 | |||||||
| chr15:50919926 | G | A | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.347-4005G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919926 | |||||||
| chr15:50919980 | G | T | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-3951G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919980 | |||||||
| chr15:50919999 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-3932C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50919999 | |||||||
| chr15:50920019 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-3912G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920019 | |||||||
| chr15:50920047 | A | G | 5 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3884A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920047 | |||||||
| chr15:50920050 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
6 | NA18940.hp2 NA18941.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-3881C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920050 | |||||||
| chr15:50920075 | T | TA | 7 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG01981.hp1 HG02738.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-3836dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920075 | ||||||
| chr15:50920075 | T | TC | 4 | a0001c0001t0005g0332 a0001c0001t0005g0334 a0002c0003t0003g0165 others(1): Show |
4 | HG01109.hp1 HG01255.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3856_347-3855i others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920075 | |||||||
| chr15:50920075 | TA | T | 100 | a0001c0001t0001g0199 a0002c0002t0002g0009 a0002c0002t0002g0010 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.347-3836delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920075 | ||||||
| chr15:50920076 | A | C | 126 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(123): Show |
127 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.347-3855A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920076 | |||||||
| chr15:50920077 | A | C | 98 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.347-3854A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920077 | |||||||
| chr15:50920078 | A | C | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-3853A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920078 | |||||||
| chr15:50920109 | C | CCTT | 79 | a0001c0001t0003g0328 a0002c0002t0002g0049 a0002c0002t0002g0082 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.347-3821_347-3819d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920109 | ||||||
| chr15:50920110 | C | CT | 11 | a0001c0001t0001g0229 a0001c0001t0001g0276 a0001c0001t0001g0277 others(8): Show |
11 | HG00140.hp2 HG01978.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-3800dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920110 | ||||||
| chr15:50920110 | CT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(43): Show |
47 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.347-3800delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920110 | ||||||
| chr15:50920111 | T | TTC | 119 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(116): Show |
119 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.347-3819_347-3818i others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920111 | ||||||
| chr15:50920112 | T | TC | 26 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(23): Show |
26 | HG01109.hp1 HG01167.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-3819_347-3818i others(3): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920112 | |||||||
| chr15:50920145 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347-3786G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920145 | |||||||
| chr15:50920277 | C | G | 1 | a0001c0001t0004g0366 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.347-3654C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920277 | |||||||
| chr15:50920338 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-3593C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920338 | |||||||
| chr15:50920415 | C | CT | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0195 others(105): Show |
110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.347-3503dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50920415 | ||||||
| chr15:50920964 | G | A | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.347-2967G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50920964 | |||||||
| chr15:50921028 | C | T | 2 | a0001c0001t0019g0215 a0001c0001t0019g0230 |
2 | NA18986.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.347-2903C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921028 | |||||||
| chr15:50921080 | G | A | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.347-2851G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921080 | |||||||
| chr15:50921116 | A | AT | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.347-2807dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50921116 | ||||||
| chr15:50921162 | A | G | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-2769A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921162 | |||||||
| chr15:50921183 | T | A | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-2748T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921183 | |||||||
| chr15:50921321 | T | G | 1 | a0002c0002t0002g0016 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-2610T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921321 | |||||||
| chr15:50921332 | T | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2599T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921332 | |||||||
| chr15:50921410 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2521G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921410 | |||||||
| chr15:50921427 | A | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.347-2504A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921427 | |||||||
| chr15:50921598 | G | C | 1 | a0002c0002t0002g0109 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.347-2333G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921598 | |||||||
| chr15:50921680 | T | C | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.347-2251T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921680 | |||||||
| chr15:50921705 | A | G | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.347-2226A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921705 | |||||||
| chr15:50921791 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-2140G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50921791 | |||||||
| chr15:50922163 | C | CA | 95 | a0001c0001t0001g0227 a0001c0001t0001g0276 a0001c0001t0001g0283 others(92): Show |
96 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.347-1747dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | ||||||
| chr15:50922163 | C | CAA | 86 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(83): Show |
86 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.347-1748_347-1747d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | ||||||
| chr15:50922163 | C | CAAA | 15 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0039 others(12): Show |
15 | HG00423.hp1 HG02071.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.347-1749_347-1747d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922163 | ||||||
| chr15:50922186 | T | C | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.347-1745T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922186 | |||||||
| chr15:50922191 | C | T | 3 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0016g0116 |
3 | NA18950.hp1 NA18971.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.347-1740C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922191 | |||||||
| chr15:50922338 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.347-1593C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922338 | |||||||
| chr15:50922361 | G | A | 1 | a0002c0002t0002g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.347-1570G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922361 | |||||||
| chr15:50922437 | C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.347-1494C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922437 | |||||||
| chr15:50922524 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.347-1407A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922524 | |||||||
| chr15:50922526 | G | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.347-1405G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922526 | |||||||
| chr15:50922729 | T | C | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.347-1202T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922729 | |||||||
| chr15:50922782 | C | CT | 96 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(93): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.347-1136dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50922782 | ||||||
| chr15:50922793 | T | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-1138T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922793 | |||||||
| chr15:50922880 | C | A | 40 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.347-1051C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922880 | |||||||
| chr15:50922881 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.347-1050C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922881 | |||||||
| chr15:50922978 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-953C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50922978 | |||||||
| chr15:50923007 | A | G | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.347-924A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923007 | |||||||
| chr15:50923050 | A | T | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.347-881A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923050 | |||||||
| chr15:50923094 | G | A | 2 | a0002c0002t0017g0055 a0002c0002t0017g0056 |
2 | HG00741.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.347-837G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923094 | |||||||
| chr15:50923139 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.347-792A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923139 | |||||||
| chr15:50923352 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-579G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923352 | |||||||
| chr15:50923461 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-470C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923461 | |||||||
| chr15:50923467 | C | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.347-464C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923467 | |||||||
| chr15:50923494 | A | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-437A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923494 | |||||||
| chr15:50923537 | GT | G | 9 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(6): Show |
9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-386delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr15 | 50923537 | ||||||
| chr15:50923829 | G | C | 1 | a0002c0002t0002g0040 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.347-102G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 3/20 | chr15 | 50923829 | |||||||
| chr15:50924239 | T | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.420+235T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924239 | |||||||
| chr15:50924289 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.420+285G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924289 | |||||||
| chr15:50924489 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+485A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924489 | |||||||
| chr15:50924552 | TAGAG | T | 3 | a0001c0001t0004g0349 a0001c0001t0004g0351 a0001c0001t0004g0352 |
3 | HG02976.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-538_421-535del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | 50924552 | ||||||
| chr15:50924623 | C | T | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.421-475C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924623 | |||||||
| chr15:50924677 | A | G | 1 | a0001c0001t0005g0334 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421-421A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924677 | |||||||
| chr15:50924759 | T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-339T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924759 | |||||||
| chr15:50924899 | CTTTA | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-195_421-192del others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr15 | 50924899 | ||||||
| chr15:50924929 | A | C | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-169A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50924929 | |||||||
| chr15:50925045 | T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.421-53T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50925045 | |||||||
| chr15:50925078 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0233 |
2 | NA18942.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.421-20T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 4/20 | chr15 | 50925078 | |||||||
| chr15:50925230 | T | G | 3 | a0002c0003t0006g0188 a0002c0003t0006g0189 a0002c0003t0006g0192 |
3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.542+11T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925230 | |||||||
| chr15:50925267 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542+48C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925267 | |||||||
| chr15:50925278 | G | A | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.542+59G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925278 | |||||||
| chr15:50925477 | A | G | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.542+258A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925477 | |||||||
| chr15:50925632 | C | CT | 70 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0292 others(67): Show |
71 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.542+428dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925632 | ||||||
| chr15:50925632 | C | CTT | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.542+427_542+428dup others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925632 | ||||||
| chr15:50925796 | AT | A | 185 | a0001c0001t0001g0223 a0001c0001t0001g0228 a0002c0002t0002g0009 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.542+594delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50925796 | ||||||
| chr15:50925877 | G | A | 1 | a0002c0003t0003g0163 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.542+658G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925877 | |||||||
| chr15:50925926 | G | C | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.542+707G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925926 | |||||||
| chr15:50925933 | T | A | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.542+714T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50925933 | |||||||
| chr15:50926065 | T | G | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.542+846T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926065 | |||||||
| chr15:50926206 | C | T | 23 | a0001c0001t0005g0302 a0001c0001t0005g0303 a0001c0001t0005g0304 others(20): Show |
23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.542+987C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926206 | |||||||
| chr15:50926207 | G | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+988G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926207 | |||||||
| chr15:50926347 | C | T | 10 | a0001c0001t0005g0302 a0001c0001t0005g0303 a0001c0001t0005g0304 others(7): Show |
10 | HG01496.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+1128C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926347 | |||||||
| chr15:50926428 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.542+1209G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926428 | |||||||
| chr15:50926603 | T | A | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+1384T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926603 | |||||||
| chr15:50926648 | G | T | 2 | a0002c0002t0002g0080 a0002c0002t0002g0083 |
2 | HG01070.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.542+1429G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926648 | |||||||
| chr15:50926940 | A | T | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+1721A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926940 | |||||||
| chr15:50926993 | T | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.542+1774T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50926993 | |||||||
| chr15:50927045 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.542+1826A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927045 | |||||||
| chr15:50927087 | T | C | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.542+1868T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927087 | |||||||
| chr15:50927096 | A | C | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.542+1877A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927096 | |||||||
| chr15:50927285 | TATGGCCA others(6): Show |
T | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.543-1723_543-1711d others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927285 | |||||||
| chr15:50927516 | G | GT | 105 | a0001c0001t0001g0200 a0001c0001t0001g0282 a0001c0001t0009g0318 others(102): Show |
105 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.543-1477dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927516 | ||||||
| chr15:50927516 | G | GTT | 120 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(117): Show |
121 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.543-1478_543-1477d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927516 | ||||||
| chr15:50927671 | C | CT | 14 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(11): Show |
14 | HG01167.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.543-1327dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927671 | ||||||
| chr15:50927765 | G | A | 57 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0129 others(54): Show |
58 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.543-1244G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927765 | |||||||
| chr15:50927890 | T | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.543-1119T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50927890 | |||||||
| chr15:50927937 | A | ATTTGCAG others(7): Show |
1 | a0002c0003t0003g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.543-1071_543-1070i others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50927937 | ||||||
| chr15:50928114 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543-895C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928114 | |||||||
| chr15:50928186 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.543-823C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928186 | |||||||
| chr15:50928193 | A | G | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.543-816A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928193 | |||||||
| chr15:50928230 | A | T | 25 | a0001c0001t0001g0270 a0001c0001t0005g0301 a0001c0001t0005g0302 others(22): Show |
25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.543-779A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928230 | |||||||
| chr15:50928390 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.543-619C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928390 | |||||||
| chr15:50928402 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-607C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928402 | |||||||
| chr15:50928566 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.543-443G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928566 | |||||||
| chr15:50928571 | A | T | 1 | a0001c0001t0004g0379 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.543-438A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928571 | |||||||
| chr15:50928714 | GT | G | 119 | a0001c0001t0001g0228 a0001c0001t0004g0349 a0001c0001t0004g0380 others(116): Show |
119 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.543-282delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50928714 | ||||||
| chr15:50928714 | GTT | G | 81 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.543-283_543-282del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr15 | 50928714 | ||||||
| chr15:50928792 | G | A | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.543-217G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928792 | |||||||
| chr15:50928813 | C | T | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.543-196C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 5/20 | chr15 | 50928813 | |||||||
| chr15:50929392 | A | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0324 |
2 | HG01261.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.702+224A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929392 | |||||||
| chr15:50929404 | A | G | 11 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(8): Show |
11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+236A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929404 | |||||||
| chr15:50929526 | G | A | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+358G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929526 | |||||||
| chr15:50929711 | T | C | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.702+543T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929711 | |||||||
| chr15:50929742 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.702+574A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929742 | |||||||
| chr15:50929861 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.702+693G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929861 | |||||||
| chr15:50929940 | G | T | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.702+772G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50929940 | |||||||
| chr15:50930035 | A | G | 8 | a0002c0002t0002g0093 a0002c0002t0002g0098 a0002c0002t0002g0099 others(5): Show |
8 | HG00438.hp2 NA18747.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-770A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930035 | |||||||
| chr15:50930264 | A | ACCATGTT others(356): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
5 | NA18941.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(357): Show |
1 | a0001c0001t0001g0285 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(344): Show |
6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(351): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(350): Show |
1 | a0005c0007t0011g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(357): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(351): Show |
1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(358): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(352): Show |
1 | a0002c0006t0015g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(359): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(353): Show |
1 | a0002c0006t0015g0348 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.703-519_703-518ins others(360): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(354): Show |
2 | a0002c0003t0003g0141 a0002c0003t0003g0175 |
2 | HG00408.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(361): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(356): Show |
130 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0196 others(127): Show |
131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(356): Show |
1 | a0001c0001t0001g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(363): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(357): Show |
24 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(21): Show |
24 | HG00609.hp2 HG01261.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(357): Show |
1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.703-519_703-518ins others(364): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(358): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0265 |
2 | HG03942.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(365): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930264 | A | ACCATGTT others(359): Show |
3 | a0001c0001t0001g0229 a0001c0001t0001g0281 a0001c0001t0001g0299 |
3 | HG01981.hp1 HG02293.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.703-519_703-518ins others(366): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr15 | 50930264 | ||||||
| chr15:50930309 | C | T | 2 | a0002c0003t0003g0029 a0002c0003t0003g0030 |
2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.703-496C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930309 | |||||||
| chr15:50930347 | G | A | 1 | a0002c0003t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-458G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930347 | |||||||
| chr15:50930674 | G | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-131G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930674 | |||||||
| chr15:50930770 | G | A | 1 | a0002c0003t0003g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.703-35G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 6/20 | chr15 | 50930770 | |||||||
| chr15:50931046 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.869+75T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931046 | |||||||
| chr15:50931179 | C | A | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.869+208C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931179 | |||||||
| chr15:50931180 | A | T | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.869+209A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931180 | |||||||
| chr15:50931252 | C | G | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.869+281C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931252 | |||||||
| chr15:50931363 | T | G | 1 | a0001c0001t0004g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.869+392T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931363 | |||||||
| chr15:50931425 | G | A | 13 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0331 others(10): Show |
13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.869+454G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931425 | |||||||
| chr15:50931436 | C | T | 1 | a0005c0007t0011g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.869+465C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931436 | |||||||
| chr15:50931524 | C | T | 1 | a0002c0003t0010g0032 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.869+553C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931524 | |||||||
| chr15:50931560 | T | C | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG01993.hp1 HG02074.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+589T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931560 | |||||||
| chr15:50931732 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(276): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.869+761G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50931732 | |||||||
| chr15:50932072 | C | T | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.869+1101C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932072 | |||||||
| chr15:50932140 | C | T | 1 | a0002c0003t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.869+1169C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932140 | |||||||
| chr15:50932235 | T | C | 1 | a0002c0003t0003g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.869+1264T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932235 | |||||||
| chr15:50932268 | C | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.869+1297C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932268 | |||||||
| chr15:50932269 | G | A | 1 | a0001c0001t0004g0359 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.869+1298G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932269 | |||||||
| chr15:50932290 | T | C | 2 | a0001c0001t0003g0311 a0001c0001t0003g0312 |
2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.869+1319T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932290 | |||||||
| chr15:50932366 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.869+1395A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932366 | |||||||
| chr15:50932417 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0323 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+1446G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932417 | |||||||
| chr15:50932445 | A | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+1474A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932445 | |||||||
| chr15:50932472 | G | A | 5 | a0001c0001t0005g0302 a0001c0001t0005g0304 a0001c0001t0005g0305 others(2): Show |
5 | HG01496.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+1501G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932472 | |||||||
| chr15:50932484 | A | G | 1 | a0001c0001t0005g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869+1513A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932484 | |||||||
| chr15:50932699 | G | T | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.869+1728G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932699 | |||||||
| chr15:50932824 | A | G | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1800A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932824 | |||||||
| chr15:50932929 | C | T | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.870-1695C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932929 | |||||||
| chr15:50932950 | C | A | 4 | a0002c0003t0003g0148 a0002c0003t0003g0173 a0002c0003t0003g0176 others(1): Show |
4 | HG02027.hp2 NA18964.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-1674C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50932950 | |||||||
| chr15:50933219 | A | G | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.870-1405A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933219 | |||||||
| chr15:50933486 | T | C | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1138T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933486 | |||||||
| chr15:50933560 | A | G | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.870-1064A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933560 | |||||||
| chr15:50933571 | T | A | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.870-1053T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933571 | |||||||
| chr15:50933572 | T | G | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.870-1052T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933572 | |||||||
| chr15:50933573 | T | A | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-1051T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933573 | |||||||
| chr15:50933578 | T | G | 34 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0236 others(31): Show |
34 | HG00423.hp2 HG00621.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.870-1046T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933578 | |||||||
| chr15:50933628 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(196): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.870-996A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933628 | |||||||
| chr15:50933652 | G | A | 3 | a0004c0005t0001g0237 a0004c0005t0001g0238 a0004c0005t0001g0266 |
3 | NA18944.hp2 NA18962.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.870-972G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933652 | |||||||
| chr15:50933902 | A | G | 213 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0253 others(210): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.870-722A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50933902 | |||||||
| chr15:50934038 | T | C | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.870-586T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934038 | |||||||
| chr15:50934070 | TAC | T | 5 | a0001c0001t0001g0252 a0001c0001t0001g0264 a0001c0001t0001g0267 others(2): Show |
5 | HG01261.hp2 NA19001.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-553_870-552del others(2): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934070 | |||||||
| chr15:50934285 | A | G | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-339A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934285 | |||||||
| chr15:50934390 | G | A | 1 | a0002c0003t0003g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.870-234G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934390 | |||||||
| chr15:50934415 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.870-209G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 7/20 | chr15 | 50934415 | |||||||
| chr15:50935024 | C | T | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.943+327C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935024 | |||||||
| chr15:50935055 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935055 | |||||||
| chr15:50935276 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+579A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935276 | |||||||
| chr15:50935363 | A | AGAGACAA others(2075): Show |
1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943+682_943+683ins others(2082): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | ||||||
| chr15:50935363 | A | AGAGACAA others(2075): Show |
5 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+682_943+683ins others(2082): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | ||||||
| chr15:50935363 | A | AGAGACAA others(2076): Show |
1 | a0002c0003t0006g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.943+682_943+683ins others(2083): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50935363 | ||||||
| chr15:50935940 | T | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.943+1243T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50935940 | |||||||
| chr15:50936255 | A | C | 109 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(106): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.943+1558A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936255 | |||||||
| chr15:50936303 | G | A | 6 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+1606G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936303 | |||||||
| chr15:50936311 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.943+1614T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936311 | |||||||
| chr15:50936337 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.943+1640T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936337 | |||||||
| chr15:50936504 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG00609.hp2 NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.943+1807A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936504 | |||||||
| chr15:50936511 | C | G | 1 | a0001c0001t0004g0357 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943+1814C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936511 | |||||||
| chr15:50936636 | C | G | 1 | a0001c0001t0004g0365 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.943+1939C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936636 | |||||||
| chr15:50936739 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.943+2042A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936739 | |||||||
| chr15:50936896 | T | C | 1 | a0002c0002t0002g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.943+2199T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936896 | |||||||
| chr15:50936939 | CA | C | 25 | a0001c0001t0005g0301 a0001c0001t0005g0303 a0001c0001t0005g0304 others(22): Show |
25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.943+2254delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr15 | 50936939 | ||||||
| chr15:50936956 | T | A | 1 | a0002c0002t0012g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.943+2259T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936956 | |||||||
| chr15:50936980 | C | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.943+2283C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50936980 | |||||||
| chr15:50937284 | T | C | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.943+2587T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937284 | |||||||
| chr15:50937611 | G | A | 60 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.943+2914G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937611 | |||||||
| chr15:50937826 | G | C | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+3129G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937826 | |||||||
| chr15:50937919 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0001g0277 |
3 | HG01952.hp1 HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.943+3222G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50937919 | |||||||
| chr15:50938106 | A | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.944-3336A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938106 | |||||||
| chr15:50938358 | T | G | 230 | a0001c0001t0001g0258 a0001c0001t0003g0307 a0001c0001t0003g0309 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.944-3084T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938358 | |||||||
| chr15:50938577 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2865T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938577 | |||||||
| chr15:50938579 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2863T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938579 | |||||||
| chr15:50938582 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2860A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938582 | |||||||
| chr15:50938584 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2858T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938584 | |||||||
| chr15:50938585 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2857T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938585 | |||||||
| chr15:50938586 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2856T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938586 | |||||||
| chr15:50938589 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2853C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938589 | |||||||
| chr15:50938591 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2851A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938591 | |||||||
| chr15:50938592 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2850T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938592 | |||||||
| chr15:50938596 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2846G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938596 | |||||||
| chr15:50938598 | AGTAGGGA others(15): Show |
A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2843_944-2822d others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938598 | |||||||
| chr15:50938626 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2816T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938626 | |||||||
| chr15:50938632 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2810T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938632 | |||||||
| chr15:50938637 | A | C | 101 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.944-2805A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938637 | |||||||
| chr15:50938640 | G | T | 1 | a0001c0001t0004g0362 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944-2802G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938640 | |||||||
| chr15:50938643 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.944-2799C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938643 | |||||||
| chr15:50938644 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2798G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938644 | |||||||
| chr15:50938653 | G | GATCACCT others(8): Show |
1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2789_944-2788i others(17): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938653 | |||||||
| chr15:50938655 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2787T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938655 | |||||||
| chr15:50938659 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2783A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938659 | |||||||
| chr15:50938664 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2778A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938664 | |||||||
| chr15:50938672 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2770T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938672 | |||||||
| chr15:50938674 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2768G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938674 | |||||||
| chr15:50938677 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2765A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938677 | |||||||
| chr15:50938681 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2761A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938681 | |||||||
| chr15:50938682 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2760G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938682 | |||||||
| chr15:50938683 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2759A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938683 | |||||||
| chr15:50938687 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2755T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938687 | |||||||
| chr15:50938688 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2754C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938688 | |||||||
| chr15:50938689 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2753C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938689 | |||||||
| chr15:50938691 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2751C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938691 | |||||||
| chr15:50938693 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2749C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938693 | |||||||
| chr15:50938694 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2748C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938694 | |||||||
| chr15:50938695 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2747T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938695 | |||||||
| chr15:50938696 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2746G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938696 | |||||||
| chr15:50938699 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2743C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938699 | |||||||
| chr15:50938704 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2738A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938704 | |||||||
| chr15:50938705 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2737T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938705 | |||||||
| chr15:50938706 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2736A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938706 | |||||||
| chr15:50938707 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938707 | |||||||
| chr15:50938710 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2732A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938710 | |||||||
| chr15:50938711 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2731G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938711 | |||||||
| chr15:50938712 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.944-2730G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938712 | |||||||
| chr15:50938713 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2729C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938713 | |||||||
| chr15:50938714 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2728C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938714 | |||||||
| chr15:50938717 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2725T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938717 | |||||||
| chr15:50938719 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2723C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938719 | |||||||
| chr15:50938721 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2721T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938721 | |||||||
| chr15:50938722 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2720C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938722 | |||||||
| chr15:50938723 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2719A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938723 | |||||||
| chr15:50938728 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2714G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938728 | |||||||
| chr15:50938729 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2713T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938729 | |||||||
| chr15:50938734 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.944-2708G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938734 | |||||||
| chr15:50938768 | T | C | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.944-2674T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50938768 | |||||||
| chr15:50939195 | G | A | 1 | a0001c0001t0003g0327 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.944-2247G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939195 | |||||||
| chr15:50939337 | A | G | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.944-2105A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939337 | |||||||
| chr15:50939339 | G | A | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.944-2103G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939339 | |||||||
| chr15:50939351 | T | C | 190 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.944-2091T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939351 | |||||||
| chr15:50939416 | A | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-2026A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939416 | |||||||
| chr15:50939420 | C | T | 5 | a0002c0002t0002g0107 a0002c0002t0002g0108 a0002c0002t0002g0109 others(2): Show |
5 | HG02155.hp1 NA18941.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.944-2022C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939420 | |||||||
| chr15:50939659 | T | C | 2 | a0002c0002t0002g0080 a0002c0003t0003g0149 |
2 | HG01070.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.944-1783T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939659 | |||||||
| chr15:50939792 | A | G | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.944-1650A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939792 | |||||||
| chr15:50939854 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.944-1588G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939854 | |||||||
| chr15:50939939 | G | A | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.944-1503G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50939939 | |||||||
| chr15:50940005 | G | T | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-1437G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940005 | |||||||
| chr15:50940129 | T | C | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.944-1313T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940129 | |||||||
| chr15:50940359 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.944-1083T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940359 | |||||||
| chr15:50940947 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.944-495A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940947 | |||||||
| chr15:50940980 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.944-462C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50940980 | |||||||
| chr15:50941116 | T | C | 1 | a0002c0002t0002g0016 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.944-326T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50941116 | |||||||
| chr15:50941234 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0323 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-208A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 8/20 | chr15 | 50941234 | |||||||
| chr15:50941615 | T | C | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1066+51T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941615 | |||||||
| chr15:50941625 | T | C | 1 | a0002c0003t0003g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1067-41T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941625 | |||||||
| chr15:50941650 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1067-16G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 9/20 | chr15 | 50941650 | |||||||
| chr15:50941893 | T | C | 2 | a0002c0002t0002g0009 a0002c0002t0002g0091 |
2 | NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1176+118T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50941893 | |||||||
| chr15:50941981 | A | G | 190 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1176+206A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50941981 | |||||||
| chr15:50942012 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1176+237G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942012 | |||||||
| chr15:50942398 | A | G | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1176+623A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942398 | |||||||
| chr15:50942475 | T | A | 1 | a0002c0003t0003g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1176+700T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942475 | |||||||
| chr15:50942750 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1176+975A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50942750 | |||||||
| chr15:50943003 | T | C | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1176+1228T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943003 | |||||||
| chr15:50943012 | G | A | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1176+1237G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943012 | |||||||
| chr15:50943272 | A | G | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1176+1497A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943272 | |||||||
| chr15:50943638 | C | T | 3 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 |
3 | HG00140.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1176+1863C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943638 | |||||||
| chr15:50943835 | T | C | 3 | a0002c0002t0002g0049 a0002c0002t0002g0060 a0002c0002t0002g0121 |
3 | NA18980.hp2 NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1176+2060T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50943835 | |||||||
| chr15:50944107 | C | T | 216 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(213): Show |
217 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1176+2332C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944107 | |||||||
| chr15:50944155 | G | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1176+2380G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944155 | |||||||
| chr15:50944212 | A | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1176+2437A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944212 | |||||||
| chr15:50944223 | C | T | 1 | a0002c0003t0003g0164 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1176+2448C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944223 | |||||||
| chr15:50944318 | A | G | 1 | a0001c0001t0004g0365 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1176+2543A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944318 | |||||||
| chr15:50944511 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1176+2736A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944511 | |||||||
| chr15:50944562 | G | C | 1 | a0002c0003t0003g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1176+2787G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944562 | |||||||
| chr15:50944586 | TA | T | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1176+2823delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50944586 | ||||||
| chr15:50944640 | C | T | 109 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(106): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1176+2865C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944640 | |||||||
| chr15:50944641 | C | T | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1176+2866C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944641 | |||||||
| chr15:50944724 | C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1176+2949C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944724 | |||||||
| chr15:50944846 | G | T | 1 | a0001c0001t0004g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1176+3071G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944846 | |||||||
| chr15:50944974 | T | C | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1177-3046T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50944974 | |||||||
| chr15:50945007 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1177-3013G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945007 | |||||||
| chr15:50945013 | A | T | 1 | a0002c0002t0024g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1177-3007A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945013 | |||||||
| chr15:50945045 | G | T | 2 | a0002c0003t0003g0137 a0002c0003t0003g0138 |
2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1177-2975G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945045 | |||||||
| chr15:50945152 | T | C | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1177-2868T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945152 | |||||||
| chr15:50945285 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1177-2735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945285 | |||||||
| chr15:50945522 | C | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-2498C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945522 | |||||||
| chr15:50945660 | C | G | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-2360C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945660 | |||||||
| chr15:50945713 | T | C | 40 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1177-2307T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945713 | |||||||
| chr15:50945833 | C | T | 2 | a0002c0003t0003g0135 a0002c0003t0003g0162 |
2 | NA18978.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1177-2187C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945833 | |||||||
| chr15:50945863 | A | G | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-2157A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945863 | |||||||
| chr15:50945898 | G | A | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-2122G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945898 | |||||||
| chr15:50945978 | T | C | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1177-2042T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50945978 | |||||||
| chr15:50946028 | A | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1177-1992A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946028 | |||||||
| chr15:50946154 | A | C | 3 | a0002c0003t0006g0188 a0002c0003t0006g0189 a0002c0003t0006g0192 |
3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1177-1866A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946154 | |||||||
| chr15:50946285 | A | G | 2 | a0002c0002t0002g0014 a0002c0002t0002g0075 |
2 | NA18942.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1177-1735A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946285 | |||||||
| chr15:50946497 | T | C | 3 | a0001c0001t0003g0313 a0002c0006t0015g0347 a0002c0006t0015g0348 |
3 | HG01433.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1177-1523T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946497 | |||||||
| chr15:50946559 | C | T | 3 | a0001c0001t0004g0378 a0001c0001t0004g0379 a0001c0001t0004g0387 |
3 | HG02602.hp2 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1177-1461C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946559 | |||||||
| chr15:50946560 | G | A | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1177-1460G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946560 | |||||||
| chr15:50946563 | GA | G | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1177-1447delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50946563 | ||||||
| chr15:50946607 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-1413T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946607 | |||||||
| chr15:50946712 | A | G | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1177-1308A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946712 | |||||||
| chr15:50946758 | A | T | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-1262A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946758 | |||||||
| chr15:50946787 | G | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-1233G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946787 | |||||||
| chr15:50946882 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG00609.hp2 NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1177-1138C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946882 | |||||||
| chr15:50946894 | T | G | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-1126T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946894 | |||||||
| chr15:50946896 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1177-1124C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946896 | |||||||
| chr15:50946968 | C | T | 192 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1177-1052C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50946968 | |||||||
| chr15:50947107 | G | A | 4 | a0002c0002t0002g0107 a0002c0002t0002g0108 a0002c0002t0002g0109 others(1): Show |
4 | NA18941.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177-913G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947107 | |||||||
| chr15:50947151 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1177-869C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947151 | |||||||
| chr15:50947193 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-827A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947193 | |||||||
| chr15:50947323 | G | A | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1177-697G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947323 | |||||||
| chr15:50947415 | CA | C | 113 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0003g0307 others(110): Show |
113 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177-586delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50947415 | ||||||
| chr15:50947415 | CAA | C | 78 | a0002c0002t0002g0043 a0002c0002t0002g0074 a0002c0002t0002g0108 others(75): Show |
79 | HG00099.hp2 HG00408.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-587_1177-586d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr15 | 50947415 | ||||||
| chr15:50947494 | T | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177-526T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947494 | |||||||
| chr15:50947550 | C | G | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1177-470C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947550 | |||||||
| chr15:50947838 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1177-182C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50947838 | |||||||
| chr15:50948011 | T | C | 1 | a0002c0003t0020g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1177-9T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50948011 | |||||||
| chr15:50948016 | A | G | 1 | a0002c0002t0002g0054 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.1177-4A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 10/20 | chr15 | 50948016 | |||||||
| chr15:50948201 | ATGCAGTG others(4): Show |
A | 100 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1316+44_1316+54del others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948201 | ||||||
| chr15:50948249 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1316+90G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948249 | |||||||
| chr15:50948339 | C | CTTT | 9 | a0001c0001t0003g0307 a0001c0001t0003g0310 a0001c0001t0003g0311 others(6): Show |
9 | HG01516.hp1 HG02293.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316+196_1316+198d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | ||||||
| chr15:50948339 | CT | C | 163 | a0001c0001t0001g0256 a0002c0002t0002g0009 a0002c0002t0002g0010 others(160): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1316+198delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | ||||||
| chr15:50948339 | CTT | C | 17 | a0002c0002t0002g0015 a0002c0003t0003g0136 a0002c0003t0003g0170 others(14): Show |
17 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1316+197_1316+198d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | ||||||
| chr15:50948339 | CTTT | C | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+196_1316+198d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948339 | ||||||
| chr15:50948503 | G | A | 190 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1316+344G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948503 | |||||||
| chr15:50948597 | A | C | 1 | a0002c0002t0021g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316+438A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948597 | |||||||
| chr15:50948675 | A | G | 1 | a0002c0003t0003g0147 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1316+516A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948675 | |||||||
| chr15:50948723 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316+564A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948723 | |||||||
| chr15:50948823 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1316+664T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948823 | |||||||
| chr15:50948840 | C | T | 1 | a0002c0003t0003g0161 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1316+681C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948840 | |||||||
| chr15:50948894 | A | C | 230 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1316+735A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948894 | |||||||
| chr15:50948972 | CA | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0001t0005g0335 others(9): Show |
12 | HG01257.hp2 HG02145.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1316+829delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50948972 | ||||||
| chr15:50948986 | A | G | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+827A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50948986 | |||||||
| chr15:50949067 | T | C | 1 | a0002c0002t0002g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1317-759T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949067 | |||||||
| chr15:50949087 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1317-739C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949087 | |||||||
| chr15:50949412 | C | CA | 34 | a0001c0001t0001g0259 a0001c0001t0001g0295 a0001c0001t0001g0298 others(31): Show |
34 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1317-398dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr15 | 50949412 | ||||||
| chr15:50949429 | G | A | 1 | a0002c0003t0003g0028 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1317-397G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949429 | |||||||
| chr15:50949431 | A | G | 1 | a0002c0003t0003g0028 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1317-395A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949431 | |||||||
| chr15:50949447 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1317-379C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949447 | |||||||
| chr15:50949512 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-314A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949512 | |||||||
| chr15:50949531 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1317-295G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949531 | |||||||
| chr15:50949575 | T | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1317-251T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949575 | |||||||
| chr15:50949582 | G | C | 1 | a0002c0003t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1317-244G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949582 | |||||||
| chr15:50949714 | G | A | 5 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-112G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 11/20 | chr15 | 50949714 | |||||||
| chr15:50949949 | T | C | 3 | a0002c0002t0002g0049 a0002c0002t0002g0060 a0002c0002t0002g0121 |
3 | NA18980.hp2 NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1429+11T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 12/20 | chr15 | 50949949 | |||||||
| chr15:50950423 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+254C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950423 | |||||||
| chr15:50950428 | G | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+259G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950428 | |||||||
| chr15:50950463 | A | G | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+294A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950463 | |||||||
| chr15:50950585 | T | G | 99 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1548+416T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950585 | |||||||
| chr15:50950652 | A | T | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1548+483A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50950652 | |||||||
| chr15:50951064 | C | CA | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+897dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951064 | ||||||
| chr15:50951374 | G | A | 2 | a0002c0003t0003g0129 a0002c0003t0003g0152 |
2 | NA18947.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1548+1205G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951374 | |||||||
| chr15:50951726 | C | CT | 30 | a0001c0001t0001g0254 a0001c0001t0001g0300 a0001c0001t0005g0329 others(27): Show |
30 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1548+1575dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951726 | ||||||
| chr15:50951726 | C | CTT | 70 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(67): Show |
71 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1548+1574_1548+157 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50951726 | ||||||
| chr15:50951726 | C | T | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1548+1557C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951726 | |||||||
| chr15:50951767 | A | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1548+1598A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951767 | |||||||
| chr15:50951786 | G | A | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1548+1617G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951786 | |||||||
| chr15:50951792 | A | T | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1548+1623A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951792 | |||||||
| chr15:50951816 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1548+1647T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50951816 | |||||||
| chr15:50952077 | T | G | 1 | a0001c0001t0004g0388 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1548+1908T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952077 | |||||||
| chr15:50952098 | A | G | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548+1929A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952098 | |||||||
| chr15:50952180 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1548+2011A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952180 | |||||||
| chr15:50952220 | G | C | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1548+2051G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952220 | |||||||
| chr15:50952238 | C | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548+2069C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952238 | |||||||
| chr15:50952239 | G | A | 2 | a0002c0002t0002g0064 a0002c0002t0002g0065 |
2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1548+2070G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952239 | |||||||
| chr15:50952292 | C | T | 1 | a0002c0003t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1548+2123C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952292 | |||||||
| chr15:50952466 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+2297C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952466 | |||||||
| chr15:50952509 | CA | C | 8 | a0001c0001t0001g0249 a0001c0001t0001g0255 a0001c0001t0004g0369 others(5): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548+2357delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50952509 | ||||||
| chr15:50952624 | T | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0260 |
2 | NA18947.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1548+2455T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952624 | |||||||
| chr15:50952625 | C | G | 1 | a0001c0001t0004g0386 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1548+2456C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952625 | |||||||
| chr15:50952765 | C | CT | 230 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1548+2597dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50952765 | ||||||
| chr15:50952804 | G | A | 2 | a0002c0003t0006g0187 a0002c0003t0006g0190 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1548+2635G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50952804 | |||||||
| chr15:50953262 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1548+3093G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953262 | |||||||
| chr15:50953483 | T | C | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1548+3314T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953483 | |||||||
| chr15:50953654 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+3485C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953654 | |||||||
| chr15:50953678 | C | T | 1 | a0001c0001t0003g0328 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1548+3509C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50953678 | |||||||
| chr15:50954217 | AT | A | 110 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(107): Show |
110 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1548+4053delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50954217 | ||||||
| chr15:50954578 | G | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0051 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1549-3914G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954578 | |||||||
| chr15:50954767 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1549-3725C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954767 | |||||||
| chr15:50954840 | T | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-3652T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954840 | |||||||
| chr15:50954857 | A | G | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1549-3635A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954857 | |||||||
| chr15:50954914 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549-3578A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954914 | |||||||
| chr15:50954914 | A | T | 1 | a0001c0001t0005g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1549-3578A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954914 | |||||||
| chr15:50954939 | C | T | 3 | a0002c0002t0012g0111 a0002c0006t0015g0347 a0002c0006t0015g0348 |
3 | HG02257.hp1 HG03209.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1549-3553C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50954939 | |||||||
| chr15:50955630 | A | G | 1 | a0001c0001t0004g0362 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1549-2862A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955630 | |||||||
| chr15:50955731 | C | G | 1 | a0001c0001t0028g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1549-2761C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955731 | |||||||
| chr15:50955945 | C | T | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-2547C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955945 | |||||||
| chr15:50955997 | G | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1549-2495G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50955997 | |||||||
| chr15:50956024 | G | T | 1 | a0002c0002t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1549-2468G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956024 | |||||||
| chr15:50956025 | C | T | 1 | a0002c0002t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1549-2467C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956025 | |||||||
| chr15:50956061 | G | A | 7 | a0002c0003t0003g0148 a0002c0003t0003g0150 a0002c0003t0003g0153 others(4): Show |
7 | HG02027.hp2 NA18612.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1549-2431G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956061 | |||||||
| chr15:50956106 | T | C | 130 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(127): Show |
130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1549-2386T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956106 | |||||||
| chr15:50956120 | G | T | 12 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(9): Show |
12 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1549-2372G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956120 | |||||||
| chr15:50956473 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1549-2019T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956473 | |||||||
| chr15:50956500 | A | T | 1 | a0002c0002t0002g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1549-1992A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956500 | |||||||
| chr15:50956640 | C | G | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1549-1852C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956640 | |||||||
| chr15:50956877 | G | A | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1615G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956877 | |||||||
| chr15:50956931 | T | C | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1561T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956931 | |||||||
| chr15:50956964 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1549-1528C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956964 | |||||||
| chr15:50956967 | T | G | 39 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1549-1525T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956967 | |||||||
| chr15:50956986 | C | CAAAACTC others(320): Show |
1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1549-1491_1549-149 others(331): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50956986 | ||||||
| chr15:50956997 | A | G | 1 | a0002c0003t0003g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1549-1495A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956997 | |||||||
| chr15:50956998 | T | A | 1 | a0002c0003t0003g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1549-1494T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50956998 | |||||||
| chr15:50957049 | A | G | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1549-1443A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957049 | |||||||
| chr15:50957065 | T | G | 3 | a0001c0001t0001g0256 a0005c0007t0011g0184 a0005c0007t0011g0185 |
3 | HG01891.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1549-1427T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957065 | |||||||
| chr15:50957092 | C | T | 1 | a0009c0012t0001g0289 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1549-1400C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957092 | |||||||
| chr15:50957238 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1549-1254C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957238 | |||||||
| chr15:50957332 | C | A | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-1160C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957332 | |||||||
| chr15:50957362 | C | T | 2 | a0002c0002t0002g0059 a0002c0002t0002g0070 |
2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1549-1130C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957362 | |||||||
| chr15:50957504 | G | A | 1 | a0004c0005t0001g0237 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1549-988G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957504 | |||||||
| chr15:50957654 | G | T | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1549-838G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957654 | |||||||
| chr15:50957671 | C | CT | 33 | a0001c0001t0001g0221 a0001c0001t0001g0247 a0001c0001t0001g0248 others(30): Show |
33 | HG00621.hp2 HG01123.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.1549-798dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | ||||||
| chr15:50957671 | C | CTT | 13 | a0001c0001t0003g0307 a0001c0001t0005g0337 a0002c0003t0003g0028 others(10): Show |
13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1549-799_1549-798d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | ||||||
| chr15:50957671 | C | CTTT | 31 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0003g0312 others(28): Show |
31 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1549-800_1549-798d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | ||||||
| chr15:50957671 | CT | C | 6 | a0001c0001t0004g0359 a0002c0002t0002g0012 a0002c0002t0002g0105 others(3): Show |
6 | HG02280.hp1 HG02897.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549-798delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | ||||||
| chr15:50957671 | CTTTTTTT others(4): Show |
C | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1549-808_1549-798d others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr15 | 50957671 | ||||||
| chr15:50957677 | T | C | 2 | a0002c0002t0002g0010 a0002c0002t0002g0011 |
2 | NA18959.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1549-815T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957677 | |||||||
| chr15:50957700 | G | A | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1549-792G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957700 | |||||||
| chr15:50957822 | G | A | 2 | a0002c0002t0002g0072 a0002c0003t0003g0031 |
2 | NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1549-670G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957822 | |||||||
| chr15:50957827 | C | A | 1 | a0001c0001t0008g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1549-665C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957827 | |||||||
| chr15:50957940 | G | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1549-552G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50957940 | |||||||
| chr15:50958015 | G | C | 1 | a0002c0003t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1549-477G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958015 | |||||||
| chr15:50958048 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1549-444C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958048 | |||||||
| chr15:50958139 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1549-353G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958139 | |||||||
| chr15:50958200 | A | G | 2 | a0002c0003t0003g0128 a0002c0003t0003g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1549-292A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958200 | |||||||
| chr15:50958251 | A | G | 20 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(17): Show |
20 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549-241A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958251 | |||||||
| chr15:50958400 | C | T | 1 | a0002c0002t0002g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1549-92C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958400 | |||||||
| chr15:50958413 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1549-79G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 13/20 | chr15 | 50958413 | |||||||
| chr15:50958924 | C | G | 1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1851+130C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958924 | |||||||
| chr15:50958925 | T | G | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1851+131T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958925 | |||||||
| chr15:50958935 | A | G | 4 | a0001c0001t0008g0216 a0001c0001t0008g0217 a0001c0001t0008g0218 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+141A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958935 | |||||||
| chr15:50958972 | G | A | 98 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1851+178G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50958972 | |||||||
| chr15:50959115 | A | G | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1851+321A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959115 | |||||||
| chr15:50959152 | A | G | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959152 | |||||||
| chr15:50959242 | A | G | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+448A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959242 | |||||||
| chr15:50959296 | G | C | 6 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+502G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959296 | |||||||
| chr15:50959426 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1851+632T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959426 | |||||||
| chr15:50959676 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1851+882T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959676 | |||||||
| chr15:50959878 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1851+1084A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959878 | |||||||
| chr15:50959899 | A | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1851+1105A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50959899 | |||||||
| chr15:50960004 | GA | G | 100 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(97): Show |
100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1851+1218delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960004 | ||||||
| chr15:50960040 | A | G | 2 | a0002c0003t0006g0187 a0002c0003t0006g0190 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1851+1246A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960040 | |||||||
| chr15:50960157 | A | G | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1851+1363A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960157 | |||||||
| chr15:50960344 | A | G | 1 | a0001c0001t0003g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1851+1550A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960344 | |||||||
| chr15:50960408 | A | G | 1 | a0002c0002t0002g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1851+1614A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960408 | |||||||
| chr15:50960455 | T | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+1661T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960455 | |||||||
| chr15:50960467 | G | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1851+1673G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50960467 | |||||||
| chr15:50960488 | TA | T | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1851+1696delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960488 | ||||||
| chr15:50960819 | C | CA | 10 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0253 others(7): Show |
10 | HG01981.hp1 HG02293.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+2035dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50960819 | ||||||
| chr15:50961109 | A | G | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+2315A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961109 | |||||||
| chr15:50961222 | A | G | 11 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(8): Show |
11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851+2428A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961222 | |||||||
| chr15:50961314 | C | CTACAAGC others(81): Show |
5 | a0001c0001t0001g0222 a0001c0001t0001g0269 a0004c0005t0001g0237 others(2): Show |
5 | HG04115.hp2 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+2525_1851+261 others(92): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50961314 | ||||||
| chr15:50961729 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1851+2935A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961729 | |||||||
| chr15:50961876 | C | A | 11 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(8): Show |
11 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851+3082C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50961876 | |||||||
| chr15:50962017 | A | AAATAC | 99 | a0001c0001t0003g0313 a0001c0010t0002g0355 a0002c0002t0002g0009 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1851+3244_1851+324 others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | ||||||
| chr15:50962017 | A | AAATACAA others(3): Show |
20 | a0002c0002t0002g0015 a0002c0002t0002g0066 a0002c0002t0002g0085 others(17): Show |
20 | HG00621.hp2 HG01167.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1851+3239_1851+324 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | ||||||
| chr15:50962017 | A | AAATACAA others(8): Show |
11 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0006g0188 others(8): Show |
11 | HG01943.hp2 HG02004.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1851+3234_1851+324 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962017 | ||||||
| chr15:50962152 | A | G | 2 | a0001c0001t0005g0329 a0001c0001t0005g0332 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1851+3358A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962152 | |||||||
| chr15:50962209 | A | G | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1851+3415A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962209 | |||||||
| chr15:50962305 | A | G | 130 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(127): Show |
130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1851+3511A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962305 | |||||||
| chr15:50962446 | C | A | 7 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0067 others(4): Show |
7 | HG00544.hp2 HG00621.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1851+3652C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962446 | |||||||
| chr15:50962472 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1851+3678C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962472 | |||||||
| chr15:50962572 | C | T | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+3778C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962572 | |||||||
| chr15:50962722 | C | T | 1 | a0001c0001t0003g0328 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1851+3928C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962722 | |||||||
| chr15:50962822 | G | A | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1851+4028G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962822 | |||||||
| chr15:50962829 | G | A | 7 | a0001c0001t0003g0307 a0001c0001t0003g0310 a0001c0001t0003g0311 others(4): Show |
7 | HG01516.hp1 HG02293.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1851+4035G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962829 | |||||||
| chr15:50962834 | A | G | 2 | a0002c0003t0003g0140 a0002c0003t0003g0181 |
2 | NA18747.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1851+4040A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962834 | |||||||
| chr15:50962889 | C | CA | 57 | a0001c0001t0001g0195 a0001c0001t0001g0199 a0001c0001t0001g0205 others(54): Show |
57 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1851+4122dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAA | 10 | a0001c0001t0001g0255 a0001c0001t0003g0328 a0001c0001t0004g0352 others(7): Show |
10 | HG01891.hp1 HG02027.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+4121_1851+412 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAA | 28 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0004g0365 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1851+4120_1851+412 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0004g0367 others(8): Show |
12 | HG01891.hp2 HG02257.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1851+4119_1851+412 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0004g0350 a0001c0001t0004g0351 a0001c0001t0004g0356 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851+4113_1851+412 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1851+4112_1851+412 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0004g0353 a0001c0001t0005g0334 a0001c0001t0005g0341 |
3 | HG01109.hp1 HG02809.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1851+4109_1851+412 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(8): Show |
5 | a0001c0001t0004g0354 a0001c0001t0005g0305 a0001c0001t0005g0321 others(2): Show |
5 | HG01496.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851+4108_1851+412 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0005g0322 a0001c0001t0005g0329 a0001c0001t0005g0330 |
3 | HG02145.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1851+4107_1851+412 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0005g0304 a0001c0001t0005g0332 |
2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1851+4106_1851+412 others(21): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0004g0362 a0001c0001t0005g0335 a0001c0001t0005g0337 |
3 | HG01884.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1851+4105_1851+412 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0301 a0001c0001t0005g0336 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1851+4104_1851+412 others(23): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0004g0359 a0001c0001t0009g0319 a0001c0001t0009g0320 |
3 | HG02622.hp2 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1851+4102_1851+412 others(25): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0004g0358 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1851+4101_1851+412 others(26): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0005g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1851+4100_1851+412 others(27): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0004g0357 a0001c0001t0005g0339 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1851+4098_1851+412 others(29): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0009g0338 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1851+4096_1851+412 others(31): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0009g0318 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(36): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(37): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0004g0364 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1851+4122_1851+412 others(40): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CA | C | 34 | a0001c0001t0001g0286 a0001c0001t0003g0307 a0001c0001t0003g0310 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1851+4122delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CAA | C | 46 | a0002c0002t0002g0016 a0002c0003t0003g0126 a0002c0003t0003g0127 others(43): Show |
47 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1851+4121_1851+412 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CAAAA | C | 10 | a0002c0003t0003g0026 a0002c0003t0003g0027 a0002c0003t0003g0028 others(7): Show |
10 | HG00621.hp2 HG02004.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+4119_1851+412 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CAAAAAAA others(2): Show |
C | 6 | a0002c0003t0006g0187 a0002c0003t0006g0188 a0002c0003t0006g0189 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1851+4114_1851+412 others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CAAAAAAA others(3): Show |
C | 1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1851+4113_1851+412 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962889 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0252 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1851+4112_1851+412 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50962889 | ||||||
| chr15:50962917 | T | A | 1 | a0001c0001t0004g0353 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1851+4123T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50962917 | |||||||
| chr15:50963020 | C | T | 4 | a0002c0003t0003g0133 a0002c0003t0003g0143 a0002c0003t0003g0149 others(1): Show |
4 | HG00609.hp1 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+4226C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963020 | |||||||
| chr15:50963181 | CAG | C | 23 | a0001c0001t0005g0302 a0001c0001t0005g0303 a0001c0001t0005g0304 others(20): Show |
23 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1851+4392_1851+439 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50963181 | ||||||
| chr15:50963195 | A | T | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+4401A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963195 | |||||||
| chr15:50963284 | T | A | 1 | a0002c0002t0002g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1851+4490T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963284 | |||||||
| chr15:50963289 | G | T | 3 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0332 |
3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1851+4495G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963289 | |||||||
| chr15:50963555 | C | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-4708C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963555 | |||||||
| chr15:50963667 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1852-4596A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963667 | |||||||
| chr15:50963677 | G | A | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1852-4586G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963677 | |||||||
| chr15:50963815 | T | C | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-4448T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963815 | |||||||
| chr15:50963845 | C | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-4418C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963845 | |||||||
| chr15:50963904 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1852-4359A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963904 | |||||||
| chr15:50963907 | A | G | 1 | a0002c0002t0016g0073 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1852-4356A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963907 | |||||||
| chr15:50963919 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-4344G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963919 | |||||||
| chr15:50963947 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-4316A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963947 | |||||||
| chr15:50963974 | G | A | 10 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(7): Show |
10 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1852-4289G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50963974 | |||||||
| chr15:50964086 | A | G | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1852-4177A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964086 | |||||||
| chr15:50964144 | G | C | 3 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0332 |
3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1852-4119G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964144 | |||||||
| chr15:50964190 | A | C | 1 | a0002c0002t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1852-4073A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964190 | |||||||
| chr15:50964315 | G | A | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-3948G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964315 | |||||||
| chr15:50964505 | T | C | 1 | a0002c0002t0016g0116 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1852-3758T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964505 | |||||||
| chr15:50964612 | G | C | 12 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(9): Show |
12 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1852-3651G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964612 | |||||||
| chr15:50964623 | G | A | 3 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1852-3640G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964623 | |||||||
| chr15:50964687 | A | G | 2 | a0001c0001t0004g0366 a0001c0001t0004g0376 |
2 | HG01515.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1852-3576A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964687 | |||||||
| chr15:50964953 | T | A | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3310T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964953 | |||||||
| chr15:50964954 | A | C | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3309A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964954 | |||||||
| chr15:50964955 | C | CA | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-3308_1852-330 others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964955 | |||||||
| chr15:50964955 | C | CACACACA others(14): Show |
2 | a0002c0002t0017g0055 a0002c0003t0006g0186 |
2 | HG01167.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1852-3308_1852-330 others(25): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50964955 | |||||||
| chr15:50964955 | C | CCA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0197 a0001c0001t0001g0198 others(39): Show |
43 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1852-3272_1852-327 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACA | 64 | a0001c0001t0001g0196 a0001c0001t0001g0257 a0001c0001t0001g0269 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1852-3274_1852-327 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACA | 15 | a0001c0001t0001g0199 a0001c0001t0004g0354 a0001c0001t0004g0358 others(12): Show |
15 | HG01496.hp1 HG02055.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1852-3276_1852-327 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(1): Show |
21 | a0001c0001t0003g0342 a0001c0001t0004g0350 a0001c0001t0004g0351 others(18): Show |
21 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1852-3278_1852-327 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(3): Show |
12 | a0001c0001t0004g0349 a0001c0001t0004g0352 a0001c0001t0004g0357 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1852-3280_1852-327 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(5): Show |
26 | a0001c0001t0004g0359 a0001c0001t0004g0366 a0001c0001t0004g0367 others(23): Show |
26 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1852-3282_1852-327 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(7): Show |
35 | a0001c0001t0004g0365 a0001c0001t0004g0371 a0001c0001t0004g0373 others(32): Show |
35 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1852-3284_1852-327 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(9): Show |
36 | a0001c0001t0004g0368 a0001c0001t0004g0378 a0001c0001t0004g0379 others(33): Show |
36 | HG00438.hp1 HG00438.hp2 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.1852-3286_1852-327 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(11): Show |
16 | a0001c0001t0001g0286 a0002c0002t0002g0014 a0002c0002t0002g0040 others(13): Show |
16 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1852-3288_1852-327 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(13): Show |
10 | a0001c0001t0004g0377 a0002c0002t0002g0036 a0002c0002t0002g0044 others(7): Show |
10 | HG00639.hp2 HG00741.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1852-3290_1852-327 others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(15): Show |
3 | a0002c0002t0002g0051 a0002c0002t0002g0057 a0002c0003t0022g0007 |
3 | HG01074.hp1 HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1852-3292_1852-327 others(26): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCACACAC others(17): Show |
4 | a0002c0003t0006g0188 a0002c0003t0006g0189 a0003c0004t0018g0019 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-3294_1852-327 others(28): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCACACA others(26): Show |
1 | a0002c0003t0003g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(37): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCACAC others(13): Show |
1 | a0002c0003t0003g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(24): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCACAC others(19): Show |
3 | a0002c0003t0003g0031 a0002c0003t0010g0032 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(30): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCACAC others(23): Show |
3 | a0002c0003t0003g0028 a0002c0003t0003g0029 a0002c0003t0003g0030 |
3 | HG01943.hp2 HG02004.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(34): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCACAC others(25): Show |
3 | a0002c0003t0003g0027 a0002c0003t0010g0033 a0002c0003t0020g0008 |
3 | HG03710.hp1 HG06807.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1852-3307_1852-330 others(36): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCCCCC others(21): Show |
1 | a0002c0003t0014g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(32): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | C | CCCCCCCC others(22): Show |
1 | a0002c0003t0014g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1852-3307_1852-330 others(33): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | CCACACA | C | 4 | a0001c0001t0001g0277 a0001c0001t0001g0344 a0001c0001t0001g0345 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-3276_1852-327 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50964955 | CCACACAC others(7): Show |
C | 2 | a0001c0001t0009g0318 a0001c0001t0009g0338 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1852-3284_1852-327 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50964955 | ||||||
| chr15:50965007 | C | T | 13 | a0001c0001t0005g0321 a0001c0001t0005g0329 a0001c0001t0005g0330 others(10): Show |
13 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1852-3256C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965007 | |||||||
| chr15:50965020 | G | A | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1852-3243G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965020 | |||||||
| chr15:50965115 | T | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-3148T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965115 | |||||||
| chr15:50965121 | G | A | 9 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(6): Show |
9 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1852-3142G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965121 | |||||||
| chr15:50965134 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1852-3129C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965134 | |||||||
| chr15:50965221 | T | TGGC | 3 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1852-3041_1852-303 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50965221 | ||||||
| chr15:50965222 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1852-3041G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965222 | |||||||
| chr15:50965424 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1852-2839A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965424 | |||||||
| chr15:50965494 | C | T | 1 | a0001c0001t0019g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1852-2769C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965494 | |||||||
| chr15:50965593 | A | G | 63 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-2670A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965593 | |||||||
| chr15:50965770 | T | A | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-2493T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965770 | |||||||
| chr15:50965889 | T | C | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-2374T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965889 | |||||||
| chr15:50965948 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1852-2315C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965948 | |||||||
| chr15:50965996 | T | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1852-2267T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50965996 | |||||||
| chr15:50966066 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1852-2197C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966066 | |||||||
| chr15:50966118 | A | G | 64 | a0002c0002t0002g0085 a0002c0003t0003g0126 a0002c0003t0003g0127 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1852-2145A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966118 | |||||||
| chr15:50966196 | G | C | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-2067G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966196 | |||||||
| chr15:50966375 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0026g0294 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1852-1888G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966375 | |||||||
| chr15:50966415 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1852-1848T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966415 | |||||||
| chr15:50966457 | G | A | 2 | a0004c0005t0001g0237 a0004c0005t0001g0238 |
2 | NA18944.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1852-1806G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966457 | |||||||
| chr15:50966464 | C | G | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1852-1799C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966464 | |||||||
| chr15:50966466 | A | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1852-1797A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966466 | |||||||
| chr15:50966473 | C | T | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1852-1790C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966473 | |||||||
| chr15:50966531 | C | CT | 7 | a0001c0001t0001g0292 a0001c0001t0001g0343 a0001c0001t0004g0353 others(4): Show |
7 | HG00733.hp2 HG02738.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1710dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | ||||||
| chr15:50966531 | CT | C | 211 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0236 others(208): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1852-1710delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | ||||||
| chr15:50966531 | CTT | C | 8 | a0002c0002t0002g0070 a0002c0002t0002g0075 a0002c0002t0002g0099 others(5): Show |
8 | HG02922.hp2 NA18747.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1852-1711_1852-171 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr15 | 50966531 | ||||||
| chr15:50966685 | C | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-1578C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50966685 | |||||||
| chr15:50967149 | A | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-1114A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967149 | |||||||
| chr15:50967397 | C | T | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1852-866C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967397 | |||||||
| chr15:50967437 | C | T | 1 | a0002c0003t0003g0154 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1852-826C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967437 | |||||||
| chr15:50967555 | A | G | 2 | a0004c0005t0001g0237 a0004c0005t0001g0238 |
2 | NA18944.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1852-708A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967555 | |||||||
| chr15:50967580 | A | G | 1 | a0011c0009t0003g0145 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1852-683A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50967580 | |||||||
| chr15:50968196 | A | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1852-67A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 14/20 | chr15 | 50968196 | |||||||
| chr15:50968678 | T | A | 230 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1966+301T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968678 | |||||||
| chr15:50968827 | A | G | 1 | a0001c0001t0004g0359 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1966+450A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968827 | |||||||
| chr15:50968832 | G | T | 1 | a0001c0001t0027g0224 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1966+455G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968832 | |||||||
| chr15:50968851 | T | TC | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+475dupC | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50968851 | ||||||
| chr15:50968898 | G | A | 25 | a0001c0001t0001g0270 a0001c0001t0005g0301 a0001c0001t0005g0302 others(22): Show |
25 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1966+521G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50968898 | |||||||
| chr15:50969001 | T | C | 1 | a0001c0010t0002g0355 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1966+624T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969001 | |||||||
| chr15:50969032 | T | A | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+655T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969032 | |||||||
| chr15:50969111 | G | A | 1 | a0002c0003t0003g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1966+734G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969111 | |||||||
| chr15:50969232 | T | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+855T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969232 | |||||||
| chr15:50969246 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1966+869G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969246 | |||||||
| chr15:50969314 | G | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+937G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969314 | |||||||
| chr15:50969512 | A | AATTTT | 229 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1966+1136_1966+114 others(9): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50969512 | ||||||
| chr15:50969530 | A | G | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1966+1153A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969530 | |||||||
| chr15:50969660 | C | CT | 45 | a0001c0001t0001g0196 a0001c0001t0001g0296 a0001c0001t0004g0350 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1966+1300dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50969660 | ||||||
| chr15:50969759 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1382T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969759 | |||||||
| chr15:50969773 | C | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+1396C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969773 | |||||||
| chr15:50969801 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1424A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969801 | |||||||
| chr15:50969804 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1427G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969804 | |||||||
| chr15:50969807 | G | A | 1 | a0001c0001t0004g0381 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1966+1430G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969807 | |||||||
| chr15:50969807 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1430G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969807 | |||||||
| chr15:50969808 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1966+1431G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969808 | |||||||
| chr15:50969850 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966+1473A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969850 | |||||||
| chr15:50969861 | A | G | 198 | a0001c0001t0001g0292 a0001c0001t0004g0380 a0001c0001t0004g0381 others(195): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1966+1484A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969861 | |||||||
| chr15:50969910 | T | C | 2 | a0002c0003t0003g0136 a0002c0003t0003g0156 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1966+1533T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969910 | |||||||
| chr15:50969936 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1966+1559G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969936 | |||||||
| chr15:50969954 | C | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+1577C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50969954 | |||||||
| chr15:50970111 | G | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+1734G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970111 | |||||||
| chr15:50970171 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1966+1794T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970171 | |||||||
| chr15:50970215 | T | C | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1966+1838T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970215 | |||||||
| chr15:50970503 | C | G | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+2126C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970503 | |||||||
| chr15:50970550 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1966+2173G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970550 | |||||||
| chr15:50970566 | A | G | 5 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0298 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+2189A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970566 | |||||||
| chr15:50970576 | T | C | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+2199T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970576 | |||||||
| chr15:50970593 | G | T | 39 | a0001c0001t0004g0349 a0001c0001t0004g0350 a0001c0001t0004g0351 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1966+2216G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970593 | |||||||
| chr15:50970927 | CA | C | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1966+2551delA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970927 | |||||||
| chr15:50970998 | G | T | 1 | a0002c0003t0002g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1966+2621G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50970998 | |||||||
| chr15:50971108 | A | G | 1 | a0002c0003t0003g0164 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1966+2731A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971108 | |||||||
| chr15:50971299 | G | C | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+2922G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971299 | |||||||
| chr15:50971634 | T | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+3257T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971634 | |||||||
| chr15:50971712 | C | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+3335C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971712 | |||||||
| chr15:50971724 | G | A | 1 | a0001c0001t0005g0337 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1966+3347G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971724 | |||||||
| chr15:50971929 | C | A | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1966+3552C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971929 | |||||||
| chr15:50971950 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+3573T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971950 | |||||||
| chr15:50971967 | G | A | 110 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(107): Show |
110 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1966+3590G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50971967 | |||||||
| chr15:50972056 | C | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+3679C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972056 | |||||||
| chr15:50972086 | T | C | 1 | a0001c0001t0004g0349 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1966+3709T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972086 | |||||||
| chr15:50972198 | GTTTC | G | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1966+3841_1966+384 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50972198 | ||||||
| chr15:50972222 | T | C | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+3845T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972222 | |||||||
| chr15:50972267 | G | A | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1966+3890G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972267 | |||||||
| chr15:50972342 | G | T | 1 | a0001c0001t0004g0373 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1966+3965G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972342 | |||||||
| chr15:50972368 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1966+3991C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972368 | |||||||
| chr15:50972401 | G | A | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+4024G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972401 | |||||||
| chr15:50972463 | C | T | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+4086C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972463 | |||||||
| chr15:50972816 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+4439A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972816 | |||||||
| chr15:50972848 | A | T | 1 | a0002c0003t0003g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1966+4471A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972848 | |||||||
| chr15:50972942 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1966+4565A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972942 | |||||||
| chr15:50972949 | G | A | 1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1966+4572G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50972949 | |||||||
| chr15:50973042 | G | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1966+4665G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973042 | |||||||
| chr15:50973347 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0323 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1966+4970C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973347 | |||||||
| chr15:50973662 | C | T | 1 | a0002c0003t0003g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1966+5285C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973662 | |||||||
| chr15:50973696 | T | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1966+5319T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973696 | |||||||
| chr15:50973789 | A | G | 57 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0129 others(54): Show |
58 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1966+5412A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973789 | |||||||
| chr15:50973842 | G | A | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1966+5465G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973842 | |||||||
| chr15:50973914 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1966+5537T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50973914 | |||||||
| chr15:50974008 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
6 | NA18940.hp2 NA18941.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1966+5631T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974008 | |||||||
| chr15:50974020 | C | T | 3 | a0002c0003t0006g0188 a0002c0003t0006g0189 a0002c0003t0006g0192 |
3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1966+5643C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974020 | |||||||
| chr15:50974266 | A | AT | 46 | a0001c0001t0001g0195 a0001c0001t0001g0227 a0001c0001t0001g0232 others(43): Show |
46 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.1966+5907dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50974266 | ||||||
| chr15:50974266 | AT | A | 11 | a0001c0001t0001g0262 a0002c0003t0006g0186 a0002c0003t0006g0187 others(8): Show |
11 | HG01167.hp1 HG01167.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1966+5907delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50974266 | ||||||
| chr15:50974720 | G | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+6343G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974720 | |||||||
| chr15:50974776 | T | G | 1 | a0002c0002t0002g0095 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1966+6399T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974776 | |||||||
| chr15:50974850 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1966+6473T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974850 | |||||||
| chr15:50974940 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0210 others(10): Show |
14 | HG02148.hp2 HG02155.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.1966+6563T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50974940 | |||||||
| chr15:50975080 | C | T | 12 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(9): Show |
12 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1966+6703C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975080 | |||||||
| chr15:50975153 | C | T | 1 | a0002c0003t0003g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1966+6776C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975153 | |||||||
| chr15:50975164 | A | G | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1966+6787A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975164 | |||||||
| chr15:50975180 | T | C | 1 | a0002c0002t0002g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1966+6803T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975180 | |||||||
| chr15:50975200 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1966+6823G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975200 | |||||||
| chr15:50975227 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+6850G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975227 | |||||||
| chr15:50975253 | A | C | 3 | a0001c0001t0004g0349 a0001c0001t0004g0351 a0001c0001t0004g0352 |
3 | HG02976.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1966+6876A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975253 | |||||||
| chr15:50975383 | C | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1966+7006C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975383 | |||||||
| chr15:50975552 | CTG | C | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1966+7177_1966+717 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975552 | ||||||
| chr15:50975946 | A | G | 4 | a0002c0002t0002g0040 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG00735.hp2 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1966+7569A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975946 | |||||||
| chr15:50975956 | C | CAG | 9 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0236 others(6): Show |
9 | HG00639.hp2 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1966+7603_1966+760 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | ||||||
| chr15:50975956 | CAG | C | 177 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1966+7603_1966+760 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | ||||||
| chr15:50975956 | CAGAGAGA others(9): Show |
C | 1 | a0002c0002t0002g0043 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1966+7589_1966+760 others(20): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50975956 | ||||||
| chr15:50975970 | G | C | 3 | a0002c0003t0006g0188 a0002c0003t0006g0189 a0002c0003t0006g0192 |
3 | HG02109.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1966+7593G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50975970 | |||||||
| chr15:50976097 | C | CA | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1966+7728dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50976097 | ||||||
| chr15:50976234 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1967-7788A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976234 | |||||||
| chr15:50976255 | G | A | 20 | a0002c0003t0003g0127 a0002c0003t0003g0130 a0002c0003t0003g0133 others(17): Show |
21 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1967-7767G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976255 | |||||||
| chr15:50976538 | G | A | 1 | a0002c0002t0002g0012 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1967-7484G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976538 | |||||||
| chr15:50976791 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1967-7231A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976791 | |||||||
| chr15:50976792 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0004g0359 a0001c0001t0004g0362 others(1): Show |
4 | HG02280.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-7230A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50976792 | |||||||
| chr15:50977084 | T | C | 2 | a0001c0001t0004g0366 a0001c0001t0004g0376 |
2 | HG01515.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1967-6938T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977084 | |||||||
| chr15:50977107 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1967-6915G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977107 | |||||||
| chr15:50977185 | A | G | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1967-6837A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977185 | |||||||
| chr15:50977193 | G | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-6829G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977193 | |||||||
| chr15:50977201 | A | C | 1 | a0002c0002t0002g0037 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1967-6821A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977201 | |||||||
| chr15:50977278 | T | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-6744T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977278 | |||||||
| chr15:50977432 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1967-6590A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977432 | |||||||
| chr15:50977478 | C | A | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1967-6544C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977478 | |||||||
| chr15:50977497 | A | C | 1 | a0002c0003t0003g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1967-6525A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977497 | |||||||
| chr15:50977563 | T | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-6459T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50977563 | |||||||
| chr15:50977706 | G | GT | 12 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0200 others(9): Show |
12 | HG00639.hp1 HG01081.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1967-6296dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977706 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0307 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1967-6305_1967-629 others(14): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977706 | G | GTTTTTTT others(4): Show |
20 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0003g0312 others(17): Show |
20 | HG01123.hp2 HG01433.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1967-6306_1967-629 others(15): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977706 | G | GTTTTTTT others(5): Show |
11 | a0001c0001t0003g0310 a0001c0001t0003g0327 a0001c0001t0003g0328 others(8): Show |
11 | HG01109.hp1 HG01255.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1967-6307_1967-629 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977706 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0005g0302 a0001c0001t0005g0304 a0001c0001t0005g0305 |
3 | HG03139.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1967-6309_1967-629 others(18): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977706 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0005g0322 a0001c0001t0029g0306 |
2 | HG01496.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1967-6310_1967-629 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977706 | ||||||
| chr15:50977708 | T | TTTTTTTT others(1): Show |
64 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977708 | ||||||
| chr15:50977709 | T | TTTTTTTG | 10 | a0002c0002t0002g0053 a0002c0002t0002g0054 a0002c0002t0002g0110 others(7): Show |
10 | HG01167.hp1 HG02071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977709 | ||||||
| chr15:50977709 | T | TTTTTTTT others(1): Show |
6 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-6306_1967-630 others(12): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977709 | ||||||
| chr15:50977710 | T | TTTTTTG | 99 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1967-6307_1967-630 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977710 | ||||||
| chr15:50977710 | T | TTTTTTTG | 8 | a0002c0002t0002g0089 a0002c0003t0003g0025 a0002c0003t0003g0026 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967-6306_1967-630 others(11): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50977710 | ||||||
| chr15:50978030 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1967-5992C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978030 | |||||||
| chr15:50978168 | T | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5854T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978168 | |||||||
| chr15:50978209 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5813G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978209 | |||||||
| chr15:50978495 | T | C | 4 | a0001c0001t0005g0329 a0001c0001t0005g0330 a0001c0001t0005g0332 others(1): Show |
4 | HG01255.hp1 HG02055.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-5527T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978495 | |||||||
| chr15:50978685 | C | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-5337C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978685 | |||||||
| chr15:50978686 | C | G | 3 | a0002c0003t0010g0032 a0002c0003t0010g0033 a0002c0003t0010g0034 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967-5336C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978686 | |||||||
| chr15:50978866 | A | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1967-5156A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978866 | |||||||
| chr15:50978980 | G | A | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1967-5042G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50978980 | |||||||
| chr15:50979032 | G | C | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-4990G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979032 | |||||||
| chr15:50979059 | G | A | 1 | a0002c0002t0002g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1967-4963G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979059 | |||||||
| chr15:50979138 | GTA | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1967-4882_1967-488 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50979138 | ||||||
| chr15:50979226 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-4796A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979226 | |||||||
| chr15:50979381 | C | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1967-4641C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979381 | |||||||
| chr15:50979384 | G | A | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1967-4638G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979384 | |||||||
| chr15:50979611 | A | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-4411A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979611 | |||||||
| chr15:50979611 | A | G | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-4411A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979611 | |||||||
| chr15:50979857 | T | C | 1 | a0002c0002t0002g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1967-4165T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50979857 | |||||||
| chr15:50980043 | G | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-3979G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980043 | |||||||
| chr15:50980448 | G | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-3574G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980448 | |||||||
| chr15:50980476 | G | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-3546G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980476 | |||||||
| chr15:50980509 | T | A | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-3513T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980509 | |||||||
| chr15:50980634 | C | G | 1 | a0003c0004t0007g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1967-3388C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980634 | |||||||
| chr15:50980685 | T | C | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-3337T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980685 | |||||||
| chr15:50980792 | C | T | 1 | a0001c0001t0005g0331 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967-3230C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980792 | |||||||
| chr15:50980897 | A | G | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-3125A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980897 | |||||||
| chr15:50980979 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1967-3043G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50980979 | |||||||
| chr15:50981201 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1967-2821A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981201 | |||||||
| chr15:50981209 | G | A | 2 | a0002c0002t0021g0006 a0008c0008t0002g0005 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1967-2813G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981209 | |||||||
| chr15:50981486 | G | T | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1967-2536G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981486 | |||||||
| chr15:50981522 | A | T | 15 | a0001c0001t0001g0214 a0001c0001t0001g0234 a0001c0001t0001g0235 others(12): Show |
15 | HG00423.hp2 HG01261.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1967-2500A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981522 | |||||||
| chr15:50981915 | G | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-2107G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981915 | |||||||
| chr15:50981931 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967-2091C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50981931 | |||||||
| chr15:50982009 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967-2013C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982009 | |||||||
| chr15:50982086 | C | CA | 41 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0229 others(38): Show |
41 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1967-1913dupA | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | ||||||
| chr15:50982086 | C | CAA | 118 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0001t0005g0332 others(115): Show |
118 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1967-1914_1967-191 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | ||||||
| chr15:50982086 | C | CAAA | 59 | a0002c0002t0002g0046 a0002c0002t0002g0062 a0002c0002t0002g0082 others(56): Show |
60 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1967-1915_1967-191 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | ||||||
| chr15:50982086 | C | CAAAA | 10 | a0002c0003t0003g0142 a0002c0003t0003g0144 a0002c0003t0003g0152 others(7): Show |
10 | HG00735.hp1 HG01109.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1967-1916_1967-191 others(8): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982086 | ||||||
| chr15:50982140 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967-1882A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982140 | |||||||
| chr15:50982238 | T | G | 1 | a0002c0003t0003g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1967-1784T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982238 | |||||||
| chr15:50982251 | A | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1967-1771A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982251 | |||||||
| chr15:50982308 | C | T | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1967-1714C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982308 | |||||||
| chr15:50982309 | G | A | 1 | a0001c0001t0028g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1967-1713G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982309 | |||||||
| chr15:50982350 | G | A | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1967-1672G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982350 | |||||||
| chr15:50982693 | CATT | C | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1967-1322_1967-132 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr15 | 50982693 | ||||||
| chr15:50982853 | A | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-1169A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50982853 | |||||||
| chr15:50983100 | G | A | 1 | a0005c0007t0011g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1967-922G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983100 | |||||||
| chr15:50983188 | C | T | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1967-834C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983188 | |||||||
| chr15:50983280 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1967-742G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983280 | |||||||
| chr15:50983372 | C | G | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967-650C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983372 | |||||||
| chr15:50983469 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1967-553G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983469 | |||||||
| chr15:50983510 | A | G | 2 | a0002c0003t0003g0171 a0002c0003t0003g0172 |
2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1967-512A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983510 | |||||||
| chr15:50983526 | T | C | 1 | a0001c0001t0004g0380 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1967-496T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983526 | |||||||
| chr15:50983568 | G | C | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1967-454G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983568 | |||||||
| chr15:50983604 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1967-418A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983604 | |||||||
| chr15:50983632 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1967-390C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983632 | |||||||
| chr15:50983705 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1967-317C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983705 | |||||||
| chr15:50983895 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0261 |
2 | NA18967.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1967-127A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983895 | |||||||
| chr15:50983911 | T | A | 4 | a0001c0001t0004g0378 a0001c0001t0004g0379 a0001c0001t0004g0387 others(1): Show |
4 | HG02602.hp2 HG03669.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967-111T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983911 | |||||||
| chr15:50983919 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1967-103G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983919 | |||||||
| chr15:50983931 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1967-91A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 15/20 | chr15 | 50983931 | |||||||
| chr15:50984317 | T | A | 1 | a0002c0002t0002g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2090+172T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984317 | |||||||
| chr15:50984328 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2090+183T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984328 | |||||||
| chr15:50984521 | A | T | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2090+376A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984521 | |||||||
| chr15:50984577 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2090+432G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984577 | |||||||
| chr15:50984614 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+469G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984614 | |||||||
| chr15:50984769 | C | T | 1 | a0002c0002t0002g0072 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2090+624C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984769 | |||||||
| chr15:50984785 | T | A | 1 | a0002c0003t0022g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2090+640T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984785 | |||||||
| chr15:50984834 | T | G | 2 | a0001c0001t0004g0349 a0001c0001t0004g0352 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2090+689T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984834 | |||||||
| chr15:50984878 | A | G | 193 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2090+733A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984878 | |||||||
| chr15:50984881 | A | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+736A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984881 | |||||||
| chr15:50984983 | T | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+838T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50984983 | |||||||
| chr15:50985017 | G | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+872G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985017 | |||||||
| chr15:50985084 | G | T | 1 | a0002c0003t0003g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2090+939G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985084 | |||||||
| chr15:50985126 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2090+981A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985126 | |||||||
| chr15:50985159 | G | GT | 27 | a0001c0010t0002g0355 a0002c0002t0002g0010 a0002c0002t0002g0011 others(24): Show |
27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2090+1022dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50985159 | ||||||
| chr15:50985349 | A | T | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+1204A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985349 | |||||||
| chr15:50985392 | C | T | 1 | a0002c0003t0003g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2090+1247C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985392 | |||||||
| chr15:50985527 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+1382G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985527 | |||||||
| chr15:50985592 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2090+1447G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985592 | |||||||
| chr15:50985593 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2090+1448T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985593 | |||||||
| chr15:50985615 | G | A | 60 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2090+1470G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985615 | |||||||
| chr15:50985664 | G | A | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1519G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985664 | |||||||
| chr15:50985702 | T | C | 1 | a0002c0003t0003g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2090+1557T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985702 | |||||||
| chr15:50985741 | G | A | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1596G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985741 | |||||||
| chr15:50985742 | A | C | 2 | a0002c0003t0014g0017 a0002c0003t0014g0018 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2090+1597A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985742 | |||||||
| chr15:50985791 | C | T | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+1646C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50985791 | |||||||
| chr15:50986008 | G | C | 3 | a0002c0002t0002g0074 a0002c0002t0002g0082 a0002c0002t0002g0120 |
3 | HG00621.hp1 NA18965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2090+1863G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986008 | |||||||
| chr15:50986018 | G | A | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+1873G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986018 | |||||||
| chr15:50986075 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2090+1930T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986075 | |||||||
| chr15:50986191 | CT | C | 60 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2090+2048delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50986191 | ||||||
| chr15:50986216 | G | A | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2090+2071G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986216 | |||||||
| chr15:50986237 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+2092A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986237 | |||||||
| chr15:50986338 | C | T | 2 | a0002c0002t0002g0113 a0002c0002t0002g0119 |
2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2090+2193C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986338 | |||||||
| chr15:50986449 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0246 a0001c0001t0001g0297 |
3 | HG00408.hp1 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2090+2304A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986449 | |||||||
| chr15:50986452 | A | G | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2090+2307A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986452 | |||||||
| chr15:50986484 | C | G | 1 | a0001c0001t0004g0350 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2090+2339C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986484 | |||||||
| chr15:50986521 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2090+2376C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986521 | |||||||
| chr15:50986607 | C | T | 1 | a0001c0001t0004g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2090+2462C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986607 | |||||||
| chr15:50986608 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2090+2463G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986608 | |||||||
| chr15:50986621 | T | C | 2 | a0003c0004t0007g0021 a0003c0004t0007g0022 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2090+2476T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986621 | |||||||
| chr15:50986636 | C | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+2491C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986636 | |||||||
| chr15:50986855 | A | G | 1 | a0002c0003t0014g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2090+2710A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986855 | |||||||
| chr15:50986941 | A | C | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+2796A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50986941 | |||||||
| chr15:50987052 | C | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG00544.hp1 HG01069.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090+2907C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987052 | |||||||
| chr15:50987145 | G | A | 1 | a0002c0003t0002g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2090+3000G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987145 | |||||||
| chr15:50987190 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | NA19012.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2090+3045C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987190 | |||||||
| chr15:50987217 | C | A | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2090+3072C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987217 | |||||||
| chr15:50987402 | C | A | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2090+3257C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987402 | |||||||
| chr15:50987409 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2090+3264A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987409 | |||||||
| chr15:50987558 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0300 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2090+3413G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50987558 | |||||||
| chr15:50988066 | G | A | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2090+3921G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988066 | |||||||
| chr15:50988137 | T | A | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2090+3992T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988137 | |||||||
| chr15:50988224 | G | T | 1 | a0002c0002t0002g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2090+4079G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988224 | |||||||
| chr15:50988385 | A | G | 230 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.2090+4240A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988385 | |||||||
| chr15:50988403 | CT | C | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2090+4260delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988403 | ||||||
| chr15:50988407 | TGG | T | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2090+4264_2090+426 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988407 | ||||||
| chr15:50988427 | G | T | 1 | a0001c0001t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2090+4282G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988427 | |||||||
| chr15:50988507 | G | A | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2090+4362G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988507 | |||||||
| chr15:50988532 | C | T | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2090+4387C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988532 | |||||||
| chr15:50988733 | C | CT | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090+4589dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50988733 | ||||||
| chr15:50988735 | A | G | 1 | a0002c0002t0002g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2090+4590A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988735 | |||||||
| chr15:50988782 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0209 others(41): Show |
45 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2091-4588T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50988782 | |||||||
| chr15:50989004 | G | A | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2091-4366G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989004 | |||||||
| chr15:50989034 | G | A | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2091-4336G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989034 | |||||||
| chr15:50989409 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2091-3961G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989409 | |||||||
| chr15:50989426 | G | T | 61 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(58): Show |
62 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2091-3944G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989426 | |||||||
| chr15:50989487 | CT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0323 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091-3871delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50989487 | ||||||
| chr15:50989635 | G | C | 1 | a0002c0002t0002g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2091-3735G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989635 | |||||||
| chr15:50989743 | G | A | 1 | a0006c0013t0005g0333 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2091-3627G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989743 | |||||||
| chr15:50989746 | G | T | 2 | a0002c0003t0003g0136 a0002c0003t0003g0156 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2091-3624G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989746 | |||||||
| chr15:50989826 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2091-3544T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989826 | |||||||
| chr15:50989830 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2091-3540A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989830 | |||||||
| chr15:50989896 | G | T | 4 | a0001c0001t0009g0318 a0001c0001t0009g0319 a0001c0001t0009g0320 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091-3474G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989896 | |||||||
| chr15:50989926 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2091-3444G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50989926 | |||||||
| chr15:50990016 | G | A | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2091-3354G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990016 | |||||||
| chr15:50990114 | T | C | 1 | a0002c0003t0006g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2091-3256T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990114 | |||||||
| chr15:50990174 | G | A | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2091-3196G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990174 | |||||||
| chr15:50990316 | A | G | 1 | a0002c0002t0002g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2091-3054A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990316 | |||||||
| chr15:50990344 | T | TTTA | 21 | a0001c0001t0001g0204 a0001c0001t0001g0222 a0001c0001t0001g0233 others(18): Show |
21 | HG00609.hp2 HG01167.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2091-2996_2091-299 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | T | TTTATTA | 30 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(27): Show |
30 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2091-2999_2091-299 others(10): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | T | TTTATTAT others(2): Show |
70 | a0001c0001t0001g0279 a0001c0001t0005g0301 a0001c0001t0005g0303 others(67): Show |
71 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.2091-3002_2091-299 others(13): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | T | TTTATTAT others(5): Show |
36 | a0001c0001t0005g0302 a0001c0001t0005g0304 a0001c0001t0009g0318 others(33): Show |
36 | HG00438.hp2 HG01175.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.2091-3005_2091-299 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | T | TTTATTAT others(8): Show |
76 | a0001c0001t0005g0305 a0001c0001t0005g0322 a0001c0001t0009g0319 others(73): Show |
76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2091-3008_2091-299 others(19): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | T | TTTATTAT others(11): Show |
4 | a0002c0002t0002g0050 a0002c0002t0002g0089 a0002c0003t0002g0123 others(1): Show |
4 | HG02080.hp1 HG02615.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-3011_2091-299 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990344 | TTTA | T | 5 | a0002c0003t0003g0031 a0002c0003t0022g0007 a0002c0006t0015g0347 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2091-2996_2091-299 others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990344 | ||||||
| chr15:50990360 | T | TTATTATT others(5): Show |
1 | a0008c0008t0002g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2091-2999_2091-299 others(16): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990360 | ||||||
| chr15:50990628 | C | T | 1 | a0001c0001t0003g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2091-2742C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990628 | |||||||
| chr15:50990635 | CTCAGCGT others(20): Show |
C | 3 | a0002c0002t0002g0014 a0002c0002t0002g0053 a0002c0002t0002g0075 |
3 | NA18942.hp2 NA18946.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2091-2733_2091-270 others(31): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50990635 | ||||||
| chr15:50990641 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2091-2729G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990641 | |||||||
| chr15:50990678 | G | A | 9 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0232 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2091-2692G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990678 | |||||||
| chr15:50990737 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2091-2633G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50990737 | |||||||
| chr15:50991319 | T | C | 2 | a0002c0006t0015g0347 a0002c0006t0015g0348 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2091-2051T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991319 | |||||||
| chr15:50991369 | A | C | 37 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(34): Show |
37 | HG01109.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.2091-2001A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991369 | |||||||
| chr15:50991891 | A | AT | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091-1473dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991891 | ||||||
| chr15:50991923 | G | A | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2091-1447G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50991923 | |||||||
| chr15:50991962 | CT | C | 93 | a0001c0001t0001g0236 a0001c0001t0004g0354 a0001c0001t0004g0359 others(90): Show |
94 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2091-1390delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991962 | ||||||
| chr15:50991962 | CTT | C | 6 | a0002c0003t0003g0153 a0002c0003t0003g0183 a0002c0003t0022g0007 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091-1391_2091-139 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr15 | 50991962 | ||||||
| chr15:50992009 | C | T | 24 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(21): Show |
24 | HG01109.hp1 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2091-1361C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992009 | |||||||
| chr15:50992098 | G | A | 1 | a0002c0003t0003g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2091-1272G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992098 | |||||||
| chr15:50992108 | T | A | 1 | a0002c0002t0002g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2091-1262T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992108 | |||||||
| chr15:50992213 | A | G | 1 | a0002c0002t0016g0116 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2091-1157A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992213 | |||||||
| chr15:50992483 | G | A | 81 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(78): Show |
82 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2091-887G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992483 | |||||||
| chr15:50992503 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2091-867T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992503 | |||||||
| chr15:50992930 | T | A | 191 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2091-440T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 16/20 | chr15 | 50992930 | |||||||
| chr15:50993838 | G | C | 1 | a0001c0001t0001g0252 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2346+213G>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993838 | |||||||
| chr15:50993896 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2346+271A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993896 | |||||||
| chr15:50993929 | C | T | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2346+304C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993929 | |||||||
| chr15:50993967 | C | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2346+342C>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50993967 | |||||||
| chr15:50994339 | A | G | 1 | a0002c0002t0002g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2346+714A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994339 | |||||||
| chr15:50994379 | C | T | 75 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(72): Show |
76 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.2346+754C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994379 | |||||||
| chr15:50994858 | G | A | 14 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(11): Show |
14 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2346+1233G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994858 | |||||||
| chr15:50994886 | G | A | 217 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(214): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2346+1261G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50994886 | |||||||
| chr15:50995358 | C | T | 6 | a0001c0001t0001g0221 a0001c0001t0008g0216 a0001c0001t0008g0217 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2346+1733C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995358 | |||||||
| chr15:50995362 | G | T | 2 | a0001c0001t0004g0367 a0001c0001t0004g0368 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2346+1737G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995362 | |||||||
| chr15:50995399 | C | CT | 109 | a0001c0001t0001g0195 a0001c0001t0005g0331 a0001c0010t0002g0355 others(106): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2346+1790dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995399 | ||||||
| chr15:50995399 | C | CTT | 7 | a0002c0002t0024g0047 a0002c0003t0003g0026 a0002c0003t0003g0027 others(4): Show |
7 | HG00621.hp2 HG01943.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2346+1789_2346+179 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995399 | ||||||
| chr15:50995483 | C | T | 1 | a0002c0003t0003g0146 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2347-1843C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995483 | |||||||
| chr15:50995651 | G | T | 3 | a0002c0003t0001g0076 a0002c0003t0001g0078 a0002c0003t0001g0079 |
3 | HG00438.hp1 HG01358.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2347-1675G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995651 | |||||||
| chr15:50995672 | C | T | 8 | a0002c0002t0002g0106 a0002c0003t0006g0186 a0002c0003t0006g0187 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2347-1654C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995672 | |||||||
| chr15:50995719 | A | G | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1607A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995719 | |||||||
| chr15:50995883 | A | G | 1 | a0002c0002t0002g0053 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2347-1443A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50995883 | |||||||
| chr15:50995980 | C | CT | 32 | a0001c0001t0001g0002 a0001c0001t0001g0196 a0001c0001t0001g0225 others(29): Show |
33 | HG00544.hp1 HG01243.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.2347-1320dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | ||||||
| chr15:50995980 | CT | C | 84 | a0001c0001t0001g0261 a0001c0001t0003g0311 a0001c0001t0004g0350 others(81): Show |
85 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2347-1320delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | ||||||
| chr15:50995980 | CTT | C | 19 | a0001c0001t0005g0336 a0002c0002t0002g0074 a0002c0003t0003g0025 others(16): Show |
19 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2347-1321_2347-132 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | ||||||
| chr15:50995980 | CTTTTTTT others(11): Show |
C | 1 | a0002c0003t0003g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2347-1337_2347-132 others(22): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50995980 | ||||||
| chr15:50996069 | A | G | 6 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2347-1257A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996069 | |||||||
| chr15:50996092 | A | G | 1 | a0002c0003t0003g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2347-1234A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996092 | |||||||
| chr15:50996113 | C | G | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2347-1213C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996113 | |||||||
| chr15:50996113 | C | T | 1 | a0002c0003t0003g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2347-1213C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996113 | |||||||
| chr15:50996155 | A | AT | 60 | a0001c0001t0001g0227 a0001c0001t0001g0271 a0001c0001t0001g0281 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2347-1150dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | ||||||
| chr15:50996155 | AT | A | 124 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0311 others(121): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2347-1150delT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | ||||||
| chr15:50996155 | ATT | A | 37 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(34): Show |
37 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.2347-1151_2347-115 others(6): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr15 | 50996155 | ||||||
| chr15:50996350 | G | A | 1 | a0002c0002t0002g0070 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2347-976G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996350 | |||||||
| chr15:50996352 | T | C | 2 | a0003c0004t0007g0021 a0003c0004t0007g0022 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2347-974T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996352 | |||||||
| chr15:50996370 | G | A | 1 | a0002c0002t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2347-956G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996370 | |||||||
| chr15:50996454 | G | A | 188 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(185): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2347-872G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996454 | |||||||
| chr15:50996571 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2347-755A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996571 | |||||||
| chr15:50996577 | T | C | 3 | a0002c0002t0002g0110 a0002c0002t0002g0113 a0002c0002t0002g0119 |
3 | HG02071.hp2 NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2347-749T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996577 | |||||||
| chr15:50996594 | C | G | 3 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 |
3 | HG00140.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2347-732C>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996594 | |||||||
| chr15:50996595 | C | T | 40 | a0001c0001t0004g0207 a0001c0001t0004g0349 a0001c0001t0004g0350 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2347-731C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996595 | |||||||
| chr15:50996959 | A | G | 1 | a0001c0001t0004g0357 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2347-367A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50996959 | |||||||
| chr15:50997145 | T | C | 3 | a0003c0004t0007g0021 a0003c0004t0007g0022 a0003c0004t0007g0023 |
3 | HG02922.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2347-181T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997145 | |||||||
| chr15:50997198 | T | C | 101 | a0001c0010t0002g0355 a0002c0002t0002g0009 a0002c0002t0002g0010 others(98): Show |
101 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2347-128T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997198 | |||||||
| chr15:50997201 | T | G | 1 | a0002c0002t0002g0119 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2347-125T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 17/20 | chr15 | 50997201 | |||||||
| chr15:50997959 | T | A | 2 | a0002c0003t0003g0137 a0002c0003t0003g0138 |
2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2904+76T>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50997959 | |||||||
| chr15:50998193 | TTGG | T | 201 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(198): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.2904+314_2904+316d others(5): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr15 | 50998193 | ||||||
| chr15:50998371 | C | T | 1 | a0001c0001t0004g0374 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2904+488C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998371 | |||||||
| chr15:50998503 | A | G | 1 | a0001c0001t0005g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2905-569A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998503 | |||||||
| chr15:50998599 | T | C | 227 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(224): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.2905-473T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998599 | |||||||
| chr15:50998638 | AG | A | 8 | a0002c0003t0003g0025 a0002c0003t0003g0026 a0002c0003t0003g0027 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2905-433delG | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998638 | |||||||
| chr15:50998780 | A | G | 2 | a0005c0007t0011g0184 a0005c0007t0011g0185 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2905-292A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998780 | |||||||
| chr15:50998859 | A | C | 62 | a0002c0003t0003g0126 a0002c0003t0003g0127 a0002c0003t0003g0128 others(59): Show |
63 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2905-213A>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998859 | |||||||
| chr15:50998997 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2905-75T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50998997 | |||||||
| chr15:50999064 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2905-8A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 18/20 | chr15 | 50999064 | |||||||
| chr15:50999379 | G | A | 201 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(198): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.3095+117G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999379 | |||||||
| chr15:50999401 | A | T | 1 | a0002c0002t0002g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3095+139A>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999401 | |||||||
| chr15:50999423 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3095+161A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999423 | |||||||
| chr15:50999703 | CTTTTT | C | 10 | a0001c0001t0001g0222 a0001c0001t0001g0236 a0001c0001t0001g0265 others(7): Show |
10 | HG01257.hp2 HG03834.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.3095+445_3095+449d others(7): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 50999703 | ||||||
| chr15:50999904 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3095+642T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 50999904 | |||||||
| chr15:51000141 | C | CT | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(333): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.3096-865dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000141 | ||||||
| chr15:51000141 | C | CTT | 26 | a0001c0001t0001g0195 a0001c0001t0001g0229 a0001c0001t0001g0277 others(23): Show |
26 | HG01081.hp1 HG01123.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.3096-866_3096-865d others(4): Show |
AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000141 | ||||||
| chr15:51000306 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3096-720A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 51000306 | |||||||
| chr15:51000658 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3096-368C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | chr15 | 51000658 | |||||||
| chr15:51000967 | G | GT | 227 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(224): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.3096-57dupT | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr15 | 51000967 | ||||||
| chr15:51001371 | T | G | 1 | a0001c0001t0004g0380 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3253+188T>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001371 | |||||||
| chr15:51001447 | A | G | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3253+264A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001447 | |||||||
| chr15:51001531 | C | T | 1 | a0002c0003t0003g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3253+348C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001531 | |||||||
| chr15:51001752 | T | C | 4 | a0002c0003t0003g0130 a0002c0003t0003g0141 a0002c0003t0003g0142 others(1): Show |
4 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.3253+569T>C | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001752 | |||||||
| chr15:51001966 | C | T | 5 | a0003c0004t0007g0021 a0003c0004t0007g0023 a0003c0004t0007g0024 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3254-536C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51001966 | |||||||
| chr15:51002004 | G | A | 7 | a0002c0003t0006g0186 a0002c0003t0006g0187 a0002c0003t0006g0188 others(4): Show |
7 | HG01167.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3254-498G>A | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002004 | |||||||
| chr15:51002004 | G | T | 1 | a0002c0003t0003g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-498G>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002004 | |||||||
| chr15:51002250 | C | T | 1 | a0002c0003t0003g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-252C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002250 | |||||||
| chr15:51002274 | C | T | 1 | a0002c0003t0003g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3254-228C>T | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002274 | |||||||
| chr15:51002300 | A | G | 88 | a0001c0001t0003g0307 a0001c0001t0003g0309 a0001c0001t0003g0310 others(85): Show |
89 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3254-202A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002300 | |||||||
| chr15:51002367 | A | G | 2 | a0002c0003t0006g0187 a0002c0003t0006g0190 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3254-135A>G | AP4E1 | ENSG00000081014.11 | transcript | ENST00000261842.10 | protein_coding | 20/20 | chr15 | 51002367 |