Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 163 |
| ensemblid | ENSG00000006125.18 |
| hgncid | 563 |
| symbol | AP2B1 |
| name | adaptor related protein complex 2 subunit beta 1 |
| refseq_nuc | NM_001030006.2 |
| refseq_prot | NP_001025177.1 |
| ensembl_nuc | ENST00000610402.5 |
| ensembl_prot | ENSP00000483185.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 35587322 |
| end | 35726413 |
| strand | + |
| ver | v1.2 |
| region | chr17:35587322-35726413 |
| region5000 | chr17:35582322-35731413 |
| regionname0 | AP2B1_chr17_35587322_35726413 |
| regionname5000 | AP2B1_chr17_35582322_35731413 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 951 | 371 | 86 | 64 | 171 | 14 | 34 | 135 | AP2B1_chr17_35582322_35731413 | AP2B1 | MTDSK others(946): Show |
chr17 | 35582322 | 35731413 |
| a0002 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | MTDSK others(946): Show |
chr17 | 35582322 | 35731413 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2853 | 219 | 40 | 39 | 104 | 10 | 24 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0002 | 0/0 | 2853 | 128 | 40 | 21 | 55 | 2 | 10 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0003 | 0/0 | 2853 | 12 | 0 | 0 | 12 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0004 | 0/0 | 2853 | 9 | 3 | 4 | 0 | 2 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0005 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0006 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0001c0008 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 | ||
| a0002c0007 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | ATGAC others(2848): Show |
chr17 | 35582322 | 35731413 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5700 | 4 | 1 | 2 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0002 | 0/0 | 5700 | 72 | 19 | 9 | 34 | 2 | 8 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0003 | 0/0 | 5700 | 44 | 1 | 2 | 36 | 1 | 4 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0004 | 0/0 | 5700 | 36 | 2 | 5 | 26 | 1 | 2 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0005 | 0/1 | 5700 | 26 | 0 | 8 | 4 | 4 | 9 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0006 | 0/0 | 5700 | 13 | 2 | 10 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0007 | 0/0 | 5700 | 7 | 4 | 3 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0008 | 0/0 | 5700 | 6 | 6 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0009 | 0/0 | 5700 | 4 | 4 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0015 | 0/0 | 5700 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0016 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0017 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0018 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0019 | 0/0 | 5700 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0020 | 0/0 | 5700 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0001t0021 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0001 | 0/0 | 5700 | 119 | 37 | 21 | 50 | 2 | 9 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0002 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0010 | 0/0 | 5700 | 3 | 3 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0011 | 0/0 | 5700 | 2 | 0 | 0 | 2 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0012 | 0/0 | 5700 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0013 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0002t0014 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0003t0001 | 0/0 | 5700 | 12 | 0 | 0 | 12 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0004t0002 | 0/0 | 5700 | 9 | 3 | 4 | 0 | 2 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0005t0002 | 0/0 | 5700 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0006t0004 | 0/0 | 5700 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0001c0008t0002 | 0/0 | 5700 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| a0002c0007t0003 | 0/0 | 5700 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | AGACC others(5695): Show |
chr17 | 35582322 | 35731413 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0001g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0017g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0020g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0001t0021g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0012g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0013g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0002t0014g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0005t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0006t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0001c0008t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| a0002c0007t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0351 | EUR | GBR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0154 | EUR | GBR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | GBR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0136 | EUR | GBR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00280 | hp1 | a0001 | c0001 | t0020 | g0151 | EUR | FIN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | FIN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0093 | EUR | FIN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | FIN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00673 | hp1 | a0001 | c0001 | t0017 | g0027 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | CHS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0338 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0361 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0363 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0354 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0315 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0183 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0163 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0365 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01099 | hp2 | a0001 | c0004 | t0002 | g0166 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0346 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0366 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0348 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0182 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0167 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0077 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0343 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01515 | hp1 | a0001 | c0004 | t0002 | g0164 | EUR | IBS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0152 | EUR | IBS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0246 | EUR | IBS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0176 | EUR | IBS | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01891 | hp1 | a0001 | c0005 | t0002 | g0118 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0074 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0340 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0144 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0071 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0073 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0341 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0069 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0121 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02055 | hp2 | a0001 | c0008 | t0002 | g0124 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0300 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CDX | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | CDX | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | CDX | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | CDX | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0362 | AMR | PEL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0347 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0155 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0135 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0316 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0160 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0125 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0131 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0339 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0364 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0127 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02886 | hp2 | a0001 | c0002 | t0010 | g0253 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0357 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02965 | hp2 | a0001 | c0002 | t0010 | g0240 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0060 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0138 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0126 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0058 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0355 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0359 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0287 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0061 | AFR | ESN | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | GWD | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03579 | hp2 | a0001 | c0002 | t0010 | g0254 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0064 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0150 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0133 | SAS | STU | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | STU | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03704 | hp2 | a0001 | c0002 | t0012 | g0217 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0137 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0153 | SAS | BEB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | STU | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | STU | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0367 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | CHB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18942 | hp2 | a0001 | c0002 | t0011 | g0236 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18943 | hp1 | a0001 | c0002 | t0014 | g0284 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0302 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18971 | hp1 | a0001 | c0001 | t0021 | g0139 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19002 | hp1 | a0001 | c0002 | t0013 | g0216 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0307 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19056 | hp2 | a0001 | c0001 | t0016 | g0054 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19066 | hp2 | a0001 | c0001 | t0018 | g0083 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19068 | hp2 | a0002 | c0007 | t0003 | g0041 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19081 | hp2 | a0001 | c0002 | t0011 | g0190 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0301 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0295 | AFR | YRI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | ASW | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0349 | AFR | ASW | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0224 | EUR | TSI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0146 | EUR | TSI | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0089 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0165 | AMR | CLM | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA21309 | hp1 | a0001 | c0006 | t0004 | g0063 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | LWK | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0140 | REF | REF | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0317 | REF | REF | AP2B1_chr17_35582322_35731413 | AP2B1 | chr17 | 35582322 | 35731413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:35709304 | A | T | 1 | a0002 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2535A>T | p.Lys845Asn | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/22 | 2665/5700 | 2535/2856 | 845/951 | chr17 | 35709304 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:35627454 | A | G | 1 | a0001c0008 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1008A>G | p.Leu336Leu | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 8/22 | 1138/5700 | 1008/2856 | 336/951 | chr17 | 35627454 | |||
| chr17:35636421 | T | C | 1 | a0001c0005 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1236T>C | p.Val412Val | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/22 | 1366/5700 | 1236/2856 | 412/951 | chr17 | 35636421 | |||
| chr17:35639610 | C | T | 1 | a0001c0003 | 12 | HG02040.hp1 HG02071.hp2 NA18960.hp1 others(9): Show |
synonymous_variant | LOW | c.1287C>T | p.Ile429Ile | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/22 | 1417/5700 | 1287/2856 | 429/951 | chr17 | 35639610 | |||
| chr17:35639637 | G | A | 1 | a0001c0006 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1314G>A | p.Ser438Ser | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/22 | 1444/5700 | 1314/2856 | 438/951 | chr17 | 35639637 | |||
| chr17:35671783 | G | C | 2 | a0001c0002 a0001c0003 |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
synonymous_variant | LOW | c.2061G>C | p.Val687Val | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/22 | 2191/5700 | 2061/2856 | 687/951 | chr17 | 35671783 | |||
| chr17:35671885 | T | C | 1 | a0001c0004 | 9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
synonymous_variant | LOW | c.2163T>C | p.Tyr721Tyr | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/22 | 2293/5700 | 2163/2856 | 721/951 | chr17 | 35671885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:35587338 | C | A | 1 | a0001c0002t0011 | 2 | NA18942.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-114C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/22 | 6693 | chr17 | 35587338 | ||||||
| chr17:35723855 | C | T | 1 | a0001c0001t0008 | 6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*156C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 156 | chr17 | 35723855 | ||||||
| chr17:35723915 | C | T | 3 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0021 |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*216C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 216 | chr17 | 35723915 | ||||||
| chr17:35724105 | T | G | 1 | a0001c0001t0020 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 406 | chr17 | 35724105 | ||||||
| chr17:35724157 | A | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*458A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 458 | chr17 | 35724157 | ||||||
| chr17:35724277 | G | A | 1 | a0001c0001t0006 | 13 | HG01069.hp1 HG01070.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 578 | chr17 | 35724277 | ||||||
| chr17:35724473 | C | T | 1 | a0001c0001t0008 | 6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*774C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 774 | chr17 | 35724473 | ||||||
| chr17:35724524 | G | A | 1 | a0001c0002t0012 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 825 | chr17 | 35724524 | ||||||
| chr17:35724771 | C | G | 1 | a0001c0001t0015 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1072 | chr17 | 35724771 | ||||||
| chr17:35724896 | T | G | 1 | a0001c0001t0016 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1197 | chr17 | 35724896 | ||||||
| chr17:35725138 | G | A | 3 | a0001c0001t0003 a0001c0001t0017 a0002c0007t0003 |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1439G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1439 | chr17 | 35725138 | ||||||
| chr17:35725330 | T | G | 1 | a0001c0001t0018 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1631T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1631 | chr17 | 35725330 | ||||||
| chr17:35725489 | C | T | 1 | a0001c0002t0010 | 3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1790C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1790 | chr17 | 35725489 | ||||||
| chr17:35725494 | C | T | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0020 others(1): Show |
34 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1795C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1795 | chr17 | 35725494 | ||||||
| chr17:35725617 | G | A | 1 | a0001c0001t0021 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1918G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1918 | chr17 | 35725617 | ||||||
| chr17:35725690 | T | C | 1 | a0001c0002t0013 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1991T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 1991 | chr17 | 35725690 | ||||||
| chr17:35725782 | A | G | 1 | a0001c0002t0014 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2083A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 2083 | chr17 | 35725782 | ||||||
| chr17:35725855 | T | G | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0016 others(1): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2156T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 2156 | chr17 | 35725855 | ||||||
| chr17:35725987 | C | T | 1 | a0001c0001t0009 | 4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2288C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 2288 | chr17 | 35725987 | ||||||
| chr17:35726019 | A | G | 1 | a0001c0001t0019 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2320A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 2320 | chr17 | 35726019 | ||||||
| chr17:35726347 | C | T | 1 | a0001c0001t0017 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2648C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 22/22 | 2648 | chr17 | 35726347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:35587472 | G | A | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-24+44G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35587472 | |||||||
| chr17:35587644 | A | C | 1 | a0001c0001t0002g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24+216A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35587644 | |||||||
| chr17:35588026 | G | C | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-24+598G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588026 | |||||||
| chr17:35588031 | G | C | 1 | a0001c0001t0016g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-24+603G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588031 | |||||||
| chr17:35588066 | CT | C | 304 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(301): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-24+652delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35588066 | ||||||
| chr17:35588066 | CTT | C | 8 | a0001c0001t0002g0055 a0001c0001t0008g0056 a0001c0001t0008g0057 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+651_-24+652del others(2): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35588066 | ||||||
| chr17:35588215 | G | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+787G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588215 | |||||||
| chr17:35588227 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-24+799A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588227 | |||||||
| chr17:35588278 | G | T | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-24+850G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588278 | |||||||
| chr17:35588336 | C | T | 1 | a0001c0002t0001g0314 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-24+908C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588336 | |||||||
| chr17:35588581 | A | G | 3 | a0001c0002t0001g0311 a0001c0002t0001g0312 a0001c0002t0001g0313 |
3 | HG02615.hp2 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+1153A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588581 | |||||||
| chr17:35588588 | T | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+1160T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588588 | |||||||
| chr17:35588694 | G | C | 1 | a0001c0002t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-24+1266G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588694 | |||||||
| chr17:35588833 | T | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24+1405T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588833 | |||||||
| chr17:35588838 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-24+1410A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588838 | |||||||
| chr17:35588989 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-24+1561G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35588989 | |||||||
| chr17:35589257 | CCTCTCAC others(25): Show |
C | 1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-24+1830_-24+1861d others(34): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35589257 | |||||||
| chr17:35589297 | C | G | 1 | a0001c0001t0006g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-24+1869C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35589297 | |||||||
| chr17:35589493 | G | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-24+2065G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35589493 | |||||||
| chr17:35589569 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-24+2141T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35589569 | |||||||
| chr17:35589676 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-24+2248G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35589676 | |||||||
| chr17:35589924 | C | CT | 25 | a0001c0001t0004g0352 a0001c0001t0004g0353 a0001c0001t0007g0007 others(22): Show |
25 | HG00438.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-24+2515dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35589924 | ||||||
| chr17:35589924 | C | CTT | 123 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(120): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-24+2514_-24+2515d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35589924 | ||||||
| chr17:35589924 | C | CTTT | 18 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(15): Show |
18 | HG01884.hp2 HG02055.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24+2513_-24+2515d others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35589924 | ||||||
| chr17:35590071 | G | A | 1 | a0001c0001t0003g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-24+2643G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590071 | |||||||
| chr17:35590170 | C | T | 1 | a0001c0001t0006g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-24+2742C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590170 | |||||||
| chr17:35590171 | G | A | 33 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24+2743G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590171 | |||||||
| chr17:35590235 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2807C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590235 | |||||||
| chr17:35590303 | A | C | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+2875A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590303 | |||||||
| chr17:35590408 | A | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24+2980A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590408 | |||||||
| chr17:35590847 | T | TTAAGACT others(7): Show |
1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-23-3160_-23-3147d others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35590847 | ||||||
| chr17:35590932 | T | C | 1 | a0001c0001t0004g0354 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-23-3076T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590932 | |||||||
| chr17:35590935 | G | A | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.-23-3073G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35590935 | |||||||
| chr17:35591057 | C | T | 148 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(145): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-23-2951C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591057 | |||||||
| chr17:35591156 | A | G | 1 | a0001c0001t0004g0351 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-23-2852A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591156 | |||||||
| chr17:35591171 | C | CA | 12 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0004g0352 others(9): Show |
12 | HG00438.hp1 HG00733.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-23-2815dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35591171 | ||||||
| chr17:35591171 | CA | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0065 a0001c0001t0002g0168 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-23-2815delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35591171 | ||||||
| chr17:35591171 | CAA | C | 74 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0066 others(71): Show |
75 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-23-2816_-23-2815d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35591171 | ||||||
| chr17:35591190 | A | G | 1 | a0001c0004t0002g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-23-2818A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591190 | |||||||
| chr17:35591255 | G | A | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-2753G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591255 | |||||||
| chr17:35591292 | A | G | 29 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(26): Show |
31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-23-2716A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591292 | |||||||
| chr17:35591391 | T | C | 1 | a0001c0001t0002g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-23-2617T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591391 | |||||||
| chr17:35591761 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-2247A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591761 | |||||||
| chr17:35591802 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-23-2206C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35591802 | |||||||
| chr17:35592030 | A | G | 2 | a0001c0002t0001g0286 a0001c0002t0001g0287 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-23-1978A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592030 | |||||||
| chr17:35592125 | TTTTTC | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-23-1874_-23-1870d others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35592125 | ||||||
| chr17:35592291 | G | A | 1 | a0001c0001t0003g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-23-1717G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592291 | |||||||
| chr17:35592307 | T | TA | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-1700dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35592307 | ||||||
| chr17:35592456 | G | C | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.-23-1552G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592456 | |||||||
| chr17:35592457 | A | T | 1 | a0001c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-23-1551A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592457 | |||||||
| chr17:35592563 | G | A | 2 | a0001c0001t0003g0012 a0001c0001t0003g0013 |
2 | NA18946.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-23-1445G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592563 | |||||||
| chr17:35592621 | C | T | 1 | a0001c0002t0001g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-23-1387C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592621 | |||||||
| chr17:35592773 | C | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.-23-1235C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592773 | |||||||
| chr17:35592832 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0187 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-23-1176T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35592832 | |||||||
| chr17:35593017 | A | C | 172 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(169): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-23-991A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593017 | |||||||
| chr17:35593077 | C | T | 1 | a0001c0002t0014g0284 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-23-931C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593077 | |||||||
| chr17:35593340 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-23-668G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593340 | |||||||
| chr17:35593400 | T | A | 1 | a0001c0001t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-23-608T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593400 | |||||||
| chr17:35593449 | T | TAAA | 319 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0001 others(316): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.-23-554_-23-552dup others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 35593449 | ||||||
| chr17:35593601 | A | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23-407A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593601 | |||||||
| chr17:35593700 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-308A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593700 | |||||||
| chr17:35593863 | G | A | 1 | a0001c0004t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-23-145G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 1/21 | chr17 | 35593863 | |||||||
| chr17:35594123 | A | C | 1 | a0001c0001t0003g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.37+56A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594123 | |||||||
| chr17:35594141 | C | T | 334 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(331): Show |
337 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.37+74C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594141 | |||||||
| chr17:35594287 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.37+220T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594287 | |||||||
| chr17:35594293 | T | C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 |
3 | HG00323.hp2 NA18984.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.37+226T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594293 | |||||||
| chr17:35594313 | T | A | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.37+246T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594313 | |||||||
| chr17:35594319 | T | C | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+252T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594319 | |||||||
| chr17:35594488 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.37+421C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594488 | |||||||
| chr17:35594594 | A | AAAAAGC | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+530_37+535dupAA others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35594594 | ||||||
| chr17:35594744 | G | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+677G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594744 | |||||||
| chr17:35594838 | G | T | 184 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(181): Show |
185 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.37+771G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35594838 | |||||||
| chr17:35595036 | A | G | 11 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.37+969A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595036 | |||||||
| chr17:35595130 | G | A | 332 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(329): Show |
335 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.37+1063G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595130 | |||||||
| chr17:35595377 | C | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.37+1310C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595377 | |||||||
| chr17:35595392 | T | A | 331 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(328): Show |
334 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.37+1325T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595392 | |||||||
| chr17:35595402 | C | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+1335C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595402 | |||||||
| chr17:35595409 | C | T | 336 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.37+1342C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595409 | |||||||
| chr17:35595414 | G | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+1347G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595414 | |||||||
| chr17:35595648 | G | C | 16 | a0001c0001t0004g0321 a0001c0001t0004g0322 a0001c0001t0004g0323 others(13): Show |
16 | HG00544.hp2 NA18612.hp1 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.37+1581G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595648 | |||||||
| chr17:35595723 | T | C | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.37+1656T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595723 | |||||||
| chr17:35595725 | T | G | 1 | a0001c0001t0005g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.37+1658T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595725 | |||||||
| chr17:35595933 | A | AAAACTCT others(318): Show |
2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.37+1883_37+1884ins others(325): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35595933 | ||||||
| chr17:35595981 | C | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.37+1914C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35595981 | |||||||
| chr17:35596180 | A | G | 1 | a0001c0001t0009g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.38-2050A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596180 | |||||||
| chr17:35596350 | G | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-1880G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596350 | |||||||
| chr17:35596375 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-1855T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596375 | |||||||
| chr17:35596471 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.38-1759A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596471 | |||||||
| chr17:35596518 | TC | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0173 a0001c0001t0002g0175 |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1711delC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596518 | |||||||
| chr17:35596519 | C | CT | 180 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(177): Show |
181 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.38-1697dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35596519 | ||||||
| chr17:35596519 | C | CTT | 12 | a0001c0001t0002g0122 a0001c0002t0001g0198 a0001c0002t0001g0199 others(9): Show |
12 | HG00558.hp2 HG01884.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.38-1698_38-1697dup others(2): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35596519 | ||||||
| chr17:35596519 | CT | C | 77 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(74): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.38-1697delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35596519 | ||||||
| chr17:35596533 | T | G | 11 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.38-1697T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596533 | |||||||
| chr17:35596545 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-1685G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596545 | |||||||
| chr17:35596588 | G | A | 148 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(145): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.38-1642G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596588 | |||||||
| chr17:35596604 | G | A | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.38-1626G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596604 | |||||||
| chr17:35596671 | C | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.38-1559C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596671 | |||||||
| chr17:35596701 | C | T | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.38-1529C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596701 | |||||||
| chr17:35596725 | C | T | 5 | a0001c0001t0004g0347 a0001c0001t0004g0354 a0001c0001t0007g0346 others(2): Show |
5 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1505C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596725 | |||||||
| chr17:35596795 | C | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.38-1435C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596795 | |||||||
| chr17:35596803 | C | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.38-1427C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596803 | |||||||
| chr17:35596810 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-1420C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596810 | |||||||
| chr17:35596927 | T | G | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.38-1303T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596927 | |||||||
| chr17:35596975 | G | T | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.38-1255G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35596975 | |||||||
| chr17:35597145 | C | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-1085C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597145 | |||||||
| chr17:35597147 | A | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-1083A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597147 | |||||||
| chr17:35597259 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.38-971A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597259 | |||||||
| chr17:35597289 | A | G | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38-941A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597289 | |||||||
| chr17:35597296 | G | GT | 10 | a0001c0001t0003g0048 a0001c0001t0004g0334 a0001c0001t0004g0345 others(7): Show |
10 | HG00597.hp1 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-926dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 35597296 | ||||||
| chr17:35597358 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.38-872G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597358 | |||||||
| chr17:35597469 | A | G | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38-761A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597469 | |||||||
| chr17:35597568 | G | A | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.38-662G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597568 | |||||||
| chr17:35597658 | T | A | 1 | a0001c0001t0005g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.38-572T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597658 | |||||||
| chr17:35597828 | C | G | 332 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(329): Show |
335 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.38-402C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597828 | |||||||
| chr17:35597833 | G | A | 1 | a0001c0002t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.38-397G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597833 | |||||||
| chr17:35597871 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.38-359C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597871 | |||||||
| chr17:35597878 | G | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.38-352G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35597878 | |||||||
| chr17:35598042 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-188C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35598042 | |||||||
| chr17:35598170 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-60A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 2/21 | chr17 | 35598170 | |||||||
| chr17:35598341 | A | T | 1 | a0001c0003t0001g0310 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.143+6A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598341 | |||||||
| chr17:35598374 | T | C | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.143+39T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598374 | |||||||
| chr17:35598503 | C | T | 5 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+168C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598503 | |||||||
| chr17:35598524 | A | T | 1 | a0001c0002t0001g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.143+189A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598524 | |||||||
| chr17:35598560 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.143+225C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598560 | |||||||
| chr17:35598736 | A | G | 190 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(187): Show |
191 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.143+401A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598736 | |||||||
| chr17:35598743 | G | A | 336 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.143+408G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598743 | |||||||
| chr17:35598878 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.143+543G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598878 | |||||||
| chr17:35598887 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.143+552A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35598887 | |||||||
| chr17:35599179 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.143+844G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599179 | |||||||
| chr17:35599218 | C | T | 1 | a0001c0001t0005g0154 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143+883C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599218 | |||||||
| chr17:35599364 | G | A | 284 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.143+1029G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599364 | |||||||
| chr17:35599667 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0170 a0001c0001t0002g0173 others(1): Show |
5 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+1332G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599667 | |||||||
| chr17:35599670 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+1335G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599670 | |||||||
| chr17:35599766 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.143+1431C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599766 | |||||||
| chr17:35599779 | A | C | 5 | a0001c0001t0002g0356 a0001c0001t0002g0357 a0001c0001t0002g0358 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+1444A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599779 | |||||||
| chr17:35599965 | A | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+1630A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35599965 | |||||||
| chr17:35600057 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+1722A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600057 | |||||||
| chr17:35600106 | GA | G | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.143+1772delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600106 | |||||||
| chr17:35600107 | A | G | 271 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(268): Show |
273 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.143+1772A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600107 | |||||||
| chr17:35600198 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.143+1863C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600198 | |||||||
| chr17:35600393 | T | G | 1 | a0001c0001t0004g0318 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143+2058T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600393 | |||||||
| chr17:35600500 | A | G | 10 | a0001c0001t0002g0066 a0001c0001t0002g0101 a0001c0001t0002g0102 others(7): Show |
10 | HG00438.hp2 NA18940.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+2165A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600500 | |||||||
| chr17:35600503 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.143+2168C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600503 | |||||||
| chr17:35600766 | A | G | 8 | a0001c0002t0001g0269 a0001c0002t0001g0270 a0001c0002t0001g0272 others(5): Show |
8 | HG01993.hp2 HG02074.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.143+2431A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600766 | |||||||
| chr17:35600773 | G | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.143+2438G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600773 | |||||||
| chr17:35600821 | TAA | T | 39 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(36): Show |
39 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.143+2487_143+2488d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600821 | |||||||
| chr17:35600878 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG00544.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.143+2543G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600878 | |||||||
| chr17:35600885 | C | G | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.143+2550C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600885 | |||||||
| chr17:35600901 | G | A | 1 | a0001c0001t0005g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.143+2566G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600901 | |||||||
| chr17:35600903 | G | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+2568G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35600903 | |||||||
| chr17:35601002 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143+2667G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601002 | |||||||
| chr17:35601039 | G | T | 1 | a0001c0005t0002g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.143+2704G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601039 | |||||||
| chr17:35601139 | G | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.143+2804G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601139 | |||||||
| chr17:35601149 | A | G | 1 | a0001c0002t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143+2814A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601149 | |||||||
| chr17:35601453 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143+3118C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601453 | |||||||
| chr17:35601468 | T | C | 1 | a0001c0001t0005g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143+3133T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601468 | |||||||
| chr17:35601641 | G | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.143+3306G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601641 | |||||||
| chr17:35601754 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143+3419G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601754 | |||||||
| chr17:35601778 | C | CT | 73 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(70): Show |
74 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.143+3459dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35601778 | ||||||
| chr17:35601778 | CT | C | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(10): Show |
13 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.143+3459delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35601778 | ||||||
| chr17:35601894 | C | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.143+3559C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601894 | |||||||
| chr17:35601926 | T | C | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.143+3591T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601926 | |||||||
| chr17:35601955 | T | G | 3 | a0001c0001t0004g0335 a0001c0001t0004g0336 a0001c0001t0004g0345 |
3 | NA18967.hp2 NA18977.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.143+3620T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35601955 | |||||||
| chr17:35602146 | T | G | 1 | a0001c0002t0001g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.144-3559T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602146 | |||||||
| chr17:35602272 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.144-3433G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602272 | |||||||
| chr17:35602275 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144-3430G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602275 | |||||||
| chr17:35602296 | C | T | 1 | a0001c0002t0001g0273 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.144-3409C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602296 | |||||||
| chr17:35602355 | A | G | 1 | a0001c0001t0015g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144-3350A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602355 | |||||||
| chr17:35602468 | G | T | 336 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.144-3237G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602468 | |||||||
| chr17:35602478 | A | G | 25 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.144-3227A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602478 | |||||||
| chr17:35602490 | C | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-3215C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602490 | |||||||
| chr17:35602563 | A | G | 152 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.144-3142A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602563 | |||||||
| chr17:35602812 | T | G | 8 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
8 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-2893T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602812 | |||||||
| chr17:35602874 | A | G | 1 | a0001c0001t0003g0046 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.144-2831A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602874 | |||||||
| chr17:35602917 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144-2788C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602917 | |||||||
| chr17:35602925 | CGTT | C | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2776_144-2774d others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35602925 | ||||||
| chr17:35602926 | G | A | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-2779G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35602926 | |||||||
| chr17:35603002 | A | G | 11 | a0001c0001t0002g0174 a0001c0001t0002g0367 a0001c0004t0002g0125 others(8): Show |
11 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-2703A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603002 | |||||||
| chr17:35603180 | G | C | 1 | a0001c0001t0021g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.144-2525G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603180 | |||||||
| chr17:35603293 | A | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-2412A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603293 | |||||||
| chr17:35603439 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.144-2266G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603439 | |||||||
| chr17:35603494 | A | C | 1 | a0001c0001t0002g0100 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.144-2211A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603494 | |||||||
| chr17:35603574 | A | G | 1 | a0001c0001t0005g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.144-2131A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603574 | |||||||
| chr17:35603592 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2113C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603592 | |||||||
| chr17:35603795 | G | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(1): Show |
4 | HG02071.hp1 HG02132.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-1910G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603795 | |||||||
| chr17:35603822 | C | T | 3 | a0001c0001t0004g0335 a0001c0001t0004g0336 a0001c0001t0004g0345 |
3 | NA18967.hp2 NA18977.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.144-1883C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35603822 | |||||||
| chr17:35604057 | C | CCATGTTA others(3895): Show |
6 | a0001c0001t0004g0321 a0001c0001t0004g0328 a0001c0001t0004g0329 others(3): Show |
6 | NA18612.hp1 NA18942.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-1641_144-1640i others(3904): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35604057 | ||||||
| chr17:35604057 | C | CCATGTTA others(3896): Show |
1 | a0001c0001t0004g0333 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.144-1641_144-1640i others(3905): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35604057 | ||||||
| chr17:35604065 | G | C | 326 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(323): Show |
329 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.144-1640G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604065 | |||||||
| chr17:35604114 | A | T | 1 | a0001c0001t0008g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.144-1591A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604114 | |||||||
| chr17:35604158 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144-1547T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604158 | |||||||
| chr17:35604168 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-1537C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604168 | |||||||
| chr17:35604175 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.144-1530G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604175 | |||||||
| chr17:35604196 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-1509A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604196 | |||||||
| chr17:35604298 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-1407G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604298 | |||||||
| chr17:35604308 | T | C | 10 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-1397T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604308 | |||||||
| chr17:35604309 | A | G | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.144-1396A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604309 | |||||||
| chr17:35604396 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.144-1309A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604396 | |||||||
| chr17:35604513 | T | A | 2 | a0001c0001t0004g0337 a0001c0001t0004g0350 |
2 | NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.144-1192T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604513 | |||||||
| chr17:35604566 | T | TGGCTAAC | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.144-1138_144-1132d others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35604566 | ||||||
| chr17:35604772 | G | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.144-933G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604772 | |||||||
| chr17:35604810 | C | T | 1 | a0001c0001t0021g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.144-895C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35604810 | |||||||
| chr17:35605012 | C | T | 1 | a0001c0001t0006g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.144-693C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605012 | |||||||
| chr17:35605038 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-667A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605038 | |||||||
| chr17:35605129 | C | T | 2 | a0001c0002t0001g0275 a0001c0002t0001g0278 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.144-576C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605129 | |||||||
| chr17:35605191 | C | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0170 a0001c0001t0002g0173 others(1): Show |
5 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-514C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605191 | |||||||
| chr17:35605216 | TTCTTTTC others(5): Show |
T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.144-475_144-464del others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35605216 | ||||||
| chr17:35605240 | CT | C | 39 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(36): Show |
39 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.144-454delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 35605240 | ||||||
| chr17:35605251 | T | C | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.144-454T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605251 | |||||||
| chr17:35605253 | C | T | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.144-452C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605253 | |||||||
| chr17:35605306 | T | C | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-399T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605306 | |||||||
| chr17:35605352 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.144-353G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605352 | |||||||
| chr17:35605478 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-227G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605478 | |||||||
| chr17:35605616 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-89A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605616 | |||||||
| chr17:35605672 | A | G | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.144-33A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 3/21 | chr17 | 35605672 | |||||||
| chr17:35605868 | G | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+28G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35605868 | |||||||
| chr17:35605987 | A | C | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.279+147A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35605987 | |||||||
| chr17:35605997 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.279+157C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35605997 | |||||||
| chr17:35606116 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+276A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606116 | |||||||
| chr17:35606178 | A | C | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+338A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606178 | |||||||
| chr17:35606181 | A | G | 1 | a0001c0001t0005g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.279+341A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606181 | |||||||
| chr17:35606195 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0015g0131 |
3 | HG01109.hp2 HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.279+355G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606195 | |||||||
| chr17:35606214 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+374A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606214 | |||||||
| chr17:35606242 | A | AT | 72 | a0001c0001t0002g0001 a0001c0001t0002g0065 a0001c0001t0002g0066 others(69): Show |
73 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.279+417dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35606242 | ||||||
| chr17:35606261 | A | G | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.279+421A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606261 | |||||||
| chr17:35606375 | G | A | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+535G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606375 | |||||||
| chr17:35606407 | T | C | 1 | a0001c0002t0001g0282 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+567T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606407 | |||||||
| chr17:35606471 | T | G | 1 | a0001c0001t0004g0322 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.279+631T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606471 | |||||||
| chr17:35606547 | T | G | 1 | a0001c0002t0001g0276 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+707T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606547 | |||||||
| chr17:35606572 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+732A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606572 | |||||||
| chr17:35606906 | A | AT | 7 | a0001c0001t0002g0106 a0001c0001t0002g0172 a0001c0001t0003g0042 others(4): Show |
7 | HG02074.hp1 HG02602.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+1081dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35606906 | ||||||
| chr17:35606940 | T | C | 1 | a0001c0001t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.279+1100T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606940 | |||||||
| chr17:35606957 | G | A | 1 | a0001c0001t0008g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+1117G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606957 | |||||||
| chr17:35606966 | C | T | 1 | a0001c0002t0014g0284 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.279+1126C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606966 | |||||||
| chr17:35606999 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0170 a0001c0001t0002g0173 others(1): Show |
5 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-1143G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35606999 | |||||||
| chr17:35607106 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.280-1036T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607106 | |||||||
| chr17:35607185 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.280-957G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607185 | |||||||
| chr17:35607220 | AGTT | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-918_280-916del others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35607220 | ||||||
| chr17:35607235 | G | GT | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02027.hp2 NA18981.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-904dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35607235 | ||||||
| chr17:35607320 | A | G | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-822A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607320 | |||||||
| chr17:35607351 | C | T | 1 | a0001c0002t0001g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.280-791C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607351 | |||||||
| chr17:35607476 | T | C | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.280-666T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607476 | |||||||
| chr17:35607774 | C | CT | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(10): Show |
13 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.280-348dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35607774 | ||||||
| chr17:35607774 | CT | C | 183 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(180): Show |
184 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(181): Show |
intron_variant | MODIFIER | c.280-348delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 35607774 | ||||||
| chr17:35607893 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.280-249A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607893 | |||||||
| chr17:35607966 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.280-176A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 4/21 | chr17 | 35607966 | |||||||
| chr17:35608510 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.525+123T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35608510 | |||||||
| chr17:35608651 | T | C | 1 | a0001c0001t0003g0022 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.525+264T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35608651 | |||||||
| chr17:35608677 | C | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+290C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35608677 | |||||||
| chr17:35609026 | G | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.525+639G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609026 | |||||||
| chr17:35609104 | A | G | 1 | a0001c0001t0002g0360 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.525+717A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609104 | |||||||
| chr17:35609348 | A | AT | 154 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(151): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.525+977dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35609348 | ||||||
| chr17:35609348 | A | ATT | 178 | a0001c0001t0002g0122 a0001c0001t0002g0168 a0001c0001t0003g0009 others(175): Show |
179 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.525+976_525+977dup others(2): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35609348 | ||||||
| chr17:35609348 | A | ATTT | 8 | a0001c0001t0004g0326 a0001c0001t0004g0337 a0001c0001t0004g0345 others(5): Show |
8 | HG02074.hp1 HG02559.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+975_525+977dup others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35609348 | ||||||
| chr17:35609433 | G | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.525+1046G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609433 | |||||||
| chr17:35609446 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+1059A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609446 | |||||||
| chr17:35609548 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1161C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609548 | |||||||
| chr17:35609589 | C | T | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.525+1202C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609589 | |||||||
| chr17:35609604 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1217C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609604 | |||||||
| chr17:35609636 | C | T | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+1249C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609636 | |||||||
| chr17:35609739 | T | C | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.525+1352T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35609739 | |||||||
| chr17:35610142 | A | ATTTATTT | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.525+1766_525+1772d others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35610142 | ||||||
| chr17:35610213 | C | T | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.525+1826C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610213 | |||||||
| chr17:35610247 | C | T | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+1860C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610247 | |||||||
| chr17:35610362 | G | A | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.525+1975G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610362 | |||||||
| chr17:35610568 | G | A | 1 | a0002c0007t0003g0041 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.525+2181G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610568 | |||||||
| chr17:35610604 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0173 a0001c0001t0002g0175 |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+2217A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610604 | |||||||
| chr17:35610629 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18944.hp1 NA19002.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.525+2242C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610629 | |||||||
| chr17:35610633 | T | C | 1 | a0001c0002t0001g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.525+2246T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610633 | |||||||
| chr17:35610674 | G | A | 179 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(176): Show |
180 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.525+2287G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610674 | |||||||
| chr17:35610688 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.525+2301A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610688 | |||||||
| chr17:35610764 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+2377G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610764 | |||||||
| chr17:35610855 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.525+2468C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610855 | |||||||
| chr17:35610888 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.525+2501C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35610888 | |||||||
| chr17:35610907 | C | CA | 321 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(318): Show |
324 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.525+2537dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35610907 | ||||||
| chr17:35610907 | C | CAA | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+2536_525+2537d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35610907 | ||||||
| chr17:35611021 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+2634G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611021 | |||||||
| chr17:35611070 | T | G | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.525+2683T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611070 | |||||||
| chr17:35611183 | C | G | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.525+2796C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611183 | |||||||
| chr17:35611272 | T | G | 1 | a0001c0002t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.525+2885T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611272 | |||||||
| chr17:35611356 | C | T | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.525+2969C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611356 | |||||||
| chr17:35611380 | C | A | 5 | a0001c0001t0004g0347 a0001c0001t0004g0354 a0001c0001t0007g0346 others(2): Show |
5 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+2993C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611380 | |||||||
| chr17:35611464 | C | CGT | 9 | a0001c0001t0003g0008 a0001c0001t0004g0343 a0001c0001t0004g0354 others(6): Show |
9 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3093_525+3094d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35611464 | ||||||
| chr17:35611464 | C | CGTGT | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.525+3091_525+3094d others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35611464 | ||||||
| chr17:35611480 | T | C | 1 | a0001c0002t0001g0194 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.525+3093T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611480 | |||||||
| chr17:35611482 | C | T | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG00735.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.525+3095C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611482 | |||||||
| chr17:35611487 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.525+3100G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611487 | |||||||
| chr17:35611492 | C | T | 13 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(10): Show |
14 | HG00735.hp1 HG01106.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+3105C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611492 | |||||||
| chr17:35611543 | C | T | 1 | a0001c0004t0002g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.525+3156C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611543 | |||||||
| chr17:35611585 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3198G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611585 | |||||||
| chr17:35611663 | A | G | 1 | a0001c0001t0004g0326 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.525+3276A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611663 | |||||||
| chr17:35611677 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3290G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611677 | |||||||
| chr17:35611791 | T | C | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.525+3404T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611791 | |||||||
| chr17:35611878 | T | C | 2 | a0001c0002t0001g0275 a0001c0002t0001g0278 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.525+3491T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611878 | |||||||
| chr17:35611893 | T | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3506T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611893 | |||||||
| chr17:35611982 | G | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.525+3595G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35611982 | |||||||
| chr17:35612289 | C | G | 5 | a0001c0001t0004g0347 a0001c0001t0004g0354 a0001c0001t0007g0346 others(2): Show |
5 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+3902C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612289 | |||||||
| chr17:35612445 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.525+4058C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612445 | |||||||
| chr17:35612636 | A | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(140): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.525+4249A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612636 | |||||||
| chr17:35612642 | C | T | 184 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(181): Show |
185 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.525+4255C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612642 | |||||||
| chr17:35612697 | G | T | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+4310G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612697 | |||||||
| chr17:35612877 | TGC | T | 12 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(9): Show |
13 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+4493_525+4494d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612877 | ||||||
| chr17:35612878 | G | GCA | 19 | a0001c0001t0002g0055 a0001c0001t0002g0085 a0001c0001t0002g0119 others(16): Show |
19 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+4492_525+4493i others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612878 | ||||||
| chr17:35612878 | G | GCACA | 4 | a0001c0001t0006g0077 a0001c0001t0006g0089 a0001c0001t0007g0006 others(1): Show |
4 | HG01123.hp1 HG01257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+4492_525+4493i others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612878 | ||||||
| chr17:35612878 | G | GCACACAC others(3): Show |
1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.525+4492_525+4493i others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612878 | ||||||
| chr17:35612880 | G | A | 139 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(136): Show |
140 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+4493G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612880 | |||||||
| chr17:35612880 | GCACACA | G | 35 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(32): Show |
35 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.525+4516_525+4521d others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612880 | ||||||
| chr17:35612880 | GCACACAC others(1): Show |
G | 10 | a0001c0001t0004g0158 a0001c0001t0004g0347 a0001c0001t0004g0354 others(7): Show |
10 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+4514_525+4521d others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612880 | ||||||
| chr17:35612880 | GCACACAC others(3): Show |
G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+4512_525+4521d others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612880 | ||||||
| chr17:35612892 | A | G | 1 | a0001c0002t0001g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.525+4505A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612892 | |||||||
| chr17:35612928 | A | G | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.525+4541A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612928 | |||||||
| chr17:35612938 | G | A | 1 | a0001c0002t0001g0195 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.525+4551G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35612938 | |||||||
| chr17:35612998 | GA | G | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+4621delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35612998 | ||||||
| chr17:35613000 | A | G | 2 | a0001c0001t0005g0135 a0001c0001t0005g0155 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.525+4613A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613000 | |||||||
| chr17:35613196 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.525+4809G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613196 | |||||||
| chr17:35613299 | T | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 |
3 | HG00323.hp2 NA18984.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.525+4912T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613299 | |||||||
| chr17:35613325 | C | G | 1 | a0001c0002t0001g0248 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.525+4938C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613325 | |||||||
| chr17:35613481 | C | G | 1 | a0001c0002t0001g0247 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.525+5094C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613481 | |||||||
| chr17:35613557 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.525+5170A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613557 | |||||||
| chr17:35613661 | A | T | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.525+5274A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613661 | |||||||
| chr17:35613766 | A | G | 1 | a0001c0001t0004g0325 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.525+5379A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613766 | |||||||
| chr17:35613940 | T | A | 1 | a0001c0002t0001g0252 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.525+5553T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613940 | |||||||
| chr17:35613947 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+5560G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35613947 | |||||||
| chr17:35614032 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+5645A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614032 | |||||||
| chr17:35614051 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+5664A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614051 | |||||||
| chr17:35614085 | A | G | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.525+5698A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614085 | |||||||
| chr17:35614101 | C | T | 143 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(140): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.525+5714C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614101 | |||||||
| chr17:35614302 | G | A | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.525+5915G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614302 | |||||||
| chr17:35614541 | G | C | 334 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(331): Show |
337 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.525+6154G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614541 | |||||||
| chr17:35614541 | G | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+6154G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614541 | |||||||
| chr17:35614655 | T | TA | 26 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(23): Show |
26 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.525+6293dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35614655 | ||||||
| chr17:35614655 | T | TAA | 33 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.525+6292_525+6293d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35614655 | ||||||
| chr17:35614655 | T | TAAA | 108 | a0001c0001t0005g0137 a0001c0002t0001g0005 a0001c0002t0001g0184 others(105): Show |
109 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.525+6291_525+6293d others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35614655 | ||||||
| chr17:35614655 | T | TAAAA | 21 | a0001c0001t0004g0158 a0001c0001t0007g0346 a0001c0001t0007g0348 others(18): Show |
21 | HG01168.hp2 HG01169.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+6290_525+6293d others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35614655 | ||||||
| chr17:35614655 | T | TAAAAA | 44 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(41): Show |
44 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.525+6289_525+6293d others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35614655 | ||||||
| chr17:35614725 | A | T | 41 | a0001c0002t0001g0062 a0001c0002t0001g0191 a0001c0002t0001g0192 others(38): Show |
41 | HG00558.hp2 HG01891.hp2 HG01993.hp2 others(38): Show |
intron_variant | MODIFIER | c.525+6338A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614725 | |||||||
| chr17:35614944 | A | G | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.525+6557A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35614944 | |||||||
| chr17:35615017 | C | T | 3 | a0001c0002t0001g0241 a0001c0002t0001g0242 a0001c0002t0001g0243 |
3 | HG02451.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.525+6630C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615017 | |||||||
| chr17:35615071 | G | A | 1 | a0001c0002t0001g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.525+6684G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615071 | |||||||
| chr17:35615214 | A | G | 36 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(33): Show |
36 | HG00558.hp1 HG00673.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.525+6827A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615214 | |||||||
| chr17:35615218 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0049 |
3 | HG01070.hp1 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.525+6831A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615218 | |||||||
| chr17:35615242 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.525+6855G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615242 | |||||||
| chr17:35615374 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+6987G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615374 | |||||||
| chr17:35615461 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.525+7074A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615461 | |||||||
| chr17:35615484 | A | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+7097A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615484 | |||||||
| chr17:35615521 | T | C | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.525+7134T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615521 | |||||||
| chr17:35615568 | T | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+7181T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615568 | |||||||
| chr17:35615740 | A | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.525+7353A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35615740 | |||||||
| chr17:35616103 | G | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.525+7716G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616103 | |||||||
| chr17:35616118 | G | T | 1 | a0001c0001t0003g0046 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.525+7731G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616118 | |||||||
| chr17:35616142 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0009g0160 a0001c0001t0009g0161 a0001c0002t0001g0192 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+7786_525+7794d others(11): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(3): Show |
C | 34 | a0001c0001t0004g0320 a0001c0001t0004g0330 a0001c0001t0004g0341 others(31): Show |
34 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.525+7785_525+7794d others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(4): Show |
C | 135 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0180 others(132): Show |
136 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.525+7784_525+7794d others(13): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(5): Show |
C | 31 | a0001c0001t0001g0128 a0001c0001t0002g0078 a0001c0001t0002g0082 others(28): Show |
31 | HG00438.hp2 HG01123.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.525+7783_525+7794d others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(6): Show |
C | 100 | a0001c0001t0002g0001 a0001c0001t0002g0065 a0001c0001t0002g0066 others(97): Show |
101 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.525+7782_525+7794d others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(7): Show |
C | 11 | a0001c0001t0002g0055 a0001c0001t0002g0168 a0001c0001t0002g0170 others(8): Show |
11 | HG00140.hp1 HG02622.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+7781_525+7794d others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(8): Show |
C | 12 | a0001c0001t0002g0004 a0001c0001t0002g0169 a0001c0001t0002g0172 others(9): Show |
13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+7780_525+7794d others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.525+7779_525+7794d others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(11): Show |
C | 7 | a0001c0001t0005g0135 a0001c0002t0001g0193 a0001c0002t0001g0194 others(4): Show |
7 | HG02698.hp1 HG03195.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+7777_525+7794d others(20): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0021g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.525+7774_525+7794d others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(17): Show |
C | 1 | a0001c0001t0003g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.525+7771_525+7794d others(26): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616142 | CTTTTTTT others(18): Show |
C | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.525+7770_525+7794d others(27): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616142 | ||||||
| chr17:35616187 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.525+7800C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616187 | |||||||
| chr17:35616205 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+7818C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616205 | |||||||
| chr17:35616217 | T | TG | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+7831dupG | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35616217 | ||||||
| chr17:35616219 | C | T | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.525+7832C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616219 | |||||||
| chr17:35616233 | C | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.525+7846C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616233 | |||||||
| chr17:35616250 | C | T | 39 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(36): Show |
39 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.525+7863C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616250 | |||||||
| chr17:35616296 | C | T | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.525+7909C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616296 | |||||||
| chr17:35616302 | C | G | 1 | a0001c0001t0002g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.525+7915C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616302 | |||||||
| chr17:35616322 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.525+7935G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616322 | |||||||
| chr17:35616365 | T | G | 1 | a0001c0001t0005g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.525+7978T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616365 | |||||||
| chr17:35616491 | A | T | 1 | a0001c0002t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.526-7906A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616491 | |||||||
| chr17:35616746 | AC | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.526-7650delC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616746 | |||||||
| chr17:35616762 | G | C | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.526-7635G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616762 | |||||||
| chr17:35616776 | A | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-7621A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616776 | |||||||
| chr17:35616789 | C | T | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-7608C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616789 | |||||||
| chr17:35616891 | T | G | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.526-7506T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616891 | |||||||
| chr17:35616930 | C | T | 1 | a0001c0002t0010g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.526-7467C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616930 | |||||||
| chr17:35616960 | C | T | 1 | a0001c0002t0001g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.526-7437C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35616960 | |||||||
| chr17:35617036 | C | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(145): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.526-7361C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617036 | |||||||
| chr17:35617129 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.526-7268T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617129 | |||||||
| chr17:35617187 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526-7210C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617187 | |||||||
| chr17:35617213 | G | C | 39 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(36): Show |
39 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.526-7184G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617213 | |||||||
| chr17:35617331 | C | T | 1 | a0001c0001t0020g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.526-7066C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617331 | |||||||
| chr17:35617353 | C | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.526-7044C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617353 | |||||||
| chr17:35617564 | C | CT | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-6832dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35617564 | ||||||
| chr17:35617571 | T | A | 184 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(181): Show |
185 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.526-6826T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617571 | |||||||
| chr17:35617754 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.526-6643T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617754 | |||||||
| chr17:35617813 | G | C | 1 | a0001c0001t0002g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.526-6584G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617813 | |||||||
| chr17:35617991 | CTATGTA | C | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-6405_526-6400d others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617991 | |||||||
| chr17:35617999 | T | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-6398T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35617999 | |||||||
| chr17:35618000 | C | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-6397C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35618000 | |||||||
| chr17:35618100 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-6297A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35618100 | |||||||
| chr17:35618413 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.526-5984C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35618413 | |||||||
| chr17:35618926 | A | C | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.526-5471A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35618926 | |||||||
| chr17:35618950 | A | G | 1 | a0001c0001t0005g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.526-5447A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35618950 | |||||||
| chr17:35619053 | T | A | 3 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0277 |
3 | HG02572.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.526-5344T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619053 | |||||||
| chr17:35619088 | A | G | 87 | a0001c0002t0001g0005 a0001c0002t0001g0184 a0001c0002t0001g0185 others(84): Show |
88 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.526-5309A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619088 | |||||||
| chr17:35619095 | T | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-5302T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619095 | |||||||
| chr17:35619101 | G | T | 1 | a0001c0002t0001g0273 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.526-5296G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619101 | |||||||
| chr17:35619163 | C | T | 34 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(31): Show |
34 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.526-5234C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619163 | |||||||
| chr17:35619449 | C | G | 1 | a0001c0001t0003g0040 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.526-4948C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619449 | |||||||
| chr17:35619481 | T | TA | 135 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(132): Show |
136 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.526-4906dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35619481 | ||||||
| chr17:35619562 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.526-4835G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619562 | |||||||
| chr17:35619724 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-4673A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619724 | |||||||
| chr17:35619764 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.526-4633G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619764 | |||||||
| chr17:35619858 | T | G | 1 | a0001c0004t0002g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.526-4539T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619858 | |||||||
| chr17:35619909 | C | T | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.526-4488C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35619909 | |||||||
| chr17:35620048 | A | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-4349A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35620048 | |||||||
| chr17:35620193 | A | G | 184 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(181): Show |
185 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.526-4204A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35620193 | |||||||
| chr17:35620400 | A | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-3997A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35620400 | |||||||
| chr17:35620426 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.526-3971C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35620426 | |||||||
| chr17:35620749 | T | A | 1 | a0001c0001t0017g0027 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.526-3648T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35620749 | |||||||
| chr17:35621092 | G | A | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.526-3305G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35621092 | |||||||
| chr17:35621517 | C | T | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-2880C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35621517 | |||||||
| chr17:35621726 | A | G | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0181 |
3 | HG00280.hp2 HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.526-2671A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35621726 | |||||||
| chr17:35622055 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
5 | NA18972.hp1 NA18975.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2342T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622055 | |||||||
| chr17:35622064 | T | G | 139 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.526-2333T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622064 | |||||||
| chr17:35622119 | T | C | 1 | a0001c0002t0001g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.526-2278T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622119 | |||||||
| chr17:35622193 | A | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-2204A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622193 | |||||||
| chr17:35622203 | G | A | 152 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.526-2194G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622203 | |||||||
| chr17:35622365 | A | G | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-2032A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622365 | |||||||
| chr17:35622596 | G | T | 1 | a0001c0001t0004g0320 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.526-1801G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622596 | |||||||
| chr17:35622598 | G | T | 1 | a0001c0002t0001g0233 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.526-1799G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622598 | |||||||
| chr17:35622672 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.526-1725T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622672 | |||||||
| chr17:35622687 | C | T | 1 | a0001c0001t0009g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.526-1710C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622687 | |||||||
| chr17:35622688 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526-1709G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622688 | |||||||
| chr17:35622740 | C | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-1657C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622740 | |||||||
| chr17:35622816 | C | T | 5 | a0001c0002t0001g0198 a0001c0002t0001g0199 a0001c0002t0001g0225 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-1581C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622816 | |||||||
| chr17:35622885 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.526-1512C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622885 | |||||||
| chr17:35622907 | C | T | 1 | a0001c0001t0003g0037 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.526-1490C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622907 | |||||||
| chr17:35622935 | G | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-1462G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35622935 | |||||||
| chr17:35623097 | A | AT | 229 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(226): Show |
231 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.526-1285dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35623097 | ||||||
| chr17:35623097 | A | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.526-1300A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623097 | |||||||
| chr17:35623097 | AT | A | 28 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(25): Show |
29 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.526-1285delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 35623097 | ||||||
| chr17:35623265 | T | A | 13 | a0001c0001t0004g0321 a0001c0001t0004g0322 a0001c0001t0004g0325 others(10): Show |
13 | HG00544.hp2 NA18612.hp1 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-1132T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623265 | |||||||
| chr17:35623285 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.526-1112C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623285 | |||||||
| chr17:35623480 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.526-917C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623480 | |||||||
| chr17:35623603 | T | A | 1 | a0001c0001t0004g0341 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.526-794T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623603 | |||||||
| chr17:35623675 | G | C | 1 | a0001c0001t0003g0009 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.526-722G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623675 | |||||||
| chr17:35623718 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.526-679G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623718 | |||||||
| chr17:35623799 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-598T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623799 | |||||||
| chr17:35623958 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.526-439A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35623958 | |||||||
| chr17:35624209 | A | C | 185 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(182): Show |
186 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.526-188A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35624209 | |||||||
| chr17:35624221 | A | T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.526-176A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35624221 | |||||||
| chr17:35624379 | T | C | 1 | a0001c0001t0003g0018 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.526-18T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 5/21 | chr17 | 35624379 | |||||||
| chr17:35624605 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.716+18G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624605 | |||||||
| chr17:35624627 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.716+40T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624627 | |||||||
| chr17:35624653 | A | G | 2 | a0001c0001t0002g0094 a0001c0001t0002g0109 |
2 | NA18948.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.716+66A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624653 | |||||||
| chr17:35624731 | T | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.716+144T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624731 | |||||||
| chr17:35624737 | A | T | 3 | a0001c0002t0001g0224 a0001c0002t0001g0232 a0001c0002t0001g0246 |
3 | HG01109.hp1 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.716+150A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624737 | |||||||
| chr17:35624795 | A | G | 1 | a0001c0001t0005g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.716+208A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624795 | |||||||
| chr17:35624800 | G | A | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.716+213G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35624800 | |||||||
| chr17:35625084 | C | G | 152 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.716+497C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625084 | |||||||
| chr17:35625202 | T | A | 1 | a0001c0002t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.716+615T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625202 | |||||||
| chr17:35625240 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.716+653C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625240 | |||||||
| chr17:35625325 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.716+738G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625325 | |||||||
| chr17:35625382 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.716+795G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625382 | |||||||
| chr17:35625619 | G | A | 4 | a0001c0003t0001g0300 a0001c0003t0001g0301 a0001c0003t0001g0302 others(1): Show |
4 | HG02071.hp2 NA18962.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.717-1002G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625619 | |||||||
| chr17:35625677 | T | C | 152 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.717-944T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625677 | |||||||
| chr17:35625763 | G | T | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717-858G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35625763 | |||||||
| chr17:35626106 | CATT | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.717-512_717-510del others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 35626106 | ||||||
| chr17:35626143 | A | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.717-478A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35626143 | |||||||
| chr17:35626194 | G | A | 1 | a0001c0002t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717-427G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35626194 | |||||||
| chr17:35626336 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.717-285G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35626336 | |||||||
| chr17:35626365 | G | A | 184 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(181): Show |
185 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.717-256G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35626365 | |||||||
| chr17:35626473 | A | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.717-148A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 6/21 | chr17 | 35626473 | |||||||
| chr17:35627108 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.938+266G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 7/21 | chr17 | 35627108 | |||||||
| chr17:35627245 | C | CT | 80 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(77): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.939-116dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 35627245 | ||||||
| chr17:35627245 | C | CTT | 196 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(193): Show |
198 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.939-117_939-116dup others(2): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 35627245 | ||||||
| chr17:35627245 | C | CTTT | 59 | a0001c0001t0002g0066 a0001c0001t0002g0075 a0001c0001t0002g0078 others(56): Show |
59 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.939-118_939-116dup others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 35627245 | ||||||
| chr17:35627245 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.939-124_939-116del others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 35627245 | ||||||
| chr17:35627508 | C | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
splice_region_variant&intron_variant | LOW | c.1059+3C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 8/21 | chr17 | 35627508 | |||||||
| chr17:35627542 | A | G | 1 | a0001c0001t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1059+37A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 8/21 | chr17 | 35627542 | |||||||
| chr17:35627569 | G | A | 1 | a0001c0001t0002g0356 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-62G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 8/21 | chr17 | 35627569 | |||||||
| chr17:35627882 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1155+156C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35627882 | |||||||
| chr17:35627991 | C | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155+265C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35627991 | |||||||
| chr17:35628035 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1155+309A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628035 | |||||||
| chr17:35628036 | A | G | 3 | a0001c0002t0001g0222 a0001c0002t0001g0223 a0001c0002t0001g0231 |
3 | HG02970.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1155+310A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628036 | |||||||
| chr17:35628135 | G | A | 1 | a0001c0001t0008g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1155+409G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628135 | |||||||
| chr17:35628224 | G | A | 136 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(133): Show |
137 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1155+498G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628224 | |||||||
| chr17:35628358 | T | A | 152 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1155+632T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628358 | |||||||
| chr17:35628392 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1155+666A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628392 | |||||||
| chr17:35628470 | G | A | 1 | a0001c0001t0002g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1155+744G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628470 | |||||||
| chr17:35628475 | C | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1155+749C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628475 | |||||||
| chr17:35628610 | CG | C | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155+885delG | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628610 | |||||||
| chr17:35628618 | CA | C | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155+899delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35628618 | ||||||
| chr17:35628737 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1155+1011C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35628737 | |||||||
| chr17:35629141 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1155+1415G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629141 | |||||||
| chr17:35629154 | G | T | 2 | a0001c0002t0001g0005 a0001c0002t0012g0217 |
3 | HG01257.hp2 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1155+1428G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629154 | |||||||
| chr17:35629190 | C | G | 1 | a0001c0002t0001g0365 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1155+1464C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629190 | |||||||
| chr17:35629333 | T | A | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | NA18943.hp2 NA18987.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155+1607T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629333 | |||||||
| chr17:35629355 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155+1629G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629355 | |||||||
| chr17:35629389 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1155+1663T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629389 | |||||||
| chr17:35629402 | A | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1155+1676A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629402 | |||||||
| chr17:35629529 | TATGA | T | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155+1808_1155+181 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35629529 | ||||||
| chr17:35629606 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1155+1880G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629606 | |||||||
| chr17:35629659 | G | A | 1 | a0001c0001t0003g0029 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1155+1933G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629659 | |||||||
| chr17:35629768 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1155+2042A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629768 | |||||||
| chr17:35629864 | C | T | 332 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(329): Show |
335 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.1155+2138C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35629864 | |||||||
| chr17:35630051 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1155+2325G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630051 | |||||||
| chr17:35630405 | C | T | 3 | a0001c0002t0001g0192 a0001c0002t0001g0259 a0001c0002t0001g0264 |
3 | HG02055.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1155+2679C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630405 | |||||||
| chr17:35630471 | G | C | 1 | a0001c0001t0002g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1155+2745G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630471 | |||||||
| chr17:35630599 | T | A | 1 | a0001c0002t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1155+2873T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630599 | |||||||
| chr17:35630760 | C | G | 3 | a0001c0002t0001g0192 a0001c0002t0001g0259 a0001c0002t0001g0264 |
3 | HG02055.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1155+3034C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630760 | |||||||
| chr17:35630861 | G | C | 1 | a0001c0001t0005g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1155+3135G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35630861 | |||||||
| chr17:35630898 | GT | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155+3175delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35630898 | ||||||
| chr17:35631039 | G | T | 45 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1155+3313G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631039 | |||||||
| chr17:35631133 | A | G | 5 | a0001c0002t0001g0198 a0001c0002t0001g0199 a0001c0002t0001g0225 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155+3407A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631133 | |||||||
| chr17:35631149 | A | G | 180 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(177): Show |
181 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.1155+3423A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631149 | |||||||
| chr17:35631297 | G | A | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1155+3571G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631297 | |||||||
| chr17:35631318 | A | C | 1 | a0001c0002t0013g0216 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1155+3592A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631318 | |||||||
| chr17:35631327 | T | C | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155+3601T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631327 | |||||||
| chr17:35631401 | T | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155+3675T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631401 | |||||||
| chr17:35631403 | T | C | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1155+3677T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631403 | |||||||
| chr17:35631489 | A | G | 7 | a0001c0003t0001g0215 a0001c0003t0001g0298 a0001c0003t0001g0305 others(4): Show |
7 | HG02040.hp1 NA18960.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155+3763A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631489 | |||||||
| chr17:35631647 | A | G | 1 | a0001c0002t0001g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1155+3921A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631647 | |||||||
| chr17:35631827 | G | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+4101G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35631827 | |||||||
| chr17:35632088 | A | AT | 201 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(198): Show |
203 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1156-4239dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35632088 | ||||||
| chr17:35632088 | A | ATT | 10 | a0001c0002t0001g0193 a0001c0004t0002g0125 a0001c0004t0002g0126 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1156-4240_1156-423 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35632088 | ||||||
| chr17:35632112 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-4229G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632112 | |||||||
| chr17:35632168 | T | A | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-4173T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632168 | |||||||
| chr17:35632198 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1156-4143A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632198 | |||||||
| chr17:35632226 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-4115C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632226 | |||||||
| chr17:35632228 | G | A | 155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1156-4113G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632228 | |||||||
| chr17:35632415 | G | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1156-3926G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632415 | |||||||
| chr17:35632485 | T | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1156-3856T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632485 | |||||||
| chr17:35632512 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1156-3829T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632512 | |||||||
| chr17:35632678 | A | G | 181 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.1156-3663A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632678 | |||||||
| chr17:35632683 | A | T | 1 | a0001c0002t0001g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1156-3658A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632683 | |||||||
| chr17:35632754 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1156-3587A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632754 | |||||||
| chr17:35632802 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1156-3539C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632802 | |||||||
| chr17:35632818 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1156-3523G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632818 | |||||||
| chr17:35632870 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1156-3471G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632870 | |||||||
| chr17:35632878 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-3463A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35632878 | |||||||
| chr17:35633084 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1156-3257C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633084 | |||||||
| chr17:35633089 | G | A | 2 | a0001c0001t0004g0337 a0001c0001t0004g0350 |
2 | NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1156-3252G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633089 | |||||||
| chr17:35633129 | G | A | 1 | a0001c0002t0010g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1156-3212G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633129 | |||||||
| chr17:35633305 | A | T | 4 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(1): Show |
4 | HG01074.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-3036A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633305 | |||||||
| chr17:35633357 | C | CA | 134 | a0001c0001t0004g0318 a0001c0001t0005g0141 a0001c0002t0001g0005 others(131): Show |
135 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.1156-2970dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35633357 | ||||||
| chr17:35633488 | T | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1156-2853T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633488 | |||||||
| chr17:35633490 | G | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1156-2851G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633490 | |||||||
| chr17:35633666 | A | G | 1 | a0001c0002t0012g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1156-2675A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633666 | |||||||
| chr17:35633873 | G | C | 1 | a0001c0001t0008g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1156-2468G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633873 | |||||||
| chr17:35633912 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1156-2429C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35633912 | |||||||
| chr17:35634006 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1156-2335G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634006 | |||||||
| chr17:35634020 | G | A | 3 | a0001c0002t0001g0266 a0001c0002t0001g0267 a0001c0002t0001g0282 |
3 | HG01891.hp2 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1156-2321G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634020 | |||||||
| chr17:35634212 | G | C | 1 | a0001c0002t0001g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1156-2129G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634212 | |||||||
| chr17:35634273 | G | C | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-2068G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634273 | |||||||
| chr17:35634316 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1156-2025A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634316 | |||||||
| chr17:35634694 | C | T | 1 | a0001c0004t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1156-1647C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634694 | |||||||
| chr17:35634890 | T | C | 1 | a0001c0001t0003g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1156-1451T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634890 | |||||||
| chr17:35634953 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1156-1388C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634953 | |||||||
| chr17:35634990 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1156-1351C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35634990 | |||||||
| chr17:35635040 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1156-1301C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635040 | |||||||
| chr17:35635067 | T | G | 335 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(332): Show |
338 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.1156-1274T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635067 | |||||||
| chr17:35635068 | T | G | 1 | a0001c0002t0001g0221 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1156-1273T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635068 | |||||||
| chr17:35635146 | C | T | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1156-1195C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635146 | |||||||
| chr17:35635149 | G | C | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-1192G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635149 | |||||||
| chr17:35635184 | G | A | 8 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
8 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1156-1157G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635184 | |||||||
| chr17:35635262 | C | T | 155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1156-1079C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635262 | |||||||
| chr17:35635348 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1156-993C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635348 | |||||||
| chr17:35635377 | CTTTGT | C | 32 | a0001c0001t0004g0316 a0001c0001t0004g0319 a0001c0001t0004g0320 others(29): Show |
32 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1156-945_1156-941d others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35635377 | ||||||
| chr17:35635481 | T | A | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1156-860T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635481 | |||||||
| chr17:35635497 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1156-844C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635497 | |||||||
| chr17:35635503 | C | A | 1 | a0001c0002t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1156-838C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635503 | |||||||
| chr17:35635540 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-801C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635540 | |||||||
| chr17:35635574 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1156-767G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635574 | |||||||
| chr17:35635634 | G | A | 1 | a0001c0002t0001g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1156-707G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635634 | |||||||
| chr17:35635726 | C | T | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1156-615C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635726 | |||||||
| chr17:35635836 | A | C | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1156-505A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635836 | |||||||
| chr17:35635877 | C | T | 3 | a0001c0002t0010g0240 a0001c0002t0010g0253 a0001c0002t0010g0254 |
3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1156-464C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635877 | |||||||
| chr17:35635878 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1156-463G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635878 | |||||||
| chr17:35635967 | G | C | 1 | a0001c0002t0001g0197 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1156-374G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635967 | |||||||
| chr17:35635968 | C | A | 1 | a0001c0002t0001g0197 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1156-373C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35635968 | |||||||
| chr17:35635997 | A | AT | 310 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(307): Show |
312 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.1156-331dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 35635997 | ||||||
| chr17:35636119 | T | G | 3 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0277 |
3 | HG02572.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1156-222T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 9/21 | chr17 | 35636119 | |||||||
| chr17:35636592 | AT | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1271+138delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 35636592 | ||||||
| chr17:35636679 | A | G | 3 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0001g0257 |
3 | HG02559.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1271+223A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35636679 | |||||||
| chr17:35636859 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+403G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35636859 | |||||||
| chr17:35637017 | A | C | 3 | a0001c0002t0001g0230 a0001c0002t0001g0249 a0001c0002t0001g0279 |
3 | HG01934.hp2 NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1271+561A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637017 | |||||||
| chr17:35637178 | C | T | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1271+722C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637178 | |||||||
| chr17:35637209 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1271+753T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637209 | |||||||
| chr17:35637520 | C | G | 139 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(136): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1271+1064C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637520 | |||||||
| chr17:35637652 | T | G | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+1196T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637652 | |||||||
| chr17:35637690 | A | AT | 140 | a0001c0001t0004g0335 a0001c0001t0004g0336 a0001c0001t0004g0337 others(137): Show |
141 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1271+1249dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 35637690 | ||||||
| chr17:35637690 | AT | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1271+1249delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 35637690 | ||||||
| chr17:35637764 | C | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1271+1308C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637764 | |||||||
| chr17:35637831 | G | C | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1271+1375G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637831 | |||||||
| chr17:35637842 | A | G | 1 | a0001c0002t0001g0194 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1271+1386A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35637842 | |||||||
| chr17:35638105 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1272-1490G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638105 | |||||||
| chr17:35638232 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1272-1363G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638232 | |||||||
| chr17:35638405 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1272-1190T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638405 | |||||||
| chr17:35638564 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1031G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638564 | |||||||
| chr17:35638682 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1272-913G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638682 | |||||||
| chr17:35638720 | C | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-875C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638720 | |||||||
| chr17:35638737 | C | T | 2 | a0001c0002t0001g0288 a0001c0002t0001g0366 |
2 | HG01169.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1272-858C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638737 | |||||||
| chr17:35638768 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1272-827G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638768 | |||||||
| chr17:35638789 | GA | G | 326 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(323): Show |
329 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.1272-788delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 35638789 | ||||||
| chr17:35638789 | GAA | G | 9 | a0001c0001t0002g0070 a0001c0001t0002g0174 a0001c0001t0002g0367 others(6): Show |
9 | HG01070.hp1 HG02015.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-789_1272-788d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 35638789 | ||||||
| chr17:35638791 | A | G | 1 | a0001c0001t0003g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1272-804A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638791 | |||||||
| chr17:35638928 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1272-667C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35638928 | |||||||
| chr17:35639205 | A | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1272-390A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35639205 | |||||||
| chr17:35639362 | A | G | 6 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(3): Show |
6 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272-233A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35639362 | |||||||
| chr17:35639391 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-204G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35639391 | |||||||
| chr17:35639515 | G | A | 1 | a0001c0002t0001g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1272-80G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 10/21 | chr17 | 35639515 | |||||||
| chr17:35639916 | A | G | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1437+156A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35639916 | |||||||
| chr17:35640028 | T | C | 155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1437+268T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640028 | |||||||
| chr17:35640089 | A | G | 1 | a0001c0002t0001g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1437+329A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640089 | |||||||
| chr17:35640118 | T | C | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1437+358T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640118 | |||||||
| chr17:35640164 | G | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1437+404G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640164 | |||||||
| chr17:35640219 | T | G | 2 | a0001c0001t0004g0347 a0001c0001t0004g0354 |
2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1437+459T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640219 | |||||||
| chr17:35640227 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437+467A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640227 | |||||||
| chr17:35640231 | T | A | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1437+471T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640231 | |||||||
| chr17:35640231 | T | TTTA | 55 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(52): Show |
55 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1437+473_1437+474i others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 35640231 | ||||||
| chr17:35640235 | T | A | 56 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(53): Show |
56 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1437+475T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640235 | |||||||
| chr17:35640235 | T | TTTA | 187 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(184): Show |
188 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.1437+477_1437+478i others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 35640235 | ||||||
| chr17:35640239 | T | A | 243 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(240): Show |
244 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.1437+479T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640239 | |||||||
| chr17:35640239 | T | TTA | 25 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1437+480_1437+481i others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 35640239 | ||||||
| chr17:35640239 | T | TTTA | 67 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(64): Show |
69 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1437+481_1437+482i others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 35640239 | ||||||
| chr17:35640243 | T | A | 335 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(332): Show |
338 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.1437+483T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640243 | |||||||
| chr17:35640247 | T | A | 190 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0004g0158 others(187): Show |
191 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.1437+487T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640247 | |||||||
| chr17:35640251 | T | A | 3 | a0001c0002t0010g0240 a0001c0002t0010g0253 a0001c0002t0010g0254 |
3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1437+491T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640251 | |||||||
| chr17:35640427 | A | G | 1 | a0001c0002t0001g0273 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1437+667A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640427 | |||||||
| chr17:35640624 | G | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1437+864G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640624 | |||||||
| chr17:35640912 | G | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1438-965G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640912 | |||||||
| chr17:35640913 | A | G | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1438-964A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640913 | |||||||
| chr17:35640989 | C | G | 1 | a0001c0001t0008g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1438-888C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35640989 | |||||||
| chr17:35641032 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1438-845T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641032 | |||||||
| chr17:35641083 | A | G | 22 | a0001c0002t0001g0062 a0001c0002t0001g0191 a0001c0002t0001g0233 others(19): Show |
22 | HG00558.hp2 HG01993.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1438-794A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641083 | |||||||
| chr17:35641095 | C | T | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0363 |
3 | HG00738.hp2 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1438-782C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641095 | |||||||
| chr17:35641197 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1438-680A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641197 | |||||||
| chr17:35641238 | C | A | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438-639C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641238 | |||||||
| chr17:35641343 | C | T | 1 | a0001c0001t0021g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1438-534C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641343 | |||||||
| chr17:35641353 | G | A | 3 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0277 |
3 | HG02572.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1438-524G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641353 | |||||||
| chr17:35641362 | C | G | 1 | a0001c0002t0001g0366 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1438-515C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641362 | |||||||
| chr17:35641617 | T | G | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1438-260T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641617 | |||||||
| chr17:35641665 | G | C | 1 | a0001c0001t0003g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1438-212G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641665 | |||||||
| chr17:35641842 | A | G | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1438-35A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641842 | |||||||
| chr17:35641852 | A | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1438-25A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 11/21 | chr17 | 35641852 | |||||||
| chr17:35641995 | C | G | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+20C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35641995 | |||||||
| chr17:35642034 | A | G | 1 | a0001c0002t0001g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1536+59A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642034 | |||||||
| chr17:35642042 | C | T | 1 | a0001c0001t0009g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1536+67C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642042 | |||||||
| chr17:35642308 | AGTACCAT | A | 181 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.1536+336_1536+342d others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35642308 | ||||||
| chr17:35642388 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1536+413A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642388 | |||||||
| chr17:35642392 | T | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1536+417T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642392 | |||||||
| chr17:35642414 | G | T | 1 | a0001c0002t0001g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1536+439G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642414 | |||||||
| chr17:35642427 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1536+452T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642427 | |||||||
| chr17:35642449 | T | C | 2 | a0001c0002t0001g0208 a0001c0002t0001g0252 |
2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1536+474T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642449 | |||||||
| chr17:35642455 | T | C | 3 | a0001c0002t0001g0266 a0001c0002t0001g0267 a0001c0002t0001g0282 |
3 | HG01891.hp2 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1536+480T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642455 | |||||||
| chr17:35642507 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1536+532G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642507 | |||||||
| chr17:35642622 | A | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1536+647A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642622 | |||||||
| chr17:35642669 | T | TA | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536+695dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35642669 | ||||||
| chr17:35642672 | G | A | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+697G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642672 | |||||||
| chr17:35642674 | T | C | 5 | a0001c0002t0001g0198 a0001c0002t0001g0199 a0001c0002t0001g0225 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1536+699T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642674 | |||||||
| chr17:35642817 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1536+842C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642817 | |||||||
| chr17:35642825 | TA | T | 155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1536+857delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35642825 | ||||||
| chr17:35642892 | T | C | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1536+917T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35642892 | |||||||
| chr17:35643027 | C | CT | 9 | a0001c0001t0003g0009 a0001c0001t0008g0056 a0001c0001t0008g0057 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.1536+1066dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35643027 | ||||||
| chr17:35643089 | C | T | 3 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0001g0257 |
3 | HG02559.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1536+1114C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643089 | |||||||
| chr17:35643103 | C | T | 3 | a0001c0002t0001g0213 a0001c0002t0001g0218 a0001c0002t0001g0220 |
3 | NA18981.hp1 NA18990.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1536+1128C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643103 | |||||||
| chr17:35643179 | T | TA | 47 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(44): Show |
47 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1536+1216dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35643179 | ||||||
| chr17:35643238 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1536+1263T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643238 | |||||||
| chr17:35643688 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+1713C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643688 | |||||||
| chr17:35643753 | AGTC | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536+1782_1536+178 others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35643753 | ||||||
| chr17:35643792 | G | A | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+1817G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643792 | |||||||
| chr17:35643916 | A | T | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.1536+1941A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643916 | |||||||
| chr17:35643952 | A | G | 1 | a0001c0001t0017g0027 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1536+1977A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35643952 | |||||||
| chr17:35644083 | T | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1536+2108T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644083 | |||||||
| chr17:35644197 | G | A | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1536+2222G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644197 | |||||||
| chr17:35644202 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1536+2227T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644202 | |||||||
| chr17:35644544 | A | AT | 18 | a0001c0001t0002g0168 a0001c0001t0003g0043 a0001c0001t0003g0050 others(15): Show |
18 | HG01934.hp1 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1536+2587dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35644544 | ||||||
| chr17:35644640 | C | T | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1536+2665C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644640 | |||||||
| chr17:35644802 | G | A | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+2827G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644802 | |||||||
| chr17:35644895 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1536+2920A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644895 | |||||||
| chr17:35644947 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536+2972G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35644947 | |||||||
| chr17:35645170 | A | C | 50 | a0001c0001t0003g0047 a0001c0001t0004g0158 a0001c0001t0004g0316 others(47): Show |
50 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1536+3195A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645170 | |||||||
| chr17:35645210 | A | T | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1536+3235A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645210 | |||||||
| chr17:35645548 | G | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1536+3573G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645548 | |||||||
| chr17:35645615 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1536+3640C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645615 | |||||||
| chr17:35645670 | A | G | 1 | a0001c0001t0003g0015 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1536+3695A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645670 | |||||||
| chr17:35645771 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1536+3796C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645771 | |||||||
| chr17:35645862 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1536+3887A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35645862 | |||||||
| chr17:35646015 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1536+4040T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646015 | |||||||
| chr17:35646142 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1536+4167A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646142 | |||||||
| chr17:35646292 | G | A | 181 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.1537-4238G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646292 | |||||||
| chr17:35646395 | GT | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1537-4133delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35646395 | ||||||
| chr17:35646443 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-4087C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646443 | |||||||
| chr17:35646586 | A | AT | 102 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0065 others(99): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1537-3927dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35646586 | ||||||
| chr17:35646586 | AT | A | 9 | a0001c0001t0001g0129 a0001c0001t0002g0355 a0001c0001t0002g0356 others(6): Show |
9 | HG01361.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-3927delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35646586 | ||||||
| chr17:35646603 | T | TG | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-3926dupG | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35646603 | ||||||
| chr17:35646643 | T | C | 66 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(63): Show |
67 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1537-3887T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646643 | |||||||
| chr17:35646656 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-3874G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646656 | |||||||
| chr17:35646677 | C | T | 1 | a0001c0002t0001g0220 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1537-3853C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646677 | |||||||
| chr17:35646732 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-3798A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35646732 | |||||||
| chr17:35647151 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1537-3379C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647151 | |||||||
| chr17:35647195 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1537-3335A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647195 | |||||||
| chr17:35647391 | C | A | 10 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(7): Show |
10 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-3139C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647391 | |||||||
| chr17:35647462 | G | A | 144 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(141): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1537-3068G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647462 | |||||||
| chr17:35647642 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1537-2888G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647642 | |||||||
| chr17:35647713 | A | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-2817A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647713 | |||||||
| chr17:35647873 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1537-2657T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647873 | |||||||
| chr17:35647891 | G | GT | 331 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(328): Show |
334 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.1537-2626dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35647891 | ||||||
| chr17:35647891 | G | T | 1 | a0001c0001t0003g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1537-2639G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35647891 | |||||||
| chr17:35648034 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1537-2496G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648034 | |||||||
| chr17:35648121 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-2409T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648121 | |||||||
| chr17:35648174 | A | C | 1 | a0001c0001t0002g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1537-2356A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648174 | |||||||
| chr17:35648181 | A | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0170 a0001c0001t0002g0173 others(1): Show |
5 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1537-2349A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648181 | |||||||
| chr17:35648213 | A | T | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1537-2317A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648213 | |||||||
| chr17:35648274 | G | T | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1537-2256G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648274 | |||||||
| chr17:35648386 | C | T | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-2144C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648386 | |||||||
| chr17:35648387 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1537-2143G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648387 | |||||||
| chr17:35648524 | GCATA | G | 56 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1537-1971_1537-196 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648524 | ||||||
| chr17:35648524 | GCATACAT others(1): Show |
G | 280 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(277): Show |
282 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.1537-1975_1537-196 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648524 | ||||||
| chr17:35648740 | A | G | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537-1790A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648740 | |||||||
| chr17:35648742 | A | G | 2 | a0001c0003t0001g0215 a0001c0003t0001g0298 |
2 | NA18987.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1537-1788A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648742 | |||||||
| chr17:35648743 | A | AGT | 14 | a0001c0001t0004g0337 a0001c0001t0004g0347 a0001c0001t0004g0350 others(11): Show |
14 | HG00733.hp2 HG01192.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1537-1757_1537-175 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGT | 36 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(33): Show |
36 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1537-1759_1537-175 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGTGT | 31 | a0001c0001t0004g0341 a0001c0001t0009g0159 a0001c0001t0009g0160 others(28): Show |
31 | HG01981.hp1 HG01993.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.1537-1761_1537-175 others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGTGTG others(1): Show |
66 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(63): Show |
66 | HG00438.hp1 HG00738.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1537-1763_1537-175 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGTGTG others(3): Show |
22 | a0001c0002t0001g0192 a0001c0002t0001g0200 a0001c0002t0001g0222 others(19): Show |
22 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1537-1765_1537-175 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGTGTG others(5): Show |
13 | a0001c0002t0001g0005 a0001c0002t0001g0184 a0001c0002t0001g0191 others(10): Show |
14 | HG01256.hp1 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1537-1767_1537-175 others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | AGTGTGTG others(7): Show |
1 | a0001c0002t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1537-1769_1537-175 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | A | T | 2 | a0001c0003t0001g0215 a0001c0003t0001g0298 |
2 | NA18987.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1537-1787A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648743 | |||||||
| chr17:35648743 | AGTGT | A | 3 | a0001c0001t0002g0086 a0001c0001t0002g0115 a0001c0001t0002g0117 |
3 | HG01081.hp2 HG01243.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1537-1759_1537-175 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | AGTGTGT | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(69): Show |
73 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1537-1761_1537-175 others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | AGTGTGTG others(1): Show |
A | 71 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1537-1763_1537-175 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648743 | AGTGTGTG others(7): Show |
A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-1769_1537-175 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 35648743 | ||||||
| chr17:35648773 | T | A | 1 | a0001c0001t0003g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1537-1757T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648773 | |||||||
| chr17:35648798 | A | T | 1 | a0001c0002t0001g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1537-1732A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35648798 | |||||||
| chr17:35649094 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1537-1436G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649094 | |||||||
| chr17:35649222 | T | G | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1537-1308T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649222 | |||||||
| chr17:35649263 | G | T | 1 | a0001c0002t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1537-1267G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649263 | |||||||
| chr17:35649265 | T | A | 1 | a0001c0002t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1537-1265T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649265 | |||||||
| chr17:35649274 | T | A | 1 | a0001c0004t0002g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1537-1256T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649274 | |||||||
| chr17:35649276 | TC | T | 9 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-1253delC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649276 | |||||||
| chr17:35649277 | C | T | 331 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(328): Show |
334 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.1537-1253C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649277 | |||||||
| chr17:35649291 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1537-1239G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649291 | |||||||
| chr17:35649431 | G | A | 1 | a0001c0001t0004g0343 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1537-1099G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649431 | |||||||
| chr17:35649516 | C | T | 130 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(127): Show |
131 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.1537-1014C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649516 | |||||||
| chr17:35649554 | G | A | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537-976G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649554 | |||||||
| chr17:35649566 | G | C | 1 | a0001c0002t0001g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1537-964G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649566 | |||||||
| chr17:35649600 | C | T | 70 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(67): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1537-930C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649600 | |||||||
| chr17:35649604 | T | G | 1 | a0001c0002t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1537-926T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649604 | |||||||
| chr17:35649605 | C | A | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1537-925C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649605 | |||||||
| chr17:35649765 | A | G | 1 | a0001c0002t0001g0312 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1537-765A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649765 | |||||||
| chr17:35649870 | T | C | 1 | a0001c0002t0001g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1537-660T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649870 | |||||||
| chr17:35649914 | G | A | 3 | a0001c0004t0002g0164 a0001c0004t0002g0165 a0001c0004t0002g0176 |
3 | HG01123.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1537-616G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649914 | |||||||
| chr17:35649961 | A | T | 1 | a0001c0001t0004g0332 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1537-569A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35649961 | |||||||
| chr17:35650142 | G | A | 10 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-388G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650142 | |||||||
| chr17:35650282 | G | C | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1537-248G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650282 | |||||||
| chr17:35650283 | C | A | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1537-247C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650283 | |||||||
| chr17:35650471 | T | C | 1 | a0001c0001t0008g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1537-59T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650471 | |||||||
| chr17:35650516 | T | G | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1537-14T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650516 | |||||||
| chr17:35650519 | C | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-11C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 12/21 | chr17 | 35650519 | |||||||
| chr17:35650876 | G | T | 1 | a0001c0001t0006g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1796+87G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35650876 | |||||||
| chr17:35650959 | A | C | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1796+170A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35650959 | |||||||
| chr17:35651005 | G | C | 1 | a0001c0002t0010g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1796+216G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651005 | |||||||
| chr17:35651079 | T | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1796+290T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651079 | |||||||
| chr17:35651166 | A | G | 1 | a0001c0001t0003g0034 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1796+377A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651166 | |||||||
| chr17:35651204 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+415T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651204 | |||||||
| chr17:35651248 | C | A | 1 | a0001c0001t0015g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1796+459C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651248 | |||||||
| chr17:35651283 | T | TA | 18 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(15): Show |
18 | HG01074.hp2 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1796+504dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35651283 | ||||||
| chr17:35651283 | TA | T | 10 | a0001c0001t0002g0090 a0001c0001t0020g0151 a0001c0002t0001g0289 others(7): Show |
10 | HG00280.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1796+504delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35651283 | ||||||
| chr17:35651438 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1796+649G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651438 | |||||||
| chr17:35651439 | A | G | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1796+650A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651439 | |||||||
| chr17:35651441 | A | C | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1796+652A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651441 | |||||||
| chr17:35651521 | T | C | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1796+732T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651521 | |||||||
| chr17:35651635 | G | A | 2 | a0001c0002t0001g0200 a0001c0002t0001g0203 |
2 | HG01074.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1796+846G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651635 | |||||||
| chr17:35651664 | G | A | 1 | a0001c0002t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1796+875G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651664 | |||||||
| chr17:35651714 | G | GA | 148 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(145): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1796+935dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35651714 | ||||||
| chr17:35651785 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1796+996C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651785 | |||||||
| chr17:35651787 | G | C | 1 | a0001c0001t0002g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1796+998G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651787 | |||||||
| chr17:35651871 | AAACATGT | A | 13 | a0001c0001t0006g0064 a0001c0001t0006g0069 a0001c0001t0006g0071 others(10): Show |
13 | HG01069.hp1 HG01070.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1796+1083_1796+108 others(11): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35651871 | |||||||
| chr17:35652060 | A | G | 3 | a0001c0001t0004g0323 a0001c0001t0004g0324 a0001c0001t0004g0334 |
3 | NA18946.hp2 NA18988.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1796+1271A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652060 | |||||||
| chr17:35652102 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1796+1313C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652102 | |||||||
| chr17:35652120 | A | T | 10 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796+1331A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652120 | |||||||
| chr17:35652122 | A | G | 1 | a0001c0002t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1796+1333A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652122 | |||||||
| chr17:35652129 | C | T | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1796+1340C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652129 | |||||||
| chr17:35652781 | A | G | 3 | a0001c0002t0001g0224 a0001c0002t0001g0232 a0001c0002t0001g0246 |
3 | HG01109.hp1 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1796+1992A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35652781 | |||||||
| chr17:35653344 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+2555C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653344 | |||||||
| chr17:35653547 | C | T | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1796+2758C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653547 | |||||||
| chr17:35653626 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0015g0131 |
3 | HG01109.hp2 HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1796+2837A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653626 | |||||||
| chr17:35653658 | T | C | 1 | a0001c0002t0001g0275 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1796+2869T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653658 | |||||||
| chr17:35653720 | G | T | 1 | a0001c0001t0003g0023 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1796+2931G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653720 | |||||||
| chr17:35653843 | G | A | 4 | a0001c0001t0003g0029 a0001c0001t0003g0031 a0001c0001t0003g0051 others(1): Show |
4 | HG00673.hp1 HG02129.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+3054G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35653843 | |||||||
| chr17:35654221 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1797-3378C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654221 | |||||||
| chr17:35654229 | T | A | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1797-3370T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654229 | |||||||
| chr17:35654284 | A | G | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1797-3315A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654284 | |||||||
| chr17:35654359 | C | T | 1 | a0001c0001t0004g0354 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1797-3240C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654359 | |||||||
| chr17:35654364 | G | GT | 10 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(7): Show |
10 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1797-3228dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35654364 | ||||||
| chr17:35654568 | G | A | 1 | a0001c0002t0001g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1797-3031G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654568 | |||||||
| chr17:35654677 | C | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797-2922C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654677 | |||||||
| chr17:35654685 | C | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1797-2914C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654685 | |||||||
| chr17:35654737 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0108 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1797-2862G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654737 | |||||||
| chr17:35654749 | T | C | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1797-2850T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654749 | |||||||
| chr17:35654876 | TGC | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797-2722_1797-272 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654876 | |||||||
| chr17:35654893 | A | G | 36 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(33): Show |
36 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1797-2706A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654893 | |||||||
| chr17:35654944 | T | C | 2 | a0001c0002t0001g0224 a0001c0002t0001g0246 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1797-2655T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654944 | |||||||
| chr17:35654950 | C | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1797-2649C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654950 | |||||||
| chr17:35654988 | C | T | 1 | a0001c0001t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1797-2611C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654988 | |||||||
| chr17:35654989 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-2610G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35654989 | |||||||
| chr17:35655044 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1797-2555A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655044 | |||||||
| chr17:35655099 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1797-2500A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655099 | |||||||
| chr17:35655147 | T | G | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1797-2452T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655147 | |||||||
| chr17:35655462 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797-2137G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655462 | |||||||
| chr17:35655494 | T | C | 1 | a0001c0001t0004g0335 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1797-2105T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655494 | |||||||
| chr17:35655526 | A | G | 1 | a0001c0004t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1797-2073A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655526 | |||||||
| chr17:35655560 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797-2039A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655560 | |||||||
| chr17:35655600 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1797-1999A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655600 | |||||||
| chr17:35655672 | C | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0013 |
2 | NA18946.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1797-1927C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655672 | |||||||
| chr17:35655739 | A | G | 3 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0001g0257 |
3 | HG02559.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1797-1860A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655739 | |||||||
| chr17:35655889 | G | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1797-1710G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35655889 | |||||||
| chr17:35656065 | A | G | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797-1534A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656065 | |||||||
| chr17:35656185 | G | T | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1797-1414G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656185 | |||||||
| chr17:35656265 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-1334C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656265 | |||||||
| chr17:35656268 | T | TAGGGGGC others(1): Show |
155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1797-1329_1797-132 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35656268 | ||||||
| chr17:35656268 | T | TAGGGGGC others(9): Show |
181 | a0001c0001t0003g0021 a0001c0001t0004g0158 a0001c0001t0004g0316 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.1797-1322_1797-132 others(20): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35656268 | ||||||
| chr17:35656348 | C | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1797-1251C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656348 | |||||||
| chr17:35656516 | C | A | 1 | a0001c0001t0002g0111 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1797-1083C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656516 | |||||||
| chr17:35656692 | G | A | 5 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1797-907G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656692 | |||||||
| chr17:35656705 | T | A | 1 | a0001c0002t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1797-894T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656705 | |||||||
| chr17:35656707 | C | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(51): Show |
55 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1797-892C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656707 | |||||||
| chr17:35656727 | CA | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797-864delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35656727 | ||||||
| chr17:35656789 | G | A | 43 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(40): Show |
43 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1797-810G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656789 | |||||||
| chr17:35656822 | T | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1797-777T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656822 | |||||||
| chr17:35656842 | G | A | 1 | a0001c0001t0009g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1797-757G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656842 | |||||||
| chr17:35656884 | C | CA | 319 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(316): Show |
322 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.1797-699dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35656884 | ||||||
| chr17:35656884 | C | CAA | 18 | a0001c0001t0002g0066 a0001c0001t0002g0112 a0001c0001t0002g0113 others(15): Show |
18 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1797-700_1797-699d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 35656884 | ||||||
| chr17:35656972 | A | G | 47 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(44): Show |
47 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1797-627A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656972 | |||||||
| chr17:35656977 | T | C | 1 | a0001c0002t0011g0236 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1797-622T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35656977 | |||||||
| chr17:35657153 | C | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1797-446C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35657153 | |||||||
| chr17:35657300 | T | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-299T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35657300 | |||||||
| chr17:35657305 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1797-294T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35657305 | |||||||
| chr17:35657487 | C | G | 3 | a0001c0001t0005g0136 a0001c0001t0005g0147 a0001c0001t0005g0152 |
3 | HG00140.hp2 HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1797-112C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 13/21 | chr17 | 35657487 | |||||||
| chr17:35657920 | A | G | 3 | a0001c0002t0001g0192 a0001c0002t0001g0259 a0001c0002t0001g0264 |
3 | HG02055.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1989+129A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35657920 | |||||||
| chr17:35657950 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1989+159A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35657950 | |||||||
| chr17:35658019 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1989+228C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35658019 | |||||||
| chr17:35658263 | C | CT | 13 | a0001c0001t0002g0085 a0001c0001t0002g0112 a0001c0001t0002g0113 others(10): Show |
13 | HG00323.hp2 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1989+481dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35658263 | ||||||
| chr17:35658282 | C | CT | 253 | a0001c0001t0001g0129 a0001c0001t0002g0004 a0001c0001t0002g0087 others(250): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1989+504dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35658282 | ||||||
| chr17:35658282 | C | CTT | 71 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(68): Show |
72 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1989+503_1989+504d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35658282 | ||||||
| chr17:35658329 | G | A | 5 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0001c0001t0002g0115 others(2): Show |
5 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+538G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35658329 | |||||||
| chr17:35658503 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1989+712G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35658503 | |||||||
| chr17:35658830 | C | T | 180 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(177): Show |
181 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.1989+1039C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35658830 | |||||||
| chr17:35658958 | C | T | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989+1167C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35658958 | |||||||
| chr17:35659043 | A | G | 2 | a0001c0001t0003g0042 a0002c0007t0003g0041 |
2 | NA18964.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1989+1252A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659043 | |||||||
| chr17:35659128 | G | A | 2 | a0001c0002t0001g0191 a0001c0002t0001g0238 |
2 | NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1989+1337G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659128 | |||||||
| chr17:35659250 | A | G | 1 | a0001c0002t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1989+1459A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659250 | |||||||
| chr17:35659315 | G | C | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1989+1524G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659315 | |||||||
| chr17:35659750 | C | G | 2 | a0001c0001t0004g0327 a0001c0001t0004g0353 |
2 | NA18954.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1989+1959C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659750 | |||||||
| chr17:35659889 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1989+2098A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659889 | |||||||
| chr17:35659957 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1989+2166G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35659957 | |||||||
| chr17:35660015 | T | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1989+2224T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660015 | |||||||
| chr17:35660234 | G | A | 1 | a0001c0001t0003g0030 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1989+2443G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660234 | |||||||
| chr17:35660280 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1989+2489G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660280 | |||||||
| chr17:35660290 | G | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989+2499G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660290 | |||||||
| chr17:35660470 | T | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1989+2679T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660470 | |||||||
| chr17:35660481 | C | CT | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1989+2708dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35660481 | ||||||
| chr17:35660481 | C | CTT | 8 | a0001c0001t0004g0335 a0001c0001t0004g0337 a0001c0001t0004g0342 others(5): Show |
8 | HG01891.hp1 NA18961.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.1989+2707_1989+270 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35660481 | ||||||
| chr17:35660481 | CT | C | 50 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(47): Show |
50 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1989+2708delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35660481 | ||||||
| chr17:35660483 | T | C | 2 | a0001c0001t0002g0168 a0001c0003t0001g0307 |
2 | HG03927.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1989+2692T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660483 | |||||||
| chr17:35660545 | G | GT | 3 | a0001c0002t0001g0222 a0001c0002t0001g0223 a0001c0002t0001g0231 |
3 | HG02970.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1989+2755dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35660545 | ||||||
| chr17:35660631 | C | T | 1 | a0001c0001t0004g0343 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1989+2840C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35660631 | |||||||
| chr17:35661035 | G | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1989+3244G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35661035 | |||||||
| chr17:35661399 | G | C | 1 | a0001c0001t0007g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1989+3608G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35661399 | |||||||
| chr17:35661434 | C | A | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.1989+3643C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35661434 | |||||||
| chr17:35661567 | A | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1989+3776A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35661567 | |||||||
| chr17:35661940 | C | A | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1989+4149C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35661940 | |||||||
| chr17:35662068 | C | G | 1 | a0001c0002t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1989+4277C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662068 | |||||||
| chr17:35662106 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989+4315C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662106 | |||||||
| chr17:35662272 | A | G | 1 | a0001c0001t0006g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1989+4481A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662272 | |||||||
| chr17:35662289 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1989+4498G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662289 | |||||||
| chr17:35662306 | CTT | C | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1989+4518_1989+451 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35662306 | ||||||
| chr17:35662322 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1989+4531A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662322 | |||||||
| chr17:35662389 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1989+4598A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662389 | |||||||
| chr17:35662500 | C | T | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1989+4709C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662500 | |||||||
| chr17:35662532 | G | GT | 9 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0003g0008 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1989+4760dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35662532 | ||||||
| chr17:35662532 | G | T | 5 | a0001c0001t0007g0007 a0001c0001t0007g0156 a0001c0001t0007g0157 others(2): Show |
5 | HG01106.hp1 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+4741G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662532 | |||||||
| chr17:35662532 | GT | G | 191 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(188): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1989+4760delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35662532 | ||||||
| chr17:35662538 | T | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1989+4747T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662538 | |||||||
| chr17:35662539 | T | G | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1989+4748T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662539 | |||||||
| chr17:35662565 | T | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1989+4774T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662565 | |||||||
| chr17:35662611 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989+4820G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662611 | |||||||
| chr17:35662675 | C | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.1989+4884C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662675 | |||||||
| chr17:35662676 | A | G | 3 | a0001c0001t0004g0316 a0001c0001t0004g0341 a0001c0001t0004g0343 |
3 | HG01261.hp1 HG01981.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1989+4885A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662676 | |||||||
| chr17:35662693 | A | C | 1 | a0001c0001t0003g0018 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1989+4902A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662693 | |||||||
| chr17:35662740 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1989+4949G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662740 | |||||||
| chr17:35662852 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1989+5061G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662852 | |||||||
| chr17:35662996 | A | G | 2 | a0001c0001t0004g0337 a0001c0001t0004g0350 |
2 | NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1989+5205A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35662996 | |||||||
| chr17:35663023 | T | C | 5 | a0001c0002t0001g0206 a0001c0002t0001g0224 a0001c0002t0001g0232 others(2): Show |
5 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+5232T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35663023 | |||||||
| chr17:35663272 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1989+5481G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35663272 | |||||||
| chr17:35663447 | AC | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1989+5659delC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35663447 | ||||||
| chr17:35663633 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1989+5842A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35663633 | |||||||
| chr17:35663712 | T | G | 3 | a0001c0002t0001g0224 a0001c0002t0001g0232 a0001c0002t0001g0246 |
3 | HG01109.hp1 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1989+5921T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35663712 | |||||||
| chr17:35664482 | A | G | 1 | a0001c0001t0004g0322 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1990-6375A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664482 | |||||||
| chr17:35664492 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1990-6365A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664492 | |||||||
| chr17:35664522 | T | C | 1 | a0001c0002t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1990-6335T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664522 | |||||||
| chr17:35664572 | A | G | 3 | a0001c0001t0002g0081 a0001c0001t0002g0086 a0001c0001t0002g0088 |
3 | HG00735.hp1 HG01106.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1990-6285A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664572 | |||||||
| chr17:35664631 | C | T | 41 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(38): Show |
41 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1990-6226C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664631 | |||||||
| chr17:35664786 | G | T | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-6071G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664786 | |||||||
| chr17:35664907 | A | C | 1 | a0001c0002t0001g0363 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1990-5950A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664907 | |||||||
| chr17:35664921 | C | T | 4 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0104 others(1): Show |
4 | NA18940.hp1 NA19007.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990-5936C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664921 | |||||||
| chr17:35664933 | C | G | 1 | a0001c0001t0003g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1990-5924C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664933 | |||||||
| chr17:35664954 | C | T | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1990-5903C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35664954 | |||||||
| chr17:35665009 | C | T | 50 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1990-5848C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35665009 | |||||||
| chr17:35665126 | C | CT | 133 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(130): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1990-5713dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35665126 | ||||||
| chr17:35665126 | C | CTT | 158 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0001c0001t0002g0115 others(155): Show |
159 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1990-5714_1990-571 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35665126 | ||||||
| chr17:35665126 | C | CTTT | 6 | a0001c0001t0007g0346 a0001c0001t0007g0348 a0001c0002t0001g0191 others(3): Show |
6 | HG00597.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1990-5715_1990-571 others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35665126 | ||||||
| chr17:35665196 | G | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1990-5661G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35665196 | |||||||
| chr17:35665710 | T | G | 2 | a0001c0001t0005g0132 a0001c0001t0005g0143 |
2 | NA18989.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1990-5147T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35665710 | |||||||
| chr17:35665831 | T | C | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1990-5026T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35665831 | |||||||
| chr17:35666010 | G | A | 1 | a0001c0004t0002g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1990-4847G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666010 | |||||||
| chr17:35666037 | CTT | C | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | NA18943.hp2 NA18987.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1990-4819_1990-481 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666037 | |||||||
| chr17:35666131 | G | A | 3 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0277 |
3 | HG02572.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1990-4726G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666131 | |||||||
| chr17:35666133 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-4724G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666133 | |||||||
| chr17:35666166 | C | G | 1 | a0001c0001t0008g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1990-4691C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666166 | |||||||
| chr17:35666208 | A | G | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-4649A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666208 | |||||||
| chr17:35666236 | CCT | C | 4 | a0001c0001t0017g0027 a0001c0002t0001g0266 a0001c0002t0001g0267 others(1): Show |
4 | HG00673.hp1 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-4620_1990-461 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666236 | |||||||
| chr17:35666274 | GAC | G | 41 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(38): Show |
41 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1990-4579_1990-457 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35666274 | ||||||
| chr17:35666395 | C | G | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1990-4462C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666395 | |||||||
| chr17:35666437 | G | A | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1990-4420G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666437 | |||||||
| chr17:35666457 | A | T | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1990-4400A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666457 | |||||||
| chr17:35666553 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1990-4304C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666553 | |||||||
| chr17:35666659 | C | G | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1990-4198C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666659 | |||||||
| chr17:35666696 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1990-4161A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35666696 | |||||||
| chr17:35667017 | A | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1990-3840A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667017 | |||||||
| chr17:35667547 | C | T | 140 | a0001c0001t0004g0338 a0001c0002t0001g0005 a0001c0002t0001g0062 others(137): Show |
141 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1990-3310C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667547 | |||||||
| chr17:35667678 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-3179A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667678 | |||||||
| chr17:35667860 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1990-2997A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667860 | |||||||
| chr17:35667884 | T | C | 1 | a0001c0003t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1990-2973T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667884 | |||||||
| chr17:35667896 | C | T | 5 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0001c0001t0002g0115 others(2): Show |
5 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1990-2961C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667896 | |||||||
| chr17:35667897 | G | T | 1 | a0001c0002t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1990-2960G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667897 | |||||||
| chr17:35667898 | T | C | 1 | a0001c0002t0001g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1990-2959T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667898 | |||||||
| chr17:35667933 | A | AT | 128 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(125): Show |
129 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1990-2902dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35667933 | ||||||
| chr17:35667933 | A | ATT | 25 | a0001c0001t0002g0004 a0001c0001t0002g0116 a0001c0001t0002g0168 others(22): Show |
26 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1990-2903_1990-290 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35667933 | ||||||
| chr17:35667933 | AT | A | 11 | a0001c0001t0005g0133 a0001c0001t0005g0148 a0001c0002t0001g0184 others(8): Show |
11 | HG01256.hp1 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1990-2902delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35667933 | ||||||
| chr17:35667961 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1990-2896G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35667961 | |||||||
| chr17:35668026 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1990-2831C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668026 | |||||||
| chr17:35668184 | G | A | 1 | a0001c0002t0001g0205 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1990-2673G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668184 | |||||||
| chr17:35668189 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-2668G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668189 | |||||||
| chr17:35668211 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1990-2646A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668211 | |||||||
| chr17:35668237 | T | C | 1 | a0001c0002t0001g0364 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1990-2620T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668237 | |||||||
| chr17:35668433 | C | T | 1 | a0001c0001t0005g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1990-2424C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668433 | |||||||
| chr17:35668682 | C | G | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1990-2175C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35668682 | |||||||
| chr17:35669083 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-1774G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669083 | |||||||
| chr17:35669142 | CT | C | 334 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(331): Show |
337 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.1990-1699delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 35669142 | ||||||
| chr17:35669158 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-1699T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669158 | |||||||
| chr17:35669265 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1990-1592T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669265 | |||||||
| chr17:35669448 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1990-1409G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669448 | |||||||
| chr17:35669462 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-1395T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669462 | |||||||
| chr17:35669539 | G | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1990-1318G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669539 | |||||||
| chr17:35669745 | A | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.1990-1112A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669745 | |||||||
| chr17:35669757 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-1100G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669757 | |||||||
| chr17:35669780 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1990-1077C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669780 | |||||||
| chr17:35669831 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-1026A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669831 | |||||||
| chr17:35669955 | T | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1990-902T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669955 | |||||||
| chr17:35669970 | A | G | 2 | a0001c0001t0007g0346 a0001c0001t0007g0348 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1990-887A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35669970 | |||||||
| chr17:35670010 | T | G | 4 | a0001c0003t0001g0300 a0001c0003t0001g0301 a0001c0003t0001g0302 others(1): Show |
4 | HG02071.hp2 NA18962.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990-847T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670010 | |||||||
| chr17:35670188 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1990-669T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670188 | |||||||
| chr17:35670313 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1990-544T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670313 | |||||||
| chr17:35670490 | A | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0100 |
2 | NA18943.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1990-367A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670490 | |||||||
| chr17:35670592 | G | C | 1 | a0001c0001t0008g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1990-265G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670592 | |||||||
| chr17:35670638 | A | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1990-219A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670638 | |||||||
| chr17:35670737 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1990-120A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 14/21 | chr17 | 35670737 | |||||||
| chr17:35670935 | T | A | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.2031+37T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 15/21 | chr17 | 35670935 | |||||||
| chr17:35671119 | G | A | 6 | a0001c0002t0001g0269 a0001c0002t0001g0270 a0001c0002t0001g0272 others(3): Show |
6 | HG02074.hp1 HG02155.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2031+221G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 15/21 | chr17 | 35671119 | |||||||
| chr17:35671574 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2032-180C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 15/21 | chr17 | 35671574 | |||||||
| chr17:35671664 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2032-90A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 15/21 | chr17 | 35671664 | |||||||
| chr17:35672145 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2178+245T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672145 | |||||||
| chr17:35672243 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2178+343C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672243 | |||||||
| chr17:35672348 | A | G | 10 | a0001c0001t0004g0158 a0001c0004t0002g0125 a0001c0004t0002g0126 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2178+448A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672348 | |||||||
| chr17:35672387 | T | C | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2178+487T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672387 | |||||||
| chr17:35672416 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2178+516G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672416 | |||||||
| chr17:35672490 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2178+590G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672490 | |||||||
| chr17:35672498 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2178+598C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672498 | |||||||
| chr17:35672837 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2178+937G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35672837 | |||||||
| chr17:35673220 | A | AT | 10 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2179-947dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 35673220 | ||||||
| chr17:35673289 | C | T | 181 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.2179-887C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673289 | |||||||
| chr17:35673377 | C | T | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2179-799C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673377 | |||||||
| chr17:35673386 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2179-790A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673386 | |||||||
| chr17:35673479 | G | A | 1 | a0001c0002t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2179-697G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673479 | |||||||
| chr17:35673599 | G | A | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2179-577G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673599 | |||||||
| chr17:35673609 | G | A | 155 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.2179-567G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673609 | |||||||
| chr17:35673629 | A | G | 2 | a0001c0003t0001g0302 a0001c0003t0001g0303 |
2 | NA18962.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2179-547A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35673629 | |||||||
| chr17:35674102 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2179-74T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35674102 | |||||||
| chr17:35674105 | T | G | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2179-71T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35674105 | |||||||
| chr17:35674120 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2179-56G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 16/21 | chr17 | 35674120 | |||||||
| chr17:35674662 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2324+341G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674662 | |||||||
| chr17:35674666 | A | G | 1 | a0001c0001t0006g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2324+345A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674666 | |||||||
| chr17:35674782 | A | G | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2324+461A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674782 | |||||||
| chr17:35674877 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2324+556G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674877 | |||||||
| chr17:35674949 | C | T | 1 | a0001c0002t0001g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2324+628C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674949 | |||||||
| chr17:35674977 | G | T | 1 | a0001c0001t0003g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2324+656G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674977 | |||||||
| chr17:35674978 | C | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2324+657C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35674978 | |||||||
| chr17:35675205 | A | T | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2324+884A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675205 | |||||||
| chr17:35675209 | A | T | 9 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2324+888A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675209 | |||||||
| chr17:35675273 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+952G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675273 | |||||||
| chr17:35675343 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2324+1022A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675343 | |||||||
| chr17:35675352 | A | G | 2 | a0001c0002t0001g0191 a0001c0002t0001g0238 |
2 | NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2324+1031A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675352 | |||||||
| chr17:35675620 | C | CT | 8 | a0001c0001t0004g0326 a0001c0001t0008g0056 a0001c0001t0008g0057 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2324+1310dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35675620 | ||||||
| chr17:35675631 | T | C | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+1310T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675631 | |||||||
| chr17:35675633 | C | T | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+1312C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675633 | |||||||
| chr17:35675645 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2324+1324T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675645 | |||||||
| chr17:35675811 | C | T | 138 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.2324+1490C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675811 | |||||||
| chr17:35675823 | CTA | C | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2324+1503_2324+150 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675823 | |||||||
| chr17:35675956 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2324+1635G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675956 | |||||||
| chr17:35675999 | T | A | 1 | a0001c0001t0005g0142 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2324+1678T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35675999 | |||||||
| chr17:35676071 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2324+1750A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676071 | |||||||
| chr17:35676139 | T | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2324+1818T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676139 | |||||||
| chr17:35676379 | C | T | 4 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(1): Show |
4 | HG01074.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2324+2058C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676379 | |||||||
| chr17:35676385 | A | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2324+2064A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676385 | |||||||
| chr17:35676678 | A | C | 1 | a0001c0001t0003g0020 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2324+2357A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676678 | |||||||
| chr17:35676791 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2324+2470A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676791 | |||||||
| chr17:35676792 | T | TTC | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2324+2471_2324+247 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676792 | |||||||
| chr17:35676793 | A | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2324+2472A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676793 | |||||||
| chr17:35676845 | G | C | 1 | a0001c0002t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2324+2524G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676845 | |||||||
| chr17:35676861 | C | T | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2324+2540C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676861 | |||||||
| chr17:35676977 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2324+2656C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35676977 | |||||||
| chr17:35677053 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2324+2732A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35677053 | |||||||
| chr17:35677320 | T | G | 1 | a0001c0001t0006g0071 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2324+2999T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35677320 | |||||||
| chr17:35677624 | T | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2324+3303T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35677624 | |||||||
| chr17:35677860 | GT | G | 317 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(314): Show |
320 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.2324+3555delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35677860 | ||||||
| chr17:35677860 | GTT | G | 7 | a0001c0001t0002g0065 a0001c0001t0002g0084 a0001c0001t0008g0056 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2324+3554_2324+355 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35677860 | ||||||
| chr17:35677946 | G | A | 5 | a0001c0002t0001g0198 a0001c0002t0001g0199 a0001c0002t0001g0225 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2324+3625G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35677946 | |||||||
| chr17:35678067 | C | A | 1 | a0001c0002t0001g0282 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2324+3746C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678067 | |||||||
| chr17:35678108 | C | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2324+3787C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678108 | |||||||
| chr17:35678245 | T | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2324+3924T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678245 | |||||||
| chr17:35678494 | C | T | 336 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(333): Show |
339 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2324+4173C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678494 | |||||||
| chr17:35678566 | A | G | 2 | a0001c0002t0001g0361 a0001c0002t0001g0364 |
2 | HG00733.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2325-4129A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678566 | |||||||
| chr17:35678582 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2325-4113G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35678582 | |||||||
| chr17:35678959 | GTTGT | G | 181 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(178): Show |
182 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.2325-3717_2325-371 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35678959 | ||||||
| chr17:35679092 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2325-3603T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679092 | |||||||
| chr17:35679212 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2325-3483G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679212 | |||||||
| chr17:35679231 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2325-3464C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679231 | |||||||
| chr17:35679281 | T | A | 4 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(1): Show |
4 | HG01074.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2325-3414T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679281 | |||||||
| chr17:35679391 | C | CT | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2325-3290dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35679391 | ||||||
| chr17:35679391 | CT | C | 11 | a0001c0001t0002g0106 a0001c0001t0004g0318 a0001c0001t0004g0319 others(8): Show |
11 | HG00673.hp2 HG01891.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.2325-3290delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35679391 | ||||||
| chr17:35679510 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2325-3185A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679510 | |||||||
| chr17:35679548 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2325-3147T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679548 | |||||||
| chr17:35679549 | C | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2325-3146C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679549 | |||||||
| chr17:35679587 | C | CT | 284 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.2325-3108_2325-310 others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679587 | |||||||
| chr17:35679640 | G | C | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2325-3055G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679640 | |||||||
| chr17:35679718 | G | T | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2325-2977G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679718 | |||||||
| chr17:35679742 | CTG | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2325-2950_2325-294 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35679742 | ||||||
| chr17:35679896 | T | C | 88 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2325-2799T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679896 | |||||||
| chr17:35679927 | CT | C | 316 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(313): Show |
319 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.2325-2752delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35679927 | ||||||
| chr17:35679927 | CTT | C | 13 | a0001c0001t0002g0106 a0001c0001t0003g0051 a0001c0001t0007g0006 others(10): Show |
13 | HG01517.hp1 HG01884.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.2325-2753_2325-275 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35679927 | ||||||
| chr17:35679979 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2325-2716T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35679979 | |||||||
| chr17:35680046 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2325-2649A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680046 | |||||||
| chr17:35680381 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2325-2314G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680381 | |||||||
| chr17:35680524 | C | T | 1 | a0001c0002t0001g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2325-2171C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680524 | |||||||
| chr17:35680543 | A | G | 3 | a0001c0001t0005g0136 a0001c0001t0005g0147 a0001c0001t0005g0152 |
3 | HG00140.hp2 HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2325-2152A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680543 | |||||||
| chr17:35680547 | T | C | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2325-2148T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680547 | |||||||
| chr17:35680578 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2325-2117C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680578 | |||||||
| chr17:35680686 | G | T | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2325-2009G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680686 | |||||||
| chr17:35680687 | T | G | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2325-2008T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680687 | |||||||
| chr17:35680692 | T | TG | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2325-2003_2325-200 others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680692 | |||||||
| chr17:35680693 | T | TTTG | 44 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(41): Show |
44 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2325-2000_2325-199 others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35680693 | ||||||
| chr17:35680694 | T | TTG | 60 | a0001c0001t0002g0112 a0001c0001t0002g0117 a0001c0001t0002g0122 others(57): Show |
60 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.2325-2000_2325-199 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35680694 | ||||||
| chr17:35680695 | T | TG | 73 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(70): Show |
75 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.2325-2000_2325-199 others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680695 | |||||||
| chr17:35680696 | T | G | 10 | a0001c0001t0009g0159 a0001c0002t0001g0289 a0001c0002t0001g0290 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2325-1999T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680696 | |||||||
| chr17:35680696 | T | TG | 129 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(126): Show |
130 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.2325-1999_2325-199 others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680696 | |||||||
| chr17:35680697 | T | G | 9 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0355 others(6): Show |
9 | HG01069.hp2 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2325-1998T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680697 | |||||||
| chr17:35680698 | T | G | 8 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(5): Show |
9 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2325-1997T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680698 | |||||||
| chr17:35680700 | G | T | 195 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2325-1995G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680700 | |||||||
| chr17:35680701 | T | G | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2325-1994T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680701 | |||||||
| chr17:35680704 | T | G | 14 | a0001c0002t0001g0260 a0001c0002t0001g0264 a0001c0002t0001g0289 others(11): Show |
14 | HG00738.hp1 HG01081.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2325-1991T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680704 | |||||||
| chr17:35680705 | T | G | 4 | a0001c0001t0007g0156 a0001c0001t0007g0346 a0001c0001t0007g0348 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1990T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680705 | |||||||
| chr17:35680706 | T | G | 41 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(38): Show |
41 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.2325-1989T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680706 | |||||||
| chr17:35680708 | T | G | 3 | a0001c0001t0009g0159 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02257.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2325-1987T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680708 | |||||||
| chr17:35680719 | G | T | 1 | a0001c0001t0009g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2325-1976G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680719 | |||||||
| chr17:35680720 | A | T | 1 | a0001c0001t0009g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2325-1975A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680720 | |||||||
| chr17:35680783 | G | A | 86 | a0001c0002t0001g0005 a0001c0002t0001g0184 a0001c0002t0001g0185 others(83): Show |
87 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.2325-1912G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680783 | |||||||
| chr17:35680792 | G | C | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.2325-1903G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35680792 | |||||||
| chr17:35681336 | G | T | 1 | a0001c0001t0003g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2325-1359G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35681336 | |||||||
| chr17:35681337 | G | T | 1 | a0001c0001t0003g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2325-1358G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35681337 | |||||||
| chr17:35681701 | C | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2325-994C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35681701 | |||||||
| chr17:35681790 | T | C | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2325-905T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35681790 | |||||||
| chr17:35682010 | T | C | 132 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(129): Show |
133 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.2325-685T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682010 | |||||||
| chr17:35682073 | G | A | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2325-622G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682073 | |||||||
| chr17:35682193 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2325-502T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682193 | |||||||
| chr17:35682229 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2325-466C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682229 | |||||||
| chr17:35682260 | CA | C | 334 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(331): Show |
337 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.2325-421delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35682260 | ||||||
| chr17:35682331 | CCT | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(44): Show |
48 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2325-361_2325-360d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35682331 | ||||||
| chr17:35682332 | CT | C | 18 | a0001c0001t0002g0081 a0001c0001t0002g0085 a0001c0001t0002g0086 others(15): Show |
18 | HG00438.hp2 HG00735.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2325-362delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682332 | |||||||
| chr17:35682334 | C | CT | 33 | a0001c0001t0002g0177 a0001c0001t0002g0180 a0001c0001t0005g0133 others(30): Show |
33 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.2325-336dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35682334 | ||||||
| chr17:35682334 | CT | C | 107 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2325-336delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35682334 | ||||||
| chr17:35682334 | CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2325-349_2325-336d others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 35682334 | ||||||
| chr17:35682335 | T | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(44): Show |
48 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2325-360T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682335 | |||||||
| chr17:35682345 | T | G | 1 | a0001c0001t0003g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2325-350T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682345 | |||||||
| chr17:35682377 | T | C | 132 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(129): Show |
133 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.2325-318T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682377 | |||||||
| chr17:35682398 | A | C | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2325-297A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682398 | |||||||
| chr17:35682412 | G | A | 2 | a0001c0001t0002g0180 a0001c0005t0002g0118 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2325-283G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682412 | |||||||
| chr17:35682429 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.2325-266G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682429 | |||||||
| chr17:35682431 | C | T | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2325-264C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682431 | |||||||
| chr17:35682500 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2325-195G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682500 | |||||||
| chr17:35682543 | C | T | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2325-152C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682543 | |||||||
| chr17:35682682 | T | C | 3 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0049 |
3 | HG01070.hp1 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2325-13T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 17/21 | chr17 | 35682682 | |||||||
| chr17:35682859 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+35A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35682859 | |||||||
| chr17:35682870 | A | AATT | 10 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(7): Show |
11 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.2454+65_2454+67dup others(3): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35682870 | ||||||
| chr17:35683236 | T | A | 1 | a0001c0002t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2454+412T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683236 | |||||||
| chr17:35683243 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2454+419G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683243 | |||||||
| chr17:35683481 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2454+657G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683481 | |||||||
| chr17:35683577 | T | A | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2454+753T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683577 | |||||||
| chr17:35683815 | C | T | 2 | a0001c0002t0001g0200 a0001c0002t0001g0203 |
2 | HG01074.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2454+991C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683815 | |||||||
| chr17:35683912 | T | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+1088T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35683912 | |||||||
| chr17:35684026 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2454+1202A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684026 | |||||||
| chr17:35684135 | A | G | 2 | a0001c0001t0004g0347 a0001c0001t0004g0354 |
2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2454+1311A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684135 | |||||||
| chr17:35684281 | A | G | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+1457A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684281 | |||||||
| chr17:35684284 | G | C | 1 | a0001c0002t0001g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2454+1460G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684284 | |||||||
| chr17:35684303 | A | C | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2454+1479A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684303 | |||||||
| chr17:35684326 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2454+1502A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684326 | |||||||
| chr17:35684581 | G | T | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+1757G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684581 | |||||||
| chr17:35684800 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2454+1976A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684800 | |||||||
| chr17:35684808 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+1984C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684808 | |||||||
| chr17:35684809 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2454+1985G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684809 | |||||||
| chr17:35684881 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2454+2057A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684881 | |||||||
| chr17:35684942 | C | A | 1 | a0001c0002t0001g0363 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2454+2118C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35684942 | |||||||
| chr17:35685315 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2454+2491A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685315 | |||||||
| chr17:35685339 | G | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2454+2515G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685339 | |||||||
| chr17:35685537 | A | G | 89 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(86): Show |
89 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.2454+2713A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685537 | |||||||
| chr17:35685773 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+2949C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685773 | |||||||
| chr17:35685865 | C | T | 1 | a0001c0002t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2454+3041C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685865 | |||||||
| chr17:35685932 | T | C | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+3108T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685932 | |||||||
| chr17:35685973 | C | T | 1 | a0001c0004t0002g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2454+3149C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35685973 | |||||||
| chr17:35686060 | G | T | 1 | a0001c0001t0009g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2454+3236G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686060 | |||||||
| chr17:35686093 | G | T | 1 | a0001c0001t0003g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2454+3269G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686093 | |||||||
| chr17:35686419 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2454+3595C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686419 | |||||||
| chr17:35686471 | G | C | 1 | a0001c0004t0002g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2454+3647G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686471 | |||||||
| chr17:35686471 | GACAGTGG others(12): Show |
G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2454+3650_2454+366 others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35686471 | ||||||
| chr17:35686527 | T | C | 6 | a0001c0001t0004g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(3): Show |
6 | HG02717.hp1 HG02818.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2454+3703T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686527 | |||||||
| chr17:35686573 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2454+3749G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686573 | |||||||
| chr17:35686617 | A | C | 144 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(141): Show |
145 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.2454+3793A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686617 | |||||||
| chr17:35686653 | A | T | 1 | a0001c0001t0005g0141 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2454+3829A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686653 | |||||||
| chr17:35686791 | C | T | 1 | a0001c0001t0008g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2454+3967C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686791 | |||||||
| chr17:35686813 | A | C | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.2454+3989A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686813 | |||||||
| chr17:35686839 | G | A | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2454+4015G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686839 | |||||||
| chr17:35686852 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.2454+4028G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686852 | |||||||
| chr17:35686882 | C | T | 1 | a0001c0004t0002g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2454+4058C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686882 | |||||||
| chr17:35686909 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2454+4085G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686909 | |||||||
| chr17:35686925 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+4101T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35686925 | |||||||
| chr17:35687065 | A | C | 1 | a0001c0003t0001g0204 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2454+4241A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687065 | |||||||
| chr17:35687135 | T | A | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2454+4311T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687135 | |||||||
| chr17:35687316 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2454+4492C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687316 | |||||||
| chr17:35687327 | C | T | 2 | a0001c0001t0004g0329 a0001c0001t0004g0331 |
2 | NA18968.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2454+4503C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687327 | |||||||
| chr17:35687467 | A | G | 2 | a0001c0001t0005g0132 a0001c0001t0005g0143 |
2 | NA18989.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2454+4643A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687467 | |||||||
| chr17:35687540 | A | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2454+4716A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687540 | |||||||
| chr17:35687552 | AT | A | 45 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2454+4739delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35687552 | ||||||
| chr17:35687861 | A | G | 2 | a0001c0002t0001g0062 a0001c0002t0001g0247 |
2 | NA18984.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2454+5037A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35687861 | |||||||
| chr17:35688072 | T | C | 2 | a0001c0002t0001g0224 a0001c0002t0001g0246 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2454+5248T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688072 | |||||||
| chr17:35688195 | TC | T | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2454+5372delC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688195 | |||||||
| chr17:35688271 | A | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0187 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2454+5447A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688271 | |||||||
| chr17:35688441 | ACT | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0015g0131 |
3 | HG01109.hp2 HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2454+5620_2454+562 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35688441 | ||||||
| chr17:35688513 | T | C | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.2454+5689T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688513 | |||||||
| chr17:35688659 | A | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2454+5835A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688659 | |||||||
| chr17:35688695 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2454+5871G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688695 | |||||||
| chr17:35688836 | C | T | 1 | a0001c0002t0001g0291 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2454+6012C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688836 | |||||||
| chr17:35688857 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+6033A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688857 | |||||||
| chr17:35688880 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18944.hp1 NA19002.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2454+6056C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35688880 | |||||||
| chr17:35689082 | G | T | 2 | a0001c0001t0004g0347 a0001c0001t0004g0354 |
2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2454+6258G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689082 | |||||||
| chr17:35689107 | C | T | 196 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2454+6283C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689107 | |||||||
| chr17:35689183 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+6359G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689183 | |||||||
| chr17:35689396 | T | C | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2454+6572T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689396 | |||||||
| chr17:35689400 | G | A | 1 | a0001c0001t0005g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2454+6576G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689400 | |||||||
| chr17:35689444 | T | G | 45 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(42): Show |
45 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2454+6620T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689444 | |||||||
| chr17:35689543 | A | G | 2 | a0001c0002t0001g0274 a0001c0002t0001g0277 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2454+6719A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689543 | |||||||
| chr17:35689828 | C | T | 1 | a0001c0002t0001g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2454+7004C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689828 | |||||||
| chr17:35689883 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+7059T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689883 | |||||||
| chr17:35689916 | C | T | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+7092C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689916 | |||||||
| chr17:35689919 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+7095G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35689919 | |||||||
| chr17:35690037 | T | C | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2454+7213T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690037 | |||||||
| chr17:35690119 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+7295T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690119 | |||||||
| chr17:35690208 | A | G | 4 | a0001c0001t0007g0156 a0001c0001t0007g0346 a0001c0001t0007g0348 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+7384A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690208 | |||||||
| chr17:35690250 | T | G | 3 | a0001c0002t0010g0240 a0001c0002t0010g0253 a0001c0002t0010g0254 |
3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2454+7426T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690250 | |||||||
| chr17:35690325 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2454+7501A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690325 | |||||||
| chr17:35690360 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2454+7536G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690360 | |||||||
| chr17:35690406 | G | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2454+7582G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690406 | |||||||
| chr17:35690434 | T | G | 140 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(137): Show |
141 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.2454+7610T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690434 | |||||||
| chr17:35690633 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+7809T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35690633 | |||||||
| chr17:35691095 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2454+8271T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691095 | |||||||
| chr17:35691471 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+8647C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691471 | |||||||
| chr17:35691583 | A | G | 3 | a0001c0002t0001g0266 a0001c0002t0001g0267 a0001c0002t0001g0282 |
3 | HG01891.hp2 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2454+8759A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691583 | |||||||
| chr17:35691663 | C | T | 136 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(133): Show |
137 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.2454+8839C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691663 | |||||||
| chr17:35691721 | AAAAATAT others(7): Show |
A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+8909_2454+892 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35691721 | ||||||
| chr17:35691755 | A | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2454+8931A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691755 | |||||||
| chr17:35691760 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+8936G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691760 | |||||||
| chr17:35691766 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+8942G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35691766 | |||||||
| chr17:35691976 | C | CT | 25 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.2454+9159dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35691976 | ||||||
| chr17:35692032 | A | G | 1 | a0001c0004t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2454+9208A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692032 | |||||||
| chr17:35692241 | T | C | 4 | a0001c0001t0007g0156 a0001c0001t0007g0346 a0001c0001t0007g0348 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+9417T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692241 | |||||||
| chr17:35692318 | A | G | 1 | a0001c0001t0009g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2454+9494A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692318 | |||||||
| chr17:35692369 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2454+9545A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692369 | |||||||
| chr17:35692469 | G | T | 196 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2454+9645G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692469 | |||||||
| chr17:35692486 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2454+9662G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692486 | |||||||
| chr17:35692555 | T | G | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.2454+9731T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692555 | |||||||
| chr17:35692563 | T | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+9739T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692563 | |||||||
| chr17:35692901 | C | T | 5 | a0001c0001t0004g0328 a0001c0001t0004g0329 a0001c0001t0004g0331 others(2): Show |
5 | NA18959.hp1 NA18968.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454+10077C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35692901 | |||||||
| chr17:35693030 | G | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2454+10206G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35693030 | |||||||
| chr17:35693031 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2454+10207G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35693031 | |||||||
| chr17:35693152 | G | T | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2454+10328G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35693152 | |||||||
| chr17:35693589 | C | T | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+10765C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35693589 | |||||||
| chr17:35693760 | ACTT | A | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2454+10939_2454+10 others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35693760 | ||||||
| chr17:35693817 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2454+10993A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35693817 | |||||||
| chr17:35694038 | A | T | 1 | a0001c0001t0002g0111 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2454+11214A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694038 | |||||||
| chr17:35694083 | C | T | 197 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2454+11259C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694083 | |||||||
| chr17:35694214 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2454+11390T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694214 | |||||||
| chr17:35694288 | C | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+11464C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694288 | |||||||
| chr17:35694411 | C | CT | 131 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(128): Show |
131 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.2454+11601dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35694411 | ||||||
| chr17:35694411 | C | CTT | 141 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(138): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2454+11600_2454+11 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35694411 | ||||||
| chr17:35694411 | C | CTTT | 45 | a0001c0001t0002g0181 a0001c0001t0003g0008 a0001c0001t0003g0010 others(42): Show |
45 | HG00558.hp1 HG00673.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.2454+11599_2454+11 others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35694411 | ||||||
| chr17:35694426 | A | T | 337 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(334): Show |
340 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2454+11602A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694426 | |||||||
| chr17:35694427 | A | T | 339 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(336): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.2454+11603A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694427 | |||||||
| chr17:35694433 | T | TA | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+11611dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35694433 | ||||||
| chr17:35694577 | G | C | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454+11753G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694577 | |||||||
| chr17:35694975 | C | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2454+12151C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35694975 | |||||||
| chr17:35695143 | T | C | 1 | a0001c0002t0001g0288 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2454+12319T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695143 | |||||||
| chr17:35695305 | C | T | 1 | a0001c0002t0001g0273 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2454+12481C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695305 | |||||||
| chr17:35695442 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2454+12618G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695442 | |||||||
| chr17:35695481 | A | C | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2454+12657A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695481 | |||||||
| chr17:35695511 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+12687C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695511 | |||||||
| chr17:35695801 | A | G | 1 | a0001c0002t0001g0364 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2454+12977A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35695801 | |||||||
| chr17:35696413 | C | CT | 121 | a0001c0001t0002g0355 a0001c0001t0003g0021 a0001c0001t0003g0043 others(118): Show |
122 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.2455-12792dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35696413 | ||||||
| chr17:35696413 | C | CTT | 6 | a0001c0002t0001g0197 a0001c0002t0001g0211 a0001c0002t0001g0245 others(3): Show |
6 | HG02738.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.2455-12793_2455-12 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35696413 | ||||||
| chr17:35696413 | CT | C | 27 | a0001c0001t0002g0084 a0001c0001t0002g0177 a0001c0001t0002g0178 others(24): Show |
27 | HG00323.hp2 HG01256.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2455-12792delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35696413 | ||||||
| chr17:35696743 | G | A | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-12481G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35696743 | |||||||
| chr17:35696928 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-12296C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35696928 | |||||||
| chr17:35696955 | T | C | 1 | a0001c0001t0003g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2455-12269T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35696955 | |||||||
| chr17:35697082 | T | A | 1 | a0001c0002t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2455-12142T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697082 | |||||||
| chr17:35697133 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2455-12091A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697133 | |||||||
| chr17:35697167 | T | C | 3 | a0001c0002t0001g0237 a0001c0002t0001g0239 a0001c0002t0001g0309 |
3 | HG00558.hp2 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2455-12057T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697167 | |||||||
| chr17:35697522 | A | C | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2455-11702A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697522 | |||||||
| chr17:35697565 | C | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2455-11659C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697565 | |||||||
| chr17:35697687 | G | A | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2455-11537G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697687 | |||||||
| chr17:35697688 | C | A | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2455-11536C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697688 | |||||||
| chr17:35697765 | C | T | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2455-11459C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697765 | |||||||
| chr17:35697783 | G | A | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2455-11441G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697783 | |||||||
| chr17:35697908 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-11316T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697908 | |||||||
| chr17:35697987 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2455-11237T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35697987 | |||||||
| chr17:35698071 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-11153A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698071 | |||||||
| chr17:35698083 | T | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2455-11141T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698083 | |||||||
| chr17:35698163 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2455-11061A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698163 | |||||||
| chr17:35698414 | A | G | 1 | a0001c0001t0004g0347 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2455-10810A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698414 | |||||||
| chr17:35698441 | T | C | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-10783T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698441 | |||||||
| chr17:35698448 | T | C | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-10776T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698448 | |||||||
| chr17:35698803 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2455-10421T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35698803 | |||||||
| chr17:35699011 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2455-10213G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699011 | |||||||
| chr17:35699316 | A | G | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2455-9908A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699316 | |||||||
| chr17:35699398 | A | T | 2 | a0001c0002t0001g0211 a0001c0002t0001g0212 |
2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2455-9826A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699398 | |||||||
| chr17:35699451 | C | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2455-9773C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699451 | |||||||
| chr17:35699578 | C | T | 132 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(129): Show |
133 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.2455-9646C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699578 | |||||||
| chr17:35699613 | G | C | 1 | a0001c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2455-9611G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699613 | |||||||
| chr17:35699669 | T | C | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.2455-9555T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699669 | |||||||
| chr17:35699698 | A | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-9526A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699698 | |||||||
| chr17:35699778 | G | C | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2455-9446G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699778 | |||||||
| chr17:35699938 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2455-9286A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699938 | |||||||
| chr17:35699957 | A | T | 2 | a0001c0001t0004g0337 a0001c0001t0004g0350 |
2 | NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2455-9267A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35699957 | |||||||
| chr17:35700108 | A | AAAAT | 9 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.2455-9108_2455-910 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35700108 | ||||||
| chr17:35700209 | G | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-9015G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700209 | |||||||
| chr17:35700251 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2455-8973G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700251 | |||||||
| chr17:35700331 | C | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0367 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2455-8893C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700331 | |||||||
| chr17:35700586 | G | T | 36 | a0001c0001t0004g0316 a0001c0001t0004g0318 a0001c0001t0004g0319 others(33): Show |
36 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.2455-8638G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700586 | |||||||
| chr17:35700588 | C | G | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-8636C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700588 | |||||||
| chr17:35700634 | T | C | 1 | a0001c0001t0004g0354 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2455-8590T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700634 | |||||||
| chr17:35700750 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2455-8474A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700750 | |||||||
| chr17:35700808 | T | C | 1 | a0001c0003t0001g0204 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2455-8416T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700808 | |||||||
| chr17:35700945 | T | C | 140 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(137): Show |
141 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.2455-8279T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35700945 | |||||||
| chr17:35701172 | T | TAC | 340 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(337): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2455-8044_2455-804 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35701172 | ||||||
| chr17:35701450 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2455-7774C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35701450 | |||||||
| chr17:35701527 | A | G | 46 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(43): Show |
46 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.2455-7697A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35701527 | |||||||
| chr17:35701602 | G | T | 3 | a0001c0002t0010g0240 a0001c0002t0010g0253 a0001c0002t0010g0254 |
3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2455-7622G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35701602 | |||||||
| chr17:35701709 | C | T | 1 | a0001c0002t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2455-7515C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35701709 | |||||||
| chr17:35701882 | A | G | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2455-7342A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35701882 | |||||||
| chr17:35701940 | CATT | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-7280_2455-727 others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35701940 | ||||||
| chr17:35702305 | T | C | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2455-6919T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35702305 | |||||||
| chr17:35702460 | G | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-6764G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35702460 | |||||||
| chr17:35702669 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2455-6555A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35702669 | |||||||
| chr17:35702717 | A | G | 4 | a0001c0001t0007g0156 a0001c0001t0007g0346 a0001c0001t0007g0348 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-6507A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35702717 | |||||||
| chr17:35702792 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2455-6432G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35702792 | |||||||
| chr17:35703001 | G | A | 5 | a0001c0001t0002g0356 a0001c0001t0002g0357 a0001c0001t0002g0358 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2455-6223G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703001 | |||||||
| chr17:35703039 | G | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-6185G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703039 | |||||||
| chr17:35703068 | C | T | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-6156C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703068 | |||||||
| chr17:35703213 | C | T | 2 | a0001c0002t0001g0237 a0001c0002t0001g0239 |
2 | NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2455-6011C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703213 | |||||||
| chr17:35703229 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2455-5995C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703229 | |||||||
| chr17:35703264 | C | CA | 324 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(321): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.2455-5942dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703264 | ||||||
| chr17:35703264 | C | CAA | 14 | a0001c0001t0002g0123 a0001c0001t0002g0367 a0001c0001t0003g0052 others(11): Show |
14 | HG01256.hp1 HG01981.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2455-5943_2455-594 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703264 | ||||||
| chr17:35703282 | A | T | 1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2455-5942A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703282 | |||||||
| chr17:35703283 | G | A | 1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2455-5941G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703283 | |||||||
| chr17:35703294 | G | T | 1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2455-5930G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703294 | |||||||
| chr17:35703302 | CACTCG | C | 16 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(13): Show |
16 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2455-5917_2455-591 others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703302 | ||||||
| chr17:35703378 | A | G | 1 | a0001c0002t0001g0314 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2455-5846A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703378 | |||||||
| chr17:35703393 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2455-5831A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703393 | |||||||
| chr17:35703402 | C | G | 131 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(128): Show |
132 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.2455-5822C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703402 | |||||||
| chr17:35703434 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2455-5790G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703434 | |||||||
| chr17:35703435 | C | T | 139 | a0001c0002t0001g0005 a0001c0002t0001g0062 a0001c0002t0001g0184 others(136): Show |
140 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.2455-5789C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703435 | |||||||
| chr17:35703491 | A | G | 1 | a0001c0001t0005g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2455-5733A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703491 | |||||||
| chr17:35703514 | A | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2455-5710A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703514 | |||||||
| chr17:35703834 | A | AAGTAAAT others(12): Show |
1 | a0001c0001t0002g0085 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2455-5387_2455-538 others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703834 | ||||||
| chr17:35703834 | A | AAGTTAAA others(12): Show |
1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2455-5386_2455-538 others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703834 | ||||||
| chr17:35703834 | A | AAGTTAAA others(13): Show |
331 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(328): Show |
334 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.2455-5386_2455-538 others(24): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703834 | ||||||
| chr17:35703834 | A | AAGTTAAA others(13): Show |
7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2455-5386_2455-538 others(24): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35703834 | ||||||
| chr17:35703888 | T | C | 2 | a0001c0002t0001g0286 a0001c0002t0001g0287 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2455-5336T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35703888 | |||||||
| chr17:35704680 | T | C | 1 | a0001c0002t0001g0194 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2455-4544T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35704680 | |||||||
| chr17:35704874 | T | C | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2455-4350T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35704874 | |||||||
| chr17:35705039 | A | G | 5 | a0001c0001t0004g0328 a0001c0001t0004g0329 a0001c0001t0004g0331 others(2): Show |
5 | NA18959.hp1 NA18968.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-4185A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705039 | |||||||
| chr17:35705087 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2455-4137G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705087 | |||||||
| chr17:35705420 | A | G | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2455-3804A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705420 | |||||||
| chr17:35705543 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-3681A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705543 | |||||||
| chr17:35705577 | A | G | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-3647A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705577 | |||||||
| chr17:35705581 | G | A | 1 | a0001c0003t0001g0204 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2455-3643G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705581 | |||||||
| chr17:35705679 | G | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG01109.hp1 HG01109.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-3545G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705679 | |||||||
| chr17:35705858 | A | T | 18 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0169 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.2455-3366A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705858 | |||||||
| chr17:35705878 | C | T | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2455-3346C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35705878 | |||||||
| chr17:35706025 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-3199A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706025 | |||||||
| chr17:35706053 | C | T | 144 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(141): Show |
145 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.2455-3171C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706053 | |||||||
| chr17:35706247 | T | TA | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2455-2976dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35706247 | ||||||
| chr17:35706440 | A | T | 6 | a0001c0001t0002g0355 a0001c0001t0002g0356 a0001c0001t0002g0357 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-2784A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706440 | |||||||
| chr17:35706625 | T | C | 1 | a0001c0001t0003g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2455-2599T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706625 | |||||||
| chr17:35706637 | C | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2455-2587C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706637 | |||||||
| chr17:35706769 | T | C | 1 | a0001c0001t0004g0316 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2455-2455T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706769 | |||||||
| chr17:35706789 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2455-2435C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706789 | |||||||
| chr17:35706803 | A | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2455-2421A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706803 | |||||||
| chr17:35706806 | A | AAT | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-2407_2455-240 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35706806 | ||||||
| chr17:35706819 | T | A | 196 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2455-2405T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706819 | |||||||
| chr17:35706871 | C | T | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2455-2353C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35706871 | |||||||
| chr17:35707040 | C | T | 342 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(339): Show |
345 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.2455-2184C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707040 | |||||||
| chr17:35707084 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-2140G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707084 | |||||||
| chr17:35707134 | C | CTTGTTG | 134 | a0001c0001t0003g0021 a0001c0002t0001g0005 a0001c0002t0001g0062 others(131): Show |
135 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.2455-2072_2455-206 others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35707134 | ||||||
| chr17:35707134 | C | CTTGTTGT others(2): Show |
6 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0293 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2455-2075_2455-206 others(13): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35707134 | ||||||
| chr17:35707273 | C | T | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2455-1951C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707273 | |||||||
| chr17:35707298 | A | C | 1 | a0001c0001t0019g0093 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2455-1926A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707298 | |||||||
| chr17:35707373 | G | A | 16 | a0001c0001t0004g0321 a0001c0001t0004g0322 a0001c0001t0004g0323 others(13): Show |
16 | HG00544.hp2 NA18612.hp1 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.2455-1851G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707373 | |||||||
| chr17:35707457 | C | CT | 152 | a0001c0001t0002g0004 a0001c0001t0002g0075 a0001c0001t0002g0168 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2455-1752dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35707457 | ||||||
| chr17:35707457 | CT | C | 48 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(45): Show |
48 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.2455-1752delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr17 | 35707457 | ||||||
| chr17:35707458 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2455-1766T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707458 | |||||||
| chr17:35707496 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-1728A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707496 | |||||||
| chr17:35707513 | C | T | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2455-1711C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707513 | |||||||
| chr17:35707748 | C | A | 1 | a0002c0007t0003g0041 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2455-1476C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707748 | |||||||
| chr17:35707763 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2455-1461A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707763 | |||||||
| chr17:35707860 | G | C | 1 | a0002c0007t0003g0041 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2455-1364G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707860 | |||||||
| chr17:35707861 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-1363C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707861 | |||||||
| chr17:35707893 | C | G | 5 | a0001c0002t0001g0260 a0001c0002t0001g0362 a0001c0002t0001g0364 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-1331C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35707893 | |||||||
| chr17:35708159 | C | T | 1 | a0001c0001t0005g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2455-1065C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708159 | |||||||
| chr17:35708250 | C | T | 1 | a0001c0001t0005g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2455-974C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708250 | |||||||
| chr17:35708297 | A | T | 1 | a0001c0002t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2455-927A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708297 | |||||||
| chr17:35708455 | A | C | 1 | a0001c0001t0002g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2455-769A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708455 | |||||||
| chr17:35708553 | T | G | 6 | a0001c0001t0004g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(3): Show |
6 | HG02717.hp1 HG02818.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2455-671T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708553 | |||||||
| chr17:35708643 | A | C | 1 | a0001c0002t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2455-581A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708643 | |||||||
| chr17:35708663 | T | C | 7 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2455-561T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35708663 | |||||||
| chr17:35709069 | T | G | 1 | a0001c0002t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2455-155T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35709069 | |||||||
| chr17:35709085 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2455-139G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35709085 | |||||||
| chr17:35709109 | C | T | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2455-115C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 18/21 | chr17 | 35709109 | |||||||
| chr17:35709406 | T | TA | 12 | a0001c0002t0001g0191 a0001c0002t0001g0235 a0001c0002t0001g0238 others(9): Show |
12 | HG01993.hp2 HG02074.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.2539+107dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 35709406 | ||||||
| chr17:35709671 | A | G | 197 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2539+363A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | chr17 | 35709671 | |||||||
| chr17:35709786 | CTCCCGAT others(22): Show |
C | 2 | a0001c0002t0001g0275 a0001c0002t0001g0278 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2540-443_2540-415d others(31): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 35709786 | ||||||
| chr17:35709856 | A | T | 3 | a0001c0002t0001g0230 a0001c0002t0001g0249 a0001c0002t0001g0279 |
3 | HG01934.hp2 NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2540-378A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | chr17 | 35709856 | |||||||
| chr17:35709959 | C | T | 3 | a0001c0002t0001g0192 a0001c0002t0001g0259 a0001c0002t0001g0264 |
3 | HG02055.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2540-275C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | chr17 | 35709959 | |||||||
| chr17:35709969 | A | G | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2540-265A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 19/21 | chr17 | 35709969 | |||||||
| chr17:35710338 | A | C | 1 | a0001c0002t0001g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2626+18A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35710338 | |||||||
| chr17:35710401 | C | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2626+81C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35710401 | |||||||
| chr17:35710728 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2626+408T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35710728 | |||||||
| chr17:35710754 | G | C | 1 | a0001c0002t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2626+434G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35710754 | |||||||
| chr17:35711050 | G | A | 1 | a0001c0002t0001g0262 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2626+730G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711050 | |||||||
| chr17:35711410 | C | CA | 50 | a0001c0001t0002g0109 a0001c0001t0002g0174 a0001c0001t0002g0181 others(47): Show |
50 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2626+1105dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 35711410 | ||||||
| chr17:35711410 | C | CAA | 6 | a0001c0001t0003g0016 a0001c0001t0004g0320 a0001c0001t0004g0343 others(3): Show |
6 | HG00323.hp2 HG01261.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2626+1104_2626+110 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 35711410 | ||||||
| chr17:35711426 | C | A | 2 | a0001c0001t0019g0093 a0001c0002t0001g0293 |
2 | HG00323.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2626+1106C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711426 | |||||||
| chr17:35711475 | A | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2626+1155A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711475 | |||||||
| chr17:35711538 | G | A | 69 | a0001c0001t0003g0047 a0001c0001t0004g0158 a0001c0001t0004g0316 others(66): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.2626+1218G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711538 | |||||||
| chr17:35711617 | A | C | 3 | a0001c0002t0001g0201 a0001c0002t0001g0209 a0001c0002t0001g0281 |
3 | HG00597.hp1 NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2626+1297A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711617 | |||||||
| chr17:35711618 | G | A | 3 | a0001c0002t0001g0201 a0001c0002t0001g0209 a0001c0002t0001g0281 |
3 | HG00597.hp1 NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2626+1298G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711618 | |||||||
| chr17:35711629 | C | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2626+1309C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711629 | |||||||
| chr17:35711678 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0049 |
3 | HG01070.hp1 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2626+1358A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711678 | |||||||
| chr17:35711713 | C | T | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2626+1393C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711713 | |||||||
| chr17:35711714 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2626+1394G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711714 | |||||||
| chr17:35711751 | A | G | 1 | a0001c0002t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2626+1431A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711751 | |||||||
| chr17:35711994 | A | T | 10 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2626+1674A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35711994 | |||||||
| chr17:35712013 | G | A | 6 | a0001c0001t0004g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(3): Show |
6 | HG02717.hp1 HG02818.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2626+1693G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712013 | |||||||
| chr17:35712017 | G | T | 1 | a0001c0002t0001g0244 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2626+1697G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712017 | |||||||
| chr17:35712068 | C | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2626+1748C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712068 | |||||||
| chr17:35712127 | T | G | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2626+1807T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712127 | |||||||
| chr17:35712411 | G | A | 36 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0011 others(33): Show |
36 | HG00558.hp1 HG00673.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.2626+2091G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712411 | |||||||
| chr17:35712487 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2626+2167G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712487 | |||||||
| chr17:35712583 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2626+2263C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712583 | |||||||
| chr17:35712622 | C | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2626+2302C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712622 | |||||||
| chr17:35712623 | C | T | 2 | a0001c0001t0006g0077 a0001c0001t0006g0089 |
2 | HG01123.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2626+2303C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712623 | |||||||
| chr17:35712668 | G | A | 6 | a0001c0004t0002g0163 a0001c0004t0002g0164 a0001c0004t0002g0165 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2626+2348G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712668 | |||||||
| chr17:35712977 | G | T | 1 | a0001c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2626+2657G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35712977 | |||||||
| chr17:35713167 | G | A | 1 | a0001c0002t0001g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2626+2847G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713167 | |||||||
| chr17:35713513 | C | G | 1 | a0001c0001t0003g0029 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2626+3193C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713513 | |||||||
| chr17:35713524 | A | G | 2 | a0001c0004t0002g0125 a0001c0004t0002g0126 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2626+3204A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713524 | |||||||
| chr17:35713662 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2626+3342A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713662 | |||||||
| chr17:35713724 | A | G | 9 | a0001c0002t0001g0233 a0001c0002t0001g0289 a0001c0002t0001g0290 others(6): Show |
9 | HG02129.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2626+3404A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713724 | |||||||
| chr17:35713767 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2627-3428T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35713767 | |||||||
| chr17:35714195 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2627-3000C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714195 | |||||||
| chr17:35714290 | T | C | 1 | a0001c0004t0002g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2627-2905T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714290 | |||||||
| chr17:35714618 | G | A | 1 | a0001c0002t0001g0296 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2627-2577G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714618 | |||||||
| chr17:35714760 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2627-2435C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714760 | |||||||
| chr17:35714772 | A | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-2423A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714772 | |||||||
| chr17:35714797 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2627-2398A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35714797 | |||||||
| chr17:35715006 | A | G | 2 | a0001c0002t0001g0224 a0001c0002t0001g0246 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2627-2189A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715006 | |||||||
| chr17:35715050 | T | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-2145T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715050 | |||||||
| chr17:35715109 | G | A | 1 | a0001c0002t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2627-2086G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715109 | |||||||
| chr17:35715171 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2627-2024G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715171 | |||||||
| chr17:35715195 | G | T | 3 | a0001c0001t0004g0323 a0001c0001t0004g0324 a0001c0001t0004g0334 |
3 | NA18946.hp2 NA18988.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2627-2000G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715195 | |||||||
| chr17:35715285 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-1910A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715285 | |||||||
| chr17:35715312 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2627-1883A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715312 | |||||||
| chr17:35715384 | C | T | 1 | a0001c0001t0005g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2627-1811C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715384 | |||||||
| chr17:35715407 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-1788C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715407 | |||||||
| chr17:35715449 | G | A | 88 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2627-1746G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715449 | |||||||
| chr17:35715527 | A | ATT | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-1664_2627-166 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 35715527 | ||||||
| chr17:35715619 | C | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2627-1576C>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715619 | |||||||
| chr17:35715712 | G | A | 1 | a0001c0001t0009g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2627-1483G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715712 | |||||||
| chr17:35715737 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2627-1458T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715737 | |||||||
| chr17:35715958 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2627-1237C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715958 | |||||||
| chr17:35715979 | G | A | 1 | a0001c0002t0001g0195 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2627-1216G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35715979 | |||||||
| chr17:35716002 | T | C | 204 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(201): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2627-1193T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716002 | |||||||
| chr17:35716140 | A | G | 1 | a0001c0001t0005g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2627-1055A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716140 | |||||||
| chr17:35716310 | C | A | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627-885C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716310 | |||||||
| chr17:35716365 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2627-830A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716365 | |||||||
| chr17:35716390 | G | A | 1 | a0001c0001t0004g0353 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2627-805G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716390 | |||||||
| chr17:35716495 | A | G | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2627-700A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716495 | |||||||
| chr17:35716566 | A | T | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2627-629A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716566 | |||||||
| chr17:35716609 | GA | G | 192 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(189): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2627-574delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 35716609 | ||||||
| chr17:35716698 | G | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2627-497G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716698 | |||||||
| chr17:35716806 | G | A | 233 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(230): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2627-389G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716806 | |||||||
| chr17:35716922 | A | G | 1 | a0001c0002t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2627-273A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 20/21 | chr17 | 35716922 | |||||||
| chr17:35717400 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2781+51G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35717400 | |||||||
| chr17:35717503 | A | G | 1 | a0001c0002t0001g0296 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2781+154A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35717503 | |||||||
| chr17:35717790 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2781+441G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35717790 | |||||||
| chr17:35718004 | A | G | 4 | a0001c0002t0001g0260 a0001c0002t0001g0362 a0001c0002t0001g0365 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781+655A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718004 | |||||||
| chr17:35718070 | T | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2781+721T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718070 | |||||||
| chr17:35718114 | A | C | 1 | a0001c0001t0006g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2781+765A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718114 | |||||||
| chr17:35718159 | G | C | 1 | a0001c0001t0003g0018 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2781+810G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718159 | |||||||
| chr17:35718176 | ACT | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2781+830_2781+831d others(4): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718176 | ||||||
| chr17:35718201 | G | A | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2781+852G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718201 | |||||||
| chr17:35718312 | C | CTG | 54 | a0001c0001t0002g0055 a0001c0001t0002g0085 a0001c0001t0002g0098 others(51): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.2781+1008_2781+100 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | C | CTGTG | 10 | a0001c0001t0002g0123 a0001c0001t0004g0321 a0001c0001t0004g0329 others(7): Show |
10 | HG01993.hp2 HG02071.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2781+1006_2781+100 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTG | C | 40 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0066 others(37): Show |
40 | HG00438.hp2 HG00597.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2781+1008_2781+100 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTG | C | 33 | a0001c0001t0002g0004 a0001c0001t0002g0120 a0001c0001t0002g0168 others(30): Show |
34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2781+1006_2781+100 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTG | C | 24 | a0001c0001t0001g0128 a0001c0001t0002g0177 a0001c0001t0002g0178 others(21): Show |
24 | HG00597.hp1 HG01884.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.2781+1004_2781+100 others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTGT others(1): Show |
C | 45 | a0001c0001t0002g0094 a0001c0001t0002g0109 a0001c0001t0002g0355 others(42): Show |
45 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.2781+1002_2781+100 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0003g0050 others(3): Show |
6 | HG00673.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2781+1000_2781+100 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0007g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2781+998_2781+1009 others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTGT others(7): Show |
C | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2781+996_2781+1009 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718312 | CTGTGTGT others(11): Show |
C | 26 | a0001c0001t0004g0158 a0001c0001t0005g0002 a0001c0001t0005g0003 others(23): Show |
28 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.2781+992_2781+1009 others(21): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718312 | ||||||
| chr17:35718509 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2781+1160G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718509 | |||||||
| chr17:35718601 | T | A | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2781+1252T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718601 | |||||||
| chr17:35718663 | CAT | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2781+1316_2781+131 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718663 | ||||||
| chr17:35718767 | G | GT | 10 | a0001c0001t0002g0085 a0001c0001t0003g0047 a0001c0001t0003g0050 others(7): Show |
10 | HG01943.hp2 HG01952.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2781+1430dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35718767 | ||||||
| chr17:35718767 | G | T | 5 | a0001c0002t0001g0198 a0001c0002t0001g0199 a0001c0002t0001g0225 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2781+1418G>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718767 | |||||||
| chr17:35718917 | T | A | 1 | a0001c0002t0001g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2781+1568T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718917 | |||||||
| chr17:35718957 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2781+1608G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35718957 | |||||||
| chr17:35719015 | A | G | 4 | a0001c0002t0001g0062 a0001c0002t0001g0230 a0001c0002t0001g0249 others(1): Show |
4 | HG01934.hp2 NA18944.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.2781+1666A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719015 | |||||||
| chr17:35719359 | C | CA | 9 | a0001c0001t0002g0085 a0001c0001t0003g0050 a0001c0001t0003g0051 others(6): Show |
9 | HG01168.hp2 HG01169.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2781+2022dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35719359 | ||||||
| chr17:35719402 | T | A | 9 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2781+2053T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719402 | |||||||
| chr17:35719449 | G | A | 6 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2781+2100G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719449 | |||||||
| chr17:35719508 | T | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781+2159T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719508 | |||||||
| chr17:35719541 | A | C | 1 | a0001c0002t0001g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2781+2192A>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719541 | |||||||
| chr17:35719628 | CT | C | 8 | a0001c0001t0002g0004 a0001c0001t0002g0168 a0001c0001t0002g0170 others(5): Show |
9 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2781+2282delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35719628 | ||||||
| chr17:35719738 | G | A | 1 | a0001c0001t0003g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2781+2389G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719738 | |||||||
| chr17:35719813 | T | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2781+2464T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35719813 | |||||||
| chr17:35720018 | A | G | 3 | a0001c0004t0002g0125 a0001c0004t0002g0126 a0001c0004t0002g0127 |
3 | HG02717.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2781+2669A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720018 | |||||||
| chr17:35720134 | T | C | 1 | a0001c0001t0004g0326 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2781+2785T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720134 | |||||||
| chr17:35720163 | G | C | 10 | a0001c0002t0001g0185 a0001c0002t0001g0201 a0001c0002t0001g0205 others(7): Show |
10 | HG00597.hp1 HG02056.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.2781+2814G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720163 | |||||||
| chr17:35720210 | A | G | 8 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2781+2861A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720210 | |||||||
| chr17:35720324 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2781+2975T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720324 | |||||||
| chr17:35720332 | T | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2781+2983T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720332 | |||||||
| chr17:35720541 | T | TTATATAT others(7): Show |
1 | a0001c0001t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2782-3081_2782-308 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720541 | ||||||
| chr17:35720541 | T | TTATATAT others(11): Show |
1 | a0001c0002t0001g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2782-3081_2782-308 others(22): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720541 | ||||||
| chr17:35720543 | A | T | 1 | a0001c0001t0005g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2782-3082A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720543 | |||||||
| chr17:35720545 | T | A | 33 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.2782-3080T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720545 | |||||||
| chr17:35720545 | T | TTA | 10 | a0001c0001t0002g0004 a0001c0001t0002g0170 a0001c0001t0002g0175 others(7): Show |
11 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.2782-3052_2782-305 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATA | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0003g0017 others(1): Show |
4 | HG03225.hp2 NA18965.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2782-3054_2782-305 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(1): Show |
6 | a0001c0001t0002g0115 a0001c0001t0002g0168 a0001c0001t0003g0039 others(3): Show |
6 | HG00673.hp1 HG01081.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2782-3058_2782-305 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(3): Show |
2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2782-3060_2782-305 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(5): Show |
1 | a0001c0001t0003g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2782-3062_2782-305 others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(7): Show |
2 | a0001c0001t0002g0112 a0001c0001t0003g0016 |
2 | HG00323.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2782-3064_2782-305 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(9): Show |
2 | a0001c0001t0003g0019 a0001c0002t0001g0289 |
2 | HG02132.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2782-3066_2782-305 others(20): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2782-3068_2782-305 others(22): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2782-3070_2782-305 others(24): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTATATAT others(15): Show |
1 | a0001c0001t0002g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2782-3072_2782-305 others(26): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTTTATAT others(9): Show |
2 | a0001c0002t0001g0291 a0001c0002t0001g0292 |
2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2782-3079_2782-307 others(20): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | T | TTTTATAT others(11): Show |
1 | a0001c0002t0001g0294 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2782-3079_2782-307 others(22): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | TTA | T | 12 | a0001c0001t0002g0356 a0001c0001t0002g0359 a0001c0002t0001g0196 others(9): Show |
12 | HG01891.hp2 HG01993.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2782-3052_2782-305 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720545 | TTATA | T | 5 | a0001c0002t0001g0191 a0001c0002t0001g0234 a0001c0002t0001g0238 others(2): Show |
5 | HG03041.hp1 HG03491.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2782-3054_2782-305 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720545 | ||||||
| chr17:35720547 | A | T | 2 | a0001c0002t0001g0290 a0001c0002t0001g0293 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2782-3078A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720547 | |||||||
| chr17:35720558 | T | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(53): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2782-3067T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720558 | |||||||
| chr17:35720565 | ATATATAT others(7): Show |
A | 9 | a0001c0001t0006g0069 a0001c0001t0006g0071 a0001c0001t0006g0072 others(6): Show |
9 | HG01069.hp1 HG01070.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.2782-3058_2782-304 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720565 | ||||||
| chr17:35720565 | ATATATAT others(8): Show |
A | 3 | a0001c0001t0002g0123 a0001c0001t0006g0064 a0001c0001t0006g0121 |
3 | HG02004.hp1 HG03654.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2782-3058_2782-304 others(19): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720565 | ||||||
| chr17:35720567 | A | T | 1 | a0001c0002t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2782-3058A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720567 | |||||||
| chr17:35720567 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0009g0161 a0001c0001t0009g0162 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2782-3056_2782-304 others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720567 | ||||||
| chr17:35720567 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0009g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2782-3056_2782-304 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720567 | ||||||
| chr17:35720567 | ATATATAT others(7): Show |
A | 19 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(16): Show |
19 | HG00323.hp1 HG00544.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.2782-3056_2782-304 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720567 | ||||||
| chr17:35720567 | ATATATAT others(8): Show |
A | 17 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0070 others(14): Show |
18 | HG00735.hp1 HG01106.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.2782-3056_2782-304 others(19): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720567 | ||||||
| chr17:35720567 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0002g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2782-3056_2782-304 others(20): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720567 | ||||||
| chr17:35720568 | TATA | T | 3 | a0001c0002t0001g0264 a0001c0002t0001g0283 a0001c0002t0011g0190 |
3 | NA18992.hp1 NA19081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2782-3056_2782-305 others(7): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720568 | |||||||
| chr17:35720569 | A | T | 4 | a0001c0002t0001g0230 a0001c0002t0001g0279 a0001c0002t0001g0288 others(1): Show |
4 | HG00733.hp2 HG01934.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2782-3056A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720569 | |||||||
| chr17:35720569 | ATATATTT others(4): Show |
A | 2 | a0001c0001t0007g0006 a0001c0001t0007g0007 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2782-3054_2782-304 others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720569 | ||||||
| chr17:35720569 | ATATATTT others(6): Show |
A | 2 | a0001c0001t0002g0090 a0001c0001t0006g0079 |
2 | HG02257.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2782-3054_2782-304 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720569 | ||||||
| chr17:35720569 | ATATATTT others(7): Show |
A | 5 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0107 others(2): Show |
5 | HG00438.hp2 HG00597.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2782-3054_2782-304 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720569 | ||||||
| chr17:35720569 | ATATATTT others(8): Show |
A | 1 | a0001c0001t0002g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2782-3054_2782-304 others(19): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720569 | ||||||
| chr17:35720570 | TA | T | 7 | a0001c0002t0001g0186 a0001c0002t0001g0237 a0001c0002t0001g0239 others(4): Show |
7 | HG02132.hp1 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2782-3054delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720570 | |||||||
| chr17:35720571 | A | T | 15 | a0001c0002t0001g0062 a0001c0002t0001g0184 a0001c0002t0001g0187 others(12): Show |
15 | HG00733.hp2 HG01256.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.2782-3054A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720571 | |||||||
| chr17:35720571 | ATATTTTT others(2): Show |
A | 15 | a0001c0001t0004g0319 a0001c0001t0004g0320 a0001c0001t0004g0321 others(12): Show |
15 | HG00673.hp2 HG01168.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.2782-3052_2782-304 others(13): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720571 | ||||||
| chr17:35720571 | ATATTTTT others(3): Show |
A | 4 | a0001c0001t0004g0158 a0001c0001t0004g0328 a0001c0001t0004g0332 others(1): Show |
4 | HG01943.hp2 HG02818.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-3052_2782-304 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720571 | ||||||
| chr17:35720572 | TA | T | 3 | a0001c0001t0002g0360 a0001c0002t0001g0259 a0001c0002t0001g0312 |
3 | HG02615.hp2 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2782-3052delA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720572 | |||||||
| chr17:35720573 | A | AT | 7 | a0001c0002t0001g0197 a0001c0002t0001g0228 a0001c0002t0001g0244 others(4): Show |
7 | HG00735.hp2 HG01517.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2782-3025dupT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT | 9 | a0001c0001t0003g0008 a0001c0001t0003g0020 a0001c0001t0003g0032 others(6): Show |
9 | HG01192.hp1 HG02056.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(11): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(4): Show |
2 | a0001c0001t0005g0134 a0001c0001t0005g0143 |
2 | HG02004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0051 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0015 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(19): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(10): Show |
1 | a0001c0001t0005g0154 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(21): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(27): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(25): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(3): Show |
1 | a0001c0001t0005g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0009 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(5): Show |
4 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0005g0146 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(16): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(6): Show |
1 | a0001c0001t0005g0149 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(1): Show |
8 | a0001c0001t0003g0023 a0001c0001t0003g0046 a0001c0001t0005g0003 others(5): Show |
8 | HG00741.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(12): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(4): Show |
2 | a0001c0001t0003g0047 a0001c0001t0020g0151 |
2 | HG00280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(15): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATAT others(7): Show |
1 | a0001c0001t0015g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(18): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATT | 6 | a0001c0001t0003g0012 a0001c0001t0003g0034 a0001c0001t0003g0042 others(3): Show |
6 | HG02165.hp1 NA18946.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(10): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATATATTT others(3): Show |
1 | a0001c0001t0005g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(14): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | ATT | 9 | a0001c0001t0003g0033 a0001c0002t0001g0211 a0001c0002t0001g0212 others(6): Show |
9 | HG00438.hp1 HG00558.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.2782-3026_2782-302 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | A | T | 44 | a0001c0002t0001g0062 a0001c0002t0001g0184 a0001c0002t0001g0186 others(41): Show |
44 | HG00733.hp2 HG01109.hp1 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.2782-3052A>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720573 | |||||||
| chr17:35720573 | AT | A | 18 | a0001c0001t0002g0358 a0001c0001t0005g0155 a0001c0002t0001g0005 others(15): Show |
19 | HG00597.hp1 HG01074.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2782-3025delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | ATTTT | A | 7 | a0001c0001t0004g0341 a0001c0001t0008g0061 a0001c0003t0001g0204 others(4): Show |
7 | HG01074.hp2 HG01123.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.2782-3028_2782-302 others(8): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720573 | ATTTTTTT | A | 10 | a0001c0001t0004g0335 a0001c0001t0004g0337 a0001c0001t0004g0342 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.2782-3031_2782-302 others(11): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720573 | ||||||
| chr17:35720574 | T | TA | 3 | a0001c0001t0002g0169 a0001c0001t0002g0173 a0001c0001t0007g0157 |
3 | HG01069.hp2 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(5): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATA | 3 | a0001c0001t0002g0119 a0001c0001t0002g0171 a0001c0001t0003g0029 |
3 | HG00280.hp2 NA19001.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(9): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA | 10 | a0001c0001t0002g0120 a0001c0001t0002g0172 a0001c0001t0002g0181 others(7): Show |
10 | HG00558.hp1 HG01891.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(11): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(2): Show |
4 | a0001c0001t0002g0355 a0001c0001t0005g0003 a0001c0001t0005g0136 others(1): Show |
4 | HG00140.hp2 HG00639.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2782-3051_2782-305 others(13): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(6): Show |
1 | a0001c0001t0003g0024 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(17): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(8): Show |
1 | a0001c0001t0005g0147 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(19): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(10): Show |
1 | a0001c0002t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(21): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(12): Show |
1 | a0001c0001t0003g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(23): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720574 | T | TATATATA others(14): Show |
1 | a0001c0002t0001g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2782-3051_2782-305 others(25): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720574 | |||||||
| chr17:35720575 | T | A | 31 | a0001c0001t0002g0004 a0001c0001t0002g0112 a0001c0001t0002g0113 others(28): Show |
33 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2782-3050T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720575 | |||||||
| chr17:35720576 | T | A | 16 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0171 others(13): Show |
16 | HG00280.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2782-3049T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720576 | |||||||
| chr17:35720577 | T | A | 24 | a0001c0001t0002g0004 a0001c0001t0002g0112 a0001c0001t0002g0113 others(21): Show |
26 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2782-3048T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720577 | |||||||
| chr17:35720578 | T | A | 9 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0173 others(6): Show |
9 | HG01069.hp2 HG01099.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2782-3047T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720578 | |||||||
| chr17:35720579 | T | A | 24 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(21): Show |
24 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.2782-3046T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720579 | |||||||
| chr17:35720580 | T | A | 9 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0004g0345 others(6): Show |
9 | HG00741.hp1 HG01891.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2782-3045T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720580 | |||||||
| chr17:35720581 | T | A | 20 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(17): Show |
20 | HG01081.hp2 HG01243.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.2782-3044T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720581 | |||||||
| chr17:35720582 | T | A | 8 | a0001c0001t0004g0335 a0001c0001t0004g0342 a0001c0001t0004g0347 others(5): Show |
8 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2782-3043T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720582 | |||||||
| chr17:35720583 | T | A | 14 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(11): Show |
14 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2782-3042T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720583 | |||||||
| chr17:35720584 | T | A | 1 | a0001c0002t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2782-3041T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720584 | |||||||
| chr17:35720585 | T | A | 8 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
8 | HG01081.hp2 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2782-3040T>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720585 | |||||||
| chr17:35720620 | G | A | 190 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0055 others(187): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2782-3005G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720620 | |||||||
| chr17:35720637 | A | ATC | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-2985_2782-298 others(6): Show |
AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35720637 | ||||||
| chr17:35720786 | A | G | 1 | a0001c0002t0001g0362 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2782-2839A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720786 | |||||||
| chr17:35720838 | C | T | 4 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0001c0001t0009g0161 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2782-2787C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35720838 | |||||||
| chr17:35721123 | T | TA | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2782-2498dupA | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35721123 | ||||||
| chr17:35721175 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-2450G>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35721175 | |||||||
| chr17:35721243 | C | T | 1 | a0001c0004t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2782-2382C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35721243 | |||||||
| chr17:35721529 | G | A | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0004g0320 others(1): Show |
4 | HG00673.hp2 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-2096G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35721529 | |||||||
| chr17:35721597 | G | A | 7 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0007g0156 others(4): Show |
7 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2782-2028G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35721597 | |||||||
| chr17:35722001 | G | A | 1 | a0001c0002t0001g0286 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2782-1624G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722001 | |||||||
| chr17:35722020 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2782-1605C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722020 | |||||||
| chr17:35722180 | G | A | 1 | a0001c0001t0005g0154 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2782-1445G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722180 | |||||||
| chr17:35722262 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0018g0083 |
2 | NA19066.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2782-1363A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722262 | |||||||
| chr17:35722370 | GT | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01109.hp2 HG01361.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782-1247delT | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35722370 | ||||||
| chr17:35722508 | T | G | 1 | a0001c0002t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2782-1117T>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722508 | |||||||
| chr17:35722563 | G | A | 1 | a0001c0006t0004g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2782-1062G>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722563 | |||||||
| chr17:35722605 | A | AC | 227 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2782-1019dupC | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 35722605 | ||||||
| chr17:35722628 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2782-997C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722628 | |||||||
| chr17:35722665 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2782-960T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722665 | |||||||
| chr17:35722677 | C | T | 3 | a0001c0002t0010g0240 a0001c0002t0010g0253 a0001c0002t0010g0254 |
3 | HG02886.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2782-948C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722677 | |||||||
| chr17:35722759 | C | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2782-866C>A | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722759 | |||||||
| chr17:35722764 | A | G | 42 | a0001c0001t0004g0158 a0001c0001t0004g0316 a0001c0001t0004g0318 others(39): Show |
42 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2782-861A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722764 | |||||||
| chr17:35722874 | T | C | 1 | a0001c0008t0002g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2782-751T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722874 | |||||||
| chr17:35722931 | C | T | 226 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(223): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2782-694C>T | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722931 | |||||||
| chr17:35722973 | A | G | 24 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0132 others(21): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2782-652A>G | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35722973 | |||||||
| chr17:35723399 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0065 others(62): Show |
66 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2782-226T>C | AP2B1 | ENSG00000006125.18 | transcript | ENST00000610402.5 | protein_coding | 21/21 | chr17 | 35723399 |