Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55814 |
| ensemblid | ENSG00000145734.20 |
| hgncid | 13652 |
| symbol | BDP1 |
| name | B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB |
| refseq_nuc | NM_018429.3 |
| refseq_prot | NP_060899.2 |
| ensembl_nuc | ENST00000358731.9 |
| ensembl_prot | ENSP00000351575.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 71455651 |
| end | 71567820 |
| strand | + |
| ver | v1.2 |
| region | chr5:71455651-71567820 |
| region5000 | chr5:71450651-71572820 |
| regionname0 | BDP1_chr5_71455651_71567820 |
| regionname5000 | BDP1_chr5_71450651_71572820 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2624 | 88 | 4 | 15 | 55 | 1 | 13 | 40 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0002 | 0/0 | 2624 | 75 | 6 | 13 | 49 | 2 | 5 | 38 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0003 | 0/0 | 2624 | 58 | 19 | 10 | 19 | 3 | 7 | 14 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0004 | 0/0 | 2624 | 11 | 3 | 3 | 3 | 0 | 2 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0005 | 0/0 | 2624 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0006 | 0/0 | 2624 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0007 | 0/0 | 2624 | 8 | 0 | 6 | 0 | 1 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0008 | 0/0 | 2624 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0009 | 0/0 | 2624 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0010 | 0/1 | 2624 | 5 | 0 | 3 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0011 | 0/0 | 2624 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0012 | 0/0 | 2624 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0013 | 0/0 | 2624 | 5 | 0 | 0 | 4 | 0 | 1 | 4 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0014 | 0/0 | 2624 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0015 | 0/0 | 2624 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0016 | 0/0 | 2624 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0017 | 0/0 | 2624 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0018 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0019 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0020 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0021 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0022 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0023 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0024 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0025 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0026 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0027 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0028 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0029 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0030 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0031 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0032 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0033 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0034 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0035 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0036 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0037 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0038 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0039 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0040 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0041 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(2619): Show |
chr5 | 71450651 | 71572820 |
| a0042 | 0/0 | 1589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | MFRRA others(1584): Show |
chr5 | 71450651 | 71572820 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 7872 | 84 | 3 | 15 | 54 | 1 | 11 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0001c0021 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0001c0022 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0001c0026 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0001c0030 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0002c0002 | 0/0 | 7872 | 73 | 6 | 13 | 47 | 2 | 5 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0002c0039 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0002c0041 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0003c0003 | 0/0 | 7872 | 57 | 18 | 10 | 19 | 3 | 7 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0003c0049 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0004c0004 | 0/0 | 7872 | 11 | 3 | 3 | 3 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0005c0005 | 0/0 | 7872 | 10 | 9 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0006c0007 | 0/0 | 7872 | 7 | 7 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0006c0024 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0006c0028 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0007c0006 | 0/0 | 7872 | 8 | 0 | 6 | 0 | 1 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0008c0009 | 0/0 | 7872 | 6 | 6 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0008c0048 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0009c0008 | 0/0 | 7872 | 6 | 5 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0010c0011 | 0/1 | 7872 | 5 | 0 | 3 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0011c0010 | 0/0 | 7872 | 5 | 4 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0012c0012 | 0/0 | 7872 | 5 | 5 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0013c0013 | 0/0 | 7872 | 5 | 0 | 0 | 4 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0014c0014 | 0/0 | 7872 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0015c0016 | 0/0 | 7872 | 2 | 0 | 0 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0016c0017 | 0/0 | 7872 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0017c0015 | 0/0 | 7872 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0018c0046 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0019c0042 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0020c0020 | 0/0 | 7872 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0021c0035 | 0/0 | 7872 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0022c0031 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0023c0018 | 0/0 | 7872 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0024c0033 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0025c0043 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0026c0032 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0027c0019 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0028c0037 | 0/0 | 7872 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0029c0050 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0030c0051 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0031c0038 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0032c0027 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0033c0047 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0034c0029 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0035c0034 | 0/0 | 7872 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0036c0040 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0037c0023 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0038c0036 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0039c0044 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0040c0045 | 0/0 | 7872 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0041c0052 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7867): Show |
chr5 | 71450651 | 71572820 | ||
| a0042c0025 | 0/0 | 7865 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | ATGTT others(7860): Show |
chr5 | 71450651 | 71572820 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 11037 | 80 | 3 | 14 | 52 | 1 | 10 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0001t0011 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0001t0019 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0001t0020 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0001t0022 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0021t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0022t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0026t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0001c0030t0002 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0002t0001 | 0/0 | 11037 | 55 | 6 | 11 | 31 | 2 | 5 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0002t0003 | 0/0 | 11037 | 11 | 0 | 1 | 10 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0002t0005 | 0/0 | 11037 | 6 | 0 | 0 | 6 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0002t0012 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0039t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0002c0041t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0003t0001 | 0/0 | 11037 | 52 | 14 | 10 | 18 | 3 | 7 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0003t0006 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0003t0008 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0003t0013 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0003t0018 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0003c0049t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0004c0004t0004 | 0/0 | 11037 | 9 | 1 | 3 | 3 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0004c0004t0010 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0005c0005t0001 | 0/0 | 11037 | 8 | 8 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0005c0005t0015 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0005c0005t0017 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0006c0007t0002 | 0/0 | 11037 | 7 | 7 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0006c0024t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0006c0028t0021 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0007c0006t0002 | 0/0 | 11037 | 8 | 0 | 6 | 0 | 1 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0008c0009t0002 | 0/0 | 11037 | 6 | 6 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0008c0048t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0009c0008t0002 | 0/0 | 11037 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0009c0008t0007 | 0/0 | 11030 | 4 | 4 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11025): Show |
chr5 | 71450651 | 71572820 |
| a0010c0011t0001 | 0/0 | 11037 | 4 | 0 | 3 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0010c0011t0014 | 0/1 | 11037 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0011c0010t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0011c0010t0006 | 0/0 | 11037 | 4 | 3 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0012c0012t0003 | 0/0 | 11037 | 5 | 5 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0013c0013t0001 | 0/0 | 11037 | 5 | 0 | 0 | 4 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0014c0014t0001 | 0/0 | 11037 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0015c0016t0001 | 0/0 | 11037 | 2 | 0 | 0 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0016c0017t0009 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0017c0015t0001 | 0/0 | 11037 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0018c0046t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0019c0042t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0020c0020t0023 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0021c0035t0001 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0022c0031t0016 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0023c0018t0001 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0024c0033t0003 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0025c0043t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0026c0032t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0027c0019t0024 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0028c0037t0003 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0029c0050t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0030c0051t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0031c0038t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0032c0027t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0033c0047t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0034c0029t0004 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0035c0034t0003 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0036c0040t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0037c0023t0002 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0038c0036t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0039c0044t0005 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0040c0045t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0041c0052t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11032): Show |
chr5 | 71450651 | 71572820 |
| a0042c0025t0002 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | GAGGG others(11025): Show |
chr5 | 71450651 | 71572820 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0019g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0022g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0021t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0022t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0026t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0030t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0012g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0039t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0041t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0049t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0010g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0015g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0017g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0024t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0028t0021g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0048t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0011t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0011t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0011t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0011t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0011t0014g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0010t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0010t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0010t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0010t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0010t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0012t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0012t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0012t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0012t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0012t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0014c0014t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0014c0014t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0015c0016t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0015c0016t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0016c0017t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0016c0017t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0017c0015t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0017c0015t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0018c0046t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0019c0042t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0020c0020t0023g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0021c0035t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0022c0031t0016g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0023c0018t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0024c0033t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0025c0043t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0026c0032t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0027c0019t0024g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0028c0037t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0029c0050t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0030c0051t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0031c0038t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0032c0027t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0033c0047t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0034c0029t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0035c0034t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0036c0040t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0037c0023t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0038c0036t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0039c0044t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0040c0045t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0041c0052t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0042c0025t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0257 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00099 | hp2 | a0018 | c0046 | t0002 | g0030 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0261 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0294 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0152 | EUR | FIN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00280 | hp2 | a0007 | c0006 | t0002 | g0050 | EUR | FIN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0174 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0213 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00621 | hp1 | a0019 | c0042 | t0001 | g0191 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00642 | hp1 | a0010 | c0011 | t0001 | g0176 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00642 | hp2 | a0020 | c0020 | t0023 | g0120 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00733 | hp1 | a0014 | c0014 | t0001 | g0006 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0177 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00741 | hp1 | a0005 | c0005 | t0015 | g0309 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00741 | hp2 | a0011 | c0010 | t0006 | g0249 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01069 | hp1 | a0007 | c0006 | t0002 | g0052 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0289 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0290 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01071 | hp2 | a0007 | c0006 | t0002 | g0051 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0271 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0260 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01167 | hp1 | a0009 | c0008 | t0002 | g0008 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0057 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01192 | hp1 | a0007 | c0006 | t0002 | g0084 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0264 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01243 | hp2 | a0021 | c0035 | t0001 | g0124 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0256 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01257 | hp1 | a0007 | c0006 | t0002 | g0049 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0262 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0258 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01433 | hp1 | a0004 | c0004 | t0004 | g0315 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01496 | hp2 | a0002 | c0002 | t0012 | g0158 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01884 | hp1 | a0022 | c0031 | t0016 | g0011 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0238 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01943 | hp1 | a0004 | c0004 | t0004 | g0312 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01975 | hp1 | a0010 | c0011 | t0001 | g0193 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01978 | hp1 | a0023 | c0018 | t0001 | g0190 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01978 | hp2 | a0004 | c0004 | t0004 | g0311 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01981 | hp1 | a0010 | c0011 | t0001 | g0192 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0283 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02027 | hp1 | a0004 | c0004 | t0004 | g0310 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02027 | hp2 | a0002 | c0039 | t0001 | g0208 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02055 | hp1 | a0003 | c0003 | t0018 | g0306 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0304 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0282 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02071 | hp2 | a0001 | c0001 | t0022 | g0014 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02080 | hp1 | a0024 | c0033 | t0003 | g0139 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02148 | hp1 | a0007 | c0006 | t0002 | g0047 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0243 | EAS | CDX | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02257 | hp1 | a0026 | c0032 | t0001 | g0115 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02258 | hp1 | a0027 | c0019 | t0024 | g0119 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02258 | hp2 | a0011 | c0010 | t0006 | g0241 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02280 | hp2 | a0012 | c0012 | t0003 | g0205 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02300 | hp1 | a0028 | c0037 | t0003 | g0206 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02451 | hp1 | a0012 | c0012 | t0003 | g0167 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0297 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0246 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02572 | hp2 | a0008 | c0009 | t0002 | g0078 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02602 | hp1 | a0029 | c0050 | t0001 | g0287 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02602 | hp2 | a0015 | c0016 | t0001 | g0195 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02615 | hp1 | a0011 | c0010 | t0001 | g0004 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02615 | hp2 | a0003 | c0003 | t0006 | g0240 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02622 | hp1 | a0016 | c0017 | t0009 | g0117 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0280 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02683 | hp1 | a0015 | c0016 | t0001 | g0180 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02683 | hp2 | a0030 | c0051 | t0001 | g0263 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02735 | hp1 | a0031 | c0038 | t0001 | g0143 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02735 | hp2 | a0032 | c0027 | t0002 | g0012 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0291 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0284 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02809 | hp2 | a0005 | c0005 | t0001 | g0298 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02886 | hp1 | a0005 | c0005 | t0017 | g0296 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0295 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02895 | hp2 | a0006 | c0007 | t0002 | g0007 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02896 | hp1 | a0005 | c0005 | t0001 | g0236 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02896 | hp2 | a0006 | c0024 | t0002 | g0109 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02922 | hp1 | a0012 | c0012 | t0003 | g0166 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02922 | hp2 | a0008 | c0048 | t0002 | g0010 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02965 | hp1 | a0003 | c0003 | t0008 | g0278 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02965 | hp2 | a0006 | c0028 | t0021 | g0009 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02970 | hp1 | a0008 | c0009 | t0002 | g0031 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02970 | hp2 | a0003 | c0003 | t0008 | g0276 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02976 | hp1 | a0009 | c0008 | t0007 | g0100 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0277 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0247 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03041 | hp1 | a0006 | c0007 | t0002 | g0110 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03098 | hp1 | a0009 | c0008 | t0002 | g0095 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03098 | hp2 | a0011 | c0010 | t0006 | g0308 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03130 | hp1 | a0006 | c0007 | t0002 | g0112 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03130 | hp2 | a0033 | c0047 | t0001 | g0229 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03139 | hp1 | a0008 | c0009 | t0002 | g0033 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03139 | hp2 | a0012 | c0012 | t0003 | g0148 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03195 | hp1 | a0008 | c0009 | t0002 | g0029 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0285 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03209 | hp1 | a0006 | c0007 | t0002 | g0113 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0274 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03225 | hp2 | a0009 | c0008 | t0007 | g0102 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03239 | hp2 | a0001 | c0021 | t0002 | g0059 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03453 | hp2 | a0014 | c0014 | t0001 | g0005 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03486 | hp1 | a0004 | c0004 | t0010 | g0320 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03486 | hp2 | a0006 | c0007 | t0002 | g0108 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03490 | hp1 | a0010 | c0011 | t0001 | g0203 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0292 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0293 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03516 | hp1 | a0006 | c0007 | t0002 | g0114 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03516 | hp2 | a0011 | c0010 | t0006 | g0305 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03540 | hp1 | a0016 | c0017 | t0009 | g0116 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0235 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03579 | hp1 | a0009 | c0008 | t0007 | g0103 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0255 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03669 | hp2 | a0034 | c0029 | t0004 | g0316 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03710 | hp2 | a0004 | c0004 | t0004 | g0314 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03927 | hp2 | a0013 | c0013 | t0001 | g0145 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03942 | hp1 | a0001 | c0022 | t0002 | g0086 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0017 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04184 | hp1 | a0035 | c0034 | t0003 | g0140 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04184 | hp2 | a0007 | c0006 | t0002 | g0048 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04199 | hp1 | a0004 | c0004 | t0004 | g0313 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0268 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0270 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0231 | EAS | CHB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0234 | AFR | YRI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0275 | AFR | YRI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18939 | hp2 | a0036 | c0040 | t0001 | g0153 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18943 | hp1 | a0003 | c0003 | t0013 | g0251 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18957 | hp2 | a0002 | c0041 | t0001 | g0147 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18959 | hp2 | a0002 | c0002 | t0005 | g0178 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18963 | hp1 | a0002 | c0002 | t0005 | g0187 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18966 | hp1 | a0001 | c0030 | t0002 | g0036 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18974 | hp1 | a0017 | c0015 | t0001 | g0222 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0216 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18982 | hp2 | a0037 | c0023 | t0002 | g0073 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18984 | hp1 | a0038 | c0036 | t0001 | g0149 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18989 | hp2 | a0013 | c0013 | t0001 | g0134 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18991 | hp2 | a0002 | c0002 | t0005 | g0183 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18998 | hp2 | a0039 | c0044 | t0005 | g0194 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18999 | hp2 | a0002 | c0002 | t0005 | g0299 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19004 | hp1 | a0013 | c0013 | t0001 | g0003 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19006 | hp2 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19030 | hp1 | a0040 | c0045 | t0002 | g0096 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19043 | hp1 | a0009 | c0008 | t0007 | g0101 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19054 | hp1 | a0013 | c0013 | t0001 | g0218 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19054 | hp2 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19063 | hp1 | a0002 | c0002 | t0005 | g0179 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19064 | hp1 | a0017 | c0015 | t0001 | g0225 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19070 | hp1 | a0041 | c0052 | t0001 | g0227 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0272 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19082 | hp1 | a0004 | c0004 | t0004 | g0318 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19087 | hp1 | a0004 | c0004 | t0004 | g0319 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19088 | hp2 | a0013 | c0013 | t0001 | g0003 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19091 | hp1 | a0042 | c0025 | t0002 | g0070 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20129 | hp1 | a0004 | c0004 | t0010 | g0321 | AFR | ASW | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20129 | hp2 | a0008 | c0009 | t0002 | g0032 | AFR | ASW | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | TSI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01123 | hp1 | a0007 | c0006 | t0002 | g0018 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02109 | hp2 | a0025 | c0043 | t0001 | g0141 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02486 | hp1 | a0012 | c0012 | t0003 | g0210 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0307 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02559 | hp1 | a0003 | c0049 | t0001 | g0250 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0237 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03471 | hp1 | a0008 | c0009 | t0002 | g0023 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0279 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG06807 | hp1 | a0004 | c0004 | t0004 | g0317 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20300 | hp2 | a0006 | c0007 | t0002 | g0111 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA21309 | hp1 | a0001 | c0026 | t0002 | g0013 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| homoSapiens | chm13v2 | a0010 | c0011 | t0014 | g0135 | REF | REF | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71455954 | A | G | 1 | a0041 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.77A>G | p.Asn26Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 304/11037 | 77/7875 | 26/2624 | chr5 | 71455954 | |||
| chr5:71455991 | T | G | 37 | a0001 a0002 a0004 others(34): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
missense_variant | MODERATE | c.114T>G | p.Asp38Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 341/11037 | 114/7875 | 38/2624 | chr5 | 71455991 | |||
| chr5:71458621 | T | G | 1 | a0023 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.255T>G | p.Ser85Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 482/11037 | 255/7875 | 85/2624 | chr5 | 71458621 | |||
| chr5:71458648 | A | T | 1 | a0013 | 5 | HG03927.hp2 NA18989.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.282A>T | p.Arg94Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 509/11037 | 282/7875 | 94/2624 | chr5 | 71458648 | |||
| chr5:71458740 | C | T | 1 | a0009 | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.374C>T | p.Ala125Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 601/11037 | 374/7875 | 125/2624 | chr5 | 71458740 | |||
| chr5:71467391 | G | A | 2 | a0020 a0027 |
2 | HG00642.hp2 HG02258.hp1 |
missense_variant | MODERATE | c.823G>A | p.Val275Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/39 | 1050/11037 | 823/7875 | 275/2624 | chr5 | 71467391 | |||
| chr5:71491003 | G | T | 2 | a0016 a0033 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1512G>T | p.Arg504Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/39 | 1739/11037 | 1512/7875 | 504/2624 | chr5 | 71491003 | |||
| chr5:71502714 | A | G | 2 | a0007 a0018 |
9 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(6): Show |
missense_variant | MODERATE | c.2164A>G | p.Lys722Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2391/11037 | 2164/7875 | 722/2624 | chr5 | 71502714 | |||
| chr5:71502726 | A | T | 1 | a0040 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2176A>T | p.Ile726Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2403/11037 | 2176/7875 | 726/2624 | chr5 | 71502726 | |||
| chr5:71504648 | C | T | 15 | a0002 a0010 a0012 others(12): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
missense_variant | MODERATE | c.2269C>T | p.Arg757Cys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/39 | 2496/11037 | 2269/7875 | 757/2624 | chr5 | 71504648 | |||
| chr5:71504711 | G | A | 12 | a0001 a0004 a0006 others(9): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
missense_variant | MODERATE | c.2332G>A | p.Val778Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/39 | 2559/11037 | 2332/7875 | 778/2624 | chr5 | 71504711 | |||
| chr5:71509484 | G | T | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2392G>T | p.Ala798Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2619/11037 | 2392/7875 | 798/2624 | chr5 | 71509484 | |||
| chr5:71509491 | A | G | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2399A>G | p.Lys800Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2626/11037 | 2399/7875 | 800/2624 | chr5 | 71509491 | |||
| chr5:71509494 | T | C | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2402T>C | p.Leu801Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2629/11037 | 2402/7875 | 801/2624 | chr5 | 71509494 | |||
| chr5:71509498 | C | G | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2406C>G | p.Asn802Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2633/11037 | 2406/7875 | 802/2624 | chr5 | 71509498 | |||
| chr5:71509499 | C | A | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2407C>A | p.Gln803Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2634/11037 | 2407/7875 | 803/2624 | chr5 | 71509499 | |||
| chr5:71509502 | G | T | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2410G>T | p.Val804Phe | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2637/11037 | 2410/7875 | 804/2624 | chr5 | 71509502 | |||
| chr5:71509503 | T | A | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2411T>A | p.Val804Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2638/11037 | 2411/7875 | 804/2624 | chr5 | 71509503 | |||
| chr5:71509509 | T | G | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2417T>G | p.Ile806Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2644/11037 | 2417/7875 | 806/2624 | chr5 | 71509509 | |||
| chr5:71509512 | T | G | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2420T>G | p.Leu807Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2647/11037 | 2420/7875 | 807/2624 | chr5 | 71509512 | |||
| chr5:71509515 | G | C | 1 | a0038 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2423G>C | p.Arg808Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2650/11037 | 2423/7875 | 808/2624 | chr5 | 71509515 | |||
| chr5:71510016 | A | T | 1 | a0039 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.2924A>T | p.Asp975Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3151/11037 | 2924/7875 | 975/2624 | chr5 | 71510016 | |||
| chr5:71510135 | A | C | 1 | a0020 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3043A>C | p.Thr1015Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3270/11037 | 3043/7875 | 1015/2624 | chr5 | 71510135 | |||
| chr5:71510157 | G | A | 1 | a0033 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.3065G>A | p.Arg1022Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3292/11037 | 3065/7875 | 1022/2624 | chr5 | 71510157 | |||
| chr5:71510304 | G | C | 1 | a0016 | 2 | HG02622.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.3212G>C | p.Ser1071Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3439/11037 | 3212/7875 | 1071/2624 | chr5 | 71510304 | |||
| chr5:71510360 | G | T | 1 | a0025 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3268G>T | p.Asp1090Tyr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3495/11037 | 3268/7875 | 1090/2624 | chr5 | 71510360 | |||
| chr5:71510399 | A | G | 1 | a0034 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3307A>G | p.Asn1103Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3534/11037 | 3307/7875 | 1103/2624 | chr5 | 71510399 | |||
| chr5:71510456 | G | A | 1 | a0018 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.3364G>A | p.Gly1122Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3591/11037 | 3364/7875 | 1122/2624 | chr5 | 71510456 | |||
| chr5:71510630 | G | A | 13 | a0001 a0004 a0006 others(10): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
missense_variant | MODERATE | c.3538G>A | p.Gly1180Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3765/11037 | 3538/7875 | 1180/2624 | chr5 | 71510630 | |||
| chr5:71510694 | A | C | 1 | a0030 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3602A>C | p.Glu1201Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3829/11037 | 3602/7875 | 1201/2624 | chr5 | 71510694 | |||
| chr5:71510780 | A | G | 1 | a0021 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.3688A>G | p.Ile1230Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3915/11037 | 3688/7875 | 1230/2624 | chr5 | 71510780 | |||
| chr5:71510810 | G | T | 1 | a0019 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.3718G>T | p.Val1240Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3945/11037 | 3718/7875 | 1240/2624 | chr5 | 71510810 | |||
| chr5:71510822 | T | A | 13 | a0001 a0004 a0006 others(10): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
missense_variant | MODERATE | c.3730T>A | p.Phe1244Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3957/11037 | 3730/7875 | 1244/2624 | chr5 | 71510822 | |||
| chr5:71510884 | C | G | 36 | a0001 a0002 a0004 others(33): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
missense_variant | MODERATE | c.3792C>G | p.Ile1264Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4019/11037 | 3792/7875 | 1264/2624 | chr5 | 71510884 | |||
| chr5:71510931 | C | G | 1 | a0015 | 2 | HG02602.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.3839C>G | p.Ala1280Gly | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4066/11037 | 3839/7875 | 1280/2624 | chr5 | 71510931 | |||
| chr5:71511131 | G | A | 36 | a0001 a0002 a0004 others(33): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
missense_variant | MODERATE | c.4039G>A | p.Val1347Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4266/11037 | 4039/7875 | 1347/2624 | chr5 | 71511131 | |||
| chr5:71512419 | T | C | 1 | a0037 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.4238T>C | p.Ile1413Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/39 | 4465/11037 | 4238/7875 | 1413/2624 | chr5 | 71512419 | |||
| chr5:71513342 | A | G | 10 | a0001 a0006 a0007 others(7): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
missense_variant | MODERATE | c.4405A>G | p.Lys1469Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/39 | 4632/11037 | 4405/7875 | 1469/2624 | chr5 | 71513342 | |||
| chr5:71515109 | G | T | 1 | a0027 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.4636G>T | p.Val1546Phe | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/39 | 4863/11037 | 4636/7875 | 1546/2624 | chr5 | 71515109 | |||
| chr5:71516170 | GGACAGAG others(10): Show |
G | 1 | a0042 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.4764_4780delGAGGCA others(11): Show |
p.Gln1590fs | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 4991/11037 | 4764/7875 | 1588/2624 | INFO_REALIGN_3_PRIME | chr5 | 71516170 | ||
| chr5:71516213 | T | G | 1 | a0042 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.4802T>G | p.Ile1601Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 5029/11037 | 4802/7875 | 1601/2624 | chr5 | 71516213 | |||
| chr5:71516218 | G | GCAAGGAT others(3): Show |
1 | a0042 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.4807_4808insCAAGGA others(4): Show |
p.Glu1603fs | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 5035/11037 | 4808/7875 | 1603/2624 | chr5 | 71516218 | |||
| chr5:71522303 | C | A | 2 | a0004 a0034 |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
missense_variant | MODERATE | c.5006C>A | p.Pro1669Gln | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5233/11037 | 5006/7875 | 1669/2624 | chr5 | 71522303 | |||
| chr5:71522323 | C | G | 1 | a0012 | 5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
missense_variant | MODERATE | c.5026C>G | p.Gln1676Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5253/11037 | 5026/7875 | 1676/2624 | chr5 | 71522323 | |||
| chr5:71522328 | G | C | 2 | a0021 a0026 |
2 | HG01243.hp2 HG02257.hp1 |
missense_variant | MODERATE | c.5031G>C | p.Met1677Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5258/11037 | 5031/7875 | 1677/2624 | chr5 | 71522328 | |||
| chr5:71522774 | A | C | 1 | a0035 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.5212A>C | p.Thr1738Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/39 | 5439/11037 | 5212/7875 | 1738/2624 | chr5 | 71522774 | |||
| chr5:71524099 | C | T | 1 | a0029 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.5548C>T | p.Arg1850Trp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/39 | 5775/11037 | 5548/7875 | 1850/2624 | chr5 | 71524099 | |||
| chr5:71541468 | A | C | 38 | a0001 a0002 a0004 others(35): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
missense_variant | MODERATE | c.6037A>C | p.Ile2013Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 29/39 | 6264/11037 | 6037/7875 | 2013/2624 | chr5 | 71541468 | |||
| chr5:71542154 | G | A | 1 | a0017 | 2 | NA18974.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.6301G>A | p.Ala2101Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/39 | 6528/11037 | 6301/7875 | 2101/2624 | chr5 | 71542154 | |||
| chr5:71545076 | A | G | 1 | a0027 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.6601A>G | p.Met2201Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/39 | 6828/11037 | 6601/7875 | 2201/2624 | chr5 | 71545076 | |||
| chr5:71548685 | A | G | 1 | a0022 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.6748A>G | p.Thr2250Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/39 | 6975/11037 | 6748/7875 | 2250/2624 | chr5 | 71548685 | |||
| chr5:71548691 | A | C | 1 | a0027 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.6754A>C | p.Thr2252Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/39 | 6981/11037 | 6754/7875 | 2252/2624 | chr5 | 71548691 | |||
| chr5:71549573 | A | G | 1 | a0006 | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
missense_variant | MODERATE | c.6962A>G | p.Lys2321Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/39 | 7189/11037 | 6962/7875 | 2321/2624 | chr5 | 71549573 | |||
| chr5:71553120 | T | C | 1 | a0028 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.7000T>C | p.Cys2334Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7227/11037 | 7000/7875 | 2334/2624 | chr5 | 71553120 | |||
| chr5:71553142 | G | T | 1 | a0036 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.7022G>T | p.Gly2341Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7249/11037 | 7022/7875 | 2341/2624 | chr5 | 71553142 | |||
| chr5:71553309 | T | G | 1 | a0013 | 5 | HG03927.hp2 NA18989.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.7189T>G | p.Tyr2397Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7416/11037 | 7189/7875 | 2397/2624 | chr5 | 71553309 | |||
| chr5:71560035 | A | G | 1 | a0032 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.7294A>G | p.Thr2432Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/39 | 7521/11037 | 7294/7875 | 2432/2624 | chr5 | 71560035 | |||
| chr5:71562441 | A | G | 2 | a0023 a0031 |
2 | HG01978.hp1 HG02735.hp1 |
missense_variant | MODERATE | c.7664A>G | p.Asn2555Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7891/11037 | 7664/7875 | 2555/2624 | chr5 | 71562441 | |||
| chr5:71562515 | A | G | 1 | a0010 | 4 | HG00642.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.7738A>G | p.Thr2580Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7965/11037 | 7738/7875 | 2580/2624 | chr5 | 71562515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71502698 | T | A | 1 | a0001c0021 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2148T>A | p.Gly716Gly | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2375/11037 | 2148/7875 | 716/2624 | chr5 | 71502698 | |||
| chr5:71509474 | G | A | 1 | a0038c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2382G>A | p.Glu794Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2609/11037 | 2382/7875 | 794/2624 | chr5 | 71509474 | |||
| chr5:71509480 | T | C | 1 | a0038c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2388T>C | p.Asn796Asn | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2615/11037 | 2388/7875 | 796/2624 | chr5 | 71509480 | |||
| chr5:71509495 | T | A | 1 | a0038c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2403T>A | p.Leu801Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2630/11037 | 2403/7875 | 801/2624 | chr5 | 71509495 | |||
| chr5:71509534 | A | C | 1 | a0038c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2442A>C | p.Pro814Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2669/11037 | 2442/7875 | 814/2624 | chr5 | 71509534 | |||
| chr5:71509627 | A | G | 1 | a0001c0030 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.2535A>G | p.Ala845Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2762/11037 | 2535/7875 | 845/2624 | chr5 | 71509627 | |||
| chr5:71510602 | G | A | 1 | a0008c0048 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.3510G>A | p.Glu1170Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3737/11037 | 3510/7875 | 1170/2624 | chr5 | 71510602 | |||
| chr5:71510746 | G | A | 1 | a0001c0022 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3654G>A | p.Lys1218Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3881/11037 | 3654/7875 | 1218/2624 | chr5 | 71510746 | |||
| chr5:71513209 | G | A | 1 | a0006c0024 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.4272G>A | p.Lys1424Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/39 | 4499/11037 | 4272/7875 | 1424/2624 | chr5 | 71513209 | |||
| chr5:71522929 | A | G | 1 | a0006c0028 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.5367A>G | p.Gln1789Gln | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/39 | 5594/11037 | 5367/7875 | 1789/2624 | chr5 | 71522929 | |||
| chr5:71524101 | G | T | 1 | a0002c0041 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.5550G>T | p.Arg1850Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/39 | 5777/11037 | 5550/7875 | 1850/2624 | chr5 | 71524101 | |||
| chr5:71532319 | T | G | 1 | a0014c0014 | 2 | HG00733.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.5784T>G | p.Thr1928Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/39 | 6011/11037 | 5784/7875 | 1928/2624 | chr5 | 71532319 | |||
| chr5:71532424 | G | A | 1 | a0033c0047 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.5889G>A | p.Pro1963Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/39 | 6116/11037 | 5889/7875 | 1963/2624 | chr5 | 71532424 | |||
| chr5:71539065 | C | A | 2 | a0004c0004 a0034c0029 |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
synonymous_variant | LOW | c.5916C>A | p.Ile1972Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/39 | 6143/11037 | 5916/7875 | 1972/2624 | chr5 | 71539065 | |||
| chr5:71544406 | C | T | 16 | a0001c0001 a0001c0021 a0001c0022 others(13): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
synonymous_variant | LOW | c.6462C>T | p.Leu2154Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/39 | 6689/11037 | 6462/7875 | 2154/2624 | chr5 | 71544406 | |||
| chr5:71553134 | T | G | 1 | a0003c0049 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.7014T>G | p.Thr2338Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7241/11037 | 7014/7875 | 2338/2624 | chr5 | 71553134 | |||
| chr5:71553194 | G | T | 19 | a0001c0001 a0001c0021 a0001c0022 others(16): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
synonymous_variant | LOW | c.7074G>T | p.Pro2358Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7301/11037 | 7074/7875 | 2358/2624 | chr5 | 71553194 | |||
| chr5:71560232 | A | G | 1 | a0002c0039 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.7491A>G | p.Leu2497Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/39 | 7718/11037 | 7491/7875 | 2497/2624 | chr5 | 71560232 | |||
| chr5:71562367 | C | T | 17 | a0002c0002 a0002c0039 a0002c0041 others(14): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
synonymous_variant | LOW | c.7590C>T | p.Arg2530Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7817/11037 | 7590/7875 | 2530/2624 | chr5 | 71562367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71455691 | A | G | 1 | a0004c0004t0010 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-187A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 187 | chr5 | 71455691 | ||||||
| chr5:71455798 | A | T | 3 | a0016c0017t0009 a0020c0020t0023 a0027c0019t0024 |
4 | HG00642.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-80A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 80 | chr5 | 71455798 | ||||||
| chr5:71455820 | C | A | 1 | a0001c0001t0011 | 1 | NA19054.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 58 | chr5 | 71455820 | ||||||
| chr5:71455876 | C | T | 1 | a0001c0001t0022 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 2 | chr5 | 71455876 | ||||||
| chr5:71565377 | A | G | 1 | a0027c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 492 | chr5 | 71565377 | ||||||
| chr5:71565662 | G | A | 3 | a0004c0004t0004 a0004c0004t0010 a0034c0029t0004 |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*777G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 777 | chr5 | 71565662 | ||||||
| chr5:71565925 | A | G | 2 | a0002c0002t0005 a0039c0044t0005 |
7 | NA18959.hp2 NA18963.hp1 NA18978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1040A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1040 | chr5 | 71565925 | ||||||
| chr5:71565930 | T | G | 3 | a0004c0004t0004 a0004c0004t0010 a0034c0029t0004 |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1045 | chr5 | 71565930 | ||||||
| chr5:71566023 | A | T | 2 | a0003c0003t0006 a0011c0010t0006 |
5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1138A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1138 | chr5 | 71566023 | ||||||
| chr5:71566107 | A | G | 1 | a0027c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1222 | chr5 | 71566107 | ||||||
| chr5:71566127 | A | T | 1 | a0020c0020t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1242 | chr5 | 71566127 | ||||||
| chr5:71566232 | C | T | 25 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(22): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1347C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1347 | chr5 | 71566232 | ||||||
| chr5:71566560 | A | G | 1 | a0003c0003t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1675 | chr5 | 71566560 | ||||||
| chr5:71566620 | C | T | 1 | a0003c0003t0008 | 2 | HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1735C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1735 | chr5 | 71566620 | ||||||
| chr5:71566910 | T | C | 1 | a0027c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2025 | chr5 | 71566910 | ||||||
| chr5:71566977 | C | A | 1 | a0002c0002t0012 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2092C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2092 | chr5 | 71566977 | ||||||
| chr5:71567047 | C | T | 25 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(22): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2162C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2162 | chr5 | 71567047 | ||||||
| chr5:71567052 | C | T | 6 | a0002c0002t0003 a0002c0002t0012 a0012c0012t0003 others(3): Show |
20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2167C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2167 | chr5 | 71567052 | ||||||
| chr5:71567264 | C | T | 1 | a0005c0005t0017 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2379C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2379 | chr5 | 71567264 | ||||||
| chr5:71567329 | G | A | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2444 | chr5 | 71567329 | ||||||
| chr5:71567402 | A | G | 1 | a0006c0028t0021 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2517 | chr5 | 71567402 | ||||||
| chr5:71567443 | A | G | 1 | a0022c0031t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2558A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2558 | chr5 | 71567443 | ||||||
| chr5:71567532 | AAGTTTTT | A | 1 | a0009c0008t0007 | 4 | HG02976.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2649_*2655delGTTT others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2649 | INFO_REALIGN_3_PRIME | chr5 | 71567532 | |||||
| chr5:71567605 | C | T | 1 | a0001c0001t0020 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2720C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2720 | chr5 | 71567605 | ||||||
| chr5:71567652 | C | A | 1 | a0003c0003t0013 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2767C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2767 | chr5 | 71567652 | ||||||
| chr5:71567654 | A | G | 1 | a0005c0005t0015 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2769A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2769 | chr5 | 71567654 | ||||||
| chr5:71567775 | G | T | 3 | a0004c0004t0004 a0004c0004t0010 a0034c0029t0004 |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2890G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2890 | chr5 | 71567775 | ||||||
| chr5:71567789 | T | A | 2 | a0016c0017t0009 a0020c0020t0023 |
3 | HG00642.hp2 HG02622.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2904T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2904 | chr5 | 71567789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71456153 | C | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+64C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456153 | |||||||
| chr5:71456941 | C | A | 142 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(139): Show |
144 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.212+852C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456941 | |||||||
| chr5:71456996 | A | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG02056.hp2 NA18950.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+907A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456996 | |||||||
| chr5:71457030 | A | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.212+941A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457030 | |||||||
| chr5:71457059 | T | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212+970T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457059 | |||||||
| chr5:71457101 | GTT | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+1013_212+1014d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457101 | |||||||
| chr5:71457195 | G | C | 10 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(7): Show |
10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+1106G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457195 | |||||||
| chr5:71457275 | C | A | 1 | a0006c0007t0002g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.212+1186C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457275 | |||||||
| chr5:71457307 | G | GT | 16 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0123 others(13): Show |
16 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.212+1235dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr5 | 71457307 | ||||||
| chr5:71457307 | GT | G | 6 | a0002c0002t0001g0133 a0006c0028t0021g0009 a0008c0048t0002g0010 others(3): Show |
6 | HG01167.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.212+1235delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr5 | 71457307 | ||||||
| chr5:71457414 | C | T | 1 | a0002c0002t0005g0299 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.213-1165C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457414 | |||||||
| chr5:71457418 | C | G | 1 | a0005c0005t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.213-1161C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457418 | |||||||
| chr5:71457481 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.213-1098A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457481 | |||||||
| chr5:71458107 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.213-472G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458107 | |||||||
| chr5:71458370 | TAA | T | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.213-208_213-207del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458370 | |||||||
| chr5:71458371 | A | G | 4 | a0008c0009t0002g0023 a0008c0009t0002g0031 a0008c0009t0002g0033 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-208A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458371 | |||||||
| chr5:71458429 | C | T | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.213-150C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458429 | |||||||
| chr5:71458493 | T | C | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.213-86T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458493 | |||||||
| chr5:71459179 | A | G | 2 | a0004c0004t0004g0318 a0004c0004t0004g0319 |
2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.489+324A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459179 | |||||||
| chr5:71459254 | G | T | 6 | a0003c0003t0001g0289 a0003c0003t0001g0290 a0003c0003t0001g0291 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+399G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459254 | |||||||
| chr5:71459318 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.489+463C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459318 | |||||||
| chr5:71459381 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+526G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459381 | |||||||
| chr5:71459579 | C | G | 7 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(4): Show |
7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+724C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459579 | |||||||
| chr5:71459734 | C | T | 1 | a0002c0002t0001g0288 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.489+879C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459734 | |||||||
| chr5:71460026 | A | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.489+1171A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460026 | |||||||
| chr5:71460047 | T | A | 2 | a0020c0020t0023g0120 a0027c0019t0024g0119 |
2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1192T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460047 | |||||||
| chr5:71460071 | G | C | 2 | a0020c0020t0023g0120 a0027c0019t0024g0119 |
2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1216G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460071 | |||||||
| chr5:71460240 | T | C | 247 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.489+1385T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460240 | |||||||
| chr5:71460252 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.489+1397C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460252 | |||||||
| chr5:71460272 | C | G | 1 | a0029c0050t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+1417C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460272 | |||||||
| chr5:71460294 | C | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.489+1439C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460294 | |||||||
| chr5:71460321 | G | A | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.489+1466G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460321 | |||||||
| chr5:71460335 | G | A | 2 | a0020c0020t0023g0120 a0027c0019t0024g0119 |
2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1480G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460335 | |||||||
| chr5:71460737 | G | A | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-1080G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460737 | |||||||
| chr5:71460763 | G | A | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-1054G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460763 | |||||||
| chr5:71460875 | T | TA | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.490-933dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr5 | 71460875 | ||||||
| chr5:71461131 | C | T | 4 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0106 others(1): Show |
4 | HG00621.hp2 NA18949.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-686C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461131 | |||||||
| chr5:71461193 | A | T | 4 | a0009c0008t0007g0100 a0009c0008t0007g0101 a0009c0008t0007g0102 others(1): Show |
4 | HG02976.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-624A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461193 | |||||||
| chr5:71461442 | C | CA | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0002c0002t0001g0137 others(3): Show |
6 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-362dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr5 | 71461442 | ||||||
| chr5:71461456 | C | A | 1 | a0001c0001t0022g0014 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-361C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461456 | |||||||
| chr5:71461530 | C | T | 2 | a0006c0007t0002g0113 a0006c0007t0002g0114 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-287C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461530 | |||||||
| chr5:71461605 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.490-212C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461605 | |||||||
| chr5:71461958 | C | CT | 207 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(204): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.599+53dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | ||||||
| chr5:71461958 | C | CTT | 13 | a0001c0001t0002g0016 a0001c0001t0002g0097 a0001c0001t0002g0098 others(10): Show |
13 | HG00673.hp1 HG02071.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+52_599+53dupTT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | ||||||
| chr5:71461958 | CT | C | 16 | a0003c0003t0001g0232 a0004c0004t0004g0310 a0004c0004t0004g0311 others(13): Show |
16 | HG00642.hp2 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.599+53delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | ||||||
| chr5:71461960 | T | C | 1 | a0003c0003t0001g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.599+34T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71461960 | |||||||
| chr5:71462147 | G | A | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.599+221G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462147 | |||||||
| chr5:71462272 | A | G | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.599+346A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462272 | |||||||
| chr5:71462643 | A | G | 6 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0226 others(3): Show |
6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+717A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462643 | |||||||
| chr5:71462759 | C | CA | 7 | a0001c0001t0019g0017 a0002c0002t0001g0133 a0002c0002t0001g0138 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+844dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71462759 | ||||||
| chr5:71462859 | G | A | 1 | a0007c0006t0002g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.599+933G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462859 | |||||||
| chr5:71462990 | G | A | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.599+1064G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462990 | |||||||
| chr5:71463004 | A | G | 6 | a0009c0008t0002g0008 a0009c0008t0002g0095 a0009c0008t0007g0100 others(3): Show |
6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.600-1054A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463004 | |||||||
| chr5:71463396 | G | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600-662G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463396 | |||||||
| chr5:71463493 | A | T | 100 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(97): Show |
101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.600-565A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463493 | |||||||
| chr5:71463537 | C | T | 5 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(2): Show |
5 | HG02071.hp1 HG02074.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.600-521C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463537 | |||||||
| chr5:71463600 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
4 | HG02015.hp2 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-458T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463600 | |||||||
| chr5:71463609 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.600-449C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463609 | |||||||
| chr5:71463829 | TA | T | 110 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(107): Show |
111 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.600-212delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71463829 | ||||||
| chr5:71463829 | TAA | T | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.600-213_600-212del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71463829 | ||||||
| chr5:71463870 | A | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0093 a0001c0001t0002g0094 others(2): Show |
6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.600-188A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463870 | |||||||
| chr5:71463873 | T | C | 1 | a0003c0003t0001g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-185T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463873 | |||||||
| chr5:71463930 | C | T | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.600-128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463930 | |||||||
| chr5:71463937 | G | A | 1 | a0008c0009t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600-121G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463937 | |||||||
| chr5:71464164 | A | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.659+47A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464164 | |||||||
| chr5:71464256 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.659+139G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464256 | |||||||
| chr5:71464411 | C | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.659+294C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464411 | |||||||
| chr5:71464595 | G | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.659+478G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464595 | |||||||
| chr5:71464640 | C | T | 1 | a0003c0003t0001g0285 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.659+523C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464640 | |||||||
| chr5:71464715 | G | GT | 35 | a0001c0001t0002g0016 a0001c0001t0002g0079 a0001c0001t0002g0080 others(32): Show |
35 | HG00423.hp2 HG00597.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.659+620dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | ||||||
| chr5:71464715 | G | GTT | 10 | a0002c0002t0001g0144 a0004c0004t0004g0317 a0004c0004t0004g0319 others(7): Show |
10 | HG01167.hp1 HG01257.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.659+619_659+620dup others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | ||||||
| chr5:71464715 | G | GTTT | 85 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(82): Show |
86 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.659+618_659+620dup others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | ||||||
| chr5:71464715 | G | GTTTT | 15 | a0002c0002t0001g0209 a0002c0002t0001g0211 a0002c0002t0001g0212 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.659+617_659+620dup others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | ||||||
| chr5:71464952 | C | T | 1 | a0012c0012t0003g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.659+835C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464952 | |||||||
| chr5:71464959 | G | C | 1 | a0003c0003t0001g0291 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.659+842G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464959 | |||||||
| chr5:71464964 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.659+847G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464964 | |||||||
| chr5:71465022 | T | G | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.659+905T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465022 | |||||||
| chr5:71465095 | T | G | 7 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(4): Show |
7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.659+978T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465095 | |||||||
| chr5:71465131 | A | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.660-965A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465131 | |||||||
| chr5:71465464 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | NA18945.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.660-632A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465464 | |||||||
| chr5:71465609 | A | C | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.660-487A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465609 | |||||||
| chr5:71465612 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.660-484G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465612 | |||||||
| chr5:71465623 | C | G | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.660-473C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465623 | |||||||
| chr5:71465665 | G | A | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.660-431G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465665 | |||||||
| chr5:71465711 | T | A | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.660-385T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465711 | |||||||
| chr5:71465813 | G | A | 1 | a0034c0029t0004g0316 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.660-283G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465813 | |||||||
| chr5:71465887 | A | G | 1 | a0002c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.660-209A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465887 | |||||||
| chr5:71466330 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.785+109C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466330 | |||||||
| chr5:71466364 | A | G | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.785+143A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466364 | |||||||
| chr5:71466426 | G | A | 6 | a0009c0008t0002g0008 a0009c0008t0002g0095 a0009c0008t0007g0100 others(3): Show |
6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+205G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466426 | |||||||
| chr5:71466463 | A | T | 1 | a0010c0011t0001g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.785+242A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466463 | |||||||
| chr5:71466620 | A | G | 112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(109): Show |
114 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.785+399A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466620 | |||||||
| chr5:71466749 | GT | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.785+537delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr5 | 71466749 | ||||||
| chr5:71466897 | G | A | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.786-457G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466897 | |||||||
| chr5:71466954 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.786-400A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466954 | |||||||
| chr5:71467075 | C | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0201 a0002c0002t0001g0202 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-279C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467075 | |||||||
| chr5:71467084 | T | C | 2 | a0020c0020t0023g0120 a0027c0019t0024g0119 |
2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.786-270T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467084 | |||||||
| chr5:71467108 | G | A | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.786-246G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467108 | |||||||
| chr5:71467125 | T | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.786-229T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467125 | |||||||
| chr5:71467232 | G | A | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.786-122G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467232 | |||||||
| chr5:71467261 | A | G | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.786-93A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467261 | |||||||
| chr5:71467283 | T | C | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786-71T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467283 | |||||||
| chr5:71467297 | T | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.786-57T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467297 | |||||||
| chr5:71467622 | C | T | 1 | a0008c0009t0002g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+135C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467622 | |||||||
| chr5:71467634 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.919+147C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467634 | |||||||
| chr5:71467731 | C | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+244C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467731 | |||||||
| chr5:71468022 | T | A | 1 | a0002c0002t0001g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.919+535T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468022 | |||||||
| chr5:71468135 | C | T | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.919+648C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468135 | |||||||
| chr5:71468175 | C | T | 1 | a0005c0005t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.919+688C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468175 | |||||||
| chr5:71468258 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.919+771G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468258 | |||||||
| chr5:71468453 | A | T | 1 | a0024c0033t0003g0139 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.919+966A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468453 | |||||||
| chr5:71468453 | AT | A | 14 | a0001c0001t0002g0118 a0002c0002t0001g0144 a0003c0003t0001g0304 others(11): Show |
15 | HG01257.hp2 HG01884.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+981delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71468453 | ||||||
| chr5:71468468 | T | A | 6 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0226 others(3): Show |
6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+981T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468468 | |||||||
| chr5:71468607 | C | CT | 216 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(213): Show |
219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.919+1136dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71468607 | ||||||
| chr5:71468731 | C | T | 12 | a0003c0003t0001g0233 a0003c0003t0001g0273 a0003c0003t0001g0274 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+1244C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468731 | |||||||
| chr5:71468782 | T | G | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919+1295T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468782 | |||||||
| chr5:71468826 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.919+1339C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468826 | |||||||
| chr5:71468906 | C | T | 1 | a0003c0003t0001g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.919+1419C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468906 | |||||||
| chr5:71468917 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.919+1430T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468917 | |||||||
| chr5:71468924 | A | C | 27 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.919+1437A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468924 | |||||||
| chr5:71468983 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-1412T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468983 | |||||||
| chr5:71469054 | T | A | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.920-1341T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469054 | |||||||
| chr5:71469322 | A | G | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-1073A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469322 | |||||||
| chr5:71469366 | T | C | 1 | a0004c0004t0010g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-1029T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469366 | |||||||
| chr5:71469425 | C | G | 3 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0033c0047t0001g0229 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-970C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469425 | |||||||
| chr5:71469645 | G | A | 5 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0021c0035t0001g0124 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-750G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469645 | |||||||
| chr5:71469725 | T | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.920-670T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469725 | |||||||
| chr5:71469762 | C | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.920-633C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469762 | |||||||
| chr5:71469770 | C | T | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-625C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469770 | |||||||
| chr5:71469813 | C | T | 1 | a0002c0002t0001g0200 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-582C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469813 | |||||||
| chr5:71469842 | C | CT | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-537dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71469842 | ||||||
| chr5:71469878 | G | A | 1 | a0004c0004t0010g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-517G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469878 | |||||||
| chr5:71469911 | G | T | 10 | a0002c0002t0001g0144 a0002c0002t0001g0196 a0002c0002t0001g0197 others(7): Show |
10 | HG01257.hp2 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-484G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469911 | |||||||
| chr5:71469934 | C | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-461C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469934 | |||||||
| chr5:71469945 | G | A | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.920-450G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469945 | |||||||
| chr5:71470088 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.920-307G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470088 | |||||||
| chr5:71470130 | C | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.920-265C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470130 | |||||||
| chr5:71470293 | C | A | 1 | a0005c0005t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.920-102C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470293 | |||||||
| chr5:71470595 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0019g0017 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1014+106T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470595 | |||||||
| chr5:71470612 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+123A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470612 | |||||||
| chr5:71470655 | C | T | 1 | a0006c0007t0002g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014+166C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470655 | |||||||
| chr5:71470744 | C | T | 6 | a0005c0005t0015g0309 a0016c0017t0009g0116 a0016c0017t0009g0117 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+255C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470744 | |||||||
| chr5:71470833 | C | T | 1 | a0003c0003t0001g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1014+344C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470833 | |||||||
| chr5:71470891 | C | CT | 22 | a0001c0026t0002g0013 a0004c0004t0004g0310 a0004c0004t0004g0311 others(19): Show |
22 | HG01433.hp1 HG01884.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014+415dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71470891 | ||||||
| chr5:71470892 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1014+403T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470892 | |||||||
| chr5:71470913 | A | T | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1014+424A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470913 | |||||||
| chr5:71471138 | C | CT | 18 | a0001c0001t0002g0063 a0001c0001t0002g0091 a0001c0001t0002g0094 others(15): Show |
18 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1014+671dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | ||||||
| chr5:71471138 | C | CTT | 10 | a0004c0004t0004g0313 a0004c0004t0004g0314 a0004c0004t0004g0315 others(7): Show |
10 | HG01433.hp1 HG02965.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+670_1014+671d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | ||||||
| chr5:71471138 | CT | C | 10 | a0001c0001t0002g0126 a0002c0002t0001g0146 a0002c0002t0001g0301 others(7): Show |
10 | HG00099.hp2 HG01070.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+671delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | ||||||
| chr5:71471150 | T | G | 1 | a0013c0013t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1014+661T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471150 | |||||||
| chr5:71471173 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+684C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471173 | |||||||
| chr5:71471174 | G | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+685G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471174 | |||||||
| chr5:71471287 | C | T | 6 | a0005c0005t0015g0309 a0016c0017t0009g0116 a0016c0017t0009g0117 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+798C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471287 | |||||||
| chr5:71471289 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+800C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471289 | |||||||
| chr5:71471329 | A | T | 3 | a0005c0005t0001g0236 a0005c0005t0001g0237 a0005c0005t0001g0238 |
3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1014+840A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471329 | |||||||
| chr5:71471423 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1014+934C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471423 | |||||||
| chr5:71471442 | T | C | 256 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(253): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1014+953T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471442 | |||||||
| chr5:71471540 | G | A | 10 | a0002c0002t0001g0144 a0002c0002t0001g0196 a0002c0002t0001g0197 others(7): Show |
10 | HG01257.hp2 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+1051G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471540 | |||||||
| chr5:71471641 | C | G | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+1152C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471641 | |||||||
| chr5:71471817 | A | G | 6 | a0001c0001t0002g0058 a0001c0001t0002g0060 a0001c0001t0002g0061 others(3): Show |
6 | HG01346.hp1 HG03239.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014+1328A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471817 | |||||||
| chr5:71472030 | T | A | 1 | a0029c0050t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014+1541T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472030 | |||||||
| chr5:71472049 | C | A | 1 | a0001c0001t0019g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1014+1560C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472049 | |||||||
| chr5:71472317 | C | T | 2 | a0005c0005t0015g0309 a0033c0047t0001g0229 |
2 | HG00741.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1014+1828C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472317 | |||||||
| chr5:71472839 | A | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+2350A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472839 | |||||||
| chr5:71472853 | C | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1014+2364C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472853 | |||||||
| chr5:71472876 | TTC | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1014+2399_1014+240 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472876 | ||||||
| chr5:71472887 | TC | T | 24 | a0001c0001t0002g0016 a0001c0001t0002g0019 a0001c0001t0002g0020 others(21): Show |
24 | HG01358.hp2 HG02015.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1014+2399delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472887 | |||||||
| chr5:71472888 | C | CTT | 91 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(88): Show |
92 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1014+2421_1014+242 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472888 | ||||||
| chr5:71472888 | C | CTTT | 11 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0189 others(8): Show |
11 | HG00423.hp1 HG01099.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+2420_1014+242 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472888 | ||||||
| chr5:71472995 | A | G | 1 | a0003c0003t0001g0294 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1014+2506A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472995 | |||||||
| chr5:71473044 | G | A | 1 | a0012c0012t0003g0148 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1014+2555G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473044 | |||||||
| chr5:71473072 | A | G | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014+2583A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473072 | |||||||
| chr5:71473119 | A | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1014+2630A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473119 | |||||||
| chr5:71473262 | A | AT | 7 | a0003c0003t0001g0231 a0003c0003t0001g0232 a0003c0003t0001g0266 others(4): Show |
7 | HG02056.hp1 HG04199.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014+2803dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473262 | AT | A | 7 | a0003c0003t0001g0004 a0003c0003t0006g0240 a0005c0005t0001g0295 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014+2803delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473262 | ATTTT | A | 8 | a0002c0002t0001g0230 a0002c0002t0001g0302 a0002c0002t0001g0303 others(5): Show |
8 | HG01884.hp1 HG01975.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1014+2800_1014+280 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473262 | ATTTTT | A | 99 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(96): Show |
100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1014+2799_1014+280 others(9): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473262 | ATTTTTT | A | 9 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0091 others(6): Show |
9 | HG01243.hp2 HG01257.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+2798_1014+280 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473262 | ATTTTTTT | A | 125 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(122): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1014+2797_1014+280 others(11): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | ||||||
| chr5:71473316 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+2827C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473316 | |||||||
| chr5:71473826 | G | A | 1 | a0002c0002t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1014+3337G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473826 | |||||||
| chr5:71473834 | C | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1014+3345C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473834 | |||||||
| chr5:71473851 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0118 |
2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1014+3362C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473851 | |||||||
| chr5:71473990 | G | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1014+3501G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473990 | |||||||
| chr5:71474048 | C | T | 1 | a0003c0003t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1014+3559C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474048 | |||||||
| chr5:71474080 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+3591T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474080 | |||||||
| chr5:71474595 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1014+4106C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474595 | |||||||
| chr5:71474677 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0011g0065 |
3 | NA18992.hp1 NA19054.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1014+4188G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474677 | |||||||
| chr5:71474707 | T | TGTG | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+4223_1014+422 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71474707 | ||||||
| chr5:71474769 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1014+4280C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474769 | |||||||
| chr5:71474859 | AT | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+4371delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474859 | |||||||
| chr5:71474860 | T | A | 111 | a0001c0001t0002g0106 a0002c0002t0001g0133 a0002c0002t0001g0137 others(108): Show |
112 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1014+4371T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474860 | |||||||
| chr5:71474893 | C | G | 1 | a0003c0003t0001g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014+4404C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474893 | |||||||
| chr5:71474907 | G | C | 1 | a0003c0003t0001g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014+4418G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474907 | |||||||
| chr5:71475034 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1014+4545C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475034 | |||||||
| chr5:71475071 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+4582C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475071 | |||||||
| chr5:71475085 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1014+4596T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475085 | |||||||
| chr5:71475330 | G | A | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014+4841G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475330 | |||||||
| chr5:71475463 | T | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+4974T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475463 | |||||||
| chr5:71475492 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+5003A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475492 | |||||||
| chr5:71475519 | A | T | 9 | a0002c0002t0001g0138 a0002c0002t0001g0215 a0002c0002t0001g0223 others(6): Show |
9 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+5030A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475519 | |||||||
| chr5:71475866 | A | G | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1014+5377A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475866 | |||||||
| chr5:71475964 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+5475A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475964 | |||||||
| chr5:71476204 | C | T | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1014+5715C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476204 | |||||||
| chr5:71476386 | A | G | 1 | a0004c0004t0004g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1014+5897A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476386 | |||||||
| chr5:71476550 | C | CT | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1014+6070dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71476550 | ||||||
| chr5:71476550 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1014+6061C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476550 | |||||||
| chr5:71476623 | C | G | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+6134C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476623 | |||||||
| chr5:71476698 | C | G | 1 | a0019c0042t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1014+6209C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476698 | |||||||
| chr5:71476698 | C | T | 6 | a0005c0005t0015g0309 a0016c0017t0009g0116 a0016c0017t0009g0117 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+6209C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476698 | |||||||
| chr5:71476729 | A | G | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1014+6240A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476729 | |||||||
| chr5:71476764 | C | T | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1014+6275C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476764 | |||||||
| chr5:71476814 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1014+6325C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476814 | |||||||
| chr5:71476841 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1014+6352C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476841 | |||||||
| chr5:71476848 | C | T | 2 | a0002c0002t0001g0215 a0002c0002t0001g0230 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1014+6359C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476848 | |||||||
| chr5:71477003 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1014+6514C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477003 | |||||||
| chr5:71477058 | C | A | 1 | a0005c0005t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1014+6569C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477058 | |||||||
| chr5:71477280 | C | A | 3 | a0002c0002t0001g0154 a0002c0002t0001g0155 a0036c0040t0001g0153 |
3 | HG02080.hp2 NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1015-6562C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477280 | |||||||
| chr5:71477361 | T | C | 142 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(139): Show |
144 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1015-6481T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477361 | |||||||
| chr5:71477492 | T | C | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1015-6350T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477492 | |||||||
| chr5:71477507 | G | T | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-6335G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477507 | |||||||
| chr5:71477581 | T | A | 1 | a0002c0002t0001g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1015-6261T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477581 | |||||||
| chr5:71477617 | A | ATGTTTTC others(4): Show |
1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-6224_1015-622 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477617 | ||||||
| chr5:71477617 | A | ATTTTTTC others(4): Show |
131 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(128): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1015-6218_1015-620 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477617 | ||||||
| chr5:71477624 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0122 a0022c0031t0016g0011 |
2 | HG00438.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1015-6208_1015-620 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477624 | ||||||
| chr5:71477810 | G | T | 1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1015-6032G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477810 | |||||||
| chr5:71477978 | C | T | 13 | a0001c0001t0002g0034 a0001c0001t0002g0053 a0001c0001t0002g0054 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1015-5864C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477978 | |||||||
| chr5:71477989 | G | A | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-5853G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477989 | |||||||
| chr5:71477999 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-5843C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477999 | |||||||
| chr5:71478045 | G | T | 1 | a0011c0010t0006g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-5797G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478045 | |||||||
| chr5:71478177 | G | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-5665G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478177 | |||||||
| chr5:71478198 | G | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-5644G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478198 | |||||||
| chr5:71478262 | A | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-5580A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478262 | |||||||
| chr5:71478347 | A | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1015-5495A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478347 | |||||||
| chr5:71478461 | C | G | 1 | a0003c0003t0001g0264 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1015-5381C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478461 | |||||||
| chr5:71478549 | A | G | 1 | a0019c0042t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1015-5293A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478549 | |||||||
| chr5:71478559 | A | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1015-5283A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478559 | |||||||
| chr5:71478644 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-5198C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478644 | |||||||
| chr5:71478653 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1015-5189T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478653 | |||||||
| chr5:71478659 | A | AT | 19 | a0001c0001t0002g0063 a0001c0026t0002g0013 a0002c0002t0001g0223 others(16): Show |
19 | HG00673.hp1 HG01433.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.1015-5171dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71478659 | ||||||
| chr5:71478840 | G | A | 293 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(290): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1015-5002G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478840 | |||||||
| chr5:71478973 | T | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-4869T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478973 | |||||||
| chr5:71479073 | C | T | 1 | a0013c0013t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1015-4769C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479073 | |||||||
| chr5:71479111 | C | T | 2 | a0010c0011t0001g0192 a0010c0011t0001g0193 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1015-4731C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479111 | |||||||
| chr5:71479586 | G | A | 5 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1015-4256G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479586 | |||||||
| chr5:71479776 | G | A | 1 | a0003c0003t0001g0242 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1015-4066G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479776 | |||||||
| chr5:71479811 | A | G | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-4031A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479811 | |||||||
| chr5:71479844 | C | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3998C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479844 | |||||||
| chr5:71479895 | T | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3947T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479895 | |||||||
| chr5:71479931 | TCC | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-3910_1015-390 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479931 | |||||||
| chr5:71479933 | C | T | 1 | a0015c0016t0001g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1015-3909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479933 | |||||||
| chr5:71479939 | G | A | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-3903G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479939 | |||||||
| chr5:71479975 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3867C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479975 | |||||||
| chr5:71480030 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1015-3812C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480030 | |||||||
| chr5:71480148 | G | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-3694G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480148 | |||||||
| chr5:71480193 | C | G | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-3649C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480193 | |||||||
| chr5:71480204 | G | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-3638G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480204 | |||||||
| chr5:71480249 | T | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-3593T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480249 | |||||||
| chr5:71480255 | C | T | 3 | a0002c0002t0001g0199 a0021c0035t0001g0124 a0026c0032t0001g0115 |
3 | HG01243.hp2 HG02257.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1015-3587C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480255 | |||||||
| chr5:71480257 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1015-3585C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480257 | |||||||
| chr5:71480277 | A | AT | 22 | a0003c0003t0001g0255 a0003c0003t0001g0262 a0003c0003t0001g0264 others(19): Show |
22 | HG00741.hp1 HG01192.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-3535dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | AT | A | 65 | a0002c0002t0001g0137 a0002c0002t0001g0150 a0002c0002t0001g0154 others(62): Show |
66 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1015-3535delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | ATT | A | 46 | a0002c0002t0001g0133 a0002c0002t0001g0144 a0002c0002t0001g0151 others(43): Show |
46 | HG00280.hp1 HG00673.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.1015-3536_1015-353 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | ATTTTTTT others(5): Show |
A | 1 | a0006c0007t0002g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1015-3546_1015-353 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0002g0016 a0001c0001t0002g0046 a0001c0001t0002g0054 others(12): Show |
15 | HG01192.hp1 HG02109.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1015-3547_1015-353 others(17): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | ATTTTTTT others(7): Show |
A | 108 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(105): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1015-3548_1015-353 others(18): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480277 | ATTTTTTT others(8): Show |
A | 1 | a0002c0002t0001g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1015-3549_1015-353 others(19): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | ||||||
| chr5:71480291 | T | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-3551T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480291 | |||||||
| chr5:71480381 | G | A | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1015-3461G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480381 | |||||||
| chr5:71480559 | T | C | 2 | a0002c0002t0001g0224 a0002c0002t0001g0226 |
2 | NA18943.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1015-3283T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480559 | |||||||
| chr5:71480570 | AT | A | 240 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(237): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1015-3258delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480570 | ||||||
| chr5:71480756 | G | A | 1 | a0007c0006t0002g0047 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1015-3086G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480756 | |||||||
| chr5:71480882 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1015-2960A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480882 | |||||||
| chr5:71480943 | A | C | 1 | a0004c0004t0004g0312 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1015-2899A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480943 | |||||||
| chr5:71481099 | G | A | 1 | a0025c0043t0001g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1015-2743G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481099 | |||||||
| chr5:71481129 | G | T | 2 | a0003c0003t0001g0289 a0003c0003t0001g0290 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1015-2713G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481129 | |||||||
| chr5:71481130 | C | T | 1 | a0001c0001t0020g0057 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1015-2712C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481130 | |||||||
| chr5:71481131 | G | A | 1 | a0002c0002t0001g0288 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1015-2711G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481131 | |||||||
| chr5:71481246 | C | CT | 13 | a0002c0002t0001g0157 a0004c0004t0004g0310 a0004c0004t0004g0311 others(10): Show |
13 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-2585dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481246 | ||||||
| chr5:71481391 | G | GA | 93 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0142 others(90): Show |
94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1015-2427dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | ||||||
| chr5:71481391 | G | GAA | 22 | a0002c0002t0001g0133 a0002c0002t0001g0172 a0002c0002t0001g0173 others(19): Show |
22 | HG00673.hp1 HG01261.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-2428_1015-242 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | ||||||
| chr5:71481391 | GA | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-2427delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | ||||||
| chr5:71481425 | G | A | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1015-2417G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481425 | |||||||
| chr5:71481434 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1015-2408C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481434 | |||||||
| chr5:71481883 | A | G | 1 | a0003c0003t0001g0239 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1015-1959A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481883 | |||||||
| chr5:71481984 | T | C | 1 | a0025c0043t0001g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1015-1858T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481984 | |||||||
| chr5:71482060 | A | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1015-1782A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482060 | |||||||
| chr5:71482187 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1015-1655C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482187 | |||||||
| chr5:71482318 | G | C | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-1524G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482318 | |||||||
| chr5:71482329 | G | C | 1 | a0003c0003t0018g0306 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1015-1513G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482329 | |||||||
| chr5:71482495 | G | A | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-1347G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482495 | |||||||
| chr5:71482633 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-1209A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482633 | |||||||
| chr5:71482658 | T | C | 1 | a0002c0002t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1015-1184T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482658 | |||||||
| chr5:71482777 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-1065G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482777 | |||||||
| chr5:71483210 | T | C | 123 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(120): Show |
125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1015-632T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71483210 | |||||||
| chr5:71483784 | A | T | 2 | a0023c0018t0001g0190 a0031c0038t0001g0143 |
2 | HG01978.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1015-58A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71483784 | |||||||
| chr5:71483920 | A | G | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1069+24A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71483920 | |||||||
| chr5:71484038 | T | G | 2 | a0004c0004t0010g0320 a0004c0004t0010g0321 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1069+142T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484038 | |||||||
| chr5:71484393 | C | G | 256 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(253): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1069+497C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484393 | |||||||
| chr5:71484428 | A | G | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1069+532A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484428 | |||||||
| chr5:71484572 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1069+676A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484572 | |||||||
| chr5:71484592 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069+696A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484592 | |||||||
| chr5:71484639 | A | G | 3 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0272 |
3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1069+743A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484639 | |||||||
| chr5:71484762 | C | T | 287 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(284): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1069+866C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484762 | |||||||
| chr5:71484803 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1069+907C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484803 | |||||||
| chr5:71484824 | A | G | 5 | a0003c0003t0006g0240 a0011c0010t0006g0241 a0011c0010t0006g0249 others(2): Show |
5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+928A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484824 | |||||||
| chr5:71484946 | C | G | 1 | a0005c0005t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1069+1050C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484946 | |||||||
| chr5:71485247 | C | T | 6 | a0002c0002t0001g0197 a0002c0002t0001g0219 a0002c0002t0001g0220 others(3): Show |
6 | HG02071.hp1 HG02074.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070-1237C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485247 | |||||||
| chr5:71485327 | A | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1070-1157A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485327 | |||||||
| chr5:71485337 | T | A | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1070-1147T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485337 | |||||||
| chr5:71485591 | T | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1070-893T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485591 | |||||||
| chr5:71485642 | C | T | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1070-842C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485642 | |||||||
| chr5:71485824 | G | A | 10 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(7): Show |
10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070-660G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485824 | |||||||
| chr5:71485853 | A | G | 8 | a0003c0003t0001g0231 a0003c0003t0001g0242 a0003c0003t0001g0248 others(5): Show |
8 | HG02056.hp1 HG02080.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-631A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485853 | |||||||
| chr5:71485927 | T | C | 245 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(242): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1070-557T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485927 | |||||||
| chr5:71486385 | TAAAC | T | 8 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-94_1070-91del others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr5 | 71486385 | ||||||
| chr5:71486453 | C | G | 1 | a0002c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1070-31C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71486453 | |||||||
| chr5:71486813 | A | C | 1 | a0016c0017t0009g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1213+186A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486813 | |||||||
| chr5:71486851 | C | G | 1 | a0001c0001t0002g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1213+224C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486851 | |||||||
| chr5:71486878 | C | G | 1 | a0015c0016t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1213+251C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486878 | |||||||
| chr5:71487279 | T | C | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1213+652T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487279 | |||||||
| chr5:71487327 | C | T | 3 | a0004c0004t0004g0314 a0006c0007t0002g0007 a0006c0028t0021g0009 |
3 | HG02895.hp2 HG02965.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1213+700C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487327 | |||||||
| chr5:71487599 | C | T | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1213+972C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487599 | |||||||
| chr5:71487673 | C | G | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1213+1046C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487673 | |||||||
| chr5:71487755 | C | T | 1 | a0003c0003t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1213+1128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487755 | |||||||
| chr5:71487772 | A | G | 1 | a0002c0002t0001g0303 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1213+1145A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487772 | |||||||
| chr5:71487787 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1213+1160A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487787 | |||||||
| chr5:71488370 | G | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1214-1034G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488370 | |||||||
| chr5:71488431 | C | CT | 13 | a0003c0003t0001g0291 a0004c0004t0004g0310 a0004c0004t0004g0311 others(10): Show |
13 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1214-959dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr5 | 71488431 | ||||||
| chr5:71488663 | A | G | 1 | a0003c0003t0001g0254 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1214-741A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488663 | |||||||
| chr5:71488799 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1214-605C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488799 | |||||||
| chr5:71488889 | G | A | 1 | a0003c0003t0001g0283 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1214-515G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488889 | |||||||
| chr5:71488983 | C | A | 1 | a0001c0001t0002g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1214-421C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488983 | |||||||
| chr5:71488992 | G | A | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1214-412G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488992 | |||||||
| chr5:71489148 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1214-256T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489148 | |||||||
| chr5:71489202 | A | G | 2 | a0023c0018t0001g0190 a0031c0038t0001g0143 |
2 | HG01978.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1214-202A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489202 | |||||||
| chr5:71489232 | C | T | 1 | a0003c0003t0001g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1214-172C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489232 | |||||||
| chr5:71489233 | G | A | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1214-171G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489233 | |||||||
| chr5:71489381 | A | G | 1 | a0006c0028t0021g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1214-23A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489381 | |||||||
| chr5:71489824 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1492+142G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71489824 | |||||||
| chr5:71489996 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1492+314A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71489996 | |||||||
| chr5:71490186 | C | T | 7 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(4): Show |
7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1492+504C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490186 | |||||||
| chr5:71490204 | A | G | 1 | a0001c0001t0020g0057 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1492+522A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490204 | |||||||
| chr5:71490336 | T | C | 1 | a0002c0002t0012g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1493-648T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490336 | |||||||
| chr5:71490386 | A | G | 6 | a0009c0008t0002g0008 a0009c0008t0002g0095 a0009c0008t0007g0100 others(3): Show |
6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-598A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490386 | |||||||
| chr5:71490619 | G | T | 1 | a0002c0002t0003g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1493-365G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490619 | |||||||
| chr5:71490888 | T | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1493-96T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490888 | |||||||
| chr5:71490899 | G | GAC | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1493-84_1493-83ins others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr5 | 71490899 | ||||||
| chr5:71490921 | T | C | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1493-63T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490921 | |||||||
| chr5:71491164 | A | C | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640+33A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491164 | |||||||
| chr5:71491196 | TC | T | 5 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0021c0035t0001g0124 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+66delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491196 | |||||||
| chr5:71491369 | T | C | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1640+238T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491369 | |||||||
| chr5:71491478 | CTTGCTGT others(67): Show |
C | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1640+349_1640+422d others(76): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr5 | 71491478 | ||||||
| chr5:71491715 | G | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1640+584G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491715 | |||||||
| chr5:71491759 | G | C | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1640+628G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491759 | |||||||
| chr5:71491873 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1640+742A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491873 | |||||||
| chr5:71492222 | G | T | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1640+1091G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492222 | |||||||
| chr5:71492263 | G | A | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1640+1132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492263 | |||||||
| chr5:71492274 | A | G | 3 | a0004c0004t0004g0310 a0004c0004t0004g0318 a0004c0004t0004g0319 |
3 | HG02027.hp1 NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1640+1143A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492274 | |||||||
| chr5:71492341 | A | G | 1 | a0013c0013t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1640+1210A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492341 | |||||||
| chr5:71492350 | A | G | 1 | a0003c0003t0001g0267 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1640+1219A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492350 | |||||||
| chr5:71492369 | G | T | 1 | a0005c0005t0001g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1640+1238G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492369 | |||||||
| chr5:71492426 | T | C | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1640+1295T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492426 | |||||||
| chr5:71492627 | G | C | 1 | a0007c0006t0002g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1640+1496G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492627 | |||||||
| chr5:71492784 | T | A | 1 | a0002c0002t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1640+1653T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492784 | |||||||
| chr5:71492802 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1640+1671G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492802 | |||||||
| chr5:71492867 | A | G | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640+1736A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492867 | |||||||
| chr5:71492920 | G | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1640+1789G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492920 | |||||||
| chr5:71493178 | G | C | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1640+2047G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493178 | |||||||
| chr5:71493525 | C | T | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1641-1725C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493525 | |||||||
| chr5:71493552 | A | C | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1641-1698A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493552 | |||||||
| chr5:71493575 | G | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1641-1675G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493575 | |||||||
| chr5:71493633 | C | A | 1 | a0005c0005t0017g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1641-1617C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493633 | |||||||
| chr5:71493766 | G | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1641-1484G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493766 | |||||||
| chr5:71493852 | G | C | 1 | a0010c0011t0001g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1641-1398G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493852 | |||||||
| chr5:71493897 | T | A | 2 | a0013c0013t0001g0003 a0013c0013t0001g0134 |
3 | NA18989.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1641-1353T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493897 | |||||||
| chr5:71493923 | A | C | 1 | a0012c0012t0003g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1641-1327A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493923 | |||||||
| chr5:71494024 | A | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1641-1226A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494024 | |||||||
| chr5:71494039 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1641-1211C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494039 | |||||||
| chr5:71494173 | A | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1641-1077A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494173 | |||||||
| chr5:71494349 | A | C | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1641-901A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494349 | |||||||
| chr5:71494360 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1641-890G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494360 | |||||||
| chr5:71494363 | G | A | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1641-887G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494363 | |||||||
| chr5:71494443 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1641-807C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494443 | |||||||
| chr5:71494471 | G | C | 2 | a0003c0003t0001g0292 a0003c0003t0001g0293 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1641-779G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494471 | |||||||
| chr5:71494538 | A | G | 2 | a0003c0003t0001g0248 a0003c0003t0001g0269 |
2 | NA18959.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1641-712A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494538 | |||||||
| chr5:71494549 | A | G | 1 | a0002c0002t0003g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1641-701A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494549 | |||||||
| chr5:71494707 | T | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1641-543T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494707 | |||||||
| chr5:71494794 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1641-456G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494794 | |||||||
| chr5:71494871 | G | A | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1641-379G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494871 | |||||||
| chr5:71494901 | G | T | 1 | a0001c0001t0002g0067 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1641-349G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494901 | |||||||
| chr5:71495032 | G | A | 5 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0016c0017t0009g0116 others(2): Show |
5 | HG00733.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1641-218G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495032 | |||||||
| chr5:71495159 | G | T | 1 | a0002c0002t0001g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1641-91G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495159 | |||||||
| chr5:71495183 | T | A | 102 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(99): Show |
103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1641-67T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495183 | |||||||
| chr5:71495239 | C | CT | 5 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0016c0017t0009g0116 others(2): Show |
5 | HG00733.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1641-3dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr5 | 71495239 | ||||||
| chr5:71495438 | A | G | 2 | a0005c0005t0001g0235 a0005c0005t0001g0298 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1799+30A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495438 | |||||||
| chr5:71495518 | T | C | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1799+110T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495518 | |||||||
| chr5:71495558 | A | G | 2 | a0002c0002t0001g0301 a0002c0002t0001g0303 |
2 | HG02071.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1799+150A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495558 | |||||||
| chr5:71495800 | C | A | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1799+392C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495800 | |||||||
| chr5:71495937 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1799+529C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495937 | |||||||
| chr5:71496128 | G | C | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1799+720G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496128 | |||||||
| chr5:71496181 | G | A | 1 | a0002c0039t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1799+773G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496181 | |||||||
| chr5:71496241 | C | CA | 7 | a0001c0001t0002g0062 a0001c0001t0002g0118 a0001c0001t0002g0131 others(4): Show |
7 | HG01943.hp1 HG01943.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1799+849dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496241 | ||||||
| chr5:71496241 | C | CAA | 135 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1799+848_1799+849d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496241 | ||||||
| chr5:71496308 | A | G | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1799+900A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496308 | |||||||
| chr5:71496372 | C | T | 5 | a0003c0003t0001g0004 a0003c0003t0001g0255 a0003c0003t0001g0285 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800-898C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496372 | |||||||
| chr5:71496438 | A | AT | 107 | a0001c0026t0002g0013 a0002c0002t0001g0137 a0002c0002t0001g0138 others(104): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1800-815dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | ||||||
| chr5:71496438 | A | ATT | 20 | a0002c0002t0001g0133 a0002c0002t0001g0170 a0002c0002t0001g0226 others(17): Show |
20 | HG01433.hp1 HG01884.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1800-816_1800-815d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | ||||||
| chr5:71496438 | A | ATTT | 6 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0046 others(3): Show |
7 | HG00609.hp2 HG03710.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1800-817_1800-815d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | ||||||
| chr5:71496438 | A | ATTTT | 100 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0019 others(97): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1800-818_1800-815d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | ||||||
| chr5:71496438 | A | ATTTTT | 12 | a0001c0001t0002g0015 a0001c0001t0002g0053 a0001c0001t0002g0085 others(9): Show |
12 | HG00621.hp2 HG01109.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1800-819_1800-815d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | ||||||
| chr5:71496645 | C | G | 1 | a0002c0002t0003g0185 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1800-625C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496645 | |||||||
| chr5:71496714 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1800-556C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496714 | |||||||
| chr5:71496756 | T | C | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1800-514T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496756 | |||||||
| chr5:71496859 | A | G | 7 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0016c0017t0009g0116 others(4): Show |
7 | HG00733.hp1 HG01243.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1800-411A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496859 | |||||||
| chr5:71496875 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1800-395G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496875 | |||||||
| chr5:71497083 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1800-187T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497083 | |||||||
| chr5:71497115 | A | G | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1800-155A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497115 | |||||||
| chr5:71497190 | A | G | 1 | a0016c0017t0009g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1800-80A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497190 | |||||||
| chr5:71497197 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1800-73A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497197 | |||||||
| chr5:71497486 | G | A | 4 | a0003c0003t0001g0256 a0003c0003t0001g0257 a0003c0003t0001g0258 others(1): Show |
4 | HG00099.hp1 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+60G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497486 | |||||||
| chr5:71497486 | G | T | 2 | a0002c0002t0001g0150 a0002c0002t0001g0188 |
2 | NA18942.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1956+60G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497486 | |||||||
| chr5:71497744 | A | G | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1956+318A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497744 | |||||||
| chr5:71498154 | G | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1956+728G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498154 | |||||||
| chr5:71498179 | T | C | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1956+753T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498179 | |||||||
| chr5:71498302 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+876A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498302 | |||||||
| chr5:71498335 | A | T | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1956+909A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498335 | |||||||
| chr5:71498367 | G | A | 1 | a0003c0003t0001g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1956+941G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498367 | |||||||
| chr5:71498390 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1956+964C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498390 | |||||||
| chr5:71498430 | C | CT | 12 | a0003c0003t0001g0242 a0004c0004t0004g0310 a0004c0004t0004g0311 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1956+1015dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71498430 | ||||||
| chr5:71498478 | C | T | 1 | a0002c0002t0003g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1956+1052C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498478 | |||||||
| chr5:71498626 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1200G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498626 | |||||||
| chr5:71498644 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1218G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498644 | |||||||
| chr5:71498725 | C | CT | 10 | a0003c0003t0001g0269 a0006c0007t0002g0108 a0006c0007t0002g0110 others(7): Show |
10 | HG02258.hp1 HG02896.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+1315dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71498725 | ||||||
| chr5:71498755 | G | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1956+1329G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498755 | |||||||
| chr5:71498880 | C | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1956+1454C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498880 | |||||||
| chr5:71499078 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0173 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1956+1652A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499078 | |||||||
| chr5:71499138 | C | T | 7 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(4): Show |
7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1956+1712C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499138 | |||||||
| chr5:71499141 | C | T | 2 | a0002c0002t0001g0168 a0002c0002t0001g0211 |
2 | HG01261.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1956+1715C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499141 | |||||||
| chr5:71499244 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1818C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499244 | |||||||
| chr5:71499636 | A | T | 8 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1957-1926A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499636 | |||||||
| chr5:71499653 | C | T | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1957-1909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499653 | |||||||
| chr5:71499669 | T | C | 1 | a0004c0004t0004g0313 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1957-1893T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499669 | |||||||
| chr5:71499868 | G | A | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1957-1694G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499868 | |||||||
| chr5:71499978 | T | C | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1957-1584T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499978 | |||||||
| chr5:71500051 | TTC | T | 2 | a0013c0013t0001g0003 a0013c0013t0001g0134 |
3 | NA18989.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1957-1509_1957-150 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500051 | ||||||
| chr5:71500288 | T | C | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1957-1274T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500288 | |||||||
| chr5:71500316 | C | CT | 16 | a0003c0003t0001g0269 a0003c0003t0001g0304 a0003c0003t0018g0306 others(13): Show |
16 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1957-1220dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CT | C | 27 | a0001c0001t0002g0094 a0001c0001t0002g0099 a0001c0026t0002g0013 others(24): Show |
27 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1957-1220delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CTT | C | 110 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(107): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1957-1221_1957-122 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CTTT | C | 7 | a0001c0001t0002g0045 a0001c0001t0002g0081 a0001c0001t0002g0082 others(4): Show |
7 | HG01070.hp1 HG01943.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-1222_1957-122 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CTTTTTTT others(2): Show |
C | 95 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(92): Show |
96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1957-1228_1957-122 others(13): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CTTTTTTT others(3): Show |
C | 4 | a0002c0002t0001g0202 a0002c0002t0001g0215 a0002c0002t0003g0207 others(1): Show |
4 | HG01169.hp1 NA18985.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-1229_1957-122 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500316 | CTTTTTTT others(6): Show |
C | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1957-1232_1957-122 others(17): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | ||||||
| chr5:71500428 | G | A | 2 | a0004c0004t0004g0311 a0004c0004t0004g0315 |
2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1957-1134G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500428 | |||||||
| chr5:71500475 | G | A | 13 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0071 others(10): Show |
13 | HG00438.hp2 HG01943.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1957-1087G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500475 | |||||||
| chr5:71500872 | G | C | 1 | a0001c0001t0002g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1957-690G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500872 | |||||||
| chr5:71501096 | CA | C | 136 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(133): Show |
138 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1957-450delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71501096 | ||||||
| chr5:71501270 | C | T | 1 | a0003c0003t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1957-292C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501270 | |||||||
| chr5:71501280 | A | T | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1957-282A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501280 | |||||||
| chr5:71501429 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1957-133C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501429 | |||||||
| chr5:71501672 | G | C | 1 | a0002c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2048+19G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501672 | |||||||
| chr5:71501673 | T | TA | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(100): Show |
105 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.2048+40dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | ||||||
| chr5:71501673 | T | TAA | 17 | a0001c0001t0002g0063 a0001c0001t0002g0069 a0001c0001t0002g0088 others(14): Show |
17 | HG00423.hp2 HG01433.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2048+39_2048+40dup others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | ||||||
| chr5:71501673 | TA | T | 102 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(99): Show |
103 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.2048+40delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | ||||||
| chr5:71501813 | ACTCT | A | 3 | a0003c0003t0001g0242 a0003c0003t0001g0248 a0003c0003t0001g0269 |
3 | NA18959.hp1 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2048+165_2048+168d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501813 | ||||||
| chr5:71501872 | A | G | 2 | a0002c0002t0005g0183 a0002c0002t0005g0187 |
2 | NA18963.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2048+219A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501872 | |||||||
| chr5:71501875 | T | A | 1 | a0002c0002t0001g0230 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2048+222T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501875 | |||||||
| chr5:71502057 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2048+404T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502057 | |||||||
| chr5:71502189 | CT | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2049-395delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71502189 | ||||||
| chr5:71502264 | T | C | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2049-335T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502264 | |||||||
| chr5:71502314 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049-285G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502314 | |||||||
| chr5:71502421 | G | A | 100 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(97): Show |
101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2049-178G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502421 | |||||||
| chr5:71502455 | C | T | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049-144C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502455 | |||||||
| chr5:71502951 | C | T | 1 | a0006c0024t0002g0109 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2241+160C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71502951 | |||||||
| chr5:71503019 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2241+228C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503019 | |||||||
| chr5:71503064 | C | CA | 7 | a0001c0001t0002g0125 a0001c0001t0002g0128 a0002c0002t0003g0174 others(4): Show |
7 | HG00423.hp1 HG01123.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+291dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71503064 | ||||||
| chr5:71503064 | C | G | 9 | a0006c0007t0002g0007 a0006c0007t0002g0108 a0006c0007t0002g0110 others(6): Show |
9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+273C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503064 | |||||||
| chr5:71503064 | CA | C | 9 | a0001c0001t0002g0028 a0002c0002t0001g0159 a0003c0003t0001g0239 others(6): Show |
9 | HG02523.hp2 HG02622.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241+291delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71503064 | ||||||
| chr5:71503079 | A | T | 7 | a0008c0009t0002g0023 a0008c0009t0002g0029 a0008c0009t0002g0031 others(4): Show |
7 | HG02572.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+288A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503079 | |||||||
| chr5:71503503 | A | G | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2241+712A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503503 | |||||||
| chr5:71503682 | C | G | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2241+891C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503682 | |||||||
| chr5:71504048 | G | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2242-573G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504048 | |||||||
| chr5:71504064 | A | AGATT | 9 | a0006c0007t0002g0007 a0006c0007t0002g0108 a0006c0007t0002g0110 others(6): Show |
9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2242-554_2242-551d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71504064 | ||||||
| chr5:71504088 | C | T | 1 | a0007c0006t0002g0049 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2242-533C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504088 | |||||||
| chr5:71504145 | C | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2242-476C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504145 | |||||||
| chr5:71504165 | C | T | 1 | a0003c0003t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2242-456C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504165 | |||||||
| chr5:71504190 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2242-431A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504190 | |||||||
| chr5:71504260 | A | G | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2242-361A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504260 | |||||||
| chr5:71504272 | C | CA | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2242-334dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71504272 | ||||||
| chr5:71504396 | T | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2242-225T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504396 | |||||||
| chr5:71504452 | A | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2242-169A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504452 | |||||||
| chr5:71504868 | G | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2372+117G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71504868 | |||||||
| chr5:71504998 | A | G | 2 | a0007c0006t0002g0051 a0007c0006t0002g0052 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2372+247A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71504998 | |||||||
| chr5:71505145 | T | G | 6 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0226 others(3): Show |
6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2372+394T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505145 | |||||||
| chr5:71505312 | T | C | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2372+561T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505312 | |||||||
| chr5:71505497 | T | A | 1 | a0042c0025t0002g0070 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2372+746T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505497 | |||||||
| chr5:71505527 | A | G | 246 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(243): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2372+776A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505527 | |||||||
| chr5:71505542 | G | C | 4 | a0003c0003t0001g0243 a0003c0003t0001g0246 a0003c0003t0001g0252 others(1): Show |
4 | HG00597.hp2 HG02155.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+791G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505542 | |||||||
| chr5:71505584 | C | T | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2372+833C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505584 | |||||||
| chr5:71505712 | G | A | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2372+961G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505712 | |||||||
| chr5:71505761 | T | G | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2372+1010T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505761 | |||||||
| chr5:71506211 | T | C | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2372+1460T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506211 | |||||||
| chr5:71506414 | C | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2372+1663C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506414 | |||||||
| chr5:71506635 | A | G | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2372+1884A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506635 | |||||||
| chr5:71506758 | T | TTA | 108 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(105): Show |
109 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2372+2029_2372+203 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | T | TTATA | 9 | a0002c0002t0001g0160 a0002c0002t0001g0175 a0002c0002t0001g0215 others(6): Show |
9 | HG00733.hp2 HG02027.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2372+2027_2372+203 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | T | TTATATAT others(3): Show |
1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2372+2021_2372+203 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | T | TTATATAT others(13): Show |
1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2372+2011_2372+203 others(24): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | T | TTATATAT others(19): Show |
1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2372+2030_2372+203 others(30): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | T | TTATATAT others(25): Show |
1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+2030_2372+203 others(36): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506758 | TTA | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2372+2029_2372+203 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | ||||||
| chr5:71506786 | A | AAC | 6 | a0001c0001t0002g0020 a0003c0003t0001g0260 a0003c0003t0001g0272 others(3): Show |
6 | HG00642.hp2 HG01109.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2372+2072_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACAC | 17 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2372+2070_2372+207 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACAC | 8 | a0001c0001t0002g0055 a0001c0001t0002g0092 a0001c0001t0002g0099 others(5): Show |
8 | HG01358.hp2 HG01433.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2372+2068_2372+207 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(1): Show |
3 | a0004c0004t0004g0311 a0005c0005t0015g0309 a0009c0008t0002g0008 |
3 | HG00741.hp1 HG01167.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2372+2066_2372+207 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(3): Show |
4 | a0004c0004t0004g0312 a0004c0004t0004g0313 a0004c0004t0010g0321 others(1): Show |
4 | HG01943.hp1 HG02976.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372+2064_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(5): Show |
1 | a0004c0004t0004g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2372+2062_2372+207 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(9): Show |
2 | a0004c0004t0004g0310 a0004c0004t0010g0320 |
2 | HG02027.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2372+2058_2372+207 others(20): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(11): Show |
1 | a0004c0004t0004g0318 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2372+2056_2372+207 others(22): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | A | AACACACA others(13): Show |
1 | a0004c0004t0004g0319 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2372+2054_2372+207 others(24): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | AAC | A | 84 | a0002c0002t0001g0137 a0002c0002t0001g0142 a0002c0002t0001g0144 others(81): Show |
85 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2372+2072_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | AACACACA others(3): Show |
A | 22 | a0003c0003t0001g0231 a0003c0003t0001g0239 a0003c0003t0001g0242 others(19): Show |
22 | HG00597.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2372+2064_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506786 | AACACACA others(5): Show |
A | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2372+2062_2372+207 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | ||||||
| chr5:71506819 | A | C | 3 | a0002c0002t0001g0146 a0002c0002t0001g0157 a0002c0002t0001g0186 |
3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2372+2068A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506819 | |||||||
| chr5:71506821 | A | ACC | 4 | a0002c0002t0001g0151 a0002c0002t0001g0154 a0002c0002t0001g0155 others(1): Show |
4 | HG02080.hp2 NA18939.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+2071_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506821 | ||||||
| chr5:71506821 | A | C | 83 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(80): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2372+2070A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506821 | |||||||
| chr5:71506823 | A | ACACACAC others(3): Show |
4 | a0001c0001t0002g0090 a0004c0004t0004g0314 a0034c0029t0004g0316 others(1): Show |
4 | HG03669.hp2 HG03710.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | ||||||
| chr5:71506823 | A | ACACACAC others(1): Show |
14 | a0001c0001t0002g0053 a0001c0001t0002g0063 a0001c0001t0002g0068 others(11): Show |
14 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | ||||||
| chr5:71506823 | A | ACACACC | 44 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(41): Show |
46 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | ||||||
| chr5:71506823 | A | ACACC | 16 | a0001c0001t0002g0025 a0001c0001t0002g0066 a0001c0001t0002g0067 others(13): Show |
16 | HG01123.hp1 HG01496.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | ||||||
| chr5:71506823 | A | ACC | 22 | a0001c0001t0002g0015 a0001c0001t0002g0024 a0001c0001t0002g0043 others(19): Show |
22 | HG01070.hp1 HG01074.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2372+2074_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | ||||||
| chr5:71506823 | A | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2372+2072A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506823 | |||||||
| chr5:71506935 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2372+2184C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506935 | |||||||
| chr5:71506939 | G | T | 1 | a0002c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2372+2188G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506939 | |||||||
| chr5:71506957 | A | T | 1 | a0001c0001t0002g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2372+2206A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506957 | |||||||
| chr5:71507003 | G | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+2252G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507003 | |||||||
| chr5:71507163 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2373-2302A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507163 | |||||||
| chr5:71507225 | C | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2373-2240C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507225 | |||||||
| chr5:71507557 | C | T | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2373-1908C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507557 | |||||||
| chr5:71507764 | T | C | 1 | a0005c0005t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2373-1701T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507764 | |||||||
| chr5:71507768 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2373-1697A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507768 | |||||||
| chr5:71507795 | G | A | 5 | a0003c0003t0001g0004 a0003c0003t0001g0255 a0003c0003t0001g0285 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2373-1670G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507795 | |||||||
| chr5:71507865 | A | G | 1 | a0006c0007t0002g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2373-1600A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507865 | |||||||
| chr5:71507963 | G | A | 2 | a0002c0002t0001g0152 a0002c0002t0001g0160 |
2 | HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2373-1502G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507963 | |||||||
| chr5:71507995 | T | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2373-1470T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507995 | |||||||
| chr5:71508050 | C | T | 5 | a0012c0012t0003g0148 a0012c0012t0003g0166 a0012c0012t0003g0167 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2373-1415C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508050 | |||||||
| chr5:71508109 | C | T | 2 | a0002c0002t0001g0133 a0002c0002t0001g0300 |
2 | NA18993.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2373-1356C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508109 | |||||||
| chr5:71508112 | G | A | 5 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2373-1353G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508112 | |||||||
| chr5:71508471 | A | AT | 243 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(240): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2373-980dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71508471 | ||||||
| chr5:71508611 | T | C | 2 | a0024c0033t0003g0139 a0035c0034t0003g0140 |
2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2373-854T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508611 | |||||||
| chr5:71508769 | A | C | 1 | a0002c0002t0001g0172 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2373-696A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508769 | |||||||
| chr5:71508794 | G | A | 1 | a0006c0007t0002g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2373-671G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508794 | |||||||
| chr5:71509048 | G | A | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2373-417G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509048 | |||||||
| chr5:71509058 | A | G | 1 | a0003c0003t0001g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2373-407A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509058 | |||||||
| chr5:71509069 | C | G | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2373-396C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509069 | |||||||
| chr5:71509353 | T | C | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(114): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2373-112T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509353 | |||||||
| chr5:71509354 | T | C | 1 | a0042c0025t0002g0070 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2373-111T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509354 | |||||||
| chr5:71509442 | T | C | 1 | a0002c0002t0001g0199 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2373-23T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509442 | |||||||
| chr5:71509445 | GC | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2373-15delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71509445 | ||||||
| chr5:71509450 | C | T | 15 | a0001c0026t0002g0013 a0004c0004t0004g0310 a0004c0004t0004g0311 others(12): Show |
15 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.2373-15C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509450 | |||||||
| chr5:71509450 | CT | C | 71 | a0002c0002t0001g0137 a0002c0002t0001g0142 a0002c0002t0001g0144 others(68): Show |
72 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(69): Show |
splice_region_variant&intron_variant | LOW | c.2373-5delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71509450 | ||||||
| chr5:71511189 | CT | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4059+44delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr5 | 71511189 | ||||||
| chr5:71511246 | C | T | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4059+95C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511246 | |||||||
| chr5:71511661 | A | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4059+510A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511661 | |||||||
| chr5:71511738 | T | C | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.4060-503T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511738 | |||||||
| chr5:71511777 | G | C | 1 | a0001c0001t0002g0104 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4060-464G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511777 | |||||||
| chr5:71511953 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4060-288A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511953 | |||||||
| chr5:71511982 | A | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4060-259A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511982 | |||||||
| chr5:71512074 | T | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4060-167T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512074 | |||||||
| chr5:71512090 | T | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4060-151T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512090 | |||||||
| chr5:71512134 | A | G | 1 | a0003c0003t0001g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4060-107A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512134 | |||||||
| chr5:71512164 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.4060-77G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512164 | |||||||
| chr5:71512458 | T | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4247+30T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512458 | |||||||
| chr5:71512467 | A | G | 1 | a0025c0043t0001g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4247+39A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512467 | |||||||
| chr5:71512515 | C | A | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4247+87C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512515 | |||||||
| chr5:71512743 | G | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4247+315G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512743 | |||||||
| chr5:71512765 | T | G | 5 | a0005c0005t0001g0234 a0014c0014t0001g0005 a0014c0014t0001g0006 others(2): Show |
5 | HG00733.hp1 HG02258.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4247+337T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512765 | |||||||
| chr5:71513063 | C | CA | 23 | a0002c0002t0001g0151 a0002c0002t0001g0154 a0002c0002t0001g0156 others(20): Show |
23 | HG00621.hp1 HG00741.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.4248-97dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | ||||||
| chr5:71513063 | CA | C | 92 | a0001c0001t0002g0040 a0001c0001t0002g0063 a0001c0001t0002g0088 others(89): Show |
93 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.4248-97delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | ||||||
| chr5:71513063 | CAA | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(103): Show |
108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.4248-98_4248-97del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | ||||||
| chr5:71513426 | G | A | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4470+19G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513426 | |||||||
| chr5:71513442 | GT | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.4470+50delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr5 | 71513442 | ||||||
| chr5:71513513 | G | C | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4470+106G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513513 | |||||||
| chr5:71513754 | T | A | 2 | a0002c0002t0001g0215 a0002c0002t0001g0230 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.4470+347T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513754 | |||||||
| chr5:71513755 | C | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.4470+348C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513755 | |||||||
| chr5:71513775 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0173 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4470+368A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513775 | |||||||
| chr5:71513813 | A | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.4470+406A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513813 | |||||||
| chr5:71513822 | C | T | 1 | a0005c0005t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4470+415C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513822 | |||||||
| chr5:71513885 | A | T | 1 | a0003c0003t0001g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4470+478A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513885 | |||||||
| chr5:71513984 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4470+577A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513984 | |||||||
| chr5:71514011 | C | T | 30 | a0003c0003t0001g0231 a0003c0003t0001g0239 a0003c0003t0001g0242 others(27): Show |
30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4470+604C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514011 | |||||||
| chr5:71514116 | C | A | 1 | a0005c0005t0001g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4470+709C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514116 | |||||||
| chr5:71514208 | A | G | 3 | a0001c0001t0002g0076 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | HG00438.hp2 HG02040.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4471-736A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514208 | |||||||
| chr5:71514209 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4471-735G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514209 | |||||||
| chr5:71514221 | C | T | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.4471-723C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514221 | |||||||
| chr5:71514567 | T | C | 2 | a0005c0005t0001g0235 a0005c0005t0001g0298 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4471-377T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514567 | |||||||
| chr5:71514597 | G | A | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4471-347G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514597 | |||||||
| chr5:71514705 | G | T | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4471-239G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514705 | |||||||
| chr5:71514763 | T | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4471-181T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514763 | |||||||
| chr5:71514868 | T | C | 2 | a0005c0005t0001g0235 a0005c0005t0001g0298 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4471-76T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514868 | |||||||
| chr5:71515275 | T | C | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4649+153T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515275 | |||||||
| chr5:71515505 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4649+383A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515505 | |||||||
| chr5:71515541 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0082 |
2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.4649+419T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515541 | |||||||
| chr5:71515885 | C | T | 1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4650-176C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515885 | |||||||
| chr5:71515981 | A | G | 3 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0033c0047t0001g0229 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4650-80A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515981 | |||||||
| chr5:71515985 | A | G | 3 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0033c0047t0001g0229 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4650-76A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515985 | |||||||
| chr5:71515994 | A | G | 111 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4650-67A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515994 | |||||||
| chr5:71516324 | A | G | 3 | a0004c0004t0004g0310 a0016c0017t0009g0116 a0016c0017t0009g0117 |
3 | HG02027.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4860+53A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516324 | |||||||
| chr5:71516407 | G | C | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4860+136G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516407 | |||||||
| chr5:71516418 | C | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0093 a0001c0001t0002g0094 others(2): Show |
6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.4860+147C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516418 | |||||||
| chr5:71516476 | C | T | 4 | a0002c0002t0001g0168 a0002c0002t0001g0175 a0002c0002t0001g0189 others(1): Show |
4 | HG00733.hp2 HG01099.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.4860+205C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516476 | |||||||
| chr5:71516485 | A | G | 1 | a0035c0034t0003g0140 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4860+214A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516485 | |||||||
| chr5:71516517 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4860+246G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516517 | |||||||
| chr5:71516749 | T | C | 6 | a0003c0003t0001g0004 a0003c0003t0001g0232 a0003c0003t0001g0255 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4860+478T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516749 | |||||||
| chr5:71516791 | T | G | 1 | a0002c0002t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4860+520T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516791 | |||||||
| chr5:71516819 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4861-503T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516819 | |||||||
| chr5:71517049 | A | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4861-273A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517049 | |||||||
| chr5:71517160 | G | A | 2 | a0017c0015t0001g0222 a0017c0015t0001g0225 |
2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4861-162G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517160 | |||||||
| chr5:71517268 | A | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4861-54A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517268 | |||||||
| chr5:71517846 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4991+394G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71517846 | |||||||
| chr5:71517954 | T | A | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4991+502T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71517954 | |||||||
| chr5:71518018 | G | A | 1 | a0040c0045t0002g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4991+566G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518018 | |||||||
| chr5:71518062 | G | A | 1 | a0006c0007t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4991+610G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518062 | |||||||
| chr5:71518101 | T | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4991+649T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518101 | |||||||
| chr5:71518272 | T | C | 104 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(101): Show |
105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.4991+820T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518272 | |||||||
| chr5:71518342 | G | C | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4991+890G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518342 | |||||||
| chr5:71518343 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4991+891G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518343 | |||||||
| chr5:71518355 | T | A | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4991+903T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518355 | |||||||
| chr5:71518373 | T | C | 3 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0017g0296 |
3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4991+921T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518373 | |||||||
| chr5:71518654 | A | G | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4991+1202A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518654 | |||||||
| chr5:71518659 | G | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4991+1207G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518659 | |||||||
| chr5:71518835 | C | CT | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4991+1401dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71518835 | ||||||
| chr5:71518835 | CT | C | 98 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(95): Show |
99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.4991+1401delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71518835 | ||||||
| chr5:71518858 | A | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4991+1406A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518858 | |||||||
| chr5:71519111 | C | T | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.4991+1659C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519111 | |||||||
| chr5:71519292 | AC | A | 100 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(97): Show |
101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.4991+1841delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519292 | |||||||
| chr5:71519377 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4991+1925T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519377 | |||||||
| chr5:71519622 | A | G | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.4991+2170A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519622 | |||||||
| chr5:71519654 | G | A | 1 | a0004c0004t0010g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4991+2202G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519654 | |||||||
| chr5:71519668 | C | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4991+2216C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519668 | |||||||
| chr5:71519986 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4992-2303G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519986 | |||||||
| chr5:71520114 | G | C | 2 | a0017c0015t0001g0222 a0017c0015t0001g0225 |
2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4992-2175G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520114 | |||||||
| chr5:71520150 | A | T | 2 | a0003c0003t0001g0004 a0011c0010t0001g0004 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4992-2139A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520150 | |||||||
| chr5:71520157 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4992-2132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520157 | |||||||
| chr5:71520322 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4992-1967T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520322 | |||||||
| chr5:71520336 | A | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4992-1953A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520336 | |||||||
| chr5:71520379 | C | T | 2 | a0005c0005t0001g0234 a0039c0044t0005g0194 |
2 | NA18906.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4992-1910C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520379 | |||||||
| chr5:71520674 | T | TGCCAGGC others(264): Show |
2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-1600_4992-159 others(275): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71520674 | ||||||
| chr5:71520690 | A | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-1599A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520690 | |||||||
| chr5:71521057 | G | A | 1 | a0041c0052t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4992-1232G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521057 | |||||||
| chr5:71521083 | G | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG00621.hp2 NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4992-1206G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521083 | |||||||
| chr5:71521169 | A | G | 1 | a0006c0007t0002g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4992-1120A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521169 | |||||||
| chr5:71521187 | C | CA | 18 | a0001c0001t0002g0039 a0001c0001t0002g0076 a0001c0001t0002g0121 others(15): Show |
18 | HG00438.hp2 HG02040.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.4992-1087dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521187 | ||||||
| chr5:71521187 | CA | C | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4992-1087delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521187 | ||||||
| chr5:71521291 | G | GT | 21 | a0001c0001t0002g0027 a0001c0001t0002g0063 a0001c0001t0002g0122 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.4992-981dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521291 | ||||||
| chr5:71521417 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4992-872C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521417 | |||||||
| chr5:71521592 | T | C | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4992-697T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521592 | |||||||
| chr5:71521714 | C | T | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4992-575C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521714 | |||||||
| chr5:71521804 | G | A | 2 | a0004c0004t0004g0318 a0004c0004t0004g0319 |
2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4992-485G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521804 | |||||||
| chr5:71521808 | C | G | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4992-481C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521808 | |||||||
| chr5:71521960 | C | CT | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.4992-318dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521960 | ||||||
| chr5:71521982 | G | C | 3 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0272 |
3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.4992-307G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521982 | |||||||
| chr5:71522073 | A | G | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-216A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71522073 | |||||||
| chr5:71522502 | C | CA | 132 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(129): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.5193+28dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr5 | 71522502 | ||||||
| chr5:71522520 | T | G | 1 | a0002c0002t0001g0226 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5193+30T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522520 | |||||||
| chr5:71522540 | G | T | 2 | a0002c0002t0001g0165 a0002c0002t0001g0182 |
2 | HG02015.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.5193+50G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522540 | |||||||
| chr5:71522667 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5194-89A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522667 | |||||||
| chr5:71522705 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5194-51C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522705 | |||||||
| chr5:71523050 | A | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5387+101A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523050 | |||||||
| chr5:71523164 | G | C | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5387+215G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523164 | |||||||
| chr5:71523353 | C | T | 2 | a0003c0003t0001g0274 a0003c0003t0001g0307 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.5387+404C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523353 | |||||||
| chr5:71523355 | C | T | 2 | a0009c0008t0002g0008 a0009c0008t0002g0095 |
2 | HG01167.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5387+406C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523355 | |||||||
| chr5:71523409 | G | A | 17 | a0001c0001t0002g0015 a0001c0001t0002g0024 a0001c0001t0002g0035 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.5387+460G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523409 | |||||||
| chr5:71523468 | C | T | 1 | a0037c0023t0002g0073 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5388-471C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523468 | |||||||
| chr5:71524448 | A | C | 1 | a0001c0001t0002g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5772+125A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524448 | |||||||
| chr5:71524540 | C | CAAT | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+217_5772+218i others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524540 | |||||||
| chr5:71524566 | C | T | 1 | a0003c0003t0001g0261 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5772+243C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524566 | |||||||
| chr5:71524592 | A | AT | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+270dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524592 | ||||||
| chr5:71524633 | ATTTTTTA others(5): Show |
A | 2 | a0006c0007t0002g0113 a0006c0007t0002g0114 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5772+317_5772+328d others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524633 | ||||||
| chr5:71524644 | AT | A | 130 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.5772+330delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524644 | ||||||
| chr5:71524787 | C | T | 31 | a0003c0003t0001g0231 a0003c0003t0001g0239 a0003c0003t0001g0242 others(28): Show |
31 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.5772+464C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524787 | |||||||
| chr5:71524825 | T | TGGCGATG others(320): Show |
1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5772+515_5772+516i others(329): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524825 | ||||||
| chr5:71524986 | G | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5772+663G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524986 | |||||||
| chr5:71525007 | A | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(119): Show |
124 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.5772+684A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525007 | |||||||
| chr5:71525063 | T | C | 1 | a0015c0016t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5772+740T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525063 | |||||||
| chr5:71525098 | A | G | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5772+775A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525098 | |||||||
| chr5:71525158 | G | C | 8 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5772+835G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525158 | |||||||
| chr5:71525189 | A | C | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5772+866A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525189 | |||||||
| chr5:71525190 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5772+867C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525190 | |||||||
| chr5:71525223 | G | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5772+900G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525223 | |||||||
| chr5:71525245 | T | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+922T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525245 | |||||||
| chr5:71525246 | G | A | 111 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5772+923G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525246 | |||||||
| chr5:71525268 | C | CCCCCCCA others(41): Show |
1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5772+951_5772+952i others(50): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525268 | ||||||
| chr5:71525269 | CCCCCCCA others(170): Show |
C | 10 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(7): Show |
10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.5772+985_5772+1161 others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525269 | ||||||
| chr5:71525286 | C | T | 1 | a0003c0003t0001g0242 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5772+963C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525286 | |||||||
| chr5:71525303 | C | T | 111 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5772+980C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525303 | |||||||
| chr5:71525304 | G | A | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+981G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525304 | |||||||
| chr5:71525329 | G | A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5772+1006G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525329 | |||||||
| chr5:71525362 | C | G | 1 | a0002c0002t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5772+1039C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525362 | |||||||
| chr5:71525364 | C | T | 1 | a0019c0042t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5772+1041C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525364 | |||||||
| chr5:71525376 | C | T | 1 | a0005c0005t0017g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5772+1053C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525376 | |||||||
| chr5:71525381 | C | T | 1 | a0006c0007t0002g0007 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5772+1058C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525381 | |||||||
| chr5:71525414 | G | A | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+1091G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525414 | |||||||
| chr5:71525417 | C | T | 3 | a0010c0011t0001g0192 a0010c0011t0001g0193 a0027c0019t0024g0119 |
3 | HG01975.hp1 HG01981.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.5772+1094C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525417 | |||||||
| chr5:71525445 | C | T | 281 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(278): Show |
284 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.5772+1122C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525445 | |||||||
| chr5:71525446 | A | C | 282 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.5772+1123A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525446 | |||||||
| chr5:71525446 | A | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5772+1123A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525446 | |||||||
| chr5:71525447 | CCCCCCAC others(92): Show |
C | 1 | a0001c0001t0002g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1129_5772+122 others(103): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525447 | ||||||
| chr5:71525448 | C | CCCCCACC others(91): Show |
2 | a0002c0002t0001g0154 a0036c0040t0001g0153 |
2 | NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.5772+1144_5772+124 others(102): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525448 | ||||||
| chr5:71525463 | CGGACGGG others(55): Show |
C | 1 | a0002c0002t0005g0178 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5772+1143_5772+120 others(66): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525463 | ||||||
| chr5:71525467 | CGGGGCGG others(91): Show |
C | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5772+1173_5772+127 others(102): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525467 | ||||||
| chr5:71525468 | G | A | 1 | a0006c0028t0021g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5772+1145G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525468 | |||||||
| chr5:71525550 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1227C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525550 | |||||||
| chr5:71525557 | CTCCCGGA others(42): Show |
C | 117 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(114): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.5772+1242_5772+129 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525557 | ||||||
| chr5:71525565 | T | C | 128 | a0001c0001t0002g0040 a0001c0001t0002g0063 a0001c0026t0002g0013 others(125): Show |
129 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.5772+1242T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525565 | |||||||
| chr5:71525570 | C | T | 16 | a0001c0001t0002g0063 a0001c0026t0002g0013 a0004c0004t0004g0310 others(13): Show |
16 | HG01192.hp1 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5772+1247C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525570 | |||||||
| chr5:71525593 | CCCCCCAA others(41): Show |
C | 2 | a0001c0001t0002g0063 a0007c0006t0002g0084 |
2 | HG01192.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.5772+1276_5772+132 others(52): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525593 | ||||||
| chr5:71525595 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1272C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525595 | |||||||
| chr5:71525599 | A | C | 127 | a0001c0001t0002g0040 a0001c0026t0002g0013 a0002c0002t0001g0133 others(124): Show |
128 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.5772+1276A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525599 | |||||||
| chr5:71525606 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1283T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525606 | |||||||
| chr5:71525619 | C | T | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.5772+1296C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525619 | |||||||
| chr5:71525680 | C | CG | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+1363dupG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525680 | ||||||
| chr5:71525681 | G | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+1358G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525681 | |||||||
| chr5:71525707 | C | T | 1 | a0002c0002t0001g0224 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5772+1384C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525707 | |||||||
| chr5:71525716 | C | T | 1 | a0005c0005t0001g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5772+1393C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525716 | |||||||
| chr5:71525725 | A | G | 1 | a0005c0005t0001g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5772+1402A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525725 | |||||||
| chr5:71525728 | C | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+1405C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525728 | |||||||
| chr5:71525791 | T | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5772+1468T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525791 | |||||||
| chr5:71525798 | C | T | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+1475C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525798 | |||||||
| chr5:71526016 | T | C | 1 | a0012c0012t0003g0166 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5772+1693T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526016 | |||||||
| chr5:71526031 | C | CG | 11 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0122 others(8): Show |
11 | HG00438.hp2 HG01099.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.5772+1712dupG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526031 | ||||||
| chr5:71526058 | A | G | 1 | a0003c0003t0006g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5772+1735A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526058 | |||||||
| chr5:71526144 | G | T | 6 | a0003c0003t0001g0239 a0003c0003t0001g0244 a0003c0003t0001g0245 others(3): Show |
6 | NA18942.hp2 NA18943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.5772+1821G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526144 | |||||||
| chr5:71526277 | T | TGGCA | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+1956_5772+195 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526277 | ||||||
| chr5:71526316 | C | CT | 132 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(129): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.5772+2005dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526316 | ||||||
| chr5:71526615 | C | CA | 19 | a0002c0002t0001g0200 a0002c0002t0001g0215 a0002c0002t0001g0302 others(16): Show |
19 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.5772+2313dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | ||||||
| chr5:71526615 | C | CAAA | 94 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.5772+2311_5772+231 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | ||||||
| chr5:71526615 | C | CAAAA | 16 | a0001c0001t0002g0016 a0001c0001t0002g0035 a0001c0001t0002g0039 others(13): Show |
16 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.5772+2310_5772+231 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | ||||||
| chr5:71526615 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0062 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5772+2303_5772+231 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | ||||||
| chr5:71526634 | A | G | 3 | a0003c0003t0001g0289 a0003c0003t0001g0290 a0003c0003t0001g0294 |
3 | HG00140.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5772+2311A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526634 | |||||||
| chr5:71526685 | G | GT | 23 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0002c0002t0001g0157 others(20): Show |
23 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.5772+2381dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526685 | ||||||
| chr5:71526711 | G | A | 1 | a0005c0005t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5772+2388G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526711 | |||||||
| chr5:71526809 | T | C | 1 | a0003c0003t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5772+2486T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526809 | |||||||
| chr5:71526995 | A | T | 1 | a0001c0001t0002g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5772+2672A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526995 | |||||||
| chr5:71527094 | T | A | 1 | a0012c0012t0003g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5772+2771T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527094 | |||||||
| chr5:71527173 | G | A | 3 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0272 |
3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.5772+2850G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527173 | |||||||
| chr5:71527202 | C | T | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.5772+2879C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527202 | |||||||
| chr5:71527241 | C | T | 1 | a0010c0011t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5772+2918C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527241 | |||||||
| chr5:71527242 | G | A | 7 | a0008c0009t0002g0023 a0008c0009t0002g0029 a0008c0009t0002g0031 others(4): Show |
7 | HG02572.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.5772+2919G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527242 | |||||||
| chr5:71527248 | A | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(96): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.5772+2925A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527248 | |||||||
| chr5:71527260 | C | G | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+2937C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527260 | |||||||
| chr5:71527674 | A | G | 1 | a0005c0005t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5772+3351A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527674 | |||||||
| chr5:71527820 | C | CT | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(16): Show |
19 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.5772+3512dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71527820 | ||||||
| chr5:71527842 | GA | G | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5772+3520delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527842 | |||||||
| chr5:71528156 | G | C | 1 | a0002c0002t0003g0136 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3833G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528156 | |||||||
| chr5:71528157 | C | A | 1 | a0002c0002t0003g0136 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3834C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528157 | |||||||
| chr5:71528159 | A | C | 1 | a0002c0002t0003g0136 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3836A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528159 | |||||||
| chr5:71528339 | G | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5773-3969G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528339 | |||||||
| chr5:71529528 | A | G | 8 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5773-2780A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529528 | |||||||
| chr5:71529558 | G | T | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5773-2750G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529558 | |||||||
| chr5:71529561 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5773-2747C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529561 | |||||||
| chr5:71529894 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5773-2414T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529894 | |||||||
| chr5:71530018 | A | G | 1 | a0004c0004t0004g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5773-2290A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530018 | |||||||
| chr5:71530052 | C | T | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5773-2256C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530052 | |||||||
| chr5:71530224 | A | C | 1 | a0001c0001t0002g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5773-2084A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530224 | |||||||
| chr5:71530412 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5773-1896T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530412 | |||||||
| chr5:71530623 | G | A | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5773-1685G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530623 | |||||||
| chr5:71530858 | G | A | 91 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(88): Show |
93 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.5773-1450G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530858 | |||||||
| chr5:71530954 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0089 |
2 | NA18939.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.5773-1354G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530954 | |||||||
| chr5:71530968 | G | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0056 |
2 | HG00735.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.5773-1340G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530968 | |||||||
| chr5:71530979 | C | T | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5773-1329C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530979 | |||||||
| chr5:71531085 | A | T | 1 | a0006c0028t0021g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5773-1223A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531085 | |||||||
| chr5:71531303 | T | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5773-1005T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531303 | |||||||
| chr5:71531685 | T | A | 2 | a0002c0002t0001g0150 a0002c0002t0001g0188 |
2 | NA18942.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.5773-623T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531685 | |||||||
| chr5:71531801 | G | A | 5 | a0006c0007t0002g0111 a0006c0007t0002g0112 a0006c0007t0002g0113 others(2): Show |
5 | HG02896.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.5773-507G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531801 | |||||||
| chr5:71532053 | T | C | 1 | a0002c0002t0001g0196 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5773-255T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532053 | |||||||
| chr5:71532097 | C | G | 1 | a0002c0002t0001g0199 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5773-211C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532097 | |||||||
| chr5:71532106 | C | T | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5773-202C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532106 | |||||||
| chr5:71532148 | G | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0020g0057 |
3 | HG01070.hp1 HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5773-160G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532148 | |||||||
| chr5:71532464 | C | T | 1 | a0007c0006t0002g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5892+37C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532464 | |||||||
| chr5:71532579 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5892+152G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532579 | |||||||
| chr5:71532590 | TTTTG | T | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5892+173_5892+176d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71532590 | ||||||
| chr5:71532792 | A | G | 2 | a0008c0009t0002g0029 a0008c0048t0002g0010 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5892+365A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532792 | |||||||
| chr5:71532793 | T | C | 1 | a0003c0003t0001g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5892+366T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532793 | |||||||
| chr5:71532856 | G | A | 6 | a0009c0008t0002g0008 a0009c0008t0002g0095 a0009c0008t0007g0100 others(3): Show |
6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.5892+429G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532856 | |||||||
| chr5:71533053 | T | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5892+626T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533053 | |||||||
| chr5:71533156 | A | C | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5892+729A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533156 | |||||||
| chr5:71533264 | A | T | 2 | a0002c0002t0001g0201 a0002c0002t0001g0202 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5892+837A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533264 | |||||||
| chr5:71533462 | C | T | 2 | a0004c0004t0004g0318 a0004c0004t0004g0319 |
2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5892+1035C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533462 | |||||||
| chr5:71533468 | A | AT | 101 | a0001c0001t0002g0046 a0002c0002t0001g0133 a0002c0002t0001g0137 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5892+1058dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71533468 | ||||||
| chr5:71533684 | G | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5892+1257G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533684 | |||||||
| chr5:71533850 | T | G | 1 | a0001c0001t0022g0014 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5892+1423T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533850 | |||||||
| chr5:71533857 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5892+1430C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533857 | |||||||
| chr5:71534114 | G | A | 1 | a0005c0005t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5892+1687G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534114 | |||||||
| chr5:71534224 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5892+1797G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534224 | |||||||
| chr5:71534331 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5892+1904C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534331 | |||||||
| chr5:71534496 | G | GT | 68 | a0001c0001t0020g0057 a0002c0002t0001g0137 a0002c0002t0001g0142 others(65): Show |
69 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.5892+2079dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71534496 | ||||||
| chr5:71534504 | T | G | 7 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5892+2077T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534504 | |||||||
| chr5:71534504 | T | TG | 3 | a0002c0002t0005g0183 a0002c0002t0005g0187 a0013c0013t0001g0145 |
3 | HG03927.hp2 NA18963.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.5892+2077_5892+207 others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534504 | |||||||
| chr5:71534702 | C | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5892+2275C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534702 | |||||||
| chr5:71534704 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5892+2277C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534704 | |||||||
| chr5:71534767 | G | A | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5892+2340G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534767 | |||||||
| chr5:71534871 | T | C | 1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5892+2444T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534871 | |||||||
| chr5:71535039 | T | G | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5892+2612T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535039 | |||||||
| chr5:71535060 | C | G | 1 | a0001c0001t0002g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5892+2633C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535060 | |||||||
| chr5:71535128 | T | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5892+2701T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535128 | |||||||
| chr5:71535173 | T | C | 249 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(246): Show |
252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.5892+2746T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535173 | |||||||
| chr5:71535202 | AT | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0074 a0001c0001t0002g0126 others(3): Show |
6 | HG01169.hp1 HG02965.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.5892+2791delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71535202 | ||||||
| chr5:71535263 | G | A | 1 | a0001c0001t0022g0014 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5892+2836G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535263 | |||||||
| chr5:71535353 | C | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5892+2926C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535353 | |||||||
| chr5:71535526 | C | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5892+3099C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535526 | |||||||
| chr5:71535527 | G | A | 1 | a0005c0005t0017g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5892+3100G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535527 | |||||||
| chr5:71535585 | T | C | 9 | a0007c0006t0002g0018 a0007c0006t0002g0047 a0007c0006t0002g0048 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.5892+3158T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535585 | |||||||
| chr5:71535686 | A | T | 1 | a0003c0003t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5892+3259A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535686 | |||||||
| chr5:71535789 | C | G | 1 | a0003c0003t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5893-3253C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535789 | |||||||
| chr5:71535814 | C | G | 104 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(101): Show |
105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.5893-3228C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535814 | |||||||
| chr5:71536157 | A | AT | 4 | a0003c0003t0001g0256 a0003c0003t0001g0257 a0003c0003t0001g0258 others(1): Show |
4 | HG00099.hp1 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.5893-2878dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71536157 | ||||||
| chr5:71536204 | A | G | 8 | a0005c0005t0001g0235 a0005c0005t0001g0236 a0005c0005t0001g0237 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5893-2838A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536204 | |||||||
| chr5:71536371 | T | C | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5893-2671T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536371 | |||||||
| chr5:71536565 | C | T | 2 | a0006c0007t0002g0108 a0006c0007t0002g0110 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5893-2477C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536565 | |||||||
| chr5:71536623 | C | T | 10 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(7): Show |
10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.5893-2419C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536623 | |||||||
| chr5:71536702 | C | T | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5893-2340C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536702 | |||||||
| chr5:71536706 | T | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5893-2336T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536706 | |||||||
| chr5:71536784 | C | T | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5893-2258C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536784 | |||||||
| chr5:71536996 | C | CA | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5893-2045dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71536996 | ||||||
| chr5:71537140 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5893-1902C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537140 | |||||||
| chr5:71537149 | C | CA | 62 | a0002c0002t0001g0137 a0002c0002t0001g0142 a0002c0002t0001g0144 others(59): Show |
63 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.5893-1870dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71537149 | ||||||
| chr5:71537149 | CA | C | 127 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(124): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.5893-1870delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71537149 | ||||||
| chr5:71537250 | G | T | 1 | a0025c0043t0001g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5893-1792G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537250 | |||||||
| chr5:71537317 | G | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG02056.hp2 NA18950.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.5893-1725G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537317 | |||||||
| chr5:71537340 | A | G | 1 | a0003c0003t0001g0267 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5893-1702A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537340 | |||||||
| chr5:71537415 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5893-1627C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537415 | |||||||
| chr5:71537513 | T | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5893-1529T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537513 | |||||||
| chr5:71537554 | G | A | 2 | a0006c0007t0002g0007 a0006c0028t0021g0009 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5893-1488G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537554 | |||||||
| chr5:71537685 | T | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-1357T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537685 | |||||||
| chr5:71537743 | T | A | 1 | a0002c0002t0003g0136 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5893-1299T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537743 | |||||||
| chr5:71538133 | C | T | 3 | a0002c0002t0001g0186 a0021c0035t0001g0124 a0026c0032t0001g0115 |
3 | HG01243.hp2 HG01433.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5893-909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538133 | |||||||
| chr5:71538250 | A | G | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-792A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538250 | |||||||
| chr5:71538264 | G | T | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5893-778G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538264 | |||||||
| chr5:71538316 | G | A | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5893-726G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538316 | |||||||
| chr5:71538435 | CAT | C | 9 | a0002c0002t0001g0172 a0002c0002t0001g0214 a0002c0002t0005g0178 others(6): Show |
9 | NA18947.hp1 NA18949.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.5893-605_5893-604d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71538435 | ||||||
| chr5:71538655 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(89): Show |
94 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.5893-387G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538655 | |||||||
| chr5:71538674 | G | T | 1 | a0003c0003t0001g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5893-368G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538674 | |||||||
| chr5:71538704 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5893-338G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538704 | |||||||
| chr5:71538805 | A | T | 1 | a0003c0003t0001g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5893-237A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538805 | |||||||
| chr5:71538876 | A | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-166A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538876 | |||||||
| chr5:71539006 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-36G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71539006 | |||||||
| chr5:71539028 | T | G | 1 | a0003c0003t0001g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5893-14T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71539028 | |||||||
| chr5:71539089 | T | C | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5929+11T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539089 | |||||||
| chr5:71539099 | T | C | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.5929+21T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539099 | |||||||
| chr5:71539126 | T | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5929+48T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539126 | |||||||
| chr5:71539265 | G | A | 5 | a0003c0003t0006g0240 a0011c0010t0006g0241 a0011c0010t0006g0249 others(2): Show |
5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5929+187G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539265 | |||||||
| chr5:71539379 | T | G | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5930-178T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539379 | |||||||
| chr5:71539380 | G | C | 1 | a0003c0003t0001g0266 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5930-177G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539380 | |||||||
| chr5:71539474 | A | C | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5930-83A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539474 | |||||||
| chr5:71539881 | TCATGGAA others(10): Show |
T | 7 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(4): Show |
7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.6022+255_6022+271d others(19): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71539881 | ||||||
| chr5:71540074 | A | G | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6022+425A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540074 | |||||||
| chr5:71540180 | T | C | 256 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(253): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.6022+531T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540180 | |||||||
| chr5:71540279 | CTTAT | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6022+641_6022+644d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71540279 | ||||||
| chr5:71540298 | C | T | 4 | a0008c0009t0002g0023 a0008c0009t0002g0031 a0008c0009t0002g0033 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.6022+649C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540298 | |||||||
| chr5:71540321 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6022+672A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540321 | |||||||
| chr5:71540576 | T | C | 256 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(253): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.6023-878T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540576 | |||||||
| chr5:71540668 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6023-786C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540668 | |||||||
| chr5:71541131 | G | GCTGT | 256 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(253): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.6023-320_6023-317d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71541131 | ||||||
| chr5:71541180 | G | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6023-274G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71541180 | |||||||
| chr5:71541315 | A | C | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6023-139A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71541315 | |||||||
| chr5:71541762 | G | A | 1 | a0003c0003t0001g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6251+80G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 29/38 | chr5 | 71541762 | |||||||
| chr5:71542449 | C | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0129 |
2 | NA18950.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.6412+184C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542449 | |||||||
| chr5:71542565 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6412+300C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542565 | |||||||
| chr5:71542614 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.6412+349G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542614 | |||||||
| chr5:71542701 | C | CAT | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6412+451_6412+452d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr5 | 71542701 | ||||||
| chr5:71542701 | C | CATATAT | 11 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(8): Show |
11 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.6412+447_6412+452d others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr5 | 71542701 | ||||||
| chr5:71542750 | C | A | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6412+485C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542750 | |||||||
| chr5:71542870 | A | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6412+605A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542870 | |||||||
| chr5:71543220 | C | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6412+955C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543220 | |||||||
| chr5:71543256 | T | C | 1 | a0040c0045t0002g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6412+991T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543256 | |||||||
| chr5:71543377 | C | T | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6413-980C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543377 | |||||||
| chr5:71543429 | T | A | 3 | a0003c0003t0001g0255 a0003c0003t0001g0285 a0003c0049t0001g0250 |
3 | HG02559.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6413-928T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543429 | |||||||
| chr5:71543555 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6413-802C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543555 | |||||||
| chr5:71543724 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6413-633G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543724 | |||||||
| chr5:71543731 | C | T | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6413-626C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543731 | |||||||
| chr5:71543851 | A | G | 247 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.6413-506A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543851 | |||||||
| chr5:71544169 | G | C | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6413-188G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71544169 | |||||||
| chr5:71544606 | A | G | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(134): Show |
139 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.6563+99A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544606 | |||||||
| chr5:71544695 | C | T | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6563+188C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544695 | |||||||
| chr5:71544759 | AGTT | A | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 |
3 | HG00673.hp2 HG02523.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.6563+255_6563+257d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544759 | ||||||
| chr5:71544780 | C | T | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.6564-259C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544780 | |||||||
| chr5:71544812 | G | A | 1 | a0001c0022t0002g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6564-227G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544812 | |||||||
| chr5:71544858 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6564-181C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544858 | |||||||
| chr5:71544859 | G | A | 3 | a0010c0011t0001g0192 a0010c0011t0001g0193 a0010c0011t0001g0203 |
3 | HG01975.hp1 HG01981.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.6564-180G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544859 | |||||||
| chr5:71544879 | C | CA | 24 | a0002c0002t0001g0164 a0002c0002t0001g0212 a0003c0003t0001g0243 others(21): Show |
24 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.6564-133dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | ||||||
| chr5:71544879 | C | CAA | 7 | a0003c0003t0001g0274 a0003c0003t0001g0307 a0003c0003t0018g0306 others(4): Show |
7 | HG00642.hp2 HG00733.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.6564-134_6564-133d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | ||||||
| chr5:71544879 | CA | C | 75 | a0002c0002t0001g0133 a0002c0002t0001g0138 a0002c0002t0001g0144 others(72): Show |
76 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.6564-133delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | ||||||
| chr5:71544879 | CAAAAAAA others(3): Show |
C | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6564-142_6564-133d others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | ||||||
| chr5:71544904 | A | AAAAAAG | 9 | a0001c0001t0002g0042 a0001c0026t0002g0013 a0004c0004t0004g0311 others(6): Show |
9 | HG01943.hp1 HG01978.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | ||||||
| chr5:71544904 | A | AAAAAG | 25 | a0001c0001t0002g0024 a0001c0001t0002g0035 a0001c0001t0002g0040 others(22): Show |
25 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | ||||||
| chr5:71544904 | A | AAAAG | 84 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | ||||||
| chr5:71544904 | A | AAAG | 7 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0006c0024t0002g0109 others(4): Show |
7 | HG01167.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.6564-134_6564-132d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | ||||||
| chr5:71544904 | A | G | 6 | a0001c0001t0002g0080 a0001c0001t0002g0122 a0004c0004t0004g0310 others(3): Show |
6 | HG00438.hp2 HG02027.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6564-135A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544904 | |||||||
| chr5:71544907 | G | A | 1 | a0003c0003t0001g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6564-132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544907 | |||||||
| chr5:71545337 | C | A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6744+118C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545337 | |||||||
| chr5:71545373 | C | T | 2 | a0005c0005t0001g0234 a0005c0005t0015g0309 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6744+154C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545373 | |||||||
| chr5:71545528 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0019g0017 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.6744+309G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545528 | |||||||
| chr5:71545598 | T | A | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6744+379T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545598 | |||||||
| chr5:71545669 | A | G | 6 | a0003c0003t0001g0004 a0003c0003t0001g0232 a0003c0003t0001g0255 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6744+450A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545669 | |||||||
| chr5:71545773 | G | A | 1 | a0001c0001t0019g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6744+554G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545773 | |||||||
| chr5:71545780 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6744+561G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545780 | |||||||
| chr5:71545840 | T | TA | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6744+634dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71545840 | ||||||
| chr5:71545859 | G | C | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.6744+640G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545859 | |||||||
| chr5:71546237 | A | G | 9 | a0006c0007t0002g0007 a0006c0007t0002g0108 a0006c0007t0002g0110 others(6): Show |
9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.6744+1018A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546237 | |||||||
| chr5:71546249 | C | A | 111 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.6744+1030C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546249 | |||||||
| chr5:71546269 | A | G | 1 | a0001c0001t0019g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6744+1050A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546269 | |||||||
| chr5:71546276 | A | G | 1 | a0004c0004t0010g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6744+1057A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546276 | |||||||
| chr5:71546500 | C | G | 1 | a0004c0004t0004g0311 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6744+1281C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546500 | |||||||
| chr5:71546594 | G | T | 3 | a0003c0003t0001g0242 a0003c0003t0001g0248 a0003c0003t0001g0269 |
3 | NA18959.hp1 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6744+1375G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546594 | |||||||
| chr5:71546596 | C | T | 1 | a0009c0008t0002g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6744+1377C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546596 | |||||||
| chr5:71546608 | A | C | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6744+1389A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546608 | |||||||
| chr5:71546617 | C | CA | 52 | a0003c0003t0001g0004 a0003c0003t0001g0232 a0003c0003t0001g0239 others(49): Show |
52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.6744+1426dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | ||||||
| chr5:71546617 | CA | C | 83 | a0002c0002t0001g0137 a0002c0002t0001g0142 a0002c0002t0001g0146 others(80): Show |
84 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.6744+1426delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | ||||||
| chr5:71546617 | CAA | C | 44 | a0001c0022t0002g0086 a0002c0002t0001g0133 a0002c0002t0001g0138 others(41): Show |
44 | HG00609.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.6744+1425_6744+142 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | ||||||
| chr5:71546617 | CAAA | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0019 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.6744+1424_6744+142 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | ||||||
| chr5:71546617 | CAAAA | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0021 others(37): Show |
42 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.6744+1423_6744+142 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | ||||||
| chr5:71546698 | G | A | 1 | a0016c0017t0009g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6744+1479G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546698 | |||||||
| chr5:71546782 | G | T | 1 | a0019c0042t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6744+1563G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546782 | |||||||
| chr5:71546850 | CT | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6744+1638delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546850 | ||||||
| chr5:71546935 | T | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0093 a0001c0001t0002g0094 others(2): Show |
6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.6744+1716T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546935 | |||||||
| chr5:71547002 | C | T | 111 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.6745-1680C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547002 | |||||||
| chr5:71547088 | A | G | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6745-1594A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547088 | |||||||
| chr5:71547144 | C | T | 12 | a0003c0003t0001g0233 a0003c0003t0001g0273 a0003c0003t0001g0274 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6745-1538C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547144 | |||||||
| chr5:71547165 | A | T | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.6745-1517A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547165 | |||||||
| chr5:71547279 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6745-1403A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547279 | |||||||
| chr5:71547284 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6745-1398C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547284 | |||||||
| chr5:71547533 | T | G | 1 | a0007c0006t0002g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6745-1149T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547533 | |||||||
| chr5:71547536 | G | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6745-1146G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547536 | |||||||
| chr5:71547579 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6745-1103C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547579 | |||||||
| chr5:71547676 | C | A | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6745-1006C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547676 | |||||||
| chr5:71547763 | C | T | 1 | a0002c0039t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6745-919C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547763 | |||||||
| chr5:71547823 | C | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6745-859C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547823 | |||||||
| chr5:71547882 | A | C | 1 | a0002c0002t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6745-800A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547882 | |||||||
| chr5:71547952 | C | A | 1 | a0001c0001t0002g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6745-730C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547952 | |||||||
| chr5:71548048 | C | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0044 |
2 | HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.6745-634C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548048 | |||||||
| chr5:71548164 | C | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6745-518C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548164 | |||||||
| chr5:71548284 | A | G | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6745-398A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548284 | |||||||
| chr5:71548671 | T | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6745-11T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548671 | |||||||
| chr5:71548868 | G | A | 2 | a0020c0020t0023g0120 a0033c0047t0001g0229 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6808+123G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71548868 | |||||||
| chr5:71549100 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6809-320C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549100 | |||||||
| chr5:71549115 | G | C | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6809-305G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549115 | |||||||
| chr5:71549163 | A | G | 1 | a0003c0003t0001g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6809-257A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549163 | |||||||
| chr5:71549236 | T | TG | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6809-184_6809-183i others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549236 | |||||||
| chr5:71549243 | C | A | 3 | a0002c0002t0001g0146 a0002c0002t0001g0157 a0002c0002t0001g0186 |
3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.6809-177C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549243 | |||||||
| chr5:71549244 | G | A | 1 | a0004c0004t0004g0312 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6809-176G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549244 | |||||||
| chr5:71549313 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6809-107T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549313 | |||||||
| chr5:71549986 | T | C | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.6995+380T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71549986 | |||||||
| chr5:71550222 | C | G | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.6995+616C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550222 | |||||||
| chr5:71550285 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6995+679C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550285 | |||||||
| chr5:71550376 | G | A | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6995+770G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550376 | |||||||
| chr5:71550385 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6995+779A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550385 | |||||||
| chr5:71550393 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6995+787C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550393 | |||||||
| chr5:71550446 | G | A | 2 | a0002c0041t0001g0147 a0041c0052t0001g0227 |
2 | NA18957.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.6995+840G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550446 | |||||||
| chr5:71550457 | TA | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(138): Show |
143 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.6995+860delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71550457 | ||||||
| chr5:71550466 | AT | A | 103 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(100): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.6995+870delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71550466 | ||||||
| chr5:71550572 | G | C | 1 | a0002c0002t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6995+966G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550572 | |||||||
| chr5:71550865 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(134): Show |
139 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.6995+1259T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550865 | |||||||
| chr5:71550997 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6995+1391C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550997 | |||||||
| chr5:71551097 | GTTTA | G | 231 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(228): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.6995+1519_6995+152 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551097 | ||||||
| chr5:71551097 | GTTTATTT others(1): Show |
G | 19 | a0001c0001t0002g0064 a0004c0004t0004g0310 a0004c0004t0004g0311 others(16): Show |
19 | HG00597.hp1 HG00642.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.6995+1515_6995+152 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551097 | ||||||
| chr5:71551230 | T | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.6995+1624T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551230 | |||||||
| chr5:71551404 | G | T | 127 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(124): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.6996-1712G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551404 | |||||||
| chr5:71551564 | C | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6996-1552C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551564 | |||||||
| chr5:71551587 | G | A | 1 | a0026c0032t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6996-1529G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551587 | |||||||
| chr5:71551653 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1463G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551653 | |||||||
| chr5:71551665 | TTCACTTC others(30): Show |
T | 1 | a0001c0001t0002g0067 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6996-1419_6996-138 others(41): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551665 | ||||||
| chr5:71551720 | C | T | 1 | a0002c0002t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6996-1396C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551720 | |||||||
| chr5:71551752 | C | T | 1 | a0003c0003t0001g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6996-1364C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551752 | |||||||
| chr5:71551781 | C | T | 1 | a0003c0003t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6996-1335C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551781 | |||||||
| chr5:71551801 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1315C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551801 | |||||||
| chr5:71551875 | C | T | 1 | a0010c0011t0001g0193 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.6996-1241C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551875 | |||||||
| chr5:71551893 | A | AGGCGGGG others(42): Show |
1 | a0010c0011t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6996-1174_6996-112 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551893 | ||||||
| chr5:71551893 | A | G | 2 | a0001c0022t0002g0086 a0002c0002t0001g0300 |
2 | HG03942.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.6996-1223A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551893 | |||||||
| chr5:71551893 | AGGCGGGG others(42): Show |
A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-1174_6996-112 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551893 | ||||||
| chr5:71551896 | C | T | 1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6996-1220C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551896 | |||||||
| chr5:71551925 | G | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6996-1191G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551925 | |||||||
| chr5:71551956 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1160C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551956 | |||||||
| chr5:71551996 | A | G | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6996-1120A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551996 | |||||||
| chr5:71552036 | G | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6996-1080G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552036 | |||||||
| chr5:71552103 | C | T | 6 | a0009c0008t0002g0008 a0009c0008t0002g0095 a0009c0008t0007g0100 others(3): Show |
6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.6996-1013C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552103 | |||||||
| chr5:71552108 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6996-1008C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552108 | |||||||
| chr5:71552126 | G | GCTCCTCA others(33): Show |
134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.6996-968_6996-967i others(42): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71552126 | ||||||
| chr5:71552265 | G | A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-851G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552265 | |||||||
| chr5:71552413 | C | T | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6996-703C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552413 | |||||||
| chr5:71552420 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6996-696C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552420 | |||||||
| chr5:71552502 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.6996-614C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552502 | |||||||
| chr5:71552568 | G | A | 1 | a0003c0003t0001g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6996-548G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552568 | |||||||
| chr5:71552603 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 |
3 | HG00673.hp2 HG02523.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.6996-513C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552603 | |||||||
| chr5:71552604 | G | A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-512G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552604 | |||||||
| chr5:71552679 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.6996-437G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552679 | |||||||
| chr5:71552687 | T | C | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.6996-429T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552687 | |||||||
| chr5:71552690 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6996-426C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552690 | |||||||
| chr5:71552703 | G | A | 1 | a0014c0014t0001g0006 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6996-413G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552703 | |||||||
| chr5:71552718 | G | A | 9 | a0006c0007t0002g0007 a0006c0007t0002g0108 a0006c0007t0002g0110 others(6): Show |
9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.6996-398G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552718 | |||||||
| chr5:71552736 | G | C | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6996-380G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552736 | |||||||
| chr5:71552753 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6996-363G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552753 | |||||||
| chr5:71552757 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-359C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552757 | |||||||
| chr5:71552801 | G | A | 100 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(97): Show |
101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.6996-315G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552801 | |||||||
| chr5:71552816 | G | C | 67 | a0002c0002t0001g0137 a0002c0002t0001g0142 a0002c0002t0001g0144 others(64): Show |
68 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.6996-300G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552816 | |||||||
| chr5:71552834 | GGGGAGA | G | 5 | a0012c0012t0003g0148 a0012c0012t0003g0166 a0012c0012t0003g0167 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6996-266_6996-261d others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71552834 | ||||||
| chr5:71552856 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6996-260T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552856 | |||||||
| chr5:71552879 | C | T | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.6996-237C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552879 | |||||||
| chr5:71552925 | A | G | 1 | a0019c0042t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6996-191A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552925 | |||||||
| chr5:71552955 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.6996-161G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552955 | |||||||
| chr5:71553012 | A | T | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6996-104A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71553012 | |||||||
| chr5:71553405 | A | T | 10 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(7): Show |
10 | HG01167.hp1 HG02015.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.7200+85A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553405 | |||||||
| chr5:71553481 | T | C | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.7200+161T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553481 | |||||||
| chr5:71553570 | A | G | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7200+250A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553570 | |||||||
| chr5:71553591 | A | G | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7200+271A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553591 | |||||||
| chr5:71553613 | A | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7200+293A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553613 | |||||||
| chr5:71553639 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+319A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553639 | |||||||
| chr5:71553712 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7200+392A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553712 | |||||||
| chr5:71553719 | C | T | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.7200+399C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553719 | |||||||
| chr5:71553750 | C | G | 1 | a0005c0005t0015g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7200+430C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553750 | |||||||
| chr5:71553766 | C | A | 1 | a0002c0002t0001g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7200+446C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553766 | |||||||
| chr5:71553788 | T | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.7200+468T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553788 | |||||||
| chr5:71553852 | T | A | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7200+532T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553852 | |||||||
| chr5:71553868 | G | A | 1 | a0002c0002t0001g0214 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7200+548G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553868 | |||||||
| chr5:71554055 | T | G | 9 | a0002c0002t0003g0136 a0002c0002t0003g0163 a0002c0002t0003g0174 others(6): Show |
9 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7200+735T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554055 | |||||||
| chr5:71554085 | C | G | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7200+765C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554085 | |||||||
| chr5:71554255 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.7200+935T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554255 | |||||||
| chr5:71554303 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.7200+983A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554303 | |||||||
| chr5:71554766 | A | AT | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+1452dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71554766 | ||||||
| chr5:71554908 | C | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+1588C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554908 | |||||||
| chr5:71555058 | C | T | 1 | a0016c0017t0009g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7200+1738C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555058 | |||||||
| chr5:71555162 | C | T | 2 | a0004c0004t0010g0320 a0004c0004t0010g0321 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7201-1724C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555162 | |||||||
| chr5:71555261 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-1625G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555261 | |||||||
| chr5:71555467 | TTCTC | T | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.7201-1416_7201-141 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71555467 | ||||||
| chr5:71555627 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7201-1259C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555627 | |||||||
| chr5:71555628 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-1258G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555628 | |||||||
| chr5:71555676 | T | A | 1 | a0003c0003t0006g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7201-1210T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555676 | |||||||
| chr5:71555690 | C | T | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7201-1196C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555690 | |||||||
| chr5:71555705 | A | C | 307 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(304): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.7201-1181A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555705 | |||||||
| chr5:71555943 | A | G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7201-943A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555943 | |||||||
| chr5:71555944 | C | T | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-942C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555944 | |||||||
| chr5:71555959 | CAGCATAA others(35): Show |
C | 4 | a0002c0002t0003g0136 a0002c0002t0003g0177 a0002c0002t0012g0158 others(1): Show |
4 | HG00738.hp1 HG01496.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.7201-925_7201-884d others(44): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71555959 | ||||||
| chr5:71556034 | GTCTT | G | 5 | a0003c0003t0006g0240 a0011c0010t0006g0241 a0011c0010t0006g0249 others(2): Show |
5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.7201-848_7201-845d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71556034 | ||||||
| chr5:71556087 | T | C | 102 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(99): Show |
103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.7201-799T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556087 | |||||||
| chr5:71556382 | T | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7201-504T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556382 | |||||||
| chr5:71556732 | A | G | 1 | a0003c0003t0006g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7201-154A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556732 | |||||||
| chr5:71556744 | G | T | 1 | a0025c0043t0001g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7201-142G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556744 | |||||||
| chr5:71556784 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(118): Show |
123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.7201-102G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556784 | |||||||
| chr5:71556850 | A | C | 1 | a0002c0002t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7201-36A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556850 | |||||||
| chr5:71556947 | A | C | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7240+22A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71556947 | |||||||
| chr5:71557080 | A | G | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7240+155A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557080 | |||||||
| chr5:71557195 | A | G | 247 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(244): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.7240+270A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557195 | |||||||
| chr5:71557219 | G | A | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7240+294G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557219 | |||||||
| chr5:71557231 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7240+306C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557231 | |||||||
| chr5:71557235 | T | A | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+310T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557235 | |||||||
| chr5:71557315 | C | A | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7240+390C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557315 | |||||||
| chr5:71557375 | A | AT | 23 | a0003c0003t0001g0255 a0003c0003t0001g0258 a0003c0003t0001g0261 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.7240+477dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | A | ATT | 14 | a0001c0001t0002g0026 a0004c0004t0004g0311 a0004c0004t0004g0312 others(11): Show |
14 | HG01243.hp2 HG01433.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.7240+476_7240+477d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | A | ATTT | 90 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.7240+475_7240+477d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | A | ATTTT | 26 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.7240+474_7240+477d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | A | ATTTTT | 8 | a0006c0007t0002g0108 a0006c0007t0002g0110 a0006c0007t0002g0111 others(5): Show |
8 | HG02258.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.7240+473_7240+477d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | ATTTTTTT others(4): Show |
A | 3 | a0002c0002t0001g0164 a0002c0002t0003g0207 a0010c0011t0001g0192 |
3 | HG01981.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.7240+467_7240+477d others(13): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557375 | ATTTTTTT others(5): Show |
A | 98 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(95): Show |
99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.7240+466_7240+477d others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | ||||||
| chr5:71557415 | C | T | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7240+490C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557415 | |||||||
| chr5:71557424 | A | G | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.7240+499A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557424 | |||||||
| chr5:71557425 | C | T | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.7240+500C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557425 | |||||||
| chr5:71557429 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7240+504G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557429 | |||||||
| chr5:71557494 | C | T | 1 | a0002c0002t0003g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7240+569C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557494 | |||||||
| chr5:71557619 | C | T | 2 | a0016c0017t0009g0116 a0016c0017t0009g0117 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7240+694C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557619 | |||||||
| chr5:71557647 | G | A | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7240+722G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557647 | |||||||
| chr5:71557654 | GTAGAGAC others(60): Show |
G | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+730_7240+796d others(69): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557654 | |||||||
| chr5:71557945 | A | G | 9 | a0002c0002t0003g0136 a0002c0002t0003g0163 a0002c0002t0003g0174 others(6): Show |
9 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7240+1020A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557945 | |||||||
| chr5:71558016 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+1091T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558016 | |||||||
| chr5:71558051 | G | A | 12 | a0004c0004t0004g0310 a0004c0004t0004g0311 a0004c0004t0004g0312 others(9): Show |
12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.7240+1126G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558051 | |||||||
| chr5:71558169 | G | A | 101 | a0002c0002t0001g0133 a0002c0002t0001g0137 a0002c0002t0001g0138 others(98): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.7240+1244G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558169 | |||||||
| chr5:71558272 | TG | T | 244 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(241): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.7240+1349delG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558272 | ||||||
| chr5:71558342 | C | T | 10 | a0001c0001t0002g0054 a0007c0006t0002g0018 a0007c0006t0002g0047 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.7240+1417C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558342 | |||||||
| chr5:71558352 | T | G | 1 | a0002c0002t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.7240+1427T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558352 | |||||||
| chr5:71558421 | G | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7240+1496G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558421 | |||||||
| chr5:71558441 | G | A | 2 | a0011c0010t0006g0249 a0011c0010t0006g0305 |
2 | HG00741.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.7240+1516G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558441 | |||||||
| chr5:71558462 | C | T | 2 | a0004c0004t0010g0320 a0004c0004t0010g0321 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7241-1520C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558462 | |||||||
| chr5:71558541 | C | T | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7241-1441C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558541 | |||||||
| chr5:71558690 | G | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7241-1292G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558690 | |||||||
| chr5:71558715 | A | G | 1 | a0040c0045t0002g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7241-1267A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558715 | |||||||
| chr5:71558782 | C | T | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7241-1200C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558782 | |||||||
| chr5:71558820 | C | CT | 3 | a0005c0005t0001g0236 a0005c0005t0001g0237 a0005c0005t0001g0238 |
3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7241-1161dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558820 | ||||||
| chr5:71558832 | CA | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0019 others(117): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.7241-1138delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558832 | ||||||
| chr5:71558836 | A | C | 1 | a0005c0005t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7241-1146A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558836 | |||||||
| chr5:71558837 | A | C | 6 | a0016c0017t0009g0116 a0016c0017t0009g0117 a0020c0020t0023g0120 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.7241-1145A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558837 | |||||||
| chr5:71558842 | A | C | 1 | a0002c0002t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.7241-1140A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558842 | |||||||
| chr5:71558897 | T | C | 1 | a0041c0052t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7241-1085T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558897 | |||||||
| chr5:71559056 | A | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7241-926A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559056 | |||||||
| chr5:71559157 | A | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.7241-825A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559157 | |||||||
| chr5:71559279 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7241-703C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559279 | |||||||
| chr5:71559293 | C | G | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7241-689C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559293 | |||||||
| chr5:71559666 | T | C | 1 | a0033c0047t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7241-316T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559666 | |||||||
| chr5:71560317 | T | C | 2 | a0021c0035t0001g0124 a0026c0032t0001g0115 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7496+80T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560317 | |||||||
| chr5:71560343 | A | G | 1 | a0027c0019t0024g0119 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7496+106A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560343 | |||||||
| chr5:71560546 | T | C | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7496+309T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560546 | |||||||
| chr5:71560551 | A | C | 119 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(116): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.7496+314A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560551 | |||||||
| chr5:71560757 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7496+520C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560757 | |||||||
| chr5:71560836 | T | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(140): Show |
145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.7496+599T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560836 | |||||||
| chr5:71560881 | A | G | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7496+644A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560881 | |||||||
| chr5:71561103 | G | C | 2 | a0005c0005t0001g0234 a0005c0005t0015g0309 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7496+866G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561103 | |||||||
| chr5:71561349 | C | T | 2 | a0001c0001t0002g0083 a0027c0019t0024g0119 |
2 | HG02258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.7497-925C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561349 | |||||||
| chr5:71561389 | G | T | 1 | a0003c0003t0001g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.7497-885G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561389 | |||||||
| chr5:71561405 | ATAAAT | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0093 a0001c0001t0002g0094 others(2): Show |
6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.7497-864_7497-860d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71561405 | ||||||
| chr5:71561487 | T | C | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7497-787T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561487 | |||||||
| chr5:71561507 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(96): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.7497-767G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561507 | |||||||
| chr5:71561566 | G | A | 254 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(251): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.7497-708G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561566 | |||||||
| chr5:71561651 | C | T | 1 | a0020c0020t0023g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7497-623C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561651 | |||||||
| chr5:71562036 | A | G | 9 | a0006c0007t0002g0007 a0006c0007t0002g0108 a0006c0007t0002g0110 others(6): Show |
9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7497-238A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562036 | |||||||
| chr5:71562081 | A | G | 3 | a0005c0005t0001g0236 a0005c0005t0001g0237 a0005c0005t0001g0238 |
3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7497-193A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562081 | |||||||
| chr5:71562095 | G | C | 3 | a0014c0014t0001g0005 a0014c0014t0001g0006 a0027c0019t0024g0119 |
3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7497-179G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562095 | |||||||
| chr5:71562146 | C | T | 3 | a0002c0002t0001g0146 a0002c0002t0001g0157 a0002c0002t0001g0186 |
3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.7497-128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562146 | |||||||
| chr5:71562195 | C | CA | 26 | a0002c0002t0001g0198 a0002c0002t0001g0212 a0002c0002t0001g0228 others(23): Show |
26 | HG00673.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.7497-51dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | ||||||
| chr5:71562195 | CA | C | 39 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(36): Show |
39 | HG00597.hp1 HG01433.hp1 HG01943.hp1 others(36): Show |
intron_variant | MODIFIER | c.7497-51delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | ||||||
| chr5:71562195 | CAA | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(96): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.7497-52_7497-51del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | ||||||
| chr5:71562195 | CAAAAAAA others(3): Show |
C | 10 | a0002c0002t0003g0136 a0002c0002t0003g0163 a0002c0002t0003g0174 others(7): Show |
10 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.7497-60_7497-51del others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | ||||||
| chr5:71562262 | T | C | 1 | a0003c0003t0001g0294 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.7497-12T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562262 | |||||||
| chr5:71562555 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7743+35G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562555 | |||||||
| chr5:71562659 | G | A | 1 | a0009c0008t0007g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7743+139G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562659 | |||||||
| chr5:71562773 | A | G | 1 | a0007c0006t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7743+253A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562773 | |||||||
| chr5:71562941 | T | G | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7743+421T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562941 | |||||||
| chr5:71563078 | T | G | 1 | a0002c0002t0001g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7743+558T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563078 | |||||||
| chr5:71563140 | G | GT | 5 | a0001c0001t0002g0107 a0002c0002t0001g0164 a0002c0002t0001g0214 others(2): Show |
5 | HG02074.hp2 NA18947.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.7743+628dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71563140 | ||||||
| chr5:71563156 | T | C | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7743+636T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563156 | |||||||
| chr5:71563260 | G | T | 1 | a0002c0002t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.7743+740G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563260 | |||||||
| chr5:71563267 | C | T | 1 | a0032c0027t0002g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7743+747C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563267 | |||||||
| chr5:71563344 | C | T | 1 | a0001c0026t0002g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7743+824C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563344 | |||||||
| chr5:71563363 | T | G | 135 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.7743+843T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563363 | |||||||
| chr5:71563723 | G | A | 2 | a0004c0004t0010g0320 a0004c0004t0010g0321 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7744-1031G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563723 | |||||||
| chr5:71563836 | C | T | 2 | a0014c0014t0001g0005 a0014c0014t0001g0006 |
2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7744-918C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563836 | |||||||
| chr5:71563870 | C | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0097 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.7744-884C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563870 | |||||||
| chr5:71564155 | A | G | 2 | a0003c0003t0001g0259 a0030c0051t0001g0263 |
2 | HG01069.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7744-599A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564155 | |||||||
| chr5:71564211 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0128 |
2 | NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.7744-543C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564211 | |||||||
| chr5:71564215 | C | T | 1 | a0003c0003t0013g0251 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.7744-539C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564215 | |||||||
| chr5:71564236 | C | T | 1 | a0022c0031t0016g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7744-518C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564236 | |||||||
| chr5:71564252 | A | T | 2 | a0017c0015t0001g0222 a0017c0015t0001g0225 |
2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.7744-502A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564252 | |||||||
| chr5:71564329 | A | ATTC | 287 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(284): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.7744-423_7744-422i others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71564329 | ||||||
| chr5:71564357 | T | TTTAA | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7744-394_7744-393i others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71564357 | ||||||
| chr5:71564438 | T | A | 1 | a0021c0035t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7744-316T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564438 | |||||||
| chr5:71564656 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.7744-98C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564656 | |||||||
| chr5:71564666 | T | C | 133 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0015 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7744-88T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564666 |