Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8828 |
| ensemblid | ENSG00000118257.17 |
| hgncid | 8005 |
| symbol | NRP2 |
| name | neuropilin 2 |
| refseq_nuc | NM_003872.3 |
| refseq_prot | NP_003863.2 |
| ensembl_nuc | ENST00000357785.10 |
| ensembl_prot | ENSP00000350432.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 205682501 |
| end | 205798131 |
| strand | + |
| ver | v1.2 |
| region | chr2:205682501-205798131 |
| region5000 | chr2:205677501-205803131 |
| regionname0 | NRP2_chr2_205682501_205798131 |
| regionname5000 | NRP2_chr2_205677501_205803131 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 926 | 335 | 81 | 72 | 129 | 16 | 35 | 94 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0002 | 0/0 | 926 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0003 | 0/0 | 926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0004 | 0/0 | 926 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0005 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0006 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0007 | 0/0 | 926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| a0008 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | MDMFP others(921): Show |
chr2 | 205677501 | 205803131 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2778 | 100 | 2 | 28 | 48 | 8 | 14 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0002 | 0/1 | 2778 | 76 | 38 | 18 | 10 | 2 | 7 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0003 | 0/0 | 2778 | 59 | 10 | 7 | 35 | 1 | 6 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0004 | 0/0 | 2778 | 55 | 2 | 12 | 36 | 1 | 4 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0005 | 0/0 | 2778 | 9 | 3 | 3 | 0 | 2 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0006 | 0/0 | 2778 | 8 | 8 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0007 | 1/0 | 2778 | 5 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0008 | 0/0 | 2778 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0009 | 0/0 | 2778 | 4 | 1 | 3 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0010 | 0/0 | 2778 | 4 | 0 | 0 | 0 | 2 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0011 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0012 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0013 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0018 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0020 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0023 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0001c0030 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0014 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0015 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0016 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0017 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0027 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0002c0029 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0003c0025 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0003c0026 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0004c0022 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0005c0019 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0006c0028 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0007c0024 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 | ||
| a0008c0021 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | ATGGA others(2773): Show |
chr2 | 205677501 | 205803131 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6647 | 17 | 1 | 5 | 7 | 1 | 3 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0002 | 0/0 | 6647 | 10 | 0 | 2 | 5 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0003 | 0/0 | 6641 | 7 | 0 | 2 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0004 | 0/0 | 6641 | 7 | 0 | 2 | 2 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0005 | 0/0 | 6653 | 11 | 0 | 0 | 11 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0006 | 0/0 | 6641 | 7 | 0 | 2 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0007 | 0/0 | 6647 | 2 | 0 | 0 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0008 | 0/0 | 6647 | 3 | 0 | 1 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0009 | 0/0 | 6650 | 4 | 0 | 1 | 1 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0010 | 0/0 | 6653 | 9 | 0 | 2 | 7 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0011 | 0/0 | 6641 | 2 | 1 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0012 | 0/0 | 6650 | 6 | 0 | 3 | 0 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0013 | 0/0 | 6644 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0015 | 0/0 | 6650 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0018 | 0/0 | 6644 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0019 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0020 | 0/0 | 6647 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0026 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0027 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6651): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0031 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0037 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0053 | 0/0 | 6647 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0057 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0001t0058 | 0/0 | 6634 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6629): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0001 | 0/0 | 6647 | 6 | 1 | 1 | 3 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0002 | 0/0 | 6647 | 5 | 3 | 1 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0003 | 0/0 | 6641 | 4 | 0 | 1 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0004 | 0/0 | 6641 | 6 | 5 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0005 | 0/0 | 6653 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0006 | 0/0 | 6641 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0007 | 0/0 | 6647 | 9 | 4 | 5 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0008 | 0/0 | 6647 | 7 | 4 | 2 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0009 | 0/0 | 6650 | 2 | 1 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0010 | 0/0 | 6653 | 3 | 0 | 1 | 0 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0011 | 0/0 | 6641 | 2 | 1 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0012 | 0/0 | 6650 | 2 | 1 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0013 | 0/0 | 6644 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0014 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0015 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0016 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0018 | 0/0 | 6644 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0020 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0025 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6651): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0028 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0029 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0032 | 0/1 | 6641 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0033 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0042 | 0/0 | 6653 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0043 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0046 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6651): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0048 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0049 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0051 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0054 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0056 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0061 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0002t0063 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0001 | 0/0 | 6647 | 10 | 0 | 0 | 10 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0002 | 0/0 | 6647 | 5 | 0 | 1 | 1 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0003 | 0/0 | 6641 | 8 | 0 | 0 | 8 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0005 | 0/0 | 6653 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0006 | 0/0 | 6641 | 5 | 0 | 0 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0007 | 0/0 | 6647 | 3 | 1 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0008 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0009 | 0/0 | 6650 | 2 | 1 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0011 | 0/0 | 6641 | 4 | 3 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0012 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0014 | 0/0 | 6650 | 3 | 0 | 0 | 2 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0015 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0021 | 0/0 | 6653 | 2 | 0 | 0 | 2 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0024 | 0/0 | 6653 | 2 | 0 | 0 | 1 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0025 | 0/0 | 6656 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6651): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0034 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0035 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0040 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0045 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0047 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0003t0055 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0001 | 0/0 | 6647 | 8 | 0 | 5 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0002 | 0/0 | 6647 | 13 | 0 | 1 | 10 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0003 | 0/0 | 6641 | 9 | 0 | 2 | 7 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0005 | 0/0 | 6653 | 5 | 0 | 0 | 4 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0006 | 0/0 | 6641 | 5 | 0 | 1 | 4 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0008 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0010 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0012 | 0/0 | 6650 | 2 | 0 | 1 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0013 | 0/0 | 6644 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0014 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0019 | 0/0 | 6647 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0026 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0041 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0044 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0050 | 0/0 | 6644 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0059 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0004t0060 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0007 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0013 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0014 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0023 | 0/0 | 6647 | 3 | 0 | 1 | 0 | 2 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0005t0029 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0006t0007 | 0/0 | 6647 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0006t0009 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0006t0011 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0006t0036 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0006t0039 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0007t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0007t0011 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0007t0013 | 1/0 | 6644 | 2 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0007t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0008t0004 | 0/0 | 6641 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0009t0005 | 0/0 | 6653 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0009t0021 | 0/0 | 6653 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6648): Show |
chr2 | 205677501 | 205803131 |
| a0001c0009t0027 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6651): Show |
chr2 | 205677501 | 205803131 |
| a0001c0010t0009 | 0/0 | 6650 | 4 | 0 | 0 | 0 | 2 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0011t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0011t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0012t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0001c0012t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0013t0016 | 0/0 | 6644 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0018t0007 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0018t0038 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0001c0020t0012 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6645): Show |
chr2 | 205677501 | 205803131 |
| a0001c0023t0007 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0001c0030t0052 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0014t0001 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0014t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0015t0030 | 0/0 | 6647 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0016t0001 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0016t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0002c0017t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0002c0017t0062 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0027t0064 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0002c0029t0013 | 0/0 | 6644 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0003c0025t0013 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0003c0026t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0004c0022t0006 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| a0005c0019t0002 | 0/0 | 6647 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0006c0028t0016 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6639): Show |
chr2 | 205677501 | 205803131 |
| a0007c0024t0002 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6642): Show |
chr2 | 205677501 | 205803131 |
| a0008c0021t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | AGAGA others(6636): Show |
chr2 | 205677501 | 205803131 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0011g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0018g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0019g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0020g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0020g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0026g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0027g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0031g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0037g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0053g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0057g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0058g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0014g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0015g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0017g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0018g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0018g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0020g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0022g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0025g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0028g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0032g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0033g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0042g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0043g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0046g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0048g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0049g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0051g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0054g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0056g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0061g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0063g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0009g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0015g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0021g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0021g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0022g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0024g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0024g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0025g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0034g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0035g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0040g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0045g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0047g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0055g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0012g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0014g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0019g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0019g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0026g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0041g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0044g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0050g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0059g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0060g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0014g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0029g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0036g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0039g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0013g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0017g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0005g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0021g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0027g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0011t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0011t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0012t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0012t0017g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0013t0016g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0013t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0018t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0018t0038g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0020t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0023t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0030t0052g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0014t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0014t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0015t0030g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0016t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0016t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0017t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0017t0062g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0027t0064g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0029t0013g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0003c0025t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0003c0026t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0004c0022t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0005c0019t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0006c0028t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0007c0024t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0008c0021t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0029 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0327 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0213 | EUR | FIN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00280 | hp2 | a0001 | c0004 | t0013 | g0050 | EUR | FIN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00408 | hp1 | a0001 | c0004 | t0010 | g0236 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00408 | hp2 | a0001 | c0004 | t0006 | g0163 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0313 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00558 | hp1 | a0001 | c0004 | t0003 | g0315 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0169 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00639 | hp1 | a0001 | c0001 | t0031 | g0328 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00639 | hp2 | a0001 | c0004 | t0012 | g0042 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0238 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00673 | hp1 | a0001 | c0004 | t0012 | g0145 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00735 | hp1 | a0001 | c0009 | t0005 | g0001 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00735 | hp2 | a0001 | c0002 | t0008 | g0160 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0114 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00741 | hp2 | a0001 | c0002 | t0018 | g0010 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01069 | hp2 | a0001 | c0001 | t0020 | g0031 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01070 | hp1 | a0001 | c0002 | t0008 | g0012 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01070 | hp2 | a0001 | c0001 | t0012 | g0027 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0026 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0276 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0049 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01081 | hp1 | a0001 | c0003 | t0040 | g0255 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01081 | hp2 | a0001 | c0002 | t0018 | g0009 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01099 | hp1 | a0001 | c0002 | t0033 | g0293 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01099 | hp2 | a0001 | c0001 | t0037 | g0323 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01106 | hp2 | a0001 | c0009 | t0005 | g0001 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01109 | hp1 | a0002 | c0029 | t0013 | g0275 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01167 | hp1 | a0001 | c0003 | t0007 | g0332 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01169 | hp1 | a0001 | c0005 | t0023 | g0118 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01192 | hp1 | a0001 | c0003 | t0015 | g0259 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0335 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01243 | hp1 | a0001 | c0003 | t0008 | g0171 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01243 | hp2 | a0001 | c0001 | t0057 | g0032 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0008 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01255 | hp2 | a0001 | c0002 | t0009 | g0226 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01256 | hp1 | a0001 | c0002 | t0025 | g0252 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01256 | hp2 | a0001 | c0001 | t0018 | g0018 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01257 | hp1 | a0001 | c0002 | t0012 | g0108 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01261 | hp1 | a0001 | c0001 | t0020 | g0072 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01261 | hp2 | a0001 | c0009 | t0027 | g0030 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01361 | hp1 | a0001 | c0002 | t0007 | g0285 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0334 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01433 | hp1 | a0001 | c0005 | t0029 | g0117 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01433 | hp2 | a0001 | c0001 | t0058 | g0068 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0239 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01515 | hp2 | a0001 | c0005 | t0023 | g0120 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0019 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01516 | hp2 | a0001 | c0010 | t0009 | g0233 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01517 | hp1 | a0001 | c0010 | t0009 | g0231 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01517 | hp2 | a0001 | c0005 | t0023 | g0119 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0126 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01884 | hp2 | a0001 | c0002 | t0046 | g0141 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0253 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0167 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01928 | hp1 | a0001 | c0004 | t0019 | g0088 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01928 | hp2 | a0001 | c0023 | t0007 | g0287 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01934 | hp1 | a0001 | c0004 | t0003 | g0224 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01975 | hp1 | a0001 | c0002 | t0007 | g0290 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0227 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0267 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0286 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01981 | hp1 | a0001 | c0004 | t0006 | g0179 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01981 | hp2 | a0001 | c0002 | t0007 | g0289 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01993 | hp1 | a0004 | c0022 | t0006 | g0115 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0086 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02004 | hp1 | a0001 | c0004 | t0019 | g0087 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0244 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02015 | hp2 | a0001 | c0002 | t0011 | g0256 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0109 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0330 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02055 | hp1 | a0001 | c0006 | t0011 | g0337 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02055 | hp2 | a0001 | c0020 | t0012 | g0015 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0209 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02071 | hp1 | a0001 | c0003 | t0006 | g0154 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02071 | hp2 | a0001 | c0001 | t0010 | g0075 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02080 | hp1 | a0001 | c0003 | t0005 | g0082 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0217 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02083 | hp1 | a0001 | c0004 | t0006 | g0148 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0297 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02129 | hp1 | a0005 | c0019 | t0002 | g0321 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02132 | hp1 | a0001 | c0004 | t0050 | g0071 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0191 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02145 | hp2 | a0001 | c0002 | t0042 | g0212 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02148 | hp1 | a0001 | c0001 | t0019 | g0089 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02148 | hp2 | a0001 | c0002 | t0007 | g0288 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | CDX | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | CDX | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02257 | hp1 | a0002 | c0017 | t0004 | g0340 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0192 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02258 | hp1 | a0002 | c0016 | t0001 | g0273 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02258 | hp2 | a0001 | c0007 | t0017 | g0269 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02273 | hp2 | a0001 | c0002 | t0007 | g0325 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02280 | hp1 | a0002 | c0014 | t0008 | g0194 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02280 | hp2 | a0001 | c0002 | t0061 | g0189 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02293 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02293 | hp2 | a0001 | c0003 | t0011 | g0322 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0296 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02572 | hp1 | a0003 | c0025 | t0013 | g0166 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0291 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0279 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02615 | hp1 | a0001 | c0002 | t0020 | g0185 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02622 | hp1 | a0006 | c0028 | t0016 | g0142 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02622 | hp2 | a0001 | c0011 | t0004 | g0170 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02630 | hp1 | a0001 | c0008 | t0004 | g0005 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02647 | hp1 | a0001 | c0004 | t0022 | g0183 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02647 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02683 | hp1 | a0001 | c0003 | t0025 | g0301 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02683 | hp2 | a0001 | c0001 | t0012 | g0102 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02698 | hp1 | a0001 | c0003 | t0014 | g0016 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0311 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02717 | hp1 | a0001 | c0013 | t0016 | g0131 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02717 | hp2 | a0001 | c0003 | t0009 | g0292 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02723 | hp1 | a0001 | c0008 | t0004 | g0128 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02723 | hp2 | a0001 | c0007 | t0008 | g0062 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0320 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0331 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02738 | hp2 | a0001 | c0010 | t0009 | g0232 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0130 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02809 | hp2 | a0001 | c0002 | t0048 | g0124 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02818 | hp1 | a0001 | c0006 | t0009 | g0303 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02818 | hp2 | a0001 | c0008 | t0004 | g0005 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0199 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02895 | hp1 | a0001 | c0003 | t0011 | g0247 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02895 | hp2 | a0001 | c0006 | t0011 | g0338 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02896 | hp1 | a0001 | c0008 | t0004 | g0196 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02896 | hp2 | a0001 | c0002 | t0013 | g0198 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02897 | hp1 | a0001 | c0003 | t0011 | g0248 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02897 | hp2 | a0001 | c0002 | t0013 | g0197 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02922 | hp1 | a0001 | c0002 | t0063 | g0136 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02922 | hp2 | a0002 | c0015 | t0030 | g0004 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02965 | hp1 | a0001 | c0018 | t0007 | g0336 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02965 | hp2 | a0002 | c0027 | t0064 | g0176 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02970 | hp1 | a0002 | c0015 | t0030 | g0004 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02970 | hp2 | a0001 | c0007 | t0013 | g0188 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02976 | hp1 | a0001 | c0005 | t0013 | g0175 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02976 | hp2 | a0001 | c0003 | t0007 | g0249 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03041 | hp1 | a0001 | c0002 | t0054 | g0214 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03041 | hp2 | a0001 | c0002 | t0016 | g0133 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03098 | hp1 | a0001 | c0018 | t0038 | g0308 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03098 | hp2 | a0001 | c0002 | t0028 | g0186 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03130 | hp1 | a0001 | c0002 | t0028 | g0187 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03130 | hp2 | a0001 | c0003 | t0047 | g0125 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03139 | hp1 | a0001 | c0007 | t0011 | g0270 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0283 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03195 | hp2 | a0001 | c0012 | t0004 | g0137 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0274 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03209 | hp2 | a0001 | c0012 | t0017 | g0272 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03225 | hp1 | a0001 | c0003 | t0011 | g0250 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03225 | hp2 | a0003 | c0026 | t0004 | g0165 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03453 | hp1 | a0001 | c0011 | t0008 | g0134 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03453 | hp2 | a0001 | c0006 | t0007 | g0329 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03490 | hp1 | a0001 | c0004 | t0008 | g0043 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03490 | hp2 | a0001 | c0002 | t0010 | g0277 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03491 | hp2 | a0001 | c0003 | t0009 | g0342 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03492 | hp2 | a0001 | c0002 | t0010 | g0278 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03516 | hp1 | a0001 | c0006 | t0036 | g0307 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03516 | hp2 | a0001 | c0002 | t0008 | g0200 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03540 | hp1 | a0002 | c0014 | t0001 | g0195 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03540 | hp2 | a0001 | c0002 | t0022 | g0184 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03579 | hp1 | a0001 | c0003 | t0035 | g0204 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03579 | hp2 | a0001 | c0013 | t0016 | g0132 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03654 | hp1 | a0001 | c0002 | t0015 | g0300 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0310 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0280 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0242 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03704 | hp1 | a0001 | c0003 | t0024 | g0324 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03704 | hp2 | a0001 | c0001 | t0013 | g0041 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03710 | hp2 | a0007 | c0024 | t0002 | g0260 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03927 | hp1 | a0001 | c0002 | t0008 | g0123 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03942 | hp1 | a0001 | c0030 | t0052 | g0070 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03942 | hp2 | a0001 | c0005 | t0014 | g0127 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0074 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0078 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04199 | hp1 | a0001 | c0004 | t0005 | g0105 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0326 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04228 | hp2 | a0001 | c0002 | t0014 | g0159 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18747 | hp1 | a0001 | c0002 | t0006 | g0051 | EAS | CHB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0107 | EAS | CHB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18906 | hp1 | a0001 | c0006 | t0039 | g0305 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18906 | hp2 | a0001 | c0003 | t0022 | g0173 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0346 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0234 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18954 | hp2 | a0001 | c0002 | t0006 | g0146 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18957 | hp1 | a0001 | c0004 | t0003 | g0205 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18957 | hp2 | a0001 | c0003 | t0005 | g0093 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18961 | hp1 | a0001 | c0004 | t0005 | g0164 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18964 | hp2 | a0001 | c0004 | t0006 | g0112 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18965 | hp1 | a0001 | c0004 | t0003 | g0218 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18965 | hp2 | a0001 | c0004 | t0002 | g0245 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18972 | hp2 | a0001 | c0004 | t0041 | g0343 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18973 | hp1 | a0001 | c0003 | t0045 | g0100 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0317 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18978 | hp2 | a0001 | c0004 | t0005 | g0054 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0345 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0201 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18984 | hp1 | a0001 | c0004 | t0005 | g0055 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18984 | hp2 | a0001 | c0003 | t0055 | g0091 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18992 | hp2 | a0001 | c0003 | t0034 | g0333 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18993 | hp1 | a0001 | c0003 | t0014 | g0099 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0298 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18995 | hp2 | a0001 | c0003 | t0006 | g0085 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19001 | hp1 | a0001 | c0003 | t0006 | g0153 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19001 | hp2 | a0001 | c0004 | t0002 | g0211 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19002 | hp2 | a0001 | c0003 | t0006 | g0097 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19004 | hp1 | a0001 | c0004 | t0002 | g0302 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0207 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19005 | hp2 | a0001 | c0003 | t0006 | g0101 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19009 | hp1 | a0001 | c0004 | t0002 | g0220 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19009 | hp2 | a0001 | c0002 | t0006 | g0090 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19010 | hp1 | a0001 | c0001 | t0053 | g0158 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19030 | hp1 | a0001 | c0004 | t0026 | g0052 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0139 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19043 | hp1 | a0001 | c0002 | t0051 | g0182 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19043 | hp2 | a0008 | c0021 | t0004 | g0138 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19056 | hp2 | a0001 | c0004 | t0014 | g0028 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19057 | hp1 | a0001 | c0003 | t0024 | g0344 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19057 | hp2 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19058 | hp1 | a0001 | c0004 | t0005 | g0069 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19060 | hp2 | a0001 | c0004 | t0003 | g0314 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0265 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19063 | hp2 | a0001 | c0004 | t0002 | g0219 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19068 | hp1 | a0001 | c0001 | t0009 | g0319 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19070 | hp2 | a0001 | c0004 | t0044 | g0251 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19080 | hp2 | a0001 | c0004 | t0002 | g0266 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19081 | hp1 | a0001 | c0004 | t0006 | g0122 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19081 | hp2 | a0001 | c0003 | t0014 | g0094 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19082 | hp1 | a0001 | c0001 | t0010 | g0229 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19082 | hp2 | a0001 | c0004 | t0060 | g0023 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19084 | hp2 | a0001 | c0004 | t0059 | g0022 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19085 | hp2 | a0001 | c0003 | t0021 | g0058 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19088 | hp1 | a0001 | c0003 | t0021 | g0057 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19088 | hp2 | a0001 | c0001 | t0027 | g0110 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0096 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19090 | hp2 | a0001 | c0001 | t0015 | g0237 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19240 | hp1 | a0001 | c0002 | t0017 | g0254 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19240 | hp2 | a0001 | c0006 | t0011 | g0304 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20129 | hp1 | a0001 | c0006 | t0007 | g0306 | AFR | ASW | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20129 | hp2 | a0001 | c0002 | t0029 | g0135 | AFR | ASW | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0040 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0046 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20805 | hp1 | a0001 | c0001 | t0026 | g0013 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20805 | hp2 | a0001 | c0002 | t0056 | g0147 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20905 | hp1 | a0001 | c0010 | t0009 | g0230 | SAS | GIH | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01123 | hp1 | a0001 | c0005 | t0007 | g0222 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0309 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0284 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02109 | hp2 | a0001 | c0002 | t0011 | g0271 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0140 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02486 | hp2 | a0001 | c0002 | t0043 | g0258 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02559 | hp1 | a0001 | c0005 | t0004 | g0048 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0221 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03471 | hp1 | a0002 | c0016 | t0004 | g0339 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0263 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG06807 | hp1 | a0001 | c0002 | t0049 | g0172 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG06807 | hp2 | a0001 | c0005 | t0008 | g0047 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18955 | hp1 | a0001 | c0001 | t0015 | g0208 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18955 | hp2 | a0001 | c0004 | t0002 | g0312 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20300 | hp1 | a0001 | c0009 | t0021 | g0044 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0181 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA21309 | hp1 | a0002 | c0017 | t0062 | g0177 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA21309 | hp2 | a0001 | c0003 | t0012 | g0174 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0032 | g0178 | REF | REF | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0013 | g0341 | REF | REF | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205716309 | A | G | 2 | a0002 a0006 |
11 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
missense_variant | MODERATE | c.368A>G | p.Lys123Arg | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/17 | 1158/6644 | 368/2781 | 123/926 | chr2 | 205716309 | |||
| chr2:205722603 | A | G | 1 | a0003 | 2 | HG02572.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.559A>G | p.Ile187Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/17 | 1349/6644 | 559/2781 | 187/926 | chr2 | 205722603 | |||
| chr2:205723790 | C | A | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.670C>A | p.Pro224Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/17 | 1460/6644 | 670/2781 | 224/926 | chr2 | 205723790 | |||
| chr2:205740654 | C | T | 1 | a0007 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1282C>T | p.Arg428Trp | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/17 | 2072/6644 | 1282/2781 | 428/926 | chr2 | 205740654 | |||
| chr2:205749746 | C | T | 1 | a0006 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1808C>T | p.Thr603Met | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/17 | 2598/6644 | 1808/2781 | 603/926 | chr2 | 205749746 | |||
| chr2:205749769 | G | A | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1831G>A | p.Glu611Lys | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/17 | 2621/6644 | 1831/2781 | 611/926 | chr2 | 205749769 | |||
| chr2:205763908 | T | C | 1 | a0004 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2279T>C | p.Ile760Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/17 | 3069/6644 | 2279/2781 | 760/926 | chr2 | 205763908 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205697593 | C | T | 2 | a0001c0006 a0001c0018 |
10 | HG02055.hp1 HG02818.hp1 HG02895.hp2 others(7): Show |
synonymous_variant | LOW | c.123C>T | p.Thr41Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/17 | 913/6644 | 123/2781 | 41/926 | chr2 | 205697593 | |||
| chr2:205697635 | C | T | 1 | a0001c0030 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.165C>T | p.Cys55Cys | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/17 | 955/6644 | 165/2781 | 55/926 | chr2 | 205697635 | |||
| chr2:205716325 | C | T | 1 | a0001c0010 | 4 | HG01516.hp2 HG01517.hp1 HG02738.hp2 others(1): Show |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/17 | 1174/6644 | 384/2781 | 128/926 | chr2 | 205716325 | |||
| chr2:205723846 | G | A | 3 | a0001c0008 a0001c0011 a0001c0012 |
8 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.726G>A | p.Thr242Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/17 | 1516/6644 | 726/2781 | 242/926 | chr2 | 205723846 | |||
| chr2:205725962 | T | C | 3 | a0001c0005 a0001c0020 a0008c0021 |
11 | HG01123.hp1 HG01169.hp1 HG01433.hp1 others(8): Show |
synonymous_variant | LOW | c.870T>C | p.Asn290Asn | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/17 | 1660/6644 | 870/2781 | 290/926 | chr2 | 205725962 | |||
| chr2:205727971 | T | C | 8 | a0001c0001 a0001c0004 a0001c0009 others(5): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
synonymous_variant | LOW | c.1071T>C | p.Tyr357Tyr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/17 | 1861/6644 | 1071/2781 | 357/926 | chr2 | 205727971 | |||
| chr2:205740521 | A | G | 1 | a0001c0008 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1149A>G | p.Val383Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/17 | 1939/6644 | 1149/2781 | 383/926 | chr2 | 205740521 | |||
| chr2:205743315 | T | C | 25 | a0001c0001 a0001c0002 a0001c0003 others(22): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
synonymous_variant | LOW | c.1404T>C | p.Val468Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2194/6644 | 1404/2781 | 468/926 | chr2 | 205743315 | |||
| chr2:205743327 | G | A | 1 | a0001c0023 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1416G>A | p.Ser472Ser | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2206/6644 | 1416/2781 | 472/926 | chr2 | 205743327 | |||
| chr2:205743360 | C | T | 1 | a0001c0013 | 2 | HG02717.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1449C>T | p.Pro483Pro | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2239/6644 | 1449/2781 | 483/926 | chr2 | 205743360 | |||
| chr2:205743366 | G | A | 1 | a0002c0029 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1455G>A | p.Glu485Glu | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2245/6644 | 1455/2781 | 485/926 | chr2 | 205743366 | |||
| chr2:205745778 | T | G | 9 | a0001c0003 a0001c0004 a0001c0011 others(6): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
synonymous_variant | LOW | c.1674T>G | p.Pro558Pro | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/17 | 2464/6644 | 1674/2781 | 558/926 | chr2 | 205745778 | |||
| chr2:205794956 | C | T | 1 | a0002c0015 | 2 | HG02922.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.2679C>T | p.Ser893Ser | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 3469/6644 | 2679/2781 | 893/926 | chr2 | 205794956 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205682514 | G | A | 1 | a0001c0001t0031 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-777G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 777 | chr2 | 205682514 | ||||||
| chr2:205682787 | A | G | 7 | a0001c0002t0029 a0001c0002t0063 a0001c0005t0023 others(4): Show |
10 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-504A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 504 | chr2 | 205682787 | ||||||
| chr2:205682821 | T | C | 59 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(56): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
5_prime_UTR_variant | MODIFIER | c.-470T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 470 | chr2 | 205682821 | ||||||
| chr2:205682875 | A | G | 1 | a0001c0002t0028 | 2 | HG03098.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-416A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 416 | chr2 | 205682875 | ||||||
| chr2:205683023 | T | C | 1 | a0001c0002t0033 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-268T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 268 | chr2 | 205683023 | ||||||
| chr2:205683178 | A | G | 1 | a0001c0004t0044 | 1 | NA19070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 113 | chr2 | 205683178 | ||||||
| chr2:205795119 | C | A | 1 | a0001c0003t0045 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 61 | chr2 | 205795119 | ||||||
| chr2:205795203 | C | A | 1 | a0001c0003t0034 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 145 | chr2 | 205795203 | ||||||
| chr2:205795240 | G | T | 4 | a0001c0002t0022 a0001c0002t0043 a0001c0003t0022 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*182G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 182 | chr2 | 205795240 | ||||||
| chr2:205795261 | G | A | 2 | a0001c0002t0046 a0001c0003t0047 |
2 | HG01884.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 203 | chr2 | 205795261 | ||||||
| chr2:205795286 | G | A | 3 | a0001c0002t0016 a0001c0013t0016 a0006c0028t0016 |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 228 | chr2 | 205795286 | ||||||
| chr2:205795305 | G | A | 1 | a0002c0017t0062 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 247 | chr2 | 205795305 | ||||||
| chr2:205795313 | C | T | 1 | a0001c0002t0061 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 255 | chr2 | 205795313 | ||||||
| chr2:205795361 | G | GTAT | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(40): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*331_*333dupTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | |||||
| chr2:205795361 | G | GTATTAT | 24 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0015 others(21): Show |
43 | HG00639.hp2 HG00642.hp1 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*333dupTATTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | |||||
| chr2:205795361 | G | GTATTATT others(2): Show |
14 | a0001c0001t0005 a0001c0001t0010 a0001c0002t0005 others(11): Show |
43 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*325_*333dupTATTAT others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | |||||
| chr2:205795361 | G | GTATTATT others(5): Show |
4 | a0001c0001t0027 a0001c0002t0025 a0001c0003t0025 others(1): Show |
4 | HG01256.hp1 HG01261.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*322_*333dupTATTAT others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | |||||
| chr2:205795361 | GTAT | G | 40 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(37): Show |
102 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*331_*333delTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 331 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | |||||
| chr2:205795418 | C | A | 1 | a0001c0030t0052 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 360 | chr2 | 205795418 | ||||||
| chr2:205795545 | A | G | 1 | a0001c0002t0042 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 487 | chr2 | 205795545 | ||||||
| chr2:205796191 | T | C | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0053 others(13): Show |
56 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1133 | chr2 | 205796191 | ||||||
| chr2:205796244 | G | A | 2 | a0001c0002t0048 a0001c0003t0035 |
2 | HG02809.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1186G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1186 | chr2 | 205796244 | ||||||
| chr2:205796332 | G | A | 1 | a0001c0004t0059 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1274 | chr2 | 205796332 | ||||||
| chr2:205796335 | A | C | 1 | a0001c0001t0037 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1277 | chr2 | 205796335 | ||||||
| chr2:205796437 | TACACACA others(9): Show |
T | 1 | a0001c0001t0058 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380_*1395delACAC others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1380 | chr2 | 205796437 | ||||||
| chr2:205796556 | A | C | 1 | a0001c0002t0049 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1498 | chr2 | 205796556 | ||||||
| chr2:205796646 | G | A | 1 | a0001c0002t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1588 | chr2 | 205796646 | ||||||
| chr2:205796771 | G | A | 3 | a0001c0002t0051 a0001c0002t0063 a0001c0018t0038 |
3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1713G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1713 | chr2 | 205796771 | ||||||
| chr2:205796978 | A | G | 1 | a0001c0001t0057 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1920 | chr2 | 205796978 | ||||||
| chr2:205797561 | A | AAGCAGGG others(5): Show |
1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2506_*2517dupCAGG others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2518 | INFO_REALIGN_3_PRIME | chr2 | 205797561 | |||||
| chr2:205797573 | C | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(29): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2515C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2515 | chr2 | 205797573 | ||||||
| chr2:205797612 | G | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(28): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2554G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2554 | chr2 | 205797612 | ||||||
| chr2:205797619 | A | G | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(39): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2561A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2561 | chr2 | 205797619 | ||||||
| chr2:205797836 | G | T | 1 | a0001c0003t0055 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2778G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2778 | chr2 | 205797836 | ||||||
| chr2:205797890 | G | A | 1 | a0001c0004t0060 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2832G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2832 | chr2 | 205797890 | ||||||
| chr2:205798074 | A | G | 1 | a0001c0002t0056 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3016A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 3016 | chr2 | 205798074 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205683555 | A | AGT | 5 | a0001c0003t0003g0345 a0001c0003t0003g0346 a0001c0003t0009g0342 others(2): Show |
5 | HG03491.hp2 NA18951.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+222_73+223dupTG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | ||||||
| chr2:205683555 | AGT | A | 81 | a0001c0001t0002g0006 a0001c0001t0002g0210 a0001c0001t0002g0215 others(78): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.73+222_73+223delTG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | ||||||
| chr2:205683555 | AGTGT | A | 23 | a0001c0001t0004g0193 a0001c0002t0001g0190 a0001c0002t0004g0181 others(20): Show |
24 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.73+220_73+223delTG others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | ||||||
| chr2:205683555 | AGTGTGT | A | 16 | a0001c0002t0001g0168 a0001c0002t0049g0172 a0001c0003t0004g0167 others(13): Show |
17 | HG00408.hp2 HG00621.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.73+218_73+223delTG others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | ||||||
| chr2:205683555 | AGTGTGTG others(1): Show |
A | 159 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(156): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.73+216_73+223delTG others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | ||||||
| chr2:205683561 | T | C | 1 | a0001c0002t0015g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.73+198T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683561 | |||||||
| chr2:205683620 | T | C | 1 | a0001c0004t0002g0201 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.73+257T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683620 | |||||||
| chr2:205683652 | A | G | 1 | a0001c0002t0008g0200 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.73+289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683652 | |||||||
| chr2:205683719 | T | C | 124 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(121): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.73+356T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683719 | |||||||
| chr2:205683783 | A | C | 1 | a0001c0002t0008g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.73+420A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683783 | |||||||
| chr2:205683955 | G | A | 1 | a0001c0002t0048g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+592G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683955 | |||||||
| chr2:205684192 | C | T | 26 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0005g0144 others(23): Show |
27 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.73+829C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684192 | |||||||
| chr2:205684289 | G | A | 1 | a0001c0002t0008g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.73+926G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684289 | |||||||
| chr2:205684315 | A | G | 1 | a0001c0004t0006g0122 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.73+952A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684315 | |||||||
| chr2:205684330 | A | G | 1 | a0001c0001t0005g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.73+967A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684330 | |||||||
| chr2:205684583 | C | G | 6 | a0001c0002t0004g0139 a0001c0002t0008g0140 a0001c0002t0046g0141 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+1220C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684583 | |||||||
| chr2:205684615 | A | G | 4 | a0001c0005t0023g0118 a0001c0005t0023g0119 a0001c0005t0023g0120 others(1): Show |
4 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+1252A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684615 | |||||||
| chr2:205684755 | G | C | 316 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(313): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.73+1392G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684755 | |||||||
| chr2:205684859 | C | CTG | 7 | a0001c0002t0049g0172 a0001c0003t0008g0171 a0001c0003t0012g0174 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+1507_73+1508dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205684859 | ||||||
| chr2:205685073 | T | C | 1 | a0001c0003t0035g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73+1710T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685073 | |||||||
| chr2:205685138 | C | T | 5 | a0001c0002t0004g0139 a0001c0002t0008g0140 a0001c0002t0046g0141 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+1775C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685138 | |||||||
| chr2:205685158 | G | C | 2 | a0001c0004t0003g0205 a0001c0004t0003g0206 |
2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.73+1795G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685158 | |||||||
| chr2:205685389 | C | A | 2 | a0002c0016t0001g0273 a0002c0016t0004g0339 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.73+2026C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685389 | |||||||
| chr2:205685413 | C | T | 311 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(308): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.73+2050C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685413 | |||||||
| chr2:205685415 | CAT | C | 311 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(308): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.73+2054_73+2055del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205685415 | ||||||
| chr2:205685446 | C | A | 1 | a0001c0004t0002g0211 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.73+2083C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685446 | |||||||
| chr2:205685554 | C | A | 311 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(308): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.73+2191C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685554 | |||||||
| chr2:205685700 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.73+2337C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685700 | |||||||
| chr2:205685728 | G | C | 1 | a0001c0011t0004g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+2365G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685728 | |||||||
| chr2:205685902 | G | A | 1 | a0001c0003t0009g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.73+2539G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685902 | |||||||
| chr2:205685934 | C | T | 1 | a0001c0012t0017g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73+2571C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685934 | |||||||
| chr2:205685954 | G | T | 1 | a0001c0002t0048g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+2591G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685954 | |||||||
| chr2:205685974 | C | G | 1 | a0004c0022t0006g0115 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.73+2611C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685974 | |||||||
| chr2:205685982 | G | C | 1 | a0001c0011t0004g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+2619G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685982 | |||||||
| chr2:205686123 | T | A | 2 | a0001c0002t0003g0281 a0001c0002t0003g0282 |
2 | NA18953.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.73+2760T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686123 | |||||||
| chr2:205686218 | CCCT | C | 6 | a0001c0001t0004g0116 a0001c0001t0004g0193 a0001c0002t0001g0190 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+2874_73+2876del others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205686218 | ||||||
| chr2:205686241 | A | G | 1 | a0001c0006t0011g0338 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.73+2878A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686241 | |||||||
| chr2:205686395 | T | C | 1 | a0001c0001t0012g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.73+3032T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686395 | |||||||
| chr2:205686400 | A | G | 1 | a0001c0005t0013g0175 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73+3037A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686400 | |||||||
| chr2:205686504 | G | A | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.73+3141G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686504 | |||||||
| chr2:205686812 | C | T | 1 | a0001c0003t0012g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73+3449C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686812 | |||||||
| chr2:205686846 | C | G | 15 | a0001c0001t0004g0116 a0001c0001t0004g0193 a0001c0002t0001g0190 others(12): Show |
16 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.73+3483C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686846 | |||||||
| chr2:205687254 | C | T | 233 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(230): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.73+3891C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687254 | |||||||
| chr2:205687371 | C | T | 11 | a0001c0001t0002g0210 a0001c0001t0003g0202 a0001c0001t0004g0116 others(8): Show |
11 | HG01106.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.73+4008C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687371 | |||||||
| chr2:205687438 | ATT | A | 313 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+4079_73+4080del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205687438 | ||||||
| chr2:205687520 | G | A | 67 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0005g0144 others(64): Show |
68 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.73+4157G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687520 | |||||||
| chr2:205687816 | CA | C | 3 | a0001c0002t0011g0271 a0001c0007t0011g0270 a0001c0007t0017g0269 |
3 | HG02109.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.73+4454delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687816 | |||||||
| chr2:205687914 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0006g0113 a0001c0001t0006g0114 others(1): Show |
4 | HG00741.hp1 HG01952.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+4551C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687914 | |||||||
| chr2:205688002 | A | G | 313 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+4639A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688002 | |||||||
| chr2:205688116 | G | A | 1 | a0001c0001t0007g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.73+4753G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688116 | |||||||
| chr2:205688222 | T | C | 11 | a0001c0001t0002g0210 a0001c0001t0003g0202 a0001c0001t0004g0116 others(8): Show |
11 | HG01106.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.73+4859T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688222 | |||||||
| chr2:205688558 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73+5195C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688558 | |||||||
| chr2:205688620 | C | T | 2 | a0001c0002t0046g0141 a0001c0012t0004g0137 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73+5257C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688620 | |||||||
| chr2:205688691 | A | T | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73+5328A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688691 | |||||||
| chr2:205688803 | G | A | 1 | a0001c0011t0004g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+5440G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688803 | |||||||
| chr2:205688804 | G | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.73+5441G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688804 | |||||||
| chr2:205688826 | T | G | 1 | a0001c0004t0006g0122 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.73+5463T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688826 | |||||||
| chr2:205688861 | C | CA | 244 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.73+5506dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205688861 | ||||||
| chr2:205688861 | C | CAA | 7 | a0001c0003t0002g0297 a0001c0003t0003g0216 a0001c0003t0003g0217 others(4): Show |
7 | HG02080.hp2 HG02083.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5505_73+5506dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205688861 | ||||||
| chr2:205688870 | C | A | 1 | a0001c0001t0004g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73+5507C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688870 | |||||||
| chr2:205688884 | G | A | 3 | a0001c0001t0018g0018 a0001c0003t0014g0016 a0001c0020t0012g0015 |
3 | HG01256.hp2 HG02055.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.73+5521G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688884 | |||||||
| chr2:205688984 | A | G | 2 | a0001c0005t0023g0119 a0001c0005t0023g0120 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.73+5621A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688984 | |||||||
| chr2:205689035 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.73+5672T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689035 | |||||||
| chr2:205689116 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.73+5753A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689116 | |||||||
| chr2:205689280 | T | G | 1 | a0001c0011t0004g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+5917T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689280 | |||||||
| chr2:205689390 | G | A | 107 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(104): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.73+6027G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689390 | |||||||
| chr2:205689536 | A | G | 10 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(7): Show |
12 | HG02280.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.73+6173A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689536 | |||||||
| chr2:205689789 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0005g0024 others(3): Show |
6 | NA18953.hp2 NA19060.hp1 NA19070.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+6426G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689789 | |||||||
| chr2:205689798 | T | C | 7 | a0001c0002t0049g0172 a0001c0003t0008g0171 a0001c0003t0012g0174 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+6435T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689798 | |||||||
| chr2:205689820 | G | A | 266 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.73+6457G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689820 | |||||||
| chr2:205689981 | G | A | 6 | a0001c0001t0004g0116 a0001c0001t0004g0193 a0001c0002t0001g0190 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+6618G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689981 | |||||||
| chr2:205690025 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.73+6662G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690025 | |||||||
| chr2:205690033 | C | G | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73+6670C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690033 | |||||||
| chr2:205690033 | C | T | 1 | a0001c0002t0048g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+6670C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690033 | |||||||
| chr2:205690056 | G | A | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73+6693G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690056 | |||||||
| chr2:205690080 | A | T | 1 | a0001c0001t0003g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.73+6717A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690080 | |||||||
| chr2:205690112 | G | A | 7 | a0001c0002t0049g0172 a0001c0003t0008g0171 a0001c0003t0012g0174 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+6749G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690112 | |||||||
| chr2:205690447 | A | T | 338 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(335): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.73+7084A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690447 | |||||||
| chr2:205690457 | C | T | 65 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0026g0013 others(62): Show |
67 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.74-7087C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690457 | |||||||
| chr2:205690458 | G | A | 270 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(267): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.74-7086G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690458 | |||||||
| chr2:205690499 | G | A | 271 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(268): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.74-7045G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690499 | |||||||
| chr2:205690524 | T | A | 2 | a0001c0001t0002g0223 a0001c0001t0012g0102 |
2 | HG00621.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.74-7020T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690524 | |||||||
| chr2:205690579 | T | TAC | 13 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0053g0158 others(10): Show |
14 | HG00280.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.74-6915_74-6914dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | T | TACAC | 8 | a0001c0002t0002g0279 a0001c0002t0008g0160 a0001c0002t0014g0159 others(5): Show |
8 | HG00735.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.74-6917_74-6914dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TAC | T | 21 | a0001c0001t0002g0215 a0001c0001t0010g0209 a0001c0001t0010g0335 others(18): Show |
21 | HG01169.hp1 HG01192.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.74-6915_74-6914del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACAC | T | 39 | a0001c0001t0002g0257 a0001c0001t0003g0202 a0001c0001t0005g0095 others(36): Show |
40 | HG01081.hp1 HG01167.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.74-6917_74-6914del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACAC | T | 123 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(120): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.74-6919_74-6914del others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(1): Show |
T | 22 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0004g0116 others(19): Show |
22 | HG01106.hp1 HG01261.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.74-6921_74-6914del others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(3): Show |
T | 62 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0045 others(59): Show |
64 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.74-6923_74-6914del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(5): Show |
T | 3 | a0001c0002t0005g0029 a0001c0004t0006g0122 a0001c0004t0014g0028 |
3 | HG00140.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.74-6925_74-6914del others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0025 a0001c0001t0012g0026 a0001c0001t0012g0027 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-6927_74-6914del others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(9): Show |
T | 1 | a0001c0002t0015g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.74-6929_74-6914del others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(13): Show |
T | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-6933_74-6914del others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(15): Show |
T | 16 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(13): Show |
16 | HG01243.hp1 HG02109.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.74-6935_74-6914del others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(17): Show |
T | 4 | a0001c0002t0029g0135 a0001c0002t0046g0141 a0001c0002t0063g0136 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-6937_74-6914del others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690579 | TACACACA others(25): Show |
T | 1 | a0001c0012t0004g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74-6945_74-6914del others(32): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | ||||||
| chr2:205690651 | G | A | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.74-6893G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690651 | |||||||
| chr2:205690781 | A | AAAAAT | 3 | a0001c0010t0009g0230 a0002c0014t0001g0195 a0002c0014t0008g0194 |
3 | HG02280.hp1 HG03540.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.74-6742_74-6738dup others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690781 | ||||||
| chr2:205691080 | C | A | 179 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.74-6464C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691080 | |||||||
| chr2:205691160 | G | A | 1 | a0001c0012t0017g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.74-6384G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691160 | |||||||
| chr2:205691484 | T | G | 343 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(340): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.74-6060T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691484 | |||||||
| chr2:205691934 | T | C | 1 | a0001c0004t0002g0201 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.74-5610T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691934 | |||||||
| chr2:205691977 | C | T | 73 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(70): Show |
74 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.74-5567C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691977 | |||||||
| chr2:205692209 | T | C | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-5335T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692209 | |||||||
| chr2:205692428 | G | A | 3 | a0001c0010t0009g0231 a0001c0010t0009g0232 a0001c0010t0009g0233 |
3 | HG01516.hp2 HG01517.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.74-5116G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692428 | |||||||
| chr2:205692494 | G | T | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.74-5050G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692494 | |||||||
| chr2:205692606 | A | T | 1 | a0001c0001t0010g0209 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.74-4938A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692606 | |||||||
| chr2:205692781 | G | T | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-4763G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692781 | |||||||
| chr2:205692802 | C | T | 74 | a0001c0001t0001g0157 a0001c0001t0004g0116 a0001c0001t0004g0193 others(71): Show |
76 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.74-4742C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692802 | |||||||
| chr2:205692815 | G | A | 66 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(63): Show |
68 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.74-4729G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692815 | |||||||
| chr2:205693008 | C | A | 1 | a0001c0002t0020g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-4536C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693008 | |||||||
| chr2:205693052 | G | A | 1 | a0001c0004t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.74-4492G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693052 | |||||||
| chr2:205693217 | A | C | 3 | a0001c0002t0049g0172 a0001c0003t0022g0173 a0001c0011t0004g0170 |
3 | HG02622.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.74-4327A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693217 | |||||||
| chr2:205693333 | C | T | 10 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(7): Show |
10 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.74-4211C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693333 | |||||||
| chr2:205693528 | A | C | 2 | a0001c0005t0023g0118 a0001c0005t0029g0117 |
2 | HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.74-4016A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693528 | |||||||
| chr2:205693550 | G | A | 105 | a0001c0001t0001g0157 a0001c0001t0004g0116 a0001c0001t0004g0193 others(102): Show |
107 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.74-3994G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693550 | |||||||
| chr2:205693716 | C | A | 10 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(7): Show |
10 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.74-3828C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693716 | |||||||
| chr2:205693789 | C | T | 104 | a0001c0001t0001g0157 a0001c0001t0004g0116 a0001c0001t0004g0193 others(101): Show |
106 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.74-3755C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693789 | |||||||
| chr2:205693915 | A | T | 7 | a0001c0002t0049g0172 a0001c0003t0008g0171 a0001c0003t0012g0174 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-3629A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693915 | |||||||
| chr2:205694044 | G | A | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-3500G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694044 | |||||||
| chr2:205694085 | A | C | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-3459A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694085 | |||||||
| chr2:205694105 | C | T | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.74-3439C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694105 | |||||||
| chr2:205694146 | A | G | 1 | a0001c0002t0008g0140 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.74-3398A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694146 | |||||||
| chr2:205694371 | G | A | 2 | a0001c0001t0020g0031 a0001c0009t0027g0030 |
2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.74-3173G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694371 | |||||||
| chr2:205694458 | T | C | 1 | a0001c0001t0057g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.74-3086T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694458 | |||||||
| chr2:205694501 | A | G | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.74-3043A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694501 | |||||||
| chr2:205694540 | C | A | 1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.74-3004C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694540 | |||||||
| chr2:205694914 | A | G | 2 | a0001c0001t0058g0068 a0001c0002t0005g0029 |
2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.74-2630A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694914 | |||||||
| chr2:205695509 | G | C | 57 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(54): Show |
57 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.74-2035G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695509 | |||||||
| chr2:205695687 | T | G | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.74-1857T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695687 | |||||||
| chr2:205695717 | T | C | 5 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 others(2): Show |
6 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-1827T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695717 | |||||||
| chr2:205695816 | G | A | 12 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(9): Show |
12 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1728G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695816 | |||||||
| chr2:205695824 | T | C | 4 | a0001c0002t0012g0130 a0001c0002t0016g0133 a0001c0013t0016g0131 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-1720T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695824 | |||||||
| chr2:205695875 | T | C | 1 | a0001c0001t0018g0018 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.74-1669T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695875 | |||||||
| chr2:205695889 | G | A | 79 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(76): Show |
81 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.74-1655G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695889 | |||||||
| chr2:205696014 | C | T | 94 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(91): Show |
96 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.74-1530C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696014 | |||||||
| chr2:205696113 | C | T | 1 | a0001c0001t0031g0328 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.74-1431C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696113 | |||||||
| chr2:205696123 | A | G | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-1421A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696123 | |||||||
| chr2:205696160 | C | T | 1 | a0001c0003t0003g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.74-1384C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696160 | |||||||
| chr2:205696174 | A | G | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-1370A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696174 | |||||||
| chr2:205696189 | G | A | 1 | a0001c0003t0002g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.74-1355G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696189 | |||||||
| chr2:205696346 | G | A | 3 | a0001c0002t0007g0283 a0001c0002t0007g0284 a0001c0002t0008g0180 |
3 | HG02109.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.74-1198G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696346 | |||||||
| chr2:205696372 | T | C | 12 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(9): Show |
12 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1172T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696372 | |||||||
| chr2:205696700 | G | A | 6 | a0001c0001t0004g0116 a0001c0001t0004g0193 a0001c0002t0001g0190 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-844G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696700 | |||||||
| chr2:205696703 | C | T | 60 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(57): Show |
60 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.74-841C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696703 | |||||||
| chr2:205697028 | T | C | 4 | a0001c0003t0002g0297 a0001c0003t0003g0295 a0001c0003t0003g0298 others(1): Show |
4 | HG02083.hp2 HG02523.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-516T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697028 | |||||||
| chr2:205697183 | G | A | 1 | a0001c0003t0014g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.74-361G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697183 | |||||||
| chr2:205697193 | G | A | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.74-351G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697193 | |||||||
| chr2:205697309 | C | T | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.74-235C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697309 | |||||||
| chr2:205697312 | C | CTGTG | 3 | a0001c0002t0004g0181 a0001c0002t0049g0172 a0001c0003t0022g0173 |
3 | HG06807.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.74-202_74-199dupGT others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(1): Show |
5 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(2): Show |
5 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-206_74-199dupGT others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(3): Show |
2 | a0002c0014t0001g0195 a0002c0014t0008g0194 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.74-208_74-199dupGT others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(9): Show |
4 | a0001c0002t0007g0283 a0001c0002t0007g0284 a0001c0002t0008g0180 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-214_74-199dupGT others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(11): Show |
6 | a0001c0002t0022g0184 a0001c0002t0051g0182 a0001c0002t0054g0214 others(3): Show |
6 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-216_74-199dupGT others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(15): Show |
1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.74-220_74-199dupGT others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(17): Show |
2 | a0001c0002t0004g0139 a0001c0002t0046g0141 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74-222_74-199dupGT others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(19): Show |
3 | a0001c0011t0004g0170 a0002c0015t0030g0004 a0002c0027t0064g0176 |
4 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-224_74-199dupGT others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(21): Show |
3 | a0001c0003t0012g0174 a0001c0005t0013g0175 a0001c0012t0017g0272 |
3 | HG02976.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.74-226_74-199dupGT others(26): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | C | CTGTGTGT others(25): Show |
1 | a0001c0012t0004g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74-230_74-199dupGT others(30): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | CTG | C | 234 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(231): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.74-200_74-199delGT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697312 | CTGTG | C | 48 | a0001c0001t0001g0157 a0001c0001t0007g0213 a0001c0001t0012g0019 others(45): Show |
48 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.74-202_74-199delGT others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | ||||||
| chr2:205697499 | T | C | 4 | a0001c0002t0004g0181 a0001c0002t0049g0172 a0001c0003t0022g0173 others(1): Show |
4 | HG02723.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-45T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697499 | |||||||
| chr2:205697526 | C | T | 302 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(299): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.74-18C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697526 | |||||||
| chr2:205697730 | C | T | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.251+9C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697730 | |||||||
| chr2:205697842 | A | G | 1 | a0001c0006t0011g0338 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.251+121A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697842 | |||||||
| chr2:205697858 | A | G | 6 | a0001c0001t0005g0007 a0001c0003t0001g0098 a0001c0003t0005g0092 others(3): Show |
6 | HG02056.hp2 NA18957.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+137A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697858 | |||||||
| chr2:205697887 | G | T | 1 | a0001c0004t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.251+166G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697887 | |||||||
| chr2:205697958 | C | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0005g0033 others(11): Show |
14 | HG00438.hp1 HG00558.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+237C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697958 | |||||||
| chr2:205698207 | G | GA | 15 | a0001c0002t0007g0291 a0001c0002t0008g0012 a0001c0002t0028g0187 others(12): Show |
15 | HG01070.hp1 HG01099.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+496dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205698207 | ||||||
| chr2:205698218 | G | A | 14 | a0001c0002t0004g0011 a0001c0002t0006g0146 a0001c0002t0008g0123 others(11): Show |
14 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+497G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698218 | |||||||
| chr2:205698221 | T | G | 14 | a0001c0002t0004g0011 a0001c0002t0006g0146 a0001c0002t0008g0123 others(11): Show |
14 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+500T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698221 | |||||||
| chr2:205698221 | TA | T | 41 | a0001c0001t0007g0213 a0001c0001t0009g0319 a0001c0001t0012g0019 others(38): Show |
41 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.251+514delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205698221 | ||||||
| chr2:205698222 | A | T | 14 | a0001c0002t0004g0011 a0001c0002t0006g0146 a0001c0002t0008g0123 others(11): Show |
14 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+501A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698222 | |||||||
| chr2:205698299 | G | A | 232 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.251+578G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698299 | |||||||
| chr2:205698460 | G | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(7): Show |
10 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+739G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698460 | |||||||
| chr2:205698515 | A | G | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251+794A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698515 | |||||||
| chr2:205698534 | T | C | 245 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.251+813T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698534 | |||||||
| chr2:205698605 | A | G | 5 | a0001c0003t0012g0174 a0001c0005t0013g0175 a0001c0011t0004g0170 others(2): Show |
5 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+884A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698605 | |||||||
| chr2:205698738 | T | C | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251+1017T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698738 | |||||||
| chr2:205698981 | T | A | 5 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(2): Show |
6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+1260T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698981 | |||||||
| chr2:205699332 | G | T | 5 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(2): Show |
6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+1611G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699332 | |||||||
| chr2:205699417 | G | A | 2 | a0001c0002t0013g0197 a0001c0002t0013g0198 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.251+1696G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699417 | |||||||
| chr2:205699429 | T | C | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(10): Show |
13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+1708T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699429 | |||||||
| chr2:205699574 | A | G | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(10): Show |
13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+1853A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699574 | |||||||
| chr2:205699993 | A | G | 4 | a0001c0002t0003g0203 a0001c0002t0003g0281 a0001c0002t0003g0282 others(1): Show |
4 | NA18953.hp1 NA18967.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+2272A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699993 | |||||||
| chr2:205700065 | C | T | 9 | a0001c0002t0004g0139 a0001c0003t0012g0174 a0001c0008t0004g0005 others(6): Show |
10 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+2344C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700065 | |||||||
| chr2:205700211 | C | T | 2 | a0001c0003t0009g0342 a0001c0003t0025g0301 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.251+2490C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700211 | |||||||
| chr2:205700247 | C | G | 1 | a0001c0001t0005g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.251+2526C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700247 | |||||||
| chr2:205700294 | C | T | 1 | a0001c0002t0004g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251+2573C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700294 | |||||||
| chr2:205700504 | C | T | 4 | a0001c0002t0012g0130 a0001c0002t0016g0133 a0001c0013t0016g0131 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+2783C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700504 | |||||||
| chr2:205700505 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.251+2784G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700505 | |||||||
| chr2:205700541 | G | A | 1 | a0001c0004t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.251+2820G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700541 | |||||||
| chr2:205700727 | T | C | 4 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(1): Show |
5 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+3006T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700727 | |||||||
| chr2:205700736 | C | T | 1 | a0001c0002t0011g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.251+3015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700736 | |||||||
| chr2:205700776 | C | T | 45 | a0001c0001t0007g0213 a0001c0002t0002g0279 a0001c0002t0004g0011 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.251+3055C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700776 | |||||||
| chr2:205700790 | C | T | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+3069C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700790 | |||||||
| chr2:205700894 | AC | A | 8 | a0001c0002t0004g0011 a0001c0002t0007g0291 a0001c0002t0008g0012 others(5): Show |
8 | HG00741.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.251+3174delC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700894 | |||||||
| chr2:205700896 | T | G | 1 | a0001c0002t0018g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.251+3175T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700896 | |||||||
| chr2:205700927 | A | C | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(10): Show |
13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+3206A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700927 | |||||||
| chr2:205700950 | G | A | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251+3229G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700950 | |||||||
| chr2:205700953 | T | C | 1 | a0001c0002t0020g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.251+3232T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700953 | |||||||
| chr2:205700988 | G | A | 9 | a0001c0002t0004g0139 a0001c0003t0012g0174 a0001c0008t0004g0005 others(6): Show |
10 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+3267G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700988 | |||||||
| chr2:205701018 | G | A | 234 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.251+3297G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701018 | |||||||
| chr2:205701130 | T | C | 1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+3409T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701130 | |||||||
| chr2:205701247 | G | A | 1 | a0001c0006t0009g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.251+3526G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701247 | |||||||
| chr2:205701538 | C | CA | 294 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.251+3833dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205701538 | ||||||
| chr2:205701699 | A | G | 300 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(297): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.251+3978A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701699 | |||||||
| chr2:205701778 | G | A | 1 | a0001c0001t0005g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.251+4057G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701778 | |||||||
| chr2:205701790 | G | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(8): Show |
11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.251+4069G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701790 | |||||||
| chr2:205702053 | T | G | 3 | a0001c0003t0004g0167 a0003c0025t0013g0166 a0003c0026t0004g0165 |
3 | HG01891.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251+4332T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702053 | |||||||
| chr2:205702070 | C | T | 1 | a0004c0022t0006g0115 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.251+4349C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702070 | |||||||
| chr2:205702149 | G | GTTTGGGA others(363): Show |
1 | a0001c0001t0003g0318 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.251+4444_251+4445i others(372): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | ||||||
| chr2:205702149 | G | GTTTGGGA others(371): Show |
1 | a0001c0001t0002g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.251+4444_251+4445i others(380): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | ||||||
| chr2:205702149 | G | GTTTGGGA others(386): Show |
1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+4444_251+4445i others(395): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | ||||||
| chr2:205702149 | G | GTTTGGGA others(399): Show |
1 | a0001c0004t0002g0245 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.251+4444_251+4445i others(408): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | ||||||
| chr2:205702153 | G | A | 5 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(2): Show |
6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+4432G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702153 | |||||||
| chr2:205702164 | C | A | 1 | a0001c0001t0005g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.251+4443C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702164 | |||||||
| chr2:205702337 | A | G | 2 | a0001c0001t0058g0068 a0001c0002t0005g0029 |
2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.251+4616A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702337 | |||||||
| chr2:205702409 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+4688C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702409 | |||||||
| chr2:205702499 | C | T | 4 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+4778C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702499 | |||||||
| chr2:205702538 | C | G | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251+4817C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702538 | |||||||
| chr2:205702712 | G | A | 1 | a0001c0001t0004g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.251+4991G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702712 | |||||||
| chr2:205703633 | A | C | 1 | a0001c0001t0004g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+5912A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703633 | |||||||
| chr2:205703683 | T | C | 1 | a0001c0002t0020g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.251+5962T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703683 | |||||||
| chr2:205703686 | G | T | 14 | a0001c0001t0002g0210 a0001c0001t0002g0257 a0001c0001t0002g0316 others(11): Show |
14 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+5965G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703686 | |||||||
| chr2:205703693 | A | G | 6 | a0001c0003t0012g0174 a0001c0005t0013g0175 a0001c0011t0004g0170 others(3): Show |
6 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+5972A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703693 | |||||||
| chr2:205703780 | T | C | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(12): Show |
15 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+6059T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703780 | |||||||
| chr2:205703782 | G | T | 1 | a0001c0002t0004g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251+6061G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703782 | |||||||
| chr2:205703902 | G | A | 12 | a0001c0001t0015g0208 a0001c0002t0004g0139 a0001c0003t0012g0174 others(9): Show |
13 | HG01169.hp1 HG01433.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+6181G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703902 | |||||||
| chr2:205704100 | G | A | 1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+6379G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704100 | |||||||
| chr2:205704513 | G | A | 1 | a0001c0011t0004g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.251+6792G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704513 | |||||||
| chr2:205704604 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.251+6883T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704604 | |||||||
| chr2:205704609 | C | T | 1 | a0001c0001t0053g0158 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.251+6888C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704609 | |||||||
| chr2:205704610 | A | G | 299 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(296): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.251+6889A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704610 | |||||||
| chr2:205704731 | T | C | 2 | a0001c0001t0013g0041 a0001c0004t0012g0042 |
2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.251+7010T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704731 | |||||||
| chr2:205704803 | A | C | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.251+7082A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704803 | |||||||
| chr2:205704809 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251+7088C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704809 | |||||||
| chr2:205704810 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251+7089C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704810 | |||||||
| chr2:205704812 | C | T | 1 | a0001c0004t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.251+7091C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704812 | |||||||
| chr2:205704899 | C | A | 1 | a0001c0003t0055g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.251+7178C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704899 | |||||||
| chr2:205705074 | T | C | 1 | a0001c0001t0007g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.251+7353T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705074 | |||||||
| chr2:205705102 | GGATTTAA others(24): Show |
G | 1 | a0001c0002t0001g0081 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.251+7382_251+7412d others(33): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705102 | |||||||
| chr2:205705183 | G | GA | 287 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(284): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.251+7476dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | ||||||
| chr2:205705183 | G | GAA | 9 | a0001c0001t0001g0063 a0001c0001t0005g0095 a0001c0002t0006g0090 others(6): Show |
9 | HG02004.hp2 HG02523.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+7475_251+7476d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | ||||||
| chr2:205705183 | GA | G | 7 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+7476delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | ||||||
| chr2:205705230 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.251+7509A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705230 | |||||||
| chr2:205705265 | C | T | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251+7544C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705265 | |||||||
| chr2:205705459 | A | G | 6 | a0001c0001t0019g0089 a0001c0002t0007g0290 a0001c0004t0001g0086 others(3): Show |
6 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+7738A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705459 | |||||||
| chr2:205705554 | T | C | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(12): Show |
15 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+7833T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705554 | |||||||
| chr2:205705571 | C | T | 53 | a0001c0001t0007g0213 a0001c0002t0002g0279 a0001c0002t0004g0011 others(50): Show |
53 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.251+7850C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705571 | |||||||
| chr2:205705665 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251+7944G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705665 | |||||||
| chr2:205705709 | T | G | 327 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(324): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.251+7988T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705709 | |||||||
| chr2:205705895 | C | T | 1 | a0001c0003t0002g0297 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.251+8174C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705895 | |||||||
| chr2:205706081 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.251+8360C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706081 | |||||||
| chr2:205706266 | T | G | 1 | a0001c0003t0009g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.251+8545T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706266 | |||||||
| chr2:205706283 | C | T | 4 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(1): Show |
5 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+8562C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706283 | |||||||
| chr2:205706411 | A | G | 75 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0063 others(72): Show |
77 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.251+8690A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706411 | |||||||
| chr2:205706926 | C | T | 10 | a0001c0001t0005g0034 a0001c0001t0005g0037 a0001c0001t0005g0039 others(7): Show |
10 | HG00438.hp1 HG00558.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+9205C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706926 | |||||||
| chr2:205707231 | G | C | 10 | a0001c0006t0007g0306 a0001c0006t0007g0329 a0001c0006t0009g0303 others(7): Show |
10 | HG02055.hp1 HG02818.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-8962G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707231 | |||||||
| chr2:205707247 | G | A | 1 | a0001c0003t0011g0322 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.252-8946G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707247 | |||||||
| chr2:205707415 | A | G | 1 | a0001c0002t0017g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.252-8778A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707415 | |||||||
| chr2:205707728 | G | T | 2 | a0001c0001t0008g0049 a0001c0004t0013g0050 |
2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.252-8465G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707728 | |||||||
| chr2:205707770 | T | G | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252-8423T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707770 | |||||||
| chr2:205707810 | C | G | 79 | a0001c0001t0005g0007 a0001c0001t0031g0328 a0001c0002t0001g0014 others(76): Show |
79 | HG00639.hp1 HG01167.hp1 HG01192.hp1 others(76): Show |
intron_variant | MODIFIER | c.252-8383C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707810 | |||||||
| chr2:205707904 | A | G | 175 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(172): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.252-8289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707904 | |||||||
| chr2:205708062 | T | C | 1 | a0001c0002t0008g0140 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.252-8131T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708062 | |||||||
| chr2:205708125 | T | C | 2 | a0001c0005t0023g0119 a0001c0005t0023g0120 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.252-8068T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708125 | |||||||
| chr2:205708148 | G | C | 5 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(2): Show |
6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-8045G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708148 | |||||||
| chr2:205708224 | C | G | 2 | a0001c0001t0005g0104 a0001c0004t0002g0169 |
2 | HG00621.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.252-7969C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708224 | |||||||
| chr2:205708364 | C | T | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.252-7829C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708364 | |||||||
| chr2:205708408 | G | A | 1 | a0001c0001t0013g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.252-7785G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708408 | |||||||
| chr2:205708510 | T | C | 324 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(321): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.252-7683T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708510 | |||||||
| chr2:205708547 | G | A | 1 | a0001c0002t0049g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.252-7646G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708547 | |||||||
| chr2:205708673 | T | TC | 167 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(164): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.252-7520_252-7519i others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708673 | |||||||
| chr2:205708808 | A | G | 1 | a0005c0019t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.252-7385A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708808 | |||||||
| chr2:205708912 | C | A | 325 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(322): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.252-7281C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708912 | |||||||
| chr2:205709444 | C | T | 1 | a0001c0001t0008g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.252-6749C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709444 | |||||||
| chr2:205709719 | G | A | 2 | a0001c0002t0046g0141 a0001c0003t0008g0171 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-6474G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709719 | |||||||
| chr2:205709834 | T | C | 1 | a0001c0002t0011g0256 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252-6359T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709834 | |||||||
| chr2:205709906 | A | G | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-6287A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709906 | |||||||
| chr2:205709963 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.252-6230G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709963 | |||||||
| chr2:205709994 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252-6199G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709994 | |||||||
| chr2:205709995 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252-6198C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709995 | |||||||
| chr2:205710531 | G | A | 4 | a0001c0005t0023g0118 a0001c0005t0023g0119 a0001c0005t0023g0120 others(1): Show |
4 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-5662G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710531 | |||||||
| chr2:205710541 | T | G | 1 | a0001c0001t0010g0313 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.252-5652T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710541 | |||||||
| chr2:205710643 | C | G | 1 | a0001c0002t0018g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.252-5550C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710643 | |||||||
| chr2:205710644 | G | A | 6 | a0001c0001t0002g0215 a0001c0005t0014g0127 a0001c0005t0023g0118 others(3): Show |
6 | HG01169.hp1 HG01346.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-5549G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710644 | |||||||
| chr2:205710644 | G | C | 2 | a0001c0001t0013g0041 a0001c0004t0012g0042 |
2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.252-5549G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710644 | |||||||
| chr2:205710680 | A | G | 147 | a0001c0001t0002g0215 a0001c0001t0005g0007 a0001c0001t0005g0095 others(144): Show |
147 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.252-5513A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710680 | |||||||
| chr2:205710695 | C | T | 3 | a0001c0003t0003g0216 a0001c0003t0003g0217 a0001c0003t0003g0299 |
3 | HG02080.hp2 NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.252-5498C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710695 | |||||||
| chr2:205711003 | G | T | 5 | a0001c0001t0019g0089 a0001c0004t0001g0086 a0001c0004t0006g0179 others(2): Show |
5 | HG01928.hp1 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-5190G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711003 | |||||||
| chr2:205711024 | T | A | 152 | a0001c0001t0002g0215 a0001c0001t0005g0007 a0001c0001t0007g0213 others(149): Show |
152 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(149): Show |
intron_variant | MODIFIER | c.252-5169T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711024 | |||||||
| chr2:205711140 | C | T | 1 | a0001c0002t0007g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.252-5053C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711140 | |||||||
| chr2:205711365 | A | T | 1 | a0001c0004t0012g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252-4828A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711365 | |||||||
| chr2:205711459 | C | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.252-4734C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711459 | |||||||
| chr2:205711513 | G | A | 11 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(8): Show |
12 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-4680G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711513 | |||||||
| chr2:205711585 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.252-4608A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711585 | |||||||
| chr2:205711724 | C | T | 10 | a0001c0002t0004g0274 a0001c0002t0007g0126 a0001c0003t0004g0167 others(7): Show |
10 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-4469C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711724 | |||||||
| chr2:205711747 | C | T | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252-4446C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711747 | |||||||
| chr2:205711773 | T | A | 1 | a0001c0001t0004g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.252-4420T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711773 | |||||||
| chr2:205711795 | T | G | 57 | a0001c0001t0007g0213 a0001c0002t0002g0279 a0001c0002t0004g0011 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.252-4398T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711795 | |||||||
| chr2:205711873 | G | A | 1 | a0001c0004t0002g0211 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.252-4320G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711873 | |||||||
| chr2:205712101 | G | C | 6 | a0001c0002t0004g0139 a0001c0005t0013g0175 a0001c0011t0004g0170 others(3): Show |
6 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-4092G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712101 | |||||||
| chr2:205712250 | T | G | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3943T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712250 | |||||||
| chr2:205712390 | G | A | 144 | a0001c0001t0005g0007 a0001c0001t0007g0213 a0001c0001t0031g0328 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.252-3803G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712390 | |||||||
| chr2:205712430 | A | G | 5 | a0001c0002t0004g0139 a0001c0003t0012g0174 a0001c0008t0004g0005 others(2): Show |
6 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3763A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712430 | |||||||
| chr2:205712687 | A | G | 96 | a0001c0001t0001g0025 a0001c0001t0005g0007 a0001c0001t0005g0095 others(93): Show |
96 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.252-3506A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712687 | |||||||
| chr2:205712719 | G | C | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.252-3474G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712719 | |||||||
| chr2:205712804 | G | C | 168 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(165): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.252-3389G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712804 | |||||||
| chr2:205712854 | T | C | 15 | a0001c0001t0002g0210 a0001c0001t0002g0257 a0001c0001t0002g0316 others(12): Show |
15 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-3339T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712854 | |||||||
| chr2:205713079 | C | T | 6 | a0001c0002t0002g0294 a0001c0002t0003g0286 a0001c0002t0007g0285 others(3): Show |
6 | HG01346.hp1 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3114C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713079 | |||||||
| chr2:205713195 | C | T | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.252-2998C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713195 | |||||||
| chr2:205713450 | C | T | 1 | a0001c0004t0001g0096 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.252-2743C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713450 | |||||||
| chr2:205713572 | A | G | 3 | a0001c0001t0008g0049 a0001c0001t0012g0074 a0001c0004t0013g0050 |
3 | HG00280.hp2 HG01074.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.252-2621A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713572 | |||||||
| chr2:205713573 | T | G | 1 | a0001c0004t0010g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.252-2620T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713573 | |||||||
| chr2:205713699 | G | T | 2 | a0001c0002t0046g0141 a0001c0003t0008g0171 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-2494G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713699 | |||||||
| chr2:205713752 | C | A | 4 | a0001c0001t0010g0313 a0001c0004t0003g0314 a0001c0004t0003g0315 others(1): Show |
4 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-2441C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713752 | |||||||
| chr2:205714312 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0012g0026 a0001c0001t0012g0027 |
3 | HG00099.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.252-1881T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714312 | |||||||
| chr2:205714541 | G | A | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252-1652G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714541 | |||||||
| chr2:205714610 | C | T | 6 | a0001c0001t0004g0060 a0001c0001t0019g0089 a0001c0004t0001g0086 others(3): Show |
6 | HG01928.hp1 HG01981.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-1583C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714610 | |||||||
| chr2:205714643 | T | C | 328 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(325): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.252-1550T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714643 | |||||||
| chr2:205714678 | T | TGG | 12 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-1511_252-1510d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205714678 | ||||||
| chr2:205714764 | G | A | 1 | a0001c0002t0010g0276 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.252-1429G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714764 | |||||||
| chr2:205714928 | T | C | 1 | a0001c0002t0022g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.252-1265T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714928 | |||||||
| chr2:205715013 | A | G | 7 | a0001c0006t0007g0306 a0001c0006t0011g0337 a0001c0006t0011g0338 others(4): Show |
7 | HG02055.hp1 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-1180A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715013 | |||||||
| chr2:205715099 | G | A | 5 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0002c0015t0030g0004 others(2): Show |
6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-1094G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715099 | |||||||
| chr2:205715101 | G | A | 135 | a0001c0001t0005g0007 a0001c0001t0007g0213 a0001c0001t0031g0328 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.252-1092G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715101 | |||||||
| chr2:205715369 | C | T | 3 | a0001c0002t0049g0172 a0001c0003t0022g0173 a0001c0007t0008g0062 |
3 | HG02723.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252-824C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715369 | |||||||
| chr2:205715421 | C | T | 1 | a0001c0002t0011g0256 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252-772C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715421 | |||||||
| chr2:205715428 | A | G | 191 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.252-765A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715428 | |||||||
| chr2:205715431 | G | A | 1 | a0001c0002t0006g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.252-762G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715431 | |||||||
| chr2:205715467 | G | A | 1 | a0001c0002t0017g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.252-726G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715467 | |||||||
| chr2:205715990 | T | G | 190 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.252-203T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715990 | |||||||
| chr2:205716156 | C | G | 2 | a0001c0002t0046g0141 a0001c0003t0008g0171 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-37C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205716156 | |||||||
| chr2:205716577 | C | CG | 21 | a0001c0001t0001g0021 a0001c0001t0001g0111 a0001c0001t0003g0202 others(18): Show |
21 | HG00423.hp1 HG00423.hp2 HG02895.hp1 others(18): Show |
intron_variant | MODIFIER | c.433+210dupG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205716577 | ||||||
| chr2:205716585 | T | G | 1 | a0001c0001t0015g0237 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.433+211T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205716585 | |||||||
| chr2:205716999 | T | C | 5 | a0001c0001t0009g0238 a0001c0010t0009g0230 a0001c0010t0009g0231 others(2): Show |
5 | HG00642.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+625T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205716999 | |||||||
| chr2:205717119 | C | T | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433+745C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717119 | |||||||
| chr2:205717138 | A | AGTGT | 70 | a0001c0001t0002g0215 a0001c0002t0001g0014 a0001c0002t0002g0279 others(67): Show |
70 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.433+764_433+765ins others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717138 | |||||||
| chr2:205717139 | A | G | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+765A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717139 | |||||||
| chr2:205717206 | T | G | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433+832T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717206 | |||||||
| chr2:205717206 | T | TG | 186 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.433+833dupG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205717206 | ||||||
| chr2:205717313 | G | A | 1 | a0001c0001t0015g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433+939G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717313 | |||||||
| chr2:205717331 | G | A | 1 | a0001c0004t0002g0280 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.433+957G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717331 | |||||||
| chr2:205717512 | G | A | 1 | a0001c0002t0017g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433+1138G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717512 | |||||||
| chr2:205717625 | G | A | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.433+1251G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717625 | |||||||
| chr2:205717738 | G | A | 153 | a0001c0001t0002g0215 a0001c0002t0001g0014 a0001c0002t0001g0056 others(150): Show |
154 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(151): Show |
intron_variant | MODIFIER | c.433+1364G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717738 | |||||||
| chr2:205717913 | T | C | 1 | a0001c0002t0007g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433+1539T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717913 | |||||||
| chr2:205718030 | C | T | 4 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1656C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718030 | |||||||
| chr2:205718271 | A | G | 4 | a0001c0001t0003g0264 a0001c0001t0005g0007 a0001c0001t0010g0265 others(1): Show |
4 | HG02135.hp2 NA18975.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+1897A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718271 | |||||||
| chr2:205718410 | G | A | 1 | a0001c0002t0017g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433+2036G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718410 | |||||||
| chr2:205718452 | A | C | 1 | a0001c0001t0004g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.433+2078A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718452 | |||||||
| chr2:205718603 | G | A | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2229G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718603 | |||||||
| chr2:205718701 | G | A | 4 | a0001c0002t0001g0190 a0001c0002t0004g0139 a0001c0002t0004g0191 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2327G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718701 | |||||||
| chr2:205718920 | C | T | 3 | a0001c0005t0007g0222 a0001c0005t0023g0119 a0001c0005t0023g0120 |
3 | HG01123.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.433+2546C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718920 | |||||||
| chr2:205718929 | C | T | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2555C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718929 | |||||||
| chr2:205718942 | C | CA | 171 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.433+2582dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205718942 | ||||||
| chr2:205718942 | C | CAA | 147 | a0001c0001t0002g0215 a0001c0001t0005g0095 a0001c0002t0001g0014 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(144): Show |
intron_variant | MODIFIER | c.433+2581_433+2582d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205718942 | ||||||
| chr2:205718968 | A | G | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2594A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718968 | |||||||
| chr2:205719037 | A | G | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2663A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719037 | |||||||
| chr2:205719226 | A | G | 77 | a0001c0001t0002g0215 a0001c0002t0001g0014 a0001c0002t0002g0279 others(74): Show |
77 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.433+2852A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719226 | |||||||
| chr2:205719473 | C | CA | 19 | a0001c0001t0003g0264 a0001c0001t0005g0007 a0001c0001t0010g0265 others(16): Show |
19 | HG02055.hp1 HG02135.hp2 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.434-2991dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719473 | ||||||
| chr2:205719473 | CA | C | 10 | a0001c0001t0002g0246 a0001c0001t0003g0243 a0001c0001t0005g0039 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-2991delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719473 | ||||||
| chr2:205719536 | A | ATG | 3 | a0001c0002t0049g0172 a0001c0003t0022g0173 a0001c0007t0008g0062 |
3 | HG02723.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.434-2926_434-2925d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719536 | ||||||
| chr2:205719672 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0005g0144 a0001c0001t0010g0209 others(8): Show |
12 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-2806C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719672 | |||||||
| chr2:205719783 | A | G | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-2695A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719783 | |||||||
| chr2:205719811 | TA | T | 7 | a0001c0002t0007g0126 a0001c0002t0051g0182 a0001c0002t0054g0214 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.434-2663delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719811 | ||||||
| chr2:205720238 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.434-2240T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720238 | |||||||
| chr2:205720262 | CT | C | 24 | a0001c0001t0001g0143 a0001c0001t0009g0239 a0001c0001t0018g0018 others(21): Show |
25 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.434-2195delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | ||||||
| chr2:205720262 | CTTTTTTT | C | 86 | a0001c0002t0001g0014 a0001c0002t0002g0261 a0001c0002t0002g0262 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.434-2201_434-2195d others(9): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | ||||||
| chr2:205720262 | CTTTTTTT others(1): Show |
C | 68 | a0001c0002t0001g0056 a0001c0002t0001g0081 a0001c0002t0001g0083 others(65): Show |
69 | HG01081.hp1 HG01123.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.434-2202_434-2195d others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | ||||||
| chr2:205720268 | T | C | 3 | a0002c0015t0030g0004 a0002c0017t0062g0177 a0002c0027t0064g0176 |
4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-2210T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720268 | |||||||
| chr2:205720447 | A | C | 4 | a0001c0011t0004g0170 a0001c0011t0008g0134 a0001c0012t0004g0137 others(1): Show |
4 | HG02622.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-2031A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720447 | |||||||
| chr2:205720479 | G | T | 2 | a0003c0025t0013g0166 a0003c0026t0004g0165 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.434-1999G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720479 | |||||||
| chr2:205720726 | G | A | 1 | a0001c0007t0013g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434-1752G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720726 | |||||||
| chr2:205720763 | C | T | 158 | a0001c0002t0001g0014 a0001c0002t0001g0056 a0001c0002t0001g0081 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(156): Show |
intron_variant | MODIFIER | c.434-1715C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720763 | |||||||
| chr2:205720772 | A | G | 1 | a0001c0002t0016g0133 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.434-1706A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720772 | |||||||
| chr2:205720896 | C | T | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1582C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720896 | |||||||
| chr2:205721068 | A | G | 4 | a0001c0002t0001g0190 a0001c0002t0004g0139 a0001c0002t0004g0191 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1410A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721068 | |||||||
| chr2:205721125 | T | A | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1353T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721125 | |||||||
| chr2:205721196 | T | A | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.434-1282T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721196 | |||||||
| chr2:205721220 | T | C | 156 | a0001c0001t0005g0095 a0001c0002t0001g0014 a0001c0002t0001g0056 others(153): Show |
157 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(154): Show |
intron_variant | MODIFIER | c.434-1258T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721220 | |||||||
| chr2:205721249 | A | G | 73 | a0001c0002t0001g0014 a0001c0002t0002g0279 a0001c0002t0002g0294 others(70): Show |
73 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.434-1229A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721249 | |||||||
| chr2:205721273 | G | C | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.434-1205G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721273 | |||||||
| chr2:205721314 | G | C | 72 | a0001c0001t0005g0095 a0001c0001t0019g0089 a0001c0002t0001g0056 others(69): Show |
72 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(69): Show |
intron_variant | MODIFIER | c.434-1164G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721314 | |||||||
| chr2:205721379 | G | A | 1 | a0001c0003t0008g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1099G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721379 | |||||||
| chr2:205721458 | C | T | 1 | a0001c0012t0017g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.434-1020C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721458 | |||||||
| chr2:205721688 | G | A | 60 | a0001c0002t0001g0056 a0001c0002t0001g0081 a0001c0002t0001g0083 others(57): Show |
60 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.434-790G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721688 | |||||||
| chr2:205721743 | C | A | 158 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(155): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.434-735C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721743 | |||||||
| chr2:205722012 | C | T | 17 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 others(14): Show |
17 | HG01243.hp1 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.434-466C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722012 | |||||||
| chr2:205722145 | C | CCT | 31 | a0001c0001t0003g0268 a0001c0001t0004g0017 a0001c0001t0004g0060 others(28): Show |
31 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.434-309_434-308dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | ||||||
| chr2:205722145 | C | CCTCT | 10 | a0001c0001t0019g0089 a0001c0002t0004g0181 a0001c0002t0004g0274 others(7): Show |
10 | HG01928.hp1 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.434-311_434-308dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | ||||||
| chr2:205722145 | CCTCT | C | 2 | a0001c0002t0008g0123 a0001c0008t0004g0005 |
3 | HG02630.hp1 HG02818.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.434-311_434-308del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | ||||||
| chr2:205722152 | C | CTT | 12 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-325_434-324ins others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722152 | ||||||
| chr2:205722162 | CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.434-315_434-306del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722162 | |||||||
| chr2:205722165 | T | A | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-313T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722165 | |||||||
| chr2:205722165 | TCTCTCAT others(3): Show |
T | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.434-311_434-302del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722165 | ||||||
| chr2:205722167 | T | A | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-311T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722167 | |||||||
| chr2:205722169 | T | A | 3 | a0001c0008t0004g0005 a0002c0015t0030g0004 a0002c0027t0064g0176 |
5 | HG02630.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-309T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722169 | |||||||
| chr2:205722169 | T | TCTCATAC others(3): Show |
1 | a0001c0002t0009g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.434-308_434-307ins others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | ||||||
| chr2:205722169 | T | TCTCTCTC others(5): Show |
1 | a0001c0003t0022g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434-308_434-307ins others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | ||||||
| chr2:205722169 | TCATA | T | 14 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.434-306_434-303del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | ||||||
| chr2:205722169 | TCATACAC others(1): Show |
T | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-306_434-299del others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | ||||||
| chr2:205722170 | C | CTCAT | 6 | a0001c0001t0011g0331 a0001c0001t0012g0019 a0001c0002t0014g0159 others(3): Show |
6 | HG01081.hp2 HG01516.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-308_434-307ins others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722170 | |||||||
| chr2:205722170 | CAT | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0143 a0001c0001t0004g0080 others(11): Show |
14 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.434-306_434-305del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722170 | ||||||
| chr2:205722171 | A | T | 161 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.434-307A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722171 | |||||||
| chr2:205722172 | T | C | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.434-306T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722172 | |||||||
| chr2:205722172 | T | TAC | 6 | a0001c0002t0017g0254 a0001c0003t0003g0295 a0001c0003t0007g0249 others(3): Show |
6 | HG02698.hp1 HG02976.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-267_434-266dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | ||||||
| chr2:205722172 | T | TACAC | 10 | a0001c0002t0001g0056 a0001c0002t0006g0051 a0001c0002t0012g0130 others(7): Show |
10 | HG01167.hp1 HG01192.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-269_434-266dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | ||||||
| chr2:205722172 | TAC | T | 15 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0003t0014g0099 others(12): Show |
15 | HG00639.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.434-267_434-266del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | ||||||
| chr2:205722172 | TACAC | T | 4 | a0001c0003t0003g0298 a0001c0003t0006g0085 a0001c0003t0014g0094 others(1): Show |
4 | NA18973.hp1 NA18993.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-269_434-266del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | ||||||
| chr2:205722173 | A | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0143 a0001c0001t0004g0080 others(13): Show |
16 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.434-305A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722173 | |||||||
| chr2:205722174 | C | T | 162 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.434-304C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722174 | |||||||
| chr2:205722175 | A | T | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(12): Show |
15 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.434-303A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722175 | |||||||
| chr2:205722176 | C | T | 15 | a0001c0001t0001g0036 a0001c0001t0001g0143 a0001c0001t0004g0080 others(12): Show |
15 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.434-302C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722176 | |||||||
| chr2:205722177 | A | T | 2 | a0001c0001t0003g0264 a0001c0003t0047g0125 |
2 | HG02135.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.434-301A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722177 | |||||||
| chr2:205722178 | C | T | 14 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.434-300C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722178 | |||||||
| chr2:205722179 | A | T | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-299A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722179 | |||||||
| chr2:205722180 | C | T | 2 | a0001c0001t0003g0264 a0001c0003t0047g0125 |
2 | HG02135.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.434-298C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722180 | |||||||
| chr2:205722182 | C | T | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-296C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722182 | |||||||
| chr2:205722725 | G | A | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664+17G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722725 | |||||||
| chr2:205722874 | T | C | 1 | a0001c0002t0020g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.664+166T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722874 | |||||||
| chr2:205722895 | C | T | 2 | a0001c0002t0007g0288 a0001c0002t0007g0289 |
2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.664+187C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722895 | |||||||
| chr2:205722947 | G | A | 62 | a0001c0002t0001g0056 a0001c0002t0001g0081 a0001c0002t0001g0083 others(59): Show |
62 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.664+239G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722947 | |||||||
| chr2:205723099 | A | T | 1 | a0001c0003t0006g0101 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.664+391A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723099 | |||||||
| chr2:205723183 | C | T | 299 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(296): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.664+475C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723183 | |||||||
| chr2:205723246 | G | A | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.664+538G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723246 | |||||||
| chr2:205723252 | G | A | 156 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(153): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.665-533G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723252 | |||||||
| chr2:205723389 | A | G | 1 | a0001c0003t0002g0334 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.665-396A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723389 | |||||||
| chr2:205723390 | T | G | 324 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(321): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.665-395T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723390 | |||||||
| chr2:205723751 | T | C | 2 | a0001c0002t0013g0197 a0001c0002t0013g0198 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-34T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723751 | |||||||
| chr2:205723996 | G | A | 3 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0061g0189 |
3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.820+56G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205723996 | |||||||
| chr2:205724047 | C | T | 1 | a0001c0001t0009g0319 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.820+107C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724047 | |||||||
| chr2:205724153 | AAT | A | 128 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(125): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.820+222_820+223del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724153 | ||||||
| chr2:205724160 | A | G | 1 | a0006c0028t0016g0142 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.820+220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724160 | |||||||
| chr2:205724341 | G | A | 1 | a0001c0004t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.820+401G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724341 | |||||||
| chr2:205724363 | A | T | 4 | a0001c0002t0001g0190 a0001c0002t0004g0139 a0001c0002t0004g0191 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+423A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724363 | |||||||
| chr2:205724386 | T | C | 1 | a0001c0001t0004g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.820+446T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724386 | |||||||
| chr2:205724397 | A | G | 149 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(146): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.820+457A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724397 | |||||||
| chr2:205724534 | C | G | 1 | a0001c0004t0006g0122 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.820+594C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724534 | |||||||
| chr2:205724654 | C | CT | 148 | a0001c0001t0001g0045 a0001c0001t0001g0103 a0001c0001t0001g0157 others(145): Show |
148 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.820+740dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | ||||||
| chr2:205724654 | C | CTT | 33 | a0001c0001t0019g0089 a0001c0002t0002g0262 a0001c0002t0003g0203 others(30): Show |
33 | HG00735.hp2 HG01361.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.820+739_820+740dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | ||||||
| chr2:205724654 | CT | C | 12 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(9): Show |
12 | HG00408.hp1 HG00408.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.820+740delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | ||||||
| chr2:205724749 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.820+809C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724749 | |||||||
| chr2:205724896 | C | G | 333 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.820+956C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724896 | |||||||
| chr2:205725153 | C | G | 1 | a0001c0002t0022g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.821-760C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725153 | |||||||
| chr2:205725240 | C | T | 3 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 |
3 | HG02630.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.821-673C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725240 | |||||||
| chr2:205725369 | G | A | 2 | a0001c0003t0021g0057 a0001c0003t0021g0058 |
2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.821-544G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725369 | |||||||
| chr2:205725509 | G | T | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.821-404G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725509 | |||||||
| chr2:205725511 | G | A | 2 | a0001c0003t0011g0247 a0001c0003t0011g0248 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.821-402G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725511 | |||||||
| chr2:205725559 | G | A | 4 | a0001c0011t0004g0170 a0001c0011t0008g0134 a0001c0012t0004g0137 others(1): Show |
4 | HG02622.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-354G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725559 | |||||||
| chr2:205725865 | G | A | 1 | a0001c0003t0009g0292 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.821-48G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725865 | |||||||
| chr2:205725898 | G | A | 1 | a0001c0002t0008g0140 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.821-15G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725898 | |||||||
| chr2:205726155 | C | T | 59 | a0001c0002t0001g0056 a0001c0002t0001g0081 a0001c0002t0001g0083 others(56): Show |
59 | HG01081.hp1 HG01167.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.990+73C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726155 | |||||||
| chr2:205726550 | C | T | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+468C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726550 | |||||||
| chr2:205726690 | A | G | 1 | a0001c0001t0053g0158 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.990+608A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726690 | |||||||
| chr2:205726883 | C | G | 178 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(175): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.990+801C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726883 | |||||||
| chr2:205727027 | C | A | 1 | a0001c0001t0003g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.991-864C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727027 | |||||||
| chr2:205727344 | C | T | 9 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(6): Show |
9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.991-547C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727344 | |||||||
| chr2:205727419 | C | A | 1 | a0001c0002t0007g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.991-472C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727419 | |||||||
| chr2:205727532 | A | C | 1 | a0001c0003t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.991-359A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727532 | |||||||
| chr2:205727677 | A | C | 3 | a0001c0009t0005g0001 a0001c0009t0021g0044 a0001c0009t0027g0030 |
4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-214A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727677 | |||||||
| chr2:205727801 | A | G | 163 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.991-90A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727801 | |||||||
| chr2:205727810 | T | C | 76 | a0001c0001t0001g0103 a0001c0001t0005g0095 a0001c0002t0001g0056 others(73): Show |
76 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(73): Show |
intron_variant | MODIFIER | c.991-81T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727810 | |||||||
| chr2:205727825 | G | GA | 3 | a0001c0009t0005g0001 a0001c0009t0021g0044 a0001c0009t0027g0030 |
4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-59dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 205727825 | ||||||
| chr2:205728183 | G | A | 1 | a0001c0002t0005g0029 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1146+137G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728183 | |||||||
| chr2:205728195 | A | C | 1 | a0001c0001t0010g0313 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1146+149A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728195 | |||||||
| chr2:205728234 | G | A | 13 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(10): Show |
14 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146+188G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728234 | |||||||
| chr2:205728517 | T | C | 164 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1146+471T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728517 | |||||||
| chr2:205728593 | T | C | 1 | a0001c0001t0010g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1146+547T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728593 | |||||||
| chr2:205728825 | T | C | 1 | a0001c0002t0043g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1146+779T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728825 | |||||||
| chr2:205728854 | C | G | 1 | a0001c0012t0004g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1146+808C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728854 | |||||||
| chr2:205728906 | T | C | 335 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1146+860T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728906 | |||||||
| chr2:205728971 | C | T | 1 | a0001c0001t0058g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1146+925C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728971 | |||||||
| chr2:205728979 | G | A | 13 | a0001c0002t0004g0181 a0001c0002t0007g0283 a0001c0002t0007g0284 others(10): Show |
14 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146+933G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728979 | |||||||
| chr2:205728996 | A | G | 53 | a0001c0001t0012g0019 a0001c0002t0001g0014 a0001c0002t0002g0279 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1146+950A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728996 | |||||||
| chr2:205729224 | T | C | 3 | a0002c0015t0030g0004 a0002c0017t0062g0177 a0002c0027t0064g0176 |
4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+1178T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729224 | |||||||
| chr2:205729230 | T | C | 8 | a0001c0002t0016g0133 a0001c0006t0007g0306 a0001c0006t0011g0337 others(5): Show |
8 | HG02055.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146+1184T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729230 | |||||||
| chr2:205729252 | T | C | 1 | a0001c0002t0004g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1146+1206T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729252 | |||||||
| chr2:205729319 | G | A | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1146+1273G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729319 | |||||||
| chr2:205729324 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1146+1278G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729324 | |||||||
| chr2:205729347 | G | C | 2 | a0001c0002t0049g0172 a0001c0007t0008g0062 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1146+1301G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729347 | |||||||
| chr2:205729417 | G | T | 146 | a0001c0002t0001g0014 a0001c0002t0001g0081 a0001c0002t0001g0083 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(143): Show |
intron_variant | MODIFIER | c.1146+1371G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729417 | |||||||
| chr2:205729444 | G | A | 3 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 |
3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+1398G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729444 | |||||||
| chr2:205729512 | G | A | 1 | a0008c0021t0004g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1146+1466G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729512 | |||||||
| chr2:205729640 | G | T | 3 | a0001c0002t0004g0011 a0001c0002t0018g0009 a0001c0002t0018g0010 |
3 | HG00741.hp2 HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1146+1594G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729640 | |||||||
| chr2:205729855 | A | G | 5 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0003t0004g0167 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+1809A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729855 | |||||||
| chr2:205730111 | C | A | 7 | a0001c0002t0004g0181 a0001c0002t0007g0126 a0001c0002t0007g0284 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146+2065C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730111 | |||||||
| chr2:205730200 | A | T | 1 | a0001c0002t0008g0140 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1146+2154A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730200 | |||||||
| chr2:205730219 | T | C | 2 | a0001c0003t0002g0327 a0001c0003t0014g0016 |
2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1146+2173T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730219 | |||||||
| chr2:205730448 | G | A | 2 | a0001c0003t0003g0295 a0001c0003t0005g0082 |
2 | HG02080.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1146+2402G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730448 | |||||||
| chr2:205730488 | T | G | 6 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0007g0126 others(3): Show |
6 | HG01884.hp1 HG02015.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+2442T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730488 | |||||||
| chr2:205730614 | T | C | 205 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0035 others(202): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1146+2568T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730614 | |||||||
| chr2:205730708 | A | T | 1 | a0001c0003t0034g0333 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1146+2662A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730708 | |||||||
| chr2:205730812 | T | C | 1 | a0001c0001t0009g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1146+2766T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730812 | |||||||
| chr2:205730974 | C | T | 1 | a0001c0003t0022g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1146+2928C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730974 | |||||||
| chr2:205731086 | C | T | 90 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0035 others(87): Show |
90 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1146+3040C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731086 | |||||||
| chr2:205731212 | G | A | 140 | a0001c0001t0001g0020 a0001c0001t0001g0073 a0001c0001t0001g0103 others(137): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1146+3166G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731212 | |||||||
| chr2:205731338 | C | A | 58 | a0001c0001t0009g0239 a0001c0001t0011g0221 a0001c0001t0026g0013 others(55): Show |
58 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1146+3292C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731338 | |||||||
| chr2:205731395 | T | C | 64 | a0001c0001t0009g0239 a0001c0001t0011g0221 a0001c0001t0026g0013 others(61): Show |
64 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1146+3349T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731395 | |||||||
| chr2:205731410 | A | G | 6 | a0001c0001t0001g0053 a0001c0002t0008g0180 a0001c0011t0004g0170 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+3364A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731410 | |||||||
| chr2:205731420 | A | C | 1 | a0001c0004t0041g0343 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1146+3374A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731420 | |||||||
| chr2:205731566 | T | C | 5 | a0001c0001t0010g0313 a0001c0004t0003g0314 a0001c0004t0003g0315 others(2): Show |
5 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+3520T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731566 | |||||||
| chr2:205731732 | C | T | 1 | a0005c0019t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1146+3686C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731732 | |||||||
| chr2:205731939 | T | C | 96 | a0001c0001t0009g0239 a0001c0001t0011g0221 a0001c0001t0020g0031 others(93): Show |
98 | HG00735.hp1 HG00735.hp2 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1146+3893T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731939 | |||||||
| chr2:205732083 | T | G | 4 | a0001c0001t0001g0053 a0001c0002t0008g0180 a0001c0012t0004g0137 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+4037T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732083 | |||||||
| chr2:205732107 | A | G | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+4061A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732107 | |||||||
| chr2:205732371 | A | G | 2 | a0001c0003t0002g0327 a0001c0003t0014g0016 |
2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1146+4325A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732371 | |||||||
| chr2:205732455 | T | C | 3 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 |
3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+4409T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732455 | |||||||
| chr2:205732685 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1146+4639G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732685 | |||||||
| chr2:205732846 | T | C | 1 | a0001c0002t0028g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1146+4800T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732846 | |||||||
| chr2:205732877 | T | C | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1146+4831T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732877 | |||||||
| chr2:205732881 | T | TA | 8 | a0001c0001t0001g0053 a0001c0002t0008g0180 a0001c0002t0012g0130 others(5): Show |
8 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146+4842dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205732881 | ||||||
| chr2:205732931 | A | G | 1 | a0001c0003t0007g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1146+4885A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732931 | |||||||
| chr2:205733000 | G | C | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1146+4954G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733000 | |||||||
| chr2:205733009 | C | T | 247 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0073 others(244): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1146+4963C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733009 | |||||||
| chr2:205733145 | C | G | 143 | a0001c0001t0001g0020 a0001c0001t0001g0073 a0001c0001t0001g0103 others(140): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1146+5099C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733145 | |||||||
| chr2:205733303 | T | G | 4 | a0001c0002t0001g0168 a0001c0009t0005g0001 a0001c0009t0021g0044 others(1): Show |
5 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+5257T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733303 | |||||||
| chr2:205733344 | G | A | 4 | a0001c0001t0001g0053 a0001c0002t0008g0180 a0001c0012t0004g0137 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+5298G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733344 | |||||||
| chr2:205733434 | C | A | 3 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 |
3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+5388C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733434 | |||||||
| chr2:205733566 | C | T | 2 | a0001c0001t0005g0039 a0001c0001t0010g0244 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1146+5520C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733566 | |||||||
| chr2:205733569 | A | G | 2 | a0001c0002t0010g0277 a0001c0002t0010g0278 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1146+5523A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733569 | |||||||
| chr2:205733634 | A | G | 24 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0002g0261 others(21): Show |
24 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1146+5588A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733634 | |||||||
| chr2:205733718 | T | C | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(8): Show |
11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1146+5672T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733718 | |||||||
| chr2:205733829 | T | C | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+5783T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733829 | |||||||
| chr2:205733927 | G | A | 1 | a0001c0004t0005g0164 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1146+5881G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733927 | |||||||
| chr2:205733944 | C | T | 1 | a0001c0001t0058g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1146+5898C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733944 | |||||||
| chr2:205734067 | G | C | 3 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 |
3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+6021G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734067 | |||||||
| chr2:205734170 | T | TTA | 11 | a0001c0001t0001g0073 a0001c0001t0002g0235 a0001c0001t0015g0237 others(8): Show |
12 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1146+6141_1146+614 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | ||||||
| chr2:205734170 | T | TTATATA | 2 | a0001c0008t0004g0005 a0001c0008t0004g0196 |
3 | HG02630.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1146+6137_1146+614 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | ||||||
| chr2:205734170 | TTA | T | 62 | a0001c0001t0001g0053 a0001c0001t0009g0239 a0001c0001t0026g0013 others(59): Show |
63 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1146+6141_1146+614 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | ||||||
| chr2:205734215 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0053 a0001c0002t0008g0180 a0001c0012t0004g0137 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+6180_1146+618 others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734215 | ||||||
| chr2:205734339 | A | G | 1 | a0001c0001t0011g0331 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1147-6180A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734339 | |||||||
| chr2:205734375 | A | T | 1 | a0001c0003t0006g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1147-6144A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734375 | |||||||
| chr2:205734399 | G | GC | 46 | a0001c0001t0001g0067 a0001c0001t0002g0235 a0001c0001t0003g0243 others(43): Show |
47 | HG00741.hp2 HG01070.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1147-6111dupC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734399 | ||||||
| chr2:205734403 | C | CA | 20 | a0001c0002t0001g0014 a0001c0002t0002g0294 a0001c0002t0003g0203 others(17): Show |
20 | HG00735.hp2 HG01255.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1147-6116_1147-611 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734403 | |||||||
| chr2:205734406 | C | A | 1 | a0001c0002t0017g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1147-6113C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734406 | |||||||
| chr2:205734406 | C | CG | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-6113_1147-611 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734406 | |||||||
| chr2:205734416 | A | G | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-6103A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734416 | |||||||
| chr2:205734442 | G | C | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1147-6077G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734442 | |||||||
| chr2:205734477 | G | C | 11 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0002g0261 others(8): Show |
11 | HG01069.hp2 HG01261.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147-6042G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734477 | |||||||
| chr2:205734539 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1147-5980C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734539 | |||||||
| chr2:205734548 | G | T | 3 | a0001c0004t0002g0234 a0001c0004t0005g0055 a0001c0004t0008g0043 |
3 | HG03490.hp1 NA18954.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1147-5971G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734548 | |||||||
| chr2:205734704 | C | T | 241 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0073 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1147-5815C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734704 | |||||||
| chr2:205734769 | T | C | 2 | a0001c0002t0008g0012 a0001c0002t0025g0252 |
2 | HG01070.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1147-5750T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734769 | |||||||
| chr2:205734987 | C | T | 3 | a0001c0002t0007g0126 a0001c0002t0048g0124 a0001c0006t0007g0306 |
3 | HG01884.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1147-5532C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734987 | |||||||
| chr2:205735043 | G | A | 62 | a0001c0001t0009g0239 a0001c0001t0011g0221 a0001c0001t0026g0013 others(59): Show |
63 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1147-5476G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735043 | |||||||
| chr2:205735047 | C | T | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-5472C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735047 | |||||||
| chr2:205735077 | C | T | 7 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0011g0256 others(4): Show |
7 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147-5442C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735077 | |||||||
| chr2:205735234 | GA | G | 63 | a0001c0001t0009g0239 a0001c0001t0011g0221 a0001c0001t0026g0013 others(60): Show |
64 | HG00735.hp2 HG01070.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.1147-5280delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735234 | ||||||
| chr2:205735365 | T | C | 7 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0011g0256 others(4): Show |
7 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147-5154T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735365 | |||||||
| chr2:205735440 | G | GCTT | 17 | a0001c0002t0001g0168 a0001c0002t0001g0190 a0001c0002t0004g0139 others(14): Show |
19 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1147-5075_1147-507 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735440 | ||||||
| chr2:205735517 | GAATGAAT others(9): Show |
G | 17 | a0001c0002t0001g0168 a0001c0002t0001g0190 a0001c0002t0004g0139 others(14): Show |
19 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1147-4998_1147-498 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735517 | ||||||
| chr2:205735570 | G | A | 1 | a0001c0003t0006g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1147-4949G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735570 | |||||||
| chr2:205735817 | A | G | 29 | a0001c0002t0001g0168 a0001c0002t0001g0190 a0001c0002t0004g0139 others(26): Show |
31 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1147-4702A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735817 | |||||||
| chr2:205735940 | A | C | 3 | a0001c0004t0001g0003 a0001c0004t0003g0309 a0001c0004t0012g0145 |
4 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-4579A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735940 | |||||||
| chr2:205736199 | A | G | 16 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0002g0261 others(13): Show |
16 | HG01069.hp2 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1147-4320A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736199 | |||||||
| chr2:205736210 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG01943.hp2 HG02056.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1147-4309C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736210 | |||||||
| chr2:205736274 | A | G | 1 | a0001c0003t0040g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1147-4245A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736274 | |||||||
| chr2:205736517 | C | T | 2 | a0001c0004t0002g0312 a0001c0004t0003g0218 |
2 | NA18955.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1147-4002C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736517 | |||||||
| chr2:205736685 | A | G | 1 | a0001c0020t0012g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1147-3834A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736685 | |||||||
| chr2:205736785 | G | A | 3 | a0001c0004t0002g0219 a0001c0004t0002g0220 a0001c0004t0002g0245 |
3 | NA18965.hp2 NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1147-3734G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736785 | |||||||
| chr2:205736828 | C | T | 4 | a0001c0002t0003g0203 a0001c0002t0003g0281 a0001c0002t0003g0282 others(1): Show |
4 | NA18953.hp1 NA18967.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-3691C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736828 | |||||||
| chr2:205736992 | A | C | 248 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(245): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1147-3527A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736992 | |||||||
| chr2:205737034 | A | T | 3 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 |
3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1147-3485A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737034 | |||||||
| chr2:205737039 | T | A | 4 | a0001c0002t0012g0130 a0001c0013t0016g0131 a0001c0013t0016g0132 others(1): Show |
4 | HG01109.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-3480T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737039 | |||||||
| chr2:205737043 | T | C | 2 | a0002c0015t0030g0004 a0002c0027t0064g0176 |
3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-3476T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737043 | |||||||
| chr2:205737066 | T | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1147-3453T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737066 | |||||||
| chr2:205737492 | T | C | 1 | a0001c0004t0026g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1147-3027T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737492 | |||||||
| chr2:205737518 | G | A | 99 | a0001c0001t0002g0223 a0001c0001t0008g0049 a0001c0001t0008g0078 others(96): Show |
101 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1147-3001G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737518 | |||||||
| chr2:205737792 | G | A | 32 | a0001c0001t0001g0053 a0001c0002t0001g0190 a0001c0002t0004g0191 others(29): Show |
32 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.1147-2727G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737792 | |||||||
| chr2:205737805 | C | A | 26 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0007g0126 others(23): Show |
26 | HG01884.hp1 HG02015.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1147-2714C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737805 | |||||||
| chr2:205737827 | T | C | 2 | a0001c0002t0049g0172 a0002c0016t0004g0339 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1147-2692T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737827 | |||||||
| chr2:205737843 | T | C | 2 | a0001c0003t0021g0057 a0001c0003t0021g0058 |
2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1147-2676T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737843 | |||||||
| chr2:205737986 | A | C | 105 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0011g0331 others(102): Show |
107 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1147-2533A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737986 | |||||||
| chr2:205738041 | C | T | 100 | a0001c0001t0001g0053 a0001c0001t0002g0223 a0001c0001t0008g0078 others(97): Show |
102 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1147-2478C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738041 | |||||||
| chr2:205738073 | C | T | 1 | a0001c0001t0005g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1147-2446C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738073 | |||||||
| chr2:205738159 | G | A | 2 | a0001c0001t0020g0031 a0001c0001t0020g0072 |
2 | HG01069.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1147-2360G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738159 | |||||||
| chr2:205738236 | T | C | 1 | a0001c0001t0004g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1147-2283T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738236 | |||||||
| chr2:205738331 | C | T | 2 | a0001c0001t0006g0113 a0001c0001t0006g0114 |
2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1147-2188C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738331 | |||||||
| chr2:205738516 | T | A | 339 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(336): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1147-2003T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738516 | |||||||
| chr2:205738585 | T | C | 122 | a0001c0001t0002g0223 a0001c0001t0005g0095 a0001c0001t0008g0078 others(119): Show |
124 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1147-1934T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738585 | |||||||
| chr2:205738718 | C | T | 1 | a0001c0001t0010g0209 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1147-1801C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738718 | |||||||
| chr2:205738774 | G | T | 2 | a0001c0002t0008g0199 a0001c0002t0008g0200 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1147-1745G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738774 | |||||||
| chr2:205738798 | G | T | 94 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0012g0102 others(91): Show |
96 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1147-1721G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738798 | |||||||
| chr2:205738841 | T | G | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1147-1678T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738841 | |||||||
| chr2:205738859 | G | A | 3 | a0002c0014t0001g0195 a0002c0014t0008g0194 a0002c0029t0013g0275 |
3 | HG01109.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1147-1660G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738859 | |||||||
| chr2:205738868 | C | T | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147-1651C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738868 | |||||||
| chr2:205739105 | G | A | 4 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0002g0263 others(1): Show |
4 | HG01069.hp2 HG01261.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-1414G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739105 | |||||||
| chr2:205739148 | T | C | 1 | a0001c0030t0052g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1147-1371T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739148 | |||||||
| chr2:205739265 | G | A | 1 | a0001c0004t0002g0201 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1147-1254G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739265 | |||||||
| chr2:205739367 | A | G | 68 | a0001c0001t0001g0073 a0001c0001t0001g0157 a0001c0001t0002g0006 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1147-1152A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739367 | |||||||
| chr2:205739506 | C | T | 1 | a0001c0002t0004g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1147-1013C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739506 | |||||||
| chr2:205739607 | G | C | 89 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1147-912G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739607 | |||||||
| chr2:205739665 | A | G | 5 | a0001c0002t0004g0139 a0001c0002t0017g0254 a0001c0002t0049g0172 others(2): Show |
5 | HG02976.hp1 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1147-854A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739665 | |||||||
| chr2:205739682 | C | CT | 81 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(78): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1147-817dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | ||||||
| chr2:205739682 | C | CTT | 6 | a0001c0001t0008g0078 a0001c0001t0010g0317 a0001c0002t0001g0168 others(3): Show |
6 | HG01934.hp1 HG03927.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1147-818_1147-817d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | ||||||
| chr2:205739682 | CT | C | 24 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(21): Show |
25 | HG01070.hp1 HG01106.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1147-817delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | ||||||
| chr2:205739682 | CTT | C | 75 | a0001c0001t0002g0223 a0001c0001t0012g0102 a0001c0002t0008g0199 others(72): Show |
77 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1147-818_1147-817d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | ||||||
| chr2:205739682 | CTTT | C | 17 | a0001c0003t0001g0098 a0001c0003t0001g0161 a0001c0003t0003g0107 others(14): Show |
17 | HG02056.hp2 NA18747.hp2 NA18950.hp2 others(14): Show |
intron_variant | MODIFIER | c.1147-819_1147-817d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | ||||||
| chr2:205739696 | T | G | 1 | a0001c0001t0005g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1147-823T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739696 | |||||||
| chr2:205739705 | G | A | 92 | a0001c0001t0002g0223 a0001c0001t0012g0102 a0001c0002t0008g0199 others(89): Show |
94 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1147-814G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739705 | |||||||
| chr2:205739874 | C | T | 1 | a0001c0002t0006g0146 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1147-645C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739874 | |||||||
| chr2:205739875 | A | G | 336 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1147-644A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739875 | |||||||
| chr2:205740089 | C | G | 1 | a0001c0030t0052g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1147-430C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740089 | |||||||
| chr2:205740281 | T | C | 1 | a0001c0003t0003g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1147-238T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740281 | |||||||
| chr2:205740347 | AT | A | 4 | a0001c0001t0001g0020 a0001c0001t0020g0031 a0001c0001t0020g0072 others(1): Show |
4 | HG01069.hp2 HG01261.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-164delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205740347 | ||||||
| chr2:205740456 | T | G | 120 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0011g0331 others(117): Show |
122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1147-63T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740456 | |||||||
| chr2:205740499 | T | C | 4 | a0001c0003t0002g0327 a0001c0003t0014g0016 a0001c0004t0002g0227 others(1): Show |
4 | HG00140.hp2 HG01975.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-20T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740499 | |||||||
| chr2:205740879 | T | C | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+216T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205740879 | |||||||
| chr2:205740994 | T | TA | 102 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0011g0331 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1291+334dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 205740994 | ||||||
| chr2:205741034 | G | A | 102 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0011g0331 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1291+371G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741034 | |||||||
| chr2:205741099 | C | T | 93 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0012g0102 others(90): Show |
95 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1291+436C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741099 | |||||||
| chr2:205741138 | G | A | 17 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0007g0283 others(14): Show |
17 | HG01884.hp2 HG02015.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291+475G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741138 | |||||||
| chr2:205741142 | G | A | 105 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(102): Show |
106 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1291+479G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741142 | |||||||
| chr2:205741168 | T | C | 123 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1291+505T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741168 | |||||||
| chr2:205741272 | C | T | 1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1291+609C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741272 | |||||||
| chr2:205741317 | G | A | 93 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0012g0102 others(90): Show |
95 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1291+654G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741317 | |||||||
| chr2:205741329 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1291+666A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741329 | |||||||
| chr2:205741459 | A | G | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+796A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741459 | |||||||
| chr2:205741687 | C | T | 1 | a0001c0002t0009g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1291+1024C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741687 | |||||||
| chr2:205742072 | T | A | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(8): Show |
11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-1131T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742072 | |||||||
| chr2:205742152 | A | C | 1 | a0001c0002t0001g0190 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1292-1051A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742152 | |||||||
| chr2:205742163 | G | C | 135 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0012g0102 others(132): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1292-1040G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742163 | |||||||
| chr2:205742174 | T | C | 135 | a0001c0001t0002g0223 a0001c0001t0005g0095 a0001c0001t0008g0078 others(132): Show |
138 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1292-1029T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742174 | |||||||
| chr2:205742194 | T | A | 55 | a0001c0001t0001g0073 a0001c0001t0001g0157 a0001c0001t0002g0006 others(52): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1292-1009T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742194 | |||||||
| chr2:205742219 | A | G | 3 | a0001c0008t0004g0005 a0001c0008t0004g0128 a0001c0008t0004g0196 |
4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-984A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742219 | |||||||
| chr2:205742335 | T | C | 8 | a0001c0003t0004g0167 a0001c0003t0007g0249 a0001c0003t0011g0247 others(5): Show |
8 | HG01891.hp2 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-868T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742335 | |||||||
| chr2:205742339 | T | C | 1 | a0001c0003t0021g0057 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1292-864T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742339 | |||||||
| chr2:205742352 | A | G | 2 | a0002c0014t0001g0195 a0002c0014t0008g0194 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1292-851A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742352 | |||||||
| chr2:205742433 | G | A | 1 | a0001c0002t0011g0256 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1292-770G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742433 | |||||||
| chr2:205742460 | C | A | 1 | a0001c0001t0004g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1292-743C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742460 | |||||||
| chr2:205742506 | A | T | 130 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0011g0331 others(127): Show |
132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1292-697A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742506 | |||||||
| chr2:205742512 | C | G | 1 | a0001c0001t0004g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1292-691C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742512 | |||||||
| chr2:205742604 | G | A | 3 | a0001c0018t0038g0308 a0002c0015t0030g0004 a0002c0027t0064g0176 |
4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-599G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742604 | |||||||
| chr2:205742700 | T | C | 1 | a0001c0001t0007g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1292-503T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742700 | |||||||
| chr2:205742832 | T | C | 4 | a0001c0001t0003g0264 a0001c0001t0005g0007 a0001c0001t0005g0034 others(1): Show |
4 | HG02135.hp2 NA18975.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-371T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742832 | |||||||
| chr2:205742976 | C | T | 53 | a0001c0001t0001g0073 a0001c0001t0001g0157 a0001c0001t0002g0006 others(50): Show |
54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1292-227C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742976 | |||||||
| chr2:205743170 | A | G | 2 | a0001c0002t0028g0186 a0001c0002t0028g0187 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1292-33A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205743170 | |||||||
| chr2:205743580 | C | T | 2 | a0002c0017t0062g0177 a0002c0029t0013g0275 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1641+28C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743580 | |||||||
| chr2:205743658 | A | G | 1 | a0001c0002t0004g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1641+106A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743658 | |||||||
| chr2:205743672 | A | G | 3 | a0001c0001t0001g0053 a0001c0002t0007g0284 a0001c0002t0020g0185 |
3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1641+120A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743672 | |||||||
| chr2:205743740 | T | TTTTG | 119 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(116): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1641+208_1641+211d others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 205743740 | ||||||
| chr2:205743837 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1641+285G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743837 | |||||||
| chr2:205743897 | C | G | 1 | a0001c0001t0027g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1641+345C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743897 | |||||||
| chr2:205743975 | C | T | 3 | a0001c0001t0001g0053 a0001c0002t0007g0284 a0001c0002t0020g0185 |
3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1641+423C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743975 | |||||||
| chr2:205744043 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1641+491C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744043 | |||||||
| chr2:205744086 | C | T | 2 | a0001c0002t0014g0159 a0001c0005t0014g0127 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1641+534C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744086 | |||||||
| chr2:205744105 | T | C | 6 | a0001c0002t0004g0139 a0001c0002t0017g0254 a0001c0002t0049g0172 others(3): Show |
6 | HG02976.hp1 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1641+553T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744105 | |||||||
| chr2:205744198 | G | A | 1 | a0001c0004t0019g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1641+646G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744198 | |||||||
| chr2:205744250 | C | T | 1 | a0001c0010t0009g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1641+698C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744250 | |||||||
| chr2:205744360 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1641+808C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744360 | |||||||
| chr2:205744470 | C | T | 1 | a0001c0004t0006g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1641+918C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744470 | |||||||
| chr2:205744540 | C | T | 86 | a0001c0003t0001g0084 a0001c0003t0001g0098 a0001c0003t0001g0149 others(83): Show |
88 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1641+988C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744540 | |||||||
| chr2:205744567 | C | T | 1 | a0001c0002t0028g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1641+1015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744567 | |||||||
| chr2:205744702 | C | T | 4 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-1044C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744702 | |||||||
| chr2:205744796 | G | A | 1 | a0001c0006t0007g0306 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1642-950G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744796 | |||||||
| chr2:205744859 | C | T | 1 | a0001c0003t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1642-887C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744859 | |||||||
| chr2:205744860 | G | A | 1 | a0001c0003t0003g0216 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1642-886G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744860 | |||||||
| chr2:205745150 | A | G | 337 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1642-596A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745150 | |||||||
| chr2:205745233 | A | G | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1642-513A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745233 | |||||||
| chr2:205745264 | G | A | 96 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(93): Show |
97 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1642-482G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745264 | |||||||
| chr2:205745327 | A | G | 170 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0002g0215 others(167): Show |
174 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1642-419A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745327 | |||||||
| chr2:205745346 | T | C | 319 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1642-400T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745346 | |||||||
| chr2:205745405 | C | G | 13 | a0001c0001t0002g0215 a0001c0002t0007g0126 a0001c0002t0008g0180 others(10): Show |
13 | HG00140.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1642-341C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745405 | |||||||
| chr2:205745501 | T | C | 15 | a0001c0001t0001g0053 a0001c0002t0007g0284 a0001c0002t0008g0199 others(12): Show |
16 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1642-245T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745501 | |||||||
| chr2:205745610 | A | T | 3 | a0001c0009t0005g0001 a0001c0009t0021g0044 a0001c0009t0027g0030 |
4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-136A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745610 | |||||||
| chr2:205745953 | C | T | 3 | a0001c0009t0005g0001 a0001c0009t0021g0044 a0001c0009t0027g0030 |
4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+63C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205745953 | |||||||
| chr2:205745974 | G | A | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1786+84G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205745974 | |||||||
| chr2:205746045 | T | C | 1 | a0001c0002t0054g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786+155T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746045 | |||||||
| chr2:205746626 | T | C | 328 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(325): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1786+736T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746626 | |||||||
| chr2:205746639 | G | C | 2 | a0002c0014t0001g0195 a0002c0014t0008g0194 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+749G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746639 | |||||||
| chr2:205746692 | T | C | 2 | a0002c0014t0001g0195 a0002c0014t0008g0194 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+802T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746692 | |||||||
| chr2:205746734 | T | C | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1786+844T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746734 | |||||||
| chr2:205746754 | C | T | 3 | a0001c0001t0001g0053 a0001c0002t0007g0284 a0001c0002t0020g0185 |
3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1786+864C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746754 | |||||||
| chr2:205747030 | G | A | 7 | a0001c0001t0001g0053 a0001c0002t0007g0284 a0001c0002t0020g0185 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1786+1140G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747030 | |||||||
| chr2:205747107 | G | A | 1 | a0001c0001t0011g0331 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1786+1217G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747107 | |||||||
| chr2:205747109 | T | C | 2 | a0001c0003t0004g0167 a0001c0004t0022g0183 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1786+1219T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747109 | |||||||
| chr2:205747167 | A | C | 5 | a0001c0002t0004g0139 a0001c0002t0049g0172 a0001c0005t0004g0048 others(2): Show |
5 | HG02559.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+1277A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747167 | |||||||
| chr2:205747197 | G | T | 3 | a0001c0002t0042g0212 a0001c0002t0051g0182 a0001c0002t0054g0214 |
3 | HG02145.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1786+1307G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747197 | |||||||
| chr2:205747306 | G | T | 4 | a0001c0002t0016g0133 a0001c0012t0017g0272 a0001c0013t0016g0131 others(1): Show |
4 | HG02717.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1416G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747306 | |||||||
| chr2:205747454 | G | C | 2 | a0001c0002t0017g0254 a0001c0005t0013g0175 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1786+1564G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747454 | |||||||
| chr2:205747588 | C | T | 6 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0002g0261 others(3): Show |
6 | HG01069.hp2 HG01261.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+1698C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747588 | |||||||
| chr2:205747597 | C | G | 1 | a0001c0001t0002g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1786+1707C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747597 | |||||||
| chr2:205747861 | T | C | 102 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0001g0157 others(99): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1787-1864T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747861 | |||||||
| chr2:205747990 | G | A | 45 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0063 others(42): Show |
46 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1787-1735G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747990 | |||||||
| chr2:205747996 | G | A | 1 | a0001c0005t0004g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1787-1729G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747996 | |||||||
| chr2:205748071 | G | C | 117 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(114): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1787-1654G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748071 | |||||||
| chr2:205748076 | C | T | 5 | a0001c0002t0007g0283 a0001c0006t0007g0329 a0001c0018t0038g0308 others(2): Show |
6 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1787-1649C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748076 | |||||||
| chr2:205748083 | T | A | 4 | a0001c0001t0004g0040 a0001c0001t0012g0019 a0001c0001t0031g0328 others(1): Show |
4 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1642T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748083 | |||||||
| chr2:205748211 | G | A | 4 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-1514G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748211 | |||||||
| chr2:205748228 | T | C | 9 | a0001c0003t0001g0149 a0001c0003t0001g0150 a0001c0003t0001g0151 others(6): Show |
9 | NA18966.hp2 NA18967.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1787-1497T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748228 | |||||||
| chr2:205748256 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1787-1469T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748256 | |||||||
| chr2:205748262 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1787-1463G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748262 | |||||||
| chr2:205748557 | G | A | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-1168G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748557 | |||||||
| chr2:205748709 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1787-1016G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748709 | |||||||
| chr2:205748940 | C | G | 1 | a0001c0001t0015g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1787-785C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748940 | |||||||
| chr2:205749095 | A | C | 6 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0007t0008g0062 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1787-630A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749095 | |||||||
| chr2:205749123 | T | A | 2 | a0001c0004t0002g0312 a0001c0004t0003g0218 |
2 | NA18955.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1787-602T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749123 | |||||||
| chr2:205749337 | T | G | 4 | a0001c0001t0008g0046 a0001c0002t0007g0126 a0001c0002t0011g0256 others(1): Show |
4 | HG01884.hp1 HG02015.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-388T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749337 | |||||||
| chr2:205749367 | T | G | 174 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(171): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1787-358T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749367 | |||||||
| chr2:205749420 | G | A | 1 | a0001c0003t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1787-305G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749420 | |||||||
| chr2:205749426 | A | G | 141 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0157 others(138): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1787-299A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749426 | |||||||
| chr2:205749436 | A | G | 213 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1787-289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749436 | |||||||
| chr2:205749922 | T | G | 190 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(187): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1903+81T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205749922 | |||||||
| chr2:205749924 | G | T | 4 | a0001c0002t0008g0199 a0001c0002t0008g0200 a0001c0002t0013g0197 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+83G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205749924 | |||||||
| chr2:205750224 | G | A | 2 | a0001c0002t0017g0254 a0001c0005t0013g0175 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1903+383G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750224 | |||||||
| chr2:205750240 | G | C | 201 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(198): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1903+399G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750240 | |||||||
| chr2:205750342 | A | G | 178 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(175): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1903+501A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750342 | |||||||
| chr2:205750413 | G | C | 4 | a0001c0001t0008g0049 a0001c0005t0007g0222 a0001c0005t0023g0119 others(1): Show |
4 | HG01074.hp2 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+572G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750413 | |||||||
| chr2:205750454 | C | T | 1 | a0001c0002t0008g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1903+613C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750454 | |||||||
| chr2:205750537 | T | G | 6 | a0001c0002t0002g0279 a0001c0002t0005g0029 a0001c0002t0010g0276 others(3): Show |
6 | HG00140.hp1 HG01074.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903+696T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750537 | |||||||
| chr2:205750786 | T | C | 1 | a0001c0001t0009g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1903+945T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750786 | |||||||
| chr2:205750815 | T | C | 187 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(184): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1903+974T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750815 | |||||||
| chr2:205750953 | C | T | 16 | a0001c0001t0001g0067 a0001c0001t0002g0006 a0001c0001t0003g0225 others(13): Show |
17 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1903+1112C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750953 | |||||||
| chr2:205751189 | C | A | 11 | a0001c0001t0002g0246 a0001c0001t0003g0240 a0001c0003t0001g0084 others(8): Show |
11 | HG00438.hp2 HG00621.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1903+1348C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751189 | |||||||
| chr2:205751245 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1903+1404C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751245 | |||||||
| chr2:205751287 | T | C | 4 | a0001c0001t0008g0046 a0001c0002t0007g0126 a0001c0002t0011g0256 others(1): Show |
4 | HG01884.hp1 HG02015.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903+1446T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751287 | |||||||
| chr2:205751350 | T | C | 5 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0007t0008g0062 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1904-1485T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751350 | |||||||
| chr2:205751381 | T | C | 1 | a0001c0001t0006g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1904-1454T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751381 | |||||||
| chr2:205751425 | C | T | 2 | a0001c0001t0007g0213 a0001c0001t0010g0228 |
2 | HG00280.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1904-1410C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751425 | |||||||
| chr2:205751426 | G | A | 15 | a0001c0002t0008g0180 a0001c0002t0022g0184 a0001c0002t0029g0135 others(12): Show |
15 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904-1409G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751426 | |||||||
| chr2:205751485 | T | TA | 5 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0007t0008g0062 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1904-1348dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 205751485 | ||||||
| chr2:205751651 | A | G | 6 | a0001c0002t0029g0135 a0001c0002t0063g0136 a0001c0007t0013g0188 others(3): Show |
6 | HG02258.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1904-1184A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751651 | |||||||
| chr2:205752057 | A | G | 1 | a0001c0002t0004g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1904-778A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205752057 | |||||||
| chr2:205753126 | C | A | 1 | a0001c0002t0028g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2044+151C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753126 | |||||||
| chr2:205753350 | G | A | 1 | a0003c0026t0004g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2044+375G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753350 | |||||||
| chr2:205753568 | A | G | 5 | a0001c0001t0008g0046 a0001c0002t0007g0126 a0001c0002t0011g0256 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+593A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753568 | |||||||
| chr2:205753672 | C | T | 4 | a0001c0001t0003g0268 a0001c0001t0006g0113 a0001c0001t0010g0229 others(1): Show |
4 | HG00642.hp2 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+697C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753672 | |||||||
| chr2:205753719 | G | A | 1 | a0001c0009t0005g0001 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2044+744G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753719 | |||||||
| chr2:205754083 | C | T | 1 | a0001c0004t0006g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2044+1108C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754083 | |||||||
| chr2:205754126 | C | T | 1 | a0001c0003t0001g0152 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2044+1151C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754126 | |||||||
| chr2:205754199 | G | C | 7 | a0001c0001t0008g0046 a0001c0002t0007g0126 a0001c0002t0011g0256 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044+1224G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754199 | |||||||
| chr2:205754224 | G | T | 18 | a0001c0001t0001g0053 a0001c0001t0004g0040 a0001c0001t0018g0018 others(15): Show |
18 | HG01069.hp2 HG01256.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2044+1249G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754224 | |||||||
| chr2:205754599 | G | C | 1 | a0001c0002t0043g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2044+1624G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754599 | |||||||
| chr2:205754805 | G | GGT | 151 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0157 others(148): Show |
152 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2044+1843_2044+184 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205754805 | ||||||
| chr2:205754847 | G | T | 3 | a0001c0001t0008g0046 a0001c0002t0011g0256 a0001c0006t0007g0306 |
3 | HG02015.hp2 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2044+1872G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754847 | |||||||
| chr2:205754869 | C | T | 2 | a0001c0008t0004g0128 a0002c0029t0013g0275 |
2 | HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2044+1894C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754869 | |||||||
| chr2:205755044 | G | A | 1 | a0001c0006t0009g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2044+2069G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755044 | |||||||
| chr2:205755151 | A | G | 1 | a0001c0003t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2044+2176A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755151 | |||||||
| chr2:205755164 | G | A | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+2189G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755164 | |||||||
| chr2:205755256 | G | A | 1 | a0001c0002t0002g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2044+2281G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755256 | |||||||
| chr2:205755263 | G | A | 3 | a0001c0002t0007g0283 a0001c0006t0007g0329 a0002c0015t0030g0004 |
4 | HG02922.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+2288G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755263 | |||||||
| chr2:205755308 | C | G | 303 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(300): Show |
309 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.2044+2333C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755308 | |||||||
| chr2:205755513 | A | C | 1 | a0001c0004t0002g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2044+2538A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755513 | |||||||
| chr2:205755596 | T | C | 2 | a0001c0001t0004g0116 a0001c0005t0023g0118 |
2 | HG01106.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2044+2621T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755596 | |||||||
| chr2:205755609 | G | GA | 162 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0157 others(159): Show |
165 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2044+2634_2044+263 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755609 | |||||||
| chr2:205755610 | G | A | 235 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(232): Show |
240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2044+2635G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755610 | |||||||
| chr2:205755704 | A | T | 2 | a0001c0002t0008g0180 a0001c0002t0022g0184 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2044+2729A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755704 | |||||||
| chr2:205755727 | G | A | 5 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0007t0008g0062 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+2752G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755727 | |||||||
| chr2:205755941 | G | C | 1 | a0002c0014t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2044+2966G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755941 | |||||||
| chr2:205756045 | C | G | 18 | a0001c0001t0001g0067 a0001c0001t0002g0006 a0001c0001t0003g0225 others(15): Show |
19 | HG00423.hp2 HG00741.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2044+3070C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756045 | |||||||
| chr2:205756544 | G | C | 1 | a0001c0007t0017g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2044+3569G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756544 | |||||||
| chr2:205756679 | T | C | 224 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(221): Show |
229 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2044+3704T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756679 | |||||||
| chr2:205756682 | G | C | 3 | a0001c0002t0017g0254 a0001c0005t0013g0175 a0001c0012t0017g0272 |
3 | HG02976.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2044+3707G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756682 | |||||||
| chr2:205756873 | T | C | 5 | a0001c0005t0004g0048 a0001c0012t0004g0137 a0002c0014t0001g0195 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+3898T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756873 | |||||||
| chr2:205756904 | G | T | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+3929G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756904 | |||||||
| chr2:205756968 | T | C | 6 | a0001c0001t0002g0215 a0001c0001t0008g0046 a0001c0002t0011g0256 others(3): Show |
6 | HG01346.hp2 HG01975.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044+3993T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756968 | |||||||
| chr2:205756981 | C | T | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2044+4006C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756981 | |||||||
| chr2:205757007 | A | G | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2044+4032A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757007 | |||||||
| chr2:205757264 | G | A | 30 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(27): Show |
32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2044+4289G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757264 | |||||||
| chr2:205757435 | G | A | 1 | a0001c0004t0006g0179 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2044+4460G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757435 | |||||||
| chr2:205757647 | A | G | 5 | a0001c0005t0004g0048 a0001c0012t0004g0137 a0002c0014t0001g0195 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+4672A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757647 | |||||||
| chr2:205757852 | A | G | 81 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0002g0210 others(78): Show |
83 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.2044+4877A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757852 | |||||||
| chr2:205757877 | A | G | 5 | a0001c0001t0009g0239 a0001c0001t0012g0026 a0001c0001t0012g0027 others(2): Show |
5 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+4902A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757877 | |||||||
| chr2:205757886 | C | T | 1 | a0001c0001t0015g0237 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2044+4911C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757886 | |||||||
| chr2:205757897 | CT | C | 19 | a0001c0001t0002g0215 a0001c0001t0008g0046 a0001c0001t0037g0323 others(16): Show |
19 | HG01099.hp2 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2044+4935delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | ||||||
| chr2:205757897 | CTT | C | 173 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(170): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2044+4934_2044+493 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | ||||||
| chr2:205757897 | CTTT | C | 29 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(26): Show |
31 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2044+4933_2044+493 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | ||||||
| chr2:205757898 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2044+4923T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757898 | |||||||
| chr2:205757921 | A | T | 1 | a0001c0013t0016g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2044+4946A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757921 | |||||||
| chr2:205758088 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2044+5113A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758088 | |||||||
| chr2:205758185 | T | C | 2 | a0001c0001t0004g0116 a0001c0005t0023g0118 |
2 | HG01106.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2044+5210T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758185 | |||||||
| chr2:205758194 | C | A | 3 | a0001c0002t0004g0274 a0001c0002t0028g0186 a0001c0002t0028g0187 |
3 | HG03098.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2044+5219C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758194 | |||||||
| chr2:205758195 | A | G | 3 | a0001c0002t0004g0274 a0001c0002t0028g0186 a0001c0002t0028g0187 |
3 | HG03098.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2044+5220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758195 | |||||||
| chr2:205758222 | A | G | 47 | a0001c0001t0001g0067 a0001c0001t0002g0210 a0001c0001t0002g0223 others(44): Show |
49 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.2044+5247A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758222 | |||||||
| chr2:205758263 | A | G | 1 | a0001c0003t0001g0149 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2044+5288A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758263 | |||||||
| chr2:205758518 | G | C | 18 | a0001c0001t0004g0040 a0001c0001t0018g0018 a0001c0002t0002g0261 others(15): Show |
18 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2045-5156G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758518 | |||||||
| chr2:205758547 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2045-5127G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758547 | |||||||
| chr2:205758603 | G | A | 30 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(27): Show |
32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2045-5071G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758603 | |||||||
| chr2:205758605 | G | A | 30 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(27): Show |
32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2045-5069G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758605 | |||||||
| chr2:205758659 | C | T | 5 | a0001c0003t0001g0149 a0001c0003t0001g0155 a0001c0003t0001g0156 others(2): Show |
5 | NA18966.hp2 NA18978.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-5015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758659 | |||||||
| chr2:205758870 | C | G | 106 | a0001c0001t0001g0073 a0001c0001t0001g0157 a0001c0001t0002g0257 others(103): Show |
107 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2045-4804C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758870 | |||||||
| chr2:205759054 | G | T | 13 | a0001c0002t0008g0180 a0001c0002t0022g0184 a0001c0002t0051g0182 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-4620G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759054 | |||||||
| chr2:205759202 | G | A | 1 | a0001c0004t0003g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2045-4472G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759202 | |||||||
| chr2:205759208 | G | C | 4 | a0001c0002t0004g0139 a0001c0002t0007g0284 a0001c0002t0008g0140 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-4466G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759208 | |||||||
| chr2:205759302 | G | T | 1 | a0001c0004t0008g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2045-4372G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759302 | |||||||
| chr2:205759303 | T | A | 1 | a0001c0004t0008g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2045-4371T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759303 | |||||||
| chr2:205759641 | G | T | 1 | a0001c0002t0007g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2045-4033G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759641 | |||||||
| chr2:205759678 | C | T | 1 | a0001c0002t0010g0276 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2045-3996C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759678 | |||||||
| chr2:205759821 | C | T | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2045-3853C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759821 | |||||||
| chr2:205759899 | T | A | 13 | a0001c0001t0004g0040 a0001c0001t0018g0018 a0001c0002t0004g0139 others(10): Show |
13 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-3775T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759899 | |||||||
| chr2:205759902 | A | G | 1 | a0001c0003t0035g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2045-3772A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759902 | |||||||
| chr2:205760161 | G | A | 1 | a0001c0002t0008g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2045-3513G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760161 | |||||||
| chr2:205760171 | G | A | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2045-3503G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760171 | |||||||
| chr2:205760542 | C | G | 59 | a0001c0001t0001g0053 a0001c0001t0002g0210 a0001c0001t0002g0223 others(56): Show |
61 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2045-3132C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760542 | |||||||
| chr2:205760653 | T | C | 237 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(234): Show |
241 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.2045-3021T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760653 | |||||||
| chr2:205760654 | G | A | 2 | a0001c0001t0005g0039 a0001c0001t0010g0244 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.2045-3020G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760654 | |||||||
| chr2:205761000 | G | T | 1 | a0001c0001t0004g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2045-2674G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761000 | |||||||
| chr2:205761039 | C | T | 1 | a0001c0003t0022g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2045-2635C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761039 | |||||||
| chr2:205761061 | A | G | 1 | a0001c0030t0052g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2045-2613A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761061 | |||||||
| chr2:205761115 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2045-2559G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761115 | |||||||
| chr2:205761177 | C | T | 1 | a0001c0004t0003g0206 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2045-2497C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761177 | |||||||
| chr2:205761288 | T | C | 1 | a0001c0001t0008g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2045-2386T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761288 | |||||||
| chr2:205761346 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(25): Show |
30 | HG00423.hp2 HG00741.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.2045-2328C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761346 | |||||||
| chr2:205761841 | T | C | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2045-1833T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761841 | |||||||
| chr2:205761861 | G | A | 58 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0002g0210 others(55): Show |
60 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2045-1813G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761861 | |||||||
| chr2:205761960 | T | C | 68 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0002g0210 others(65): Show |
70 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.2045-1714T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761960 | |||||||
| chr2:205762133 | T | G | 1 | a0001c0002t0016g0133 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2045-1541T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762133 | |||||||
| chr2:205762205 | C | T | 2 | a0001c0002t0029g0135 a0001c0002t0063g0136 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2045-1469C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762205 | |||||||
| chr2:205762222 | T | A | 1 | a0001c0001t0058g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2045-1452T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762222 | |||||||
| chr2:205762284 | G | A | 3 | a0001c0001t0012g0019 a0001c0001t0031g0328 a0001c0001t0057g0032 |
3 | HG00639.hp1 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2045-1390G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762284 | |||||||
| chr2:205762285 | A | G | 235 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(232): Show |
240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2045-1389A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762285 | |||||||
| chr2:205762297 | C | T | 5 | a0001c0002t0051g0182 a0001c0002t0054g0214 a0001c0007t0008g0062 others(2): Show |
5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-1377C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762297 | |||||||
| chr2:205762587 | G | A | 187 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0157 others(184): Show |
189 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.2045-1087G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762587 | |||||||
| chr2:205762659 | C | T | 3 | a0001c0001t0004g0040 a0001c0001t0018g0018 a0001c0002t0020g0185 |
3 | HG01256.hp2 HG02615.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2045-1015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762659 | |||||||
| chr2:205762686 | G | A | 17 | a0001c0001t0002g0006 a0001c0001t0003g0225 a0001c0001t0006g0065 others(14): Show |
19 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2045-988G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762686 | |||||||
| chr2:205762691 | T | C | 188 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0073 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2045-983T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762691 | |||||||
| chr2:205762749 | T | C | 70 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0002g0210 others(67): Show |
72 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2045-925T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762749 | |||||||
| chr2:205762966 | C | A | 4 | a0001c0001t0003g0225 a0001c0001t0006g0114 a0001c0004t0003g0309 others(1): Show |
4 | HG00741.hp1 HG01123.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2045-708C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762966 | |||||||
| chr2:205763087 | C | G | 1 | a0001c0003t0004g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2045-587C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763087 | |||||||
| chr2:205763244 | A | C | 7 | a0001c0002t0022g0184 a0001c0003t0004g0167 a0001c0003t0007g0249 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2045-430A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763244 | |||||||
| chr2:205763289 | C | G | 1 | a0001c0001t0026g0013 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2045-385C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763289 | |||||||
| chr2:205763333 | C | A | 2 | a0001c0001t0002g0316 a0001c0001t0009g0319 |
2 | NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2045-341C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763333 | |||||||
| chr2:205763348 | A | C | 1 | a0001c0003t0002g0327 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2045-326A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763348 | |||||||
| chr2:205763403 | T | C | 8 | a0001c0002t0008g0180 a0001c0002t0022g0184 a0001c0003t0004g0167 others(5): Show |
8 | HG01891.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2045-271T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763403 | |||||||
| chr2:205763445 | T | C | 14 | a0001c0001t0001g0053 a0001c0001t0020g0031 a0001c0001t0020g0072 others(11): Show |
14 | HG01069.hp2 HG01261.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2045-229T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763445 | |||||||
| chr2:205763476 | T | G | 3 | a0001c0001t0012g0019 a0001c0001t0031g0328 a0001c0001t0057g0032 |
3 | HG00639.hp1 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2045-198T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763476 | |||||||
| chr2:205764006 | T | C | 1 | a0001c0004t0013g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2307+70T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764006 | |||||||
| chr2:205764199 | T | A | 1 | a0001c0002t0002g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2307+263T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764199 | |||||||
| chr2:205764390 | A | T | 31 | a0001c0001t0002g0006 a0001c0001t0003g0202 a0001c0001t0003g0225 others(28): Show |
32 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2307+454A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764390 | |||||||
| chr2:205764505 | C | T | 2 | a0001c0001t0004g0116 a0001c0002t0004g0192 |
2 | HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2307+569C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764505 | |||||||
| chr2:205764517 | T | G | 1 | a0001c0002t0002g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2307+581T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764517 | |||||||
| chr2:205764537 | T | C | 6 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2307+601T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764537 | |||||||
| chr2:205764617 | A | G | 329 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(326): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2307+681A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764617 | |||||||
| chr2:205764652 | T | A | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2307+716T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764652 | |||||||
| chr2:205765349 | A | AAC | 200 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2308-107_2308-106d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 205765349 | ||||||
| chr2:205765369 | T | C | 2 | a0001c0002t0007g0284 a0001c0002t0008g0140 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2308-105T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205765369 | |||||||
| chr2:205765637 | G | A | 2 | a0001c0002t0022g0184 a0001c0002t0043g0258 |
2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2404+67G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765637 | |||||||
| chr2:205765759 | G | A | 5 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404+189G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765759 | |||||||
| chr2:205765783 | G | A | 11 | a0001c0002t0001g0190 a0001c0002t0004g0191 a0001c0002t0004g0274 others(8): Show |
12 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404+213G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765783 | |||||||
| chr2:205765827 | G | A | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2404+257G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765827 | |||||||
| chr2:205766163 | C | T | 96 | a0001c0001t0002g0257 a0001c0001t0003g0202 a0001c0001t0003g0243 others(93): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2404+593C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766163 | |||||||
| chr2:205766175 | C | G | 1 | a0001c0002t0004g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2404+605C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766175 | |||||||
| chr2:205766530 | A | G | 191 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0157 others(188): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2405-253A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766530 | |||||||
| chr2:205766676 | C | G | 1 | a0001c0001t0008g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2405-107C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766676 | |||||||
| chr2:205766830 | T | A | 2 | a0001c0002t0020g0185 a0001c0002t0042g0212 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2425+27T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766830 | |||||||
| chr2:205766877 | TG | T | 6 | a0001c0001t0012g0019 a0001c0001t0018g0018 a0001c0001t0031g0328 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425+80delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205766877 | ||||||
| chr2:205766897 | A | G | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+94A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766897 | |||||||
| chr2:205766926 | C | T | 3 | a0001c0011t0004g0170 a0001c0011t0008g0134 a0006c0028t0016g0142 |
3 | HG02622.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2425+123C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766926 | |||||||
| chr2:205766945 | T | C | 6 | a0001c0001t0002g0215 a0001c0001t0004g0017 a0001c0001t0004g0193 others(3): Show |
6 | HG01081.hp1 HG01099.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425+142T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766945 | |||||||
| chr2:205767041 | A | G | 2 | a0001c0001t0019g0089 a0001c0004t0003g0224 |
2 | HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2425+238A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767041 | |||||||
| chr2:205767145 | C | CA | 82 | a0001c0001t0002g0223 a0001c0001t0002g0257 a0001c0001t0002g0316 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2425+357dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767145 | ||||||
| chr2:205767145 | CA | C | 7 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(4): Show |
8 | HG02630.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2425+357delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767145 | ||||||
| chr2:205767543 | GAGA | G | 5 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+745_2425+747d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767543 | ||||||
| chr2:205767578 | T | TA | 25 | a0001c0001t0004g0060 a0001c0001t0008g0078 a0001c0002t0013g0197 others(22): Show |
25 | HG01109.hp1 HG01891.hp2 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.2425+788dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767578 | ||||||
| chr2:205767927 | G | A | 3 | a0001c0001t0020g0031 a0001c0001t0020g0072 a0001c0002t0020g0185 |
3 | HG01069.hp2 HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2425+1124G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767927 | |||||||
| chr2:205767954 | T | C | 1 | a0001c0003t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2425+1151T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767954 | |||||||
| chr2:205768108 | C | T | 2 | a0001c0003t0021g0057 a0001c0003t0021g0058 |
2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2425+1305C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768108 | |||||||
| chr2:205768121 | A | G | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+1318A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768121 | |||||||
| chr2:205768142 | C | T | 1 | a0001c0002t0007g0284 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2425+1339C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768142 | |||||||
| chr2:205768285 | T | C | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2425+1482T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768285 | |||||||
| chr2:205768778 | G | C | 8 | a0001c0002t0004g0191 a0001c0002t0004g0274 a0001c0002t0028g0186 others(5): Show |
8 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425+1975G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768778 | |||||||
| chr2:205768783 | C | T | 7 | a0001c0002t0051g0182 a0001c0003t0007g0249 a0001c0003t0011g0247 others(4): Show |
7 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2425+1980C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768783 | |||||||
| chr2:205768784 | G | A | 1 | a0001c0013t0016g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2425+1981G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768784 | |||||||
| chr2:205768955 | A | G | 2 | a0001c0002t0008g0140 a0001c0002t0046g0141 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2425+2152A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768955 | |||||||
| chr2:205769119 | C | A | 146 | a0001c0001t0002g0006 a0001c0001t0002g0215 a0001c0001t0002g0223 others(143): Show |
149 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.2425+2316C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769119 | |||||||
| chr2:205769484 | G | C | 1 | a0001c0003t0002g0297 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2425+2681G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769484 | |||||||
| chr2:205769492 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2425+2689G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769492 | |||||||
| chr2:205769505 | T | C | 2 | a0001c0001t0001g0103 a0001c0002t0010g0276 |
2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2425+2702T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769505 | |||||||
| chr2:205769505 | T | TAC | 14 | a0001c0001t0001g0053 a0001c0001t0008g0046 a0001c0002t0008g0123 others(11): Show |
15 | HG00408.hp2 HG01169.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2425+2736_2425+273 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACAC | 18 | a0001c0001t0001g0063 a0001c0001t0002g0006 a0001c0002t0002g0261 others(15): Show |
20 | HG00140.hp1 HG00735.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2425+2734_2425+273 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACAC | 117 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0045 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.2425+2732_2425+273 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(1): Show |
75 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0036 others(72): Show |
75 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2425+2730_2425+273 others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(3): Show |
48 | a0001c0001t0002g0223 a0001c0001t0002g0257 a0001c0001t0002g0316 others(45): Show |
48 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2425+2728_2425+273 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(5): Show |
9 | a0001c0001t0001g0059 a0001c0001t0002g0215 a0001c0001t0005g0007 others(6): Show |
9 | HG01346.hp2 HG02004.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.2425+2726_2425+273 others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(7): Show |
6 | a0001c0001t0003g0264 a0001c0001t0010g0265 a0001c0003t0024g0344 others(3): Show |
6 | HG02135.hp2 HG03195.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.2425+2724_2425+273 others(18): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(9): Show |
1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2425+2722_2425+273 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | T | TACACACA others(17): Show |
1 | a0001c0001t0005g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2425+2714_2425+273 others(28): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | TAC | T | 10 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(7): Show |
10 | HG01243.hp1 HG02717.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+2736_2425+273 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769505 | TACAC | T | 13 | a0001c0002t0008g0140 a0001c0002t0016g0133 a0001c0002t0022g0184 others(10): Show |
14 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2425+2734_2425+273 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | ||||||
| chr2:205769541 | G | C | 1 | a0001c0004t0002g0280 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2425+2738G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769541 | |||||||
| chr2:205769864 | G | T | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2425+3061G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769864 | |||||||
| chr2:205769885 | C | T | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2425+3082C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769885 | |||||||
| chr2:205770145 | G | A | 125 | a0001c0001t0002g0006 a0001c0001t0002g0215 a0001c0001t0002g0257 others(122): Show |
127 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.2425+3342G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770145 | |||||||
| chr2:205770169 | C | T | 1 | a0001c0030t0052g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2425+3366C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770169 | |||||||
| chr2:205770467 | ATC | A | 99 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0053 others(96): Show |
99 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2425+3668_2425+366 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205770467 | ||||||
| chr2:205770573 | G | C | 1 | a0001c0001t0008g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2425+3770G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770573 | |||||||
| chr2:205770974 | A | G | 3 | a0001c0002t0004g0192 a0001c0003t0008g0171 a0001c0005t0004g0048 |
3 | HG01243.hp1 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2425+4171A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770974 | |||||||
| chr2:205770975 | T | C | 3 | a0001c0001t0004g0017 a0001c0002t0004g0011 a0001c0002t0033g0293 |
3 | HG01099.hp1 HG01496.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2425+4172T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770975 | |||||||
| chr2:205770988 | C | T | 1 | a0001c0005t0013g0175 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2425+4185C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770988 | |||||||
| chr2:205771107 | G | A | 8 | a0001c0002t0051g0182 a0001c0002t0063g0136 a0001c0003t0007g0249 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2425+4304G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771107 | |||||||
| chr2:205771190 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2425+4387T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771190 | |||||||
| chr2:205771209 | TC | T | 3 | a0001c0002t0008g0180 a0001c0002t0042g0212 a0003c0025t0013g0166 |
3 | HG02145.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2425+4409delC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205771209 | ||||||
| chr2:205771287 | G | A | 5 | a0001c0003t0047g0125 a0001c0013t0016g0131 a0001c0013t0016g0132 others(2): Show |
5 | HG02622.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+4484G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771287 | |||||||
| chr2:205771399 | C | A | 104 | a0001c0001t0003g0240 a0001c0001t0004g0060 a0001c0001t0005g0007 others(101): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.2425+4596C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771399 | |||||||
| chr2:205771419 | C | T | 320 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(317): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2425+4616C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771419 | |||||||
| chr2:205771664 | C | G | 1 | a0001c0001t0011g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2425+4861C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771664 | |||||||
| chr2:205771970 | C | A | 1 | a0001c0001t0010g0317 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2425+5167C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771970 | |||||||
| chr2:205772039 | T | G | 335 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2425+5236T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772039 | |||||||
| chr2:205772327 | C | T | 1 | a0001c0006t0039g0305 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2425+5524C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772327 | |||||||
| chr2:205772595 | T | C | 9 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(6): Show |
9 | HG01109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2425+5792T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772595 | |||||||
| chr2:205773102 | T | C | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+6299T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773102 | |||||||
| chr2:205773169 | C | T | 3 | a0001c0002t0008g0180 a0001c0002t0056g0147 a0003c0025t0013g0166 |
3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+6366C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773169 | |||||||
| chr2:205773438 | G | T | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2425+6635G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773438 | |||||||
| chr2:205773584 | T | C | 4 | a0001c0002t0008g0140 a0001c0003t0007g0249 a0001c0018t0007g0336 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425+6781T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773584 | |||||||
| chr2:205773608 | T | C | 1 | a0001c0002t0028g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2425+6805T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773608 | |||||||
| chr2:205773806 | C | A | 1 | a0001c0004t0050g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2425+7003C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773806 | |||||||
| chr2:205774177 | C | A | 1 | a0001c0003t0040g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2425+7374C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774177 | |||||||
| chr2:205774179 | T | G | 1 | a0001c0003t0040g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2425+7376T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774179 | |||||||
| chr2:205774218 | C | G | 1 | a0001c0004t0003g0309 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2425+7415C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774218 | |||||||
| chr2:205774383 | C | T | 11 | a0001c0002t0008g0180 a0001c0002t0013g0197 a0001c0002t0013g0198 others(8): Show |
11 | HG02572.hp1 HG02647.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.2425+7580C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774383 | |||||||
| chr2:205774571 | C | T | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+7768C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774571 | |||||||
| chr2:205774693 | CATT | C | 3 | a0001c0002t0008g0180 a0001c0002t0056g0147 a0003c0025t0013g0166 |
3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+7892_2425+789 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205774693 | ||||||
| chr2:205775062 | C | T | 4 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(1): Show |
4 | HG01069.hp2 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425+8259C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775062 | |||||||
| chr2:205775068 | T | G | 3 | a0001c0002t0008g0180 a0001c0002t0056g0147 a0003c0025t0013g0166 |
3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+8265T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775068 | |||||||
| chr2:205775107 | G | A | 86 | a0001c0001t0003g0225 a0001c0001t0003g0243 a0001c0001t0003g0264 others(83): Show |
87 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2425+8304G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775107 | |||||||
| chr2:205775354 | C | T | 1 | a0001c0013t0016g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2425+8551C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775354 | |||||||
| chr2:205775445 | T | C | 5 | a0001c0001t0001g0053 a0001c0002t0002g0261 a0001c0002t0002g0262 others(2): Show |
5 | HG02257.hp1 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+8642T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775445 | |||||||
| chr2:205775450 | C | T | 5 | a0001c0002t0042g0212 a0001c0003t0047g0125 a0001c0013t0016g0131 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+8647C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775450 | |||||||
| chr2:205775472 | C | G | 5 | a0001c0002t0004g0191 a0001c0002t0028g0186 a0001c0002t0061g0189 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+8669C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775472 | |||||||
| chr2:205775522 | C | A | 1 | a0001c0001t0003g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2425+8719C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775522 | |||||||
| chr2:205775609 | G | A | 1 | a0001c0002t0002g0294 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2425+8806G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775609 | |||||||
| chr2:205775635 | A | G | 1 | a0001c0001t0004g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2425+8832A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775635 | |||||||
| chr2:205775771 | T | C | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+8968T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775771 | |||||||
| chr2:205775778 | C | T | 3 | a0001c0002t0008g0180 a0001c0002t0056g0147 a0003c0025t0013g0166 |
3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+8975C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775778 | |||||||
| chr2:205775916 | G | A | 101 | a0001c0001t0003g0225 a0001c0001t0003g0243 a0001c0001t0003g0264 others(98): Show |
102 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.2425+9113G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775916 | |||||||
| chr2:205775979 | A | G | 4 | a0001c0001t0018g0018 a0001c0002t0004g0192 a0001c0002t0018g0009 others(1): Show |
4 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425+9176A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775979 | |||||||
| chr2:205776051 | A | C | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2425+9248A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776051 | |||||||
| chr2:205776516 | CGCA | C | 9 | a0001c0001t0004g0040 a0001c0001t0004g0116 a0001c0001t0011g0221 others(6): Show |
10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9714_2425+971 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776516 | |||||||
| chr2:205776520 | C | T | 9 | a0001c0001t0004g0040 a0001c0001t0004g0116 a0001c0001t0011g0221 others(6): Show |
10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9717C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776520 | |||||||
| chr2:205776521 | T | A | 9 | a0001c0001t0004g0040 a0001c0001t0004g0116 a0001c0001t0011g0221 others(6): Show |
10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9718T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776521 | |||||||
| chr2:205776903 | A | C | 2 | a0001c0001t0006g0114 a0001c0004t0003g0309 |
2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2425+10100A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776903 | |||||||
| chr2:205777021 | C | T | 1 | a0001c0001t0011g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2425+10218C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777021 | |||||||
| chr2:205777060 | T | C | 1 | a0001c0001t0003g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2425+10257T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777060 | |||||||
| chr2:205777260 | C | T | 112 | a0001c0001t0004g0060 a0001c0001t0005g0007 a0001c0001t0005g0024 others(109): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2425+10457C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777260 | |||||||
| chr2:205777277 | A | C | 1 | a0001c0002t0025g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2425+10474A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777277 | |||||||
| chr2:205777385 | A | C | 8 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(5): Show |
8 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425+10582A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777385 | |||||||
| chr2:205777496 | C | T | 33 | a0001c0001t0007g0213 a0001c0001t0007g0242 a0001c0001t0008g0046 others(30): Show |
33 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2425+10693C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777496 | |||||||
| chr2:205777613 | G | A | 113 | a0001c0001t0004g0060 a0001c0001t0005g0007 a0001c0001t0005g0024 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2425+10810G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777613 | |||||||
| chr2:205777728 | T | G | 10 | a0001c0002t0007g0126 a0001c0002t0011g0271 a0001c0002t0016g0133 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2425+10925T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777728 | |||||||
| chr2:205778149 | T | A | 1 | a0001c0001t0010g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2425+11346T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778149 | |||||||
| chr2:205778220 | A | AT | 15 | a0001c0001t0002g0257 a0001c0003t0001g0162 a0001c0003t0014g0094 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.2425+11433dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205778220 | ||||||
| chr2:205778220 | AT | A | 118 | a0001c0001t0003g0225 a0001c0001t0003g0243 a0001c0001t0003g0264 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2425+11433delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205778220 | ||||||
| chr2:205778249 | G | C | 2 | a0001c0001t0004g0080 a0001c0003t0011g0322 |
2 | HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2425+11446G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778249 | |||||||
| chr2:205778343 | C | T | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2425+11540C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778343 | |||||||
| chr2:205778379 | A | G | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+11576A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778379 | |||||||
| chr2:205778478 | A | G | 5 | a0001c0002t0016g0133 a0001c0003t0047g0125 a0001c0013t0016g0131 others(2): Show |
5 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+11675A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778478 | |||||||
| chr2:205778479 | G | A | 1 | a0001c0004t0060g0023 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2425+11676G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778479 | |||||||
| chr2:205778489 | C | T | 1 | a0002c0016t0001g0273 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2425+11686C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778489 | |||||||
| chr2:205778706 | T | C | 1 | a0001c0001t0005g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2425+11903T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778706 | |||||||
| chr2:205778708 | C | G | 225 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2425+11905C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778708 | |||||||
| chr2:205778756 | C | A | 1 | a0001c0001t0005g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2425+11953C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778756 | |||||||
| chr2:205778762 | A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2425+11959A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778762 | |||||||
| chr2:205778792 | A | T | 225 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2425+11989A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778792 | |||||||
| chr2:205778875 | C | T | 1 | a0001c0003t0003g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2425+12072C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778875 | |||||||
| chr2:205778956 | TG | T | 3 | a0001c0002t0051g0182 a0001c0002t0063g0136 a0001c0018t0038g0308 |
3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2425+12154delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778956 | |||||||
| chr2:205778970 | C | G | 1 | a0001c0003t0003g0295 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2425+12167C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778970 | |||||||
| chr2:205778994 | G | A | 1 | a0001c0002t0004g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2425+12191G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778994 | |||||||
| chr2:205779029 | G | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2425+12226G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779029 | |||||||
| chr2:205779032 | A | G | 1 | a0001c0002t0006g0146 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2425+12229A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779032 | |||||||
| chr2:205779201 | C | T | 1 | a0001c0002t0004g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2425+12398C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779201 | |||||||
| chr2:205779651 | C | T | 1 | a0001c0002t0006g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2426-12584C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779651 | |||||||
| chr2:205779901 | T | C | 4 | a0001c0002t0008g0140 a0001c0003t0007g0249 a0001c0018t0007g0336 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-12334T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779901 | |||||||
| chr2:205779996 | C | A | 1 | a0001c0001t0003g0240 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2426-12239C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779996 | |||||||
| chr2:205780050 | G | C | 50 | a0001c0001t0003g0225 a0001c0001t0003g0240 a0001c0001t0003g0243 others(47): Show |
50 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2426-12185G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780050 | |||||||
| chr2:205780055 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2426-12180C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780055 | |||||||
| chr2:205780256 | C | T | 1 | a0001c0006t0011g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2426-11979C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780256 | |||||||
| chr2:205780325 | A | G | 3 | a0001c0002t0051g0182 a0001c0002t0063g0136 a0001c0018t0038g0308 |
3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2426-11910A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780325 | |||||||
| chr2:205780409 | T | A | 1 | a0001c0003t0005g0093 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2426-11826T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780409 | |||||||
| chr2:205780442 | C | T | 61 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0059 others(58): Show |
63 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.2426-11793C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780442 | |||||||
| chr2:205780523 | G | C | 57 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
59 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.2426-11712G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780523 | |||||||
| chr2:205780823 | T | C | 1 | a0001c0004t0012g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2426-11412T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780823 | |||||||
| chr2:205780923 | TG | T | 3 | a0001c0002t0051g0182 a0001c0002t0063g0136 a0001c0018t0038g0308 |
3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2426-11311delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780923 | |||||||
| chr2:205781186 | A | T | 13 | a0001c0001t0003g0225 a0001c0001t0003g0264 a0001c0001t0003g0268 others(10): Show |
13 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2426-11049A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781186 | |||||||
| chr2:205781263 | A | G | 1 | a0001c0002t0012g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2426-10972A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781263 | |||||||
| chr2:205781878 | T | A | 1 | a0001c0002t0008g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2426-10357T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781878 | |||||||
| chr2:205781912 | A | G | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2426-10323A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781912 | |||||||
| chr2:205782030 | T | G | 7 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(4): Show |
7 | HG01069.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-10205T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782030 | |||||||
| chr2:205782056 | G | A | 1 | a0001c0004t0050g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426-10179G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782056 | |||||||
| chr2:205782069 | C | A | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2426-10166C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782069 | |||||||
| chr2:205782073 | A | ATT | 111 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(108): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2426-10160_2426-10 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205782073 | ||||||
| chr2:205782387 | G | T | 5 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2426-9848G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782387 | |||||||
| chr2:205782646 | T | C | 3 | a0001c0001t0018g0018 a0001c0002t0004g0192 a0001c0006t0039g0305 |
3 | HG01256.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-9589T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782646 | |||||||
| chr2:205782763 | C | T | 2 | a0001c0002t0002g0261 a0001c0002t0002g0262 |
2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2426-9472C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782763 | |||||||
| chr2:205782812 | G | A | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-9423G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782812 | |||||||
| chr2:205782827 | C | T | 1 | a0001c0001t0037g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2426-9408C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782827 | |||||||
| chr2:205782855 | GT | G | 19 | a0001c0001t0018g0018 a0001c0002t0004g0181 a0001c0002t0008g0180 others(16): Show |
19 | HG01256.hp2 HG02257.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.2426-9366delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205782855 | ||||||
| chr2:205782861 | T | C | 4 | a0001c0002t0016g0133 a0001c0013t0016g0131 a0001c0013t0016g0132 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-9374T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782861 | |||||||
| chr2:205783209 | C | T | 2 | a0001c0001t0003g0318 a0001c0003t0006g0097 |
2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2426-9026C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783209 | |||||||
| chr2:205783353 | T | A | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-8882T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783353 | |||||||
| chr2:205783429 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2426-8806T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783429 | |||||||
| chr2:205783721 | C | T | 1 | a0001c0002t0049g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2426-8514C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783721 | |||||||
| chr2:205784001 | G | GAC | 267 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(264): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.2426-8214_2426-821 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACAC | 7 | a0001c0001t0007g0213 a0001c0001t0026g0013 a0001c0003t0014g0016 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2426-8216_2426-821 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(3): Show |
1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-8222_2426-821 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(9): Show |
7 | a0001c0002t0007g0283 a0001c0002t0016g0133 a0001c0002t0046g0141 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2426-8228_2426-821 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(11): Show |
6 | a0001c0001t0002g0215 a0001c0001t0018g0018 a0001c0002t0002g0261 others(3): Show |
6 | HG01256.hp2 HG01346.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2426-8230_2426-821 others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(13): Show |
2 | a0002c0016t0001g0273 a0002c0027t0064g0176 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2426-8232_2426-821 others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(15): Show |
1 | a0001c0001t0001g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(26): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(17): Show |
3 | a0001c0002t0001g0190 a0001c0006t0039g0305 a0002c0014t0001g0195 |
3 | HG02615.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(28): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(19): Show |
7 | a0001c0001t0002g0223 a0001c0002t0015g0300 a0001c0003t0002g0326 others(4): Show |
7 | HG00621.hp1 HG00621.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(30): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(21): Show |
13 | a0001c0001t0001g0059 a0001c0002t0001g0168 a0001c0002t0008g0180 others(10): Show |
13 | HG02056.hp2 HG02083.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(32): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(23): Show |
18 | a0001c0001t0001g0025 a0001c0001t0001g0103 a0001c0001t0002g0006 others(15): Show |
20 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(34): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(25): Show |
1 | a0001c0003t0001g0084 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(36): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784001 | G | GACACACA others(27): Show |
1 | a0001c0003t0015g0259 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(38): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | ||||||
| chr2:205784351 | C | G | 1 | a0001c0002t0001g0081 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2426-7884C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784351 | |||||||
| chr2:205784383 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2426-7852T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784383 | |||||||
| chr2:205784386 | G | A | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-7849G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784386 | |||||||
| chr2:205784407 | A | C | 1 | a0001c0004t0060g0023 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2426-7828A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784407 | |||||||
| chr2:205784502 | A | T | 8 | a0001c0002t0007g0126 a0001c0002t0011g0271 a0001c0006t0007g0306 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2426-7733A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784502 | |||||||
| chr2:205784614 | T | C | 109 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(106): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.2426-7621T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784614 | |||||||
| chr2:205784867 | G | A | 1 | a0001c0001t0003g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2426-7368G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784867 | |||||||
| chr2:205784893 | A | G | 1 | a0001c0001t0031g0328 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2426-7342A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784893 | |||||||
| chr2:205784910 | C | A | 2 | a0001c0002t0004g0274 a0001c0002t0028g0187 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2426-7325C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784910 | |||||||
| chr2:205784961 | A | G | 17 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(14): Show |
18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-7274A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784961 | |||||||
| chr2:205784963 | T | C | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-7272T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784963 | |||||||
| chr2:205785019 | A | G | 112 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(109): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.2426-7216A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785019 | |||||||
| chr2:205785227 | G | C | 2 | a0001c0002t0004g0274 a0001c0002t0028g0187 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2426-7008G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785227 | |||||||
| chr2:205785417 | A | G | 1 | a0001c0009t0005g0001 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2426-6818A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785417 | |||||||
| chr2:205785580 | T | C | 1 | a0001c0001t0007g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2426-6655T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785580 | |||||||
| chr2:205785690 | C | A | 1 | a0001c0001t0026g0013 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2426-6545C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785690 | |||||||
| chr2:205785915 | G | A | 1 | a0001c0003t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2426-6320G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785915 | |||||||
| chr2:205785984 | C | T | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-6251C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785984 | |||||||
| chr2:205786076 | C | T | 2 | a0001c0002t0010g0277 a0001c0002t0010g0278 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2426-6159C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786076 | |||||||
| chr2:205786100 | G | T | 1 | a0001c0002t0002g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2426-6135G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786100 | |||||||
| chr2:205786383 | C | T | 8 | a0001c0002t0007g0285 a0001c0002t0007g0288 a0001c0002t0007g0289 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2426-5852C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786383 | |||||||
| chr2:205786519 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2426-5716C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786519 | |||||||
| chr2:205786591 | C | T | 6 | a0001c0001t0009g0239 a0001c0001t0012g0008 a0001c0002t0018g0009 others(3): Show |
6 | HG00741.hp2 HG01081.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-5644C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786591 | |||||||
| chr2:205786898 | C | T | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-5337C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786898 | |||||||
| chr2:205787159 | G | C | 3 | a0001c0013t0016g0131 a0001c0013t0016g0132 a0006c0028t0016g0142 |
3 | HG02622.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2426-5076G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787159 | |||||||
| chr2:205787190 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2426-5045C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787190 | |||||||
| chr2:205787202 | C | A | 1 | a0001c0001t0020g0031 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2426-5033C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787202 | |||||||
| chr2:205787529 | T | C | 1 | a0001c0003t0004g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2426-4706T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787529 | |||||||
| chr2:205787576 | C | G | 125 | a0001c0001t0003g0202 a0001c0001t0004g0060 a0001c0001t0005g0007 others(122): Show |
126 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2426-4659C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787576 | |||||||
| chr2:205787705 | T | TA | 23 | a0001c0001t0002g0223 a0001c0001t0018g0018 a0001c0001t0020g0031 others(20): Show |
24 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2426-4522dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787705 | ||||||
| chr2:205787713 | AGTGTC | A | 43 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0059 others(40): Show |
44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4521_2426-451 others(9): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787713 | |||||||
| chr2:205787718 | C | CTG | 14 | a0001c0001t0004g0040 a0001c0001t0004g0116 a0001c0001t0011g0221 others(11): Show |
15 | HG01106.hp1 HG01256.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2426-4481_2426-448 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | C | CTGTG | 8 | a0001c0002t0004g0181 a0001c0002t0051g0182 a0001c0002t0063g0136 others(5): Show |
8 | HG02257.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2426-4483_2426-448 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | C | CTGTGTG | 4 | a0001c0002t0029g0135 a0001c0003t0011g0247 a0001c0003t0011g0248 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-4485_2426-448 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | C | CTGTGTGT others(3): Show |
1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-4489_2426-448 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | CTG | C | 179 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(176): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2426-4481_2426-448 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | CTGTG | C | 59 | a0001c0001t0002g0223 a0001c0001t0003g0225 a0001c0001t0003g0240 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2426-4483_2426-448 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787718 | CTGTGTGT others(3): Show |
C | 1 | a0004c0022t0006g0115 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2426-4489_2426-448 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | ||||||
| chr2:205787719 | T | A | 43 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0059 others(40): Show |
44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4516T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787719 | |||||||
| chr2:205787721 | T | A | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-4514T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787721 | |||||||
| chr2:205787724 | G | C | 43 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0059 others(40): Show |
44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4511G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787724 | |||||||
| chr2:205787726 | G | C | 1 | a0001c0002t0046g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-4509G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787726 | |||||||
| chr2:205787809 | T | G | 1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2426-4426T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787809 | |||||||
| chr2:205787825 | C | A | 2 | a0001c0003t0003g0217 a0001c0004t0006g0112 |
2 | HG02080.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2426-4410C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787825 | |||||||
| chr2:205787882 | G | A | 2 | a0001c0002t0008g0180 a0003c0025t0013g0166 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2426-4353G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787882 | |||||||
| chr2:205787988 | G | A | 1 | a0001c0002t0008g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2426-4247G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787988 | |||||||
| chr2:205788000 | T | C | 2 | a0001c0001t0010g0075 a0001c0004t0010g0236 |
2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.2426-4235T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788000 | |||||||
| chr2:205788239 | T | C | 69 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0059 others(66): Show |
71 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.2426-3996T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788239 | |||||||
| chr2:205788370 | C | A | 1 | a0002c0029t0013g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2426-3865C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788370 | |||||||
| chr2:205788491 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2426-3744C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788491 | |||||||
| chr2:205788554 | C | T | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-3681C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788554 | |||||||
| chr2:205788557 | GT | G | 84 | a0001c0001t0003g0225 a0001c0001t0003g0240 a0001c0001t0003g0243 others(81): Show |
85 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2426-3675delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205788557 | ||||||
| chr2:205788696 | C | G | 1 | a0001c0001t0009g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2426-3539C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788696 | |||||||
| chr2:205788741 | G | A | 1 | a0001c0002t0028g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2426-3494G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788741 | |||||||
| chr2:205788756 | C | G | 1 | a0001c0002t0054g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2426-3479C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788756 | |||||||
| chr2:205788883 | G | A | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-3352G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788883 | |||||||
| chr2:205788914 | T | C | 2 | a0001c0001t0004g0193 a0001c0001t0037g0323 |
2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2426-3321T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788914 | |||||||
| chr2:205788915 | A | T | 2 | a0001c0001t0004g0193 a0001c0001t0037g0323 |
2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2426-3320A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788915 | |||||||
| chr2:205788982 | T | C | 1 | a0001c0001t0009g0238 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2426-3253T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788982 | |||||||
| chr2:205789191 | C | T | 6 | a0001c0001t0004g0017 a0001c0001t0004g0080 a0001c0001t0004g0193 others(3): Show |
6 | HG01099.hp2 HG01496.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-3044C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789191 | |||||||
| chr2:205789235 | C | T | 7 | a0001c0002t0011g0271 a0001c0003t0004g0167 a0001c0006t0011g0304 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-3000C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789235 | |||||||
| chr2:205789277 | C | A | 3 | a0001c0001t0011g0221 a0001c0008t0004g0005 a0001c0008t0004g0196 |
4 | HG02559.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-2958C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789277 | |||||||
| chr2:205789319 | C | T | 1 | a0001c0002t0054g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2426-2916C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789319 | |||||||
| chr2:205789399 | C | A | 91 | a0001c0001t0003g0225 a0001c0001t0003g0240 a0001c0001t0003g0243 others(88): Show |
92 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.2426-2836C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789399 | |||||||
| chr2:205789512 | C | G | 1 | a0001c0001t0057g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2426-2723C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789512 | |||||||
| chr2:205789521 | T | G | 4 | a0001c0002t0003g0203 a0001c0002t0003g0281 a0001c0002t0003g0282 others(1): Show |
4 | NA18953.hp1 NA18965.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-2714T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789521 | |||||||
| chr2:205789536 | C | T | 1 | a0001c0004t0005g0164 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2426-2699C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789536 | |||||||
| chr2:205789537 | T | A | 2 | a0001c0001t0015g0208 a0001c0001t0015g0237 |
2 | NA18955.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2426-2698T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789537 | |||||||
| chr2:205789626 | T | C | 1 | a0002c0017t0062g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2426-2609T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789626 | |||||||
| chr2:205789682 | C | T | 1 | a0001c0011t0008g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-2553C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789682 | |||||||
| chr2:205789716 | C | G | 15 | a0001c0001t0018g0018 a0001c0002t0004g0192 a0001c0002t0008g0180 others(12): Show |
16 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2426-2519C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789716 | |||||||
| chr2:205789742 | A | G | 2 | a0001c0007t0013g0188 a0001c0007t0017g0269 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2426-2493A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789742 | |||||||
| chr2:205789750 | A | G | 251 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2426-2485A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789750 | |||||||
| chr2:205789752 | T | A | 2 | a0001c0003t0007g0249 a0001c0018t0007g0336 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2426-2483T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789752 | |||||||
| chr2:205789950 | T | C | 1 | a0001c0001t0009g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2426-2285T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789950 | |||||||
| chr2:205790290 | A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-1945A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790290 | |||||||
| chr2:205790452 | T | G | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-1783T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790452 | |||||||
| chr2:205790457 | G | A | 1 | a0001c0002t0006g0146 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2426-1778G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790457 | |||||||
| chr2:205790520 | G | A | 1 | a0001c0003t0055g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1715G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790520 | |||||||
| chr2:205790524 | T | A | 1 | a0001c0003t0055g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1711T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790524 | |||||||
| chr2:205790527 | T | TATTCACA others(6): Show |
1 | a0001c0003t0055g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1708_2426-170 others(17): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790527 | |||||||
| chr2:205790529 | C | A | 1 | a0001c0003t0055g0091 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1706C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790529 | |||||||
| chr2:205790634 | C | T | 45 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0103 others(42): Show |
46 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2426-1601C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790634 | |||||||
| chr2:205790648 | G | GT | 173 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(170): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.2426-1573dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | ||||||
| chr2:205790648 | G | GTT | 16 | a0001c0001t0001g0064 a0001c0001t0006g0109 a0001c0001t0007g0213 others(13): Show |
16 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2426-1574_2426-157 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | ||||||
| chr2:205790648 | GTT | G | 9 | a0001c0002t0008g0180 a0001c0002t0016g0133 a0001c0002t0046g0141 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2426-1574_2426-157 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | ||||||
| chr2:205790831 | C | T | 1 | a0001c0004t0012g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2426-1404C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790831 | |||||||
| chr2:205790835 | C | T | 1 | a0001c0004t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2426-1400C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790835 | |||||||
| chr2:205790844 | C | T | 1 | a0001c0002t0002g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2426-1391C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790844 | |||||||
| chr2:205790963 | C | G | 1 | a0001c0003t0002g0326 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2426-1272C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790963 | |||||||
| chr2:205790967 | G | C | 257 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2426-1268G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790967 | |||||||
| chr2:205790970 | C | A | 3 | a0001c0001t0001g0103 a0001c0003t0002g0334 a0001c0009t0021g0044 |
3 | HG01361.hp2 HG02602.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2426-1265C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790970 | |||||||
| chr2:205790983 | G | C | 1 | a0001c0003t0001g0161 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2426-1252G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790983 | |||||||
| chr2:205791015 | A | G | 258 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2426-1220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791015 | |||||||
| chr2:205791071 | G | A | 1 | a0001c0003t0047g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2426-1164G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791071 | |||||||
| chr2:205791099 | A | G | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-1136A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791099 | |||||||
| chr2:205791154 | G | A | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2426-1081G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791154 | |||||||
| chr2:205791159 | G | A | 1 | a0001c0008t0004g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2426-1076G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791159 | |||||||
| chr2:205791200 | C | T | 2 | a0001c0001t0008g0049 a0001c0002t0007g0325 |
2 | HG01074.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2426-1035C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791200 | |||||||
| chr2:205791229 | T | G | 17 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(14): Show |
18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-1006T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791229 | |||||||
| chr2:205791246 | A | G | 1 | a0001c0003t0009g0292 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2426-989A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791246 | |||||||
| chr2:205791418 | C | T | 10 | a0001c0001t0007g0242 a0001c0002t0007g0285 a0001c0002t0007g0288 others(7): Show |
10 | HG00735.hp2 HG01070.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2426-817C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791418 | |||||||
| chr2:205791461 | C | G | 105 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(102): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2426-774C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791461 | |||||||
| chr2:205791572 | T | C | 3 | a0001c0005t0007g0222 a0001c0005t0023g0119 a0001c0005t0023g0120 |
3 | HG01123.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2426-663T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791572 | |||||||
| chr2:205791667 | A | G | 2 | a0001c0002t0007g0126 a0001c0006t0007g0306 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2426-568A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791667 | |||||||
| chr2:205791696 | A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-539A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791696 | |||||||
| chr2:205791744 | A | AAAC | 17 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(14): Show |
18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-489_2426-487d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205791744 | ||||||
| chr2:205791936 | T | A | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-299T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791936 | |||||||
| chr2:205791940 | A | T | 38 | a0001c0001t0007g0213 a0001c0001t0007g0242 a0001c0001t0008g0046 others(35): Show |
38 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2426-295A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791940 | |||||||
| chr2:205792070 | A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-165A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792070 | |||||||
| chr2:205792192 | T | C | 10 | a0001c0002t0008g0180 a0001c0002t0016g0133 a0001c0002t0046g0141 others(7): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2426-43T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792192 | |||||||
| chr2:205792195 | A | T | 10 | a0001c0002t0008g0180 a0001c0002t0016g0133 a0001c0002t0046g0141 others(7): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2426-40A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792195 | |||||||
| chr2:205792579 | A | T | 7 | a0001c0001t0018g0018 a0001c0001t0020g0031 a0001c0001t0020g0072 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2476+294A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792579 | |||||||
| chr2:205792927 | G | A | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2476+642G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792927 | |||||||
| chr2:205792960 | A | C | 3 | a0001c0001t0008g0049 a0001c0002t0007g0325 a0001c0002t0008g0123 |
3 | HG01074.hp2 HG02273.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2476+675A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792960 | |||||||
| chr2:205793192 | C | T | 8 | a0001c0002t0008g0180 a0001c0002t0016g0133 a0001c0002t0046g0141 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2476+907C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793192 | |||||||
| chr2:205793193 | G | T | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2476+908G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793193 | |||||||
| chr2:205793384 | C | A | 5 | a0001c0002t0013g0197 a0001c0002t0013g0198 a0001c0002t0017g0254 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+1099C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793384 | |||||||
| chr2:205793425 | T | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
13 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1140T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793425 | |||||||
| chr2:205793604 | G | T | 3 | a0001c0002t0002g0261 a0001c0002t0002g0262 a0001c0002t0002g0263 |
3 | HG02630.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2477-1150G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793604 | |||||||
| chr2:205793659 | G | A | 1 | a0001c0001t0027g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2477-1095G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793659 | |||||||
| chr2:205793668 | T | C | 1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2477-1086T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793668 | |||||||
| chr2:205793705 | A | T | 8 | a0001c0002t0008g0180 a0001c0002t0016g0133 a0001c0002t0046g0141 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2477-1049A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793705 | |||||||
| chr2:205793719 | G | A | 6 | a0001c0002t0016g0133 a0001c0002t0046g0141 a0001c0003t0047g0125 others(3): Show |
6 | HG01884.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-1035G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793719 | |||||||
| chr2:205793810 | A | G | 1 | a0001c0002t0042g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2477-944A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793810 | |||||||
| chr2:205793921 | G | A | 2 | a0001c0002t0046g0141 a0001c0003t0047g0125 |
2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2477-833G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793921 | |||||||
| chr2:205793979 | A | C | 5 | a0001c0002t0015g0300 a0001c0002t0033g0293 a0001c0003t0014g0016 others(2): Show |
5 | HG01099.hp1 HG01192.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2477-775A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793979 | |||||||
| chr2:205794120 | A | T | 5 | a0001c0001t0003g0318 a0001c0003t0006g0097 a0001c0003t0024g0324 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-634A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794120 | |||||||
| chr2:205794124 | T | A | 4 | a0001c0002t0022g0184 a0001c0002t0043g0258 a0001c0003t0022g0173 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2477-630T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794124 | |||||||
| chr2:205794155 | G | C | 1 | a0001c0001t0010g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2477-599G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794155 | |||||||
| chr2:205794179 | C | T | 1 | a0002c0027t0064g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2477-575C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794179 | |||||||
| chr2:205794244 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2477-510G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794244 | |||||||
| chr2:205794301 | G | A | 1 | a0001c0001t0004g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2477-453G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794301 | |||||||
| chr2:205794389 | C | T | 7 | a0001c0002t0004g0191 a0001c0002t0004g0274 a0001c0002t0028g0186 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2477-365C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794389 | |||||||
| chr2:205794394 | G | C | 1 | a0001c0009t0027g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2477-360G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794394 | |||||||
| chr2:205794401 | C | T | 11 | a0001c0001t0007g0242 a0001c0002t0007g0285 a0001c0002t0007g0288 others(8): Show |
11 | HG00735.hp2 HG01070.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-353C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794401 | |||||||
| chr2:205794597 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2477-157G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794597 | |||||||
| chr2:205794602 | G | A | 2 | a0001c0001t0001g0073 a0001c0003t0001g0156 |
2 | NA18978.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2477-152G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794602 | |||||||
| chr2:205794739 | T | C | 4 | a0001c0002t0004g0191 a0001c0002t0061g0189 a0001c0005t0004g0048 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2477-15T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794739 | |||||||
| chr2:205794750 | G | A | 1 | a0001c0002t0056g0147 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.2477-4G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794750 |