Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 255743 |
| ensemblid | ENSG00000168743.13 |
| hgncid | 27405 |
| symbol | NPNT |
| name | nephronectin |
| refseq_nuc | NM_001033047.3 |
| refseq_prot | NP_001028219.1 |
| ensembl_nuc | ENST00000379987.7 |
| ensembl_prot | ENSP00000369323.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105895471 |
| end | 105971671 |
| strand | + |
| ver | v1.2 |
| region | chr4:105895471-105971671 |
| region5000 | chr4:105890471-105976671 |
| regionname0 | NPNT_chr4_105895471_105971671 |
| regionname5000 | NPNT_chr4_105890471_105976671 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 565 | 103 | 28 | 27 | 27 | 6 | 15 | 19 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0002 | 0/1 | 565 | 84 | 21 | 11 | 31 | 6 | 14 | 23 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0003 | 1/0 | 565 | 27 | 17 | 6 | 0 | 2 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0004 | 0/0 | 565 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0005 | 0/0 | 565 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0006 | 0/0 | 565 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0007 | 0/0 | 565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0008 | 0/0 | 565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0009 | 0/0 | 565 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0010 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0011 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0012 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| a0013 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | MDFLL others(560): Show |
chr4 | 105890471 | 105976671 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1695 | 103 | 28 | 27 | 27 | 6 | 15 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0002c0002 | 0/1 | 1695 | 84 | 21 | 11 | 31 | 6 | 14 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0003c0003 | 1/0 | 1695 | 26 | 17 | 5 | 0 | 2 | 1 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0003c0014 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0004c0004 | 0/0 | 1695 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0005c0005 | 0/0 | 1695 | 4 | 4 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0006c0008 | 0/0 | 1695 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0007c0007 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0008c0006 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0009c0009 | 0/0 | 1695 | 2 | 0 | 0 | 2 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0010c0011 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0011c0013 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0012c0010 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 | ||
| a0013c0012 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | ATGGA others(1690): Show |
chr4 | 105890471 | 105976671 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4561 | 66 | 12 | 22 | 24 | 1 | 7 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0002 | 0/0 | 4561 | 26 | 13 | 3 | 1 | 4 | 5 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0003 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0004 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0005 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0006 | 0/0 | 4561 | 3 | 0 | 1 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0008 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 0 | 2 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0011 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0012 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0001c0001t0014 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0001 | 0/0 | 4561 | 20 | 7 | 3 | 8 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0002 | 0/0 | 4561 | 46 | 13 | 4 | 16 | 4 | 9 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0003 | 0/1 | 4561 | 13 | 0 | 2 | 7 | 0 | 3 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0006 | 0/0 | 4561 | 2 | 0 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0009 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0002c0002t0013 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0001 | 0/0 | 4561 | 4 | 4 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0002 | 0/0 | 4561 | 6 | 5 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0004 | 1/0 | 4561 | 7 | 1 | 3 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0005 | 0/0 | 4561 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0007 | 0/0 | 4561 | 2 | 0 | 1 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0003t0015 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0003c0014t0001 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0004c0004t0002 | 0/0 | 4561 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0005c0005t0001 | 0/0 | 4561 | 3 | 3 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0005c0005t0002 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0006c0008t0002 | 0/0 | 4561 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0007c0007t0002 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0008c0006t0002 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0009c0009t0001 | 0/0 | 4561 | 2 | 0 | 0 | 2 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0010c0011t0002 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0011c0013t0010 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0012c0010t0002 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| a0013c0012t0010 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | GCGCA others(4556): Show |
chr4 | 105890471 | 105976671 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0014g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0009g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0007g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0014t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0006c0008t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0007c0007t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0007c0007t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0008c0006t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0008c0006t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0009c0009t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0009c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0010c0011t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0011c0013t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0012c0010t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0013c0012t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0009 | g0227 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00099 | hp2 | a0003 | c0003 | t0004 | g0015 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00140 | hp1 | a0003 | c0003 | t0007 | g0016 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | FIN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0223 | EUR | FIN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0174 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00597 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00642 | hp2 | a0003 | c0003 | t0004 | g0226 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00735 | hp1 | a0006 | c0008 | t0002 | g0001 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0148 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00741 | hp2 | a0003 | c0003 | t0007 | g0014 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01070 | hp2 | a0010 | c0011 | t0002 | g0130 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0224 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0181 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01192 | hp2 | a0003 | c0014 | t0001 | g0131 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0046 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01346 | hp2 | a0002 | c0002 | t0006 | g0149 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0095 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0175 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0209 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0132 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0038 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02004 | hp2 | a0003 | c0003 | t0004 | g0207 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02055 | hp1 | a0003 | c0003 | t0005 | g0121 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0177 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0114 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02280 | hp2 | a0011 | c0013 | t0010 | g0136 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02451 | hp2 | a0007 | c0007 | t0002 | g0185 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02622 | hp1 | a0003 | c0003 | t0004 | g0198 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02622 | hp2 | a0002 | c0002 | t0013 | g0107 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02630 | hp2 | a0003 | c0003 | t0005 | g0127 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02723 | hp1 | a0004 | c0004 | t0002 | g0145 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02723 | hp2 | a0005 | c0005 | t0002 | g0133 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02738 | hp2 | a0003 | c0003 | t0004 | g0017 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02809 | hp2 | a0003 | c0003 | t0005 | g0197 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02818 | hp1 | a0003 | c0003 | t0005 | g0113 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0189 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02895 | hp1 | a0003 | c0003 | t0005 | g0126 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02896 | hp1 | a0008 | c0006 | t0002 | g0192 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02896 | hp2 | a0004 | c0004 | t0002 | g0146 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02897 | hp1 | a0008 | c0006 | t0002 | g0194 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02965 | hp2 | a0012 | c0010 | t0002 | g0190 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03098 | hp1 | a0006 | c0008 | t0002 | g0001 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03139 | hp1 | a0004 | c0004 | t0002 | g0152 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03195 | hp1 | a0004 | c0004 | t0002 | g0144 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03225 | hp1 | a0004 | c0004 | t0002 | g0195 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0216 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0165 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0044 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0171 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0139 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0196 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0057 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03942 | hp2 | a0002 | c0002 | t0009 | g0228 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0153 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0158 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0168 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0167 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0097 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18522 | hp1 | a0005 | c0005 | t0001 | g0135 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18906 | hp2 | a0007 | c0007 | t0002 | g0182 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0075 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18982 | hp1 | a0009 | c0009 | t0001 | g0155 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19030 | hp1 | a0003 | c0003 | t0002 | g0217 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19043 | hp2 | a0003 | c0003 | t0015 | g0129 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19074 | hp1 | a0009 | c0009 | t0001 | g0048 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19240 | hp1 | a0003 | c0003 | t0005 | g0128 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20129 | hp1 | a0013 | c0012 | t0010 | g0122 | AFR | ASW | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ASW | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0150 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02559 | hp1 | a0004 | c0004 | t0002 | g0141 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0134 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0208 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0215 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0219 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0170 | REF | REF | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0004 | g0054 | REF | REF | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105897987 | G | C | 1 | a0008 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.158G>C | p.Trp53Ser | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/12 | 340/4561 | 158/1698 | 53/565 | chr4 | 105897987 | |||
| chr4:105938382 | C | T | 1 | a0005 | 4 | HG01884.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.467C>T | p.Pro156Leu | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/12 | 649/4561 | 467/1698 | 156/565 | chr4 | 105938382 | |||
| chr4:105938392 | G | C | 4 | a0002 a0004 a0007 others(1): Show |
93 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
missense_variant | MODERATE | c.477G>C | p.Gln159His | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/12 | 659/4561 | 477/1698 | 159/565 | chr4 | 105938392 | |||
| chr4:105940089 | G | A | 1 | a0012 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.520G>A | p.Ala174Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/12 | 702/4561 | 520/1698 | 174/565 | chr4 | 105940089 | |||
| chr4:105940573 | A | G | 7 | a0001 a0002 a0004 others(4): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
missense_variant | MODERATE | c.700A>G | p.Ile234Val | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/12 | 882/4561 | 700/1698 | 234/565 | chr4 | 105940573 | |||
| chr4:105942325 | T | C | 1 | a0010 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.782T>C | p.Ile261Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/12 | 964/4561 | 782/1698 | 261/565 | chr4 | 105942325 | |||
| chr4:105942469 | G | A | 1 | a0007 | 2 | HG02451.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.926G>A | p.Arg309Lys | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/12 | 1108/4561 | 926/1698 | 309/565 | chr4 | 105942469 | |||
| chr4:105967259 | G | A | 2 | a0004 a0006 |
8 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.1417G>A | p.Gly473Ser | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/12 | 1599/4561 | 1417/1698 | 473/565 | chr4 | 105967259 | |||
| chr4:105967269 | T | C | 2 | a0011 a0013 |
2 | HG02280.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1427T>C | p.Met476Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/12 | 1609/4561 | 1427/1698 | 476/565 | chr4 | 105967269 | |||
| chr4:105968920 | G | A | 1 | a0009 | 2 | NA18982.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.1628G>A | p.Arg543His | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1810/4561 | 1628/1698 | 543/565 | chr4 | 105968920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105927367 | A | G | 1 | a0003c0014 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.204A>G | p.Glu68Glu | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/12 | 386/4561 | 204/1698 | 68/565 | chr4 | 105927367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105969030 | C | A | 1 | a0003c0003t0007 | 2 | HG00140.hp1 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*40C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 40 | chr4 | 105969030 | ||||||
| chr4:105969035 | T | G | 1 | a0001c0001t0011 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 45 | chr4 | 105969035 | ||||||
| chr4:105969193 | G | A | 2 | a0001c0001t0006 a0002c0002t0006 |
5 | HG00735.hp2 HG00741.hp1 HG01346.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 203 | chr4 | 105969193 | ||||||
| chr4:105969197 | C | G | 2 | a0011c0013t0010 a0013c0012t0010 |
2 | HG02280.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*207C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 207 | chr4 | 105969197 | ||||||
| chr4:105969213 | C | T | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*223C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 223 | chr4 | 105969213 | ||||||
| chr4:105969702 | G | A | 3 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 |
8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*712G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 712 | chr4 | 105969702 | ||||||
| chr4:105970196 | C | T | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1206 | chr4 | 105970196 | ||||||
| chr4:105970260 | G | A | 1 | a0001c0001t0008 | 2 | HG03492.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1270 | chr4 | 105970260 | ||||||
| chr4:105970374 | A | G | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
116 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1384A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1384 | chr4 | 105970374 | ||||||
| chr4:105970688 | T | A | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1698T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1698 | chr4 | 105970688 | ||||||
| chr4:105970737 | G | A | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1747G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1747 | chr4 | 105970737 | ||||||
| chr4:105970781 | C | G | 1 | a0002c0002t0013 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1791 | chr4 | 105970781 | ||||||
| chr4:105971038 | C | A | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2048C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2048 | chr4 | 105971038 | ||||||
| chr4:105971053 | T | G | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2063T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2063 | chr4 | 105971053 | ||||||
| chr4:105971151 | C | T | 1 | a0002c0002t0009 | 2 | HG00099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2161 | chr4 | 105971151 | ||||||
| chr4:105971180 | C | T | 2 | a0001c0001t0005 a0003c0003t0005 |
7 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2190C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2190 | chr4 | 105971180 | ||||||
| chr4:105971393 | T | C | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2403T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2403 | chr4 | 105971393 | ||||||
| chr4:105971401 | C | T | 1 | a0001c0001t0012 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2411C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2411 | chr4 | 105971401 | ||||||
| chr4:105971418 | G | A | 2 | a0001c0001t0003 a0002c0002t0003 |
13 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2428G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2428 | chr4 | 105971418 | ||||||
| chr4:105971489 | T | C | 5 | a0001c0001t0005 a0003c0003t0005 a0003c0003t0015 others(2): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2499T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2499 | chr4 | 105971489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105895757 | C | A | 1 | a0002c0002t0002g0007 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.71+34C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105895757 | |||||||
| chr4:105895947 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71+224C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105895947 | |||||||
| chr4:105896018 | C | T | 3 | a0002c0002t0009g0227 a0002c0002t0009g0228 a0003c0003t0004g0226 |
3 | HG00099.hp1 HG00642.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.71+295C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896018 | |||||||
| chr4:105896035 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71+312T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896035 | |||||||
| chr4:105896064 | A | G | 128 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0137 others(125): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.71+341A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896064 | |||||||
| chr4:105896077 | C | T | 1 | a0002c0002t0003g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.71+354C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896077 | |||||||
| chr4:105896105 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71+382G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896105 | |||||||
| chr4:105896258 | G | T | 1 | a0003c0003t0004g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.71+535G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896258 | |||||||
| chr4:105896335 | A | C | 8 | a0001c0001t0001g0105 a0001c0001t0002g0106 a0001c0001t0002g0220 others(5): Show |
8 | HG00280.hp2 HG01081.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+612A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896335 | |||||||
| chr4:105896376 | G | C | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+653G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896376 | |||||||
| chr4:105896589 | T | C | 19 | a0001c0001t0002g0123 a0001c0001t0005g0112 a0001c0001t0011g0116 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+866T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896589 | |||||||
| chr4:105896699 | T | C | 4 | a0002c0002t0002g0108 a0002c0002t0002g0109 a0002c0002t0002g0110 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+976T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896699 | |||||||
| chr4:105896939 | T | C | 16 | a0001c0001t0002g0124 a0001c0001t0005g0112 a0002c0002t0001g0125 others(13): Show |
16 | HG01070.hp2 HG01192.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.72-962T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896939 | |||||||
| chr4:105897099 | A | G | 9 | a0001c0001t0002g0123 a0001c0001t0002g0214 a0001c0001t0004g0218 others(6): Show |
10 | HG00735.hp1 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-802A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897099 | |||||||
| chr4:105897435 | C | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(34): Show |
39 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-466C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897435 | |||||||
| chr4:105897691 | G | A | 3 | a0001c0001t0002g0124 a0001c0001t0005g0112 a0002c0002t0013g0107 |
3 | HG02451.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.72-210G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897691 | |||||||
| chr4:105897712 | A | C | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72-189A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897712 | |||||||
| chr4:105897742 | T | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72-159T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897742 | |||||||
| chr4:105897754 | G | A | 2 | a0003c0014t0001g0131 a0010c0011t0002g0130 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.72-147G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897754 | |||||||
| chr4:105897826 | G | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(31): Show |
36 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-75G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897826 | |||||||
| chr4:105897896 | G | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.72-5G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897896 | |||||||
| chr4:105898245 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172+244T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898245 | |||||||
| chr4:105898289 | TTTCTCTC others(30): Show |
T | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172+290_172+326del others(37): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898289 | ||||||
| chr4:105898290 | TTCTCTCT others(31): Show |
T | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+311_172+348del others(38): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898290 | ||||||
| chr4:105898290 | TTCTCTCT others(33): Show |
T | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+311_172+350del others(40): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898290 | ||||||
| chr4:105898294 | CTCTCTCT others(27): Show |
C | 10 | a0001c0001t0002g0214 a0003c0003t0001g0209 a0003c0003t0002g0001 others(7): Show |
11 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+311_172+344del others(34): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898294 | ||||||
| chr4:105898296 | CTCTCTCT others(25): Show |
C | 2 | a0001c0001t0002g0124 a0013c0012t0010g0122 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.172+311_172+342del others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898296 | ||||||
| chr4:105898298 | CTCTCTCT others(23): Show |
C | 2 | a0001c0001t0002g0210 a0001c0001t0004g0218 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+311_172+340del others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898298 | ||||||
| chr4:105898300 | CTCTCTCT others(21): Show |
C | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.172+311_172+338del others(28): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898300 | ||||||
| chr4:105898308 | CTCTGTCT others(13): Show |
C | 1 | a0001c0001t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172+311_172+330del others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898308 | ||||||
| chr4:105898312 | GTCTCTCT others(11): Show |
G | 1 | a0003c0003t0004g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172+327_172+344del others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898312 | GTCTCTCT others(17): Show |
G | 2 | a0001c0001t0001g0199 a0003c0003t0005g0197 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.172+327_172+350del others(24): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898312 | GTCTCTCT others(19): Show |
G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.172+327_172+352del others(26): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898312 | GTCTCTCT others(21): Show |
G | 2 | a0001c0001t0001g0006 a0003c0003t0004g0198 |
3 | HG01069.hp1 HG01192.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.172+327_172+354del others(28): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898312 | GTCTCTCT others(23): Show |
G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+327_172+356del others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898312 | GTCTCTCT others(25): Show |
G | 6 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+327_172+358del others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | ||||||
| chr4:105898318 | CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.172+327_172+336del others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898318 | ||||||
| chr4:105898320 | C | CTCTCCTC others(4): Show |
2 | a0002c0002t0002g0139 a0002c0002t0002g0140 |
2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.172+323_172+324ins others(11): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898320 | ||||||
| chr4:105898324 | C | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+323C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898324 | |||||||
| chr4:105898326 | CTG | C | 3 | a0001c0001t0001g0103 a0003c0014t0001g0131 a0004c0004t0002g0195 |
3 | HG01106.hp2 HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172+327_172+328del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898326 | ||||||
| chr4:105898328 | G | C | 4 | a0001c0001t0002g0220 a0001c0001t0005g0112 a0002c0002t0002g0139 others(1): Show |
4 | HG02451.hp1 HG03490.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+327G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898328 | |||||||
| chr4:105898328 | G | GTC | 18 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0066 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+378_172+379dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTC | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(20): Show |
24 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.172+376_172+379dup others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCCCT others(11): Show |
1 | a0002c0002t0003g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172+331_172+332ins others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTC | 14 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0082 others(11): Show |
14 | HG01167.hp1 HG01361.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.172+374_172+379dup others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(1): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0169 others(7): Show |
11 | HG02055.hp2 HG02886.hp2 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+372_172+379dup others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(3): Show |
11 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0001g0229 others(8): Show |
11 | HG00438.hp1 HG01243.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+370_172+379dup others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(5): Show |
10 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0006g0095 others(7): Show |
10 | HG00597.hp2 HG01175.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.172+368_172+379dup others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(7): Show |
4 | a0001c0001t0002g0098 a0001c0001t0002g0184 a0002c0002t0003g0183 others(1): Show |
4 | HG00408.hp1 HG03927.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+366_172+379dup others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(9): Show |
1 | a0007c0007t0002g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.172+364_172+379dup others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(13): Show |
3 | a0001c0001t0001g0186 a0002c0002t0001g0118 a0002c0002t0001g0119 |
3 | HG01175.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.172+360_172+379dup others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(15): Show |
1 | a0002c0002t0002g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172+358_172+379dup others(22): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTCTCT others(19): Show |
1 | a0001c0001t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.172+354_172+379dup others(26): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | G | GTCTGTCT others(7): Show |
1 | a0002c0002t0002g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.172+330_172+331ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTC | G | 17 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0045 others(14): Show |
17 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+378_172+379del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTCTC | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(7): Show |
10 | HG00140.hp2 HG00597.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.172+376_172+379del others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTCTCTC | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
9 | HG01074.hp2 HG02083.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.172+374_172+379del others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTCTCTCT others(1): Show |
G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0138 others(3): Show |
7 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+372_172+379del others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTCTCTCT others(3): Show |
G | 5 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0002c0002t0001g0143 others(2): Show |
6 | HG02559.hp1 HG02698.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+370_172+379del others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898328 | GTCTCTCT others(5): Show |
G | 1 | a0001c0001t0003g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172+368_172+379del others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | ||||||
| chr4:105898330 | C | CTCTCTCT others(7): Show |
1 | a0008c0006t0002g0194 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.172+342_172+343ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898330 | ||||||
| chr4:105898330 | C | G | 1 | a0001c0001t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172+329C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898330 | |||||||
| chr4:105898332 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0193 a0008c0006t0002g0192 |
2 | HG02896.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.172+342_172+343ins others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898332 | ||||||
| chr4:105898332 | C | G | 1 | a0004c0004t0002g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172+331C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898332 | |||||||
| chr4:105898334 | C | CTCTCTCT others(3): Show |
1 | a0002c0002t0002g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.172+342_172+343ins others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898334 | ||||||
| chr4:105898334 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.172+333C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898334 | |||||||
| chr4:105898340 | C | G | 2 | a0001c0001t0002g0210 a0001c0001t0004g0218 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+339C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898340 | |||||||
| chr4:105898342 | C | G | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+341C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898342 | |||||||
| chr4:105898344 | C | G | 10 | a0001c0001t0002g0214 a0003c0003t0001g0209 a0003c0003t0002g0001 others(7): Show |
11 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+343C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898344 | |||||||
| chr4:105898350 | C | G | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+349C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898350 | |||||||
| chr4:105898352 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172+351C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898352 | |||||||
| chr4:105898354 | C | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.172+353C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898354 | |||||||
| chr4:105898362 | C | G | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01069.hp2 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+361C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898362 | |||||||
| chr4:105898380 | C | CTCTCTCT others(7): Show |
5 | a0001c0001t0002g0213 a0002c0002t0001g0125 a0003c0003t0001g0120 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+379_172+380ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | |||||||
| chr4:105898380 | C | CTCTCTCT others(5): Show |
4 | a0003c0003t0002g0189 a0003c0003t0005g0126 a0003c0003t0005g0127 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+379_172+380ins others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | |||||||
| chr4:105898380 | C | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0138 others(34): Show |
40 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.172+379C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | |||||||
| chr4:105898408 | ATGGGGAT others(29): Show |
A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0012g0079 |
3 | HG02080.hp2 HG02083.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.172+444_172+479del others(36): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898408 | ||||||
| chr4:105898456 | T | C | 5 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0226 others(2): Show |
5 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+455T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898456 | |||||||
| chr4:105898633 | C | T | 26 | a0001c0001t0002g0184 a0002c0002t0001g0164 a0002c0002t0001g0172 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.172+632C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898633 | |||||||
| chr4:105898667 | T | C | 1 | a0002c0002t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.172+666T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898667 | |||||||
| chr4:105898723 | A | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+722A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898723 | |||||||
| chr4:105898732 | T | C | 86 | a0001c0001t0001g0040 a0001c0001t0002g0184 a0001c0001t0011g0116 others(83): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.172+731T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898732 | |||||||
| chr4:105898979 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
6 | HG01069.hp1 HG01192.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+978T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898979 | |||||||
| chr4:105899104 | G | A | 7 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(4): Show |
7 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+1103G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899104 | |||||||
| chr4:105899187 | T | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(27): Show |
32 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.172+1186T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899187 | |||||||
| chr4:105899390 | A | G | 17 | a0001c0001t0002g0210 a0003c0003t0001g0114 a0003c0003t0001g0209 others(14): Show |
18 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+1389A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899390 | |||||||
| chr4:105899468 | A | G | 3 | a0002c0002t0002g0007 a0002c0002t0002g0080 a0002c0002t0002g0081 |
3 | NA18956.hp2 NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.172+1467A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899468 | |||||||
| chr4:105899545 | C | T | 17 | a0001c0001t0002g0210 a0003c0003t0001g0114 a0003c0003t0001g0209 others(14): Show |
18 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+1544C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899545 | |||||||
| chr4:105899575 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+1574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899575 | |||||||
| chr4:105899626 | G | A | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+1625G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899626 | |||||||
| chr4:105899679 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0138 others(48): Show |
54 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.172+1678T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899679 | |||||||
| chr4:105900228 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172+2227A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900228 | |||||||
| chr4:105900276 | G | A | 1 | a0002c0002t0003g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2275G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900276 | |||||||
| chr4:105900277 | A | G | 1 | a0002c0002t0003g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2276A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900277 | |||||||
| chr4:105900304 | T | C | 1 | a0002c0002t0003g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2303T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900304 | |||||||
| chr4:105900305 | C | T | 1 | a0002c0002t0003g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2304C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900305 | |||||||
| chr4:105900331 | T | C | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+2330T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900331 | |||||||
| chr4:105900421 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(27): Show |
32 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.172+2420C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900421 | |||||||
| chr4:105900487 | C | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+2486C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900487 | |||||||
| chr4:105900569 | C | T | 4 | a0003c0003t0002g0001 a0003c0003t0002g0216 a0003c0003t0002g0217 others(1): Show |
5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+2568C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900569 | |||||||
| chr4:105900595 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172+2594G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900595 | |||||||
| chr4:105900831 | GTTGT | G | 6 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+2833_172+2836d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900831 | ||||||
| chr4:105900831 | GTTGTT | G | 12 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0002c0002t0001g0125 others(9): Show |
13 | HG02055.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.172+2833_172+2837d others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900831 | ||||||
| chr4:105900834 | G | GT | 29 | a0001c0001t0001g0058 a0001c0001t0001g0076 a0001c0001t0001g0086 others(26): Show |
30 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.172+2853dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900834 | ||||||
| chr4:105900834 | GT | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0093 a0001c0001t0006g0010 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.172+2853delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900834 | ||||||
| chr4:105900840 | T | TTTG | 5 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
6 | HG01069.hp1 HG01192.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+2841_172+2842i others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900840 | ||||||
| chr4:105900841 | T | TTG | 6 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+2841_172+2842i others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900841 | ||||||
| chr4:105900964 | G | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+2963G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900964 | |||||||
| chr4:105901099 | T | C | 19 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(16): Show |
20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3098T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901099 | |||||||
| chr4:105901144 | A | G | 1 | a0003c0003t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.172+3143A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901144 | |||||||
| chr4:105901162 | C | T | 19 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(16): Show |
20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901162 | |||||||
| chr4:105901357 | A | G | 5 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0028 others(2): Show |
5 | NA18942.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+3356A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901357 | |||||||
| chr4:105901542 | G | T | 19 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(16): Show |
20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3541G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901542 | |||||||
| chr4:105901703 | A | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+3702A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901703 | |||||||
| chr4:105901796 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+3795C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901796 | |||||||
| chr4:105901807 | A | G | 1 | a0001c0001t0004g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.172+3806A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901807 | |||||||
| chr4:105902114 | G | T | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+4113G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902114 | |||||||
| chr4:105902143 | A | C | 2 | a0002c0002t0002g0161 a0002c0002t0002g0162 |
2 | NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.172+4142A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902143 | |||||||
| chr4:105902299 | C | T | 1 | a0002c0002t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.172+4298C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902299 | |||||||
| chr4:105902328 | C | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+4327C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902328 | |||||||
| chr4:105902356 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+4355G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902356 | |||||||
| chr4:105902428 | T | C | 1 | a0003c0003t0005g0126 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.172+4427T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902428 | |||||||
| chr4:105902550 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+4549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902550 | |||||||
| chr4:105902886 | A | C | 1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172+4885A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902886 | |||||||
| chr4:105903220 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+5219C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903220 | |||||||
| chr4:105903232 | C | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+5231C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903232 | |||||||
| chr4:105903410 | G | T | 1 | a0002c0002t0003g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172+5409G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903410 | |||||||
| chr4:105903481 | G | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(44): Show |
50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+5480G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903481 | |||||||
| chr4:105903582 | C | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5581C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903582 | |||||||
| chr4:105903783 | C | CT | 23 | a0001c0001t0008g0057 a0002c0002t0001g0061 a0002c0002t0002g0027 others(20): Show |
23 | HG01070.hp2 HG01081.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.172+5801dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | ||||||
| chr4:105903783 | C | CTT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(11): Show |
15 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.172+5800_172+5801d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | ||||||
| chr4:105903783 | C | CTTT | 7 | a0001c0001t0002g0123 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
7 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+5799_172+5801d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | ||||||
| chr4:105903802 | T | G | 1 | a0002c0002t0002g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.172+5801T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903802 | |||||||
| chr4:105903824 | G | A | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+5823G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903824 | |||||||
| chr4:105903883 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.172+5882C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903883 | |||||||
| chr4:105903929 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5928T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903929 | |||||||
| chr4:105903970 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5969T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903970 | |||||||
| chr4:105904064 | G | A | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+6063G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904064 | |||||||
| chr4:105904083 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6082T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904083 | |||||||
| chr4:105904100 | A | G | 1 | a0004c0004t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.172+6099A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904100 | |||||||
| chr4:105904112 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6111T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904112 | |||||||
| chr4:105904182 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6181T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904182 | |||||||
| chr4:105904230 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6229G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904230 | |||||||
| chr4:105904252 | G | C | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+6251G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904252 | |||||||
| chr4:105904323 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+6322A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904323 | |||||||
| chr4:105904374 | G | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(44): Show |
50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+6373G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904374 | |||||||
| chr4:105904578 | G | A | 2 | a0002c0002t0002g0161 a0002c0002t0002g0162 |
2 | NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.172+6577G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904578 | |||||||
| chr4:105904603 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6602A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904603 | |||||||
| chr4:105904619 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6618G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904619 | |||||||
| chr4:105904626 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6625G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904626 | |||||||
| chr4:105904686 | AT | A | 13 | a0003c0003t0001g0209 a0003c0003t0002g0001 a0003c0003t0002g0208 others(10): Show |
14 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.172+6695delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105904686 | ||||||
| chr4:105904797 | A | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+6796A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904797 | |||||||
| chr4:105904849 | T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+6848T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904849 | |||||||
| chr4:105904891 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.172+6890A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904891 | |||||||
| chr4:105904892 | C | T | 1 | a0001c0001t0014g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.172+6891C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904892 | |||||||
| chr4:105904951 | G | A | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+6950G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904951 | |||||||
| chr4:105904977 | C | T | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+6976C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904977 | |||||||
| chr4:105905026 | G | A | 4 | a0003c0003t0002g0001 a0003c0003t0002g0216 a0003c0003t0002g0217 others(1): Show |
5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+7025G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905026 | |||||||
| chr4:105905054 | A | G | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+7053A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905054 | |||||||
| chr4:105905074 | C | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+7073C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905074 | |||||||
| chr4:105905074 | CT | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7084delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105905074 | ||||||
| chr4:105905153 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.172+7152C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905153 | |||||||
| chr4:105905159 | T | C | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+7158T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905159 | |||||||
| chr4:105905204 | A | G | 2 | a0001c0001t0002g0068 a0012c0010t0002g0190 |
2 | HG02965.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.172+7203A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905204 | |||||||
| chr4:105905315 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7314G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905315 | |||||||
| chr4:105905436 | T | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7435T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905436 | |||||||
| chr4:105905550 | G | A | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+7549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905550 | |||||||
| chr4:105905816 | G | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(45): Show |
51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+7815G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905816 | |||||||
| chr4:105906176 | G | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+8175G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906176 | |||||||
| chr4:105906268 | A | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8267A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906268 | |||||||
| chr4:105906286 | C | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8285C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906286 | |||||||
| chr4:105906311 | G | A | 5 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0028 others(2): Show |
5 | NA18942.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+8310G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906311 | |||||||
| chr4:105906331 | G | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(44): Show |
50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+8330G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906331 | |||||||
| chr4:105906343 | C | A | 1 | a0001c0001t0001g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.172+8342C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906343 | |||||||
| chr4:105906486 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(26): Show |
31 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.172+8485G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906486 | |||||||
| chr4:105906500 | C | CA | 48 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(45): Show |
51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+8499_172+8500i others(3): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906500 | |||||||
| chr4:105906513 | A | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8512A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906513 | |||||||
| chr4:105906708 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8707A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906708 | |||||||
| chr4:105906773 | A | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8772A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906773 | |||||||
| chr4:105906866 | A | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+8865A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906866 | |||||||
| chr4:105906872 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8871A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906872 | |||||||
| chr4:105907269 | C | T | 2 | a0002c0002t0002g0004 a0002c0002t0002g0153 |
3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172+9268C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907269 | |||||||
| chr4:105907273 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(15): Show |
19 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.172+9272A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907273 | |||||||
| chr4:105907343 | A | G | 5 | a0003c0003t0002g0001 a0003c0003t0002g0215 a0003c0003t0002g0216 others(2): Show |
6 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+9342A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907343 | |||||||
| chr4:105907376 | T | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+9375T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907376 | |||||||
| chr4:105907471 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+9470C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907471 | |||||||
| chr4:105907630 | T | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0086 others(2): Show |
5 | NA18942.hp2 NA18957.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+9629T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907630 | |||||||
| chr4:105907638 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.172+9637T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907638 | |||||||
| chr4:105907946 | G | A | 1 | a0002c0002t0002g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.172+9945G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907946 | |||||||
| chr4:105908323 | C | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0049 a0001c0001t0002g0077 |
3 | HG02630.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172+10322C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908323 | |||||||
| chr4:105908488 | T | C | 143 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0040 others(140): Show |
148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172+10487T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908488 | |||||||
| chr4:105908569 | C | CT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0199 others(17): Show |
21 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.172+10580dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105908569 | ||||||
| chr4:105908569 | CTT | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+10579_172+1058 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105908569 | ||||||
| chr4:105908586 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+10585C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908586 | |||||||
| chr4:105908632 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172+10631C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908632 | |||||||
| chr4:105908656 | T | C | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+10655T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908656 | |||||||
| chr4:105908756 | G | C | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+10755G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908756 | |||||||
| chr4:105908829 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.172+10828C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908829 | |||||||
| chr4:105909075 | G | A | 138 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0138 others(135): Show |
143 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.172+11074G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909075 | |||||||
| chr4:105909187 | T | C | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+11186T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909187 | |||||||
| chr4:105909648 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+11647T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909648 | |||||||
| chr4:105909834 | G | T | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+11833G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909834 | |||||||
| chr4:105910030 | A | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+12029A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910030 | |||||||
| chr4:105910065 | TA | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0210 others(8): Show |
12 | HG01361.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+12076delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910065 | ||||||
| chr4:105910121 | G | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+12120G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910121 | |||||||
| chr4:105910143 | C | T | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+12142C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910143 | |||||||
| chr4:105910189 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12188G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910189 | |||||||
| chr4:105910256 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12255A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910256 | |||||||
| chr4:105910261 | G | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+12260G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910261 | |||||||
| chr4:105910443 | T | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12442T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910443 | |||||||
| chr4:105910502 | CA | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(34): Show |
39 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.172+12513delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910502 | ||||||
| chr4:105910513 | AATTGT | A | 10 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12515_172+1251 others(9): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910513 | ||||||
| chr4:105910519 | A | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12518A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910519 | |||||||
| chr4:105910526 | G | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12525G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910526 | |||||||
| chr4:105910605 | G | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+12604G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910605 | |||||||
| chr4:105910888 | A | C | 3 | a0002c0002t0002g0108 a0002c0002t0002g0109 a0002c0002t0002g0110 |
3 | HG02647.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.172+12887A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910888 | |||||||
| chr4:105910935 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+12934C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910935 | |||||||
| chr4:105911047 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.172+13046A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911047 | |||||||
| chr4:105911355 | G | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+13354G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911355 | |||||||
| chr4:105911452 | C | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+13451C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911452 | |||||||
| chr4:105911563 | G | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.172+13562G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911563 | |||||||
| chr4:105911596 | G | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+13595G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911596 | |||||||
| chr4:105911602 | A | G | 6 | a0003c0003t0002g0001 a0003c0003t0002g0215 a0003c0003t0002g0216 others(3): Show |
7 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172+13601A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911602 | |||||||
| chr4:105911792 | T | C | 1 | a0002c0002t0002g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.172+13791T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911792 | |||||||
| chr4:105911983 | T | G | 1 | a0002c0002t0003g0183 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.172+13982T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911983 | |||||||
| chr4:105912011 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172+14010T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912011 | |||||||
| chr4:105912368 | C | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+14367C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912368 | |||||||
| chr4:105912449 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+14448G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912449 | |||||||
| chr4:105912690 | TATA | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-14642_173-1464 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105912690 | ||||||
| chr4:105912753 | A | G | 1 | a0002c0002t0002g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.173-14583A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912753 | |||||||
| chr4:105912763 | C | T | 1 | a0007c0007t0002g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.173-14573C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912763 | |||||||
| chr4:105912798 | T | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-14538T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912798 | |||||||
| chr4:105912809 | G | A | 1 | a0003c0003t0002g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.173-14527G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912809 | |||||||
| chr4:105912956 | C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-14380C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912956 | |||||||
| chr4:105913004 | A | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0214 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173-14332A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913004 | |||||||
| chr4:105913143 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14193A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913143 | |||||||
| chr4:105913207 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14129T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913207 | |||||||
| chr4:105913284 | G | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14052G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913284 | |||||||
| chr4:105913381 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-13955G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913381 | |||||||
| chr4:105913466 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-13870A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913466 | |||||||
| chr4:105913467 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-13869A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913467 | |||||||
| chr4:105913500 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.173-13836A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913500 | |||||||
| chr4:105913825 | T | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-13511T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913825 | |||||||
| chr4:105914177 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-13159A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914177 | |||||||
| chr4:105914367 | C | CTA | 6 | a0001c0001t0002g0005 a0003c0003t0001g0114 a0003c0003t0001g0219 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-12968_173-1296 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914367 | ||||||
| chr4:105914369 | C | A | 16 | a0001c0001t0001g0138 a0001c0001t0002g0005 a0001c0001t0002g0123 others(13): Show |
17 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-12967C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914369 | |||||||
| chr4:105914371 | C | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0078 others(50): Show |
57 | HG00735.hp1 HG01069.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.173-12965C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914371 | |||||||
| chr4:105914373 | C | A | 102 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(99): Show |
106 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.173-12963C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914373 | |||||||
| chr4:105914375 | A | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0037 others(6): Show |
9 | HG00735.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.173-12961A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914375 | |||||||
| chr4:105914382 | T | A | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-12954T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914382 | |||||||
| chr4:105914383 | A | T | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-12953A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914383 | |||||||
| chr4:105914480 | T | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0086 others(8): Show |
11 | HG01255.hp2 HG02004.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-12856T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914480 | |||||||
| chr4:105914480 | TAGAGAGA others(6): Show |
T | 1 | a0001c0001t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.173-12854_173-1284 others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914480 | ||||||
| chr4:105914482 | G | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0020 others(26): Show |
30 | HG00140.hp2 HG01069.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.173-12854G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914482 | |||||||
| chr4:105914483 | AGAGAGAG others(6): Show |
A | 2 | a0001c0001t0002g0214 a0001c0001t0004g0218 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-12844_173-1283 others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914483 | ||||||
| chr4:105914484 | G | T | 4 | a0003c0003t0005g0113 a0003c0003t0005g0126 a0003c0003t0005g0127 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-12852G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914484 | |||||||
| chr4:105914496 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.173-12840G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914496 | |||||||
| chr4:105914502 | A | G | 2 | a0003c0003t0004g0198 a0003c0003t0005g0197 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.173-12834A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914502 | |||||||
| chr4:105914522 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-12814C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914522 | |||||||
| chr4:105914816 | C | T | 1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.173-12520C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914816 | |||||||
| chr4:105914850 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-12486G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914850 | |||||||
| chr4:105914881 | G | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-12455G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914881 | |||||||
| chr4:105915031 | A | G | 19 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(16): Show |
20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-12305A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915031 | |||||||
| chr4:105915100 | C | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(45): Show |
51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.173-12236C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915100 | |||||||
| chr4:105915144 | C | T | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-12192C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915144 | |||||||
| chr4:105915171 | A | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-12165A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915171 | |||||||
| chr4:105915620 | G | T | 1 | a0002c0002t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.173-11716G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915620 | |||||||
| chr4:105915722 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.173-11614T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915722 | |||||||
| chr4:105915737 | G | A | 30 | a0001c0001t0001g0138 a0001c0001t0002g0005 a0001c0001t0002g0123 others(27): Show |
32 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.173-11599G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915737 | |||||||
| chr4:105915780 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-11556T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915780 | |||||||
| chr4:105915881 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.173-11455T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915881 | |||||||
| chr4:105915902 | T | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-11434T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915902 | |||||||
| chr4:105915905 | A | C | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-11431A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915905 | |||||||
| chr4:105915925 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.173-11411A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915925 | |||||||
| chr4:105916132 | G | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-11204G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916132 | |||||||
| chr4:105916196 | A | T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(5): Show |
9 | HG02257.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-11140A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916196 | |||||||
| chr4:105916217 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.173-11119C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916217 | |||||||
| chr4:105916221 | C | CT | 19 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(16): Show |
20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-11103dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916221 | ||||||
| chr4:105916221 | CT | C | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-11103delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916221 | ||||||
| chr4:105916248 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173-11088C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916248 | |||||||
| chr4:105916269 | G | C | 1 | a0002c0002t0002g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.173-11067G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916269 | |||||||
| chr4:105916386 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0201 a0001c0001t0002g0005 others(1): Show |
5 | HG00741.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-10934delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916386 | ||||||
| chr4:105916461 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.173-10875A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916461 | |||||||
| chr4:105916691 | T | A | 1 | a0002c0002t0001g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.173-10645T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916691 | |||||||
| chr4:105916769 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-10567G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916769 | |||||||
| chr4:105916779 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-10557A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916779 | |||||||
| chr4:105916790 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.173-10546C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916790 | |||||||
| chr4:105916962 | G | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0214 a0001c0001t0004g0218 |
3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-10374G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916962 | |||||||
| chr4:105916987 | G | GACCTTAT others(1): Show |
19 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(16): Show |
20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-10346_173-1033 others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916987 | ||||||
| chr4:105917047 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-10289A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917047 | |||||||
| chr4:105917177 | A | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(44): Show |
50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.173-10159A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917177 | |||||||
| chr4:105917270 | T | C | 7 | a0002c0002t0002g0003 a0004c0004t0002g0141 a0004c0004t0002g0144 others(4): Show |
8 | HG02559.hp1 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.173-10066T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917270 | |||||||
| chr4:105917572 | A | C | 2 | a0002c0002t0002g0004 a0002c0002t0002g0153 |
3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.173-9764A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917572 | |||||||
| chr4:105917685 | T | G | 1 | a0004c0004t0002g0152 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.173-9651T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917685 | |||||||
| chr4:105917861 | T | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-9475T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917861 | |||||||
| chr4:105917873 | T | C | 6 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-9463T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917873 | |||||||
| chr4:105917874 | G | T | 1 | a0003c0003t0001g0209 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.173-9462G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917874 | |||||||
| chr4:105917953 | A | G | 1 | a0002c0002t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-9383A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917953 | |||||||
| chr4:105917981 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-9355G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917981 | |||||||
| chr4:105918027 | C | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-9309C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918027 | |||||||
| chr4:105918694 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.173-8642G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918694 | |||||||
| chr4:105918732 | A | C | 19 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(16): Show |
20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-8604A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918732 | |||||||
| chr4:105918740 | T | C | 3 | a0002c0002t0001g0115 a0002c0002t0001g0118 a0002c0002t0001g0125 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-8596T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918740 | |||||||
| chr4:105918924 | G | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-8412G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918924 | |||||||
| chr4:105919007 | G | T | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-8329G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919007 | |||||||
| chr4:105919240 | A | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(32): Show |
37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-8096A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919240 | |||||||
| chr4:105919241 | T | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-8095T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919241 | |||||||
| chr4:105919302 | G | C | 90 | a0001c0001t0001g0040 a0001c0001t0002g0184 a0001c0001t0011g0116 others(87): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.173-8034G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919302 | |||||||
| chr4:105919468 | G | C | 1 | a0002c0002t0002g0212 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.173-7868G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919468 | |||||||
| chr4:105919474 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-7862A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919474 | |||||||
| chr4:105919794 | TAA | T | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-7541_173-7540d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919794 | |||||||
| chr4:105919976 | AATT | A | 2 | a0002c0002t0009g0227 a0002c0002t0009g0228 |
2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.173-7356_173-7354d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105919976 | ||||||
| chr4:105920093 | C | T | 3 | a0002c0002t0002g0156 a0002c0002t0002g0159 a0002c0002t0002g0181 |
3 | HG01175.hp2 HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.173-7243C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920093 | |||||||
| chr4:105920395 | T | TA | 7 | a0001c0001t0001g0031 a0001c0001t0002g0005 a0001c0001t0002g0124 others(4): Show |
8 | HG01175.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.173-6917dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAA | 10 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(7): Show |
10 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.173-6920_173-6917d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAA | 6 | a0001c0001t0002g0204 a0003c0003t0002g0001 a0003c0003t0002g0208 others(3): Show |
7 | HG00735.hp1 HG01243.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-6921_173-6917d others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.173-6931_173-6917d others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0206 others(1): Show |
5 | HG01069.hp1 HG01192.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-6932_173-6917d others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0205 a0001c0001t0002g0202 |
2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.173-6933_173-6917d others(19): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(18): Show |
1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-6917_173-6916i others(27): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(21): Show |
4 | a0003c0003t0002g0189 a0003c0003t0005g0113 a0003c0003t0005g0127 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-6917_173-6916i others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(23): Show |
2 | a0003c0003t0001g0120 a0003c0003t0005g0126 |
2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.173-6917_173-6916i others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | T | TAAAAAAA others(29): Show |
1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.173-6917_173-6916i others(38): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920395 | TA | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.173-6917delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | ||||||
| chr4:105920465 | A | G | 2 | a0008c0006t0002g0192 a0008c0006t0002g0194 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.173-6871A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920465 | |||||||
| chr4:105920560 | C | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(32): Show |
37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-6776C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920560 | |||||||
| chr4:105920590 | A | G | 3 | a0002c0002t0001g0115 a0002c0002t0001g0118 a0002c0002t0001g0125 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-6746A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920590 | |||||||
| chr4:105920660 | C | T | 2 | a0002c0002t0002g0004 a0002c0002t0002g0153 |
3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.173-6676C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920660 | |||||||
| chr4:105920721 | G | C | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.173-6615G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920721 | |||||||
| chr4:105920758 | T | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.173-6578T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920758 | |||||||
| chr4:105920805 | G | T | 156 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0031 others(153): Show |
161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.173-6531G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920805 | |||||||
| chr4:105921235 | C | G | 2 | a0003c0003t0001g0209 a0003c0003t0002g0208 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.173-6101C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921235 | |||||||
| chr4:105921276 | G | A | 2 | a0003c0003t0001g0209 a0003c0003t0002g0208 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.173-6060G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921276 | |||||||
| chr4:105921360 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.173-5976A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921360 | |||||||
| chr4:105921408 | G | C | 19 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(16): Show |
20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-5928G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921408 | |||||||
| chr4:105921660 | T | A | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-5676T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921660 | |||||||
| chr4:105921687 | C | T | 1 | a0003c0003t0005g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.173-5649C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921687 | |||||||
| chr4:105921826 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.173-5510C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921826 | |||||||
| chr4:105922311 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-5025T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922311 | |||||||
| chr4:105922335 | G | C | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-5001G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922335 | |||||||
| chr4:105922388 | TA | T | 2 | a0002c0002t0003g0165 a0002c0002t0003g0171 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.173-4947delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922388 | |||||||
| chr4:105922389 | AT | A | 68 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0002g0005 others(65): Show |
71 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(68): Show |
intron_variant | MODIFIER | c.173-4931delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105922389 | ||||||
| chr4:105922389 | ATTTT | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(32): Show |
37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-4934_173-4931d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105922389 | ||||||
| chr4:105922557 | T | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-4779T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922557 | |||||||
| chr4:105922798 | A | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4538A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922798 | |||||||
| chr4:105922801 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG00639.hp1 HG01106.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-4535G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922801 | |||||||
| chr4:105922852 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4484A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922852 | |||||||
| chr4:105922859 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.173-4477G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922859 | |||||||
| chr4:105922891 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4445C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922891 | |||||||
| chr4:105922944 | A | G | 2 | a0002c0002t0002g0028 a0002c0002t0002g0042 |
2 | NA18998.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.173-4392A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922944 | |||||||
| chr4:105922996 | A | C | 18 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(15): Show |
19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-4340A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922996 | |||||||
| chr4:105923060 | T | C | 4 | a0003c0003t0002g0001 a0003c0003t0002g0216 a0003c0003t0002g0217 others(1): Show |
5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-4276T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923060 | |||||||
| chr4:105923315 | G | GT | 26 | a0001c0001t0001g0040 a0002c0002t0001g0041 a0002c0002t0001g0060 others(23): Show |
27 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.173-4011dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105923315 | ||||||
| chr4:105923827 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.173-3509C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923827 | |||||||
| chr4:105923996 | C | T | 2 | a0001c0001t0008g0057 a0003c0003t0002g0215 |
2 | HG03471.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.173-3340C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923996 | |||||||
| chr4:105924039 | G | GC | 28 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(25): Show |
28 | HG00639.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.173-3287dupC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924039 | ||||||
| chr4:105924039 | GC | G | 20 | a0001c0001t0001g0053 a0001c0001t0002g0005 a0001c0001t0002g0123 others(17): Show |
22 | HG00735.hp1 HG01070.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.173-3287delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924039 | ||||||
| chr4:105924041 | C | A | 1 | a0002c0002t0002g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.173-3295C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924041 | |||||||
| chr4:105924041 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.173-3295C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924041 | |||||||
| chr4:105924042 | C | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
11 | HG01070.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-3294C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924042 | |||||||
| chr4:105924049 | C | A | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.173-3287C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924049 | |||||||
| chr4:105924061 | TA | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.173-3274delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924061 | |||||||
| chr4:105924101 | A | G | 11 | a0003c0003t0001g0209 a0003c0003t0002g0208 a0003c0003t0004g0015 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-3235A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924101 | |||||||
| chr4:105924232 | T | C | 3 | a0002c0002t0002g0191 a0008c0006t0002g0192 a0008c0006t0002g0194 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173-3104T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924232 | |||||||
| chr4:105924351 | A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-2985A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924351 | |||||||
| chr4:105924455 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.173-2881C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924455 | |||||||
| chr4:105924462 | A | G | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.173-2874A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924462 | |||||||
| chr4:105924525 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.173-2811G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924525 | |||||||
| chr4:105924656 | A | G | 9 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(6): Show |
9 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-2680A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924656 | |||||||
| chr4:105924750 | GCTACAGC others(8): Show |
G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.173-2583_173-2569d others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924750 | ||||||
| chr4:105924803 | T | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.173-2533T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924803 | |||||||
| chr4:105924989 | A | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0214 a0001c0001t0004g0218 |
3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-2347A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924989 | |||||||
| chr4:105925132 | G | A | 8 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(5): Show |
8 | HG01192.hp2 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.173-2204G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925132 | |||||||
| chr4:105925384 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.173-1952T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925384 | |||||||
| chr4:105925403 | G | T | 1 | a0003c0003t0001g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.173-1933G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925403 | |||||||
| chr4:105925762 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-1574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925762 | |||||||
| chr4:105925834 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.173-1502A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925834 | |||||||
| chr4:105925846 | G | A | 1 | a0002c0002t0002g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.173-1490G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925846 | |||||||
| chr4:105925846 | G | T | 1 | a0001c0001t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.173-1490G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925846 | |||||||
| chr4:105926175 | C | T | 3 | a0002c0002t0002g0191 a0008c0006t0002g0192 a0008c0006t0002g0194 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173-1161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926175 | |||||||
| chr4:105926280 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.173-1056A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926280 | |||||||
| chr4:105926308 | T | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0086 others(2): Show |
5 | NA18942.hp2 NA18957.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-1028T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926308 | |||||||
| chr4:105926334 | A | T | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-1002A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926334 | |||||||
| chr4:105926346 | A | T | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.173-990A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926346 | |||||||
| chr4:105926522 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.173-814A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926522 | |||||||
| chr4:105926597 | C | T | 1 | a0003c0003t0002g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.173-739C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926597 | |||||||
| chr4:105926809 | CTTGAA | C | 2 | a0003c0003t0015g0129 a0012c0010t0002g0190 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.173-521_173-517del others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105926809 | ||||||
| chr4:105927044 | A | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.173-292A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105927044 | |||||||
| chr4:105927157 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.173-179C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105927157 | |||||||
| chr4:105927479 | C | T | 3 | a0002c0002t0001g0087 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | NA18979.hp2 NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.265+51C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927479 | |||||||
| chr4:105927546 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.265+118C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927546 | |||||||
| chr4:105927702 | G | A | 1 | a0005c0005t0002g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.265+274G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927702 | |||||||
| chr4:105927905 | T | C | 1 | a0002c0002t0002g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.265+477T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927905 | |||||||
| chr4:105928051 | G | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+623G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928051 | |||||||
| chr4:105928052 | C | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+624C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928052 | |||||||
| chr4:105928095 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.265+667C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928095 | |||||||
| chr4:105928176 | G | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+748G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928176 | |||||||
| chr4:105928178 | C | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+750C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928178 | |||||||
| chr4:105928181 | C | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+753C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928181 | |||||||
| chr4:105928182 | T | C | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+754T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928182 | |||||||
| chr4:105928183 | T | C | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+755T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928183 | |||||||
| chr4:105928185 | G | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+757G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928185 | |||||||
| chr4:105928187 | G | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+759G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928187 | |||||||
| chr4:105928188 | C | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+760C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928188 | |||||||
| chr4:105928352 | A | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(216): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.265+924A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928352 | |||||||
| chr4:105928384 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.265+956C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928384 | |||||||
| chr4:105928408 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+980G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928408 | |||||||
| chr4:105928471 | C | T | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+1043C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928471 | |||||||
| chr4:105928485 | T | C | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+1057T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928485 | |||||||
| chr4:105928506 | A | G | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+1078A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928506 | |||||||
| chr4:105928523 | G | C | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+1095G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928523 | |||||||
| chr4:105928613 | C | CA | 13 | a0003c0003t0001g0114 a0003c0003t0001g0120 a0003c0003t0001g0219 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+1202dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | ||||||
| chr4:105928613 | CA | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0138 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.265+1202delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | ||||||
| chr4:105928613 | CAA | C | 7 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(4): Show |
7 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+1201_265+1202d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | ||||||
| chr4:105928630 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.265+1202A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928630 | |||||||
| chr4:105928632 | A | G | 1 | a0002c0002t0002g0003 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.265+1204A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928632 | |||||||
| chr4:105928736 | T | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265+1308T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928736 | |||||||
| chr4:105928782 | CAT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.265+1357_265+1358d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928782 | ||||||
| chr4:105928929 | AC | A | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1502delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928929 | |||||||
| chr4:105928931 | A | G | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1503A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928931 | |||||||
| chr4:105928932 | G | GT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(199): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.265+1512dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928932 | ||||||
| chr4:105928932 | G | T | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1504G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928932 | |||||||
| chr4:105929055 | A | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.265+1627A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929055 | |||||||
| chr4:105929088 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.265+1660A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929088 | |||||||
| chr4:105929205 | A | T | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+1777A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929205 | |||||||
| chr4:105929231 | C | T | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+1803C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929231 | |||||||
| chr4:105929343 | A | G | 91 | a0002c0002t0001g0041 a0002c0002t0001g0060 a0002c0002t0001g0061 others(88): Show |
93 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.265+1915A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929343 | |||||||
| chr4:105929622 | AGTATACT others(101): Show |
A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.265+2196_265+2303d others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105929622 | ||||||
| chr4:105929710 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0001g0188 |
3 | HG01109.hp1 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.265+2282G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929710 | |||||||
| chr4:105929738 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.265+2310A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929738 | |||||||
| chr4:105930101 | T | C | 3 | a0002c0002t0002g0187 a0007c0007t0002g0182 a0007c0007t0002g0185 |
3 | HG02451.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.265+2673T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930101 | |||||||
| chr4:105930160 | C | T | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+2732C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930160 | |||||||
| chr4:105930250 | C | T | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+2822C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930250 | |||||||
| chr4:105930627 | G | T | 1 | a0002c0002t0002g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.265+3199G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930627 | |||||||
| chr4:105930699 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.265+3271A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930699 | |||||||
| chr4:105931207 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.265+3779C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931207 | |||||||
| chr4:105931423 | T | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+3995T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931423 | |||||||
| chr4:105931668 | CA | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.265+4262delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | ||||||
| chr4:105931668 | CAA | C | 13 | a0001c0001t0001g0023 a0001c0001t0002g0213 a0001c0001t0002g0214 others(10): Show |
14 | HG02257.hp1 HG02559.hp1 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.265+4261_265+4262d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | ||||||
| chr4:105931668 | CAAA | C | 7 | a0001c0001t0002g0005 a0003c0003t0001g0120 a0003c0003t0002g0189 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+4260_265+4262d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | ||||||
| chr4:105931711 | G | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.265+4283G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931711 | |||||||
| chr4:105931901 | T | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+4473T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931901 | |||||||
| chr4:105932089 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0188 |
2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.265+4661C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932089 | |||||||
| chr4:105932221 | AC | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.266-4787delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932221 | |||||||
| chr4:105932360 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0083 |
2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.266-4649A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932360 | |||||||
| chr4:105932722 | A | C | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-4287A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932722 | |||||||
| chr4:105932723 | G | A | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-4286G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932723 | |||||||
| chr4:105932777 | A | G | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.266-4232A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932777 | |||||||
| chr4:105932851 | G | A | 2 | a0003c0003t0015g0129 a0012c0010t0002g0190 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-4158G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932851 | |||||||
| chr4:105932964 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.266-4045A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932964 | |||||||
| chr4:105933106 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.266-3903T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933106 | |||||||
| chr4:105933108 | A | C | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-3901A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933108 | |||||||
| chr4:105933255 | G | T | 2 | a0003c0003t0015g0129 a0012c0010t0002g0190 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-3754G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933255 | |||||||
| chr4:105933277 | G | A | 2 | a0003c0003t0015g0129 a0012c0010t0002g0190 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-3732G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933277 | |||||||
| chr4:105933362 | C | A | 2 | a0002c0002t0001g0176 a0002c0002t0003g0047 |
2 | NA19072.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.266-3647C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933362 | |||||||
| chr4:105933482 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.266-3527T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933482 | |||||||
| chr4:105933629 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.266-3380T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933629 | |||||||
| chr4:105933638 | TA | T | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-3367delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105933638 | ||||||
| chr4:105933946 | T | G | 1 | a0002c0002t0002g0142 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.266-3063T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933946 | |||||||
| chr4:105933951 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.266-3058A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933951 | |||||||
| chr4:105934020 | A | G | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2989A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934020 | |||||||
| chr4:105934065 | A | G | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-2944A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934065 | |||||||
| chr4:105934068 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.266-2941A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934068 | |||||||
| chr4:105934123 | A | C | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2886A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934123 | |||||||
| chr4:105934378 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.266-2631T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934378 | |||||||
| chr4:105934379 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(201): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.266-2630G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934379 | |||||||
| chr4:105934566 | G | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.266-2443G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934566 | |||||||
| chr4:105934567 | G | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0214 a0001c0001t0004g0218 |
3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.266-2442G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934567 | |||||||
| chr4:105934817 | A | G | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2192A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934817 | |||||||
| chr4:105934904 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.266-2105A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934904 | |||||||
| chr4:105935071 | T | C | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-1938T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935071 | |||||||
| chr4:105935102 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0011g0116 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.266-1907A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935102 | |||||||
| chr4:105935355 | T | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.266-1654T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935355 | |||||||
| chr4:105935391 | C | G | 1 | a0001c0001t0006g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.266-1618C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935391 | |||||||
| chr4:105935549 | C | T | 24 | a0002c0002t0001g0061 a0002c0002t0001g0163 a0002c0002t0002g0007 others(21): Show |
24 | HG01255.hp1 HG01261.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.266-1460C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935549 | |||||||
| chr4:105935644 | A | G | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-1365A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935644 | |||||||
| chr4:105935830 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.266-1179G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935830 | |||||||
| chr4:105935928 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.266-1081C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935928 | |||||||
| chr4:105936074 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-935G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936074 | |||||||
| chr4:105936178 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.266-831T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936178 | |||||||
| chr4:105936247 | G | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.266-762G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936247 | |||||||
| chr4:105936300 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0201 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-709A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936300 | |||||||
| chr4:105936448 | T | TTGGGA | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.266-560_266-556dup others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105936448 | ||||||
| chr4:105936500 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.266-509G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936500 | |||||||
| chr4:105936522 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.266-487G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936522 | |||||||
| chr4:105936609 | G | A | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-400G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936609 | |||||||
| chr4:105936779 | G | T | 2 | a0002c0002t0002g0104 a0002c0002t0002g0212 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.266-230G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936779 | |||||||
| chr4:105936808 | A | T | 3 | a0002c0002t0001g0115 a0002c0002t0001g0118 a0002c0002t0001g0125 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.266-201A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936808 | |||||||
| chr4:105936867 | G | C | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-142G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936867 | |||||||
| chr4:105936894 | AC | A | 7 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(4): Show |
8 | HG02257.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-114delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936894 | |||||||
| chr4:105937165 | G | T | 1 | a0004c0004t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.385+37G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937165 | |||||||
| chr4:105937320 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.385+192C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937320 | |||||||
| chr4:105937537 | A | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385+409A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937537 | |||||||
| chr4:105937741 | A | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.386-560A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937741 | |||||||
| chr4:105937880 | C | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.386-421C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937880 | |||||||
| chr4:105938168 | T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.386-133T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105938168 | |||||||
| chr4:105938242 | A | G | 1 | a0002c0002t0002g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.386-59A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105938242 | |||||||
| chr4:105938441 | T | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.505+21T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938441 | |||||||
| chr4:105938535 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.505+115A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938535 | |||||||
| chr4:105938764 | A | G | 1 | a0002c0002t0002g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.505+344A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938764 | |||||||
| chr4:105938785 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.505+365A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938785 | |||||||
| chr4:105938844 | T | G | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+424T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938844 | |||||||
| chr4:105939373 | G | C | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-702G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939373 | |||||||
| chr4:105939550 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.506-525T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939550 | |||||||
| chr4:105939824 | C | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0037 others(1): Show |
4 | HG02486.hp2 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-251C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939824 | |||||||
| chr4:105939879 | T | A | 1 | a0002c0002t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.506-196T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939879 | |||||||
| chr4:105939995 | A | T | 1 | a0001c0001t0002g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.506-80A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939995 | |||||||
| chr4:105940286 | G | C | 1 | a0001c0001t0002g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.640+77G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/11 | chr4 | 105940286 | |||||||
| chr4:105940400 | A | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.641-114A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/11 | chr4 | 105940400 | |||||||
| chr4:105940725 | T | C | 1 | a0001c0001t0012g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.763+89T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940725 | |||||||
| chr4:105940740 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.763+104A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940740 | |||||||
| chr4:105940860 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0074 |
2 | HG00597.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.763+224T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940860 | |||||||
| chr4:105941003 | AT | A | 7 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0003c0014t0001g0131 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+374delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105941003 | ||||||
| chr4:105941024 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.763+388T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941024 | |||||||
| chr4:105941025 | G | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.763+389G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941025 | |||||||
| chr4:105941056 | C | T | 3 | a0002c0002t0002g0156 a0002c0002t0002g0159 a0002c0002t0002g0181 |
3 | HG01175.hp2 HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.763+420C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941056 | |||||||
| chr4:105941151 | C | A | 25 | a0002c0002t0001g0041 a0002c0002t0001g0060 a0002c0002t0001g0069 others(22): Show |
26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.763+515C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941151 | |||||||
| chr4:105941210 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.763+574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941210 | |||||||
| chr4:105941686 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.764-621A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941686 | |||||||
| chr4:105941921 | T | C | 3 | a0002c0002t0001g0115 a0002c0002t0001g0118 a0002c0002t0001g0125 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.764-386T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941921 | |||||||
| chr4:105941925 | A | AT | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-380dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105941925 | ||||||
| chr4:105942017 | G | C | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.764-290G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942017 | |||||||
| chr4:105942039 | T | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.764-268T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942039 | |||||||
| chr4:105942077 | A | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.764-230A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942077 | |||||||
| chr4:105942105 | CTG | C | 7 | a0001c0001t0001g0138 a0001c0001t0002g0005 a0001c0001t0002g0124 others(4): Show |
8 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.764-192_764-191del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942105 | ||||||
| chr4:105942111 | G | C | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-196G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942111 | |||||||
| chr4:105942113 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(183): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.764-194G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942113 | |||||||
| chr4:105942115 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.764-192G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942115 | |||||||
| chr4:105942115 | G | GTA | 7 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0207 others(4): Show |
7 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-171_764-170dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942115 | ||||||
| chr4:105942117 | A | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.764-190A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942117 | |||||||
| chr4:105942125 | A | T | 1 | a0002c0002t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.764-182A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942125 | |||||||
| chr4:105942134 | T | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.764-173T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942134 | |||||||
| chr4:105942134 | T | TAG | 6 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0102 others(3): Show |
6 | HG01070.hp1 HG02004.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-172_764-171ins others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942134 | ||||||
| chr4:105942136 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(163): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.764-171T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942136 | |||||||
| chr4:105942136 | T | TAGAC | 37 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(34): Show |
39 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942136 | T | TATAGAC | 5 | a0001c0001t0001g0093 a0002c0002t0002g0150 a0003c0003t0001g0120 others(2): Show |
5 | HG01255.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942136 | T | TATATATA others(9): Show |
1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.764-170_764-169ins others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942136 | T | TATATATA others(9): Show |
4 | a0005c0005t0001g0132 a0005c0005t0001g0134 a0005c0005t0001g0135 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942136 | T | TATATATA others(13): Show |
1 | a0003c0003t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764-170_764-169ins others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942136 | T | TATATATA others(15): Show |
1 | a0003c0003t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.764-170_764-169ins others(22): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | ||||||
| chr4:105942245 | G | A | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.764-62G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942245 | |||||||
| chr4:105942252 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.764-55T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942252 | |||||||
| chr4:105942771 | C | T | 3 | a0002c0002t0001g0061 a0002c0002t0003g0038 a0002c0002t0003g0046 |
3 | HG01255.hp1 HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1159+69C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942771 | |||||||
| chr4:105942791 | C | T | 1 | a0003c0003t0004g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1159+89C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942791 | |||||||
| chr4:105942949 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1159+247G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942949 | |||||||
| chr4:105942952 | T | A | 1 | a0001c0001t0002g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+250T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942952 | |||||||
| chr4:105942965 | A | C | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1159+263A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942965 | |||||||
| chr4:105943116 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(200): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1159+414C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943116 | |||||||
| chr4:105943209 | G | A | 1 | a0002c0002t0003g0180 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1159+507G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943209 | |||||||
| chr4:105943640 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+938A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943640 | |||||||
| chr4:105943730 | C | A | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+1028C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943730 | |||||||
| chr4:105943770 | A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+1068A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943770 | |||||||
| chr4:105944088 | T | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+1386T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944088 | |||||||
| chr4:105944234 | C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+1532C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944234 | |||||||
| chr4:105944272 | A | G | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1159+1570A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944272 | |||||||
| chr4:105944405 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+1703A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944405 | |||||||
| chr4:105944428 | T | C | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+1726T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944428 | |||||||
| chr4:105944430 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0011g0116 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1159+1728A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944430 | |||||||
| chr4:105944698 | G | A | 2 | a0003c0003t0001g0209 a0003c0003t0002g0208 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1159+1996G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944698 | |||||||
| chr4:105944769 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1159+2067G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944769 | |||||||
| chr4:105944811 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1159+2109A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944811 | |||||||
| chr4:105944898 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1159+2196G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944898 | |||||||
| chr4:105944920 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+2218T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944920 | |||||||
| chr4:105945007 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+2305T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945007 | |||||||
| chr4:105945171 | G | C | 1 | a0002c0002t0002g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1159+2469G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945171 | |||||||
| chr4:105945179 | C | CTG | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+2477_1159+247 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945179 | |||||||
| chr4:105945216 | G | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1159+2514G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945216 | |||||||
| chr4:105945257 | C | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+2555C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945257 | |||||||
| chr4:105945416 | G | A | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+2714G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945416 | |||||||
| chr4:105945483 | C | G | 1 | a0005c0005t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1159+2781C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945483 | |||||||
| chr4:105945705 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1159+3003T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945705 | |||||||
| chr4:105945791 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1159+3089A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945791 | |||||||
| chr4:105945823 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+3121A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945823 | |||||||
| chr4:105945910 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1159+3208G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945910 | |||||||
| chr4:105946057 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1159+3355A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946057 | |||||||
| chr4:105946065 | A | G | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+3363A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946065 | |||||||
| chr4:105946085 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1159+3383T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946085 | |||||||
| chr4:105946115 | G | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1159+3413G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946115 | |||||||
| chr4:105946185 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+3483A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946185 | |||||||
| chr4:105946501 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+3799C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946501 | |||||||
| chr4:105946551 | T | C | 2 | a0003c0014t0001g0131 a0010c0011t0002g0130 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1159+3849T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946551 | |||||||
| chr4:105946559 | C | T | 2 | a0003c0014t0001g0131 a0010c0011t0002g0130 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1159+3857C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946559 | |||||||
| chr4:105946683 | G | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1159+3981G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946683 | |||||||
| chr4:105946743 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1159+4041A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946743 | |||||||
| chr4:105946984 | C | G | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1159+4282C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946984 | |||||||
| chr4:105947272 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+4570G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947272 | |||||||
| chr4:105947351 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+4649C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947351 | |||||||
| chr4:105947630 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1159+4928C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947630 | |||||||
| chr4:105947658 | G | A | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+4956G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947658 | |||||||
| chr4:105947673 | G | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+4971G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947673 | |||||||
| chr4:105947703 | C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+5001C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947703 | |||||||
| chr4:105947726 | C | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1159+5024C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947726 | |||||||
| chr4:105947770 | T | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+5068T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947770 | |||||||
| chr4:105947793 | G | T | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1159+5091G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947793 | |||||||
| chr4:105947932 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+5230G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947932 | |||||||
| chr4:105948113 | A | G | 8 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(5): Show |
8 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+5411A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948113 | |||||||
| chr4:105948138 | A | G | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+5436A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948138 | |||||||
| chr4:105948140 | C | T | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+5438C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948140 | |||||||
| chr4:105948614 | C | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+5912C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948614 | |||||||
| chr4:105948620 | A | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1159+5918A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948620 | |||||||
| chr4:105948643 | T | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(201): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1159+5941T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948643 | |||||||
| chr4:105948700 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+5998A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948700 | |||||||
| chr4:105948725 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+6023A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948725 | |||||||
| chr4:105949020 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1159+6318T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949020 | |||||||
| chr4:105949191 | A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+6489A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949191 | |||||||
| chr4:105949215 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0089 |
2 | HG02129.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1159+6513A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949215 | |||||||
| chr4:105949252 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+6550G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949252 | |||||||
| chr4:105949330 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+6628A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949330 | |||||||
| chr4:105949408 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0011g0116 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1159+6706T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949408 | |||||||
| chr4:105949440 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(184): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1159+6738G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949440 | |||||||
| chr4:105949503 | C | A | 5 | a0003c0003t0002g0001 a0003c0003t0002g0215 a0003c0003t0002g0216 others(2): Show |
6 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+6801C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949503 | |||||||
| chr4:105949504 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+6802T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949504 | |||||||
| chr4:105949699 | T | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+6997T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949699 | |||||||
| chr4:105949791 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1159+7089C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949791 | |||||||
| chr4:105949818 | A | G | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+7116A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949818 | |||||||
| chr4:105949825 | A | G | 1 | a0002c0002t0001g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1159+7123A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949825 | |||||||
| chr4:105949925 | C | T | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+7223C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949925 | |||||||
| chr4:105949975 | C | T | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1159+7273C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949975 | |||||||
| chr4:105949988 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+7286G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949988 | |||||||
| chr4:105949996 | C | G | 2 | a0001c0001t0002g0124 a0001c0001t0005g0112 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1159+7294C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949996 | |||||||
| chr4:105950004 | C | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+7302C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950004 | |||||||
| chr4:105950030 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(198): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1159+7328G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950030 | |||||||
| chr4:105950049 | C | A | 2 | a0002c0002t0009g0227 a0002c0002t0009g0228 |
2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1159+7347C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950049 | |||||||
| chr4:105950197 | C | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(199): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1159+7495C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950197 | |||||||
| chr4:105950343 | GTTATTT | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+7643_1159+764 others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105950343 | ||||||
| chr4:105950350 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1159+7648T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950350 | |||||||
| chr4:105950354 | C | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(190): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1159+7652C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950354 | |||||||
| chr4:105950489 | T | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1159+7787T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950489 | |||||||
| chr4:105950498 | A | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(214): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1159+7796A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950498 | |||||||
| chr4:105950964 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1160-7507C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950964 | |||||||
| chr4:105951072 | G | T | 1 | a0002c0002t0002g0081 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1160-7399G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951072 | |||||||
| chr4:105951074 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1160-7397C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951074 | |||||||
| chr4:105951100 | C | T | 7 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-7371C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951100 | |||||||
| chr4:105951160 | A | T | 2 | a0001c0001t0002g0210 a0011c0013t0010g0136 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-7311A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951160 | |||||||
| chr4:105951219 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-7252C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951219 | |||||||
| chr4:105951220 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1160-7251G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951220 | |||||||
| chr4:105951275 | T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1160-7196T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951275 | |||||||
| chr4:105951396 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(200): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1160-7075G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951396 | |||||||
| chr4:105951417 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0094 |
2 | HG00408.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1160-7054C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951417 | |||||||
| chr4:105951704 | T | C | 25 | a0002c0002t0001g0041 a0002c0002t0001g0060 a0002c0002t0001g0069 others(22): Show |
26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-6767T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951704 | |||||||
| chr4:105952005 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
12 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160-6466G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952005 | |||||||
| chr4:105952092 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1160-6379G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952092 | |||||||
| chr4:105952274 | T | C | 1 | a0002c0002t0002g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1160-6197T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952274 | |||||||
| chr4:105952312 | G | T | 3 | a0001c0001t0002g0210 a0010c0011t0002g0130 a0011c0013t0010g0136 |
3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-6159G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952312 | |||||||
| chr4:105952369 | T | G | 3 | a0001c0001t0002g0210 a0010c0011t0002g0130 a0011c0013t0010g0136 |
3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-6102T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952369 | |||||||
| chr4:105952421 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1160-6050C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952421 | |||||||
| chr4:105952765 | A | G | 1 | a0002c0002t0002g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1160-5706A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952765 | |||||||
| chr4:105952855 | C | G | 5 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-5616C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952855 | |||||||
| chr4:105952861 | C | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-5610C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952861 | |||||||
| chr4:105952922 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-5549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952922 | |||||||
| chr4:105953044 | G | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-5427G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953044 | |||||||
| chr4:105953117 | G | A | 8 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(5): Show |
8 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160-5354G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953117 | |||||||
| chr4:105953130 | C | T | 2 | a0001c0001t0001g0138 a0003c0014t0001g0131 |
2 | HG01192.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-5341C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953130 | |||||||
| chr4:105953248 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(195): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1160-5223G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953248 | |||||||
| chr4:105953410 | G | C | 3 | a0001c0001t0002g0210 a0010c0011t0002g0130 a0011c0013t0010g0136 |
3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-5061G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953410 | |||||||
| chr4:105953843 | G | A | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1160-4628G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953843 | |||||||
| chr4:105954608 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(195): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1160-3863C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105954608 | |||||||
| chr4:105955192 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1160-3279A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955192 | |||||||
| chr4:105955459 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0011g0116 a0003c0014t0001g0131 |
3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-3012A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955459 | |||||||
| chr4:105955468 | C | T | 2 | a0002c0002t0002g0065 a0002c0002t0002g0084 |
2 | NA18979.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1160-3003C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955468 | |||||||
| chr4:105955690 | CT | C | 26 | a0001c0001t0002g0210 a0003c0003t0001g0114 a0003c0003t0001g0209 others(23): Show |
27 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1160-2772delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105955690 | ||||||
| chr4:105955724 | G | T | 9 | a0003c0003t0001g0209 a0003c0003t0002g0208 a0003c0003t0004g0015 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-2747G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955724 | |||||||
| chr4:105955742 | T | C | 25 | a0002c0002t0001g0041 a0002c0002t0001g0060 a0002c0002t0001g0069 others(22): Show |
26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-2729T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955742 | |||||||
| chr4:105955758 | T | A | 3 | a0001c0001t0001g0138 a0001c0001t0011g0116 a0003c0014t0001g0131 |
3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-2713T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955758 | |||||||
| chr4:105955806 | C | CA | 27 | a0001c0001t0001g0138 a0001c0001t0002g0210 a0001c0001t0011g0116 others(24): Show |
28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1160-2665_1160-266 others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955806 | |||||||
| chr4:105955820 | T | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0199 others(49): Show |
55 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1160-2651T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955820 | |||||||
| chr4:105956086 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0001g0188 |
3 | HG01109.hp1 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1160-2385A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956086 | |||||||
| chr4:105956152 | CTG | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(78): Show |
82 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1160-2317_1160-231 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105956152 | ||||||
| chr4:105956186 | T | G | 3 | a0001c0001t0002g0210 a0010c0011t0002g0130 a0011c0013t0010g0136 |
3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-2285T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956186 | |||||||
| chr4:105956271 | G | C | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-2200G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956271 | |||||||
| chr4:105956308 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1160-2163A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956308 | |||||||
| chr4:105956441 | G | A | 1 | a0001c0001t0006g0010 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1160-2030G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956441 | |||||||
| chr4:105956474 | A | G | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1997A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956474 | |||||||
| chr4:105956485 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1160-1986C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956485 | |||||||
| chr4:105956486 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1160-1985G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956486 | |||||||
| chr4:105956582 | A | G | 3 | a0001c0001t0002g0210 a0010c0011t0002g0130 a0011c0013t0010g0136 |
3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-1889A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956582 | |||||||
| chr4:105956684 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0222 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1160-1787A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956684 | |||||||
| chr4:105956714 | A | G | 4 | a0001c0001t0002g0210 a0002c0002t0002g0159 a0010c0011t0002g0130 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1757A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956714 | |||||||
| chr4:105956886 | G | A | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1585G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956886 | |||||||
| chr4:105956888 | C | A | 6 | a0002c0002t0002g0157 a0002c0002t0002g0158 a0002c0002t0002g0166 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1583C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956888 | |||||||
| chr4:105956979 | A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1160-1492A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956979 | |||||||
| chr4:105957254 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1160-1217G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957254 | |||||||
| chr4:105957371 | G | A | 2 | a0001c0001t0001g0138 a0003c0014t0001g0131 |
2 | HG01192.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-1100G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957371 | |||||||
| chr4:105957398 | C | CTGAT | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1069_1160-106 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105957398 | ||||||
| chr4:105957450 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160-1021T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957450 | |||||||
| chr4:105957496 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1160-975G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957496 | |||||||
| chr4:105957582 | A | G | 3 | a0002c0002t0002g0108 a0002c0002t0002g0109 a0002c0002t0002g0110 |
3 | HG02647.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1160-889A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957582 | |||||||
| chr4:105957769 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1160-702C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957769 | |||||||
| chr4:105957831 | G | A | 2 | a0010c0011t0002g0130 a0011c0013t0010g0136 |
2 | HG01070.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1160-640G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957831 | |||||||
| chr4:105957866 | A | G | 1 | a0002c0002t0001g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1160-605A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957866 | |||||||
| chr4:105957914 | G | T | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1160-557G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957914 | |||||||
| chr4:105958315 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1160-156C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958315 | |||||||
| chr4:105958422 | A | G | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-49A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958422 | |||||||
| chr4:105958427 | T | TCA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
10 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1160-27_1160-26dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105958427 | ||||||
| chr4:105958435 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0011g0116 a0003c0014t0001g0131 |
3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-36A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958435 | |||||||
| chr4:105958618 | A | G | 2 | a0001c0001t0002g0123 a0001c0001t0002g0214 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1246+61A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958618 | |||||||
| chr4:105958812 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1247-216A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958812 | |||||||
| chr4:105958899 | A | G | 41 | a0002c0002t0001g0061 a0002c0002t0001g0163 a0002c0002t0002g0007 others(38): Show |
42 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1247-129A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958899 | |||||||
| chr4:105958900 | T | C | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1247-128T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958900 | |||||||
| chr4:105959288 | A | G | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+162A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959288 | |||||||
| chr4:105959356 | A | G | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+230A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959356 | |||||||
| chr4:105959523 | C | CT | 27 | a0001c0001t0001g0094 a0001c0001t0002g0123 a0001c0001t0002g0210 others(24): Show |
28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+413dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959523 | ||||||
| chr4:105959523 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1345+397C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959523 | |||||||
| chr4:105959523 | CT | C | 25 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0002g0124 others(22): Show |
25 | HG01192.hp2 HG01255.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1345+413delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959523 | ||||||
| chr4:105959592 | T | C | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1345+466T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959592 | |||||||
| chr4:105959644 | G | A | 23 | a0003c0003t0001g0114 a0003c0003t0001g0209 a0003c0003t0001g0219 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+518G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959644 | |||||||
| chr4:105959809 | C | CT | 29 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0199 others(26): Show |
30 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.1345+701dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | ||||||
| chr4:105959809 | CT | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0001g0138 others(3): Show |
6 | HG01070.hp1 HG01258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+701delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | ||||||
| chr4:105959809 | CTT | C | 18 | a0001c0001t0002g0210 a0003c0003t0001g0209 a0003c0003t0002g0001 others(15): Show |
19 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1345+700_1345+701d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | ||||||
| chr4:105959809 | CTTT | C | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+699_1345+701d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | ||||||
| chr4:105959836 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345+710G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959836 | |||||||
| chr4:105959863 | G | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1345+737G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959863 | |||||||
| chr4:105959966 | T | C | 5 | a0001c0001t0001g0137 a0001c0001t0001g0229 a0001c0001t0006g0010 others(2): Show |
5 | HG00735.hp2 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+840T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959966 | |||||||
| chr4:105960012 | C | G | 5 | a0002c0002t0001g0087 a0002c0002t0003g0165 a0002c0002t0003g0171 others(2): Show |
5 | HG00140.hp1 HG00741.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+886C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960012 | |||||||
| chr4:105960027 | G | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1345+901G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960027 | |||||||
| chr4:105960100 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1345+974G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960100 | |||||||
| chr4:105960200 | G | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1074G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960200 | |||||||
| chr4:105960279 | T | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(39): Show |
44 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+1153T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960279 | |||||||
| chr4:105960284 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1345+1158A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960284 | |||||||
| chr4:105960498 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1345+1372A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960498 | |||||||
| chr4:105960594 | C | T | 2 | a0002c0002t0009g0227 a0002c0002t0009g0228 |
2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1345+1468C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960594 | |||||||
| chr4:105960622 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1345+1496A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960622 | |||||||
| chr4:105960761 | C | CGT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0201 a0001c0001t0002g0005 others(11): Show |
15 | HG01070.hp2 HG01192.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1345+1656_1345+165 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | ||||||
| chr4:105960761 | C | CGTGT | 8 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1345+1654_1345+165 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | ||||||
| chr4:105960761 | CGTGT | C | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1654_1345+165 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | ||||||
| chr4:105960921 | A | G | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1795A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960921 | |||||||
| chr4:105960960 | C | G | 1 | a0001c0001t0002g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1345+1834C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960960 | |||||||
| chr4:105961059 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1345+1933C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961059 | |||||||
| chr4:105961239 | A | C | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+2113A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961239 | |||||||
| chr4:105961241 | C | A | 1 | a0011c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+2115C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961241 | |||||||
| chr4:105961377 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345+2251A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961377 | |||||||
| chr4:105961401 | A | G | 6 | a0003c0003t0001g0114 a0003c0003t0001g0219 a0005c0005t0001g0132 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+2275A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961401 | |||||||
| chr4:105961437 | C | T | 32 | a0001c0001t0001g0138 a0001c0001t0002g0123 a0001c0001t0002g0124 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1345+2311C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961437 | |||||||
| chr4:105961699 | C | T | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+2573C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961699 | |||||||
| chr4:105961735 | C | T | 1 | a0001c0001t0008g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1345+2609C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961735 | |||||||
| chr4:105961987 | G | T | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+2861G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961987 | |||||||
| chr4:105962059 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0011g0116 a0003c0014t0001g0131 |
3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345+2933G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962059 | |||||||
| chr4:105962345 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0201 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1345+3219A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962345 | |||||||
| chr4:105962460 | T | C | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3334T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962460 | |||||||
| chr4:105962803 | T | C | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1345+3677T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962803 | |||||||
| chr4:105962816 | T | C | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3690T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962816 | |||||||
| chr4:105962851 | A | ATG | 7 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0076 others(4): Show |
7 | HG00099.hp1 HG00438.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345+3743_1345+374 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | ||||||
| chr4:105962851 | ATG | A | 12 | a0001c0001t0001g0138 a0003c0003t0001g0120 a0003c0003t0002g0189 others(9): Show |
12 | HG01070.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+3743_1345+374 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | ||||||
| chr4:105962851 | ATGTG | A | 12 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+3741_1345+374 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | ||||||
| chr4:105962865 | GTGTGTA | G | 16 | a0003c0003t0001g0209 a0003c0003t0002g0001 a0003c0003t0002g0208 others(13): Show |
17 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1345+3745_1345+375 others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962865 | ||||||
| chr4:105962873 | G | A | 16 | a0003c0003t0001g0209 a0003c0003t0002g0001 a0003c0003t0002g0208 others(13): Show |
17 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1345+3747G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962873 | |||||||
| chr4:105962885 | A | G | 1 | a0010c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345+3759A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962885 | |||||||
| chr4:105963019 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0002g0202 others(2): Show |
5 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+3893G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963019 | |||||||
| chr4:105963086 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0011g0116 a0003c0014t0001g0131 |
3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345+3960G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963086 | |||||||
| chr4:105963097 | C | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3971C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963097 | |||||||
| chr4:105963133 | G | A | 3 | a0002c0002t0002g0191 a0008c0006t0002g0192 a0008c0006t0002g0194 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1345+4007G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963133 | |||||||
| chr4:105963145 | A | G | 8 | a0003c0003t0001g0120 a0003c0003t0002g0189 a0003c0003t0005g0113 others(5): Show |
8 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345+4019A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963145 | |||||||
| chr4:105963200 | A | G | 31 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0124 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1346-3988A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963200 | |||||||
| chr4:105963229 | A | AT | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3959_1346-395 others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963229 | |||||||
| chr4:105963582 | G | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3606G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963582 | |||||||
| chr4:105963639 | A | C | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3549A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963639 | |||||||
| chr4:105963660 | C | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3528C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963660 | |||||||
| chr4:105963806 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1346-3382A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963806 | |||||||
| chr4:105963873 | G | A | 1 | a0002c0002t0002g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1346-3315G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963873 | |||||||
| chr4:105963877 | C | G | 1 | a0001c0001t0011g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1346-3311C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963877 | |||||||
| chr4:105963988 | C | A | 1 | a0001c0001t0002g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1346-3200C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963988 | |||||||
| chr4:105964199 | C | T | 1 | a0002c0002t0003g0183 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1346-2989C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964199 | |||||||
| chr4:105964341 | G | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-2847G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964341 | |||||||
| chr4:105964429 | G | A | 28 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0214 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-2759G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964429 | |||||||
| chr4:105964695 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1346-2493T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964695 | |||||||
| chr4:105964861 | T | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-2327T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964861 | |||||||
| chr4:105964912 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-2276A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964912 | |||||||
| chr4:105965182 | T | C | 6 | a0001c0001t0002g0049 a0003c0003t0001g0114 a0003c0003t0001g0219 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-2006T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965182 | |||||||
| chr4:105965302 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1346-1886G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965302 | |||||||
| chr4:105965360 | C | CA | 21 | a0001c0001t0001g0082 a0001c0001t0002g0064 a0001c0001t0002g0098 others(18): Show |
21 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-1811dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | ||||||
| chr4:105965360 | C | CAAA | 14 | a0001c0001t0002g0077 a0001c0001t0002g0123 a0001c0001t0002g0214 others(11): Show |
15 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1346-1813_1346-181 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | ||||||
| chr4:105965360 | CA | C | 23 | a0001c0001t0001g0058 a0001c0001t0001g0173 a0001c0001t0001g0186 others(20): Show |
23 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1346-1811delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | ||||||
| chr4:105965399 | C | T | 12 | a0001c0001t0002g0005 a0001c0001t0002g0210 a0003c0003t0001g0120 others(9): Show |
13 | HG01070.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346-1789C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965399 | |||||||
| chr4:105965733 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1346-1455A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965733 | |||||||
| chr4:105965836 | G | T | 2 | a0011c0013t0010g0136 a0013c0012t0010g0122 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1346-1352G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965836 | |||||||
| chr4:105965862 | G | A | 9 | a0001c0001t0005g0112 a0003c0003t0005g0113 a0003c0003t0005g0121 others(6): Show |
9 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-1326G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965862 | |||||||
| chr4:105966006 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(80): Show |
84 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1346-1182G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966006 | |||||||
| chr4:105966017 | G | GAGA | 135 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(132): Show |
139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1346-1167_1346-116 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966017 | ||||||
| chr4:105966148 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1346-1040T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966148 | |||||||
| chr4:105966285 | T | C | 8 | a0001c0001t0005g0112 a0003c0003t0005g0113 a0003c0003t0005g0121 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-903T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966285 | |||||||
| chr4:105966331 | A | AT | 5 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01069.hp2 HG01081.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-849dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966331 | ||||||
| chr4:105966341 | T | G | 6 | a0003c0003t0005g0113 a0003c0003t0005g0121 a0003c0003t0005g0126 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-847T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966341 | |||||||
| chr4:105966478 | A | G | 2 | a0011c0013t0010g0136 a0013c0012t0010g0122 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1346-710A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966478 | |||||||
| chr4:105966626 | C | CT | 4 | a0001c0001t0002g0123 a0001c0001t0002g0214 a0003c0003t0002g0208 others(1): Show |
4 | HG02615.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-561dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966626 | ||||||
| chr4:105966661 | C | T | 1 | a0013c0012t0010g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346-527C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966661 | |||||||
| chr4:105966670 | ATTT | A | 8 | a0001c0001t0005g0112 a0003c0003t0005g0113 a0003c0003t0005g0121 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-508_1346-506d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966670 | ||||||
| chr4:105966889 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1346-299T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966889 | |||||||
| chr4:105966918 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
123 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1346-270C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966918 | |||||||
| chr4:105966951 | T | C | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1346-237T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966951 | |||||||
| chr4:105967052 | A | G | 1 | a0003c0003t0002g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1346-136A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105967052 | |||||||
| chr4:105967106 | A | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0201 a0001c0001t0002g0024 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1346-82A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105967106 | |||||||
| chr4:105967479 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1602+35C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967479 | |||||||
| chr4:105967524 | C | G | 1 | a0003c0003t0002g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+80C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967524 | |||||||
| chr4:105967585 | C | T | 1 | a0012c0010t0002g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1602+141C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967585 | |||||||
| chr4:105967728 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1602+284G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967728 | |||||||
| chr4:105967931 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1602+487G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967931 | |||||||
| chr4:105968333 | G | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(101): Show |
106 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1603-562G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968333 | |||||||
| chr4:105968423 | C | T | 2 | a0001c0001t0002g0210 a0010c0011t0002g0130 |
2 | HG01070.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1603-472C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968423 | |||||||
| chr4:105968560 | G | T | 1 | a0009c0009t0001g0155 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1603-335G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968560 |