Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79050 |
| ensemblid | ENSG00000184967.7 |
| hgncid | 28461 |
| symbol | NOC4L |
| name | nucleolar complex associated 4 homolog |
| refseq_nuc | NM_024078.3 |
| refseq_prot | NP_076983.1 |
| ensembl_nuc | ENST00000330579.6 |
| ensembl_prot | ENSP00000328854.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 132144457 |
| end | 132152468 |
| strand | + |
| ver | v1.2 |
| region | chr12:132144457-132152468 |
| region5000 | chr12:132139457-132157468 |
| regionname0 | NOC4L_chr12_132144457_132152468 |
| regionname5000 | NOC4L_chr12_132139457_132157468 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 516 | 226 | 65 | 51 | 80 | 9 | 19 | 60 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0002 | 0/0 | 322 | 34 | 10 | 2 | 16 | 1 | 5 | 12 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(317): Show |
chr12 | 132139457 | 132157468 |
| a0003 | 0/0 | 326 | 8 | 1 | 1 | 5 | 0 | 1 | 3 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(321): Show |
chr12 | 132139457 | 132157468 |
| a0004 | 0/0 | 351 | 6 | 1 | 2 | 3 | 0 | 0 | 2 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(346): Show |
chr12 | 132139457 | 132157468 |
| a0005 | 0/0 | 317 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(312): Show |
chr12 | 132139457 | 132157468 |
| a0006 | 0/0 | 323 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(318): Show |
chr12 | 132139457 | 132157468 |
| a0007 | 0/0 | 516 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0008 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0009 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0010 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0011 | 0/0 | 516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0012 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0013 | 0/0 | 516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0014 | 0/0 | 516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0015 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0016 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| a0017 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(335): Show |
chr12 | 132139457 | 132157468 |
| a0018 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | MEREP others(511): Show |
chr12 | 132139457 | 132157468 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1548 | 181 | 55 | 50 | 53 | 7 | 14 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0003 | 0/0 | 1548 | 27 | 0 | 0 | 24 | 0 | 3 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0004 | 0/0 | 1548 | 5 | 5 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0005 | 0/0 | 1548 | 5 | 1 | 1 | 0 | 1 | 2 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0006 | 0/0 | 1548 | 3 | 2 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0015 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0020 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0023 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0026 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0001c0039 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0002c0002 | 0/0 | 1543 | 29 | 9 | 2 | 12 | 1 | 5 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1538): Show |
chr12 | 132139457 | 132157468 | ||
| a0002c0008 | 0/0 | 1543 | 3 | 0 | 0 | 3 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1538): Show |
chr12 | 132139457 | 132157468 | ||
| a0002c0016 | 0/0 | 1543 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1538): Show |
chr12 | 132139457 | 132157468 | ||
| a0002c0035 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1539): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0011 | 0/0 | 1636 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1631): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0028 | 0/0 | 1680 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1675): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0029 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1763): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0030 | 0/0 | 3645 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(3640): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0031 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1807): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0032 | 0/0 | 1856 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1851): Show |
chr12 | 132139457 | 132157468 | ||
| a0003c0033 | 0/0 | 2120 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(2115): Show |
chr12 | 132139457 | 132157468 | ||
| a0004c0007 | 0/0 | 1549 | 3 | 0 | 0 | 3 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1544): Show |
chr12 | 132139457 | 132157468 | ||
| a0004c0010 | 0/0 | 1549 | 2 | 1 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1544): Show |
chr12 | 132139457 | 132157468 | ||
| a0004c0041 | 0/0 | 1549 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1544): Show |
chr12 | 132139457 | 132157468 | ||
| a0005c0013 | 0/0 | 1543 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1538): Show |
chr12 | 132139457 | 132157468 | ||
| a0005c0036 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1539): Show |
chr12 | 132139457 | 132157468 | ||
| a0005c0037 | 0/0 | 1543 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1538): Show |
chr12 | 132139457 | 132157468 | ||
| a0006c0012 | 0/0 | 1592 | 2 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1587): Show |
chr12 | 132139457 | 132157468 | ||
| a0006c0034 | 0/0 | 1592 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1587): Show |
chr12 | 132139457 | 132157468 | ||
| a0007c0009 | 0/0 | 1548 | 2 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0008c0025 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0009c0038 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0010c0021 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0011c0040 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0012c0017 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0013c0022 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0014c0014 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0015c0024 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0016c0019 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 | ||
| a0017c0027 | 0/0 | 1810 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1805): Show |
chr12 | 132139457 | 132157468 | ||
| a0018c0018 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | ATGGA others(1543): Show |
chr12 | 132139457 | 132157468 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1650 | 180 | 55 | 49 | 53 | 7 | 14 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0001t0002 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0003t0001 | 0/0 | 1650 | 27 | 0 | 0 | 24 | 0 | 3 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0004t0001 | 0/0 | 1650 | 5 | 5 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0005t0001 | 0/0 | 1650 | 5 | 1 | 1 | 0 | 1 | 2 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0006t0001 | 0/0 | 1650 | 3 | 2 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0015t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0020t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0023t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0026t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0001c0039t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0002c0002t0001 | 0/0 | 1645 | 27 | 8 | 2 | 12 | 1 | 4 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0002c0002t0003 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0002c0002t0004 | 0/0 | 1645 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0002c0008t0001 | 0/0 | 1645 | 3 | 0 | 0 | 3 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0002c0016t0001 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0002c0035t0001 | 0/0 | 1646 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1641): Show |
chr12 | 132139457 | 132157468 |
| a0003c0011t0001 | 0/0 | 1738 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1733): Show |
chr12 | 132139457 | 132157468 |
| a0003c0028t0001 | 0/0 | 1782 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1777): Show |
chr12 | 132139457 | 132157468 |
| a0003c0029t0001 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1865): Show |
chr12 | 132139457 | 132157468 |
| a0003c0030t0001 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(3742): Show |
chr12 | 132139457 | 132157468 |
| a0003c0031t0001 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1909): Show |
chr12 | 132139457 | 132157468 |
| a0003c0032t0001 | 0/0 | 1958 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1953): Show |
chr12 | 132139457 | 132157468 |
| a0003c0033t0001 | 0/0 | 2222 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(2217): Show |
chr12 | 132139457 | 132157468 |
| a0004c0007t0001 | 0/0 | 1651 | 3 | 0 | 0 | 3 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1646): Show |
chr12 | 132139457 | 132157468 |
| a0004c0010t0001 | 0/0 | 1651 | 2 | 1 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1646): Show |
chr12 | 132139457 | 132157468 |
| a0004c0041t0001 | 0/0 | 1651 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1646): Show |
chr12 | 132139457 | 132157468 |
| a0005c0013t0001 | 0/0 | 1645 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0005c0036t0001 | 0/0 | 1646 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1641): Show |
chr12 | 132139457 | 132157468 |
| a0005c0037t0001 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1640): Show |
chr12 | 132139457 | 132157468 |
| a0006c0012t0001 | 0/0 | 1694 | 2 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1689): Show |
chr12 | 132139457 | 132157468 |
| a0006c0034t0001 | 0/0 | 1694 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1689): Show |
chr12 | 132139457 | 132157468 |
| a0007c0009t0001 | 0/0 | 1650 | 2 | 0 | 1 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0008c0025t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0009c0038t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0010c0021t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0011c0040t0001 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0012c0017t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0013c0022t0001 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0014c0014t0001 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0015c0024t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0016c0019t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| a0017c0027t0001 | 0/0 | 1912 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1907): Show |
chr12 | 132139457 | 132157468 |
| a0018c0018t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | GAGAA others(1645): Show |
chr12 | 132139457 | 132157468 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0024 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0005t0001g0001 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0006t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0006t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0015t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0020t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0023t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0026t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0001c0039t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0016t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0002c0035t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0011t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0011t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0028t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0029t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0030t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0031t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0032t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0003c0033t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0010t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0010t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0004c0041t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0005c0013t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0005c0013t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0005c0036t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0005c0037t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0006c0012t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0006c0012t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0006c0034t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0007c0009t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0007c0009t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0008c0025t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0009c0038t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0010c0021t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0011c0040t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0012c0017t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0013c0022t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0014c0014t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0015c0024t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0016c0019t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0017c0027t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| a0018c0018t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0001 | EUR | GBR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0192 | EUR | FIN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00423 | hp1 | a0003 | c0011 | t0001 | g0208 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00642 | hp2 | a0004 | c0010 | t0001 | g0003 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CHS | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00733 | hp2 | a0006 | c0012 | t0001 | g0176 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00735 | hp2 | a0004 | c0041 | t0001 | g0002 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01106 | hp2 | a0003 | c0028 | t0001 | g0201 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01258 | hp1 | a0001 | c0005 | t0001 | g0043 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02027 | hp2 | a0008 | c0025 | t0001 | g0106 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02056 | hp1 | a0003 | c0033 | t0001 | g0223 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02074 | hp2 | a0005 | c0013 | t0001 | g0103 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02080 | hp2 | a0004 | c0007 | t0001 | g0001 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02132 | hp2 | a0005 | c0013 | t0001 | g0100 | EAS | KHV | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02258 | hp2 | a0002 | c0016 | t0001 | g0150 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02293 | hp1 | a0007 | c0009 | t0001 | g0006 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0152 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02647 | hp2 | a0009 | c0038 | t0001 | g0155 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02683 | hp1 | a0006 | c0012 | t0001 | g0177 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0219 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02809 | hp1 | a0010 | c0021 | t0001 | g0087 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0153 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02970 | hp1 | a0003 | c0030 | t0001 | g0072 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02976 | hp2 | a0001 | c0023 | t0001 | g0088 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03017 | hp2 | a0011 | c0040 | t0001 | g0084 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03098 | hp1 | a0006 | c0034 | t0001 | g0071 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03239 | hp2 | a0002 | c0002 | t0004 | g0094 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03453 | hp2 | a0012 | c0017 | t0001 | g0156 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03492 | hp1 | a0003 | c0032 | t0001 | g0122 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0114 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03516 | hp1 | a0004 | c0010 | t0001 | g0077 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03669 | hp1 | a0001 | c0005 | t0001 | g0199 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03669 | hp2 | a0013 | c0022 | t0001 | g0128 | SAS | PJL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG04184 | hp1 | a0007 | c0009 | t0001 | g0026 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG04199 | hp2 | a0014 | c0014 | t0001 | g0026 | SAS | STU | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | CHB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18941 | hp1 | a0003 | c0011 | t0001 | g0207 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18941 | hp2 | a0002 | c0035 | t0001 | g0067 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18947 | hp2 | a0004 | c0007 | t0001 | g0044 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18966 | hp1 | a0005 | c0037 | t0001 | g0066 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18971 | hp1 | a0015 | c0024 | t0001 | g0012 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18971 | hp2 | a0001 | c0026 | t0001 | g0006 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18979 | hp1 | a0002 | c0008 | t0001 | g0210 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18979 | hp2 | a0016 | c0019 | t0001 | g0076 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18980 | hp1 | a0003 | c0031 | t0001 | g0078 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18986 | hp2 | a0002 | c0008 | t0001 | g0209 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19000 | hp1 | a0017 | c0027 | t0001 | g0175 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19005 | hp2 | a0001 | c0015 | t0001 | g0069 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19043 | hp1 | a0018 | c0018 | t0001 | g0118 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19056 | hp1 | a0004 | c0007 | t0001 | g0126 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19056 | hp2 | a0005 | c0036 | t0001 | g0174 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19066 | hp1 | a0002 | c0008 | t0001 | g0211 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19070 | hp2 | a0003 | c0029 | t0001 | g0221 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19080 | hp1 | a0001 | c0020 | t0001 | g0186 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | YRI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | ASW | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20752 | hp1 | a0001 | c0006 | t0001 | g0154 | EUR | TSI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | GIH | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0001 | SAS | GIH | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0145 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | USA | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | USA | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA21309 | hp1 | a0001 | c0039 | t0001 | g0151 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0024 | REF | REF | NOC4L_chr12_132139457_132157468 | NOC4L | chr12 | 132139457 | 132157468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132144900 | G | A | 2 | a0007 a0014 |
3 | HG02293.hp1 HG04184.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.164G>A | p.Arg55His | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/15 | 196/1650 | 164/1551 | 55/516 | chr12 | 132144900 | |||
| chr12:132147642 | G | C | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.463G>C | p.Gly155Arg | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 5/15 | 495/1650 | 463/1551 | 155/516 | chr12 | 132147642 | |||
| chr12:132147688 | A | G | 1 | a0011 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.509A>G | p.Gln170Arg | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 5/15 | 541/1650 | 509/1551 | 170/516 | chr12 | 132147688 | |||
| chr12:132147730 | C | G | 1 | a0009 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.551C>G | p.Thr184Ser | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 5/15 | 583/1650 | 551/1551 | 184/516 | chr12 | 132147730 | |||
| chr12:132148794 | G | T | 1 | a0014 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.800G>T | p.Ser267Ile | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/15 | 832/1650 | 800/1551 | 267/516 | chr12 | 132148794 | |||
| chr12:132148815 | T | C | 1 | a0018 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.821T>C | p.Leu274Pro | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/15 | 853/1650 | 821/1551 | 274/516 | chr12 | 132148815 | |||
| chr12:132148890 | A | ACCTTGGT others(37): Show |
1 | a0006 | 1 | HG03098.hp1 | frameshift_variant&splice_region_variant | HIGH | c.899_900insTGGTGAGT others(36): Show |
p.Gly302fs | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/15 | 932/1650 | 900/1551 | 300/516 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||
| chr12:132151278 | G | A | 2 | a0002 a0016 |
2 | NA18941.hp2 NA18979.hp2 |
missense_variant | MODERATE | c.983G>A | p.Arg328Gln | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/15 | 1015/1650 | 983/1551 | 328/516 | chr12 | 132151278 | |||
| chr12:132151328 | G | GC | 3 | a0002 a0004 a0005 |
8 | HG00642.hp2 HG00735.hp2 HG02080.hp2 others(5): Show |
frameshift_variant | HIGH | c.1036dupC | p.Arg346fs | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/15 | 1069/1650 | 1037/1551 | 346/516 | INFO_REALIGN_3_PRIME | chr12 | 132151328 | ||
| chr12:132151530 | C | G | 1 | a0018 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1120C>G | p.Arg374Gly | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 12/15 | 1152/1650 | 1120/1551 | 374/516 | chr12 | 132151530 | |||
| chr12:132151531 | G | A | 1 | a0015 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.1121G>A | p.Arg374His | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 12/15 | 1153/1650 | 1121/1551 | 374/516 | chr12 | 132151531 | |||
| chr12:132151614 | C | T | 1 | a0013 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1204C>T | p.Arg402Trp | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 12/15 | 1236/1650 | 1204/1551 | 402/516 | chr12 | 132151614 | |||
| chr12:132151746 | G | A | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1243G>A | p.Ala415Thr | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/15 | 1275/1650 | 1243/1551 | 415/516 | chr12 | 132151746 | |||
| chr12:132152291 | C | T | 1 | a0011 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1441C>T | p.Arg481Trp | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 15/15 | 1473/1650 | 1441/1551 | 481/516 | chr12 | 132152291 | |||
| chr12:132152313 | C | T | 1 | a0008 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1463C>T | p.Pro488Leu | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 15/15 | 1495/1650 | 1463/1551 | 488/516 | chr12 | 132152313 | |||
| chr12:132152317 | G | C | 1 | a0010 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1467G>C | p.Glu489Asp | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 15/15 | 1499/1650 | 1467/1551 | 489/516 | chr12 | 132152317 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132144509 | C | G | 1 | a0002c0008 | 3 | NA18979.hp1 NA18986.hp2 NA19066.hp1 |
synonymous_variant | LOW | c.21C>G | p.Ala7Ala | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 1/15 | 53/1650 | 21/1551 | 7/516 | chr12 | 132144509 | |||
| chr12:132145590 | G | A | 1 | a0001c0015 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.270G>A | p.Val90Val | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/15 | 302/1650 | 270/1551 | 90/516 | chr12 | 132145590 | |||
| chr12:132147310 | C | T | 2 | a0001c0005 a0004c0041 |
6 | HG00099.hp2 HG00735.hp2 HG01258.hp1 others(3): Show |
synonymous_variant | LOW | c.375C>T | p.Phe125Phe | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/15 | 407/1650 | 375/1551 | 125/516 | chr12 | 132147310 | |||
| chr12:132147328 | G | A | 2 | a0001c0006 a0002c0016 |
4 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.393G>A | p.Ala131Ala | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/15 | 425/1650 | 393/1551 | 131/516 | chr12 | 132147328 | |||
| chr12:132147713 | C | T | 1 | a0001c0039 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.534C>T | p.Asp178Asp | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 5/15 | 566/1650 | 534/1551 | 178/516 | chr12 | 132147713 | |||
| chr12:132148647 | C | T | 1 | a0001c0004 | 5 | HG02258.hp1 HG02630.hp2 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.777C>T | p.Phe259Phe | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 8/15 | 809/1650 | 777/1551 | 259/516 | chr12 | 132148647 | |||
| chr12:132148894 | C | T | 2 | a0001c0001 a0004c0010 |
8 | HG02630.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.900C>T | p.Leu300Leu | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/15 | 932/1650 | 900/1551 | 300/516 | chr12 | 132148894 | |||
| chr12:132151036 | C | T | 10 | a0001c0003 a0001c0026 a0003c0029 others(7): Show |
39 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
synonymous_variant | LOW | c.957C>T | p.His319His | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 10/15 | 989/1650 | 957/1551 | 319/516 | chr12 | 132151036 | |||
| chr12:132151342 | C | T | 1 | a0001c0023 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1047C>T | p.His349His | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/15 | 1079/1650 | 1047/1551 | 349/516 | chr12 | 132151342 | |||
| chr12:132151343 | C | T | 1 | a0011c0040 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1048C>T | p.Leu350Leu | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/15 | 1080/1650 | 1048/1551 | 350/516 | chr12 | 132151343 | |||
| chr12:132151358 | C | T | 1 | a0005c0037 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1063C>T | p.Leu355Leu | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/15 | 1095/1650 | 1063/1551 | 355/516 | chr12 | 132151358 | |||
| chr12:132151544 | G | A | 1 | a0001c0020 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.1134G>A | p.Thr378Thr | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 12/15 | 1166/1650 | 1134/1551 | 378/516 | chr12 | 132151544 | |||
| chr12:132151610 | C | T | 1 | a0001c0026 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1200C>T | p.Ala400Ala | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 12/15 | 1232/1650 | 1200/1551 | 400/516 | chr12 | 132151610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132144466 | C | T | 1 | a0002c0002t0004 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 1/15 | 23 | chr12 | 132144466 | ||||||
| chr12:132144481 | G | A | 1 | a0001c0001t0002 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 1/15 | 8 | chr12 | 132144481 | ||||||
| chr12:132152456 | T | C | 1 | a0002c0002t0003 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 15/15 | 55 | chr12 | 132152456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132144701 | G | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01167.hp1 HG01243.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+96G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 1/14 | chr12 | 132144701 | |||||||
| chr12:132144982 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.238+8C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132144982 | |||||||
| chr12:132145080 | C | G | 11 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(8): Show |
11 | HG02027.hp1 HG02056.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+106C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145080 | |||||||
| chr12:132145106 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.238+132C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145106 | |||||||
| chr12:132145334 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01167.hp1 HG01243.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-225C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145334 | |||||||
| chr12:132145345 | G | A | 1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.239-214G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145345 | |||||||
| chr12:132145355 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(48): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.239-204G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145355 | |||||||
| chr12:132145362 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18947.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.239-197G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145362 | |||||||
| chr12:132145529 | C | T | 6 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0001c0003t0001g0222 others(3): Show |
6 | HG02027.hp1 HG02056.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-30C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145529 | |||||||
| chr12:132145548 | C | T | 3 | a0002c0008t0001g0209 a0002c0008t0001g0210 a0002c0008t0001g0211 |
3 | NA18979.hp1 NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.239-11C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 2/14 | chr12 | 132145548 | |||||||
| chr12:132145809 | C | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01167.hp1 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+144C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132145809 | |||||||
| chr12:132146127 | A | G | 15 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0157 others(12): Show |
18 | HG01099.hp1 HG01123.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.345+462A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146127 | |||||||
| chr12:132146241 | C | T | 1 | a0012c0017t0001g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.345+576C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146241 | |||||||
| chr12:132146277 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(32): Show |
47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.345+612C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146277 | |||||||
| chr12:132146289 | G | A | 3 | a0002c0002t0001g0183 a0002c0002t0001g0184 a0002c0002t0001g0185 |
3 | HG00609.hp2 NA19004.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.345+624G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146289 | |||||||
| chr12:132146466 | G | C | 1 | a0004c0007t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.345+801G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146466 | |||||||
| chr12:132146470 | A | G | 1 | a0009c0038t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.345+805A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146470 | |||||||
| chr12:132146476 | T | C | 1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.346-805T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146476 | |||||||
| chr12:132146507 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | NA18956.hp1 NA18991.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.346-774T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146507 | |||||||
| chr12:132146527 | G | A | 1 | a0001c0020t0001g0186 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.346-754G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146527 | |||||||
| chr12:132146543 | TTCCATAG others(9): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.346-736_346-721del others(16): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 132146543 | ||||||
| chr12:132146607 | C | T | 2 | a0003c0011t0001g0207 a0003c0011t0001g0208 |
2 | HG00423.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.346-674C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146607 | |||||||
| chr12:132146611 | G | A | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG00621.hp1 NA18950.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-670G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146611 | |||||||
| chr12:132146673 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.346-608C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146673 | |||||||
| chr12:132146700 | C | G | 5 | a0001c0006t0001g0152 a0001c0006t0001g0153 a0001c0006t0001g0154 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-581C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146700 | |||||||
| chr12:132146781 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.346-500G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146781 | |||||||
| chr12:132146879 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.346-402G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146879 | |||||||
| chr12:132146954 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.346-327C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132146954 | |||||||
| chr12:132147195 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.346-86T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132147195 | |||||||
| chr12:132147240 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.346-41G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132147240 | |||||||
| chr12:132147275 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | splice_region_variant&intron_variant | LOW | c.346-6T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 3/14 | chr12 | 132147275 | |||||||
| chr12:132147431 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0046 others(5): Show |
13 | NA18747.hp1 NA18950.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.453+43G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/14 | chr12 | 132147431 | |||||||
| chr12:132147500 | A | G | 1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.453+112A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/14 | chr12 | 132147500 | |||||||
| chr12:132147541 | G | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0002t0001g0158 |
3 | HG02809.hp2 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.454-92G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/14 | chr12 | 132147541 | |||||||
| chr12:132147600 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0214 a0001c0001t0001g0215 others(11): Show |
16 | HG02027.hp1 HG02056.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.454-33C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 4/14 | chr12 | 132147600 | |||||||
| chr12:132147875 | C | T | 1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.604-5C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 5/14 | chr12 | 132147875 | |||||||
| chr12:132148188 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+82C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148188 | |||||||
| chr12:132148199 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.738+93C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148199 | |||||||
| chr12:132148252 | C | T | 1 | a0002c0002t0003g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738+146C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148252 | |||||||
| chr12:132148365 | T | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(87): Show |
108 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(105): Show |
intron_variant | MODIFIER | c.739-244T>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148365 | |||||||
| chr12:132148386 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.739-223G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148386 | |||||||
| chr12:132148391 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-218T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148391 | |||||||
| chr12:132148437 | C | T | 3 | a0002c0008t0001g0209 a0002c0008t0001g0210 a0002c0008t0001g0211 |
3 | NA18979.hp1 NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.739-172C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148437 | |||||||
| chr12:132148534 | G | A | 1 | a0002c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.739-75G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148534 | |||||||
| chr12:132148534 | G | C | 3 | a0001c0001t0001g0188 a0003c0011t0001g0207 a0003c0011t0001g0208 |
3 | HG00423.hp1 NA18941.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.739-75G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148534 | |||||||
| chr12:132148597 | A | C | 1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.739-12A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148597 | |||||||
| chr12:132148601 | C | T | 1 | a0001c0004t0001g0168 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.739-8C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 7/14 | chr12 | 132148601 | |||||||
| chr12:132148664 | G | A | 1 | a0001c0004t0001g0161 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.789+5G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 8/14 | chr12 | 132148664 | |||||||
| chr12:132148671 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.789+12G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 8/14 | chr12 | 132148671 | |||||||
| chr12:132148725 | C | T | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0091 others(8): Show |
13 | HG01099.hp1 HG01123.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.790-59C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 8/14 | chr12 | 132148725 | |||||||
| chr12:132148777 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.790-7C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 8/14 | chr12 | 132148777 | |||||||
| chr12:132148890 | A | ACCTCGGT others(255): Show |
1 | a0017c0027t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(260): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(81): Show |
2 | a0003c0011t0001g0207 a0003c0011t0001g0208 |
2 | HG00423.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.901+17_901+18insAC others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(37): Show |
2 | a0006c0012t0001g0176 a0006c0012t0001g0177 |
2 | HG00733.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.901+17_901+18insAC others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(125): Show |
1 | a0003c0028t0001g0201 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.901+17_901+18insAC others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(213): Show |
1 | a0003c0029t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.901+17_901+18insAC others(218): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(2090): Show |
1 | a0003c0030t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(2095): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(257): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(301): Show |
1 | a0003c0032t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.901+61_901+62insGC others(306): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | A | ACCTCGGT others(565): Show |
1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.901+8_901+9insTGCC others(568): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(37): Show |
A | 6 | a0002c0002t0001g0061 a0002c0002t0001g0098 a0002c0002t0001g0158 others(3): Show |
6 | HG02451.hp2 HG02738.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+18_901+61delGC others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(81): Show |
A | 2 | a0002c0002t0001g0065 a0002c0002t0001g0097 |
2 | HG01943.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.901+18_901+105delG others(87): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(125): Show |
A | 2 | a0002c0002t0001g0095 a0002c0002t0004g0094 |
2 | HG03239.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.901+18_901+149del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(169): Show |
A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0099 |
2 | HG02723.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.901+18_901+193del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(213): Show |
A | 3 | a0002c0002t0001g0089 a0002c0002t0001g0187 a0002c0002t0001g0218 |
3 | NA18986.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.901+18_901+237del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(257): Show |
A | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.901+62_901+325del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(301): Show |
A | 2 | a0002c0002t0001g0090 a0002c0002t0003g0145 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.901+62_901+369del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(389): Show |
A | 1 | a0002c0002t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.901+62_901+457del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(433): Show |
A | 1 | a0002c0002t0001g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.901+62_901+501del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(521): Show |
A | 1 | a0005c0013t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.901+62_901+589del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1220): Show |
A | 2 | a0002c0002t0001g0171 a0002c0035t0001g0067 |
2 | NA18612.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.901+62_902-798del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1264): Show |
A | 1 | a0005c0037t0001g0066 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.901+62_902-754del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1396): Show |
A | 2 | a0002c0002t0001g0101 a0002c0002t0001g0102 |
2 | NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.901+62_902-622del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1440): Show |
A | 3 | a0002c0002t0001g0183 a0002c0002t0001g0184 a0005c0036t0001g0174 |
3 | HG00609.hp2 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.901+62_902-578del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1484): Show |
A | 3 | a0002c0002t0001g0185 a0002c0002t0001g0190 a0005c0013t0001g0103 |
3 | HG02074.hp2 NA19004.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.901+62_902-534del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1528): Show |
A | 3 | a0002c0002t0001g0104 a0002c0002t0001g0191 a0002c0008t0001g0209 |
3 | HG00673.hp1 NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.901+62_902-490del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1572): Show |
A | 2 | a0002c0008t0001g0210 a0002c0008t0001g0211 |
2 | NA18979.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.901+62_902-446del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148890 | ACCTCGGT others(1660): Show |
A | 1 | a0002c0002t0001g0192 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.901+23_902-397del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148890 | ||||||
| chr12:132148904 | C | CGCCGCCT others(160): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(165): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | CGCCGCCT others(415): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(420): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | CGCCGCCT others(893): Show |
1 | a0001c0001t0001g0009 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.901+17_901+18insAC others(898): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | CGCCGCCT others(163): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.901+17_901+18insAC others(168): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | CGCCGCCT others(484): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.901+17_901+18insAC others(489): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | CGCCGCCT others(170): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.901+23_901+24insCA others(175): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148904 | ||||||
| chr12:132148904 | C | G | 1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.901+9C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148904 | |||||||
| chr12:132148904 | C | T | 3 | a0001c0001t0001g0170 a0001c0003t0001g0219 a0001c0003t0001g0220 |
3 | HG02735.hp2 NA18951.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.901+9C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148904 | |||||||
| chr12:132148908 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.901+13G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148908 | |||||||
| chr12:132148913 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.901+18G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148913 | |||||||
| chr12:132148913 | G | GCTCACAC others(521): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(526): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148913 | ||||||
| chr12:132148916 | CACACCAC others(430): Show |
C | 1 | a0001c0004t0001g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.901+22_901+458del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148916 | |||||||
| chr12:132148916 | CACACCAC others(518): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.901+22_901+546del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148916 | |||||||
| chr12:132148917 | A | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0031 others(22): Show |
26 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.901+22A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148917 | |||||||
| chr12:132148917 | ACACCACA others(169): Show |
A | 1 | a0001c0001t0001g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.901+23_901+198del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148917 | |||||||
| chr12:132148918 | C | CACCACAC others(521): Show |
1 | a0001c0001t0001g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(526): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | CACCACAC others(565): Show |
1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.901+61_901+62insGC others(570): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | CACCACAC others(873): Show |
1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.901+61_901+62insGC others(878): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.901+61_901+62insGC others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | CACCACAC others(298): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.901+61_901+62insGC others(303): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | CACCACAC others(75): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+56_901+57insTC others(80): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(37): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.901+23C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148918 | |||||||
| chr12:132148918 | CACCACAC others(37): Show |
C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0002g0012 others(1): Show |
4 | HG01255.hp1 HG02056.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+110_901+153del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | CACCACAC others(81): Show |
C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0073 others(3): Show |
6 | HG02886.hp1 HG02896.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.901+66_901+153delC others(87): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | CACCACAC others(169): Show |
C | 2 | a0001c0001t0001g0144 a0004c0010t0001g0077 |
2 | HG01081.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.901+106_901+281del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | CACCACAC others(213): Show |
C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0062 others(5): Show |
9 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.901+62_901+281del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | CACCACAC others(1660): Show |
C | 1 | a0001c0020t0001g0186 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.901+62_902-358del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148918 | CACCACAC others(1704): Show |
C | 1 | a0001c0003t0001g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.901+62_902-314del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148918 | ||||||
| chr12:132148920 | CCACACCC others(1088): Show |
C | 1 | a0001c0001t0001g0013 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.901+62_902-930del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148920 | ||||||
| chr12:132148924 | ACCCCTAA others(126): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.901+33_901+165del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148924 | ||||||
| chr12:132148939 | G | A | 1 | a0001c0015t0001g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.901+44G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148939 | |||||||
| chr12:132148948 | C | CGCCGCCT others(213): Show |
1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.901+65_901+66insAC others(218): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148948 | ||||||
| chr12:132148948 | C | CGCCGCCT others(37): Show |
2 | a0001c0003t0001g0028 a0001c0003t0001g0131 |
3 | HG00558.hp2 NA18973.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.901+61_901+62insGC others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148948 | ||||||
| chr12:132148948 | C | CGCCGCCT others(433): Show |
1 | a0001c0003t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901+61_901+62insGC others(438): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148948 | ||||||
| chr12:132148948 | C | CGCCTCGC others(31): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+56_901+57insTC others(36): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148948 | ||||||
| chr12:132148948 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0214 |
2 | HG02630.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.901+53C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148948 | |||||||
| chr12:132148957 | A | ACTCACAC others(301): Show |
1 | a0008c0025t0001g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.901+65_901+66insAC others(306): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | A | ACTCACAC others(169): Show |
1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.901+65_901+66insAC others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | A | ACTCACAC others(609): Show |
1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901+65_901+66insAC others(614): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | A | ACTCCTAC others(257): Show |
1 | a0001c0001t0001g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.901+94_901+95insAC others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | A | G | 49 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0029 others(46): Show |
56 | HG00609.hp1 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.901+62A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148957 | |||||||
| chr12:132148957 | ACTCCTAC others(345): Show |
A | 1 | a0001c0003t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.901+66_901+417del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | ACTCCTAC others(1352): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.901+66_902-662del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148957 | ACTCCTAC others(1704): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.901+66_902-310del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148957 | ||||||
| chr12:132148960 | C | CACACCAC others(78): Show |
1 | a0001c0001t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(83): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(34): Show |
1 | a0001c0001t0001g0001 | 2 | NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.901+65_901+66insAC others(39): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(166): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(171): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(122): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(127): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(122): Show |
2 | a0001c0001t0001g0018 a0001c0003t0001g0114 |
2 | HG03492.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.901+65_901+66insAC others(127): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(254): Show |
1 | a0001c0001t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.901+65_901+66insAC others(259): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148960 | C | CACACCAC others(365): Show |
1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+65_901+66insAC others(370): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148960 | |||||||
| chr12:132148961 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.901+66C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148961 | |||||||
| chr12:132148961 | C | CTACCACA others(81): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.901+96_901+97insGG others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148961 | ||||||
| chr12:132148962 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.901+67T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148962 | |||||||
| chr12:132148962 | T | TACCACAC others(213): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0120 |
2 | NA18975.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.901+109_901+110ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(213): Show |
1 | a0001c0003t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.901+109_901+110ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(37): Show |
3 | a0001c0001t0001g0049 a0001c0003t0001g0220 a0003c0031t0001g0078 |
3 | NA18980.hp1 NA18995.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.901+105_901+106ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(81): Show |
1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.901+105_901+106ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(125): Show |
1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.901+105_901+106ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(169): Show |
1 | a0001c0001t0001g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.901+105_901+106ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(37): Show |
1 | a0001c0001t0001g0003 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.901+96_901+97insGG others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(125): Show |
1 | a0001c0001t0001g0001 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.901+96_901+97insGG others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TACCACAC others(169): Show |
1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.901+96_901+97insGG others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | T | TCAC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(5): Show |
9 | HG01934.hp1 HG02572.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.901+67_901+68insCA others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148962 | |||||||
| chr12:132148962 | TACCACAC others(257): Show |
T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.901+106_901+369del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | TACCACAC others(1176): Show |
T | 2 | a0001c0001t0001g0003 a0004c0010t0001g0003 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.901+106_902-798del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | TACCACAC others(1264): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.901+106_902-710del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | TACCACAC others(1352): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.901+106_902-622del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148962 | TACCACAC others(1572): Show |
T | 1 | a0001c0001t0001g0004 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.901+106_902-402del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148962 | ||||||
| chr12:132148963 | A | ACCACACC others(40): Show |
1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.901+95_901+96insGC others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148963 | ||||||
| chr12:132148964 | CCACACCC others(35): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.901+70_901+111delC others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148964 | |||||||
| chr12:132148989 | TGCCGCCG others(128): Show |
T | 1 | a0001c0023t0001g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.901+101_901+235del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148989 | ||||||
| chr12:132148992 | C | CGCCGCCT others(78): Show |
1 | a0001c0006t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.901+105_901+106ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148992 | ||||||
| chr12:132148992 | C | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0159 others(3): Show |
6 | HG00099.hp2 HG00673.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+97C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148992 | |||||||
| chr12:132148992 | CGCCGCCT others(741): Show |
C | 1 | a0009c0038t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.901+106_901+853del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148992 | ||||||
| chr12:132148993 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.901+98G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132148993 | |||||||
| chr12:132148995 | C | CGCCTCGC others(917): Show |
1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.901+105_901+106ins others(924): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132148995 | ||||||
| chr12:132149001 | A | ACTCACAC others(125): Show |
1 | a0001c0001t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149001 | ||||||
| chr12:132149001 | A | ACTCACAC others(37): Show |
1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149001 | ||||||
| chr12:132149001 | A | ACTCACAC others(169): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149001 | ||||||
| chr12:132149001 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
82 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.901+106A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149001 | |||||||
| chr12:132149001 | ACTCCTAC others(213): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.901+110_901+329del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149001 | ||||||
| chr12:132149001 | ACTCCTAC others(1440): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.901+110_902-530del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149001 | ||||||
| chr12:132149003 | TCCTACCA others(1709): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.901+110_902-261del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149003 | ||||||
| chr12:132149004 | C | CACACCAC others(78): Show |
1 | a0001c0001t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(553): Show |
1 | a0001c0001t0001g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.901+109_901+110ins others(560): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(386): Show |
1 | a0001c0003t0001g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(393): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(78): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.901+109_901+110ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(166): Show |
1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(173): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(31): Show |
1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901+109_901+110ins others(38): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACACCAC others(34): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0166 |
2 | HG01167.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.901+109_901+110ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149004 | C | CACCACCA others(79): Show |
1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901+109_901+110ins others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149004 | |||||||
| chr12:132149005 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.901+110C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149005 | |||||||
| chr12:132149006 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.901+111T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149006 | |||||||
| chr12:132149006 | T | TACCACAC others(37): Show |
1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901+149_901+150ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TACCACAC others(81): Show |
1 | a0001c0001t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.901+149_901+150ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TACCACAC others(301): Show |
1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.901+149_901+150ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TACCACAC others(386): Show |
1 | a0001c0001t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.901+149_901+150ins others(393): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TACCACAC others(163): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+149_901+150ins others(170): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TACCACAC others(565): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.901+149_901+150ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149006 | T | TCAC | 8 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0032 others(5): Show |
9 | HG00673.hp2 HG01167.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.901+111_901+112ins others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149006 | |||||||
| chr12:132149006 | TACCACAC others(1044): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.901+150_902-886del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149006 | ||||||
| chr12:132149008 | C | CCACACCC others(161): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901+144_901+145ins others(168): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149008 | ||||||
| chr12:132149008 | CCACACCC others(79): Show |
C | 1 | a0001c0001t0001g0020 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.901+114_901+199del others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149008 | |||||||
| chr12:132149036 | C | CGCCGCCT others(345): Show |
1 | a0001c0001t0001g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.901+193_901+194ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149036 | ||||||
| chr12:132149036 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+149_901+150ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149036 | ||||||
| chr12:132149036 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.901+149_901+150ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149036 | ||||||
| chr12:132149036 | C | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0025 others(11): Show |
15 | HG00544.hp2 HG00558.hp2 HG03130.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+141C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149036 | |||||||
| chr12:132149036 | CGCCGCCT others(697): Show |
C | 1 | a0007c0009t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.901+150_901+853del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149036 | ||||||
| chr12:132149045 | A | ACTCACAC others(37): Show |
2 | a0001c0001t0001g0086 a0001c0005t0001g0001 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.901+193_901+194ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | ACTCACAC others(82): Show |
1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.901+193_901+194ins others(89): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | ACTCACAC others(281): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+158_901+159ins others(288): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | ACTCCTAC others(435): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.901+153_901+154ins others(442): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | ACTCCTAC others(521): Show |
1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.901+153_901+154ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | ACTCCTAC others(257): Show |
1 | a0001c0001t0001g0006 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.901+153_901+154ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.901+150A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149045 | |||||||
| chr12:132149045 | ACTCACAC others(1088): Show |
A | 1 | a0001c0001t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.901+194_902-798del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149045 | ACTCACAC others(1396): Show |
A | 1 | a0002c0002t0001g0189 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.901+194_902-490del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149045 | ||||||
| chr12:132149048 | C | CCT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0058 |
4 | NA18747.hp1 NA19065.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+153_901+154ins others(2): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149048 | |||||||
| chr12:132149048 | CACACCAC others(1173): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.901+154_902-753del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149048 | |||||||
| chr12:132149049 | A | ACACCACA others(82): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901+193_901+194ins others(89): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149049 | ||||||
| chr12:132149049 | A | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(26): Show |
29 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.901+154A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149049 | |||||||
| chr12:132149050 | C | CACCACAC others(257): Show |
1 | a0001c0001t0001g0005 | 2 | NA18970.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.901+197_901+198ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149050 | ||||||
| chr12:132149050 | C | CACCACAC others(431): Show |
1 | a0003c0011t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.901+193_901+194ins others(438): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149050 | ||||||
| chr12:132149050 | C | CCACACCC others(255): Show |
1 | a0001c0001t0001g0014 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.901+155_901+156ins others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149050 | |||||||
| chr12:132149050 | C | CCACACCC others(79): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0058 |
3 | NA19065.hp2 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.901+155_901+156ins others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149050 | |||||||
| chr12:132149050 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(33): Show |
36 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.901+155C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149050 | |||||||
| chr12:132149050 | CACCACAC others(37): Show |
C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0022 |
2 | HG01433.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.901+238_901+281del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149050 | ||||||
| chr12:132149050 | CACCACAC others(81): Show |
C | 1 | a0002c0002t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.901+194_901+281del others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149050 | ||||||
| chr12:132149061 | T | TAATCCCC others(606): Show |
1 | a0003c0011t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.901+193_901+194ins others(613): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149061 | ||||||
| chr12:132149080 | C | CGCCGCCT others(521): Show |
1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.901+193_901+194ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149080 | ||||||
| chr12:132149080 | C | CGCCGCCT others(125): Show |
1 | a0004c0007t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.901+193_901+194ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149080 | ||||||
| chr12:132149080 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0041 others(10): Show |
13 | HG01243.hp1 HG01943.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+185C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149080 | |||||||
| chr12:132149083 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.901+188C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149083 | |||||||
| chr12:132149089 | A | ACTCACAC others(37): Show |
1 | a0001c0001t0001g0010 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.901+197_901+198ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149089 | ||||||
| chr12:132149089 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.901+194A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149089 | |||||||
| chr12:132149093 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
129 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.901+198C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149093 | |||||||
| chr12:132149094 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.901+199T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149094 | |||||||
| chr12:132149094 | T | TACCACAC others(389): Show |
1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.901+241_901+242ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | T | TACCACAC others(169): Show |
1 | a0001c0001t0001g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.901+237_901+238ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | T | TACCACAC others(169): Show |
1 | a0001c0001t0001g0003 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.901+237_901+238ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | T | TACCACAC others(346): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.901+231_901+232ins others(353): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | T | TACCACAC others(37): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.901+228_901+229ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | TACCACAC others(213): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.901+238_901+457del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | TACCACAC others(1308): Show |
T | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.901+238_902-534del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149094 | TACCACAC others(1616): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.901+238_902-226del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149094 | ||||||
| chr12:132149096 | C | CCACACCC others(340): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+237_901+238ins others(347): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149096 | ||||||
| chr12:132149096 | CCACACCC others(35): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.901+202_901+243del others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149096 | |||||||
| chr12:132149100 | A | ACCCCTAA others(38): Show |
1 | a0001c0001t0001g0004 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.901+237_901+238ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149100 | ||||||
| chr12:132149114 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.901+219C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149114 | |||||||
| chr12:132149122 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+227G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149122 | |||||||
| chr12:132149124 | C | CGCCGCCT others(81): Show |
1 | a0001c0003t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901+241_901+242ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149124 | ||||||
| chr12:132149124 | C | CGCCGCCT others(609): Show |
1 | a0001c0001t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901+237_901+238ins others(616): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149124 | ||||||
| chr12:132149124 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0029 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.901+237_901+238ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149124 | ||||||
| chr12:132149124 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0083 others(5): Show |
8 | HG00741.hp2 HG02109.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.901+229C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149124 | |||||||
| chr12:132149125 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0217 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.901+230G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149125 | |||||||
| chr12:132149133 | A | ACTCATAC others(125): Show |
1 | a0001c0001t0001g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.901+241_901+242ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149133 | ||||||
| chr12:132149133 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(71): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.901+238A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149133 | |||||||
| chr12:132149133 | A | T | 1 | a0001c0001t0001g0004 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.901+238A>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149133 | |||||||
| chr12:132149133 | ACTCCTAC others(37): Show |
A | 1 | a0002c0002t0004g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901+242_901+285del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149133 | ||||||
| chr12:132149133 | ACTCCTAC others(477): Show |
A | 1 | a0014c0014t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.901+242_901+725del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149133 | ||||||
| chr12:132149136 | C | CACACCAC others(167): Show |
1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.901+241_901+242ins others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149136 | |||||||
| chr12:132149136 | C | CACACCAC others(169): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.901+241_901+242ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149136 | |||||||
| chr12:132149137 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.901+242C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149137 | |||||||
| chr12:132149138 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.901+243T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149138 | |||||||
| chr12:132149138 | T | CACCACAC others(213): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.901+242_901+243ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149138 | |||||||
| chr12:132149138 | T | CACCACAC others(37): Show |
1 | a0001c0001t0001g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.901+242_901+243ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149138 | |||||||
| chr12:132149138 | T | TACCACAC others(213): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.901+281_901+282ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149138 | T | TACCACAC others(1093): Show |
1 | a0013c0022t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.901+281_901+282ins others(1100): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149138 | T | TACCACAC others(81): Show |
1 | a0001c0015t0001g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.901+285_901+286ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149138 | T | TACCACAC others(37): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.901+272_901+273ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149138 | T | TACCACAC others(81): Show |
1 | a0003c0028t0001g0201 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.901+272_901+273ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149138 | T | TACCACAC others(917): Show |
1 | a0001c0001t0001g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.901+272_901+273ins others(924): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149138 | ||||||
| chr12:132149166 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+271G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149166 | |||||||
| chr12:132149168 | C | CGCCGCCT others(1480): Show |
1 | a0001c0001t0001g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.901+281_901+282ins others(1487): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149168 | ||||||
| chr12:132149168 | C | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0062 others(5): Show |
8 | HG01261.hp2 HG02300.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.901+273C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149168 | |||||||
| chr12:132149169 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+274G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149169 | |||||||
| chr12:132149169 | G | GCCGCCTC others(433): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+281_901+282ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149169 | ||||||
| chr12:132149173 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.901+278C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149173 | |||||||
| chr12:132149177 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
41 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.901+282G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149177 | |||||||
| chr12:132149177 | G | GCTCCTAC others(169): Show |
1 | a0001c0001t0001g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.901+285_901+286ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149177 | ||||||
| chr12:132149178 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+283C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149178 | |||||||
| chr12:132149180 | CACACCAC others(1305): Show |
C | 1 | a0001c0004t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.901+286_902-489del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149180 | |||||||
| chr12:132149181 | A | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(10): Show |
13 | HG00423.hp2 HG00733.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.901+286A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149181 | |||||||
| chr12:132149182 | C | CACCACAC others(37): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+314_901+315ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149182 | ||||||
| chr12:132149182 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.901+325_901+326ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149182 | ||||||
| chr12:132149182 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0137 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.901+360_901+361ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149182 | ||||||
| chr12:132149182 | C | CACCACAC others(125): Show |
2 | a0001c0003t0001g0028 a0001c0003t0001g0131 |
2 | HG00558.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.901+316_901+317ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149182 | ||||||
| chr12:132149182 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(22): Show |
25 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.901+287C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149182 | |||||||
| chr12:132149193 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+298T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149193 | |||||||
| chr12:132149203 | G | GGTGAGTG others(1087): Show |
1 | a0001c0006t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.901+325_901+326ins others(1094): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149203 | ||||||
| chr12:132149209 | TGCC | T | 4 | a0001c0001t0001g0007 a0001c0006t0001g0152 a0001c0006t0001g0153 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+321_901+323del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149209 | ||||||
| chr12:132149212 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.901+325_901+326ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149212 | ||||||
| chr12:132149212 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.901+325_901+326ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149212 | ||||||
| chr12:132149212 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.901+325_901+326ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149212 | ||||||
| chr12:132149212 | C | G | 18 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0125 others(15): Show |
18 | HG00544.hp2 HG00741.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.901+317C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149212 | |||||||
| chr12:132149216 | G | T | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.901+321G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149216 | |||||||
| chr12:132149221 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
79 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.901+326G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149221 | |||||||
| chr12:132149221 | G | GCTCCTAC others(37): Show |
1 | a0001c0005t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.901+329_901+330ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149221 | ||||||
| chr12:132149221 | G | GCTCCTAC others(213): Show |
1 | a0001c0001t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.901+329_901+330ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149221 | ||||||
| chr12:132149224 | CACACCAC others(562): Show |
C | 1 | a0007c0009t0001g0006 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.901+330_901+898del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149224 | |||||||
| chr12:132149225 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(27): Show |
30 | HG00099.hp2 HG00558.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.901+330A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149225 | |||||||
| chr12:132149226 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0001 | 2 | NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.901+369_901+370ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149226 | ||||||
| chr12:132149226 | C | CACCACAC others(81): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.901+413_901+414ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149226 | ||||||
| chr12:132149226 | C | CACCCCTA others(242): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901+334_901+335ins others(249): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149226 | ||||||
| chr12:132149226 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
40 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.901+331C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149226 | |||||||
| chr12:132149236 | C | G | 1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+341C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149236 | |||||||
| chr12:132149237 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+342T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149237 | |||||||
| chr12:132149253 | TGCC | T | 3 | a0001c0001t0001g0062 a0001c0023t0001g0088 a0002c0002t0001g0096 |
3 | HG02559.hp1 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.901+365_901+367del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149253 | ||||||
| chr12:132149256 | C | CGCCGCCT others(2105): Show |
1 | a0001c0005t0001g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.901+369_901+370ins others(2112): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149256 | ||||||
| chr12:132149256 | C | CGCCGCCT others(389): Show |
1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149256 | ||||||
| chr12:132149256 | C | CGCCGCCT others(125): Show |
1 | a0003c0029t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.901+417_901+418ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149256 | ||||||
| chr12:132149256 | C | CGCCGCCT others(257): Show |
1 | a0001c0026t0001g0006 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.901+373_901+374ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149256 | ||||||
| chr12:132149256 | C | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 others(11): Show |
14 | HG00735.hp1 HG01261.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.901+361C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149256 | |||||||
| chr12:132149265 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
69 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.901+370G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149265 | |||||||
| chr12:132149265 | G | ACTCACAC others(128): Show |
1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.901+369_901+370ins others(135): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149265 | |||||||
| chr12:132149265 | G | GCTCACAC others(257): Show |
1 | a0008c0025t0001g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149265 | G | GCTCACAC others(125): Show |
1 | a0001c0001t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.901+448_901+449ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149265 | G | GCTCACAC others(169): Show |
1 | a0001c0001t0001g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.901+404_901+405ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149265 | G | GCTCCTAC others(81): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.901+373_901+374ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149265 | G | GCTCCTAC others(125): Show |
1 | a0001c0001t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.901+373_901+374ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149265 | G | GCTCCTAC others(81): Show |
1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.901+373_901+374ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149265 | ||||||
| chr12:132149269 | A | ATACCACA others(81): Show |
1 | a0001c0004t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.901+374_901+375ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149269 | |||||||
| chr12:132149269 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(30): Show |
33 | HG01123.hp2 HG01243.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.901+374A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149269 | |||||||
| chr12:132149270 | C | CACCACAC others(477): Show |
1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(484): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(125): Show |
1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.901+413_901+414ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(81): Show |
1 | a0001c0005t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.901+501_901+502ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.901+448_901+449ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCACAC others(78): Show |
1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.901+408_901+409ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | CACCGACA others(38): Show |
1 | a0001c0001t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.901+378_901+379ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149270 | ||||||
| chr12:132149270 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
46 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.901+375C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149270 | |||||||
| chr12:132149290 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.901+395C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149290 | |||||||
| chr12:132149297 | TGCC | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0002c0002t0001g0089 |
3 | HG02559.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.901+409_901+411del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149297 | ||||||
| chr12:132149298 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.901+403G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149298 | |||||||
| chr12:132149300 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149300 | ||||||
| chr12:132149300 | C | CGCCGCCT others(829): Show |
1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.901+413_901+414ins others(836): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149300 | ||||||
| chr12:132149300 | C | CGCCGCCT others(1005): Show |
1 | a0001c0001t0001g0196 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.901+417_901+418ins others(1012): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149300 | ||||||
| chr12:132149300 | C | G | 14 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0041 others(11): Show |
14 | HG00642.hp1 HG01123.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+405C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149300 | |||||||
| chr12:132149300 | CGCCGCCT others(389): Show |
C | 1 | a0001c0001t0001g0001 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.901+414_901+809del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149300 | ||||||
| chr12:132149301 | G | GCCGCCTC others(78): Show |
1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+452_901+453ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149301 | ||||||
| chr12:132149309 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
65 | HG00609.hp1 HG01123.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.901+414G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149309 | |||||||
| chr12:132149309 | G | ACTCCTAC others(257): Show |
1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.901+413_901+414ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149309 | |||||||
| chr12:132149309 | G | GCTCACAC others(697): Show |
1 | a0001c0001t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.901+457_901+458ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149309 | ||||||
| chr12:132149309 | G | GCTCACAC others(697): Show |
1 | a0001c0001t0001g0005 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.901+457_901+458ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149309 | ||||||
| chr12:132149309 | G | GCTCCTAC others(257): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.901+417_901+418ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149309 | ||||||
| chr12:132149312 | CACACCAC others(733): Show |
C | 1 | a0001c0001t0001g0005 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.901+418_902-929del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149312 | |||||||
| chr12:132149313 | A | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(28): Show |
33 | HG00423.hp2 HG00544.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.901+418A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149313 | |||||||
| chr12:132149314 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0182 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.901+545_901+546ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149314 | ||||||
| chr12:132149314 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.901+462_901+463ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149314 | ||||||
| chr12:132149314 | C | CACCACAC others(829): Show |
1 | a0001c0003t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.901+448_901+449ins others(836): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149314 | ||||||
| chr12:132149314 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.901+448_901+449ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149314 | ||||||
| chr12:132149314 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(36): Show |
41 | HG00423.hp2 HG00544.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.901+419C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149314 | |||||||
| chr12:132149325 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0159 a0002c0002t0001g0065 |
3 | HG02976.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.901+430T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149325 | |||||||
| chr12:132149329 | CCCCTCGG others(691): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.901+438_902-951del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149329 | ||||||
| chr12:132149335 | G | A | 1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+440G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149335 | |||||||
| chr12:132149342 | G | A | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+447G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149342 | |||||||
| chr12:132149344 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0006 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.901+457_901+458ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149344 | ||||||
| chr12:132149344 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.901+457_901+458ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149344 | ||||||
| chr12:132149344 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.901+492_901+493ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149344 | ||||||
| chr12:132149344 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.901+462_901+463ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149344 | ||||||
| chr12:132149344 | C | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(17): Show |
20 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.901+449C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149344 | |||||||
| chr12:132149345 | G | A | 2 | a0001c0001t0001g0036 a0006c0034t0001g0071 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.901+450G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149345 | |||||||
| chr12:132149347 | C | CGCCTCAC others(159): Show |
1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901+457_901+458ins others(166): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149347 | ||||||
| chr12:132149353 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
69 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.901+458G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149353 | |||||||
| chr12:132149353 | G | GCTCACAC others(125): Show |
1 | a0001c0003t0001g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.901+536_901+537ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149353 | ||||||
| chr12:132149353 | G | GCTCATAC others(37): Show |
1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.901+462_901+463ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149353 | ||||||
| chr12:132149354 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.901+459C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149354 | |||||||
| chr12:132149354 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+459C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149354 | |||||||
| chr12:132149356 | C | CCT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0070 others(1): Show |
4 | HG00423.hp2 HG01993.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+461_901+462ins others(2): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149356 | |||||||
| chr12:132149356 | CACACCAC others(78): Show |
C | 1 | a0002c0002t0001g0218 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.901+462_901+546del others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149356 | |||||||
| chr12:132149357 | A | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(38): Show |
44 | HG00558.hp2 HG00621.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.901+462A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149357 | |||||||
| chr12:132149358 | C | CACCACAC others(80): Show |
1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.901+473_901+474ins others(87): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(37): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0040 |
3 | HG03516.hp2 NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.901+501_901+502ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(125): Show |
1 | a0001c0005t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.901+501_901+502ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(345): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0058 |
3 | NA19065.hp2 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.901+501_901+502ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(257): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.901+501_901+502ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.901+501_901+502ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(2325): Show |
1 | a0001c0001t0001g0181 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.901+545_901+546ins others(2332): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.901+492_901+493ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149358 | C | CCACACCC others(343): Show |
1 | a0001c0001t0001g0006 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.901+463_901+464ins others(350): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149358 | |||||||
| chr12:132149358 | C | CCACACCC others(167): Show |
1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.901+463_901+464ins others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149358 | |||||||
| chr12:132149358 | C | CCACACCC others(79): Show |
1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.901+463_901+464ins others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149358 | |||||||
| chr12:132149358 | C | CCACACCC others(167): Show |
1 | a0001c0001t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.901+463_901+464ins others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149358 | |||||||
| chr12:132149358 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
54 | HG00558.hp2 HG00621.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.901+463C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149358 | |||||||
| chr12:132149358 | CACCACAC others(1308): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.901+555_902-217del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149358 | ||||||
| chr12:132149367 | C | T | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.901+472C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149367 | |||||||
| chr12:132149369 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.901+474T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149369 | |||||||
| chr12:132149385 | TGCC | T | 4 | a0001c0001t0001g0007 a0001c0023t0001g0088 a0002c0002t0001g0068 others(1): Show |
4 | HG02145.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+497_901+499del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149385 | ||||||
| chr12:132149386 | G | A | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+491G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149386 | |||||||
| chr12:132149388 | C | CGCCGCCT others(81): Show |
1 | a0004c0007t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.901+501_901+502ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149388 | ||||||
| chr12:132149388 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.901+536_901+537ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149388 | ||||||
| chr12:132149388 | C | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.901+493C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149388 | |||||||
| chr12:132149389 | G | A | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+494G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149389 | |||||||
| chr12:132149393 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.901+498C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149393 | |||||||
| chr12:132149397 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
58 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.901+502G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149397 | |||||||
| chr12:132149397 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.901+502G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149397 | |||||||
| chr12:132149397 | G | GCTCATAC others(462): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+506_901+507ins others(469): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149397 | ||||||
| chr12:132149397 | G | GCTCCTAC others(81): Show |
1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.901+505_901+506ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149397 | ||||||
| chr12:132149397 | GCTCACAC others(169): Show |
G | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.901+590_901+765del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149397 | ||||||
| chr12:132149401 | A | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
34 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.901+506A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149401 | |||||||
| chr12:132149402 | C | CACCACAC others(1181): Show |
1 | a0001c0001t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.901+545_901+546ins others(1188): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149402 | ||||||
| chr12:132149402 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.901+545_901+546ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149402 | ||||||
| chr12:132149402 | C | CACCACAC others(433): Show |
1 | a0001c0003t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.901+545_901+546ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149402 | ||||||
| chr12:132149402 | C | CACCACAC others(81): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.901+545_901+546ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149402 | ||||||
| chr12:132149402 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0027 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.901+624_901+625ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149402 | ||||||
| chr12:132149402 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(39): Show |
43 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.901+507C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149402 | |||||||
| chr12:132149412 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+517C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149412 | |||||||
| chr12:132149413 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+518T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149413 | |||||||
| chr12:132149429 | TGCC | T | 3 | a0001c0023t0001g0088 a0002c0002t0001g0068 a0002c0002t0001g0089 |
3 | HG02145.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.901+541_901+543del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149429 | ||||||
| chr12:132149432 | C | CGCCGCCT others(697): Show |
1 | a0001c0001t0001g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.901+580_901+581ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149432 | ||||||
| chr12:132149432 | C | CGCCGCCT others(1771): Show |
1 | a0003c0030t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.901+549_901+550ins others(1778): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149432 | ||||||
| chr12:132149432 | C | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0082 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.901+537C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149432 | |||||||
| chr12:132149432 | CGCCGCCT others(257): Show |
C | 1 | a0002c0002t0001g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.901+546_901+809del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149432 | ||||||
| chr12:132149433 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+538G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149433 | |||||||
| chr12:132149437 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0167 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.901+542C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149437 | |||||||
| chr12:132149441 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): Show |
49 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.901+546G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149441 | |||||||
| chr12:132149441 | G | GCTCCTAC others(78): Show |
1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901+549_901+550ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149441 | ||||||
| chr12:132149442 | C | G | 1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.901+547C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149442 | |||||||
| chr12:132149445 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
29 | HG00558.hp1 HG02258.hp1 HG02300.hp1 others(26): Show |
intron_variant | MODIFIER | c.901+550A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149445 | |||||||
| chr12:132149446 | C | CACCACAC others(81): Show |
1 | a0010c0021t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.901+589_901+590ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901+589_901+590ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.901+589_901+590ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(125): Show |
1 | a0001c0005t0001g0001 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.901+589_901+590ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(1225): Show |
1 | a0003c0032t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.901+593_901+594ins others(1232): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(80): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.901+580_901+581ins others(87): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(521): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.901+580_901+581ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CACCACAC others(389): Show |
1 | a0001c0003t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.901+580_901+581ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149446 | ||||||
| chr12:132149446 | C | CCACACCC others(255): Show |
1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.901+551_901+552ins others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149446 | |||||||
| chr12:132149446 | C | CCACACCC others(433): Show |
1 | a0001c0001t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.901+551_901+552ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149446 | |||||||
| chr12:132149446 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
50 | HG00558.hp1 HG01071.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.901+551C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149446 | |||||||
| chr12:132149450 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.901+555A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149450 | |||||||
| chr12:132149454 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.901+559C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149454 | |||||||
| chr12:132149473 | TGCC | T | 3 | a0001c0001t0001g0062 a0001c0023t0001g0088 a0002c0002t0001g0068 |
3 | HG02145.hp1 HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.901+585_901+587del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149473 | ||||||
| chr12:132149476 | C | CGCCGCCT others(122): Show |
1 | a0001c0001t0001g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.901+589_901+590ins others(129): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149476 | ||||||
| chr12:132149476 | C | CGCCGCCT others(433): Show |
1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.901+589_901+590ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149476 | ||||||
| chr12:132149476 | C | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(19): Show |
25 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.901+581C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149476 | |||||||
| chr12:132149481 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.901+586C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149481 | |||||||
| chr12:132149485 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(36): Show |
40 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.901+590G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149485 | |||||||
| chr12:132149485 | G | GCTCACAC others(521): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.901+624_901+625ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149485 | ||||||
| chr12:132149485 | G | GCTCACAC others(252): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+604_901+605ins others(259): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149485 | ||||||
| chr12:132149485 | G | GCTCCTAC others(81): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.901+593_901+594ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149485 | ||||||
| chr12:132149485 | GCTCACAC others(37): Show |
G | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.901+678_901+721del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149485 | ||||||
| chr12:132149486 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+591C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149486 | |||||||
| chr12:132149488 | CACACCAC others(601): Show |
C | 1 | a0016c0019t0001g0076 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.901+594_902-885del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149488 | |||||||
| chr12:132149489 | A | ATACCACA others(37): Show |
1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901+594_901+595ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149489 | |||||||
| chr12:132149489 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.901+594A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149489 | |||||||
| chr12:132149490 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0011 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.901+637_901+638ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149490 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0010 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.901+637_901+638ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149490 | C | CACCACAC others(256): Show |
1 | a0001c0001t0001g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.901+633_901+634ins others(263): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149490 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901+624_901+625ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149490 | C | CACCACAC others(81): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.901+624_901+625ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149490 | C | CCACACCC others(79): Show |
1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.901+595_901+596ins others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149490 | |||||||
| chr12:132149490 | C | CCACACCC others(475): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.901+595_901+596ins others(482): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149490 | |||||||
| chr12:132149490 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
44 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.901+595C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149490 | |||||||
| chr12:132149490 | CACCACAC others(169): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.901+625_901+800del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149490 | ||||||
| chr12:132149491 | A | ACCACACC others(169): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.901+624_901+625ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149491 | ||||||
| chr12:132149492 | CCACACCC others(516): Show |
C | 1 | a0002c0002t0001g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901+634_902-930del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149492 | ||||||
| chr12:132149500 | CTAATCCC others(561): Show |
C | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.901+606_902-913del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149500 | |||||||
| chr12:132149501 | T | C | 1 | a0004c0010t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.901+606T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149501 | |||||||
| chr12:132149505 | C | CCCCTCGG others(740): Show |
1 | a0001c0001t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.901+624_901+625ins others(747): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149505 | ||||||
| chr12:132149518 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.901+623G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149518 | |||||||
| chr12:132149520 | C | CGCCGCCT others(296): Show |
1 | a0001c0001t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.901+633_901+634ins others(303): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149520 | ||||||
| chr12:132149520 | C | CGCCGCCT others(213): Show |
1 | a0003c0029t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.901+633_901+634ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149520 | ||||||
| chr12:132149520 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0049 others(8): Show |
15 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+625C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149520 | |||||||
| chr12:132149521 | G | A | 2 | a0001c0001t0001g0062 a0018c0018t0001g0118 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.901+626G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149521 | |||||||
| chr12:132149529 | A | ACTCACAC others(82): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.901+649_901+650ins others(89): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | ACTCACAC others(169): Show |
1 | a0001c0001t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.901+677_901+678ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | ACTCACAC others(81): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.901+677_901+678ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | ACTCCTAC others(81): Show |
1 | a0001c0003t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.901+637_901+638ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | ACTCCTAC others(1709): Show |
1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.901+637_901+638ins others(1716): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | ACTCCTAC others(81): Show |
1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.901+637_901+638ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149529 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.901+634A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149529 | |||||||
| chr12:132149529 | ACTCACAC others(81): Show |
G | 1 | a0004c0010t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.901+634_901+721del others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149529 | |||||||
| chr12:132149529 | ACTCACAC others(257): Show |
G | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.901+634_901+897del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149529 | |||||||
| chr12:132149529 | ACTCACAC others(560): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.901+678_902-842del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149529 | ||||||
| chr12:132149532 | C | CCT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0003t0001g0052 |
3 | NA18973.hp1 NA19030.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.901+637_901+638ins others(2): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149532 | |||||||
| chr12:132149533 | A | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(41): Show |
52 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.901+638A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149533 | |||||||
| chr12:132149534 | C | CACCACAC others(36): Show |
1 | a0003c0011t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.901+649_901+650ins others(43): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149534 | ||||||
| chr12:132149534 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.901+681_901+682ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149534 | ||||||
| chr12:132149534 | C | CACCACAC others(301): Show |
1 | a0001c0001t0001g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.901+677_901+678ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149534 | ||||||
| chr12:132149534 | C | CACCACAC others(609): Show |
1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.901+677_901+678ins others(616): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149534 | ||||||
| chr12:132149534 | C | CCACACCC others(255): Show |
1 | a0001c0001t0001g0001 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.901+639_901+640ins others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149534 | |||||||
| chr12:132149534 | C | CCACACCC others(79): Show |
1 | a0001c0003t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.901+639_901+640ins others(86): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149534 | |||||||
| chr12:132149534 | C | CCACACCC others(343): Show |
1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.901+639_901+640ins others(350): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149534 | |||||||
| chr12:132149534 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(49): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.901+639C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149534 | |||||||
| chr12:132149536 | CCACACCC others(472): Show |
C | 1 | a0002c0002t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.901+678_902-930del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149536 | ||||||
| chr12:132149536 | CCACACCC others(516): Show |
C | 1 | a0001c0001t0001g0013 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.901+678_902-886del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149536 | ||||||
| chr12:132149545 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+650T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149545 | |||||||
| chr12:132149563 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.901+668C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149563 | |||||||
| chr12:132149564 | C | CGCCGCCT others(2017): Show |
1 | a0001c0001t0001g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.901+677_901+678ins others(2024): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149564 | ||||||
| chr12:132149564 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.901+677_901+678ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149564 | ||||||
| chr12:132149564 | C | CGCCTCAC others(207): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+672_901+673ins others(214): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149564 | ||||||
| chr12:132149564 | C | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0038 others(6): Show |
13 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.901+669C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149564 | |||||||
| chr12:132149564 | CGCCGCCT others(169): Show |
C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0025 |
2 | HG01123.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.901+678_901+853del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149564 | ||||||
| chr12:132149565 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.901+670G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149565 | |||||||
| chr12:132149568 | G | T | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.901+673G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149568 | |||||||
| chr12:132149573 | A | ACTCACAC others(565): Show |
1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.901+721_901+722ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | A | ACTCACAC others(1841): Show |
1 | a0003c0032t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.901+725_901+726ins others(1848): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | A | ACTCCTAC others(125): Show |
1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.901+681_901+682ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | A | ACTCCTAC others(81): Show |
1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.901+681_901+682ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | A | ACTCCTAC others(81): Show |
1 | a0001c0001t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.901+681_901+682ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.901+678A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149573 | |||||||
| chr12:132149573 | ACTCACAC others(560): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.901+766_902-754del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149573 | ACTCACAC others(1000): Show |
A | 1 | a0002c0002t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.901+683_902-397del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149573 | ||||||
| chr12:132149576 | CACACCAC others(513): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.901+682_902-885del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149576 | |||||||
| chr12:132149576 | CACACCAC others(557): Show |
C | 1 | a0001c0001t0001g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.901+682_902-841del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149576 | |||||||
| chr12:132149577 | A | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.901+682A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149577 | |||||||
| chr12:132149578 | C | CACCACAC others(2369): Show |
1 | a0001c0001t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.901+721_901+722ins others(2376): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0014 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.901+721_901+722ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CACCACAC others(2633): Show |
1 | a0001c0001t0001g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.901+765_901+766ins others(2640): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.901+725_901+726ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CACCACAC others(917): Show |
1 | a0001c0005t0001g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.901+712_901+713ins others(924): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CACCACAC others(37): Show |
1 | a0001c0006t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.901+712_901+713ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149578 | ||||||
| chr12:132149578 | C | CCACACCC others(739): Show |
1 | a0001c0001t0001g0010 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.901+683_901+684ins others(746): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149578 | |||||||
| chr12:132149578 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
70 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.901+683C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149578 | |||||||
| chr12:132149578 | C | TACCACAC others(81): Show |
1 | a0001c0001t0001g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.901+682_901+683ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149578 | |||||||
| chr12:132149580 | C | CCCCTAAT others(418): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901+686_901+687ins others(425): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149580 | ||||||
| chr12:132149582 | A | C | 1 | a0002c0002t0001g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.901+687A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149582 | |||||||
| chr12:132149587 | C | CCTAATCC others(213): Show |
1 | a0001c0001t0001g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.901+712_901+713ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149587 | ||||||
| chr12:132149589 | T | C | 2 | a0001c0001t0001g0041 a0002c0002t0001g0065 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.901+694T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149589 | |||||||
| chr12:132149605 | TGCCGCCG others(1091): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.901+717_902-272del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149605 | ||||||
| chr12:132149606 | G | A | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+711G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149606 | |||||||
| chr12:132149608 | C | CGCCGCCT others(345): Show |
1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.901+765_901+766ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149608 | ||||||
| chr12:132149608 | C | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
19 | HG00140.hp1 HG00544.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.901+713C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149608 | |||||||
| chr12:132149608 | CGCCGCCT others(125): Show |
C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0002c0002t0001g0098 |
3 | HG02145.hp2 HG03834.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.901+766_901+897del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149608 | ||||||
| chr12:132149609 | G | A | 2 | a0006c0034t0001g0071 a0018c0018t0001g0118 |
2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.901+714G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149609 | |||||||
| chr12:132149613 | C | T | 2 | a0001c0001t0001g0032 a0002c0002t0001g0096 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.901+718C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149613 | |||||||
| chr12:132149617 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(38): Show |
43 | HG00558.hp1 HG00621.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.901+722G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149617 | |||||||
| chr12:132149617 | G | GCTCACAC others(37): Show |
1 | a0001c0001t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.901+726_901+769dup others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149617 | ||||||
| chr12:132149617 | G | GCTCACAC others(34): Show |
1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.901+760_901+761ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149617 | ||||||
| chr12:132149617 | G | GCTCCTAC others(829): Show |
1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.901+725_901+726ins others(836): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149617 | ||||||
| chr12:132149620 | CACACCAC others(122): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.901+726_901+854del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149620 | |||||||
| chr12:132149621 | A | ATACCACA others(213): Show |
1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.901+726_901+727ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149621 | |||||||
| chr12:132149621 | A | ATACCACA others(213): Show |
1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.901+726_901+727ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149621 | |||||||
| chr12:132149621 | A | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0031 others(19): Show |
23 | HG00621.hp1 HG01123.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.901+726A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149621 | |||||||
| chr12:132149621 | ACACCACA others(37): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.901+727_901+770del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149621 | |||||||
| chr12:132149622 | C | CACCACAC others(433): Show |
1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.901+765_901+766ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CACCACAC others(213): Show |
1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901+765_901+766ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.901+765_901+766ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.901+765_901+766ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CACCACAC others(949): Show |
1 | a0001c0006t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.901+760_901+761ins others(956): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.901+756_901+757ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149622 | ||||||
| chr12:132149622 | C | CCACACCC others(519): Show |
1 | a0001c0001t0001g0017 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.901+727_901+728ins others(526): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149622 | |||||||
| chr12:132149622 | C | CCACACCC others(299): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.901+727_901+728ins others(306): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149622 | |||||||
| chr12:132149622 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(31): Show |
36 | HG00621.hp1 HG01123.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.901+727C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149622 | |||||||
| chr12:132149623 | A | ACCACACC others(303): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.901+765_901+766ins others(310): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149623 | ||||||
| chr12:132149624 | CCACACCC others(384): Show |
C | 2 | a0001c0001t0001g0013 a0002c0002t0001g0061 |
2 | HG02451.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.901+766_902-930del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149624 | ||||||
| chr12:132149632 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+737C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149632 | |||||||
| chr12:132149633 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.901+738T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149633 | |||||||
| chr12:132149649 | TGCCGCCG others(519): Show |
T | 1 | a0002c0002t0001g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.901+761_902-800del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149649 | ||||||
| chr12:132149652 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.901+769_901+770ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149652 | ||||||
| chr12:132149652 | C | CGCCGCCT others(3195): Show |
1 | a0003c0028t0001g0201 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.901+765_901+766ins others(3202): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149652 | ||||||
| chr12:132149652 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.901+765_901+766ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149652 | ||||||
| chr12:132149652 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0031 others(17): Show |
20 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.901+757C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149652 | |||||||
| chr12:132149652 | CGCCGCCT others(37): Show |
C | 1 | a0001c0001t0001g0048 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.901+770_901+813del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149652 | ||||||
| chr12:132149652 | CGCCGCCT others(81): Show |
C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0139 a0001c0001t0001g0188 others(1): Show |
4 | HG01884.hp2 HG01943.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+766_901+853del others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149652 | ||||||
| chr12:132149661 | A | ACTCACAC others(37): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149661 | ||||||
| chr12:132149661 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(73): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.901+766A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149661 | |||||||
| chr12:132149661 | ACTCCTAC others(604): Show |
A | 1 | a0002c0002t0001g0218 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.901+770_902-706del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149661 | ||||||
| chr12:132149661 | ACTCCTAC others(692): Show |
A | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.901+770_902-618del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149661 | ||||||
| chr12:132149661 | ACTCCTAC others(736): Show |
A | 1 | a0001c0001t0001g0200 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.901+770_902-574del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149661 | ||||||
| chr12:132149664 | C | CACACCAC others(1399): Show |
1 | a0001c0001t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(1406): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(78): Show |
1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.901+769_901+770ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(515): Show |
1 | a0001c0001t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(522): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(474): Show |
1 | a0001c0001t0001g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.901+769_901+770ins others(481): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(650): Show |
1 | a0001c0001t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.901+769_901+770ins others(657): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(510): Show |
1 | a0001c0001t0001g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(517): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(166): Show |
1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.901+769_901+770ins others(173): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(694): Show |
1 | a0001c0001t0001g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(701): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149664 | C | CACACCAC others(210): Show |
1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.901+769_901+770ins others(217): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149664 | |||||||
| chr12:132149665 | C | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
94 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.901+770C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149665 | |||||||
| chr12:132149666 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
85 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.901+771T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149666 | |||||||
| chr12:132149666 | T | TACCACAC others(81): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.901+800_901+801ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(81): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(1005): Show |
1 | a0001c0001t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(1012): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(37): Show |
1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(82): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(89): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(257): Show |
1 | a0001c0003t0001g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(169): Show |
1 | a0001c0003t0001g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.901+800_901+801ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(125): Show |
1 | a0003c0030t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(433): Show |
1 | a0001c0001t0001g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TACCACAC others(565): Show |
1 | a0001c0001t0001g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.901+800_901+801ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | T | TCAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.901+771_901+772ins others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149666 | |||||||
| chr12:132149666 | TACCACAC others(428): Show |
T | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.901+801_902-851del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | TACCACAC others(692): Show |
T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.901+801_902-587del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | TACCACAC others(868): Show |
T | 1 | a0001c0003t0001g0011 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.901+801_902-411del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149666 | TACCACAC others(1044): Show |
T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0085 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.901+801_902-235del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149666 | ||||||
| chr12:132149668 | C | CCACACCC others(76): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(83): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149668 | ||||||
| chr12:132149668 | CCACACCC others(340): Show |
C | 3 | a0001c0004t0001g0030 a0002c0002t0001g0095 a0002c0002t0001g0187 |
3 | HG03041.hp2 NA18612.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.901+801_902-939del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149668 | ||||||
| chr12:132149672 | A | ACCCCTAA others(258): Show |
1 | a0001c0003t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.901+800_901+801ins others(265): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149672 | ||||||
| chr12:132149673 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.901+778C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149673 | |||||||
| chr12:132149677 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+782T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149677 | |||||||
| chr12:132149693 | TGCGGCCG others(343): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.901+801_902-936del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149693 | ||||||
| chr12:132149694 | G | A | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+799G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149694 | |||||||
| chr12:132149695 | C | CCACCGCC others(248): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+800_901+801ins others(255): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149695 | |||||||
| chr12:132149696 | G | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
129 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.901+801G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149696 | |||||||
| chr12:132149696 | G | GGCCGCCT others(37): Show |
1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.901+809_901+810ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149696 | ||||||
| chr12:132149696 | G | GGCCGCCT others(2266): Show |
1 | a0001c0006t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.901+809_901+810ins others(2273): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149696 | ||||||
| chr12:132149696 | G | T | 1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901+801G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149696 | |||||||
| chr12:132149705 | A | ACTCACAC others(345): Show |
1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.901+844_901+845ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149705 | A | ACTCACAC others(81): Show |
1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.901+844_901+845ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149705 | A | ACTCCTAC others(389): Show |
1 | a0001c0001t0001g0005 | 2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.901+813_901+814ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149705 | A | ACTCCTAC others(213): Show |
1 | a0001c0005t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.901+813_901+814ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149705 | A | ACTCCTAC others(37): Show |
1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.901+813_901+814ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149705 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.901+810A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149705 | |||||||
| chr12:132149705 | ACTCACAC others(648): Show |
A | 1 | a0001c0003t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.901+845_902-587del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149705 | ||||||
| chr12:132149706 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+811C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149706 | |||||||
| chr12:132149708 | CACACCAC others(777): Show |
C | 1 | a0002c0002t0001g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.901+814_902-489del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149708 | |||||||
| chr12:132149709 | A | ATACCACA others(81): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.901+814_901+815ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149709 | |||||||
| chr12:132149709 | A | ATACCACA others(81): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+814_901+815ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149709 | |||||||
| chr12:132149709 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(27): Show |
32 | HG00099.hp1 HG00323.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.901+814A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149709 | |||||||
| chr12:132149710 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.901+844_901+845ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(37): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0105 a0001c0001t0001g0111 others(2): Show |
5 | NA18747.hp2 NA18953.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+844_901+845ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.901+844_901+845ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(1709): Show |
1 | a0001c0001t0001g0006 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.901+844_901+845ins others(1716): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.901+844_901+845ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(653): Show |
1 | a0001c0001t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.901+844_901+845ins others(660): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.901+853_901+854ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CACCACAC others(213): Show |
1 | a0004c0007t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.901+858_901+859ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149710 | ||||||
| chr12:132149710 | C | CCACACCC others(123): Show |
1 | a0001c0001t0001g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.901+815_901+816ins others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149710 | |||||||
| chr12:132149710 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
48 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.901+815C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149710 | |||||||
| chr12:132149710 | C | TACCACAC others(609): Show |
1 | a0017c0027t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.901+814_901+815ins others(616): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149710 | |||||||
| chr12:132149712 | C | CCACACCC others(32): Show |
1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901+844_901+845ins others(39): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149712 | ||||||
| chr12:132149739 | C | CCGCCGCC others(34): Show |
1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901+844_901+845ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149739 | |||||||
| chr12:132149740 | G | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
134 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.901+845G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149740 | |||||||
| chr12:132149740 | G | GGCCGCCT others(37): Show |
1 | a0001c0003t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.901+942_901+985dup others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149740 | ||||||
| chr12:132149740 | G | GGCCGCCT others(521): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+897_901+898ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149740 | ||||||
| chr12:132149740 | G | GGCCGCCT others(81): Show |
1 | a0008c0025t0001g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.901+888_901+889ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149740 | ||||||
| chr12:132149740 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901+845G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149740 | |||||||
| chr12:132149740 | GGCCGCCT others(1000): Show |
G | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.901+863_902-217del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149740 | ||||||
| chr12:132149741 | G | A | 1 | a0018c0018t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.901+846G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149741 | |||||||
| chr12:132149744 | G | T | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.901+849G>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149744 | |||||||
| chr12:132149745 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.901+850C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149745 | |||||||
| chr12:132149749 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(40): Show |
48 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.901+854G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149749 | |||||||
| chr12:132149749 | G | GCTCACAC others(301): Show |
1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.901+888_901+889ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149749 | ||||||
| chr12:132149749 | G | GCTCATAC others(389): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.901+858_901+859ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149749 | ||||||
| chr12:132149753 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(21): Show |
28 | HG00735.hp2 HG01123.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.901+858A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149753 | |||||||
| chr12:132149754 | C | CACACACC others(36): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.901+861_901+862ins others(43): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149754 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.901+945_901+946ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149754 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901+891_901+892ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149754 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.901+888_901+889ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149754 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.901+888_901+889ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149754 | C | CCACACCC others(35): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0165 |
2 | HG02273.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.901+859_901+860ins others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149754 | |||||||
| chr12:132149754 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
44 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.901+859C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149754 | |||||||
| chr12:132149754 | CACCACAC others(868): Show |
C | 1 | a0002c0002t0004g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901+903_902-309del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149754 | ||||||
| chr12:132149756 | CCACACCC others(252): Show |
C | 2 | a0002c0002t0001g0173 a0012c0017t0001g0156 |
2 | HG02738.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.901+986_902-842del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149756 | ||||||
| chr12:132149784 | C | CGCCGCCT others(257): Show |
1 | a0001c0001t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.901+897_901+898ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149784 | ||||||
| chr12:132149784 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.901+897_901+898ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149784 | ||||||
| chr12:132149784 | C | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(13): Show |
16 | HG00099.hp1 HG00621.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.901+889C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149784 | |||||||
| chr12:132149793 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(27): Show |
32 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.901+898G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149793 | |||||||
| chr12:132149793 | G | GCTCACAC others(169): Show |
1 | a0001c0004t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.901+945_901+946ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149793 | ||||||
| chr12:132149793 | G | GCTCCTAC others(125): Show |
1 | a0001c0003t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.901+901_901+902ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149793 | ||||||
| chr12:132149797 | A | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0031 others(16): Show |
19 | HG00544.hp2 HG01123.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.901+902A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149797 | |||||||
| chr12:132149798 | C | CACCACAC others(1181): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.901+941_901+942ins others(1188): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149798 | ||||||
| chr12:132149798 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.901+976_901+977ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149798 | ||||||
| chr12:132149798 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.901+945_901+946ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149798 | ||||||
| chr12:132149798 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
37 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.901+903C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149798 | |||||||
| chr12:132149807 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901+912C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149807 | |||||||
| chr12:132149808 | C | G | 1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+913C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149808 | |||||||
| chr12:132149818 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.901+923C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149818 | |||||||
| chr12:132149828 | C | CGCCGCCT others(125): Show |
1 | a0001c0026t0001g0006 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.901+985_901+986ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149828 | ||||||
| chr12:132149828 | C | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG00735.hp1 HG02572.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.901+933C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149828 | |||||||
| chr12:132149833 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901+938C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149833 | |||||||
| chr12:132149837 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(36): Show |
41 | HG00558.hp2 HG00673.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.901+942G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149837 | |||||||
| chr12:132149837 | G | GCTCACAC others(81): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.901+1029_901+1030i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149837 | ||||||
| chr12:132149838 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+943C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149838 | |||||||
| chr12:132149841 | A | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0031 others(20): Show |
24 | HG00673.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.901+946A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149841 | |||||||
| chr12:132149842 | C | CACCACAC others(423): Show |
1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901+989_901+990ins others(430): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149842 | ||||||
| chr12:132149842 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.901+1029_901+1030i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149842 | ||||||
| chr12:132149842 | C | CACCACAC others(521): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.901+985_901+986ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149842 | ||||||
| chr12:132149842 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.901+985_901+986ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149842 | ||||||
| chr12:132149842 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.901+976_901+977ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149842 | ||||||
| chr12:132149842 | C | CCACACCC others(299): Show |
1 | a0001c0005t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.901+947_901+948ins others(306): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149842 | |||||||
| chr12:132149842 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(29): Show |
34 | HG00673.hp2 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.901+947C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149842 | |||||||
| chr12:132149844 | CCACACCC others(164): Show |
C | 1 | a0005c0013t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.901+986_902-930del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149844 | ||||||
| chr12:132149846 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.901+951A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149846 | |||||||
| chr12:132149852 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.901+957C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149852 | |||||||
| chr12:132149853 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901+958T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149853 | |||||||
| chr12:132149872 | C | CGCCGCCT others(81): Show |
1 | a0001c0003t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.901+989_901+990ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149872 | ||||||
| chr12:132149872 | C | CGCCGCCT others(961): Show |
1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.901+985_901+986ins others(968): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149872 | ||||||
| chr12:132149872 | C | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0025 others(11): Show |
17 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.901+977C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149872 | |||||||
| chr12:132149879 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.901+984T>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149879 | |||||||
| chr12:132149881 | A | ACTCCTAC others(81): Show |
1 | a0001c0001t0001g0014 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.901+1029_901+1030i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149881 | ||||||
| chr12:132149881 | A | ACTCCTAC others(125): Show |
1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901+1029_901+1030i others(134): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149881 | ||||||
| chr12:132149881 | A | ACTCCTAC others(81): Show |
1 | a0001c0006t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.901+1020_901+1021i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149881 | ||||||
| chr12:132149881 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.901+986A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149881 | |||||||
| chr12:132149881 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.901+986A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149881 | |||||||
| chr12:132149881 | ACTCCTAC others(164): Show |
A | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901+990_902-926del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149881 | ||||||
| chr12:132149881 | ACTCCTAC others(692): Show |
A | 1 | a0002c0002t0001g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.901+990_902-398del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149881 | ||||||
| chr12:132149884 | C | CACACCAC others(34): Show |
1 | a0001c0001t0001g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.901+989_901+990ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149884 | |||||||
| chr12:132149884 | C | CACACCAC others(166): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.901+989_901+990ins others(173): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149884 | |||||||
| chr12:132149884 | C | CACACCAC others(34): Show |
2 | a0001c0001t0001g0040 a0004c0007t0001g0126 |
2 | HG03516.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.901+989_901+990ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149884 | |||||||
| chr12:132149885 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.901+990C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149885 | |||||||
| chr12:132149885 | C | CTACCACA others(37): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01934.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.901+1020_901+1021i others(46): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149885 | ||||||
| chr12:132149885 | CTACCACA others(736): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.902-1012_902-270de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149885 | ||||||
| chr12:132149886 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.901+991T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149886 | |||||||
| chr12:132149886 | T | TACCACAC others(33): Show |
1 | a0001c0001t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.901+1029_901+1030i others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TACCACAC others(81): Show |
1 | a0010c0021t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.901+1029_901+1030i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TACCACAC others(213): Show |
1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.901+1033_901+1034i others(222): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TACCACAC others(125): Show |
1 | a0001c0001t0001g0011 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.901+1020_901+1021i others(134): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TACCACAC others(1395): Show |
1 | a0001c0006t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.901+1020_901+1021i others(1404): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TACCACAC others(81): Show |
1 | a0001c0001t0001g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.901+1020_901+1021i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | T | TCAC | 4 | a0001c0001t0001g0040 a0001c0001t0001g0202 a0004c0007t0001g0126 others(1): Show |
4 | HG01069.hp1 HG02683.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+991_901+992ins others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149886 | |||||||
| chr12:132149886 | TACCACAC others(164): Show |
T | 1 | a0001c0001t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.901+1035_902-881de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149886 | TACCACAC others(252): Show |
T | 1 | a0001c0001t0001g0020 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.901+1035_902-793de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149886 | ||||||
| chr12:132149888 | C | CCACACCC others(32): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901+1020_901+1021i others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149888 | ||||||
| chr12:132149888 | CCACACCC others(120): Show |
C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0002c0002t0001g0097 |
3 | HG01943.hp2 HG02056.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.901+1035_902-925de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149888 | ||||||
| chr12:132149897 | T | C | 1 | a0004c0010t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.901+1002T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149897 | |||||||
| chr12:132149907 | G | A | 1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.901+1012G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149907 | |||||||
| chr12:132149916 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.901+1029_901+1030i others(43): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149916 | ||||||
| chr12:132149916 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.901+1034_901+1035i others(46): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149916 | ||||||
| chr12:132149916 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0025 others(8): Show |
13 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.901+1021C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149916 | |||||||
| chr12:132149920 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.901+1025G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149920 | |||||||
| chr12:132149925 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
50 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.901+1030G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149925 | |||||||
| chr12:132149925 | G | GCTCACAC others(32): Show |
1 | a0001c0001t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.901+1034_901+1035i others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149925 | ||||||
| chr12:132149929 | A | ACACCACA others(170): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.901+1034_901+1035i others(179): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149929 | |||||||
| chr12:132149929 | A | ACACCACA others(81): Show |
1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.901+1034_901+1035i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149929 | |||||||
| chr12:132149929 | A | ACACCACA others(125): Show |
1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.901+1034_901+1035i others(134): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149929 | |||||||
| chr12:132149929 | A | ACACCACA others(81): Show |
1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.901+1034_901+1035i others(90): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149929 | |||||||
| chr12:132149929 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.901+1034A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149929 | |||||||
| chr12:132149930 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.901+1035T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149930 | |||||||
| chr12:132149930 | TACCACAC others(252): Show |
T | 1 | a0009c0038t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.902-1012_902-754de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149930 | ||||||
| chr12:132149930 | TACCACAC others(340): Show |
T | 1 | a0002c0016t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902-1012_902-666de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149930 | ||||||
| chr12:132149930 | TACCACAC others(428): Show |
T | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902-1012_902-578de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149930 | ||||||
| chr12:132149932 | CCACACCC others(76): Show |
C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0083 others(2): Show |
5 | HG01123.hp1 HG02145.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.902-1012_902-930de others(84): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149932 | ||||||
| chr12:132149933 | C | T | 1 | a0001c0003t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.901+1038C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149933 | |||||||
| chr12:132149951 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.902-1030G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149951 | |||||||
| chr12:132149960 | C | CGCCGCCT others(521): Show |
1 | a0001c0001t0001g0116 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.902-1013_902-1012i others(530): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149960 | ||||||
| chr12:132149960 | C | CGCCGCCT others(3601): Show |
1 | a0001c0001t0001g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.902-1013_902-1012i others(3610): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149960 | ||||||
| chr12:132149960 | C | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0021 others(11): Show |
15 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.902-1021C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149960 | |||||||
| chr12:132149969 | A | ACTCCTAC others(565): Show |
1 | a0001c0001t0001g0023 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.902-1009_902-1008i others(574): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149969 | ||||||
| chr12:132149969 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.902-1012A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149969 | |||||||
| chr12:132149969 | ACTCACAC others(76): Show |
A | 2 | a0001c0001t0001g0033 a0014c0014t0001g0026 |
2 | HG01255.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.902-959_902-877del others(83): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149969 | ||||||
| chr12:132149969 | ACTCACAC others(472): Show |
A | 1 | a0001c0003t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.902-959_902-481del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149969 | ||||||
| chr12:132149971 | TCACACCA others(123): Show |
T | 1 | a0001c0004t0001g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.902-1009_902-880de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149971 | |||||||
| chr12:132149972 | CACACCAC others(73): Show |
C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0031 |
2 | HG01123.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.902-1008_902-929de others(81): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149972 | |||||||
| chr12:132149972 | CACACCAC others(161): Show |
C | 1 | a0001c0001t0001g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.902-1008_902-841de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149972 | |||||||
| chr12:132149972 | CACACCAC others(249): Show |
C | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.902-1008_902-753de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149972 | |||||||
| chr12:132149972 | CACACCAC others(513): Show |
C | 1 | a0002c0002t0003g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.902-1008_902-489de others(1): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149972 | |||||||
| chr12:132149973 | A | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
38 | HG00558.hp1 HG00558.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.902-1008A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149973 | |||||||
| chr12:132149974 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.902-969_902-968ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149974 | ||||||
| chr12:132149974 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
47 | HG00558.hp1 HG00558.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.902-1007C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132149974 | |||||||
| chr12:132149976 | CCACACCC others(32): Show |
C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0119 others(3): Show |
6 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-959_902-921del others(39): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132149976 | ||||||
| chr12:132150001 | TGCCGCCG others(35): Show |
T | 1 | a0001c0023t0001g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.902-973_902-932del others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150001 | ||||||
| chr12:132150004 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(10): Show |
13 | HG00609.hp1 HG00621.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.902-977C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150004 | |||||||
| chr12:132150013 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
50 | HG00558.hp1 HG00735.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.902-968G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150013 | |||||||
| chr12:132150015 | T | TCACAC | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.902-964_902-960dup others(5): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACAC others(90): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.902-961_902-960ins others(97): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(42): Show |
1 | a0001c0001t0001g0009 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(42): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0003t0001g0008 |
3 | NA18966.hp2 NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.902-960_902-959ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(1409): Show |
1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(1416): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(262): Show |
1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(269): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(482): Show |
1 | a0001c0001t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(489): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(2672): Show |
1 | a0001c0003t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(2679): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(1098): Show |
1 | a0001c0001t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(1105): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(42): Show |
1 | a0001c0001t0001g0006 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(174): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(181): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(174): Show |
1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(181): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(42): Show |
5 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0003t0001g0003 others(2): Show |
5 | HG00609.hp1 HG00673.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.902-960_902-959ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(86): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(394): Show |
1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(401): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(1362): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(1369): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(86): Show |
3 | a0001c0001t0001g0010 a0001c0015t0001g0069 a0001c0026t0001g0006 |
3 | NA18971.hp2 NA19005.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.902-960_902-959ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(4585): Show |
1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(4592): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(86): Show |
1 | a0001c0003t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(658): Show |
1 | a0001c0001t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(665): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(218): Show |
1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(225): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(438): Show |
1 | a0013c0022t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(445): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(2858): Show |
1 | a0015c0024t0001g0012 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(2865): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(702): Show |
1 | a0001c0001t0001g0014 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(709): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(130): Show |
1 | a0001c0003t0001g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(137): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(1259): Show |
1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(1266): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(42): Show |
1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(218): Show |
1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(225): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(86): Show |
1 | a0001c0003t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(570): Show |
1 | a0003c0032t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(577): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(218): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(225): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(253): Show |
1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(260): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(513): Show |
1 | a0001c0001t0001g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(520): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(86): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(350): Show |
1 | a0001c0003t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(357): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(1363): Show |
1 | a0001c0001t0001g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(1370): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(2990): Show |
1 | a0001c0001t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(2997): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(746): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(753): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(2154): Show |
1 | a0001c0003t0001g0142 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(2161): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(615): Show |
1 | a0001c0005t0001g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(622): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(306): Show |
1 | a0003c0028t0001g0201 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(313): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCACACCA others(130): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.902-960_902-959ins others(137): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATAC | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.902-964_902-963ins others(5): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATACCA others(482): Show |
1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.902-964_902-963ins others(489): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATACCA others(42): Show |
1 | a0006c0012t0001g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.902-964_902-963ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATACCA others(614): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.902-964_902-963ins others(621): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATACCA others(42): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.902-964_902-963ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCATACCA others(438): Show |
1 | a0001c0001t0001g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.902-964_902-963ins others(445): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTAC | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(20): Show |
25 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.902-965_902-964ins others(5): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(86): Show |
1 | a0001c0005t0001g0001 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.902-965_902-964ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(86): Show |
1 | a0001c0001t0001g0003 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.902-965_902-964ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(218): Show |
1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.902-965_902-964ins others(225): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(42): Show |
4 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0006t0001g0153 others(1): Show |
4 | HG02273.hp2 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.902-965_902-964ins others(49): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(86): Show |
1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(1317): Show |
1 | a0001c0001t0001g0001 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(1324): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(1669): Show |
1 | a0001c0001t0001g0001 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.902-965_902-964ins others(1676): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(86): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(86): Show |
1 | a0003c0029t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.902-965_902-964ins others(93): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(81): Show |
1 | a0001c0001t0001g0127 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(262): Show |
1 | a0001c0001t0001g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(269): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150015 | T | TCCTACCA others(438): Show |
1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.902-965_902-964ins others(445): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150015 | ||||||
| chr12:132150016 | CACACCCC others(29): Show |
C | 2 | a0001c0001t0001g0188 a0004c0010t0001g0077 |
2 | HG03516.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.902-964_902-929del others(36): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150016 | |||||||
| chr12:132150016 | CACACCCC others(337): Show |
C | 1 | a0002c0002t0001g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.902-964_902-621del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150016 | |||||||
| chr12:132150016 | CACACCCC others(513): Show |
C | 1 | a0018c0018t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.902-964_902-445del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150016 | |||||||
| chr12:132150019 | A | ACCACACC others(87): Show |
1 | a0001c0001t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.902-960_902-959ins others(94): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150019 | ||||||
| chr12:132150038 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.902-943A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150038 | |||||||
| chr12:132150043 | C | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(17): Show |
20 | HG00673.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.902-938C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150043 | |||||||
| chr12:132150046 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.902-935C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150046 | |||||||
| chr12:132150052 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
29 | HG00423.hp2 HG00609.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.902-929G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150052 | |||||||
| chr12:132150054 | TCAC | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0031 others(2): Show |
5 | HG01123.hp2 HG03516.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-926_902-924del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150054 | |||||||
| chr12:132150056 | A | ATACCACA others(296): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.902-925_902-924ins others(303): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150056 | |||||||
| chr12:132150056 | A | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(18): Show |
22 | HG00642.hp1 HG01261.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.902-925A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150056 | |||||||
| chr12:132150057 | C | CACCACAC others(345): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.902-842_902-841ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150057 | ||||||
| chr12:132150057 | C | CACCACAC others(433): Show |
1 | a0008c0025t0001g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.902-842_902-841ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150057 | ||||||
| chr12:132150057 | C | CACCACAC others(119): Show |
1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.902-891_902-890ins others(126): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150057 | ||||||
| chr12:132150057 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
31 | HG00423.hp2 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.902-924C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150057 | |||||||
| chr12:132150059 | C | CCACACCC others(291): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.902-871_902-870ins others(298): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150059 | ||||||
| chr12:132150087 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.902-886_902-885ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150087 | ||||||
| chr12:132150087 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.902-887_902-847dup others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150087 | ||||||
| chr12:132150087 | C | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(16): Show |
19 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.902-894C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150087 | |||||||
| chr12:132150096 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(35): Show |
40 | HG00609.hp1 HG00621.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.902-885G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150096 | |||||||
| chr12:132150096 | G | GCTCACAC others(81): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.902-851_902-850ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150096 | ||||||
| chr12:132150100 | A | ATACCACA others(37): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.902-881_902-880ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150100 | |||||||
| chr12:132150100 | A | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(25): Show |
28 | HG00423.hp2 HG00558.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.902-881A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150100 | |||||||
| chr12:132150101 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.902-842_902-841ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150101 | ||||||
| chr12:132150101 | C | CACCACAC others(519): Show |
1 | a0003c0011t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902-782_902-781ins others(526): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150101 | ||||||
| chr12:132150101 | C | CCACACCC others(911): Show |
1 | a0001c0004t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.902-880_902-879ins others(918): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150101 | |||||||
| chr12:132150101 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
37 | HG00423.hp2 HG00558.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.902-880C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150101 | |||||||
| chr12:132150131 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0010 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.902-842_902-841ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150131 | ||||||
| chr12:132150131 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.902-842_902-841ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150131 | ||||||
| chr12:132150131 | C | CGCCGCCT others(2325): Show |
1 | a0001c0001t0001g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.902-798_902-797ins others(2332): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150131 | ||||||
| chr12:132150131 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(13): Show |
16 | HG00099.hp2 HG00609.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.902-850C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150131 | |||||||
| chr12:132150132 | G | GCCGCCTC others(213): Show |
1 | a0001c0001t0001g0009 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.902-838_902-837ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150132 | ||||||
| chr12:132150140 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
49 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.902-841G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150140 | |||||||
| chr12:132150140 | G | GCTCACAC others(169): Show |
1 | a0001c0001t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.902-710_902-709ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150140 | ||||||
| chr12:132150140 | G | GCTCACAC others(477): Show |
1 | a0004c0007t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.902-763_902-762ins others(484): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150140 | ||||||
| chr12:132150144 | A | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(29): Show |
34 | HG01123.hp2 HG01261.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.902-837A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150144 | |||||||
| chr12:132150145 | C | CACCACAC others(34): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.902-798_902-797ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150145 | ||||||
| chr12:132150145 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.902-798_902-797ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150145 | ||||||
| chr12:132150145 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.902-750_902-749ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150145 | ||||||
| chr12:132150145 | C | CACCACAC others(125): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.902-763_902-762ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150145 | ||||||
| chr12:132150145 | C | CCACCACA others(38): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.902-836_902-835ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150145 | |||||||
| chr12:132150145 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
48 | HG00423.hp2 HG01123.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.902-836C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150145 | |||||||
| chr12:132150145 | C | TACCACAC others(257): Show |
1 | a0001c0001t0001g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.902-837_902-836ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150145 | |||||||
| chr12:132150175 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.902-798_902-797ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150175 | ||||||
| chr12:132150175 | C | CGCCGCCT others(423): Show |
1 | a0001c0001t0001g0010 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.902-789_902-788ins others(430): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150175 | ||||||
| chr12:132150175 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.902-794_902-793ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150175 | ||||||
| chr12:132150175 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(9): Show |
13 | HG00621.hp2 HG00735.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.902-806C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150175 | |||||||
| chr12:132150175 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.902-806C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150175 | |||||||
| chr12:132150180 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.902-801C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150180 | |||||||
| chr12:132150184 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(42): Show |
50 | HG00558.hp1 HG00621.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.902-797G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150184 | |||||||
| chr12:132150184 | G | GCTCACAC others(428): Show |
1 | a0001c0001t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.902-706_902-705ins others(435): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150184 | ||||||
| chr12:132150188 | A | ATACCACA others(169): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.902-793_902-792ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150188 | |||||||
| chr12:132150188 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
24 | HG00544.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.902-793A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150188 | |||||||
| chr12:132150189 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0196 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.902-784_902-783ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150189 | ||||||
| chr12:132150189 | C | CACCACAC others(213): Show |
1 | a0001c0001t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.902-754_902-753ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150189 | ||||||
| chr12:132150189 | C | CACCACAC others(1392): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.902-671_902-670ins others(1399): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150189 | ||||||
| chr12:132150189 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.902-763_902-762ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150189 | ||||||
| chr12:132150189 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0008 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.902-763_902-762ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150189 | ||||||
| chr12:132150189 | C | CCACACCC others(255): Show |
1 | a0001c0003t0001g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.902-792_902-791ins others(262): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150189 | |||||||
| chr12:132150189 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(32): Show |
35 | HG00544.hp2 HG00558.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.902-792C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150189 | |||||||
| chr12:132150196 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.902-785C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150196 | |||||||
| chr12:132150219 | C | CGCCGCCT others(257): Show |
1 | a0001c0001t0001g0146 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.902-754_902-753ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(1885): Show |
1 | a0001c0005t0001g0001 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.902-754_902-753ins others(1892): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(1049): Show |
1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.902-754_902-753ins others(1056): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(37): Show |
1 | a0004c0007t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.902-754_902-753ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(1401): Show |
1 | a0001c0001t0001g0005 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.902-710_902-709ins others(1408): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(1225): Show |
1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.902-662_902-661ins others(1232): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | CGCCGCCT others(37): Show |
1 | a0001c0026t0001g0006 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.902-719_902-718ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150219 | ||||||
| chr12:132150219 | C | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
21 | HG00323.hp2 HG00423.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.902-762C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150219 | |||||||
| chr12:132150228 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(39): Show |
47 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.902-753G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150228 | |||||||
| chr12:132150229 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.902-752C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150229 | |||||||
| chr12:132150232 | A | ATACCACA others(203): Show |
1 | a0001c0001t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.902-749_902-748ins others(210): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150232 | |||||||
| chr12:132150232 | A | ATACCACA others(291): Show |
1 | a0001c0001t0001g0010 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.902-749_902-748ins others(298): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150232 | |||||||
| chr12:132150232 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(30): Show |
36 | HG00423.hp1 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.902-749A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150232 | |||||||
| chr12:132150233 | C | CACCACAC others(213): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.902-710_902-709ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150233 | ||||||
| chr12:132150233 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.902-710_902-709ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150233 | ||||||
| chr12:132150233 | C | CACCACAC others(213): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.902-710_902-709ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150233 | ||||||
| chr12:132150233 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.902-719_902-718ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150233 | ||||||
| chr12:132150233 | C | CCACACCC others(343): Show |
1 | a0001c0005t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.902-748_902-747ins others(350): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150233 | |||||||
| chr12:132150233 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(40): Show |
48 | HG00423.hp1 HG00558.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.902-748C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150233 | |||||||
| chr12:132150263 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.902-710_902-709ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150263 | ||||||
| chr12:132150263 | C | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.902-718C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150263 | |||||||
| chr12:132150272 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
53 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.902-709G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150272 | |||||||
| chr12:132150276 | A | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(25): Show |
29 | HG00621.hp1 HG01255.hp1 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.902-705A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150276 | |||||||
| chr12:132150277 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.902-666_902-665ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(1183): Show |
1 | a0001c0001t0001g0004 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.902-666_902-665ins others(1190): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.902-666_902-665ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(1225): Show |
1 | a0003c0029t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.902-574_902-573ins others(1232): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(125): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.902-631_902-630ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(521): Show |
1 | a0001c0003t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.902-631_902-630ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.902-631_902-630ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(81): Show |
1 | a0001c0003t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.902-675_902-674ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(345): Show |
1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.902-675_902-674ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(169): Show |
1 | a0010c0021t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.902-675_902-674ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.902-675_902-674ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150277 | ||||||
| chr12:132150277 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
36 | HG00621.hp1 HG01255.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.902-704C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150277 | |||||||
| chr12:132150278 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.902-703A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150278 | |||||||
| chr12:132150288 | T | C | 1 | a0004c0010t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.902-693T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150288 | |||||||
| chr12:132150307 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.902-666_902-665ins others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150307 | ||||||
| chr12:132150307 | C | CGCCGCCT others(521): Show |
1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.902-666_902-665ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150307 | ||||||
| chr12:132150307 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.902-666_902-665ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150307 | ||||||
| chr12:132150307 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.902-631_902-630ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150307 | ||||||
| chr12:132150307 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.902-661_902-660ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150307 | ||||||
| chr12:132150307 | C | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0020 others(20): Show |
24 | HG00323.hp2 HG00621.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.902-674C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150307 | |||||||
| chr12:132150316 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(44): Show |
50 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.902-665G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150316 | |||||||
| chr12:132150316 | G | GCTCACAC others(345): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.902-622_902-621ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150316 | ||||||
| chr12:132150316 | G | GCTCACAC others(120): Show |
1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.902-622_902-621ins others(127): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150316 | ||||||
| chr12:132150316 | G | GCTCACAC others(3293): Show |
1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.902-618_902-617ins others(3300): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150316 | ||||||
| chr12:132150320 | A | ATACCACA others(82): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.902-661_902-660ins others(89): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150320 | |||||||
| chr12:132150320 | A | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(23): Show |
26 | HG00099.hp1 HG01243.hp2 HG02293.hp1 others(23): Show |
intron_variant | MODIFIER | c.902-661A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150320 | |||||||
| chr12:132150321 | C | CACCACAC others(1885): Show |
1 | a0001c0001t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.902-652_902-651ins others(1892): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CACCACAC others(1709): Show |
1 | a0001c0001t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.902-622_902-621ins others(1716): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CACCACAC others(477): Show |
1 | a0001c0001t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.902-622_902-621ins others(484): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CACCACAC others(169): Show |
1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.902-622_902-621ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.902-618_902-617ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.902-631_902-630ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150321 | ||||||
| chr12:132150321 | C | CCACACCC others(123): Show |
1 | a0001c0003t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.902-660_902-659ins others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150321 | |||||||
| chr12:132150321 | C | CCACACCC others(123): Show |
1 | a0001c0001t0001g0027 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.902-660_902-659ins others(130): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150321 | |||||||
| chr12:132150321 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
34 | HG00099.hp1 HG01243.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.902-660C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150321 | |||||||
| chr12:132150331 | CTAATCCC others(302): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.902-649_902-341del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150331 | |||||||
| chr12:132150338 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.902-643C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150338 | |||||||
| chr12:132150351 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.902-622_902-621ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150351 | ||||||
| chr12:132150351 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0001 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.902-622_902-621ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150351 | ||||||
| chr12:132150351 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.902-543_902-542ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150351 | ||||||
| chr12:132150351 | C | CGCCGCCT others(75): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.902-618_902-617ins others(82): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150351 | ||||||
| chr12:132150351 | C | CGCCGCCT others(477): Show |
1 | a0003c0028t0001g0201 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.902-618_902-617ins others(484): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150351 | ||||||
| chr12:132150351 | C | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(17): Show |
20 | HG00609.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.902-630C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150351 | |||||||
| chr12:132150352 | G | GCCGCCTC others(38): Show |
1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.902-627_902-583dup others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150352 | ||||||
| chr12:132150352 | G | GCCGCCTC others(81): Show |
1 | a0001c0001t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.902-578_902-577ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150352 | ||||||
| chr12:132150360 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
56 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.902-621G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150360 | |||||||
| chr12:132150360 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.902-621G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150360 | |||||||
| chr12:132150360 | G | GCTCACAC others(169): Show |
1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.902-587_902-586ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150360 | ||||||
| chr12:132150360 | G | GCTCATAC others(37): Show |
1 | a0001c0001t0001g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.902-617_902-616ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150360 | ||||||
| chr12:132150360 | G | GCTCCTAC others(345): Show |
1 | a0001c0001t0001g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.902-618_902-617ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150360 | ||||||
| chr12:132150361 | C | T | 1 | a0001c0039t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.902-620C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150361 | |||||||
| chr12:132150364 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
32 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.902-617A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150364 | |||||||
| chr12:132150365 | C | CACCACAC others(433): Show |
1 | a0001c0001t0001g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.902-608_902-607ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.902-578_902-577ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.902-578_902-577ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(389): Show |
1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.902-578_902-577ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(256): Show |
1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.902-574_902-573ins others(263): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(2319): Show |
1 | a0001c0001t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.902-583_902-582ins others(2326): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CACCACAC others(1797): Show |
1 | a0001c0001t0001g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.902-587_902-586ins others(1804): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150365 | ||||||
| chr12:132150365 | C | CCACACCC others(121): Show |
1 | a0017c0027t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.902-616_902-615ins others(128): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150365 | |||||||
| chr12:132150365 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
44 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.902-616C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150365 | |||||||
| chr12:132150395 | C | CGCCGCCT others(2017): Show |
1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.902-578_902-577ins others(2024): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150395 | ||||||
| chr12:132150395 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.902-578_902-577ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150395 | ||||||
| chr12:132150395 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0010 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.902-543_902-542ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150395 | ||||||
| chr12:132150395 | C | CGCCGCCT others(741): Show |
1 | a0001c0001t0001g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.902-543_902-542ins others(748): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150395 | ||||||
| chr12:132150395 | C | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.902-586C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150395 | |||||||
| chr12:132150396 | G | GCCGCCTC others(345): Show |
1 | a0001c0001t0001g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.902-490_902-489ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150396 | ||||||
| chr12:132150404 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
63 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.902-577G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150404 | |||||||
| chr12:132150404 | G | GCTCACAC others(565): Show |
1 | a0001c0001t0001g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.902-446_902-445ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150404 | ||||||
| chr12:132150404 | G | GCTCCTAC others(1126): Show |
1 | a0003c0030t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.902-574_902-573ins others(1133): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150404 | ||||||
| chr12:132150405 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.902-576C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150405 | |||||||
| chr12:132150408 | A | ATACCACA others(125): Show |
1 | a0001c0001t0001g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.902-573_902-572ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150408 | |||||||
| chr12:132150408 | A | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(29): Show |
36 | HG00323.hp2 HG01071.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.902-573A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150408 | |||||||
| chr12:132150409 | C | CACCACAC others(968): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.902-562_902-561ins others(975): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150409 | ||||||
| chr12:132150409 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.902-530_902-529ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150409 | ||||||
| chr12:132150409 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.902-543_902-542ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150409 | ||||||
| chr12:132150409 | C | CCACACCC others(35): Show |
1 | a0001c0003t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.902-572_902-571ins others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150409 | |||||||
| chr12:132150409 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
55 | HG00323.hp2 HG00423.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.902-572C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150409 | |||||||
| chr12:132150409 | CACCACAC others(169): Show |
C | 1 | a0012c0017t0001g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.902-528_902-353del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150409 | ||||||
| chr12:132150409 | CACCACAC others(257): Show |
C | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.902-480_902-217del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150409 | ||||||
| chr12:132150413 | A | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0212 |
2 | HG02273.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.902-568A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150413 | |||||||
| chr12:132150420 | T | TAATCCCC others(37): Show |
1 | a0001c0001t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.902-543_902-542ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150420 | ||||||
| chr12:132150437 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0070 |
3 | HG02559.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.902-544G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150437 | |||||||
| chr12:132150437 | G | GCCGCCGC others(258): Show |
1 | a0001c0001t0001g0003 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.902-534_902-533ins others(265): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150437 | ||||||
| chr12:132150439 | C | CGCCGCCT others(472): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.902-534_902-533ins others(479): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150439 | ||||||
| chr12:132150439 | C | CGCCGCCT others(1182): Show |
1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.902-534_902-533ins others(1189): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150439 | ||||||
| chr12:132150439 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.902-455_902-454ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150439 | ||||||
| chr12:132150439 | C | CGCCGCCT others(785): Show |
1 | a0001c0003t0001g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.902-499_902-498ins others(792): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150439 | ||||||
| chr12:132150439 | C | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(20): Show |
26 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.902-542C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150439 | |||||||
| chr12:132150440 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0062 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.902-541G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150440 | |||||||
| chr12:132150442 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.902-539C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150442 | |||||||
| chr12:132150444 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.902-537C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150444 | |||||||
| chr12:132150448 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
54 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.902-533G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150448 | |||||||
| chr12:132150448 | G | GCTCACAC others(1049): Show |
1 | a0004c0007t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.902-490_902-489ins others(1056): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150448 | ||||||
| chr12:132150448 | G | GCTCACAC others(301): Show |
1 | a0001c0003t0001g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.902-490_902-489ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150448 | ||||||
| chr12:132150448 | G | GCTCACAC others(37): Show |
1 | a0001c0001t0001g0008 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.902-499_902-498ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150448 | ||||||
| chr12:132150451 | C | CCT | 3 | a0001c0001t0001g0002 a0001c0003t0001g0130 a0006c0034t0001g0071 |
3 | HG00544.hp2 HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.902-530_902-529ins others(2): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150451 | |||||||
| chr12:132150452 | A | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(31): Show |
35 | HG00558.hp2 HG00621.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.902-529A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150452 | |||||||
| chr12:132150453 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0137 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.902-490_902-489ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(213): Show |
1 | a0001c0001t0001g0004 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.902-490_902-489ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(1177): Show |
1 | a0003c0011t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.902-474_902-473ins others(1184): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(697): Show |
1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.902-446_902-445ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(1137): Show |
1 | a0001c0001t0001g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.902-485_902-484ins others(1144): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.902-486_902-485ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CACCACAC others(565): Show |
1 | a0010c0021t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.902-499_902-498ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150453 | C | CCACACCC others(35): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.902-528_902-527ins others(42): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150453 | |||||||
| chr12:132150453 | C | CCACACCC others(167): Show |
1 | a0001c0003t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.902-528_902-527ins others(174): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150453 | |||||||
| chr12:132150453 | C | CCACACCC others(387): Show |
1 | a0001c0001t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.902-528_902-527ins others(394): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150453 | |||||||
| chr12:132150453 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(40): Show |
46 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.902-528C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150453 | |||||||
| chr12:132150453 | C | TACCACAC others(3249): Show |
1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.902-529_902-528ins others(3256): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150453 | |||||||
| chr12:132150453 | CACCACAC others(213): Show |
C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.902-436_902-217del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150453 | ||||||
| chr12:132150457 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0212 |
2 | HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.902-524A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150457 | |||||||
| chr12:132150481 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0062 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.902-500G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150481 | |||||||
| chr12:132150483 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.902-490_902-489ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150483 | ||||||
| chr12:132150483 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.902-490_902-489ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150483 | ||||||
| chr12:132150483 | C | CGCCGCCT others(553): Show |
1 | a0001c0001t0001g0017 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.902-490_902-489ins others(560): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150483 | ||||||
| chr12:132150483 | C | CGCCGCCT others(433): Show |
1 | a0001c0003t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.902-455_902-454ins others(440): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150483 | ||||||
| chr12:132150483 | C | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0020 others(19): Show |
22 | HG00140.hp1 HG00738.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.902-498C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150483 | |||||||
| chr12:132150484 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0062 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.902-497G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150484 | |||||||
| chr12:132150488 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.902-493C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150488 | |||||||
| chr12:132150492 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
50 | HG00621.hp1 HG01106.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.902-489G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150492 | |||||||
| chr12:132150492 | G | GCTCACAC others(169): Show |
1 | a0001c0001t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.902-446_902-445ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150492 | ||||||
| chr12:132150492 | G | GCTCACAC others(125): Show |
1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.902-455_902-454ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150492 | ||||||
| chr12:132150492 | G | GCTCACAC others(213): Show |
1 | a0001c0003t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.902-455_902-454ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150492 | ||||||
| chr12:132150493 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.902-488C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150493 | |||||||
| chr12:132150494 | TCAC | T | 3 | a0001c0004t0001g0161 a0002c0002t0001g0065 a0002c0002t0003g0145 |
3 | HG03098.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.902-486_902-484del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150494 | |||||||
| chr12:132150496 | A | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(25): Show |
30 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.902-485A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150496 | |||||||
| chr12:132150497 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.902-446_902-445ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150497 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.902-446_902-445ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150497 | C | CACCACAC others(81): Show |
1 | a0001c0001t0001g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.902-411_902-410ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150497 | C | CACCACAC others(125): Show |
1 | a0001c0001t0001g0011 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.902-442_902-441ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150497 | C | CACCACAC others(565): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.902-455_902-454ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150497 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(36): Show |
42 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.902-484C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150497 | |||||||
| chr12:132150497 | C | TACCACAC others(5405): Show |
1 | a0001c0001t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.902-485_902-484ins others(5412): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150497 | |||||||
| chr12:132150497 | CACCACAC others(169): Show |
C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0119 |
2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.902-396_902-221del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150497 | ||||||
| chr12:132150508 | T | C | 2 | a0001c0001t0001g0038 a0002c0002t0001g0065 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.902-473T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150508 | |||||||
| chr12:132150525 | G | A | 2 | a0001c0001t0001g0007 a0006c0034t0001g0071 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.902-456G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150525 | |||||||
| chr12:132150527 | C | CGCCGCCT others(34): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.902-447_902-407dup others(41): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150527 | ||||||
| chr12:132150527 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.902-411_902-410ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150527 | ||||||
| chr12:132150527 | C | G | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(19): Show |
23 | HG00673.hp2 HG01081.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.902-454C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150527 | |||||||
| chr12:132150528 | G | A | 2 | a0001c0001t0001g0007 a0006c0034t0001g0071 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.902-453G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150528 | |||||||
| chr12:132150528 | G | GCCGCCTC others(299): Show |
1 | a0003c0011t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902-430_902-429ins others(306): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150528 | ||||||
| chr12:132150536 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
53 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.902-445G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150536 | |||||||
| chr12:132150536 | G | GCTCACAC others(125): Show |
1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.902-402_902-401ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150536 | ||||||
| chr12:132150536 | G | GCTCACAC others(1533): Show |
1 | a0001c0026t0001g0006 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.902-397_902-396ins others(1540): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150536 | ||||||
| chr12:132150536 | G | GCTCCTAC others(3337): Show |
1 | a0001c0001t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.902-442_902-441ins others(3344): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150536 | ||||||
| chr12:132150536 | G | GCTCCTAC others(213): Show |
1 | a0001c0001t0001g0003 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.902-442_902-441ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150536 | ||||||
| chr12:132150537 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.902-444C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150537 | |||||||
| chr12:132150538 | TCAC | T | 3 | a0001c0001t0001g0024 a0001c0004t0001g0168 a0018c0018t0001g0118 |
3 | HG00558.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.902-442_902-440del others(3): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150538 | |||||||
| chr12:132150540 | A | C | 34 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(31): Show |
34 | HG00621.hp1 HG01167.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.902-441A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150540 | |||||||
| chr12:132150541 | C | CACCACAC others(257): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.902-402_902-401ins others(264): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(213): Show |
1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(37): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(171): Show |
1 | a0001c0003t0001g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.902-402_902-401ins others(178): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(301): Show |
1 | a0001c0003t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.902-402_902-401ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(1269): Show |
1 | a0003c0033t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(1276): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | CACCACAC others(1534): Show |
1 | a0001c0001t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(1541): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
51 | HG00621.hp1 HG01123.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.902-440C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150541 | |||||||
| chr12:132150541 | CACCACAC others(37): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.902-308_902-265del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | CACCACAC others(37): Show |
T | 1 | a0001c0001t0001g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.902-440_902-397del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150541 | |||||||
| chr12:132150541 | CACCACAC others(81): Show |
C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0002c0002t0001g0098 others(1): Show |
4 | HG02738.hp2 HG03834.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-352_902-265del others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150541 | CACCACAC others(125): Show |
C | 1 | a0005c0013t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.902-396_902-265del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150541 | ||||||
| chr12:132150543 | C | CCACACCC others(32): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(39): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150543 | ||||||
| chr12:132150550 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.902-431C>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150550 | |||||||
| chr12:132150552 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902-429T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150552 | |||||||
| chr12:132150569 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0073 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.902-412G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150569 | |||||||
| chr12:132150571 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150571 | ||||||
| chr12:132150571 | C | CGCCGCCT others(125): Show |
1 | a0003c0031t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.902-402_902-401ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150571 | ||||||
| chr12:132150571 | C | CGCCGCCT others(868): Show |
1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.902-397_902-396ins others(875): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150571 | ||||||
| chr12:132150571 | C | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(21): Show |
28 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.902-410C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150571 | |||||||
| chr12:132150572 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0073 |
2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.902-409G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150572 | |||||||
| chr12:132150572 | G | GCCGCCCT others(852): Show |
1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.902-404_902-403ins others(859): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150572 | ||||||
| chr12:132150574 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.902-407C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150574 | |||||||
| chr12:132150576 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.902-405C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150576 | |||||||
| chr12:132150580 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(57): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.902-401G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150580 | |||||||
| chr12:132150580 | G | GCTCACAC others(2809): Show |
1 | a0001c0001t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(2816): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150580 | G | GCTCACAC others(122): Show |
1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.902-397_902-396ins others(129): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150580 | G | GCTCACAC others(1489): Show |
1 | a0001c0001t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(1496): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150580 | G | GCTCACAC others(78): Show |
1 | a0001c0006t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(85): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150580 | G | GCTCACAC others(339): Show |
1 | a0001c0006t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(346): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150580 | G | GCTCACAC others(38): Show |
1 | a0001c0001t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.902-397_902-396ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150580 | ||||||
| chr12:132150582 | TCATACCA others(130): Show |
T | 1 | a0002c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.902-396_902-260del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150582 | ||||||
| chr12:132150584 | A | ACACCACA others(5848): Show |
1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(5855): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150584 | |||||||
| chr12:132150584 | A | ACACCACA others(37): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.902-397_902-396ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150584 | |||||||
| chr12:132150584 | A | ACACCACA others(389): Show |
1 | a0001c0001t0001g0005 | 2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.902-397_902-396ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150584 | |||||||
| chr12:132150584 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(34): Show |
40 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.902-397A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150584 | |||||||
| chr12:132150585 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.902-396T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150585 | |||||||
| chr12:132150585 | T | TACCACAC others(125): Show |
1 | a0001c0001t0001g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.902-358_902-357ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150585 | ||||||
| chr12:132150585 | T | TACCACAC others(37): Show |
1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150585 | ||||||
| chr12:132150585 | T | TACCACAC others(3820): Show |
1 | a0001c0001t0001g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(3827): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150585 | ||||||
| chr12:132150585 | TACCACAC others(125): Show |
T | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.902-352_902-221del | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150585 | ||||||
| chr12:132150613 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.902-368G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150613 | |||||||
| chr12:132150615 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.902-358_902-357ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150615 | ||||||
| chr12:132150615 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150615 | ||||||
| chr12:132150615 | C | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(25): Show |
31 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.902-366C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150615 | |||||||
| chr12:132150616 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.902-365G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150616 | |||||||
| chr12:132150623 | C | CGCTCACA others(81): Show |
1 | a0003c0032t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150623 | ||||||
| chr12:132150624 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(58): Show |
64 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.902-357G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150624 | |||||||
| chr12:132150624 | G | GCTCAACC others(784): Show |
1 | a0006c0012t0001g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.902-353_902-352ins others(791): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150624 | ||||||
| chr12:132150624 | G | GCTCCTAC others(301): Show |
1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.902-354_902-353ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150624 | ||||||
| chr12:132150624 | G | GCTCCTAC others(345): Show |
1 | a0001c0001t0001g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.902-354_902-353ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150624 | ||||||
| chr12:132150628 | A | ACACCACA others(213): Show |
1 | a0001c0004t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.902-353_902-352ins others(220): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150628 | A | ACACCACA others(1798): Show |
1 | a0001c0003t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(1805): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150628 | A | ACACCACA others(119): Show |
1 | a0001c0001t0001g0001 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(126): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150628 | A | ACACCACA others(81): Show |
1 | a0001c0001t0001g0006 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.902-353_902-352ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150628 | A | ACACCACA others(873): Show |
1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.902-353_902-352ins others(880): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150628 | A | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(30): Show |
33 | HG00544.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.902-353A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150628 | |||||||
| chr12:132150629 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.902-352T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150629 | |||||||
| chr12:132150629 | T | CACCACAC others(4698): Show |
1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.902-353_902-352ins others(4705): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150629 | |||||||
| chr12:132150633 | A | C | 1 | a0002c0002t0001g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.902-348A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150633 | |||||||
| chr12:132150639 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.902-342C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150639 | |||||||
| chr12:132150657 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.902-324G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150657 | |||||||
| chr12:132150659 | C | CGCCGCCT others(917): Show |
1 | a0001c0001t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(924): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150659 | ||||||
| chr12:132150659 | C | CGCCGCCT others(125): Show |
1 | a0001c0003t0001g0053 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150659 | ||||||
| chr12:132150659 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0008 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150659 | ||||||
| chr12:132150659 | C | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0031 others(20): Show |
23 | HG00609.hp1 HG00642.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.902-322C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150659 | |||||||
| chr12:132150660 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.902-321G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150660 | |||||||
| chr12:132150660 | G | GCCGCCTC others(169): Show |
1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.902-314_902-313ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150660 | ||||||
| chr12:132150662 | C | T | 2 | a0001c0001t0001g0036 a0002c0002t0001g0061 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.902-319C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150662 | |||||||
| chr12:132150668 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
73 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.902-313G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150668 | |||||||
| chr12:132150668 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.902-313G>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150668 | |||||||
| chr12:132150668 | G | GCTCACAC others(1708): Show |
1 | a0001c0001t0001g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(1715): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150668 | ||||||
| chr12:132150668 | G | GCTCACAC others(878): Show |
1 | a0001c0001t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(885): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150668 | ||||||
| chr12:132150668 | G | GCTCCTAC others(1665): Show |
1 | a0001c0001t0001g0002 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.902-310_902-309ins others(1672): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150668 | ||||||
| chr12:132150672 | A | ACACCACA others(2545): Show |
1 | a0001c0001t0001g0009 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(2552): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(3821): Show |
1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(3828): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(653): Show |
1 | a0001c0001t0001g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(660): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(37): Show |
1 | a0001c0001t0001g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(81): Show |
1 | a0003c0030t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(301): Show |
1 | a0001c0001t0001g0027 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(389): Show |
1 | a0008c0025t0001g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(301): Show |
1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(308): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(81): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(1357): Show |
1 | a0001c0001t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(1364): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(249): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(256): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(81): Show |
1 | a0001c0001t0001g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(2325): Show |
1 | a0001c0003t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.902-309_902-308ins others(2332): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ACACCACA others(81): Show |
1 | a0001c0003t0001g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.902-309_902-308ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150672 | A | ATACCACA others(81): Show |
1 | a0006c0012t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.902-270_902-269ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150672 | ||||||
| chr12:132150672 | A | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.902-309A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150672 | |||||||
| chr12:132150673 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.902-308T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150673 | |||||||
| chr12:132150673 | TACCACAC others(37): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.902-260_902-217del others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150673 | ||||||
| chr12:132150677 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0162 |
2 | HG01261.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.902-304A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150677 | |||||||
| chr12:132150679 | A | ACCCCTAA others(38): Show |
1 | a0001c0001t0001g0003 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.902-270_902-269ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150679 | ||||||
| chr12:132150701 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0062 |
3 | HG02559.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.902-280G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150701 | |||||||
| chr12:132150703 | C | CGCCGCCT others(81): Show |
1 | a0001c0001t0001g0017 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.902-270_902-269ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150703 | ||||||
| chr12:132150703 | C | CGCCGCCT others(37): Show |
1 | a0001c0001t0001g0001 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.902-270_902-269ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150703 | ||||||
| chr12:132150703 | C | CGCCGCCT others(38): Show |
1 | a0001c0003t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.902-254_902-253ins others(45): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150703 | ||||||
| chr12:132150703 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0048 others(8): Show |
11 | HG00642.hp2 HG00673.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.902-278C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150703 | |||||||
| chr12:132150704 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0062 |
3 | HG02559.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.902-277G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150704 | |||||||
| chr12:132150706 | C | T | 1 | a0005c0037t0001g0066 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.902-275C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150706 | |||||||
| chr12:132150708 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.902-273C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150708 | |||||||
| chr12:132150712 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
71 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.902-269G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150712 | |||||||
| chr12:132150712 | G | GCTCACAC others(37): Show |
1 | a0001c0001t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150712 | ||||||
| chr12:132150712 | G | GCTCACAC others(37): Show |
1 | a0001c0003t0001g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.902-235_902-234ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150712 | ||||||
| chr12:132150712 | G | GCTCACAC others(125): Show |
1 | a0001c0001t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.902-235_902-234ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150712 | ||||||
| chr12:132150712 | G | GCTCACAC others(697): Show |
1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.902-235_902-234ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150712 | ||||||
| chr12:132150712 | G | GCTCCTAC others(2363): Show |
1 | a0001c0001t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.902-266_902-265ins others(2370): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150712 | ||||||
| chr12:132150713 | C | G | 1 | a0004c0041t0001g0002 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.902-268C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150713 | |||||||
| chr12:132150716 | A | ATACCACA others(37): Show |
1 | a0001c0001t0001g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.902-265_902-264ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150716 | |||||||
| chr12:132150716 | A | ATACCACA others(917): Show |
1 | a0001c0001t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.902-265_902-264ins others(924): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150716 | |||||||
| chr12:132150716 | A | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0031 others(21): Show |
25 | HG01106.hp1 HG01123.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.902-265A>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150716 | |||||||
| chr12:132150717 | C | CACCACAC others(37): Show |
1 | a0001c0001t0001g0146 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(1885): Show |
1 | a0001c0001t0001g0148 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(1892): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(961): Show |
1 | a0001c0004t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(968): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(2261): Show |
1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(2268): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(2413): Show |
1 | a0001c0001t0001g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(2420): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(345): Show |
1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(352): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(37): Show |
1 | a0001c0005t0001g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.902-221_902-220ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(37): Show |
1 | a0006c0034t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.902-235_902-234ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | CACCACAC others(1181): Show |
1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.902-235_902-234ins others(1188): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150717 | ||||||
| chr12:132150717 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
65 | HG00099.hp2 HG00741.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.902-264C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150717 | |||||||
| chr12:132150747 | C | CGCCGCCT others(697): Show |
1 | a0001c0001t0001g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(704): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(2545): Show |
1 | a0001c0001t0001g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(2552): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(37): Show |
2 | a0001c0001t0001g0113 a0001c0003t0001g0045 |
2 | HG01243.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.902-226_902-225ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(169): Show |
1 | a0001c0003t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(389): Show |
1 | a0001c0001t0001g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(125): Show |
1 | a0001c0001t0001g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(132): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(389): Show |
1 | a0001c0001t0001g0157 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(396): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(699): Show |
1 | a0001c0001t0001g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.902-226_902-225ins others(706): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1225): Show |
1 | a0001c0001t0001g0181 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(1232): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(565): Show |
1 | a0001c0001t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.902-226_902-225ins others(572): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(169): Show |
1 | a0004c0007t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1005): Show |
1 | a0001c0003t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(1012): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(3380): Show |
1 | a0001c0001t0001g0182 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(3387): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1665): Show |
1 | a0001c0001t0001g0116 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(1672): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(477): Show |
1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(484): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1735): Show |
1 | a0001c0015t0001g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(1742): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(4569): Show |
1 | a0001c0001t0001g0196 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(4576): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(37): Show |
1 | a0001c0003t0001g0117 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(44): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(169): Show |
1 | a0001c0001t0001g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(176): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1005): Show |
1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(1012): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(521): Show |
1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(528): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | CGCCGCCT others(1227): Show |
1 | a0001c0005t0001g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.902-220_902-219ins others(1234): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150747 | ||||||
| chr12:132150747 | C | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(54): Show |
79 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.902-234C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150747 | |||||||
| chr12:132150748 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.902-233G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150748 | |||||||
| chr12:132150756 | G | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0073 others(22): Show |
27 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.902-225G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150756 | |||||||
| chr12:132150756 | G | GCTCACAC others(2017): Show |
1 | a0001c0001t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.902-217_902-216ins others(2024): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150756 | ||||||
| chr12:132150761 | C | CACCACAC others(81): Show |
1 | a0001c0006t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.902-217_902-216ins others(88): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 132150761 | ||||||
| chr12:132150761 | C | T | 3 | a0001c0001t0001g0121 a0001c0006t0001g0152 a0001c0006t0001g0153 |
3 | HG02647.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.902-220C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150761 | |||||||
| chr12:132150806 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.902-175C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150806 | |||||||
| chr12:132150856 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.902-125G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150856 | |||||||
| chr12:132150975 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02004.hp2 | splice_region_variant&intron_variant | LOW | c.902-6C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150975 | |||||||
| chr12:132150976 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
splice_region_variant&intron_variant | LOW | c.902-5T>C | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | 132150976 | |||||||
| chr12:132151127 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.962+86C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 10/14 | chr12 | 132151127 | |||||||
| chr12:132151217 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.963-41G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 10/14 | chr12 | 132151217 | |||||||
| chr12:132151233 | G | A | 2 | a0001c0001t0001g0041 a0001c0003t0001g0222 |
2 | HG02027.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.963-25G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 10/14 | chr12 | 132151233 | |||||||
| chr12:132151234 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.963-24C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 10/14 | chr12 | 132151234 | |||||||
| chr12:132151381 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+13G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/14 | chr12 | 132151381 | |||||||
| chr12:132151406 | C | G | 1 | a0013c0022t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1073+38C>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/14 | chr12 | 132151406 | |||||||
| chr12:132151444 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(86): Show |
112 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.1074-40A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/14 | chr12 | 132151444 | |||||||
| chr12:132151452 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1074-32G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 11/14 | chr12 | 132151452 | |||||||
| chr12:132151829 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG02965.hp1 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1317+9G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151829 | |||||||
| chr12:132151855 | G | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(62): Show |
80 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1317+35G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151855 | |||||||
| chr12:132151935 | A | G | 3 | a0001c0004t0001g0030 a0001c0004t0001g0161 a0001c0004t0001g0163 |
4 | HG02630.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+115A>G | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151935 | |||||||
| chr12:132151980 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0003c0031t0001g0078 |
3 | NA18980.hp1 NA18998.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1318-104C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151980 | |||||||
| chr12:132151985 | C | T | 1 | a0001c0003t0001g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1318-99C>T | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151985 | |||||||
| chr12:132151987 | A | AC | 5 | a0001c0001t0001g0059 a0001c0001t0001g0120 a0001c0001t0001g0204 others(2): Show |
5 | HG00741.hp2 HG02071.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-93dupC | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 132151987 | ||||||
| chr12:132151992 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1318-92G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 13/14 | chr12 | 132151992 | |||||||
| chr12:132152235 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1431+38G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 14/14 | chr12 | 132152235 | |||||||
| chr12:132152240 | G | A | 2 | a0001c0001t0001g0160 a0002c0002t0001g0158 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1432-42G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 14/14 | chr12 | 132152240 | |||||||
| chr12:132152261 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0041 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1432-21G>A | NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 14/14 | chr12 | 132152261 |