Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7064 |
| ensemblid | ENSG00000172009.15 |
| hgncid | 11793 |
| symbol | THOP1 |
| name | thimet oligopeptidase 1 |
| refseq_nuc | NM_003249.5 |
| refseq_prot | NP_003240.1 |
| ensembl_nuc | ENST00000307741.11 |
| ensembl_prot | ENSP00000304467.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 2785503 |
| end | 2815807 |
| strand | + |
| ver | v1.2 |
| region | chr19:2785503-2815807 |
| region5000 | chr19:2780503-2820807 |
| regionname0 | THOP1_chr19_2785503_2815807 |
| regionname5000 | THOP1_chr19_2780503_2820807 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 689 | 356 | 84 | 58 | 153 | 17 | 42 | 124 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0002 | 0/0 | 684 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(679): Show |
chr19 | 2780503 | 2820807 |
| a0003 | 0/0 | 689 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0004 | 0/0 | 689 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0005 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0006 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0007 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0008 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(684): Show |
chr19 | 2780503 | 2820807 |
| a0009 | 0/0 | 661 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | MKPPA others(656): Show |
chr19 | 2780503 | 2820807 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2067 | 342 | 77 | 54 | 151 | 17 | 41 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0002 | 0/0 | 2067 | 7 | 7 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0004 | 0/0 | 2067 | 2 | 0 | 2 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0007 | 0/0 | 2067 | 2 | 0 | 2 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0009 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0015 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0001c0016 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0002c0005 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2047): Show |
chr19 | 2780503 | 2820807 | ||
| a0002c0006 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2047): Show |
chr19 | 2780503 | 2820807 | ||
| a0003c0003 | 0/0 | 2067 | 4 | 0 | 0 | 4 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0004c0011 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0005c0013 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0006c0010 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0007c0014 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0008c0012 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2062): Show |
chr19 | 2780503 | 2820807 | ||
| a0009c0008 | 0/0 | 2153 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | ATGAA others(2148): Show |
chr19 | 2780503 | 2820807 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4761 | 117 | 16 | 33 | 43 | 12 | 11 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0002 | 0/0 | 4761 | 108 | 17 | 14 | 56 | 3 | 18 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0003 | 0/0 | 4761 | 50 | 6 | 1 | 36 | 0 | 7 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0004 | 0/0 | 4762 | 10 | 8 | 1 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0005 | 0/0 | 4761 | 9 | 9 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0007 | 0/0 | 4762 | 7 | 0 | 1 | 5 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0008 | 0/0 | 4762 | 3 | 3 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0009 | 0/0 | 4762 | 6 | 1 | 2 | 2 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0010 | 0/0 | 4761 | 3 | 3 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0011 | 0/0 | 4762 | 3 | 3 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0012 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0013 | 0/0 | 4761 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0014 | 0/0 | 4761 | 2 | 1 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0015 | 0/0 | 4761 | 2 | 0 | 0 | 0 | 0 | 2 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0016 | 0/0 | 4761 | 2 | 0 | 0 | 1 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0017 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0018 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0019 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0020 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0021 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0023 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0024 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0025 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0026 | 0/0 | 4761 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0027 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0028 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0029 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0030 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0031 | 0/0 | 4761 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0032 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0033 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0001t0035 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0002t0006 | 0/0 | 4762 | 7 | 7 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0001c0004t0001 | 0/0 | 4761 | 2 | 0 | 2 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0007t0001 | 0/0 | 4761 | 2 | 0 | 2 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0009t0001 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0015t0001 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0001c0016t0001 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0002c0005t0008 | 0/0 | 4747 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4742): Show |
chr19 | 2780503 | 2820807 |
| a0002c0006t0008 | 0/0 | 4747 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4742): Show |
chr19 | 2780503 | 2820807 |
| a0002c0006t0022 | 0/0 | 4747 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4742): Show |
chr19 | 2780503 | 2820807 |
| a0003c0003t0002 | 0/0 | 4761 | 3 | 0 | 0 | 3 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0003c0003t0012 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4757): Show |
chr19 | 2780503 | 2820807 |
| a0004c0011t0002 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0005c0013t0003 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0006c0010t0002 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0007c0014t0034 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0008c0012t0003 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4756): Show |
chr19 | 2780503 | 2820807 |
| a0009c0008t0001 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | AGCAT others(4842): Show |
chr19 | 2780503 | 2820807 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 27 | 1 | 5 | 16 | 0 | 4 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0004 | 0/0 | 7 | 1 | 3 | 3 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0031 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0002 | 0/0 | 16 | 0 | 2 | 9 | 2 | 3 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0005g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0008g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0009g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0013g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0014g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0015g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0016g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0016g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0018g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0021g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0024g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0025g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0026g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0027g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0028g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0029g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0030g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0031g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0032g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0033g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0001t0035g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0002t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0002t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0002t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0002t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0004t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0007t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0009t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0001c0016t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0002c0005t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0002c0005t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0002c0006t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0002c0006t0022g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0003c0003t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0003c0003t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0004c0011t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0005c0013t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0006c0010t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0007c0014t0034g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0008c0012t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| a0009c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | GBR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00280 | hp2 | a0001 | c0001 | t0016 | g0022 | EUR | FIN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00621 | hp1 | a0001 | c0001 | t0012 | g0216 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0001 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01258 | hp2 | a0001 | c0007 | t0001 | g0001 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01261 | hp2 | a0001 | c0001 | t0026 | g0129 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01516 | hp1 | a0001 | c0001 | t0014 | g0021 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0190 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02004 | hp1 | a0001 | c0001 | t0031 | g0004 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02071 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02083 | hp2 | a0001 | c0015 | t0001 | g0001 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02132 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0118 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02165 | hp2 | a0004 | c0011 | t0002 | g0175 | EAS | CDX | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02523 | hp2 | a0001 | c0001 | t0023 | g0167 | EAS | KHV | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02572 | hp1 | a0001 | c0001 | t0027 | g0062 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02572 | hp2 | a0001 | c0001 | t0021 | g0039 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02615 | hp1 | a0001 | c0002 | t0006 | g0156 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0007 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02630 | hp2 | a0006 | c0010 | t0002 | g0009 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02723 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0058 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0063 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02896 | hp1 | a0001 | c0001 | t0032 | g0049 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02922 | hp2 | a0002 | c0006 | t0022 | g0048 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03098 | hp1 | a0002 | c0006 | t0008 | g0057 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03098 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03195 | hp2 | a0007 | c0014 | t0034 | g0067 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03453 | hp2 | a0002 | c0005 | t0008 | g0053 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0013 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0013 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0155 | AFR | ESN | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0055 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0218 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03927 | hp2 | a0001 | c0009 | t0001 | g0126 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18522 | hp2 | a0001 | c0001 | t0030 | g0170 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18906 | hp2 | a0002 | c0005 | t0008 | g0054 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18940 | hp1 | a0003 | c0003 | t0012 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18959 | hp1 | a0001 | c0001 | t0020 | g0130 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18962 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18971 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18978 | hp1 | a0001 | c0001 | t0028 | g0103 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18995 | hp1 | a0001 | c0001 | t0016 | g0198 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18998 | hp2 | a0001 | c0001 | t0009 | g0134 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19000 | hp1 | a0001 | c0001 | t0029 | g0094 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19043 | hp1 | a0008 | c0012 | t0003 | g0025 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0021 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19070 | hp1 | a0001 | c0016 | t0001 | g0125 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19086 | hp2 | a0003 | c0003 | t0002 | g0206 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19090 | hp2 | a0001 | c0001 | t0018 | g0027 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20752 | hp1 | a0009 | c0008 | t0001 | g0001 | EUR | TSI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | GIH | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20905 | hp2 | a0001 | c0001 | t0035 | g0003 | SAS | GIH | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02109 | hp1 | a0001 | c0002 | t0006 | g0154 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02486 | hp1 | a0005 | c0013 | t0003 | g0025 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02559 | hp1 | a0001 | c0001 | t0033 | g0157 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | USA | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | USA | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18955 | hp1 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | LWK | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0031 | REF | REF | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | THOP1_chr19_2780503_2820807 | THOP1 | chr19 | 2780503 | 2820807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2790510 | C | T | 1 | a0007 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.106C>T | p.Arg36Cys | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/13 | 266/4761 | 106/2070 | 36/689 | chr19 | 2790510 | |||
| chr19:2805036 | C | G | 2 | a0005 a0008 |
2 | HG02486.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.610C>G | p.Leu204Val | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/13 | 770/4761 | 610/2070 | 204/689 | chr19 | 2805036 | |||
| chr19:2807751 | C | T | 1 | a0003 | 4 | NA18940.hp1 NA18955.hp1 NA18971.hp1 others(1): Show |
missense_variant | MODERATE | c.1196C>T | p.Ala399Val | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/13 | 1356/4761 | 1196/2070 | 399/689 | chr19 | 2807751 | |||
| chr19:2808311 | G | A | 1 | a0008 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1322G>A | p.Arg441His | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/13 | 1482/4761 | 1322/2070 | 441/689 | chr19 | 2808311 | |||
| chr19:2808316 | A | C | 1 | a0004 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1327A>C | p.Ile443Leu | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/13 | 1487/4761 | 1327/2070 | 443/689 | chr19 | 2808316 | |||
| chr19:2810693 | A | G | 1 | a0006 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1696A>G | p.Thr566Ala | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/13 | 1856/4761 | 1696/2070 | 566/689 | chr19 | 2810693 | |||
| chr19:2811719 | TGTCCTGA others(122): Show |
T | 1 | a0002 | 4 | HG02922.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1903_1908+123del | p.Ser635_Lys636del | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/13 | 2063/4761 | 1903/2070 | 635/689 | INFO_REALIGN_3_PRIME | chr19 | 2811719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2790443 | C | T | 1 | a0001c0016 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.39C>T | p.Asp13Asp | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/13 | 199/4761 | 39/2070 | 13/689 | chr19 | 2790443 | |||
| chr19:2790470 | C | T | 1 | a0001c0015 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.66C>T | p.Asn22Asn | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/13 | 226/4761 | 66/2070 | 22/689 | chr19 | 2790470 | |||
| chr19:2790620 | G | A | 1 | a0001c0004 | 2 | HG00738.hp2 HG01981.hp2 |
synonymous_variant | LOW | c.216G>A | p.Glu72Glu | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/13 | 376/4761 | 216/2070 | 72/689 | chr19 | 2790620 | |||
| chr19:2794804 | C | T | 3 | a0005c0013 a0007c0014 a0008c0012 |
3 | HG02486.hp1 HG03195.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.270C>T | p.Pro90Pro | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/13 | 430/4761 | 270/2070 | 90/689 | chr19 | 2794804 | |||
| chr19:2806925 | C | T | 1 | a0001c0002 | 7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
synonymous_variant | LOW | c.759C>T | p.Cys253Cys | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/13 | 919/4761 | 759/2070 | 253/689 | chr19 | 2806925 | |||
| chr19:2806949 | G | T | 1 | a0001c0007 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.783G>T | p.Thr261Thr | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/13 | 943/4761 | 783/2070 | 261/689 | chr19 | 2806949 | |||
| chr19:2811656 | C | T | 1 | a0001c0009 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1830C>T | p.Tyr610Tyr | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/13 | 1990/4761 | 1830/2070 | 610/689 | chr19 | 2811656 | |||
| chr19:2813264 | G | A | 1 | a0002c0005 | 2 | HG03453.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.2058G>A | p.Pro686Pro | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2218/4761 | 2058/2070 | 686/689 | chr19 | 2813264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2785559 | C | T | 1 | a0001c0001t0035 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/13 | 104 | chr19 | 2785559 | ||||||
| chr19:2785599 | C | G | 1 | a0007c0014t0034 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/13 | 64 | chr19 | 2785599 | ||||||
| chr19:2813309 | C | T | 1 | a0001c0001t0033 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 33 | chr19 | 2813309 | ||||||
| chr19:2813312 | T | TC | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0018 others(1): Show |
4 | HG00621.hp1 HG02615.hp2 NA18940.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*39dupC | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 40 | INFO_REALIGN_3_PRIME | chr19 | 2813312 | |||||
| chr19:2813339 | G | A | 1 | a0001c0001t0019 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 63 | chr19 | 2813339 | ||||||
| chr19:2813344 | A | T | 1 | a0001c0001t0032 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 68 | chr19 | 2813344 | ||||||
| chr19:2813404 | G | A | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 128 | chr19 | 2813404 | ||||||
| chr19:2813458 | C | T | 1 | a0001c0001t0011 | 3 | HG02145.hp1 HG02809.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 182 | chr19 | 2813458 | ||||||
| chr19:2813521 | G | A | 1 | a0001c0001t0020 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 245 | chr19 | 2813521 | ||||||
| chr19:2813539 | G | A | 1 | a0001c0001t0021 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 263 | chr19 | 2813539 | ||||||
| chr19:2813612 | G | T | 1 | a0001c0001t0010 | 3 | HG02257.hp1 HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*336G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 336 | chr19 | 2813612 | ||||||
| chr19:2813654 | T | C | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(4): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 378 | chr19 | 2813654 | ||||||
| chr19:2813690 | G | A | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(4): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 414 | chr19 | 2813690 | ||||||
| chr19:2813804 | C | T | 1 | a0001c0001t0016 | 2 | HG00280.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*528C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 528 | chr19 | 2813804 | ||||||
| chr19:2813805 | G | A | 8 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(5): Show |
28 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*529G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 529 | chr19 | 2813805 | ||||||
| chr19:2813811 | C | G | 1 | a0001c0001t0031 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 535 | chr19 | 2813811 | ||||||
| chr19:2813817 | G | A | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*541G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 541 | chr19 | 2813817 | ||||||
| chr19:2813823 | C | A | 1 | a0001c0001t0023 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 547 | chr19 | 2813823 | ||||||
| chr19:2813853 | G | C | 9 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(6): Show |
31 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*577G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 577 | chr19 | 2813853 | ||||||
| chr19:2813855 | C | CT | 8 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(5): Show |
28 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*579_*580insT | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 580 | chr19 | 2813855 | ||||||
| chr19:2813889 | A | G | 9 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(6): Show |
31 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*613A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 613 | chr19 | 2813889 | ||||||
| chr19:2813940 | C | T | 1 | a0002c0006t0022 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 664 | chr19 | 2813940 | ||||||
| chr19:2813959 | A | G | 8 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(5): Show |
28 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 683 | chr19 | 2813959 | ||||||
| chr19:2814183 | C | T | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0012 others(11): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*907C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 907 | chr19 | 2814183 | ||||||
| chr19:2814184 | G | A | 1 | a0001c0001t0024 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*908G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 908 | chr19 | 2814184 | ||||||
| chr19:2814197 | C | CG | 4 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0028 others(1): Show |
15 | HG01934.hp1 HG01952.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*928dupG | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 929 | INFO_REALIGN_3_PRIME | chr19 | 2814197 | |||||
| chr19:2814334 | G | A | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1058G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1058 | chr19 | 2814334 | ||||||
| chr19:2814687 | C | T | 1 | a0001c0001t0005 | 9 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1411C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1411 | chr19 | 2814687 | ||||||
| chr19:2814721 | G | A | 1 | a0001c0001t0025 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1445 | chr19 | 2814721 | ||||||
| chr19:2814784 | C | T | 1 | a0001c0001t0027 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1508 | chr19 | 2814784 | ||||||
| chr19:2815004 | C | T | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1728C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1728 | chr19 | 2815004 | ||||||
| chr19:2815048 | T | C | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(4): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1772T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1772 | chr19 | 2815048 | ||||||
| chr19:2815118 | C | T | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1842C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1842 | chr19 | 2815118 | ||||||
| chr19:2815242 | G | A | 1 | a0001c0001t0026 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1966G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 1966 | chr19 | 2815242 | ||||||
| chr19:2815374 | A | G | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
233 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*2098A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2098 | chr19 | 2815374 | ||||||
| chr19:2815413 | C | T | 3 | a0001c0001t0004 a0001c0001t0032 a0002c0006t0022 |
12 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2137C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2137 | chr19 | 2815413 | ||||||
| chr19:2815422 | G | A | 1 | a0001c0001t0018 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2146 | chr19 | 2815422 | ||||||
| chr19:2815433 | C | T | 1 | a0001c0001t0028 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2157C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2157 | chr19 | 2815433 | ||||||
| chr19:2815496 | T | C | 1 | a0001c0001t0010 | 3 | HG02257.hp1 HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2220T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2220 | chr19 | 2815496 | ||||||
| chr19:2815500 | G | A | 1 | a0001c0001t0030 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2224G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2224 | chr19 | 2815500 | ||||||
| chr19:2815562 | G | A | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2286G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2286 | chr19 | 2815562 | ||||||
| chr19:2815739 | A | G | 1 | a0001c0001t0014 | 2 | HG01516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2463A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 13/13 | 2463 | chr19 | 2815739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2785783 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.16+105C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2785783 | |||||||
| chr19:2785809 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.16+131G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2785809 | |||||||
| chr19:2785956 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.16+278C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2785956 | |||||||
| chr19:2786017 | G | A | 1 | a0001c0001t0005g0046 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.16+339G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786017 | |||||||
| chr19:2786101 | TG | T | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
14 | HG00323.hp1 HG00733.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.16+425delG | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786101 | ||||||
| chr19:2786103 | GT | G | 28 | a0001c0001t0002g0068 a0001c0001t0003g0024 a0001c0001t0003g0059 others(25): Show |
34 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.16+427delT | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786103 | ||||||
| chr19:2786104 | T | A | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
14 | HG00323.hp1 HG00733.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.16+426T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786104 | |||||||
| chr19:2786108 | TG | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(2): Show |
7 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+436delG | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786108 | ||||||
| chr19:2786112 | G | A | 28 | a0001c0001t0002g0068 a0001c0001t0003g0024 a0001c0001t0003g0059 others(25): Show |
34 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.16+434G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786112 | |||||||
| chr19:2786141 | T | A | 3 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 |
8 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.16+463T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786141 | |||||||
| chr19:2786259 | T | C | 34 | a0001c0001t0001g0073 a0001c0001t0002g0090 a0001c0001t0003g0003 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.16+581T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786259 | |||||||
| chr19:2786399 | C | G | 98 | a0001c0001t0001g0041 a0001c0001t0001g0159 a0001c0001t0001g0166 others(95): Show |
145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.16+721C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786399 | |||||||
| chr19:2786559 | C | T | 96 | a0001c0001t0001g0041 a0001c0001t0001g0159 a0001c0001t0001g0166 others(93): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.16+881C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786559 | |||||||
| chr19:2786703 | G | T | 1 | a0001c0001t0003g0028 | 2 | NA18959.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.16+1025G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786703 | |||||||
| chr19:2786705 | T | C | 1 | a0001c0001t0003g0028 | 2 | NA18959.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.16+1027T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786705 | |||||||
| chr19:2786728 | A | C | 140 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(137): Show |
198 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.16+1050A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786728 | |||||||
| chr19:2786750 | C | G | 1 | a0001c0001t0002g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.16+1072C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786750 | |||||||
| chr19:2786765 | A | ATTTTTTT others(3): Show |
9 | a0001c0001t0002g0160 a0001c0001t0003g0024 a0001c0001t0003g0059 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+1093_16+1102dup others(10): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(4): Show |
7 | a0001c0001t0001g0153 a0001c0001t0002g0038 a0001c0001t0002g0039 others(4): Show |
9 | HG01891.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+1092_16+1102dup others(11): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0002g0162 a0001c0001t0002g0164 a0001c0001t0003g0074 others(1): Show |
4 | HG01109.hp2 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+1091_16+1102dup others(12): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(6): Show |
40 | a0001c0001t0001g0166 a0001c0001t0002g0009 a0001c0001t0002g0069 others(37): Show |
60 | HG00423.hp1 HG00558.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.16+1090_16+1102dup others(13): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(7): Show |
77 | a0001c0001t0001g0041 a0001c0001t0001g0199 a0001c0001t0001g0205 others(74): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.16+1089_16+1102dup others(14): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(8): Show |
21 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0044 others(18): Show |
28 | HG00423.hp2 HG00621.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.16+1088_16+1102dup others(15): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786765 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0011g0058 a0001c0002t0006g0037 a0001c0002t0006g0155 others(1): Show |
5 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+1102_16+1103ins others(16): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786765 | ||||||
| chr19:2786913 | GCCACCAC others(2): Show |
G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(1): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+1239_16+1247del others(9): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2786913 | ||||||
| chr19:2786988 | C | G | 1 | a0001c0001t0004g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16+1310C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786988 | |||||||
| chr19:2786990 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.16+1312C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2786990 | |||||||
| chr19:2787051 | G | A | 1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.16+1373G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787051 | |||||||
| chr19:2787188 | C | T | 1 | a0003c0003t0002g0206 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.16+1510C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787188 | |||||||
| chr19:2787193 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00140.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.16+1515C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787193 | |||||||
| chr19:2787195 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.16+1517G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787195 | |||||||
| chr19:2787331 | G | A | 161 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(158): Show |
230 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.16+1653G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787331 | |||||||
| chr19:2787435 | CA | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+1759delA | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2787435 | ||||||
| chr19:2787815 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+2137G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787815 | |||||||
| chr19:2787817 | T | C | 13 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0026 others(10): Show |
18 | HG00423.hp1 HG00621.hp2 NA18939.hp1 others(15): Show |
intron_variant | MODIFIER | c.16+2139T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787817 | |||||||
| chr19:2787834 | T | G | 98 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(95): Show |
145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.16+2156T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787834 | |||||||
| chr19:2787909 | G | A | 1 | a0001c0001t0004g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.16+2231G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2787909 | |||||||
| chr19:2788021 | G | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 others(1): Show |
9 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.16+2343G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788021 | |||||||
| chr19:2788165 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.17-2256C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788165 | |||||||
| chr19:2788500 | C | T | 20 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(17): Show |
27 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.17-1921C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788500 | |||||||
| chr19:2788743 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.17-1678T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788743 | |||||||
| chr19:2788756 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.17-1665G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788756 | |||||||
| chr19:2788793 | C | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1628C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788793 | |||||||
| chr19:2788848 | G | C | 1 | a0001c0001t0004g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.17-1573G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2788848 | |||||||
| chr19:2789264 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-1157T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789264 | |||||||
| chr19:2789273 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-1148C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789273 | |||||||
| chr19:2789339 | T | C | 73 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(70): Show |
112 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.17-1082T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789339 | |||||||
| chr19:2789404 | G | T | 1 | a0001c0001t0027g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.17-1017G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789404 | |||||||
| chr19:2789432 | AGAGAGGC others(3): Show |
A | 1 | a0001c0001t0003g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.17-987_17-978delAG others(8): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 2789432 | ||||||
| chr19:2789471 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0078 |
4 | NA18953.hp1 NA18957.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-950C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789471 | |||||||
| chr19:2789553 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-868C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789553 | |||||||
| chr19:2789617 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(1): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-804C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789617 | |||||||
| chr19:2789663 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0099 others(4): Show |
11 | HG01167.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.17-758G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789663 | |||||||
| chr19:2789728 | G | C | 1 | a0001c0001t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.17-693G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789728 | |||||||
| chr19:2789883 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.17-538G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2789883 | |||||||
| chr19:2790033 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0174 |
4 | HG02698.hp2 HG03491.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-388G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2790033 | |||||||
| chr19:2790098 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.17-323A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2790098 | |||||||
| chr19:2790188 | C | T | 1 | a0001c0001t0030g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.17-233C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2790188 | |||||||
| chr19:2790396 | G | A | 97 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(94): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.17-25G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 1/12 | chr19 | 2790396 | |||||||
| chr19:2790688 | C | T | 20 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(17): Show |
27 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.229+55C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790688 | |||||||
| chr19:2790829 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.229+196G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790829 | |||||||
| chr19:2790846 | C | T | 1 | a0001c0001t0007g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.229+213C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790846 | |||||||
| chr19:2790884 | C | CCGCTCTG others(3): Show |
1 | a0001c0001t0001g0019 | 3 | NA18942.hp2 NA19084.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.229+253_229+262dup others(10): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 2790884 | ||||||
| chr19:2790944 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.229+311G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790944 | |||||||
| chr19:2790971 | A | C | 1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.229+338A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790971 | |||||||
| chr19:2790977 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+344C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2790977 | |||||||
| chr19:2791134 | C | T | 1 | a0003c0003t0002g0206 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.229+501C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791134 | |||||||
| chr19:2791158 | C | T | 3 | a0002c0005t0008g0053 a0002c0005t0008g0054 a0002c0006t0008g0057 |
3 | HG03098.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.229+525C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791158 | |||||||
| chr19:2791357 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.229+724C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791357 | |||||||
| chr19:2791407 | T | TC | 160 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(157): Show |
229 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.229+776dupC | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 2791407 | ||||||
| chr19:2791410 | A | C | 1 | a0001c0001t0003g0077 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.229+777A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791410 | |||||||
| chr19:2791471 | T | C | 156 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(153): Show |
224 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.229+838T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791471 | |||||||
| chr19:2791535 | G | A | 1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.229+902G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791535 | |||||||
| chr19:2791614 | G | C | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.229+981G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791614 | |||||||
| chr19:2791626 | C | T | 136 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(133): Show |
197 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.229+993C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791626 | |||||||
| chr19:2791655 | G | A | 20 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(17): Show |
27 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.229+1022G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791655 | |||||||
| chr19:2791708 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0176 others(2): Show |
15 | HG00558.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.229+1075G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791708 | |||||||
| chr19:2791842 | C | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0164 a0001c0001t0021g0039 |
3 | HG02572.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.229+1209C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2791842 | |||||||
| chr19:2792036 | G | A | 136 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(133): Show |
197 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.229+1403G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792036 | |||||||
| chr19:2792070 | G | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(34): Show |
50 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.229+1437G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792070 | |||||||
| chr19:2792120 | G | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.229+1487G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792120 | |||||||
| chr19:2792130 | C | G | 97 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(94): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.229+1497C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792130 | |||||||
| chr19:2792242 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.229+1609T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792242 | |||||||
| chr19:2792267 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
7 | HG00639.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.229+1634C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792267 | |||||||
| chr19:2792301 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.229+1668C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792301 | |||||||
| chr19:2792328 | A | T | 1 | a0001c0001t0012g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.229+1695A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792328 | |||||||
| chr19:2792345 | G | A | 156 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(153): Show |
224 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.229+1712G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792345 | |||||||
| chr19:2792350 | A | G | 1 | a0001c0001t0012g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.229+1717A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792350 | |||||||
| chr19:2792467 | C | A | 1 | a0001c0001t0003g0074 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.229+1834C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792467 | |||||||
| chr19:2792472 | C | A | 1 | a0001c0001t0002g0177 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.229+1839C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792472 | |||||||
| chr19:2792472 | C | G | 11 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(8): Show |
14 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.229+1839C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792472 | |||||||
| chr19:2792500 | C | T | 3 | a0001c0002t0006g0037 a0001c0002t0006g0154 a0001c0002t0006g0156 |
4 | HG02109.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+1867C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792500 | |||||||
| chr19:2792568 | G | A | 156 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(153): Show |
224 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.229+1935G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792568 | |||||||
| chr19:2792615 | T | TTTTTTTA others(67): Show |
1 | a0001c0001t0003g0077 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.229+1988_229+1989i others(76): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 2792615 | ||||||
| chr19:2792621 | T | A | 1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.229+1988T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792621 | |||||||
| chr19:2792622 | T | A | 145 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0105 others(142): Show |
208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.229+1989T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792622 | |||||||
| chr19:2792654 | T | G | 1 | a0001c0001t0004g0015 | 3 | HG01243.hp1 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.229+2021T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792654 | |||||||
| chr19:2792916 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.230-1848C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792916 | |||||||
| chr19:2792942 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.230-1822G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792942 | |||||||
| chr19:2792944 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.230-1820G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792944 | |||||||
| chr19:2792960 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.230-1804G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2792960 | |||||||
| chr19:2793035 | C | T | 8 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(5): Show |
11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-1729C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793035 | |||||||
| chr19:2793099 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0003g0145 |
2 | HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.230-1665C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793099 | |||||||
| chr19:2793196 | A | C | 87 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(84): Show |
129 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.230-1568A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793196 | |||||||
| chr19:2793291 | T | C | 161 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(158): Show |
230 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.230-1473T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793291 | |||||||
| chr19:2793313 | G | A | 7 | a0001c0001t0008g0014 a0001c0001t0011g0055 a0001c0001t0011g0056 others(4): Show |
9 | HG02145.hp1 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-1451G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793313 | |||||||
| chr19:2793432 | C | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-1332C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793432 | |||||||
| chr19:2793684 | C | T | 3 | a0001c0001t0011g0055 a0001c0001t0011g0056 a0001c0001t0011g0058 |
3 | HG02145.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.230-1080C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793684 | |||||||
| chr19:2793685 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0013g0035 |
3 | HG01891.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.230-1079G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793685 | |||||||
| chr19:2793887 | G | T | 8 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(5): Show |
11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-877G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793887 | |||||||
| chr19:2793939 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.230-825C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2793939 | |||||||
| chr19:2794003 | C | CT | 9 | a0001c0001t0002g0174 a0001c0001t0002g0200 a0001c0001t0002g0201 others(6): Show |
9 | HG00438.hp2 HG02145.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-749dupT | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 2794003 | ||||||
| chr19:2794006 | TTTTTTTT others(3): Show |
T | 42 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(39): Show |
57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.230-741_230-732del others(10): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 2794006 | ||||||
| chr19:2794045 | C | T | 1 | a0001c0001t0002g0043 | 2 | NA18944.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.230-719C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2794045 | |||||||
| chr19:2794141 | A | G | 1 | a0001c0001t0003g0095 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.230-623A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2794141 | |||||||
| chr19:2794213 | C | A | 5 | a0001c0001t0003g0028 a0001c0001t0003g0080 a0001c0001t0003g0091 others(2): Show |
6 | HG00558.hp2 NA18959.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-551C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2794213 | |||||||
| chr19:2794325 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.230-439C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 2/12 | chr19 | 2794325 | |||||||
| chr19:2795120 | G | A | 5 | a0001c0001t0002g0174 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02698.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+208G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795120 | |||||||
| chr19:2795251 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.378+339C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795251 | |||||||
| chr19:2795360 | G | A | 1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.378+448G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795360 | |||||||
| chr19:2795378 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.378+466G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795378 | |||||||
| chr19:2795495 | T | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | NA18949.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.378+583T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795495 | |||||||
| chr19:2795518 | T | A | 161 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(158): Show |
230 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.379-563T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795518 | |||||||
| chr19:2795626 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.379-455C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795626 | |||||||
| chr19:2795644 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.379-437G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795644 | |||||||
| chr19:2795768 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0013g0035 |
3 | HG01891.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.379-313G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795768 | |||||||
| chr19:2795773 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.379-308G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795773 | |||||||
| chr19:2795959 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.379-122C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2795959 | |||||||
| chr19:2796000 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.379-81G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2796000 | |||||||
| chr19:2796023 | G | A | 97 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(94): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.379-58G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2796023 | |||||||
| chr19:2796033 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0013g0035 |
3 | HG01891.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.379-48G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 3/12 | chr19 | 2796033 | |||||||
| chr19:2796199 | G | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.486+11G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796199 | |||||||
| chr19:2796200 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.486+12G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796200 | |||||||
| chr19:2796236 | C | T | 4 | a0001c0001t0002g0018 a0001c0001t0002g0143 a0001c0001t0007g0018 others(1): Show |
5 | HG03098.hp1 NA18971.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+48C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796236 | |||||||
| chr19:2796256 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.486+68G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796256 | |||||||
| chr19:2796318 | G | A | 119 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(116): Show |
174 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.486+130G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796318 | |||||||
| chr19:2796337 | G | T | 5 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(2): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+149G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796337 | |||||||
| chr19:2796357 | G | A | 97 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(94): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.486+169G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796357 | |||||||
| chr19:2796592 | G | A | 7 | a0001c0001t0008g0014 a0001c0001t0011g0055 a0001c0001t0011g0056 others(4): Show |
9 | HG02145.hp1 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+404G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796592 | |||||||
| chr19:2796635 | G | A | 1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.486+447G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796635 | |||||||
| chr19:2796646 | C | T | 157 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0166 others(154): Show |
225 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.486+458C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796646 | |||||||
| chr19:2796698 | C | T | 7 | a0001c0001t0008g0014 a0001c0001t0011g0055 a0001c0001t0011g0056 others(4): Show |
9 | HG02145.hp1 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+510C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796698 | |||||||
| chr19:2796740 | C | T | 1 | a0001c0001t0003g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.486+552C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796740 | |||||||
| chr19:2796896 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.486+708G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2796896 | |||||||
| chr19:2797088 | G | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(34): Show |
50 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.486+900G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797088 | |||||||
| chr19:2797109 | C | A | 1 | a0001c0001t0007g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.486+921C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797109 | |||||||
| chr19:2797201 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0142 |
3 | HG00673.hp2 HG02074.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.486+1013C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797201 | |||||||
| chr19:2797372 | A | C | 5 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(2): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+1184A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797372 | |||||||
| chr19:2797416 | A | C | 1 | a0001c0001t0002g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.486+1228A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797416 | |||||||
| chr19:2797428 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+1240G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797428 | |||||||
| chr19:2797450 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.486+1262G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797450 | |||||||
| chr19:2797479 | G | A | 3 | a0005c0013t0003g0025 a0007c0014t0034g0067 a0008c0012t0003g0025 |
3 | HG02486.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.486+1291G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797479 | |||||||
| chr19:2797486 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA19009.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486+1298G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797486 | |||||||
| chr19:2797544 | C | T | 1 | a0001c0001t0016g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.486+1356C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797544 | |||||||
| chr19:2797585 | C | T | 3 | a0002c0005t0008g0053 a0002c0005t0008g0054 a0002c0006t0008g0057 |
3 | HG03098.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.486+1397C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797585 | |||||||
| chr19:2797629 | G | A | 1 | a0004c0011t0002g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.486+1441G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797629 | |||||||
| chr19:2797705 | C | T | 160 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(157): Show |
228 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.486+1517C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797705 | |||||||
| chr19:2797939 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487-1750G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2797939 | |||||||
| chr19:2798195 | A | AT | 5 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0140 others(2): Show |
6 | HG00140.hp1 HG00140.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-1485dupT | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 2798195 | ||||||
| chr19:2798223 | G | T | 1 | a0001c0001t0003g0077 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-1466G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798223 | |||||||
| chr19:2798307 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG00323.hp1 HG01361.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1382G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798307 | |||||||
| chr19:2798535 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.487-1154G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798535 | |||||||
| chr19:2798603 | G | C | 2 | a0001c0001t0002g0176 a0004c0011t0002g0175 |
2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.487-1086G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798603 | |||||||
| chr19:2798663 | C | T | 1 | a0001c0001t0013g0035 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.487-1026C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798663 | |||||||
| chr19:2798688 | T | G | 166 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(163): Show |
236 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.487-1001T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798688 | |||||||
| chr19:2798692 | G | A | 1 | a0001c0001t0013g0035 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.487-997G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798692 | |||||||
| chr19:2798778 | G | A | 5 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(2): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.487-911G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798778 | |||||||
| chr19:2798810 | C | T | 1 | a0001c0001t0008g0014 | 3 | HG02258.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.487-879C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798810 | |||||||
| chr19:2798923 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.487-766A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798923 | |||||||
| chr19:2798986 | G | A | 1 | a0001c0001t0004g0015 | 3 | HG01243.hp1 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.487-703G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2798986 | |||||||
| chr19:2799221 | G | A | 1 | a0001c0001t0002g0020 | 3 | HG03491.hp1 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.487-468G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2799221 | |||||||
| chr19:2799225 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.487-464C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2799225 | |||||||
| chr19:2799313 | A | C | 1 | a0001c0001t0004g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487-376A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2799313 | |||||||
| chr19:2799324 | CAGAAGAA others(8): Show |
C | 1 | a0001c0001t0003g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.487-362_487-348del others(15): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 2799324 | ||||||
| chr19:2799425 | G | A | 3 | a0001c0001t0011g0055 a0001c0001t0011g0056 a0001c0001t0011g0058 |
3 | HG02145.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.487-264G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2799425 | |||||||
| chr19:2799639 | G | T | 1 | a0001c0001t0010g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.487-50G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 4/12 | chr19 | 2799639 | |||||||
| chr19:2799913 | C | T | 1 | a0001c0001t0008g0014 | 3 | HG02258.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.589+122C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2799913 | |||||||
| chr19:2799981 | C | T | 100 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(97): Show |
148 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.589+190C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2799981 | |||||||
| chr19:2800082 | G | T | 2 | a0002c0005t0008g0053 a0002c0005t0008g0054 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.589+291G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800082 | |||||||
| chr19:2800088 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+297G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800088 | |||||||
| chr19:2800121 | T | G | 3 | a0005c0013t0003g0025 a0007c0014t0034g0067 a0008c0012t0003g0025 |
3 | HG02486.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589+330T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800121 | |||||||
| chr19:2800128 | A | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.589+337A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800128 | |||||||
| chr19:2800136 | T | C | 8 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(5): Show |
11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.589+345T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800136 | |||||||
| chr19:2800194 | A | T | 103 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(100): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.589+403A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800194 | |||||||
| chr19:2800383 | C | T | 1 | a0001c0001t0016g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.589+592C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800383 | |||||||
| chr19:2800505 | C | T | 1 | a0001c0001t0004g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589+714C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800505 | |||||||
| chr19:2800507 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0138 |
4 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+716A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800507 | |||||||
| chr19:2800539 | T | C | 3 | a0001c0001t0003g0080 a0001c0001t0003g0091 a0001c0001t0003g0097 |
3 | HG00558.hp2 NA19068.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.589+748T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800539 | |||||||
| chr19:2800749 | G | A | 1 | a0001c0001t0011g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.589+958G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800749 | |||||||
| chr19:2800767 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.589+976G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800767 | |||||||
| chr19:2800833 | C | T | 3 | a0001c0001t0003g0080 a0001c0001t0003g0091 a0001c0001t0003g0097 |
3 | HG00558.hp2 NA19068.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.589+1042C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800833 | |||||||
| chr19:2800836 | A | T | 10 | a0001c0001t0002g0197 a0001c0001t0002g0212 a0001c0001t0004g0015 others(7): Show |
13 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.589+1045A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800836 | |||||||
| chr19:2800856 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | NA18990.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.589+1065G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800856 | |||||||
| chr19:2800860 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.589+1069C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800860 | |||||||
| chr19:2800993 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.589+1202T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2800993 | |||||||
| chr19:2801009 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.589+1218C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801009 | |||||||
| chr19:2801157 | G | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(34): Show |
50 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.589+1366G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801157 | |||||||
| chr19:2801172 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.589+1381C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801172 | |||||||
| chr19:2801340 | C | G | 5 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(2): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.589+1549C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801340 | |||||||
| chr19:2801438 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.589+1647G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801438 | |||||||
| chr19:2801494 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.589+1703G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801494 | |||||||
| chr19:2801498 | T | C | 1 | a0001c0001t0003g0097 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.589+1707T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801498 | |||||||
| chr19:2801522 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.589+1731C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801522 | |||||||
| chr19:2801704 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+1913T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801704 | |||||||
| chr19:2801740 | G | T | 1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.589+1949G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801740 | |||||||
| chr19:2801793 | C | T | 3 | a0005c0013t0003g0025 a0007c0014t0034g0067 a0008c0012t0003g0025 |
3 | HG02486.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589+2002C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801793 | |||||||
| chr19:2801970 | C | T | 1 | a0002c0006t0008g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.589+2179C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2801970 | |||||||
| chr19:2802025 | G | A | 1 | a0001c0001t0009g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.589+2234G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802025 | |||||||
| chr19:2802065 | C | A | 1 | a0001c0001t0007g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.589+2274C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802065 | |||||||
| chr19:2802094 | T | C | 168 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0153 others(165): Show |
238 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.589+2303T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802094 | |||||||
| chr19:2802356 | A | G | 1 | a0001c0001t0011g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.589+2565A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802356 | |||||||
| chr19:2802459 | C | CCACCTCC others(9): Show |
1 | a0001c0001t0002g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.590-2518_590-2503d others(18): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802459 | ||||||
| chr19:2802459 | CCACCTCC others(9): Show |
C | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.590-2518_590-2503d others(18): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802459 | ||||||
| chr19:2802474 | A | AACACCTC others(41): Show |
1 | a0001c0001t0002g0020 | 3 | HG03491.hp1 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.590-2503_590-2456d others(50): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802474 | ||||||
| chr19:2802514 | ACGACACC others(9): Show |
A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0161 a0001c0001t0002g0162 others(2): Show |
5 | HG01109.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-2494_590-2479d others(18): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802514 | ||||||
| chr19:2802522 | CACACCTC others(9): Show |
C | 3 | a0002c0005t0008g0053 a0002c0005t0008g0054 a0002c0006t0008g0057 |
3 | HG03098.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.590-2471_590-2456d others(18): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802522 | ||||||
| chr19:2802540 | C | T | 1 | a0001c0001t0013g0035 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.590-2476C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802540 | |||||||
| chr19:2802545 | CCCGACAC others(9): Show |
C | 8 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(5): Show |
11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.590-2462_590-2447d others(18): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802545 | ||||||
| chr19:2802564 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.590-2452G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802564 | |||||||
| chr19:2802566 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.590-2450C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802566 | |||||||
| chr19:2802635 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.590-2381G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802635 | |||||||
| chr19:2802700 | G | A | 5 | a0001c0001t0003g0028 a0001c0001t0003g0080 a0001c0001t0003g0091 others(2): Show |
6 | HG00558.hp2 NA18959.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-2316G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802700 | |||||||
| chr19:2802846 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 others(1): Show |
9 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.590-2170C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802846 | |||||||
| chr19:2802856 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(31): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.590-2160C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802856 | |||||||
| chr19:2802874 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.590-2142A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802874 | |||||||
| chr19:2802982 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.590-2034G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2802982 | |||||||
| chr19:2802992 | TGGTACCG others(40): Show |
T | 1 | a0002c0006t0008g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.590-1996_590-1950d others(49): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 2802992 | ||||||
| chr19:2803022 | G | A | 5 | a0001c0001t0003g0028 a0001c0001t0003g0080 a0001c0001t0003g0091 others(2): Show |
6 | HG00558.hp2 NA18959.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-1994G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803022 | |||||||
| chr19:2803035 | C | T | 1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-1981C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803035 | |||||||
| chr19:2803101 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.590-1915G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803101 | |||||||
| chr19:2803229 | C | T | 124 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(121): Show |
179 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.590-1787C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803229 | |||||||
| chr19:2803460 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.590-1556A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803460 | |||||||
| chr19:2803539 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0185 a0001c0001t0002g0186 |
7 | HG01123.hp2 HG01361.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-1477G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803539 | |||||||
| chr19:2803551 | G | A | 1 | a0001c0001t0009g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.590-1465G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803551 | |||||||
| chr19:2803577 | G | A | 4 | a0001c0001t0004g0066 a0001c0001t0010g0063 a0001c0001t0010g0064 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-1439G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803577 | |||||||
| chr19:2803582 | C | T | 42 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(39): Show |
57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.590-1434C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803582 | |||||||
| chr19:2803621 | A | G | 1 | a0001c0001t0007g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.590-1395A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803621 | |||||||
| chr19:2803625 | A | G | 97 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(94): Show |
145 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.590-1391A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803625 | |||||||
| chr19:2803666 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.590-1350T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803666 | |||||||
| chr19:2803691 | C | A | 2 | a0001c0001t0002g0165 a0001c0001t0002g0196 |
2 | HG02895.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.590-1325C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803691 | |||||||
| chr19:2803813 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.590-1203G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803813 | |||||||
| chr19:2803836 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.590-1180C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803836 | |||||||
| chr19:2803999 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.590-1017G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2803999 | |||||||
| chr19:2804033 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0089 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.590-983G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804033 | |||||||
| chr19:2804167 | G | A | 1 | a0001c0001t0030g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.590-849G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804167 | |||||||
| chr19:2804173 | C | T | 1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-843C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804173 | |||||||
| chr19:2804302 | A | G | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.590-714A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804302 | |||||||
| chr19:2804307 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.590-709T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804307 | |||||||
| chr19:2804354 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.590-662G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804354 | |||||||
| chr19:2804569 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.590-447T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804569 | |||||||
| chr19:2804668 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.590-348G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804668 | |||||||
| chr19:2804684 | A | C | 22 | a0001c0001t0001g0153 a0001c0001t0002g0161 a0001c0001t0002g0162 others(19): Show |
28 | HG00438.hp2 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.590-332A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804684 | |||||||
| chr19:2804803 | G | A | 3 | a0001c0001t0011g0055 a0001c0001t0011g0056 a0001c0001t0011g0058 |
3 | HG02145.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.590-213G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 5/12 | chr19 | 2804803 | |||||||
| chr19:2805179 | G | T | 2 | a0001c0002t0006g0036 a0001c0002t0006g0155 |
3 | HG02723.hp1 HG03225.hp1 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.750+3G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805179 | |||||||
| chr19:2805285 | C | T | 1 | a0001c0001t0004g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.750+109C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805285 | |||||||
| chr19:2805538 | C | T | 8 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(5): Show |
10 | HG02109.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.750+362C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805538 | |||||||
| chr19:2805552 | G | C | 1 | a0001c0002t0006g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.750+376G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805552 | |||||||
| chr19:2805584 | G | T | 1 | a0001c0002t0006g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.750+408G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805584 | |||||||
| chr19:2805606 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0002g0201 a0001c0001t0002g0215 |
3 | HG03491.hp2 HG03492.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.750+430C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805606 | |||||||
| chr19:2805673 | G | T | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.750+497G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805673 | |||||||
| chr19:2805727 | C | T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0194 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.750+551C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805727 | |||||||
| chr19:2805756 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.750+580C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805756 | |||||||
| chr19:2805803 | G | A | 9 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0008g0014 others(6): Show |
11 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.750+627G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805803 | |||||||
| chr19:2805820 | A | AGGGGACG others(21): Show |
2 | a0001c0001t0003g0089 a0002c0006t0008g0057 |
2 | HG03098.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.750+762_750+789dup others(28): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805820 | ||||||
| chr19:2805820 | AGGGGACG others(21): Show |
A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0019 others(40): Show |
60 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.750+762_750+789del others(28): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805820 | ||||||
| chr19:2805820 | AGGGGACG others(49): Show |
A | 71 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(68): Show |
101 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.750+734_750+789del others(56): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805820 | ||||||
| chr19:2805847 | GGGGGGAC others(20): Show |
G | 1 | a0001c0001t0009g0001 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.750+677_750+703del others(27): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805847 | ||||||
| chr19:2805854 | CGGGCGGG others(105): Show |
C | 1 | a0001c0001t0003g0003 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.750+705_750+816del | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805854 | ||||||
| chr19:2805882 | CGGGCGGG others(77): Show |
C | 12 | a0001c0001t0002g0203 a0001c0001t0003g0024 a0001c0001t0003g0026 others(9): Show |
15 | HG00423.hp1 HG00621.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.750+733_750+816del others(84): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805882 | ||||||
| chr19:2805903 | GGGGGGAC others(20): Show |
G | 2 | a0001c0001t0001g0122 a0001c0015t0001g0001 |
2 | HG01993.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.750+733_750+759del others(27): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805903 | ||||||
| chr19:2805910 | CGGGCGGG others(49): Show |
C | 47 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0021 others(44): Show |
69 | HG00558.hp1 HG00558.hp2 HG01261.hp1 others(66): Show |
intron_variant | MODIFIER | c.750+761_750+816del others(56): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805910 | ||||||
| chr19:2805931 | GGGGGGAC others(48): Show |
G | 1 | a0001c0001t0003g0016 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.750+761_750+815del others(55): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805931 | ||||||
| chr19:2805938 | CGGGCGGG others(21): Show |
C | 2 | a0001c0001t0003g0003 a0007c0014t0034g0067 |
2 | HG03195.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.750+789_750+816del others(28): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 2805938 | ||||||
| chr19:2805966 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0117 others(4): Show |
12 | HG02970.hp2 HG03831.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.750+790T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2805966 | |||||||
| chr19:2806066 | G | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.751-851G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806066 | |||||||
| chr19:2806102 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 others(1): Show |
9 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-815C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806102 | |||||||
| chr19:2806103 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-814G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806103 | |||||||
| chr19:2806287 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.751-630C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806287 | |||||||
| chr19:2806288 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(1): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-629G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806288 | |||||||
| chr19:2806325 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.751-592C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806325 | |||||||
| chr19:2806382 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.751-535C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806382 | |||||||
| chr19:2806462 | C | T | 1 | a0001c0001t0030g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.751-455C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806462 | |||||||
| chr19:2806576 | A | G | 92 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(89): Show |
135 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.751-341A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806576 | |||||||
| chr19:2806618 | T | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0001t0001g0219 others(3): Show |
6 | HG00323.hp1 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-299T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806618 | |||||||
| chr19:2806733 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-184T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806733 | |||||||
| chr19:2806744 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-173A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806744 | |||||||
| chr19:2806745 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-172T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806745 | |||||||
| chr19:2806746 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-171A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806746 | |||||||
| chr19:2806751 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-166T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806751 | |||||||
| chr19:2806761 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-156A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806761 | |||||||
| chr19:2806764 | A | G | 1 | a0001c0001t0013g0035 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.751-153A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806764 | |||||||
| chr19:2806772 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-145T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806772 | |||||||
| chr19:2806773 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-144G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806773 | |||||||
| chr19:2806774 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-143T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806774 | |||||||
| chr19:2806775 | G | A | 2 | a0001c0001t0001g0124 a0001c0016t0001g0125 |
2 | NA18940.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.751-142G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806775 | |||||||
| chr19:2806776 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-141T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806776 | |||||||
| chr19:2806777 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-140A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806777 | |||||||
| chr19:2806779 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-138T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806779 | |||||||
| chr19:2806781 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-136A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806781 | |||||||
| chr19:2806785 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-132A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806785 | |||||||
| chr19:2806787 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-130G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806787 | |||||||
| chr19:2806788 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-129C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806788 | |||||||
| chr19:2806790 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-127G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806790 | |||||||
| chr19:2806791 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-126A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806791 | |||||||
| chr19:2806793 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-124A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806793 | |||||||
| chr19:2806800 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-117G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806800 | |||||||
| chr19:2806803 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-114A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806803 | |||||||
| chr19:2806806 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-111G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806806 | |||||||
| chr19:2806808 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-109A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806808 | |||||||
| chr19:2806815 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-102A>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806815 | |||||||
| chr19:2806817 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-100G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806817 | |||||||
| chr19:2806818 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-99G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806818 | |||||||
| chr19:2806822 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-95T>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806822 | |||||||
| chr19:2806825 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-92A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806825 | |||||||
| chr19:2806827 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-90A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806827 | |||||||
| chr19:2806835 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-82T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806835 | |||||||
| chr19:2806837 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-80G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806837 | |||||||
| chr19:2806842 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-75T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806842 | |||||||
| chr19:2806843 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-74G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806843 | |||||||
| chr19:2806845 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-72G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806845 | |||||||
| chr19:2806847 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-70C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806847 | |||||||
| chr19:2806849 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-68G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806849 | |||||||
| chr19:2806851 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-66G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806851 | |||||||
| chr19:2806853 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0010g0063 a0001c0001t0010g0064 others(1): Show |
4 | HG02257.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-64G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806853 | |||||||
| chr19:2806857 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-60T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806857 | |||||||
| chr19:2806858 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-59G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806858 | |||||||
| chr19:2806859 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-58G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806859 | |||||||
| chr19:2806865 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-52G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806865 | |||||||
| chr19:2806867 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-50G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806867 | |||||||
| chr19:2806868 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-49G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806868 | |||||||
| chr19:2806870 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-47G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806870 | |||||||
| chr19:2806871 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-46G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806871 | |||||||
| chr19:2806872 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-45A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806872 | |||||||
| chr19:2806873 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-44G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806873 | |||||||
| chr19:2806877 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-40G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806877 | |||||||
| chr19:2806882 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-35G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806882 | |||||||
| chr19:2806884 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-33C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806884 | |||||||
| chr19:2806885 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-32C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806885 | |||||||
| chr19:2806887 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-30T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806887 | |||||||
| chr19:2806888 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-29G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806888 | |||||||
| chr19:2806889 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-28G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806889 | |||||||
| chr19:2806890 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-27G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806890 | |||||||
| chr19:2806891 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-26T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806891 | |||||||
| chr19:2806893 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-24A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806893 | |||||||
| chr19:2806902 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.751-15T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 6/12 | chr19 | 2806902 | |||||||
| chr19:2807065 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886+13T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807065 | |||||||
| chr19:2807136 | G | T | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.886+84G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807136 | |||||||
| chr19:2807202 | G | A | 9 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(6): Show |
12 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.886+150G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807202 | |||||||
| chr19:2807231 | C | T | 1 | a0002c0005t0008g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.886+179C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807231 | |||||||
| chr19:2807290 | T | C | 18 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0004g0015 others(15): Show |
23 | HG00438.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.887-152T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807290 | |||||||
| chr19:2807322 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.887-120G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807322 | |||||||
| chr19:2807366 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.887-76C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807366 | |||||||
| chr19:2807377 | G | A | 76 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(73): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.887-65G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 7/12 | chr19 | 2807377 | |||||||
| chr19:2807820 | C | T | 1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1253+12C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2807820 | |||||||
| chr19:2807931 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1253+123C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2807931 | |||||||
| chr19:2808008 | C | G | 15 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(12): Show |
20 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1253+200C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808008 | |||||||
| chr19:2808061 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(1): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254-182C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808061 | |||||||
| chr19:2808095 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1254-148C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808095 | |||||||
| chr19:2808106 | CT | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(34): Show |
50 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254-136delT | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808106 | |||||||
| chr19:2808142 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0149 |
2 | HG00544.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1254-101G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808142 | |||||||
| chr19:2808164 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1254-79G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808164 | |||||||
| chr19:2808179 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1254-64C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 8/12 | chr19 | 2808179 | |||||||
| chr19:2808458 | CGGGCAG | C | 36 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(33): Show |
49 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1455+43_1455+48del others(6): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 2808458 | ||||||
| chr19:2808458 | CGGGCAGG others(5): Show |
C | 3 | a0001c0001t0004g0050 a0001c0001t0004g0051 a0001c0001t0032g0049 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1455+37_1455+48del others(12): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 2808458 | ||||||
| chr19:2808552 | T | C | 19 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(16): Show |
24 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1455+108T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808552 | |||||||
| chr19:2808572 | A | G | 3 | a0001c0001t0010g0063 a0001c0001t0010g0064 a0001c0001t0010g0065 |
3 | HG02257.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1455+128A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808572 | |||||||
| chr19:2808781 | G | A | 13 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0026 others(10): Show |
18 | HG00423.hp1 HG00621.hp2 NA18939.hp1 others(15): Show |
intron_variant | MODIFIER | c.1455+337G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808781 | |||||||
| chr19:2808801 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1455+357A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808801 | |||||||
| chr19:2808866 | C | A | 1 | a0001c0001t0032g0049 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1455+422C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808866 | |||||||
| chr19:2808867 | G | A | 1 | a0001c0009t0001g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1455+423G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808867 | |||||||
| chr19:2808962 | G | A | 5 | a0001c0002t0006g0036 a0001c0002t0006g0037 a0001c0002t0006g0154 others(2): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1455+518G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808962 | |||||||
| chr19:2808979 | G | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0099 others(4): Show |
11 | HG01167.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455+535G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2808979 | |||||||
| chr19:2809145 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1455+701G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809145 | |||||||
| chr19:2809170 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1455+726A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809170 | |||||||
| chr19:2809255 | T | C | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1455+811T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809255 | |||||||
| chr19:2809280 | GCA | G | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1455+843_1455+844d others(4): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 2809280 | ||||||
| chr19:2809335 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1455+891C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809335 | |||||||
| chr19:2809336 | G | A | 1 | a0001c0001t0008g0014 | 3 | HG02258.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1455+892G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809336 | |||||||
| chr19:2809408 | G | A | 1 | a0001c0001t0003g0083 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1456-896G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809408 | |||||||
| chr19:2809508 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1456-796G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809508 | |||||||
| chr19:2809524 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1456-780G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809524 | |||||||
| chr19:2809582 | G | A | 2 | a0001c0002t0006g0036 a0001c0002t0006g0155 |
3 | HG02723.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1456-722G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809582 | |||||||
| chr19:2809674 | A | G | 166 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(163): Show |
236 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1456-630A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809674 | |||||||
| chr19:2809734 | T | C | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1456-570T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809734 | |||||||
| chr19:2809738 | G | A | 1 | a0001c0001t0003g0026 | 2 | HG00423.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1456-566G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809738 | |||||||
| chr19:2809860 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1456-444G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2809860 | |||||||
| chr19:2810183 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1456-121G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2810183 | |||||||
| chr19:2810250 | G | A | 98 | a0001c0001t0001g0041 a0001c0001t0001g0166 a0001c0001t0001g0199 others(95): Show |
146 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1456-54G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2810250 | |||||||
| chr19:2810258 | G | A | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1456-46G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2810258 | |||||||
| chr19:2810275 | C | T | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1456-29C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 9/12 | chr19 | 2810275 | |||||||
| chr19:2810503 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0132 |
4 | NA18942.hp2 NA18973.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1642+13C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 10/12 | chr19 | 2810503 | |||||||
| chr19:2810516 | G | A | 1 | a0001c0001t0012g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1642+26G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 10/12 | chr19 | 2810516 | |||||||
| chr19:2810620 | T | C | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1643-20T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 10/12 | chr19 | 2810620 | |||||||
| chr19:2810889 | C | A | 1 | a0004c0011t0002g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1771+121C>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2810889 | |||||||
| chr19:2810891 | C | T | 2 | a0001c0002t0006g0036 a0001c0002t0006g0155 |
3 | HG02723.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1771+123C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2810891 | |||||||
| chr19:2810896 | C | CGCAGGGG others(3): Show |
1 | a0001c0001t0001g0135 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1771+130_1771+131i others(12): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | 2810896 | ||||||
| chr19:2811050 | C | T | 1 | a0004c0011t0002g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1771+282C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811050 | |||||||
| chr19:2811058 | T | C | 3 | a0001c0001t0010g0063 a0001c0001t0010g0064 a0001c0001t0010g0065 |
3 | HG02257.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1771+290T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811058 | |||||||
| chr19:2811137 | T | A | 20 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0071 others(17): Show |
27 | HG00438.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1771+369T>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811137 | |||||||
| chr19:2811207 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1772-391G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811207 | |||||||
| chr19:2811285 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1772-313G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811285 | |||||||
| chr19:2811295 | A | C | 177 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0115 others(174): Show |
248 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1772-303A>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811295 | |||||||
| chr19:2811371 | G | A | 1 | a0001c0001t0003g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1772-227G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811371 | |||||||
| chr19:2811579 | T | C | 2 | a0001c0001t0001g0100 a0007c0014t0034g0067 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1772-19T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 11/12 | chr19 | 2811579 | |||||||
| chr19:2811719 | T | TGTCCTGA others(79): Show |
1 | a0009c0008t0001g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1902_1908+79dupCAG others(83): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811719 | ||||||
| chr19:2811729 | A | AGCAAGGT others(122): Show |
1 | a0001c0007t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1908+55_1908+56ins others(129): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811729 | ||||||
| chr19:2811729 | A | AGCAAGGT others(165): Show |
1 | a0001c0001t0001g0001 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1908+55_1908+56ins others(172): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811729 | ||||||
| chr19:2811729 | AGCAAGGT others(36): Show |
A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0140 others(4): Show |
7 | HG00140.hp1 HG00140.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1908+37_1908+79del others(43): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811729 | ||||||
| chr19:2811729 | AGCAAGGT others(79): Show |
A | 9 | a0001c0001t0003g0096 a0001c0001t0004g0015 a0001c0001t0004g0066 others(6): Show |
13 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1908+77_1908+162de others(87): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811729 | ||||||
| chr19:2811747 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0023g0167 |
2 | HG02523.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1908+13T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811747 | |||||||
| chr19:2811747 | T | TGGGGACA others(208): Show |
1 | a0001c0001t0033g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1908+55_1908+56ins others(215): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811747 | ||||||
| chr19:2811771 | C | CGGCAAGG others(165): Show |
3 | a0001c0001t0002g0039 a0001c0001t0002g0164 a0001c0001t0021g0039 |
3 | HG02572.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1908+55_1908+56ins others(172): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811771 | ||||||
| chr19:2811771 | C | CGGCAAGG others(251): Show |
1 | a0001c0001t0027g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1908+55_1908+56ins others(258): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811771 | ||||||
| chr19:2811771 | C | CGGCAAGG others(36): Show |
1 | a0001c0001t0025g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1908+55_1908+56ins others(43): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811771 | ||||||
| chr19:2811771 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1908+37C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811771 | |||||||
| chr19:2811771 | CGGCAAGG others(36): Show |
C | 3 | a0001c0001t0003g0024 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02145.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908+80_1908+122de others(44): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811771 | ||||||
| chr19:2811772 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1908+38G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811772 | |||||||
| chr19:2811790 | T | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(88): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1908+56T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811790 | |||||||
| chr19:2811790 | T | TGGGGACA others(552): Show |
4 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 others(1): Show |
9 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1908+79_1908+80ins others(559): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811790 | ||||||
| chr19:2811790 | T | TGGGGACA others(36): Show |
9 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0001t0001g0153 others(6): Show |
9 | HG00323.hp1 HG01346.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1908+98_1908+99ins others(43): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811790 | ||||||
| chr19:2811790 | T | TGGGGACA others(79): Show |
1 | a0001c0001t0001g0011 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1908+98_1908+99ins others(86): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811790 | ||||||
| chr19:2811814 | T | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0099 a0001c0001t0002g0038 others(11): Show |
15 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1908+80T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811814 | |||||||
| chr19:2811814 | T | TGGCAAGG others(79): Show |
1 | a0001c0001t0001g0001 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1908+98_1908+99ins others(86): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811814 | ||||||
| chr19:2811814 | T | TGGCAAGG others(79): Show |
1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1908+98_1908+99ins others(86): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811814 | ||||||
| chr19:2811814 | TGGCAAGG others(36): Show |
T | 42 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0016 others(39): Show |
58 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1908+120_1908+162d others(45): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811814 | ||||||
| chr19:2811820 | G | A | 1 | a0007c0014t0034g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1908+86G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811820 | |||||||
| chr19:2811833 | T | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(89): Show |
134 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1908+99T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811833 | |||||||
| chr19:2811857 | C | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(89): Show |
140 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1908+123C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811857 | |||||||
| chr19:2811870 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1908+136G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811870 | |||||||
| chr19:2811876 | T | C | 135 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(132): Show |
195 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1908+142T>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811876 | |||||||
| chr19:2811876 | T | TGGGGACA others(36): Show |
1 | a0001c0001t0001g0128 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1908+162_1908+163i others(45): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811876 | ||||||
| chr19:2811891 | C | CGTCCTGA others(251): Show |
1 | a0001c0001t0030g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1908+162_1908+163i others(260): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811891 | ||||||
| chr19:2811891 | C | CGTCCTGA others(165): Show |
1 | a0001c0001t0002g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1908+162_1908+163i others(174): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811891 | ||||||
| chr19:2811891 | C | CGTCCTGA others(79): Show |
2 | a0001c0001t0003g0082 a0001c0001t0003g0089 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1908+162_1908+163i others(88): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811891 | ||||||
| chr19:2811891 | C | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0107 a0001c0001t0001g0205 others(50): Show |
71 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1908+157C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811891 | |||||||
| chr19:2811894 | C | CCTGAACG others(208): Show |
2 | a0001c0001t0002g0224 a0001c0001t0023g0167 |
2 | HG00733.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1908+162_1908+163i others(217): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAACG others(380): Show |
1 | a0001c0001t0002g0209 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1908+162_1908+163i others(389): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAACG others(165): Show |
18 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0038 others(15): Show |
22 | HG00280.hp2 HG01884.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1908+162_1908+163i others(174): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAACG others(165): Show |
2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1908+162_1908+163i others(174): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(122): Show |
4 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0189 others(1): Show |
5 | HG02074.hp2 HG02132.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1908+162_1908+163i others(131): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(380): Show |
1 | a0001c0001t0002g0141 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1908+162_1908+163i others(389): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(208): Show |
54 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(51): Show |
91 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1908+162_1908+163i others(217): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(423): Show |
1 | a0001c0001t0002g0208 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1908+162_1908+163i others(432): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(251): Show |
1 | a0001c0001t0002g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1908+162_1908+163i others(260): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | CCTGAATG others(122): Show |
2 | a0001c0001t0002g0211 a0001c0001t0003g0171 |
2 | HG01884.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1908+162_1908+163i others(131): Show |
THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 2811894 | ||||||
| chr19:2811894 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0164 a0001c0001t0004g0015 others(2): Show |
7 | HG01243.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1908+160C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811894 | |||||||
| chr19:2811897 | C | G | 1 | a0001c0001t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1908+163C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811897 | |||||||
| chr19:2811901 | A | G | 1 | a0001c0001t0028g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1908+167A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2811901 | |||||||
| chr19:2812020 | C | G | 2 | a0001c0001t0002g0165 a0001c0001t0002g0196 |
2 | HG02895.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1908+286C>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812020 | |||||||
| chr19:2812055 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1908+321G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812055 | |||||||
| chr19:2812060 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1908+326G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812060 | |||||||
| chr19:2812155 | A | G | 121 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(118): Show |
175 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1908+421A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812155 | |||||||
| chr19:2812282 | G | A | 5 | a0001c0001t0005g0006 a0001c0001t0005g0046 a0001c0001t0005g0072 others(2): Show |
10 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1908+548G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812282 | |||||||
| chr19:2812327 | C | T | 2 | a0001c0001t0001g0100 a0002c0006t0008g0057 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1908+593C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812327 | |||||||
| chr19:2812464 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1909-651C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812464 | |||||||
| chr19:2812589 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1909-526G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812589 | |||||||
| chr19:2812636 | G | A | 16 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0047 others(13): Show |
21 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1909-479G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812636 | |||||||
| chr19:2812660 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1909-455G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812660 | |||||||
| chr19:2812662 | C | T | 1 | a0001c0001t0009g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1909-453C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812662 | |||||||
| chr19:2812689 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1909-426C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812689 | |||||||
| chr19:2812692 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0059 a0001c0001t0003g0060 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909-423C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812692 | |||||||
| chr19:2812760 | C | T | 3 | a0001c0001t0010g0063 a0001c0001t0010g0064 a0001c0001t0010g0065 |
3 | HG02257.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1909-355C>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812760 | |||||||
| chr19:2812782 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1909-333G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812782 | |||||||
| chr19:2812975 | G | T | 2 | a0001c0001t0002g0183 a0001c0001t0007g0190 |
2 | HG00099.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1909-140G>T | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2812975 | |||||||
| chr19:2813002 | A | G | 122 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(119): Show |
176 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1909-113A>G | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2813002 | |||||||
| chr19:2813006 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1909-109G>A | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2813006 | |||||||
| chr19:2813012 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1909-103G>C | THOP1 | ENSG00000172009.15 | transcript | ENST00000307741.11 | protein_coding | 12/12 | chr19 | 2813012 |