Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8563 |
| ensemblid | ENSG00000100296.14 |
| hgncid | 19074 |
| symbol | THOC5 |
| name | THO complex subunit 5 |
| refseq_nuc | NM_003678.5 |
| refseq_prot | NP_003669.4 |
| ensembl_nuc | ENST00000490103.6 |
| ensembl_prot | ENSP00000420306.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29505879 |
| end | 29553757 |
| strand | - |
| ver | v1.2 |
| region | chr22:29505879-29553757 |
| region5000 | chr22:29500879-29558757 |
| regionname0 | THOC5_chr22_29505879_29553757 |
| regionname5000 | THOC5_chr22_29500879_29558757 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 683 | 192 | 63 | 36 | 55 | 10 | 26 | 40 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0002 | 0/0 | 683 | 94 | 11 | 11 | 63 | 1 | 8 | 50 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0003 | 0/0 | 683 | 88 | 18 | 20 | 40 | 4 | 6 | 25 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0004 | 0/0 | 683 | 5 | 1 | 0 | 2 | 0 | 2 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0005 | 0/0 | 683 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0006 | 0/0 | 683 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0007 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0008 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| a0009 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | MSSES others(678): Show |
chr22 | 29500879 | 29558757 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2049 | 179 | 51 | 36 | 55 | 10 | 25 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0001c0005 | 0/0 | 2049 | 13 | 12 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0002c0003 | 0/0 | 2049 | 54 | 1 | 4 | 46 | 0 | 3 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0002c0004 | 0/0 | 2049 | 40 | 10 | 7 | 17 | 1 | 5 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0003c0002 | 0/0 | 2049 | 87 | 18 | 20 | 40 | 4 | 5 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0003c0011 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0004c0006 | 0/0 | 2049 | 5 | 1 | 0 | 2 | 0 | 2 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0005c0009 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0006c0010 | 0/0 | 2049 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0007c0008 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0008c0012 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 | ||
| a0009c0007 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ATGTC others(2044): Show |
chr22 | 29500879 | 29558757 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4728 | 57 | 24 | 8 | 20 | 1 | 3 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0002 | 0/1 | 4728 | 50 | 1 | 14 | 15 | 5 | 14 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0003 | 0/0 | 4728 | 5 | 1 | 3 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0004 | 0/0 | 4724 | 20 | 1 | 0 | 15 | 0 | 4 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0006 | 0/0 | 4728 | 11 | 0 | 6 | 0 | 3 | 2 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0007 | 0/0 | 4728 | 8 | 7 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0009 | 0/0 | 4724 | 5 | 5 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0012 | 0/0 | 4728 | 4 | 4 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0013 | 0/0 | 4728 | 3 | 3 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0014 | 0/0 | 4728 | 3 | 0 | 0 | 3 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0015 | 0/0 | 4728 | 3 | 0 | 2 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0016 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0017 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0019 | 0/0 | 4728 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0020 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0021 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0023 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0027 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0029 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0030 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0001t0031 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0005t0002 | 0/0 | 4728 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0001c0005t0005 | 0/0 | 4728 | 12 | 12 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0003t0001 | 0/0 | 4728 | 46 | 1 | 4 | 38 | 0 | 3 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0003t0003 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0003t0004 | 0/0 | 4724 | 5 | 0 | 0 | 5 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0002c0003t0008 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0003t0018 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0004t0001 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0004t0003 | 0/0 | 4728 | 37 | 8 | 6 | 17 | 1 | 5 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0004t0022 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0002c0004t0028 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0001 | 0/0 | 4728 | 70 | 13 | 17 | 33 | 4 | 3 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0003 | 0/0 | 4728 | 2 | 0 | 0 | 0 | 0 | 2 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0008 | 0/0 | 4728 | 7 | 0 | 0 | 7 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0009 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0011 | 0/0 | 4724 | 4 | 3 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0024 | 0/0 | 4724 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0025 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0003c0002t0026 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0003c0011t0004 | 0/0 | 4724 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0004c0006t0010 | 0/0 | 4724 | 5 | 1 | 0 | 2 | 0 | 2 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0005c0009t0002 | 0/0 | 4728 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0006c0010t0002 | 0/0 | 4728 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0007c0008t0004 | 0/0 | 4724 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4719): Show |
chr22 | 29500879 | 29558757 |
| a0008c0012t0001 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| a0009c0007t0006 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | ACTTC others(4723): Show |
chr22 | 29500879 | 29558757 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0007g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0014g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0014g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0014g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0015g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0015g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0015g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0019g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0020g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0021g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0023g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0027g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0029g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0030g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0001t0031g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0001c0005t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0003t0018g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0022g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0002c0004t0028g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 3 | 2 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0008g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0011g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0024g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0025g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0002t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0003c0011t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0004c0006t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0004c0006t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0004c0006t0010g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0004c0006t0010g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0004c0006t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0005c0009t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0006c0010t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0007c0008t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0008c0012t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| a0009c0007t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0001 | g0001 | EUR | GBR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0328 | EUR | GBR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0339 | EUR | GBR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0332 | EUR | GBR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0173 | EUR | FIN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0322 | EUR | FIN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00323 | hp2 | a0005 | c0009 | t0002 | g0100 | EUR | FIN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0272 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00438 | hp2 | a0003 | c0002 | t0001 | g0146 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0299 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00597 | hp2 | a0003 | c0002 | t0001 | g0191 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0188 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00609 | hp2 | a0004 | c0006 | t0010 | g0132 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00621 | hp2 | a0003 | c0002 | t0001 | g0023 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00639 | hp1 | a0003 | c0002 | t0025 | g0171 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00642 | hp1 | a0002 | c0004 | t0003 | g0305 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0243 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00735 | hp1 | a0002 | c0004 | t0003 | g0240 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00741 | hp1 | a0003 | c0002 | t0024 | g0141 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG00741 | hp2 | a0003 | c0002 | t0001 | g0004 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01069 | hp1 | a0003 | c0002 | t0001 | g0005 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01070 | hp1 | a0002 | c0004 | t0003 | g0261 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01071 | hp1 | a0003 | c0002 | t0001 | g0005 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01071 | hp2 | a0002 | c0004 | t0003 | g0260 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0319 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01081 | hp1 | a0002 | c0004 | t0003 | g0264 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01081 | hp2 | a0002 | c0004 | t0022 | g0077 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01099 | hp1 | a0003 | c0002 | t0001 | g0157 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01099 | hp2 | a0003 | c0002 | t0011 | g0134 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01109 | hp1 | a0002 | c0004 | t0003 | g0241 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01109 | hp2 | a0003 | c0002 | t0001 | g0167 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01168 | hp1 | a0001 | c0001 | t0015 | g0093 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0333 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01175 | hp1 | a0003 | c0002 | t0001 | g0193 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01175 | hp2 | a0001 | c0001 | t0015 | g0113 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01192 | hp2 | a0003 | c0002 | t0001 | g0170 | AMR | PUR | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01256 | hp1 | a0003 | c0002 | t0001 | g0031 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0323 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0318 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01257 | hp2 | a0003 | c0002 | t0001 | g0133 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0325 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01258 | hp2 | a0003 | c0002 | t0001 | g0162 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01261 | hp1 | a0003 | c0002 | t0001 | g0186 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0014 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0296 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01361 | hp1 | a0001 | c0001 | t0031 | g0358 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01361 | hp2 | a0003 | c0002 | t0001 | g0149 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01433 | hp1 | a0006 | c0010 | t0002 | g0072 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0353 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01496 | hp2 | a0003 | c0002 | t0001 | g0187 | AMR | CLM | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0016 | EUR | IBS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01515 | hp2 | a0002 | c0004 | t0003 | g0285 | EUR | IBS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | IBS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0016 | EUR | IBS | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01884 | hp1 | a0003 | c0002 | t0011 | g0180 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01891 | hp1 | a0002 | c0004 | t0003 | g0195 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0327 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0357 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01934 | hp2 | a0003 | c0002 | t0001 | g0007 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0308 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0278 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01993 | hp1 | a0003 | c0002 | t0001 | g0159 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02015 | hp1 | a0003 | c0002 | t0001 | g0147 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02027 | hp1 | a0003 | c0002 | t0001 | g0148 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0271 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02055 | hp1 | a0001 | c0005 | t0005 | g0051 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0341 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02056 | hp2 | a0002 | c0004 | t0003 | g0204 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02071 | hp1 | a0003 | c0002 | t0001 | g0184 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02071 | hp2 | a0002 | c0004 | t0003 | g0015 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0270 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02080 | hp1 | a0002 | c0004 | t0003 | g0033 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0302 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02083 | hp2 | a0003 | c0002 | t0001 | g0175 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02129 | hp1 | a0003 | c0002 | t0001 | g0007 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02129 | hp2 | a0003 | c0002 | t0001 | g0176 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02135 | hp2 | a0002 | c0004 | t0003 | g0293 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0314 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0054 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02148 | hp2 | a0003 | c0002 | t0001 | g0004 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | CDX | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02155 | hp2 | a0003 | c0002 | t0001 | g0178 | EAS | CDX | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02165 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | CDX | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0269 | EAS | CDX | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02258 | hp1 | a0002 | c0004 | t0003 | g0008 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02280 | hp1 | a0001 | c0005 | t0005 | g0002 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0017 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02293 | hp1 | a0003 | c0002 | t0001 | g0007 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02451 | hp2 | a0003 | c0002 | t0001 | g0153 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | KHV | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02572 | hp1 | a0001 | c0005 | t0005 | g0057 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02602 | hp2 | a0002 | c0004 | t0003 | g0279 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02622 | hp2 | a0003 | c0002 | t0001 | g0019 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02647 | hp1 | a0002 | c0004 | t0003 | g0201 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02683 | hp2 | a0002 | c0004 | t0003 | g0196 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0289 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02738 | hp2 | a0004 | c0006 | t0010 | g0130 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02809 | hp1 | a0003 | c0002 | t0001 | g0139 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02818 | hp1 | a0003 | c0002 | t0001 | g0174 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02818 | hp2 | a0001 | c0005 | t0005 | g0011 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02886 | hp1 | a0001 | c0005 | t0005 | g0024 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02886 | hp2 | a0003 | c0002 | t0001 | g0151 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02895 | hp2 | a0003 | c0002 | t0001 | g0140 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02896 | hp1 | a0003 | c0002 | t0001 | g0138 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02896 | hp2 | a0001 | c0001 | t0027 | g0046 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02922 | hp1 | a0003 | c0002 | t0011 | g0135 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02922 | hp2 | a0001 | c0005 | t0005 | g0011 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02965 | hp1 | a0002 | c0004 | t0003 | g0008 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02965 | hp2 | a0002 | c0004 | t0028 | g0205 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02970 | hp1 | a0001 | c0005 | t0005 | g0002 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02976 | hp2 | a0003 | c0002 | t0009 | g0136 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03098 | hp2 | a0002 | c0004 | t0003 | g0199 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03139 | hp1 | a0003 | c0002 | t0026 | g0036 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03195 | hp2 | a0003 | c0002 | t0011 | g0179 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03225 | hp1 | a0001 | c0005 | t0005 | g0058 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0040 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0297 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0068 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03453 | hp2 | a0001 | c0005 | t0005 | g0002 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0331 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03491 | hp1 | a0003 | c0002 | t0003 | g0181 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03491 | hp2 | a0001 | c0001 | t0019 | g0326 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0350 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03492 | hp2 | a0003 | c0002 | t0003 | g0145 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03516 | hp2 | a0003 | c0002 | t0001 | g0192 | AFR | ESN | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03540 | hp1 | a0001 | c0005 | t0005 | g0052 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03579 | hp1 | a0002 | c0004 | t0003 | g0197 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03579 | hp2 | a0003 | c0002 | t0001 | g0137 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03654 | hp2 | a0003 | c0002 | t0001 | g0165 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03704 | hp2 | a0003 | c0011 | t0004 | g0194 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03710 | hp2 | a0004 | c0006 | t0010 | g0131 | SAS | PJL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03831 | hp1 | a0003 | c0002 | t0001 | g0155 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03834 | hp1 | a0001 | c0005 | t0002 | g0082 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03942 | hp2 | a0002 | c0004 | t0003 | g0203 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04115 | hp1 | a0002 | c0004 | t0003 | g0291 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0347 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04204 | hp1 | a0003 | c0002 | t0001 | g0030 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04228 | hp1 | a0002 | c0004 | t0003 | g0306 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0311 | SAS | STU | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0069 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0290 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18612 | hp1 | a0003 | c0002 | t0001 | g0144 | EAS | CHB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18747 | hp1 | a0003 | c0002 | t0001 | g0004 | EAS | CHB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18747 | hp2 | a0003 | c0002 | t0001 | g0012 | EAS | CHB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18906 | hp2 | a0003 | c0002 | t0001 | g0154 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18940 | hp1 | a0003 | c0002 | t0008 | g0006 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18940 | hp2 | a0002 | c0003 | t0008 | g0286 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18943 | hp1 | a0002 | c0004 | t0003 | g0275 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18944 | hp2 | a0002 | c0004 | t0003 | g0277 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18947 | hp2 | a0003 | c0002 | t0001 | g0189 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18948 | hp1 | a0002 | c0004 | t0003 | g0200 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0273 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18952 | hp2 | a0002 | c0004 | t0003 | g0015 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18953 | hp2 | a0001 | c0001 | t0014 | g0321 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18957 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18962 | hp2 | a0003 | c0002 | t0008 | g0161 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0298 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18966 | hp1 | a0003 | c0002 | t0001 | g0185 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18966 | hp2 | a0002 | c0004 | t0003 | g0303 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18970 | hp2 | a0002 | c0003 | t0004 | g0307 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18971 | hp2 | a0003 | c0002 | t0001 | g0169 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18973 | hp2 | a0003 | c0002 | t0001 | g0005 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18974 | hp2 | a0002 | c0003 | t0004 | g0242 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18975 | hp1 | a0003 | c0002 | t0001 | g0158 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18977 | hp2 | a0002 | c0004 | t0003 | g0084 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18982 | hp2 | a0003 | c0002 | t0008 | g0177 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18983 | hp2 | a0003 | c0002 | t0008 | g0006 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18984 | hp2 | a0003 | c0002 | t0001 | g0182 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18986 | hp2 | a0002 | c0004 | t0003 | g0309 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18990 | hp2 | a0002 | c0003 | t0018 | g0287 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0292 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18993 | hp1 | a0003 | c0002 | t0008 | g0190 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18993 | hp2 | a0001 | c0001 | t0014 | g0336 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18999 | hp1 | a0003 | c0002 | t0001 | g0164 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19002 | hp2 | a0002 | c0003 | t0004 | g0250 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19003 | hp2 | a0002 | c0004 | t0003 | g0259 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19005 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0168 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19012 | hp2 | a0004 | c0006 | t0010 | g0020 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0202 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0356 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19043 | hp2 | a0001 | c0005 | t0005 | g0050 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19054 | hp2 | a0003 | c0002 | t0001 | g0143 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19056 | hp1 | a0003 | c0002 | t0001 | g0012 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19062 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19064 | hp1 | a0002 | c0003 | t0004 | g0281 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19065 | hp1 | a0003 | c0002 | t0008 | g0006 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19065 | hp2 | a0002 | c0004 | t0003 | g0263 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19066 | hp1 | a0003 | c0002 | t0001 | g0163 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19066 | hp2 | a0002 | c0004 | t0003 | g0280 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19067 | hp1 | a0003 | c0002 | t0001 | g0160 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19068 | hp1 | a0003 | c0002 | t0001 | g0156 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19068 | hp2 | a0002 | c0004 | t0003 | g0295 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19070 | hp2 | a0003 | c0002 | t0008 | g0142 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19074 | hp1 | a0002 | c0004 | t0003 | g0258 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19076 | hp2 | a0001 | c0001 | t0029 | g0120 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19077 | hp1 | a0007 | c0008 | t0004 | g0218 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19077 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19081 | hp1 | a0001 | c0001 | t0014 | g0349 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19082 | hp1 | a0002 | c0003 | t0003 | g0274 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19082 | hp2 | a0003 | c0002 | t0001 | g0150 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19086 | hp1 | a0008 | c0012 | t0001 | g0294 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19087 | hp1 | a0002 | c0004 | t0003 | g0304 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19087 | hp2 | a0001 | c0001 | t0021 | g0061 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19090 | hp1 | a0002 | c0003 | t0004 | g0282 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19090 | hp2 | a0003 | c0002 | t0001 | g0172 | EAS | JPT | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0340 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA19240 | hp2 | a0003 | c0002 | t0001 | g0152 | AFR | YRI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20129 | hp1 | a0003 | c0002 | t0001 | g0237 | AFR | ASW | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20129 | hp2 | a0001 | c0001 | t0020 | g0342 | AFR | ASW | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20752 | hp1 | a0003 | c0002 | t0001 | g0001 | EUR | TSI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | TSI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20805 | hp1 | a0003 | c0002 | t0001 | g0166 | EUR | TSI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20805 | hp2 | a0001 | c0001 | t0015 | g0098 | EUR | TSI | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02109 | hp1 | a0003 | c0002 | t0001 | g0032 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02109 | hp2 | a0001 | c0005 | t0005 | g0053 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0115 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02559 | hp1 | a0002 | c0004 | t0003 | g0008 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03471 | hp1 | a0002 | c0004 | t0003 | g0198 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | USA | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | USA | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | USA | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA20300 | hp2 | a0009 | c0007 | t0006 | g0324 | AFR | USA | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA21309 | hp1 | a0004 | c0006 | t0010 | g0129 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0090 | REF | REF | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0251 | REF | REF | THOC5_chr22_29500879_29558757 | THOC5 | chr22 | 29500879 | 29558757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29512083 | C | T | 2 | a0002 a0008 |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
missense_variant | MODERATE | c.1735G>A | p.Val579Ile | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/20 | 1833/4728 | 1735/2052 | 579/683 | chr22 | 29512083 | |||
| chr22:29517044 | T | C | 1 | a0006 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1666A>G | p.Ile556Val | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/20 | 1764/4728 | 1666/2052 | 556/683 | chr22 | 29517044 | |||
| chr22:29517283 | C | T | 3 | a0002 a0003 a0008 |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
missense_variant | MODERATE | c.1573G>A | p.Val525Ile | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 16/20 | 1671/4728 | 1573/2052 | 525/683 | chr22 | 29517283 | |||
| chr22:29517289 | C | T | 1 | a0005 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1567G>A | p.Val523Met | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 16/20 | 1665/4728 | 1567/2052 | 523/683 | chr22 | 29517289 | |||
| chr22:29528135 | G | T | 1 | a0007 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1009C>A | p.Arg337Ser | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/20 | 1107/4728 | 1009/2052 | 337/683 | chr22 | 29528135 | |||
| chr22:29528167 | C | T | 1 | a0009 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.977G>A | p.Arg326Lys | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/20 | 1075/4728 | 977/2052 | 326/683 | chr22 | 29528167 | |||
| chr22:29539391 | T | C | 1 | a0008 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.538A>G | p.Met180Val | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/20 | 636/4728 | 538/2052 | 180/683 | chr22 | 29539391 | |||
| chr22:29544567 | G | C | 1 | a0004 | 5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
missense_variant | MODERATE | c.133C>G | p.Leu45Val | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/20 | 231/4728 | 133/2052 | 45/683 | chr22 | 29544567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29512036 | G | A | 1 | a0001c0005 | 13 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
synonymous_variant | LOW | c.1782C>T | p.Asn594Asn | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/20 | 1880/4728 | 1782/2052 | 594/683 | chr22 | 29512036 | |||
| chr22:29529232 | C | T | 2 | a0002c0003 a0008c0012 |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
synonymous_variant | LOW | c.855G>A | p.Thr285Thr | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/20 | 953/4728 | 855/2052 | 285/683 | chr22 | 29529232 | |||
| chr22:29531928 | T | C | 1 | a0003c0011 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.750A>G | p.Pro250Pro | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/20 | 848/4728 | 750/2052 | 250/683 | chr22 | 29531928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29505898 | T | A | 3 | a0001c0001t0023 a0003c0002t0026 a0004c0006t0010 |
7 | HG00609.hp2 HG02738.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2559A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2559 | chr22 | 29505898 | ||||||
| chr22:29505931 | C | T | 1 | a0001c0001t0020 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2526G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2526 | chr22 | 29505931 | ||||||
| chr22:29506007 | G | A | 7 | a0001c0001t0003 a0001c0001t0017 a0002c0003t0003 others(4): Show |
48 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2450C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2450 | chr22 | 29506007 | ||||||
| chr22:29506048 | C | T | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(8): Show |
45 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2409G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2409 | chr22 | 29506048 | ||||||
| chr22:29506140 | A | G | 14 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0012 others(11): Show |
62 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2317T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2317 | chr22 | 29506140 | ||||||
| chr22:29506203 | A | C | 8 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0017 others(5): Show |
51 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2254T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2254 | chr22 | 29506203 | ||||||
| chr22:29506393 | C | A | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(8): Show |
45 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2064G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 2064 | chr22 | 29506393 | ||||||
| chr22:29506484 | G | A | 2 | a0003c0002t0011 a0003c0002t0024 |
5 | HG00741.hp1 HG01099.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1973C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1973 | chr22 | 29506484 | ||||||
| chr22:29506501 | C | T | 2 | a0002c0003t0008 a0003c0002t0008 |
8 | NA18940.hp1 NA18940.hp2 NA18962.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1956G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1956 | chr22 | 29506501 | ||||||
| chr22:29506669 | T | C | 1 | a0004c0006t0010 | 5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1788A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1788 | chr22 | 29506669 | ||||||
| chr22:29506710 | G | A | 2 | a0001c0001t0006 a0009c0007t0006 |
12 | HG00140.hp1 HG01074.hp2 HG01168.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1747C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1747 | chr22 | 29506710 | ||||||
| chr22:29506782 | A | T | 1 | a0003c0002t0024 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1675 | chr22 | 29506782 | ||||||
| chr22:29506860 | ATTTC | A | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(8): Show |
45 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1593_*1596delGAAA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1593 | chr22 | 29506860 | ||||||
| chr22:29506871 | T | A | 2 | a0003c0002t0011 a0003c0002t0024 |
5 | HG00741.hp1 HG01099.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1586A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1586 | chr22 | 29506871 | ||||||
| chr22:29506931 | G | A | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(8): Show |
45 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1526C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1526 | chr22 | 29506931 | ||||||
| chr22:29507089 | C | G | 3 | a0001c0001t0023 a0003c0002t0026 a0004c0006t0010 |
7 | HG00609.hp2 HG02738.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1368G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1368 | chr22 | 29507089 | ||||||
| chr22:29507128 | T | C | 12 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(9): Show |
46 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1329A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1329 | chr22 | 29507128 | ||||||
| chr22:29507137 | C | G | 1 | a0003c0002t0025 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1320G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1320 | chr22 | 29507137 | ||||||
| chr22:29507218 | C | G | 9 | a0001c0001t0004 a0001c0001t0009 a0002c0003t0004 others(6): Show |
39 | HG00558.hp2 HG00621.hp1 HG00741.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1239G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1239 | chr22 | 29507218 | ||||||
| chr22:29507335 | G | C | 1 | a0001c0001t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1122 | chr22 | 29507335 | ||||||
| chr22:29507343 | A | G | 1 | a0001c0001t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1114 | chr22 | 29507343 | ||||||
| chr22:29507422 | C | T | 1 | a0002c0004t0022 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1035 | chr22 | 29507422 | ||||||
| chr22:29507442 | A | G | 1 | a0001c0001t0021 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1015T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 1015 | chr22 | 29507442 | ||||||
| chr22:29507507 | C | G | 1 | a0001c0001t0020 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*950G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 950 | chr22 | 29507507 | ||||||
| chr22:29507636 | G | T | 1 | a0001c0001t0013 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 821 | chr22 | 29507636 | ||||||
| chr22:29507638 | C | T | 1 | a0001c0001t0019 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 819 | chr22 | 29507638 | ||||||
| chr22:29507639 | G | A | 1 | a0001c0001t0027 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 818 | chr22 | 29507639 | ||||||
| chr22:29507848 | C | T | 2 | a0001c0001t0009 a0003c0002t0009 |
6 | HG02486.hp1 HG02976.hp2 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*609G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 609 | chr22 | 29507848 | ||||||
| chr22:29507902 | G | A | 1 | a0002c0004t0028 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 555 | chr22 | 29507902 | ||||||
| chr22:29508034 | A | G | 1 | a0002c0003t0018 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 423 | chr22 | 29508034 | ||||||
| chr22:29508094 | C | A | 1 | a0001c0001t0029 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 363 | chr22 | 29508094 | ||||||
| chr22:29508154 | C | T | 1 | a0001c0001t0014 | 3 | NA18953.hp2 NA18993.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*303G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 303 | chr22 | 29508154 | ||||||
| chr22:29508365 | G | A | 7 | a0001c0001t0002 a0001c0001t0029 a0001c0001t0030 others(4): Show |
55 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*92C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 92 | chr22 | 29508365 | ||||||
| chr22:29508367 | A | G | 5 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0016 others(2): Show |
25 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*90T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 20/20 | 90 | chr22 | 29508367 | ||||||
| chr22:29553695 | C | G | 1 | a0001c0001t0016 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/20 | 4548 | chr22 | 29553695 | ||||||
| chr22:29553717 | G | A | 1 | a0001c0001t0030 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/20 | 4570 | chr22 | 29553717 | ||||||
| chr22:29553738 | C | A | 1 | a0001c0001t0031 | 1 | HG01361.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/20 | 4591 | chr22 | 29553738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29508530 | T | C | 60 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0118 others(57): Show |
63 | HG00558.hp1 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1989-10A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508530 | |||||||
| chr22:29508671 | G | T | 1 | a0002c0004t0003g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1989-151C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508671 | |||||||
| chr22:29508776 | G | A | 1 | a0003c0002t0001g0169 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1989-256C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508776 | |||||||
| chr22:29508864 | C | T | 1 | a0002c0003t0001g0278 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1989-344G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508864 | |||||||
| chr22:29508956 | C | G | 1 | a0003c0002t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1989-436G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508956 | |||||||
| chr22:29508957 | G | A | 1 | a0003c0002t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1989-437C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508957 | |||||||
| chr22:29508980 | A | G | 2 | a0003c0002t0003g0145 a0003c0002t0003g0181 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1989-460T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29508980 | |||||||
| chr22:29509061 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0002g0003 a0001c0001t0002g0025 others(1): Show |
6 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989-541G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509061 | |||||||
| chr22:29509062 | G | A | 76 | a0001c0001t0001g0320 a0002c0003t0001g0269 a0003c0002t0001g0001 others(73): Show |
89 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1989-542C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509062 | |||||||
| chr22:29509275 | C | CA | 6 | a0001c0001t0001g0352 a0001c0001t0002g0095 a0002c0003t0001g0249 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1989-756dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509275 | |||||||
| chr22:29509275 | CA | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0233 others(4): Show |
7 | HG01517.hp1 HG03041.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1989-756delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509275 | |||||||
| chr22:29509281 | AAAAAAAA others(5): Show |
A | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989-773_1989-762d others(14): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509281 | |||||||
| chr22:29509283 | A | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1989-763T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509283 | |||||||
| chr22:29509288 | A | G | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1989-768T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509288 | |||||||
| chr22:29509339 | G | C | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1989-819C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509339 | |||||||
| chr22:29509388 | A | G | 166 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(163): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1989-868T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509388 | |||||||
| chr22:29509513 | GTTA | G | 4 | a0002c0004t0003g0196 a0002c0004t0003g0203 a0002c0004t0003g0204 others(1): Show |
4 | HG01081.hp2 HG02056.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1989-996_1989-994d others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509513 | |||||||
| chr22:29509608 | TGAGAACA others(43): Show |
T | 1 | a0003c0002t0001g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1989-1138_1989-108 others(54): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509608 | |||||||
| chr22:29509608 | TGAGAACA others(93): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1989-1188_1989-108 others(104): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509608 | |||||||
| chr22:29509620 | G | A | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989-1100C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509620 | |||||||
| chr22:29509640 | T | C | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989-1120A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509640 | |||||||
| chr22:29509640 | TTTAGACT others(93): Show |
T | 29 | a0001c0001t0001g0081 a0001c0001t0001g0217 a0001c0001t0001g0219 others(26): Show |
30 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1989-1220_1989-112 others(104): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509640 | |||||||
| chr22:29509670 | GAGGGAGA others(43): Show |
G | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1989-1200_1989-115 others(54): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509670 | |||||||
| chr22:29509716 | A | C | 1 | a0003c0002t0001g0169 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1989-1196T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509716 | |||||||
| chr22:29509720 | A | G | 62 | a0001c0001t0004g0220 a0001c0001t0004g0235 a0001c0001t0023g0356 others(59): Show |
63 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1989-1200T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509720 | |||||||
| chr22:29509746 | C | G | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1989-1226G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509746 | |||||||
| chr22:29509768 | G | A | 1 | a0002c0003t0001g0297 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1989-1248C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509768 | |||||||
| chr22:29509813 | A | G | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1988+1293T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509813 | |||||||
| chr22:29509962 | G | C | 5 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0045 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+1144C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29509962 | |||||||
| chr22:29510084 | C | G | 1 | a0003c0002t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1988+1022G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510084 | |||||||
| chr22:29510390 | A | G | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1988+716T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510390 | |||||||
| chr22:29510450 | T | C | 5 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0045 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+656A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510450 | |||||||
| chr22:29510464 | G | A | 6 | a0001c0001t0001g0039 a0004c0006t0010g0020 a0004c0006t0010g0129 others(3): Show |
6 | HG00609.hp2 HG02738.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1988+642C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510464 | |||||||
| chr22:29510502 | G | C | 1 | a0003c0002t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1988+604C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510502 | |||||||
| chr22:29510503 | C | G | 1 | a0003c0002t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1988+603G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510503 | |||||||
| chr22:29510696 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1988+410G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510696 | |||||||
| chr22:29510712 | T | C | 177 | a0001c0001t0007g0038 a0001c0001t0023g0356 a0001c0005t0005g0002 others(174): Show |
197 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1988+394A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510712 | |||||||
| chr22:29510796 | C | T | 2 | a0002c0004t0003g0198 a0002c0004t0003g0199 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1988+310G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29510796 | |||||||
| chr22:29511051 | G | C | 2 | a0001c0001t0004g0223 a0001c0001t0004g0234 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1988+55C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29511051 | |||||||
| chr22:29511088 | C | A | 1 | a0003c0002t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1988+18G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 19/19 | chr22 | 29511088 | |||||||
| chr22:29511333 | T | C | 2 | a0002c0003t0001g0270 a0002c0003t0001g0310 |
2 | HG02074.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1798-37A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511333 | |||||||
| chr22:29511384 | G | A | 1 | a0005c0009t0002g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1798-88C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511384 | |||||||
| chr22:29511387 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1798-91G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511387 | |||||||
| chr22:29511387 | C | T | 5 | a0001c0001t0002g0026 a0001c0001t0002g0060 a0001c0001t0002g0103 others(2): Show |
5 | HG01943.hp2 NA18612.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1798-91G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511387 | |||||||
| chr22:29511406 | G | A | 1 | a0001c0001t0012g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1798-110C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511406 | |||||||
| chr22:29511412 | C | T | 66 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0064 others(63): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1798-116G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511412 | |||||||
| chr22:29511481 | C | T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1798-185G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511481 | |||||||
| chr22:29511510 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0064 others(1): Show |
5 | HG00642.hp2 HG01074.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1798-214C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511510 | |||||||
| chr22:29511618 | C | A | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1798-322G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511618 | |||||||
| chr22:29511622 | G | T | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1798-326C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511622 | |||||||
| chr22:29511805 | AG | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0102 |
4 | HG01891.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+215delC | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511805 | |||||||
| chr22:29511807 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0102 |
4 | HG01891.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+214A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511807 | |||||||
| chr22:29511861 | G | T | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1797+160C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511861 | |||||||
| chr22:29511889 | G | A | 1 | a0002c0004t0003g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1797+132C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 18/19 | chr22 | 29511889 | |||||||
| chr22:29512165 | G | T | 166 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(163): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1682-29C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29512165 | |||||||
| chr22:29512379 | G | A | 1 | a0001c0001t0020g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1682-243C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29512379 | |||||||
| chr22:29512530 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1682-394G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29512530 | |||||||
| chr22:29512812 | G | A | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1682-676C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29512812 | |||||||
| chr22:29512860 | G | T | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1682-724C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29512860 | |||||||
| chr22:29513120 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1682-984C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513120 | |||||||
| chr22:29513125 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1682-989G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513125 | |||||||
| chr22:29513146 | C | G | 1 | a0001c0001t0002g0104 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1682-1010G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513146 | |||||||
| chr22:29513208 | G | A | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1682-1072C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513208 | |||||||
| chr22:29513286 | G | A | 1 | a0003c0002t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1682-1150C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513286 | |||||||
| chr22:29513351 | C | T | 3 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0353 |
3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1682-1215G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513351 | |||||||
| chr22:29513356 | C | CA | 71 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0081 others(68): Show |
72 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1682-1221dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513356 | |||||||
| chr22:29513356 | C | CAA | 6 | a0001c0001t0001g0217 a0002c0003t0001g0239 a0002c0003t0001g0262 others(3): Show |
6 | HG02080.hp2 HG02132.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1682-1222_1682-122 others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513356 | |||||||
| chr22:29513356 | CA | C | 40 | a0001c0001t0001g0039 a0001c0001t0017g0054 a0002c0004t0001g0202 others(37): Show |
43 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1682-1221delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513356 | |||||||
| chr22:29513491 | C | T | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1682-1355G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513491 | |||||||
| chr22:29513585 | G | A | 1 | a0001c0001t0020g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1682-1449C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513585 | |||||||
| chr22:29513594 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1682-1458C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513594 | |||||||
| chr22:29513611 | C | G | 2 | a0001c0001t0007g0088 a0001c0001t0007g0315 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1682-1475G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513611 | |||||||
| chr22:29513680 | C | T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1682-1544G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513680 | |||||||
| chr22:29513730 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1682-1594C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513730 | |||||||
| chr22:29513951 | AT | A | 114 | a0001c0001t0002g0059 a0001c0001t0002g0091 a0001c0001t0007g0038 others(111): Show |
130 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1682-1816delA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29513951 | |||||||
| chr22:29514001 | AG | A | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1682-1866delC | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514001 | |||||||
| chr22:29514036 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1682-1900G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514036 | |||||||
| chr22:29514106 | G | A | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1682-1970C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514106 | |||||||
| chr22:29514238 | C | T | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1682-2102G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514238 | |||||||
| chr22:29514315 | A | AT | 62 | a0001c0001t0001g0022 a0001c0001t0001g0221 a0001c0001t0001g0232 others(59): Show |
63 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1682-2180dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514315 | |||||||
| chr22:29514315 | A | ATT | 6 | a0002c0003t0001g0244 a0002c0003t0001g0267 a0002c0003t0001g0271 others(3): Show |
6 | HG02027.hp2 NA18973.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1682-2181_1682-218 others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514315 | |||||||
| chr22:29514315 | AT | A | 10 | a0001c0001t0001g0355 a0001c0001t0004g0215 a0001c0001t0023g0356 others(7): Show |
11 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1682-2180delA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514315 | |||||||
| chr22:29514457 | C | T | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1682-2321G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514457 | |||||||
| chr22:29514562 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1682-2426G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514562 | |||||||
| chr22:29514687 | C | T | 1 | a0001c0001t0023g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1681+2342G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514687 | |||||||
| chr22:29514701 | A | T | 3 | a0001c0001t0007g0088 a0001c0001t0007g0315 a0001c0001t0012g0314 |
3 | HG02145.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1681+2328T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514701 | |||||||
| chr22:29514703 | T | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1681+2326A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514703 | |||||||
| chr22:29514728 | G | A | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1681+2301C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514728 | |||||||
| chr22:29514794 | C | T | 1 | a0002c0003t0004g0250 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1681+2235G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514794 | |||||||
| chr22:29514799 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1681+2230C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514799 | |||||||
| chr22:29514801 | G | A | 115 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(112): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1681+2228C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29514801 | |||||||
| chr22:29515051 | G | T | 2 | a0003c0002t0001g0153 a0003c0002t0001g0192 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1681+1978C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515051 | |||||||
| chr22:29515592 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1681+1437G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515592 | |||||||
| chr22:29515606 | C | G | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1681+1423G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515606 | |||||||
| chr22:29515658 | C | A | 1 | a0003c0011t0004g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1681+1371G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515658 | |||||||
| chr22:29515663 | C | CA | 20 | a0001c0001t0001g0345 a0001c0001t0002g0086 a0001c0001t0002g0226 others(17): Show |
20 | HG01099.hp1 HG01099.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1681+1365dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515663 | |||||||
| chr22:29515955 | A | C | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1681+1074T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29515955 | |||||||
| chr22:29516097 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1681+932G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516097 | |||||||
| chr22:29516147 | G | GA | 81 | a0001c0001t0001g0355 a0001c0001t0002g0018 a0001c0001t0004g0220 others(78): Show |
97 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1681+881dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516147 | |||||||
| chr22:29516147 | GA | G | 44 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0076 others(41): Show |
47 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1681+881delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516147 | |||||||
| chr22:29516147 | GAA | G | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1681+880_1681+881d others(4): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516147 | |||||||
| chr22:29516166 | G | T | 2 | a0003c0002t0001g0143 a0003c0002t0001g0158 |
2 | NA18975.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1681+863C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516166 | |||||||
| chr22:29516170 | A | G | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1681+859T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516170 | |||||||
| chr22:29516441 | A | G | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1681+588T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516441 | |||||||
| chr22:29516520 | C | T | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1681+509G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516520 | |||||||
| chr22:29516686 | A | G | 3 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0353 |
3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1681+343T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516686 | |||||||
| chr22:29516848 | T | C | 17 | a0003c0002t0001g0004 a0003c0002t0001g0007 a0003c0002t0001g0030 others(14): Show |
21 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1681+181A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516848 | |||||||
| chr22:29516896 | G | A | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1681+133C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516896 | |||||||
| chr22:29516926 | C | G | 1 | a0003c0002t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1681+103G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516926 | |||||||
| chr22:29516964 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1681+65G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516964 | |||||||
| chr22:29516979 | T | C | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1681+50A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29516979 | |||||||
| chr22:29517004 | C | T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1681+25G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 17/19 | chr22 | 29517004 | |||||||
| chr22:29517391 | G | A | 2 | a0002c0003t0001g0238 a0002c0003t0001g0256 |
2 | NA18948.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1490-25C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517391 | |||||||
| chr22:29517524 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0003g0108 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1490-158C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517524 | |||||||
| chr22:29517535 | T | C | 5 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0223 others(2): Show |
5 | NA18953.hp1 NA18971.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1490-169A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517535 | |||||||
| chr22:29517583 | T | C | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1490-217A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517583 | |||||||
| chr22:29517630 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG01192.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1490-264T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517630 | |||||||
| chr22:29517753 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0313 others(3): Show |
6 | HG01496.hp1 HG02055.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1490-387C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517753 | |||||||
| chr22:29517812 | A | C | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(322): Show |
350 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1490-446T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517812 | |||||||
| chr22:29517943 | G | A | 2 | a0003c0002t0003g0145 a0003c0002t0003g0181 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1490-577C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29517943 | |||||||
| chr22:29518005 | A | G | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1490-639T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518005 | |||||||
| chr22:29518097 | G | A | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1490-731C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518097 | |||||||
| chr22:29518116 | T | C | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1490-750A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518116 | |||||||
| chr22:29518348 | G | A | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1489+658C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518348 | |||||||
| chr22:29518348 | G | T | 1 | a0004c0006t0010g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1489+658C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518348 | |||||||
| chr22:29518578 | A | C | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1489+428T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518578 | |||||||
| chr22:29518643 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1489+363G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518643 | |||||||
| chr22:29518647 | G | A | 1 | a0002c0004t0003g0305 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1489+359C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518647 | |||||||
| chr22:29518667 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1489+339G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518667 | |||||||
| chr22:29518690 | G | A | 1 | a0003c0002t0001g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1489+316C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518690 | |||||||
| chr22:29518860 | G | C | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1489+146C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 15/19 | chr22 | 29518860 | |||||||
| chr22:29519155 | C | T | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1375-35G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519155 | |||||||
| chr22:29519199 | C | T | 5 | a0002c0003t0004g0242 a0002c0003t0004g0250 a0002c0003t0004g0281 others(2): Show |
5 | NA18970.hp2 NA18974.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-79G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519199 | |||||||
| chr22:29519417 | A | G | 177 | a0001c0001t0007g0038 a0001c0001t0023g0356 a0001c0005t0005g0002 others(174): Show |
197 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1375-297T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519417 | |||||||
| chr22:29519478 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1375-358G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519478 | |||||||
| chr22:29519523 | G | A | 1 | a0002c0004t0001g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1375-403C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519523 | |||||||
| chr22:29519525 | A | T | 6 | a0001c0001t0001g0317 a0001c0001t0001g0330 a0001c0001t0001g0352 others(3): Show |
6 | HG02074.hp1 HG02135.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-405T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519525 | |||||||
| chr22:29519634 | C | CT | 135 | a0001c0001t0001g0217 a0001c0001t0001g0233 a0001c0001t0004g0212 others(132): Show |
149 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1374+373dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519634 | |||||||
| chr22:29519654 | C | T | 1 | a0003c0002t0001g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1374+354G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519654 | |||||||
| chr22:29519704 | C | T | 8 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0195 others(5): Show |
10 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1374+304G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519704 | |||||||
| chr22:29519808 | A | G | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1374+200T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519808 | |||||||
| chr22:29519836 | G | C | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1374+172C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519836 | |||||||
| chr22:29519909 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1374+99A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 14/19 | chr22 | 29519909 | |||||||
| chr22:29520408 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1278-304A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 13/19 | chr22 | 29520408 | |||||||
| chr22:29520480 | G | GT | 6 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0048 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-377dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 13/19 | chr22 | 29520480 | |||||||
| chr22:29520525 | G | C | 1 | a0008c0012t0001g0294 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1278-421C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 13/19 | chr22 | 29520525 | |||||||
| chr22:29520974 | G | A | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1277+24C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 13/19 | chr22 | 29520974 | |||||||
| chr22:29521187 | G | A | 1 | a0002c0004t0003g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1176-88C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521187 | |||||||
| chr22:29521224 | T | C | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1176-125A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521224 | |||||||
| chr22:29521256 | G | T | 1 | a0001c0001t0001g0317 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1176-157C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521256 | |||||||
| chr22:29521628 | G | A | 1 | a0001c0001t0013g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1176-529C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521628 | |||||||
| chr22:29521713 | G | C | 1 | a0001c0001t0020g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1176-614C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521713 | |||||||
| chr22:29521717 | C | T | 1 | a0003c0002t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1176-618G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521717 | |||||||
| chr22:29521734 | G | A | 1 | a0003c0002t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1176-635C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521734 | |||||||
| chr22:29521902 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1176-803C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521902 | |||||||
| chr22:29521982 | C | T | 3 | a0003c0002t0001g0031 a0003c0002t0001g0133 a0003c0002t0001g0162 |
3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1176-883G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521982 | |||||||
| chr22:29521987 | T | A | 1 | a0003c0002t0026g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1176-888A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29521987 | |||||||
| chr22:29522121 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0007g0340 a0001c0001t0007g0341 others(1): Show |
4 | HG01496.hp1 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-1022G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522121 | |||||||
| chr22:29522194 | C | CA | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(110): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1176-1096dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522194 | |||||||
| chr22:29522194 | C | CAA | 8 | a0001c0001t0001g0116 a0001c0001t0002g0003 a0001c0001t0002g0025 others(5): Show |
10 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1176-1097_1176-109 others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522194 | |||||||
| chr22:29522194 | CA | C | 125 | a0002c0003t0001g0014 a0002c0003t0001g0239 a0002c0003t0001g0243 others(122): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1176-1096delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522194 | |||||||
| chr22:29522367 | T | TAAATA | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1176-1273_1176-126 others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522367 | |||||||
| chr22:29522367 | TAAATA | T | 41 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(38): Show |
44 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1176-1273_1176-126 others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522367 | |||||||
| chr22:29522367 | TAAATAAA others(3): Show |
T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1176-1278_1176-126 others(14): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522367 | |||||||
| chr22:29522367 | TAAATAAA others(8): Show |
T | 1 | a0001c0001t0002g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1176-1283_1176-126 others(19): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522367 | |||||||
| chr22:29522493 | C | T | 22 | a0002c0004t0003g0015 a0002c0004t0003g0240 a0002c0004t0003g0241 others(19): Show |
23 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1176-1394G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522493 | |||||||
| chr22:29522565 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1176-1466A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522565 | |||||||
| chr22:29522664 | A | G | 1 | a0002c0003t0001g0299 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1176-1565T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522664 | |||||||
| chr22:29522729 | G | A | 1 | a0003c0002t0001g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1176-1630C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522729 | |||||||
| chr22:29522774 | G | A | 1 | a0003c0002t0001g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1176-1675C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522774 | |||||||
| chr22:29522871 | C | T | 6 | a0003c0002t0001g0165 a0003c0002t0008g0006 a0003c0002t0008g0142 others(3): Show |
8 | HG03654.hp2 NA18940.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1176-1772G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522871 | |||||||
| chr22:29522872 | G | A | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1176-1773C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522872 | |||||||
| chr22:29522892 | T | C | 7 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0002g0124 others(4): Show |
7 | HG01261.hp2 HG01361.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-1793A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522892 | |||||||
| chr22:29522988 | G | A | 1 | a0002c0004t0003g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1176-1889C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29522988 | |||||||
| chr22:29523135 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1176-2036C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523135 | |||||||
| chr22:29523212 | G | A | 166 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(163): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1176-2113C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523212 | |||||||
| chr22:29523344 | T | C | 166 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(163): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1176-2245A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523344 | |||||||
| chr22:29523435 | C | T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1176-2336G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523435 | |||||||
| chr22:29523477 | C | T | 54 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(51): Show |
55 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1175+2361G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523477 | |||||||
| chr22:29523839 | T | C | 3 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0353 |
3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1175+1999A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523839 | |||||||
| chr22:29523841 | T | C | 166 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(163): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1175+1997A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523841 | |||||||
| chr22:29523887 | G | C | 1 | a0004c0006t0010g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1175+1951C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523887 | |||||||
| chr22:29523939 | A | G | 4 | a0001c0001t0006g0016 a0001c0001t0006g0318 a0001c0001t0006g0323 others(1): Show |
5 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175+1899T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29523939 | |||||||
| chr22:29524073 | A | G | 1 | a0002c0003t0001g0288 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1175+1765T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524073 | |||||||
| chr22:29524309 | T | A | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(110): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1175+1529A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524309 | |||||||
| chr22:29524310 | A | G | 2 | a0002c0004t0003g0258 a0002c0004t0003g0275 |
2 | NA18943.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1175+1528T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524310 | |||||||
| chr22:29524511 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1175+1327C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524511 | |||||||
| chr22:29524585 | G | T | 2 | a0002c0003t0001g0268 a0002c0003t0001g0298 |
2 | NA18964.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1175+1253C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524585 | |||||||
| chr22:29524630 | C | T | 1 | a0002c0003t0001g0292 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1175+1208G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524630 | |||||||
| chr22:29524766 | G | A | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1175+1072C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524766 | |||||||
| chr22:29524830 | C | A | 37 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0015 others(34): Show |
40 | HG00642.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175+1008G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524830 | |||||||
| chr22:29524988 | T | C | 13 | a0003c0002t0001g0032 a0003c0002t0001g0137 a0003c0002t0001g0138 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1175+850A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29524988 | |||||||
| chr22:29525026 | A | G | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175+812T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525026 | |||||||
| chr22:29525061 | C | T | 1 | a0001c0001t0027g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1175+777G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525061 | |||||||
| chr22:29525098 | C | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0037 others(43): Show |
48 | HG00558.hp2 HG00621.hp1 HG01192.hp1 others(45): Show |
intron_variant | MODIFIER | c.1175+740G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525098 | |||||||
| chr22:29525268 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1175+570A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525268 | |||||||
| chr22:29525330 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0313 others(3): Show |
6 | HG01496.hp1 HG02055.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175+508G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525330 | |||||||
| chr22:29525349 | T | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0313 |
3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1175+489A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525349 | |||||||
| chr22:29525391 | C | A | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175+447G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525391 | |||||||
| chr22:29525507 | C | G | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175+331G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525507 | |||||||
| chr22:29525652 | A | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0348 |
2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1175+186T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525652 | |||||||
| chr22:29525682 | G | A | 1 | a0002c0004t0003g0306 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1175+156C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525682 | |||||||
| chr22:29525785 | C | A | 1 | a0003c0002t0011g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1175+53G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525785 | |||||||
| chr22:29525806 | G | A | 2 | a0002c0003t0001g0238 a0002c0003t0001g0256 |
2 | NA18948.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1175+32C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 12/19 | chr22 | 29525806 | |||||||
| chr22:29525957 | G | A | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1067-11C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29525957 | |||||||
| chr22:29526053 | CTACTAGG | C | 118 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(115): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1067-114_1067-108d others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526053 | |||||||
| chr22:29526059 | G | A | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1067-113C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526059 | |||||||
| chr22:29526060 | G | C | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1067-114C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526060 | |||||||
| chr22:29526123 | T | C | 1 | a0003c0002t0001g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1067-177A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526123 | |||||||
| chr22:29526158 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1067-212C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526158 | |||||||
| chr22:29526250 | C | T | 1 | a0004c0006t0010g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1067-304G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526250 | |||||||
| chr22:29526281 | C | T | 1 | a0002c0003t0001g0265 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1067-335G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526281 | |||||||
| chr22:29526290 | T | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0064 others(65): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1067-344A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526290 | |||||||
| chr22:29526314 | T | C | 1 | a0001c0001t0020g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1067-368A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526314 | |||||||
| chr22:29526317 | A | G | 1 | a0001c0001t0020g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1067-371T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526317 | |||||||
| chr22:29526401 | G | A | 92 | a0001c0001t0002g0092 a0001c0001t0002g0127 a0002c0003t0001g0014 others(89): Show |
96 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1067-455C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526401 | |||||||
| chr22:29526473 | A | C | 4 | a0004c0006t0010g0020 a0004c0006t0010g0130 a0004c0006t0010g0131 others(1): Show |
4 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-527T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526473 | |||||||
| chr22:29526607 | G | A | 1 | a0003c0002t0024g0141 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1067-661C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526607 | |||||||
| chr22:29526632 | AT | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG01192.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067-687delA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526632 | |||||||
| chr22:29526761 | T | C | 2 | a0002c0004t0003g0033 a0002c0004t0003g0200 |
2 | HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1067-815A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29526761 | |||||||
| chr22:29527095 | A | G | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1066+983T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527095 | |||||||
| chr22:29527367 | C | T | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1066+711G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527367 | |||||||
| chr22:29527422 | A | AAAAC | 13 | a0003c0002t0001g0032 a0003c0002t0001g0137 a0003c0002t0001g0138 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1066+652_1066+655d others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527422 | |||||||
| chr22:29527483 | T | G | 1 | a0007c0008t0004g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1066+595A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527483 | |||||||
| chr22:29527493 | A | C | 1 | a0008c0012t0001g0294 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1066+585T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527493 | |||||||
| chr22:29527667 | T | C | 1 | a0002c0003t0001g0253 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1066+411A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29527667 | |||||||
| chr22:29528026 | G | C | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1066+52C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 11/19 | chr22 | 29528026 | |||||||
| chr22:29528223 | T | C | 91 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.967-46A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 10/19 | chr22 | 29528223 | |||||||
| chr22:29528256 | A | C | 2 | a0003c0002t0001g0237 a0003c0002t0026g0036 |
2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-79T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 10/19 | chr22 | 29528256 | |||||||
| chr22:29528287 | T | C | 3 | a0001c0001t0007g0315 a0001c0001t0012g0314 a0001c0001t0023g0356 |
3 | HG02145.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-110A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 10/19 | chr22 | 29528287 | |||||||
| chr22:29528492 | AGAG | A | 6 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0045 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.926-29_926-27delCT others(1): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29528492 | |||||||
| chr22:29528666 | ATAACTCA others(4): Show |
A | 31 | a0001c0001t0001g0081 a0001c0001t0001g0217 a0001c0001t0001g0219 others(28): Show |
32 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.926-211_926-201del others(11): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29528666 | |||||||
| chr22:29528709 | G | A | 1 | a0002c0003t0001g0292 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.926-243C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29528709 | |||||||
| chr22:29528836 | T | C | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(231): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.925+326A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29528836 | |||||||
| chr22:29528987 | C | T | 3 | a0003c0002t0001g0151 a0003c0002t0001g0152 a0003c0002t0001g0187 |
3 | HG01496.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.925+175G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29528987 | |||||||
| chr22:29529054 | C | G | 3 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0353 |
3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.925+108G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 9/19 | chr22 | 29529054 | |||||||
| chr22:29529295 | T | C | 92 | a0001c0001t0002g0097 a0002c0003t0001g0014 a0002c0003t0001g0238 others(89): Show |
96 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.848-56A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29529295 | |||||||
| chr22:29529307 | A | G | 55 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(52): Show |
56 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.848-68T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29529307 | |||||||
| chr22:29529438 | G | A | 1 | a0001c0001t0012g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.848-199C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29529438 | |||||||
| chr22:29529918 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.848-679C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29529918 | |||||||
| chr22:29530142 | C | CA | 64 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0064 others(61): Show |
67 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.848-904dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29530142 | |||||||
| chr22:29530194 | T | C | 1 | a0001c0001t0006g0333 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.848-955A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29530194 | |||||||
| chr22:29530291 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.848-1052T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29530291 | |||||||
| chr22:29530505 | G | C | 1 | a0003c0002t0008g0161 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.848-1266C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29530505 | |||||||
| chr22:29530738 | T | C | 3 | a0003c0002t0001g0031 a0003c0002t0001g0133 a0003c0002t0001g0162 |
3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.847+1093A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29530738 | |||||||
| chr22:29531005 | A | G | 2 | a0002c0003t0001g0299 a0002c0003t0001g0300 |
2 | HG00558.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.847+826T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531005 | |||||||
| chr22:29531150 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.847+681C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531150 | |||||||
| chr22:29531229 | G | A | 1 | a0003c0002t0001g0148 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.847+602C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531229 | |||||||
| chr22:29531234 | G | A | 39 | a0001c0001t0001g0116 a0001c0001t0002g0003 a0001c0001t0002g0025 others(36): Show |
41 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.847+597C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531234 | |||||||
| chr22:29531252 | G | GT | 98 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0055 others(95): Show |
106 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.847+578dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531252 | |||||||
| chr22:29531254 | G | T | 98 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0055 others(95): Show |
106 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.847+577C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531254 | |||||||
| chr22:29531609 | C | T | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.847+222G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531609 | |||||||
| chr22:29531715 | T | C | 91 | a0001c0001t0004g0214 a0002c0003t0001g0014 a0002c0003t0001g0238 others(88): Show |
95 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.847+116A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 8/19 | chr22 | 29531715 | |||||||
| chr22:29531972 | A | G | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.715-9T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29531972 | |||||||
| chr22:29531978 | C | G | 1 | a0002c0004t0003g0285 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.715-15G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29531978 | |||||||
| chr22:29532101 | C | T | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.715-138G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532101 | |||||||
| chr22:29532112 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.715-149G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532112 | |||||||
| chr22:29532293 | C | A | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.715-330G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532293 | |||||||
| chr22:29532351 | C | T | 1 | a0003c0002t0001g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.715-388G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532351 | |||||||
| chr22:29532391 | T | C | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-428A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532391 | |||||||
| chr22:29532488 | C | A | 118 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(115): Show |
122 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.715-525G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532488 | |||||||
| chr22:29532911 | G | A | 1 | a0002c0004t0003g0305 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.715-948C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532911 | |||||||
| chr22:29532917 | G | A | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.715-954C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532917 | |||||||
| chr22:29532943 | A | G | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.715-980T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532943 | |||||||
| chr22:29532959 | G | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.715-996C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532959 | |||||||
| chr22:29532965 | A | T | 1 | a0002c0004t0003g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.715-1002T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29532965 | |||||||
| chr22:29533250 | G | A | 76 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.715-1287C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533250 | |||||||
| chr22:29533266 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.715-1303G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533266 | |||||||
| chr22:29533267 | G | A | 1 | a0001c0001t0029g0120 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.715-1304C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533267 | |||||||
| chr22:29533550 | A | G | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.715-1587T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533550 | |||||||
| chr22:29533587 | C | T | 6 | a0001c0001t0001g0039 a0004c0006t0010g0020 a0004c0006t0010g0129 others(3): Show |
6 | HG00609.hp2 HG02738.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-1624G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533587 | |||||||
| chr22:29533607 | A | C | 1 | a0003c0002t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-1644T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533607 | |||||||
| chr22:29533638 | G | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.715-1675C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533638 | |||||||
| chr22:29533734 | T | C | 182 | a0001c0001t0001g0039 a0001c0001t0007g0038 a0001c0001t0007g0315 others(179): Show |
202 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.715-1771A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533734 | |||||||
| chr22:29533755 | A | G | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.715-1792T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533755 | |||||||
| chr22:29533789 | A | C | 1 | a0002c0003t0004g0281 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.715-1826T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533789 | |||||||
| chr22:29533851 | A | G | 3 | a0001c0001t0002g0074 a0001c0001t0002g0091 a0001c0001t0002g0105 |
3 | NA18943.hp2 NA18984.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.715-1888T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29533851 | |||||||
| chr22:29534047 | T | G | 1 | a0001c0005t0005g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.715-2084A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534047 | |||||||
| chr22:29534075 | C | T | 182 | a0001c0001t0001g0039 a0001c0001t0007g0038 a0001c0001t0007g0315 others(179): Show |
202 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.715-2112G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534075 | |||||||
| chr22:29534088 | T | C | 32 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0002g0062 others(29): Show |
32 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-2125A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534088 | |||||||
| chr22:29534101 | A | G | 1 | a0001c0001t0012g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715-2138T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534101 | |||||||
| chr22:29534206 | T | C | 76 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.715-2243A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534206 | |||||||
| chr22:29534221 | G | A | 1 | a0002c0004t0003g0285 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.715-2258C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534221 | |||||||
| chr22:29534351 | G | GCTGGTTA others(25): Show |
1 | a0002c0003t0001g0257 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.714+2272_714+2273i others(34): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534351 | |||||||
| chr22:29534513 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.714+2111T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534513 | |||||||
| chr22:29534541 | GT | G | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.714+2082delA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534541 | |||||||
| chr22:29534570 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.714+2054C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534570 | |||||||
| chr22:29534570 | G | C | 1 | a0002c0004t0003g0306 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.714+2054C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534570 | |||||||
| chr22:29534589 | C | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.714+2035G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534589 | |||||||
| chr22:29534726 | G | A | 1 | a0001c0001t0013g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.714+1898C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534726 | |||||||
| chr22:29534747 | G | A | 1 | a0003c0002t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.714+1877C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534747 | |||||||
| chr22:29534864 | C | G | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+1760G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534864 | |||||||
| chr22:29534916 | G | A | 3 | a0001c0001t0007g0038 a0001c0001t0007g0315 a0001c0001t0012g0314 |
3 | HG02145.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.714+1708C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534916 | |||||||
| chr22:29534958 | C | CA | 19 | a0001c0001t0001g0352 a0001c0001t0002g0026 a0001c0001t0002g0094 others(16): Show |
22 | HG00621.hp1 HG01106.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.714+1665dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534958 | |||||||
| chr22:29534958 | C | CAAA | 79 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(76): Show |
83 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.714+1663_714+1665d others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534958 | |||||||
| chr22:29534958 | C | CAAAA | 9 | a0002c0003t0001g0257 a0002c0003t0001g0276 a0002c0003t0001g0283 others(6): Show |
9 | HG01978.hp1 HG02523.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1662_714+1665d others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534958 | |||||||
| chr22:29534990 | C | T | 10 | a0002c0003t0001g0238 a0002c0003t0001g0239 a0002c0003t0001g0253 others(7): Show |
10 | HG02698.hp1 NA18945.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+1634G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534990 | |||||||
| chr22:29534991 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.714+1633C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29534991 | |||||||
| chr22:29535220 | G | A | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.714+1404C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535220 | |||||||
| chr22:29535220 | G | C | 1 | a0002c0004t0003g0277 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.714+1404C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535220 | |||||||
| chr22:29535261 | C | CA | 105 | a0001c0001t0001g0222 a0001c0001t0002g0097 a0001c0001t0002g0112 others(102): Show |
110 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.714+1362dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535261 | |||||||
| chr22:29535261 | C | CAA | 13 | a0001c0001t0001g0334 a0002c0003t0001g0244 a0002c0003t0001g0278 others(10): Show |
13 | HG00597.hp1 HG00735.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.714+1361_714+1362d others(4): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535261 | |||||||
| chr22:29535302 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.714+1322G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535302 | |||||||
| chr22:29535328 | GA | G | 10 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(7): Show |
13 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.714+1295delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535328 | |||||||
| chr22:29535461 | G | C | 1 | a0001c0001t0002g0091 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.714+1163C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535461 | |||||||
| chr22:29535515 | A | G | 1 | a0003c0002t0024g0141 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.714+1109T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535515 | |||||||
| chr22:29535764 | C | T | 2 | a0001c0001t0002g0091 a0001c0001t0002g0105 |
2 | NA18943.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.714+860G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535764 | |||||||
| chr22:29535818 | G | A | 3 | a0001c0001t0007g0340 a0001c0001t0007g0341 a0001c0001t0007g0353 |
3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.714+806C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535818 | |||||||
| chr22:29535923 | C | A | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.714+701G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535923 | |||||||
| chr22:29535923 | C | G | 2 | a0001c0001t0002g0107 a0001c0001t0004g0073 |
2 | HG00280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.714+701G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29535923 | |||||||
| chr22:29536374 | A | C | 3 | a0001c0001t0007g0315 a0001c0001t0012g0314 a0001c0001t0023g0356 |
3 | HG02145.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.714+250T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29536374 | |||||||
| chr22:29536449 | C | A | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+175G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29536449 | |||||||
| chr22:29536539 | G | A | 1 | a0004c0006t0010g0020 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.714+85C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 7/19 | chr22 | 29536539 | |||||||
| chr22:29536847 | A | T | 9 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(6): Show |
9 | HG01496.hp1 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.600-109T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29536847 | |||||||
| chr22:29536870 | T | C | 1 | a0003c0002t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.600-132A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29536870 | |||||||
| chr22:29537000 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.600-262C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537000 | |||||||
| chr22:29537298 | G | A | 27 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0329 others(24): Show |
28 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.600-560C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537298 | |||||||
| chr22:29537351 | C | T | 1 | a0002c0004t0003g0295 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.600-613G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537351 | |||||||
| chr22:29537362 | C | T | 1 | a0003c0002t0001g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.600-624G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537362 | |||||||
| chr22:29537363 | G | A | 1 | a0002c0004t0003g0293 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.600-625C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537363 | |||||||
| chr22:29537368 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.600-630A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537368 | |||||||
| chr22:29537409 | G | A | 5 | a0002c0003t0004g0242 a0002c0003t0004g0250 a0002c0003t0004g0281 others(2): Show |
5 | NA18970.hp2 NA18974.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.600-671C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537409 | |||||||
| chr22:29537583 | C | T | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.600-845G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537583 | |||||||
| chr22:29537638 | T | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.600-900A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537638 | |||||||
| chr22:29537690 | G | A | 3 | a0003c0002t0001g0150 a0003c0002t0001g0173 a0003c0002t0001g0185 |
3 | HG00280.hp1 NA18966.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.600-952C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537690 | |||||||
| chr22:29537751 | G | C | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.600-1013C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537751 | |||||||
| chr22:29537762 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.600-1024G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537762 | |||||||
| chr22:29537774 | C | T | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-1036G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537774 | |||||||
| chr22:29537840 | G | A | 1 | a0001c0001t0031g0358 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.600-1102C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537840 | |||||||
| chr22:29537848 | A | G | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.600-1110T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537848 | |||||||
| chr22:29537886 | T | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.600-1148A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29537886 | |||||||
| chr22:29538273 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.599+1057G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538273 | |||||||
| chr22:29538312 | A | C | 2 | a0001c0001t0001g0338 a0001c0001t0002g0328 |
2 | HG00099.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.599+1018T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538312 | |||||||
| chr22:29538495 | G | A | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.599+835C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538495 | |||||||
| chr22:29538546 | C | G | 1 | a0003c0002t0009g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.599+784G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538546 | |||||||
| chr22:29538558 | G | A | 76 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.599+772C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538558 | |||||||
| chr22:29538582 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+748C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538582 | |||||||
| chr22:29538583 | A | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+747T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538583 | |||||||
| chr22:29538584 | A | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+746T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538584 | |||||||
| chr22:29538585 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+745C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538585 | |||||||
| chr22:29538586 | C | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+744G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538586 | |||||||
| chr22:29538589 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+741C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538589 | |||||||
| chr22:29538590 | G | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+740C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538590 | |||||||
| chr22:29538592 | A | G | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.599+738T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538592 | |||||||
| chr22:29538598 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+732C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538598 | |||||||
| chr22:29538601 | C | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+729G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538601 | |||||||
| chr22:29538603 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+727C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538603 | |||||||
| chr22:29538604 | C | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+726G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538604 | |||||||
| chr22:29538607 | G | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+723C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538607 | |||||||
| chr22:29538608 | G | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+722C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538608 | |||||||
| chr22:29538609 | G | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+721C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538609 | |||||||
| chr22:29538611 | A | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+719T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538611 | |||||||
| chr22:29538612 | A | G | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+718T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538612 | |||||||
| chr22:29538613 | C | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+717G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538613 | |||||||
| chr22:29538614 | A | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+716T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538614 | |||||||
| chr22:29538618 | T | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+712A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538618 | |||||||
| chr22:29538623 | A | T | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+707T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538623 | |||||||
| chr22:29538631 | C | A | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+699G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538631 | |||||||
| chr22:29538647 | A | C | 1 | a0002c0003t0001g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599+683T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538647 | |||||||
| chr22:29538799 | TG | T | 35 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0087 others(32): Show |
35 | HG00280.hp2 HG01081.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.599+530delC | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538799 | |||||||
| chr22:29538800 | G | GA | 67 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0037 others(64): Show |
69 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.599+529_599+530ins others(1): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538800 | G | GAA | 5 | a0001c0001t0001g0055 a0001c0001t0001g0102 a0001c0001t0001g0313 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.599+529_599+530ins others(2): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538800 | G | GAAA | 7 | a0001c0001t0001g0056 a0001c0001t0007g0315 a0001c0001t0012g0314 others(4): Show |
9 | HG02145.hp1 HG03209.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.599+529_599+530ins others(3): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538800 | G | GAAAA | 8 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.599+529_599+530ins others(4): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538800 | GGA | G | 60 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(57): Show |
64 | HG00558.hp1 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.599+528_599+529del others(2): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538800 | GGAA | G | 11 | a0002c0003t0001g0243 a0002c0003t0001g0244 a0002c0003t0001g0247 others(8): Show |
11 | HG00408.hp1 HG00673.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.599+527_599+529del others(3): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538800 | |||||||
| chr22:29538801 | G | A | 240 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(237): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.599+529C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538801 | |||||||
| chr22:29538848 | C | T | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.599+482G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538848 | |||||||
| chr22:29538881 | C | A | 1 | a0003c0002t0001g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.599+449G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29538881 | |||||||
| chr22:29539109 | C | CA | 41 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0056 others(38): Show |
41 | HG00673.hp2 HG01106.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.599+220dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29539109 | |||||||
| chr22:29539128 | A | AG | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.599+201_599+202ins others(1): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29539128 | |||||||
| chr22:29539207 | A | C | 1 | a0003c0002t0009g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.599+123T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 6/19 | chr22 | 29539207 | |||||||
| chr22:29539483 | A | G | 1 | a0003c0002t0001g0186 | 1 | HG01261.hp1 | splice_region_variant&intron_variant | LOW | c.453-7T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29539483 | |||||||
| chr22:29539715 | G | A | 75 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.453-239C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29539715 | |||||||
| chr22:29539784 | G | A | 309 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(306): Show |
334 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.453-308C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29539784 | |||||||
| chr22:29540049 | G | A | 76 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.453-573C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540049 | |||||||
| chr22:29540358 | T | C | 6 | a0001c0001t0007g0088 a0001c0001t0009g0068 a0001c0001t0009g0069 others(3): Show |
6 | HG02486.hp1 HG02630.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-882A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540358 | |||||||
| chr22:29540402 | G | A | 1 | a0001c0001t0012g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.453-926C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540402 | |||||||
| chr22:29540531 | G | T | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.453-1055C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540531 | |||||||
| chr22:29540566 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.453-1090C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540566 | |||||||
| chr22:29540569 | C | T | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.453-1093G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540569 | |||||||
| chr22:29540592 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.453-1116C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540592 | |||||||
| chr22:29540843 | C | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.453-1367G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540843 | |||||||
| chr22:29540845 | G | C | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.453-1369C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540845 | |||||||
| chr22:29540993 | C | G | 324 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(321): Show |
349 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.453-1517G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29540993 | |||||||
| chr22:29541124 | G | A | 3 | a0001c0001t0007g0038 a0001c0001t0007g0315 a0001c0001t0012g0314 |
3 | HG02145.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.453-1648C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541124 | |||||||
| chr22:29541250 | C | A | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.452+1609G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541250 | |||||||
| chr22:29541272 | G | A | 1 | a0001c0001t0004g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.452+1587C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541272 | |||||||
| chr22:29541279 | G | T | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.452+1580C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541279 | |||||||
| chr22:29541395 | T | C | 1 | a0003c0002t0001g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.452+1464A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541395 | |||||||
| chr22:29541403 | A | G | 1 | a0001c0001t0004g0216 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.452+1456T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541403 | |||||||
| chr22:29541446 | T | G | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.452+1413A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541446 | |||||||
| chr22:29541481 | G | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01884.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+1378C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541481 | |||||||
| chr22:29541506 | C | CA | 86 | a0001c0001t0002g0063 a0001c0001t0007g0315 a0001c0001t0012g0314 others(83): Show |
90 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.452+1352dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541506 | |||||||
| chr22:29541506 | CA | C | 85 | a0001c0001t0001g0039 a0001c0001t0001g0338 a0001c0001t0002g0103 others(82): Show |
98 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.452+1352delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541506 | |||||||
| chr22:29541524 | A | G | 2 | a0003c0002t0001g0150 a0003c0002t0001g0185 |
2 | NA18966.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.452+1335T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541524 | |||||||
| chr22:29541619 | T | C | 75 | a0002c0003t0001g0290 a0003c0002t0001g0001 a0003c0002t0001g0004 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.452+1240A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541619 | |||||||
| chr22:29541705 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.452+1154G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541705 | |||||||
| chr22:29541786 | G | C | 1 | a0002c0003t0001g0257 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.452+1073C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541786 | |||||||
| chr22:29541859 | TC | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0322 a0004c0006t0010g0129 |
3 | HG00323.hp1 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.452+999delG | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541859 | |||||||
| chr22:29541860 | CCA | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0316 a0001c0001t0002g0106 others(2): Show |
5 | HG01358.hp2 HG02055.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+997_452+998del others(2): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAA | C | 6 | a0001c0001t0001g0346 a0001c0001t0003g0108 a0001c0001t0003g0347 others(3): Show |
8 | HG02280.hp1 HG02970.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.452+996_452+998del others(3): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAA | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0059 others(5): Show |
8 | HG01167.hp2 HG01517.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.452+995_452+998del others(4): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAA | C | 7 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0002g0067 others(4): Show |
7 | HG01106.hp2 HG01496.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.452+994_452+998del others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAAA | C | 6 | a0001c0001t0004g0228 a0001c0001t0006g0318 a0001c0001t0006g0319 others(3): Show |
6 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.452+993_452+998del others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAAAA | C | 5 | a0001c0001t0001g0337 a0001c0001t0006g0323 a0001c0001t0009g0068 others(2): Show |
5 | HG01070.hp2 HG01256.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+992_452+998del others(7): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAAAA others(1): Show |
C | 5 | a0001c0001t0004g0206 a0001c0001t0004g0213 a0001c0001t0004g0214 others(2): Show |
5 | HG00621.hp1 HG02486.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+991_452+998del others(8): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAAAA others(2): Show |
C | 5 | a0001c0001t0004g0208 a0003c0002t0011g0134 a0003c0002t0011g0179 others(2): Show |
5 | HG01099.hp2 HG01884.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+990_452+998del others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541860 | CCAAAAAA others(3): Show |
C | 1 | a0001c0001t0027g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.452+989_452+998del others(10): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541860 | |||||||
| chr22:29541861 | C | A | 305 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(302): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.452+998G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541861 | |||||||
| chr22:29541869 | AAAAAAAA others(21): Show |
A | 2 | a0001c0001t0013g0035 a0001c0001t0013g0040 |
2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452+962_452+989del others(28): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541869 | |||||||
| chr22:29541871 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0013g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.452+960_452+987del others(28): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541871 | |||||||
| chr22:29541873 | A | T | 88 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(85): Show |
92 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.452+986T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541873 | |||||||
| chr22:29541873 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0010 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452+958_452+985del others(28): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541873 | |||||||
| chr22:29541875 | AAAAAAAA others(21): Show |
A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01884.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+956_452+983del others(28): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541875 | |||||||
| chr22:29541877 | A | T | 88 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(85): Show |
92 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.452+982T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541877 | |||||||
| chr22:29541884 | A | T | 88 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(85): Show |
92 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.452+975T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541884 | |||||||
| chr22:29541885 | A | T | 3 | a0001c0001t0017g0054 a0001c0001t0020g0342 a0004c0006t0010g0129 |
3 | HG02145.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.452+974T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541885 | |||||||
| chr22:29541886 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0344 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.452+958_452+972del others(15): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541886 | |||||||
| chr22:29541887 | A | T | 4 | a0001c0001t0001g0355 a0001c0001t0017g0054 a0001c0001t0020g0342 others(1): Show |
4 | HG02145.hp2 HG03195.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+972T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541887 | |||||||
| chr22:29541887 | AAAAAAAA others(5): Show |
A | 3 | a0003c0002t0001g0007 a0003c0002t0001g0147 a0003c0002t0001g0237 |
3 | HG02015.hp1 HG02293.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.452+960_452+971del others(12): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541887 | |||||||
| chr22:29541888 | AAAAAAAT others(2): Show |
A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0080 a0001c0001t0001g0232 others(4): Show |
7 | HG02155.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.452+962_452+970del others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541888 | |||||||
| chr22:29541888 | AAAAAAAT others(4): Show |
A | 11 | a0001c0001t0007g0038 a0003c0002t0001g0004 a0003c0002t0001g0007 others(8): Show |
13 | HG00741.hp1 HG00741.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.452+960_452+970del others(11): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541888 | |||||||
| chr22:29541888 | AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0023g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452+956_452+970del others(15): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541888 | |||||||
| chr22:29541889 | A | T | 7 | a0001c0001t0001g0313 a0001c0001t0001g0343 a0001c0001t0001g0354 others(4): Show |
7 | HG02145.hp2 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.452+970T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541889 | |||||||
| chr22:29541889 | AAAAAATA others(1): Show |
A | 20 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0075 others(17): Show |
21 | HG00558.hp2 HG01192.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.452+962_452+969del others(8): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541889 | |||||||
| chr22:29541889 | AAAAAATA others(3): Show |
A | 2 | a0003c0002t0001g0001 a0003c0002t0001g0004 |
2 | HG02148.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.452+960_452+969del others(10): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541889 | |||||||
| chr22:29541889 | AAAAAATA others(5): Show |
A | 5 | a0003c0002t0001g0137 a0003c0002t0001g0138 a0003c0002t0001g0153 others(2): Show |
5 | HG02451.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.452+958_452+969del others(12): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541889 | |||||||
| chr22:29541890 | AAAAATAT | A | 13 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0222 others(10): Show |
13 | HG00140.hp2 HG01168.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.452+962_452+968del others(7): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541890 | |||||||
| chr22:29541890 | AAAAATAT others(4): Show |
A | 18 | a0003c0002t0001g0032 a0003c0002t0001g0139 a0003c0002t0001g0140 others(15): Show |
19 | HG00438.hp2 HG00639.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.452+958_452+968del others(11): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541890 | |||||||
| chr22:29541890 | AAAAATAT others(6): Show |
A | 13 | a0002c0003t0001g0014 a0002c0003t0001g0239 a0002c0003t0001g0244 others(10): Show |
13 | HG00558.hp1 HG02132.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.452+956_452+968del others(13): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541890 | |||||||
| chr22:29541891 | A | ATATATAT others(24): Show |
1 | a0001c0001t0007g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.452+967_452+968ins others(31): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541891 | |||||||
| chr22:29541891 | A | T | 9 | a0001c0001t0001g0313 a0001c0001t0001g0343 a0001c0001t0001g0345 others(6): Show |
9 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.452+968T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541891 | |||||||
| chr22:29541891 | AAAATAT | A | 16 | a0001c0001t0001g0317 a0001c0001t0001g0329 a0001c0001t0001g0330 others(13): Show |
16 | HG00140.hp1 HG00408.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.452+962_452+967del others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541891 | |||||||
| chr22:29541891 | AAAATATA others(3): Show |
A | 6 | a0003c0002t0001g0012 a0003c0002t0001g0019 a0003c0002t0001g0160 others(3): Show |
6 | HG02071.hp1 HG02622.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.452+958_452+967del others(10): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541891 | |||||||
| chr22:29541891 | AAAATATA others(7): Show |
A | 1 | a0002c0003t0001g0290 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.452+954_452+967del others(14): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541891 | |||||||
| chr22:29541892 | AAATAT | A | 10 | a0001c0001t0001g0081 a0001c0001t0001g0221 a0001c0001t0001g0334 others(7): Show |
10 | HG00597.hp1 HG01175.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.452+962_452+966del others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541892 | |||||||
| chr22:29541892 | AAATATAT others(4): Show |
A | 16 | a0003c0002t0001g0001 a0003c0002t0001g0005 a0003c0002t0001g0031 others(13): Show |
17 | HG00280.hp1 HG00609.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.452+956_452+966del others(11): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541892 | |||||||
| chr22:29541892 | AAATATAT others(6): Show |
A | 62 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0245 others(59): Show |
63 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.452+954_452+966del others(13): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541892 | |||||||
| chr22:29541893 | A | AAAATATA others(7): Show |
1 | a0001c0001t0012g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.452+965_452+966ins others(14): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541893 | |||||||
| chr22:29541893 | A | T | 15 | a0001c0001t0001g0065 a0001c0001t0001g0313 a0001c0001t0001g0320 others(12): Show |
15 | HG00099.hp2 HG01069.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.452+966T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541893 | |||||||
| chr22:29541893 | AATATAT | A | 28 | a0001c0001t0001g0335 a0001c0001t0002g0003 a0001c0001t0002g0025 others(25): Show |
28 | HG00323.hp2 HG00673.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.452+960_452+965del others(6): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541893 | |||||||
| chr22:29541893 | AATATATA others(3): Show |
A | 10 | a0003c0002t0001g0001 a0003c0002t0001g0012 a0003c0002t0001g0023 others(7): Show |
10 | HG00621.hp2 HG01099.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.452+956_452+965del others(10): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541893 | |||||||
| chr22:29541894 | ATAT | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0002g0003 others(1): Show |
4 | NA18983.hp1 NA18986.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+962_452+964del others(3): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541894 | |||||||
| chr22:29541894 | ATATAT | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0116 others(6): Show |
10 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.452+960_452+964del others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541894 | |||||||
| chr22:29541894 | ATATATAT others(2): Show |
A | 4 | a0003c0002t0001g0001 a0003c0002t0001g0005 a0003c0002t0001g0167 others(1): Show |
5 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+956_452+964del others(9): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541894 | |||||||
| chr22:29541894 | ATATATAT others(6): Show |
A | 14 | a0002c0003t0001g0243 a0002c0003t0001g0249 a0002c0003t0001g0289 others(11): Show |
16 | HG00673.hp1 HG01891.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.452+952_452+964del others(13): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541894 | |||||||
| chr22:29541895 | T | A | 38 | a0001c0001t0001g0064 a0001c0001t0001g0316 a0001c0001t0001g0337 others(35): Show |
39 | HG00621.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.452+964A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541895 | |||||||
| chr22:29541899 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0002g0094 |
2 | HG01106.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.452+960A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541899 | |||||||
| chr22:29541901 | T | A | 6 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0094 others(3): Show |
6 | HG01106.hp1 HG01168.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.452+958A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541901 | |||||||
| chr22:29541903 | T | A | 1 | a0001c0001t0002g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.452+956A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541903 | |||||||
| chr22:29541909 | T | A | 1 | a0002c0004t0028g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.452+950A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29541909 | |||||||
| chr22:29542241 | G | A | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.452+618C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542241 | |||||||
| chr22:29542242 | C | G | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.452+617G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542242 | |||||||
| chr22:29542289 | T | G | 1 | a0001c0001t0006g0339 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.452+570A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542289 | |||||||
| chr22:29542688 | C | T | 87 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(84): Show |
91 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.452+171G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542688 | |||||||
| chr22:29542689 | G | T | 1 | a0002c0003t0001g0257 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.452+170C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542689 | |||||||
| chr22:29542763 | C | CA | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.452+95dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542763 | |||||||
| chr22:29542768 | A | G | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.452+91T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542768 | |||||||
| chr22:29542818 | G | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.452+41C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542818 | |||||||
| chr22:29542820 | A | C | 1 | a0003c0002t0001g0149 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.452+39T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 5/19 | chr22 | 29542820 | |||||||
| chr22:29543347 | C | CA | 57 | a0001c0001t0001g0337 a0001c0001t0002g0096 a0001c0001t0002g0097 others(54): Show |
66 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.354+81dupT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543347 | |||||||
| chr22:29543347 | C | CAA | 8 | a0002c0003t0001g0290 a0003c0002t0001g0140 a0003c0002t0001g0170 others(5): Show |
8 | HG00280.hp1 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.354+80_354+81dupTT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543347 | |||||||
| chr22:29543347 | C | CAAAAAA | 6 | a0001c0005t0005g0002 a0001c0005t0005g0024 a0001c0005t0005g0051 others(3): Show |
8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.354+76_354+81dupTT others(4): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543347 | |||||||
| chr22:29543347 | CA | C | 84 | a0001c0001t0001g0232 a0001c0001t0001g0320 a0001c0001t0002g0121 others(81): Show |
88 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.354+81delT | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543347 | |||||||
| chr22:29543347 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.354+72_354+81delTT others(8): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543347 | |||||||
| chr22:29543390 | G | A | 2 | a0002c0003t0001g0288 a0002c0003t0018g0287 |
2 | NA18947.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.354+39C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543390 | |||||||
| chr22:29543402 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0102 |
2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.354+27C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543402 | |||||||
| chr22:29543425 | C | T | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.354+4G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 4/19 | chr22 | 29543425 | |||||||
| chr22:29543694 | T | C | 310 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(307): Show |
335 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.241-152A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/19 | chr22 | 29543694 | |||||||
| chr22:29544023 | TATCTATC | T | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.240+430_240+436del others(7): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/19 | chr22 | 29544023 | |||||||
| chr22:29544165 | T | C | 1 | a0002c0003t0001g0290 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.240+295A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/19 | chr22 | 29544165 | |||||||
| chr22:29544295 | A | G | 1 | a0003c0002t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.240+165T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/19 | chr22 | 29544295 | |||||||
| chr22:29544407 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.240+53C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 3/19 | chr22 | 29544407 | |||||||
| chr22:29544844 | A | G | 1 | a0003c0002t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.97-241T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29544844 | |||||||
| chr22:29544960 | G | A | 181 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(178): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.97-357C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29544960 | |||||||
| chr22:29545004 | G | A | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.97-401C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545004 | |||||||
| chr22:29545039 | A | G | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-436T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545039 | |||||||
| chr22:29545335 | G | A | 1 | a0003c0002t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-732C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545335 | |||||||
| chr22:29545383 | T | G | 1 | a0003c0011t0004g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97-780A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545383 | |||||||
| chr22:29545568 | C | T | 1 | a0002c0004t0003g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.97-965G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545568 | |||||||
| chr22:29545605 | A | C | 6 | a0003c0002t0001g0137 a0003c0002t0001g0138 a0003c0002t0001g0139 others(3): Show |
6 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-1002T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545605 | |||||||
| chr22:29545948 | G | A | 354 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(351): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.97-1345C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545948 | |||||||
| chr22:29545964 | C | T | 1 | a0003c0002t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-1361G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29545964 | |||||||
| chr22:29546003 | C | T | 1 | a0002c0004t0003g0258 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.97-1400G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546003 | |||||||
| chr22:29546103 | G | A | 3 | a0002c0004t0003g0198 a0002c0004t0003g0199 a0002c0004t0028g0205 |
3 | HG02965.hp2 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.97-1500C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546103 | |||||||
| chr22:29546142 | C | T | 2 | a0002c0004t0003g0033 a0002c0004t0003g0200 |
2 | HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.97-1539G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546142 | |||||||
| chr22:29546219 | G | A | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-1616C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546219 | |||||||
| chr22:29546263 | G | T | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-1660C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546263 | |||||||
| chr22:29546285 | G | A | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.97-1682C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546285 | |||||||
| chr22:29546308 | G | A | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-1705C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546308 | |||||||
| chr22:29546317 | A | G | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-1714T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546317 | |||||||
| chr22:29546409 | T | TTTTTC | 281 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(278): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.97-1811_97-1807dup others(5): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546409 | |||||||
| chr22:29546512 | C | T | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-1909G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546512 | |||||||
| chr22:29546540 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.97-1937G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546540 | |||||||
| chr22:29546552 | TGGAGATT others(3): Show |
T | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-1959_97-1950del others(10): Show |
THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546552 | |||||||
| chr22:29546720 | G | A | 281 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(278): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.97-2117C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546720 | |||||||
| chr22:29546729 | C | T | 4 | a0003c0002t0011g0134 a0003c0002t0011g0135 a0003c0002t0011g0179 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-2126G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546729 | |||||||
| chr22:29546741 | G | C | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.97-2138C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546741 | |||||||
| chr22:29546843 | C | CT | 11 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0195 others(8): Show |
13 | HG01891.hp1 HG02056.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+2208dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546843 | |||||||
| chr22:29546843 | CT | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0338 a0001c0001t0013g0034 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2208delA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29546843 | |||||||
| chr22:29547004 | C | T | 75 | a0002c0003t0001g0290 a0003c0002t0001g0001 a0003c0002t0001g0004 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.96+2048G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547004 | |||||||
| chr22:29547096 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+1956C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547096 | |||||||
| chr22:29547105 | A | G | 1 | a0003c0002t0026g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+1947T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547105 | |||||||
| chr22:29547106 | A | G | 1 | a0003c0002t0026g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+1946T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547106 | |||||||
| chr22:29547108 | T | G | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.96+1944A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547108 | |||||||
| chr22:29547124 | G | A | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.96+1928C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547124 | |||||||
| chr22:29547136 | A | G | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.96+1916T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547136 | |||||||
| chr22:29547152 | T | C | 1 | a0003c0002t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.96+1900A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547152 | |||||||
| chr22:29547157 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0045 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1895T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547157 | |||||||
| chr22:29547222 | T | C | 9 | a0001c0005t0005g0002 a0001c0005t0005g0011 a0001c0005t0005g0024 others(6): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.96+1830A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547222 | |||||||
| chr22:29547249 | T | A | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.96+1803A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547249 | |||||||
| chr22:29547365 | C | CT | 9 | a0002c0003t0001g0238 a0002c0003t0001g0239 a0002c0003t0001g0253 others(6): Show |
9 | HG02698.hp1 NA18948.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1686dupA | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547365 | |||||||
| chr22:29547512 | G | A | 1 | a0001c0001t0009g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.96+1540C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547512 | |||||||
| chr22:29547537 | G | A | 1 | a0001c0001t0016g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.96+1515C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547537 | |||||||
| chr22:29547546 | G | C | 1 | a0001c0001t0006g0339 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.96+1506C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547546 | |||||||
| chr22:29547643 | G | A | 2 | a0003c0002t0001g0175 a0003c0002t0001g0176 |
2 | HG02083.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.96+1409C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547643 | |||||||
| chr22:29547658 | C | T | 1 | a0001c0001t0017g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.96+1394G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547658 | |||||||
| chr22:29547784 | C | A | 1 | a0002c0003t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.96+1268G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547784 | |||||||
| chr22:29547834 | A | T | 1 | a0001c0001t0007g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.96+1218T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547834 | |||||||
| chr22:29547869 | G | A | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.96+1183C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547869 | |||||||
| chr22:29547991 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.96+1061C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29547991 | |||||||
| chr22:29548282 | G | A | 5 | a0001c0001t0002g0026 a0001c0001t0002g0060 a0001c0001t0002g0103 others(2): Show |
5 | HG01943.hp2 NA18612.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+770C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548282 | |||||||
| chr22:29548424 | G | A | 75 | a0002c0003t0001g0290 a0003c0002t0001g0001 a0003c0002t0001g0004 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.96+628C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548424 | |||||||
| chr22:29548469 | C | T | 1 | a0001c0001t0021g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.96+583G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548469 | |||||||
| chr22:29548470 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.96+582C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548470 | |||||||
| chr22:29548534 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.96+518C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548534 | |||||||
| chr22:29548563 | T | A | 119 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(116): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.96+489A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548563 | |||||||
| chr22:29548600 | G | C | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+452C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548600 | |||||||
| chr22:29548812 | T | A | 75 | a0002c0003t0001g0290 a0003c0002t0001g0001 a0003c0002t0001g0004 others(72): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.96+240A>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 2/19 | chr22 | 29548812 | |||||||
| chr22:29549169 | G | A | 1 | a0003c0002t0008g0177 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-11-11C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29549169 | |||||||
| chr22:29549462 | T | C | 1 | a0002c0004t0003g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11-304A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29549462 | |||||||
| chr22:29549470 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01884.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-312A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29549470 | |||||||
| chr22:29550021 | C | G | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-863G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550021 | |||||||
| chr22:29550103 | C | T | 3 | a0001c0001t0002g0231 a0001c0001t0004g0210 a0001c0001t0004g0230 |
3 | HG03239.hp1 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-11-945G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550103 | |||||||
| chr22:29550128 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-11-970C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550128 | |||||||
| chr22:29550249 | T | C | 17 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0002g0109 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-1091A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550249 | |||||||
| chr22:29550448 | G | T | 5 | a0001c0001t0001g0047 a0001c0001t0012g0044 a0001c0001t0012g0045 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-1290C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550448 | |||||||
| chr22:29550450 | T | G | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11-1292A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550450 | |||||||
| chr22:29550490 | T | C | 2 | a0002c0004t0003g0033 a0002c0004t0003g0200 |
2 | HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-11-1332A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550490 | |||||||
| chr22:29550664 | C | T | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11-1506G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550664 | |||||||
| chr22:29550665 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-11-1507C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550665 | |||||||
| chr22:29550700 | C | T | 1 | a0003c0002t0001g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-11-1542G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550700 | |||||||
| chr22:29550928 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-11-1770G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29550928 | |||||||
| chr22:29551213 | C | G | 267 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-11-2055G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551213 | |||||||
| chr22:29551382 | C | T | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0228 |
3 | HG00558.hp2 NA18959.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-11-2224G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551382 | |||||||
| chr22:29551391 | A | G | 267 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-11-2233T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551391 | |||||||
| chr22:29551421 | C | T | 1 | a0003c0002t0001g0133 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-12+2250G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551421 | |||||||
| chr22:29551497 | T | C | 10 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(7): Show |
10 | HG01496.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+2174A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551497 | |||||||
| chr22:29551519 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-12+2152C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551519 | |||||||
| chr22:29551544 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+2127C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551544 | |||||||
| chr22:29551677 | G | A | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-12+1994C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551677 | |||||||
| chr22:29551740 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0004g0227 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-12+1931G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551740 | |||||||
| chr22:29551795 | T | TC | 95 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0043 others(92): Show |
97 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12+1875dupG | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551795 | |||||||
| chr22:29551815 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12+1856T>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551815 | |||||||
| chr22:29551817 | G | A | 13 | a0002c0004t0001g0202 a0002c0004t0003g0008 a0002c0004t0003g0033 others(10): Show |
15 | HG01891.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12+1854C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551817 | |||||||
| chr22:29551833 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0021 |
3 | HG00642.hp2 HG01074.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-12+1838G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551833 | |||||||
| chr22:29551916 | C | T | 119 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(116): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+1755G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551916 | |||||||
| chr22:29551921 | A | G | 267 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-12+1750T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551921 | |||||||
| chr22:29551931 | G | A | 267 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-12+1740C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551931 | |||||||
| chr22:29551933 | G | T | 1 | a0001c0001t0012g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+1738C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551933 | |||||||
| chr22:29551958 | G | A | 1 | a0001c0001t0023g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+1713C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29551958 | |||||||
| chr22:29552021 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0042 others(2): Show |
6 | HG01884.hp2 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+1650C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552021 | |||||||
| chr22:29552029 | G | C | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12+1642C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552029 | |||||||
| chr22:29552055 | A | G | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+1616T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552055 | |||||||
| chr22:29552129 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+1542A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552129 | |||||||
| chr22:29552266 | C | A | 1 | a0002c0003t0001g0310 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-12+1405G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552266 | |||||||
| chr22:29552277 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-12+1394C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552277 | |||||||
| chr22:29552316 | A | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.-12+1355T>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552316 | |||||||
| chr22:29552318 | C | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.-12+1353G>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552318 | |||||||
| chr22:29552358 | G | A | 2 | a0004c0006t0010g0020 a0004c0006t0010g0132 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-12+1313C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552358 | |||||||
| chr22:29552380 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0042 others(5): Show |
9 | HG01884.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+1291T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552380 | |||||||
| chr22:29552393 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-12+1278G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552393 | |||||||
| chr22:29552402 | G | A | 113 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(110): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+1269C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552402 | |||||||
| chr22:29552420 | A | G | 163 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(160): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-12+1251T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552420 | |||||||
| chr22:29552513 | C | T | 76 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12+1158G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552513 | |||||||
| chr22:29552532 | G | C | 5 | a0004c0006t0010g0020 a0004c0006t0010g0129 a0004c0006t0010g0130 others(2): Show |
5 | HG00609.hp2 HG02738.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+1139C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552532 | |||||||
| chr22:29552544 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+1127C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552544 | |||||||
| chr22:29552552 | AG | A | 74 | a0003c0002t0001g0001 a0003c0002t0001g0004 a0003c0002t0001g0005 others(71): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-12+1118delC | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552552 | |||||||
| chr22:29552556 | G | A | 32 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0221 others(29): Show |
33 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(30): Show |
intron_variant | MODIFIER | c.-12+1115C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552556 | |||||||
| chr22:29552560 | C | G | 1 | a0002c0003t0001g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-12+1111G>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552560 | |||||||
| chr22:29552568 | G | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0238 a0002c0003t0001g0239 others(86): Show |
93 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.-12+1103C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552568 | |||||||
| chr22:29552600 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+1071G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552600 | |||||||
| chr22:29552614 | C | T | 1 | a0001c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+1057G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552614 | |||||||
| chr22:29552646 | A | AC | 13 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0004g0206 others(10): Show |
13 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+1024dupG | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552646 | |||||||
| chr22:29552659 | G | A | 1 | a0002c0003t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-12+1012C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552659 | |||||||
| chr22:29552694 | G | C | 32 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0221 others(29): Show |
33 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(30): Show |
intron_variant | MODIFIER | c.-12+977C>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552694 | |||||||
| chr22:29552723 | A | AC | 24 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0316 others(21): Show |
24 | HG00621.hp2 HG00673.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+947dupG | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552723 | |||||||
| chr22:29552762 | G | A | 1 | a0002c0003t0001g0312 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-12+909C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552762 | |||||||
| chr22:29552770 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0021 |
3 | HG00642.hp2 HG01074.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-12+901T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552770 | |||||||
| chr22:29552806 | A | G | 1 | a0004c0006t0010g0020 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-12+865T>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552806 | |||||||
| chr22:29552853 | G | T | 1 | a0003c0002t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-12+818C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552853 | |||||||
| chr22:29552981 | G | A | 1 | a0003c0002t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+690C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29552981 | |||||||
| chr22:29553003 | G | T | 280 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0021 others(277): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-12+668C>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29553003 | |||||||
| chr22:29553109 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+562A>C | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29553109 | |||||||
| chr22:29553117 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-12+554G>A | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29553117 | |||||||
| chr22:29553279 | T | C | 2 | a0001c0001t0007g0315 a0001c0001t0012g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12+392A>G | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29553279 | |||||||
| chr22:29553520 | G | A | 43 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0320 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.-12+151C>T | THOC5 | ENSG00000100296.14 | transcript | ENST00000490103.6 | protein_coding | 1/19 | chr22 | 29553520 |