Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57187 |
| ensemblid | ENSG00000125676.20 |
| hgncid | 19073 |
| symbol | THOC2 |
| name | THO complex subunit 2 |
| refseq_nuc | NM_001081550.2 |
| refseq_prot | NP_001075019.1 |
| ensembl_nuc | ENST00000245838.13 |
| ensembl_prot | ENSP00000245838.8 |
| mane_status | MANE Select |
| chr | chrX |
| start | 123600569 |
| end | 123733052 |
| strand | - |
| ver | v1.2 |
| region | chrX:123600569-123733052 |
| region5000 | chrX:123595569-123738052 |
| regionname0 | THOC2_chrX_123600569_123733052 |
| regionname5000 | THOC2_chrX_123595569_123738052 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1593 | 248 | 69 | 47 | 93 | 11 | 26 | 75 | THOC2_chrX_123595569_123738052 | THOC2 | MAAAA others(1588): Show |
chrX | 123595569 | 123738052 |
| a0002 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | MAAAA others(1588): Show |
chrX | 123595569 | 123738052 |
| a0003 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | MAAAA others(1588): Show |
chrX | 123595569 | 123738052 |
| a0004 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | MAAAA others(1588): Show |
chrX | 123595569 | 123738052 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4779 | 245 | 68 | 46 | 92 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0001c0002 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0001c0005 | 0/0 | 4779 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0001c0007 | 0/0 | 4779 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0002c0006 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0003c0003 | 0/0 | 4779 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 | ||
| a0004c0004 | 0/0 | 4779 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATGGC others(4774): Show |
chrX | 123595569 | 123738052 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5600 | 245 | 68 | 46 | 92 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0001c0002t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0001c0005t0001 | 0/0 | 5600 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0001c0007t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0002c0006t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0003c0003t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| a0004c0004t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | ATCCG others(5595): Show |
chrX | 123595569 | 123738052 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0001c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0002c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| a0004c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0111 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0148 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19074 | hp1 | a0004 | c0004 | t0001 | g0237 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19077 | hp2 | a0001 | c0007 | t0001 | g0061 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | GIH | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0214 | REF | REF | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0142 | REF | REF | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:123621328 | C | T | 1 | a0004 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.4045G>A | p.Ala1349Thr | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/39 | 4075/5600 | 4045/4782 | 1349/1593 | chrX | 123621328 | |||
| chrX:123622783 | T | C | 1 | a0002 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3760A>G | p.Ser1254Gly | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 30/39 | 3790/5600 | 3760/4782 | 1254/1593 | chrX | 123622783 | |||
| chrX:123665767 | C | T | 1 | a0003 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1261G>A | p.Ala421Thr | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/39 | 1291/5600 | 1261/4782 | 421/1593 | chrX | 123665767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:123621329 | G | A | 1 | a0001c0005 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.4044C>T | p.Asn1348Asn | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/39 | 4074/5600 | 4044/4782 | 1348/1593 | chrX | 123621329 | |||
| chrX:123623133 | T | C | 1 | a0001c0007 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.3654A>G | p.Lys1218Lys | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 29/39 | 3684/5600 | 3654/4782 | 1218/1593 | chrX | 123623133 | |||
| chrX:123667141 | C | T | 1 | a0001c0002 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1155G>A | p.Lys385Lys | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/39 | 1185/5600 | 1155/4782 | 385/1593 | chrX | 123667141 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:123601370 | G | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.*19-32C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601370 | |||||||
| chrX:123601485 | AAGGGAGG others(1): Show |
A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*19-155_*19-148del others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601485 | |||||||
| chrX:123601582 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0219 |
2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.*19-244A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601582 | |||||||
| chrX:123601646 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.*19-308G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601646 | |||||||
| chrX:123601723 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*19-385C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601723 | |||||||
| chrX:123601767 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA18988.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.*19-429G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601767 | |||||||
| chrX:123601786 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.*19-448G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601786 | |||||||
| chrX:123602392 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.*19-1054C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602392 | |||||||
| chrX:123602433 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0100 |
2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.*19-1095C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602433 | |||||||
| chrX:123602455 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*19-1117G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602455 | |||||||
| chrX:123602531 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.*19-1193T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602531 | |||||||
| chrX:123602683 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.*19-1345G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602683 | |||||||
| chrX:123602831 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0239 |
3 | NA18957.hp1 NA18987.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.*19-1493G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602831 | |||||||
| chrX:123602845 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*19-1507T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602845 | |||||||
| chrX:123603134 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA18988.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.*19-1796T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603134 | |||||||
| chrX:123603933 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*19-2595T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603933 | |||||||
| chrX:123604026 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*19-2688C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604026 | |||||||
| chrX:123604320 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*19-2982A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604320 | |||||||
| chrX:123604450 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*19-3112C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604450 | |||||||
| chrX:123604742 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*19-3404A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604742 | |||||||
| chrX:123604756 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0031 |
2 | NA18987.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.*19-3418A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604756 | |||||||
| chrX:123605107 | G | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.*19-3769C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605107 | |||||||
| chrX:123605228 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.*19-3890A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605228 | |||||||
| chrX:123605248 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.*19-3910C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605248 | |||||||
| chrX:123605270 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.*19-3932A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605270 | |||||||
| chrX:123605581 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*19-4243A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605581 | |||||||
| chrX:123605612 | C | CA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*19-4275dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605612 | |||||||
| chrX:123605778 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*19-4440T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605778 | |||||||
| chrX:123605907 | TG | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0160 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.*19-4570delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605907 | |||||||
| chrX:123606171 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.*18+4747G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606171 | |||||||
| chrX:123606274 | C | CA | 15 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(12): Show |
15 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.*18+4643dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606274 | |||||||
| chrX:123606286 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0177 |
2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.*18+4632T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606286 | |||||||
| chrX:123606555 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.*18+4363G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606555 | |||||||
| chrX:123607057 | T | TA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*18+3860dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607057 | |||||||
| chrX:123607084 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.*18+3834C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607084 | |||||||
| chrX:123607298 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.*18+3620G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607298 | |||||||
| chrX:123607419 | G | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*18+3499C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607419 | |||||||
| chrX:123607444 | T | TTTTA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0094 others(19): Show |
22 | HG00738.hp1 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.*18+3470_*18+3473d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | |||||||
| chrX:123607444 | T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0128 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.*18+3466_*18+3473d others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | |||||||
| chrX:123607444 | TTTTA | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.*18+3470_*18+3473d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | |||||||
| chrX:123607444 | TTTTATTT others(1): Show |
T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01496.hp1 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*18+3466_*18+3473d others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | |||||||
| chrX:123607444 | TTTTATTT others(13): Show |
T | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*18+3454_*18+3473d others(22): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | |||||||
| chrX:123607530 | C | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0116 others(71): Show |
74 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.*18+3388G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607530 | |||||||
| chrX:123607737 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*18+3181G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607737 | |||||||
| chrX:123607912 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*18+3006G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607912 | |||||||
| chrX:123608362 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.*18+2556A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608362 | |||||||
| chrX:123608417 | A | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(12): Show |
15 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.*18+2501T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608417 | |||||||
| chrX:123608517 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.*18+2401T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608517 | |||||||
| chrX:123608519 | T | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0122 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*18+2399A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608519 | |||||||
| chrX:123608597 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0241 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.*18+2321C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608597 | |||||||
| chrX:123609022 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*18+1896G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609022 | |||||||
| chrX:123609161 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*18+1757C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609161 | |||||||
| chrX:123609378 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*18+1540A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609378 | |||||||
| chrX:123609628 | C | T | 1 | a0004c0004t0001g0237 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.*18+1290G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609628 | |||||||
| chrX:123609795 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*18+1123G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609795 | |||||||
| chrX:123609944 | G | T | 9 | a0001c0001t0001g0132 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.*18+974C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609944 | |||||||
| chrX:123610295 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.*18+613_*18+622del others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610295 | |||||||
| chrX:123610391 | T | TA | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0094 others(8): Show |
11 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.*18+526dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610391 | |||||||
| chrX:123610463 | C | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*18+455G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610463 | |||||||
| chrX:123610724 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.*18+194C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610724 | |||||||
| chrX:123611027 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4755-64A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 37/38 | chrX | 123611027 | |||||||
| chrX:123611364 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4754+76T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 37/38 | chrX | 123611364 | |||||||
| chrX:123611682 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4678-166A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123611682 | |||||||
| chrX:123611779 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4678-263A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123611779 | |||||||
| chrX:123613207 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4677+192G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123613207 | |||||||
| chrX:123613259 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0235 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4677+140G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123613259 | |||||||
| chrX:123613625 | A | G | 1 | a0001c0007t0001g0061 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4519+14T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 35/38 | chrX | 123613625 | |||||||
| chrX:123614552 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-363C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614552 | |||||||
| chrX:123614863 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.4312-674G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614863 | |||||||
| chrX:123614925 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4312-736C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614925 | |||||||
| chrX:123615084 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-895C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615084 | |||||||
| chrX:123615173 | C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4312-984G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615173 | |||||||
| chrX:123615324 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4312-1135G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615324 | |||||||
| chrX:123615348 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-1159G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615348 | |||||||
| chrX:123615469 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4312-1280A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615469 | |||||||
| chrX:123615528 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4312-1339A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615528 | |||||||
| chrX:123615535 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4312-1346C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615535 | |||||||
| chrX:123615644 | C | CA | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
118 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.4312-1456dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615644 | |||||||
| chrX:123615656 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0095 a0001c0001t0001g0100 others(4): Show |
7 | HG00323.hp1 HG02683.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.4312-1467A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615656 | |||||||
| chrX:123615656 | T | TAC | 13 | a0001c0001t0001g0094 a0001c0001t0001g0112 a0001c0001t0001g0132 others(10): Show |
13 | HG01952.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.4312-1469_4312-146 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615656 | |||||||
| chrX:123615658 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4312-1469G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615658 | |||||||
| chrX:123615680 | C | CAA | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4312-1493_4312-149 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615680 | |||||||
| chrX:123616100 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4312-1911G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616100 | |||||||
| chrX:123616190 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4312-2001A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616190 | |||||||
| chrX:123616525 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4312-2336A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616525 | |||||||
| chrX:123616630 | C | CCT | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(1): Show |
4 | HG00280.hp1 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4312-2443_4312-244 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616630 | |||||||
| chrX:123616680 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4312-2491A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616680 | |||||||
| chrX:123616728 | C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4312-2539G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616728 | |||||||
| chrX:123616803 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0089 |
2 | HG00438.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4311+2598A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616803 | |||||||
| chrX:123617372 | T | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0210 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4311+2029A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123617372 | |||||||
| chrX:123618187 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4311+1214A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618187 | |||||||
| chrX:123618195 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 |
3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4311+1206A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618195 | |||||||
| chrX:123618877 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4311+524T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618877 | |||||||
| chrX:123619030 | C | G | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4311+371G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619030 | |||||||
| chrX:123619035 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4311+366A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619035 | |||||||
| chrX:123619036 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4311+365C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619036 | |||||||
| chrX:123619095 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4311+306T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619095 | |||||||
| chrX:123619097 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01496.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.4311+304C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619097 | |||||||
| chrX:123619141 | T | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.4311+260A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619141 | |||||||
| chrX:123619269 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4311+132A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619269 | |||||||
| chrX:123619537 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4276-101A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 32/38 | chrX | 123619537 | |||||||
| chrX:123620506 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4275+401A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 32/38 | chrX | 123620506 | |||||||
| chrX:123621127 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4216+30C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/38 | chrX | 123621127 | |||||||
| chrX:123621931 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3786-344C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 30/38 | chrX | 123621931 | |||||||
| chrX:123623034 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3682+71A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 29/38 | chrX | 123623034 | |||||||
| chrX:123623501 | C | CT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.3504-219dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 28/38 | chrX | 123623501 | |||||||
| chrX:123624678 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.3058-9C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123624678 | |||||||
| chrX:123624961 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3058-292A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123624961 | |||||||
| chrX:123625115 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3058-446A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625115 | |||||||
| chrX:123625187 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0090 |
2 | NA18612.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3058-518C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625187 | |||||||
| chrX:123625520 | CT | C | 7 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0144 others(4): Show |
7 | HG01168.hp1 HG01256.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3057+391delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625520 | |||||||
| chrX:123625720 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3057+192T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625720 | |||||||
| chrX:123627033 | A | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2758-371T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627033 | |||||||
| chrX:123627099 | A | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2758-437T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627099 | |||||||
| chrX:123627186 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2757+507G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627186 | |||||||
| chrX:123627277 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2757+416G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627277 | |||||||
| chrX:123627506 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0164 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2757+187A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627506 | |||||||
| chrX:123627535 | C | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2757+158G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627535 | |||||||
| chrX:123628116 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2482-148A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628116 | |||||||
| chrX:123628170 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2482-202A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628170 | |||||||
| chrX:123628282 | T | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-314A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628282 | |||||||
| chrX:123628722 | T | TA | 8 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0147 others(5): Show |
8 | HG01978.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-755dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628722 | |||||||
| chrX:123628722 | TA | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0066 others(7): Show |
10 | HG00323.hp2 HG01074.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.2482-755delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628722 | |||||||
| chrX:123628945 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0221 |
2 | NA18959.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.2482-977A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628945 | |||||||
| chrX:123629139 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-1171T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629139 | |||||||
| chrX:123629206 | A | AAC | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(52): Show |
55 | HG00741.hp1 HG01074.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.2482-1240_2482-123 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACAC | 30 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0060 others(27): Show |
30 | HG00438.hp2 HG00673.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2482-1242_2482-123 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACAC | 18 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0069 others(15): Show |
18 | HG00735.hp2 HG01167.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.2482-1244_2482-123 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACACA others(1): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(38): Show |
41 | HG01258.hp1 HG01934.hp1 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.2482-1246_2482-123 others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACACA others(3): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(23): Show |
26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2482-1248_2482-123 others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACACA others(5): Show |
19 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
19 | HG00140.hp1 HG00438.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.2482-1250_2482-123 others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACACA others(7): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0001g0096 |
3 | HG00621.hp1 HG03195.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2482-1252_2482-123 others(18): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | A | AACACACA others(9): Show |
1 | a0001c0001t0001g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2482-1254_2482-123 others(20): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | AAC | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0122 others(10): Show |
13 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2482-1240_2482-123 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | AACAC | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 others(5): Show |
8 | HG01243.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-1242_2482-123 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | AACACAC | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0161 |
2 | HG01106.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2482-1244_2482-123 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629206 | AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2482-1252_2482-123 others(18): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | |||||||
| chrX:123629246 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0025 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2482-1279_2482-127 others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629246 | |||||||
| chrX:123629248 | T | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0203 a0001c0001t0001g0248 |
3 | HG02148.hp2 HG02630.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2482-1280A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629248 | |||||||
| chrX:123629653 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2482-1685C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629653 | |||||||
| chrX:123629923 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1765C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629923 | |||||||
| chrX:123630387 | C | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+1301G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630387 | |||||||
| chrX:123630612 | C | CA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(82): Show |
85 | HG01069.hp1 HG01099.hp1 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.2481+1075dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | |||||||
| chrX:123630612 | C | CAA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0078 others(13): Show |
16 | HG00438.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2481+1074_2481+107 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | |||||||
| chrX:123630612 | CA | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0152 others(3): Show |
6 | HG00639.hp1 HG01168.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+1075delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | |||||||
| chrX:123630612 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2481+1065_2481+107 others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | |||||||
| chrX:123630706 | C | A | 9 | a0001c0001t0001g0132 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2481+982G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630706 | |||||||
| chrX:123631072 | C | G | 74 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0127 others(71): Show |
74 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.2481+616G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631072 | |||||||
| chrX:123631217 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2481+471A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631217 | |||||||
| chrX:123631267 | C | T | 9 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0215 others(6): Show |
9 | NA18943.hp1 NA18957.hp1 NA18987.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+421G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631267 | |||||||
| chrX:123631598 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+90G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631598 | |||||||
| chrX:123631899 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2317-47A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123631899 | |||||||
| chrX:123632297 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2317-445C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632297 | |||||||
| chrX:123632319 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2317-467G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632319 | |||||||
| chrX:123632401 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2316+460A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632401 | |||||||
| chrX:123632489 | C | CA | 8 | a0001c0001t0001g0134 a0001c0001t0001g0165 a0001c0001t0001g0188 others(5): Show |
8 | HG00438.hp2 HG01928.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2316+371dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | |||||||
| chrX:123632489 | CA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2316+371delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | |||||||
| chrX:123632489 | CAA | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
24 | HG01099.hp1 HG01106.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2316+370_2316+371d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | |||||||
| chrX:123632587 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0200 a0001c0001t0001g0220 |
3 | HG02148.hp1 NA18942.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2316+274G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632587 | |||||||
| chrX:123632692 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2316+169A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632692 | |||||||
| chrX:123633081 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2137-41A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633081 | |||||||
| chrX:123633341 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2137-301C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633341 | |||||||
| chrX:123633346 | A | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2137-306T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633346 | |||||||
| chrX:123633362 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2137-322A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633362 | |||||||
| chrX:123633411 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2137-371A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633411 | |||||||
| chrX:123633489 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2137-449C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633489 | |||||||
| chrX:123634432 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2019-362T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634432 | |||||||
| chrX:123634631 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2019-561A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634631 | |||||||
| chrX:123635103 | G | GT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0019 others(3): Show |
6 | HG01978.hp2 HG02293.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018+975dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635103 | |||||||
| chrX:123635343 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2018+736T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635343 | |||||||
| chrX:123635346 | GT | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0211 |
3 | NA19002.hp2 NA19068.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2018+732delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635346 | |||||||
| chrX:123636473 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0241 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1922-298C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636473 | |||||||
| chrX:123636593 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1922-418G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636593 | |||||||
| chrX:123636944 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1922-769C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636944 | |||||||
| chrX:123637140 | G | A | 9 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0215 others(6): Show |
9 | NA18943.hp1 NA18957.hp1 NA18987.hp1 others(6): Show |
intron_variant | MODIFIER | c.1921+903C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637140 | |||||||
| chrX:123637223 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1921+820A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637223 | |||||||
| chrX:123637238 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1921+805G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637238 | |||||||
| chrX:123637263 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1921+780C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637263 | |||||||
| chrX:123637365 | CAA | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 |
3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1921+676_1921+677d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637365 | |||||||
| chrX:123637497 | A | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921+546T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637497 | |||||||
| chrX:123638666 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1840+268G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638666 | |||||||
| chrX:123638668 | A | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1840+266T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638668 | |||||||
| chrX:123638726 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1840+208C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638726 | |||||||
| chrX:123638727 | T | TAC | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1840+205_1840+206d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638727 | |||||||
| chrX:123638727 | TAC | T | 15 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(12): Show |
15 | HG01192.hp1 HG01346.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1840+205_1840+206d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638727 | |||||||
| chrX:123638750 | A | ACT | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840+182_1840+183d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | |||||||
| chrX:123638750 | A | ACTCT | 3 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1840+180_1840+183d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | |||||||
| chrX:123638750 | A | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0069 others(2): Show |
5 | HG02602.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1840+184T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | |||||||
| chrX:123638764 | T | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1840+170A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638764 | |||||||
| chrX:123638767 | C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1840+167G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638767 | |||||||
| chrX:123638769 | T | C | 2 | a0001c0001t0001g0051 a0001c0005t0001g0111 |
2 | HG01496.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1840+165A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | |||||||
| chrX:123638769 | T | TAC | 15 | a0001c0001t0001g0028 a0001c0001t0001g0108 a0001c0001t0001g0109 others(12): Show |
15 | HG01099.hp1 HG01106.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1840+163_1840+164d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | |||||||
| chrX:123638769 | TAC | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG01175.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1840+163_1840+164d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | |||||||
| chrX:123639154 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1747-127A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639154 | |||||||
| chrX:123639486 | G | C | 6 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-459C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639486 | |||||||
| chrX:123639499 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1747-472A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639499 | |||||||
| chrX:123639646 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(35): Show |
38 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.1747-619C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639646 | |||||||
| chrX:123639790 | C | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1746+748G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639790 | |||||||
| chrX:123639991 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1746+547C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639991 | |||||||
| chrX:123640004 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1746+534C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640004 | |||||||
| chrX:123640044 | A | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1746+494T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640044 | |||||||
| chrX:123640060 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1746+478C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640060 | |||||||
| chrX:123640127 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1746+411G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640127 | |||||||
| chrX:123640287 | A | ACCT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1746+250_1746+251i others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640287 | |||||||
| chrX:123640315 | T | C | 1 | a0004c0004t0001g0237 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1746+223A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640315 | |||||||
| chrX:123640333 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1746+205T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640333 | |||||||
| chrX:123640457 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1746+81G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640457 | |||||||
| chrX:123640700 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1662-78C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123640700 | |||||||
| chrX:123641033 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1662-411A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641033 | |||||||
| chrX:123641104 | A | AAT | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662-483_1662-482i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641104 | |||||||
| chrX:123641370 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1662-748A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641370 | |||||||
| chrX:123641436 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1662-814G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641436 | |||||||
| chrX:123642087 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662-1465G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642087 | |||||||
| chrX:123642099 | T | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1662-1477A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642099 | |||||||
| chrX:123642164 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662-1542C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642164 | |||||||
| chrX:123642219 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1662-1597A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642219 | |||||||
| chrX:123642286 | T | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662-1664A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642286 | |||||||
| chrX:123642380 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0055 |
3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1662-1758C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642380 | |||||||
| chrX:123642386 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662-1764G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642386 | |||||||
| chrX:123642429 | C | CA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0081 others(3): Show |
6 | HG00438.hp1 HG02074.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662-1808dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642429 | |||||||
| chrX:123642447 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1662-1825A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642447 | |||||||
| chrX:123642883 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1661+1692A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642883 | |||||||
| chrX:123643220 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1661+1355G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643220 | |||||||
| chrX:123643584 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1661+991A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643584 | |||||||
| chrX:123644490 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1661+85G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123644490 | |||||||
| chrX:123644500 | G | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1661+75C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123644500 | |||||||
| chrX:123645053 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1429-144C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 13/38 | chrX | 123645053 | |||||||
| chrX:123645106 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1429-197C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 13/38 | chrX | 123645106 | |||||||
| chrX:123645690 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1387-315C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645690 | |||||||
| chrX:123645700 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0141 a0001c0001t0001g0168 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-325C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645700 | |||||||
| chrX:123645737 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1387-362T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645737 | |||||||
| chrX:123645835 | A | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-460T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645835 | |||||||
| chrX:123645949 | C | CA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1387-575dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645949 | |||||||
| chrX:123646051 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1387-676A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646051 | |||||||
| chrX:123646265 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1387-890G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646265 | |||||||
| chrX:123646460 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0057 |
2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1387-1085C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646460 | |||||||
| chrX:123646532 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0094 |
3 | HG02622.hp1 HG03471.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1387-1157G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646532 | |||||||
| chrX:123646686 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1387-1311A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646686 | |||||||
| chrX:123647056 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1387-1681A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647056 | |||||||
| chrX:123647356 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1387-1981C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647356 | |||||||
| chrX:123647445 | G | GCATT | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1387-2074_1387-207 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647445 | |||||||
| chrX:123647522 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-2147T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647522 | |||||||
| chrX:123647770 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-2395C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647770 | |||||||
| chrX:123647771 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-2396C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647771 | |||||||
| chrX:123647840 | C | CA | 67 | a0001c0001t0001g0116 a0001c0001t0001g0126 a0001c0001t0001g0127 others(64): Show |
67 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1387-2466dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | |||||||
| chrX:123647840 | CA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1387-2466delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | |||||||
| chrX:123647840 | CAA | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0062 a0001c0001t0001g0095 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1387-2467_1387-246 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | |||||||
| chrX:123647840 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-2478_1387-246 others(17): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | |||||||
| chrX:123647940 | G | A | 11 | a0001c0001t0001g0132 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG01167.hp1 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387-2565C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647940 | |||||||
| chrX:123647986 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1387-2611G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647986 | |||||||
| chrX:123648280 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1387-2905A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648280 | |||||||
| chrX:123648420 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
128 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1387-3045A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648420 | |||||||
| chrX:123648456 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | NA18971.hp1 NA19007.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-3081C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648456 | |||||||
| chrX:123648601 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0177 |
2 | NA18985.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1387-3226C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648601 | |||||||
| chrX:123649017 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-3642G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649017 | |||||||
| chrX:123649081 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1387-3706C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649081 | |||||||
| chrX:123649586 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1387-4211T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649586 | |||||||
| chrX:123649974 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1387-4599A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649974 | |||||||
| chrX:123650101 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-4726G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650101 | |||||||
| chrX:123650164 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-4789T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650164 | |||||||
| chrX:123650170 | AG | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01358.hp1 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1387-4796delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650170 | |||||||
| chrX:123650661 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1387-5286A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650661 | |||||||
| chrX:123650675 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0221 |
2 | NA18959.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1387-5300C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650675 | |||||||
| chrX:123651057 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(7): Show |
10 | HG01891.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1387-5682G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651057 | |||||||
| chrX:123651126 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-5751T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651126 | |||||||
| chrX:123651421 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1387-6046A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651421 | |||||||
| chrX:123651539 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-6164A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651539 | |||||||
| chrX:123651674 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1387-6299C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651674 | |||||||
| chrX:123651708 | A | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1387-6333T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651708 | |||||||
| chrX:123651725 | G | GC | 12 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0088 others(9): Show |
12 | HG01081.hp2 HG01496.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1387-6351dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651725 | |||||||
| chrX:123651727 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1387-6352G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651727 | |||||||
| chrX:123651730 | C | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-6355G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651730 | |||||||
| chrX:123651731 | C | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1387-6356G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651731 | |||||||
| chrX:123651732 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1387-6357G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651732 | |||||||
| chrX:123651733 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1387-6358G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651733 | |||||||
| chrX:123652013 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1387-6638A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652013 | |||||||
| chrX:123652040 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-6665A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652040 | |||||||
| chrX:123652104 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1387-6729G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652104 | |||||||
| chrX:123652354 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387-6979G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652354 | |||||||
| chrX:123652714 | T | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0160 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-7339A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652714 | |||||||
| chrX:123652761 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1387-7386T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652761 | |||||||
| chrX:123652827 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1387-7452T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652827 | |||||||
| chrX:123653011 | C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1387-7636G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653011 | |||||||
| chrX:123653143 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1387-7768C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653143 | |||||||
| chrX:123653296 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-7921C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653296 | |||||||
| chrX:123653679 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1387-8304C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653679 | |||||||
| chrX:123653968 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1387-8593G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653968 | |||||||
| chrX:123654186 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1387-8811C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654186 | |||||||
| chrX:123654236 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1387-8861G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654236 | |||||||
| chrX:123654313 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-8938C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654313 | |||||||
| chrX:123654494 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 |
3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1387-9119G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654494 | |||||||
| chrX:123654627 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1387-9252G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654627 | |||||||
| chrX:123654630 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387-9255C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654630 | |||||||
| chrX:123654758 | C | CA | 75 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0055 others(72): Show |
75 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.1387-9384dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | |||||||
| chrX:123654758 | C | CAA | 6 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0200 others(3): Show |
6 | HG01516.hp1 HG02056.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-9385_1387-938 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | |||||||
| chrX:123654758 | CA | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1387-9384delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | |||||||
| chrX:123654758 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1387-9394_1387-938 others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | |||||||
| chrX:123655026 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1387-9651C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655026 | |||||||
| chrX:123655206 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0203 |
2 | HG01106.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1387-9831G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655206 | |||||||
| chrX:123655292 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1387-9917A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655292 | |||||||
| chrX:123655996 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1386+9646C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655996 | |||||||
| chrX:123656020 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1386+9622T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656020 | |||||||
| chrX:123656051 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1386+9591C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656051 | |||||||
| chrX:123656330 | T | TA | 8 | a0001c0001t0001g0055 a0001c0001t0001g0079 a0001c0001t0001g0140 others(5): Show |
8 | HG00741.hp2 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+9311dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | |||||||
| chrX:123656330 | TA | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0025 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1386+9311delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | |||||||
| chrX:123656352 | A | AG | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1386+9289_1386+929 others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656352 | |||||||
| chrX:123656420 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1386+9222G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656420 | |||||||
| chrX:123656462 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1386+9180T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656462 | |||||||
| chrX:123656660 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1386+8982C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656660 | |||||||
| chrX:123656723 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386+8919G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656723 | |||||||
| chrX:123656813 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+8829A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656813 | |||||||
| chrX:123656853 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0218 a0001c0001t0001g0226 |
3 | HG00738.hp1 NA18952.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1386+8789A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656853 | |||||||
| chrX:123656941 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1386+8701G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656941 | |||||||
| chrX:123656946 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+8696C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656946 | |||||||
| chrX:123657029 | A | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1386+8613T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657029 | |||||||
| chrX:123657379 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG02896.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1386+8263C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657379 | |||||||
| chrX:123657431 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+8211T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657431 | |||||||
| chrX:123657437 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1386+8205A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657437 | |||||||
| chrX:123657644 | T | TA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1386+7997dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657644 | |||||||
| chrX:123657960 | CGT | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(65): Show |
68 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1386+7680_1386+768 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123657960 | CGTGT | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
65 | HG00438.hp1 HG00438.hp2 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.1386+7678_1386+768 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123657960 | CGTGTGT | C | 72 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(69): Show |
72 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.1386+7676_1386+768 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123657960 | CGTGTGTG others(1): Show |
C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1386+7674_1386+768 others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123657960 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1386+7672_1386+768 others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123657960 | CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+7660_1386+768 others(26): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | |||||||
| chrX:123658175 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1386+7467G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658175 | |||||||
| chrX:123658244 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1386+7398G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658244 | |||||||
| chrX:123658568 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1386+7074T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658568 | |||||||
| chrX:123658873 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1386+6769T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658873 | |||||||
| chrX:123658896 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1386+6746C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658896 | |||||||
| chrX:123659142 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+6500G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659142 | |||||||
| chrX:123659261 | G | A | 10 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG00323.hp2 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+6381C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659261 | |||||||
| chrX:123659262 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386+6380C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659262 | |||||||
| chrX:123659311 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1386+6331C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659311 | |||||||
| chrX:123659347 | C | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1386+6295G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659347 | |||||||
| chrX:123659447 | T | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1386+6195A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659447 | |||||||
| chrX:123659502 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+6140G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659502 | |||||||
| chrX:123659546 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1386+6096C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659546 | |||||||
| chrX:123659556 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0160 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+6086G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659556 | |||||||
| chrX:123659565 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+6077C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659565 | |||||||
| chrX:123659663 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+5979T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659663 | |||||||
| chrX:123660111 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1386+5531A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660111 | |||||||
| chrX:123660220 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1386+5422C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660220 | |||||||
| chrX:123660301 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0106 |
2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1386+5341C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660301 | |||||||
| chrX:123660656 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+4986G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660656 | |||||||
| chrX:123660787 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1386+4855G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660787 | |||||||
| chrX:123661127 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1386+4515C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661127 | |||||||
| chrX:123661273 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1386+4369G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661273 | |||||||
| chrX:123661298 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1386+4344C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661298 | |||||||
| chrX:123661360 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+4282C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661360 | |||||||
| chrX:123661361 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0235 a0001c0001t0001g0250 |
3 | HG01515.hp1 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1386+4281G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661361 | |||||||
| chrX:123661439 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+4203G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661439 | |||||||
| chrX:123661559 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+4083C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661559 | |||||||
| chrX:123661597 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1386+4045G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661597 | |||||||
| chrX:123661649 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1386+3993A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661649 | |||||||
| chrX:123661718 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1386+3924A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661718 | |||||||
| chrX:123661737 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+3905A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661737 | |||||||
| chrX:123661753 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1386+3889C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661753 | |||||||
| chrX:123662079 | T | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1386+3563A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662079 | |||||||
| chrX:123662132 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1386+3510G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662132 | |||||||
| chrX:123662312 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1386+3330G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662312 | |||||||
| chrX:123662313 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1386+3329C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662313 | |||||||
| chrX:123662368 | C | T | 22 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0139 others(19): Show |
22 | HG00438.hp2 HG01928.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1386+3274G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662368 | |||||||
| chrX:123662402 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1386+3240G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662402 | |||||||
| chrX:123662582 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1386+3060G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662582 | |||||||
| chrX:123662587 | C | CA | 17 | a0001c0001t0001g0116 a0001c0001t0001g0128 a0001c0001t0001g0138 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1386+3054dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662587 | |||||||
| chrX:123662587 | CA | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1386+3054delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662587 | |||||||
| chrX:123662598 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1386+3044T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662598 | |||||||
| chrX:123663531 | A | AT | 8 | a0001c0001t0001g0093 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
8 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2110dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663531 | |||||||
| chrX:123663538 | T | TA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1386+2103dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | |||||||
| chrX:123663538 | T | TAA | 32 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(29): Show |
32 | HG00621.hp1 HG01978.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.1386+2102_1386+210 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | |||||||
| chrX:123663539 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+2103T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663539 | |||||||
| chrX:123663784 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1386+1858G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663784 | |||||||
| chrX:123663795 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+1847C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663795 | |||||||
| chrX:123663847 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1386+1795T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663847 | |||||||
| chrX:123664111 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0168 a0001c0001t0001g0247 |
3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1386+1531A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664111 | |||||||
| chrX:123664138 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1386+1504T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664138 | |||||||
| chrX:123665125 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(61): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1386+517G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665125 | |||||||
| chrX:123665299 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1386+343G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665299 | |||||||
| chrX:123665513 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1386+129G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665513 | |||||||
| chrX:123665576 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 |
3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1386+66T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665576 | |||||||
| chrX:123665865 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1191-28T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665865 | |||||||
| chrX:123665899 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1191-62A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665899 | |||||||
| chrX:123665910 | A | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0087 |
2 | NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1191-73T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665910 | |||||||
| chrX:123665945 | A | ATCAGTGA others(3): Show |
1 | a0001c0001t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1191-118_1191-109d others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665945 | |||||||
| chrX:123666200 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1191-363C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666200 | |||||||
| chrX:123666351 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1191-514A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666351 | |||||||
| chrX:123666633 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0082 |
2 | HG01934.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1190+473C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666633 | |||||||
| chrX:123666746 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0092 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190+360T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666746 | |||||||
| chrX:123667042 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1190+64A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123667042 | |||||||
| chrX:123667573 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1018-295T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 10/38 | chrX | 123667573 | |||||||
| chrX:123667888 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02015.hp1 HG02129.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+271T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 10/38 | chrX | 123667888 | |||||||
| chrX:123669140 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0248 |
2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.862-826T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669140 | |||||||
| chrX:123669244 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0055 |
3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.862-930T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669244 | |||||||
| chrX:123669902 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.862-1588A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669902 | |||||||
| chrX:123669987 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.862-1673G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669987 | |||||||
| chrX:123670523 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861+1146C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670523 | |||||||
| chrX:123670827 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.861+842A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670827 | |||||||
| chrX:123670945 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.861+724G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670945 | |||||||
| chrX:123671173 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.861+496G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671173 | |||||||
| chrX:123671305 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02135.hp1 NA18994.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.861+364A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671305 | |||||||
| chrX:123671371 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.861+298A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671371 | |||||||
| chrX:123671570 | C | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.861+99G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671570 | |||||||
| chrX:123671620 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.861+49A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671620 | |||||||
| chrX:123672106 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0035 others(6): Show |
9 | HG02135.hp1 HG02273.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-345C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672106 | |||||||
| chrX:123672980 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.769-1219A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672980 | |||||||
| chrX:123673150 | A | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0122 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-1389T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673150 | |||||||
| chrX:123673344 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.769-1583T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673344 | |||||||
| chrX:123673761 | C | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02809.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769-2000G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673761 | |||||||
| chrX:123673879 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.769-2118G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673879 | |||||||
| chrX:123674092 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.769-2331C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674092 | |||||||
| chrX:123674639 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.769-2878T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674639 | |||||||
| chrX:123674647 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.769-2886G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674647 | |||||||
| chrX:123674845 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.769-3084G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674845 | |||||||
| chrX:123674962 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-3201T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674962 | |||||||
| chrX:123675019 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.769-3258T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675019 | |||||||
| chrX:123675467 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.769-3706G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675467 | |||||||
| chrX:123675596 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.769-3835A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675596 | |||||||
| chrX:123675826 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.769-4065C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675826 | |||||||
| chrX:123676416 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.769-4655C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123676416 | |||||||
| chrX:123676461 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.769-4700G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123676461 | |||||||
| chrX:123677402 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.769-5641A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677402 | |||||||
| chrX:123677443 | CCTTAT | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0212 |
3 | NA18960.hp1 NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.769-5687_769-5683d others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677443 | |||||||
| chrX:123677871 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0017 others(45): Show |
48 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.769-6111dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677871 | |||||||
| chrX:123677986 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-6225C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677986 | |||||||
| chrX:123678199 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.769-6438G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678199 | |||||||
| chrX:123678267 | C | CT | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(42): Show |
45 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.769-6507dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678267 | |||||||
| chrX:123678288 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.769-6527A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678288 | |||||||
| chrX:123678308 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.769-6547G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678308 | |||||||
| chrX:123678360 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.769-6599G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678360 | |||||||
| chrX:123678728 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.769-6967A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678728 | |||||||
| chrX:123679710 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.768+6838C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679710 | |||||||
| chrX:123679713 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.768+6835C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679713 | |||||||
| chrX:123679961 | G | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+6587C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679961 | |||||||
| chrX:123680020 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG02257.hp1 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.768+6528A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680020 | |||||||
| chrX:123680061 | G | GTCCCCCA others(11): Show |
1 | a0001c0001t0001g0016 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.768+6469_768+6486d others(20): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680061 | |||||||
| chrX:123680094 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0175 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.768+6454G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680094 | |||||||
| chrX:123680191 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768+6357G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680191 | |||||||
| chrX:123680569 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.768+5979G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680569 | |||||||
| chrX:123680579 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0035 others(6): Show |
9 | HG02135.hp1 HG02273.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+5969G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680579 | |||||||
| chrX:123680584 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.768+5964G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680584 | |||||||
| chrX:123680965 | T | TTCTC | 2 | a0001c0001t0001g0020 a0001c0001t0001g0247 |
2 | HG01934.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.768+5579_768+5582d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680965 | |||||||
| chrX:123681027 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.768+5521A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681027 | |||||||
| chrX:123681591 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+4957C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681591 | |||||||
| chrX:123681721 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.768+4827A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681721 | |||||||
| chrX:123681974 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.768+4574C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681974 | |||||||
| chrX:123682487 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.768+4061G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682487 | |||||||
| chrX:123682529 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.768+4019C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682529 | |||||||
| chrX:123682838 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0160 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+3710G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682838 | |||||||
| chrX:123683035 | C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+3513G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683035 | |||||||
| chrX:123683121 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+3427A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683121 | |||||||
| chrX:123683341 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.768+3207T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683341 | |||||||
| chrX:123683584 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.768+2964A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683584 | |||||||
| chrX:123683600 | C | CT | 13 | a0001c0001t0001g0026 a0001c0001t0001g0117 a0001c0001t0001g0118 others(10): Show |
13 | HG01106.hp1 HG02055.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.768+2947dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683600 | |||||||
| chrX:123683630 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.768+2918G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683630 | |||||||
| chrX:123683667 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.768+2881G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683667 | |||||||
| chrX:123683726 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.768+2822C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683726 | |||||||
| chrX:123684081 | C | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.768+2467G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684081 | |||||||
| chrX:123684243 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.768+2305T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684243 | |||||||
| chrX:123684393 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.768+2155C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684393 | |||||||
| chrX:123684482 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.768+2066G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684482 | |||||||
| chrX:123684675 | A | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0122 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+1873T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684675 | |||||||
| chrX:123684681 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.768+1867G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684681 | |||||||
| chrX:123684694 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.768+1854C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684694 | |||||||
| chrX:123684960 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.768+1588G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684960 | |||||||
| chrX:123685035 | T | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1513A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685035 | |||||||
| chrX:123685283 | G | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1265C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685283 | |||||||
| chrX:123685400 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.768+1148C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685400 | |||||||
| chrX:123685697 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.768+851C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685697 | |||||||
| chrX:123685799 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768+749A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685799 | |||||||
| chrX:123685977 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.768+571G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685977 | |||||||
| chrX:123685985 | G | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+563C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685985 | |||||||
| chrX:123686046 | A | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0047 others(11): Show |
14 | HG00673.hp1 HG02015.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.768+502T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123686046 | |||||||
| chrX:123686106 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.768+442G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123686106 | |||||||
| chrX:123687103 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.602-389G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687103 | |||||||
| chrX:123687211 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.602-497A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687211 | |||||||
| chrX:123687659 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.602-945G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687659 | |||||||
| chrX:123687805 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.602-1091C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687805 | |||||||
| chrX:123688090 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.602-1376G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688090 | |||||||
| chrX:123688188 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-1474A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688188 | |||||||
| chrX:123688397 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0086 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-1683A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688397 | |||||||
| chrX:123688502 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.602-1788T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688502 | |||||||
| chrX:123688721 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-2007A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688721 | |||||||
| chrX:123688897 | TCTC | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(7): Show |
10 | HG01891.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.602-2186_602-2184d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688897 | |||||||
| chrX:123690013 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0157 |
3 | HG01192.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.602-3299A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690013 | |||||||
| chrX:123690212 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0195 |
3 | HG02486.hp1 HG02572.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.602-3498C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690212 | |||||||
| chrX:123690231 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.602-3517C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690231 | |||||||
| chrX:123690525 | AACC | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-3814_602-3812d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690525 | |||||||
| chrX:123690529 | A | T | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-3815T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690529 | |||||||
| chrX:123690563 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0057 |
2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.602-3849T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690563 | |||||||
| chrX:123690950 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.602-4236C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690950 | |||||||
| chrX:123690989 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.602-4275T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690989 | |||||||
| chrX:123692294 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.601+3727A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692294 | |||||||
| chrX:123692482 | G | A | 14 | a0001c0001t0001g0127 a0001c0001t0001g0192 a0001c0001t0001g0193 others(11): Show |
14 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.601+3539C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692482 | |||||||
| chrX:123692494 | C | CT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0140 a0001c0001t0001g0153 others(9): Show |
12 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+3526dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | |||||||
| chrX:123692494 | CT | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.601+3526delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | |||||||
| chrX:123692494 | CTT | C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0112 a0001c0001t0001g0117 others(3): Show |
6 | HG01168.hp1 HG01496.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+3525_601+3526d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | |||||||
| chrX:123692571 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601+3450T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692571 | |||||||
| chrX:123692739 | T | C | 1 | a0003c0003t0001g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601+3282A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692739 | |||||||
| chrX:123692784 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.601+3237G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692784 | |||||||
| chrX:123692872 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+3149T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692872 | |||||||
| chrX:123693091 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+2930G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693091 | |||||||
| chrX:123693196 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.601+2825G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693196 | |||||||
| chrX:123693241 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+2780A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693241 | |||||||
| chrX:123693270 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.601+2751G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693270 | |||||||
| chrX:123693407 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2614C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693407 | |||||||
| chrX:123693409 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2612T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693409 | |||||||
| chrX:123693410 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2611A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693410 | |||||||
| chrX:123693415 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.601+2606T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693415 | |||||||
| chrX:123693920 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.601+2101C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693920 | |||||||
| chrX:123693922 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(36): Show |
39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.601+2099G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693922 | |||||||
| chrX:123694140 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.601+1881C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694140 | |||||||
| chrX:123694338 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.601+1683C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694338 | |||||||
| chrX:123694434 | G | A | 4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+1587C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694434 | |||||||
| chrX:123694606 | T | TA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.601+1414dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694606 | |||||||
| chrX:123694620 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02300.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.601+1401C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694620 | |||||||
| chrX:123694620 | GA | G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0116 others(69): Show |
72 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.601+1400delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694620 | |||||||
| chrX:123694621 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02300.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.601+1400T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694621 | |||||||
| chrX:123695993 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.601+28T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123695993 | |||||||
| chrX:123697459 | T | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345+222A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 5/38 | chrX | 123697459 | |||||||
| chrX:123697472 | G | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345+209C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 5/38 | chrX | 123697472 | |||||||
| chrX:123698089 | TA | T | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0117 others(9): Show |
12 | HG01081.hp2 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.275-339delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698089 | |||||||
| chrX:123698330 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.275-579G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698330 | |||||||
| chrX:123698330 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0050 others(4): Show |
7 | HG00673.hp1 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-579G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698330 | |||||||
| chrX:123698362 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.275-611C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698362 | |||||||
| chrX:123698407 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.275-656C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698407 | |||||||
| chrX:123698412 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.275-661G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698412 | |||||||
| chrX:123698445 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-694C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698445 | |||||||
| chrX:123698457 | C | CA | 14 | a0001c0001t0001g0036 a0001c0001t0001g0117 a0001c0001t0001g0118 others(11): Show |
14 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.275-707dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698457 | |||||||
| chrX:123698457 | CA | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0069 others(2): Show |
5 | HG02602.hp1 HG02897.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-707delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698457 | |||||||
| chrX:123698706 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0094 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.275-955G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698706 | |||||||
| chrX:123698909 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0081 |
2 | HG02148.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.275-1158T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698909 | |||||||
| chrX:123698929 | G | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02809.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.275-1178C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698929 | |||||||
| chrX:123699215 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0025 |
2 | NA18993.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.275-1464A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699215 | |||||||
| chrX:123699387 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-1636T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699387 | |||||||
| chrX:123699491 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.275-1740C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699491 | |||||||
| chrX:123699507 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.275-1756G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699507 | |||||||
| chrX:123699645 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.275-1894G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699645 | |||||||
| chrX:123700321 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.275-2570G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700321 | |||||||
| chrX:123700411 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.275-2660C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700411 | |||||||
| chrX:123700503 | G | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-2752C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700503 | |||||||
| chrX:123700544 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.275-2793A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | |||||||
| chrX:123700544 | T | TG | 44 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(41): Show |
44 | HG00438.hp2 HG01074.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.275-2794dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | |||||||
| chrX:123700544 | TG | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
77 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.275-2794delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | |||||||
| chrX:123700551 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.275-2800C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700551 | |||||||
| chrX:123700553 | G | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0074 a0001c0001t0001g0082 others(7): Show |
10 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-2802C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700553 | |||||||
| chrX:123700554 | T | G | 25 | a0001c0001t0001g0041 a0001c0001t0001g0074 a0001c0001t0001g0082 others(22): Show |
25 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.275-2803A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700554 | |||||||
| chrX:123700554 | T | TG | 11 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0065 others(8): Show |
11 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.275-2804dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700554 | |||||||
| chrX:123700686 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.274+2768C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700686 | |||||||
| chrX:123701229 | G | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+2225C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701229 | |||||||
| chrX:123701692 | C | CA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
30 | HG01099.hp1 HG01106.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.274+1761dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701692 | |||||||
| chrX:123701711 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.274+1743A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701711 | |||||||
| chrX:123701755 | G | T | 1 | a0001c0001t0001g0220 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.274+1699C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701755 | |||||||
| chrX:123702775 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+679T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702775 | |||||||
| chrX:123702816 | G | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+638C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702816 | |||||||
| chrX:123703102 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0157 |
3 | HG01192.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.274+352C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123703102 | |||||||
| chrX:123703139 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.274+315G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123703139 | |||||||
| chrX:123703725 | C | CA | 24 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0137 others(21): Show |
24 | HG00438.hp2 HG01192.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-221dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | |||||||
| chrX:123703725 | CA | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
114 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.223-221delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | |||||||
| chrX:123703725 | CAA | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0041 others(14): Show |
17 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-222_223-221del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | |||||||
| chrX:123703725 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0019 others(2): Show |
5 | HG02293.hp2 NA18942.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-228_223-221del others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | |||||||
| chrX:123703727 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-222T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703727 | |||||||
| chrX:123703763 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.223-258C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703763 | |||||||
| chrX:123703800 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-295T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703800 | |||||||
| chrX:123703801 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-296C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703801 | |||||||
| chrX:123703890 | T | TAAAAAAA | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 others(2): Show |
5 | HG01168.hp1 HG02683.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-392_223-386dup others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0147 others(5): Show |
8 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-393_223-386dup others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(2): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(20): Show |
23 | HG01516.hp2 HG01891.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.223-394_223-386dup others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(3): Show |
44 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(41): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.223-395_223-386dup others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(4): Show |
50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(47): Show |
50 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.223-396_223-386dup others(11): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(5): Show |
25 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
25 | HG00735.hp1 HG01069.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-397_223-386dup others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(6): Show |
10 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0118 others(7): Show |
10 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-398_223-386dup others(13): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(7): Show |
4 | a0001c0001t0001g0119 a0001c0001t0001g0162 a0001c0001t0001g0168 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-399_223-386dup others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0249 |
2 | HG02055.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.223-400_223-386dup others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-401_223-386dup others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0026 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.223-402_223-386dup others(17): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | TA | T | 58 | a0001c0001t0001g0116 a0001c0001t0001g0126 a0001c0001t0001g0127 others(55): Show |
58 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.223-386delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123703890 | TAA | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0179 a0001c0001t0001g0190 others(2): Show |
5 | HG01515.hp1 HG02976.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-387_223-386del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | |||||||
| chrX:123704463 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0080 |
3 | HG00621.hp1 HG02027.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.223-958A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704463 | |||||||
| chrX:123704598 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.223-1093C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704598 | |||||||
| chrX:123704996 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.223-1491C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704996 | |||||||
| chrX:123705415 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.222+1443G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705415 | |||||||
| chrX:123705879 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.222+979G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705879 | |||||||
| chrX:123705918 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.222+940C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705918 | |||||||
| chrX:123705939 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+919A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705939 | |||||||
| chrX:123705981 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222+877C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705981 | |||||||
| chrX:123706357 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0241 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.222+501C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706357 | |||||||
| chrX:123706373 | CT | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(39): Show |
42 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(39): Show |
intron_variant | MODIFIER | c.222+484delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706373 | |||||||
| chrX:123706424 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.222+434C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706424 | |||||||
| chrX:123707502 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.131-553A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707502 | |||||||
| chrX:123707991 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-1042T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707991 | |||||||
| chrX:123708107 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.131-1158A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708107 | |||||||
| chrX:123708528 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.131-1579C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708528 | |||||||
| chrX:123708772 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-1823T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708772 | |||||||
| chrX:123708849 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.131-1900G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708849 | |||||||
| chrX:123709329 | A | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-2380T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709329 | |||||||
| chrX:123709398 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.131-2449A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709398 | |||||||
| chrX:123709460 | G | A | 2 | a0001c0001t0001g0147 a0002c0006t0001g0148 |
2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.131-2511C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709460 | |||||||
| chrX:123709584 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.131-2635G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709584 | |||||||
| chrX:123709693 | C | T | 2 | a0001c0001t0001g0147 a0002c0006t0001g0148 |
2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.131-2744G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709693 | |||||||
| chrX:123710173 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+2677T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710173 | |||||||
| chrX:123710758 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(36): Show |
39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.130+2092C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710758 | |||||||
| chrX:123711009 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+1841G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711009 | |||||||
| chrX:123711188 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+1662A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711188 | |||||||
| chrX:123711195 | G | GT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+1654dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711195 | |||||||
| chrX:123711200 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 |
3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+1650A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711200 | |||||||
| chrX:123711201 | G | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.130+1649C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711201 | |||||||
| chrX:123711237 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+1613T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711237 | |||||||
| chrX:123711238 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130+1612C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711238 | |||||||
| chrX:123711613 | G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+1237C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711613 | |||||||
| chrX:123711679 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.130+1171T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711679 | |||||||
| chrX:123711767 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0090 |
2 | NA18612.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.130+1083C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711767 | |||||||
| chrX:123711779 | A | G | 2 | a0001c0001t0001g0153 a0001c0002t0001g0154 |
2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.130+1071T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711779 | |||||||
| chrX:123711878 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.130+972C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711878 | |||||||
| chrX:123711958 | T | TA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(178): Show |
181 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.130+891dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | |||||||
| chrX:123711958 | T | TAA | 42 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0082 others(39): Show |
42 | HG00673.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.130+890_130+891dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | |||||||
| chrX:123712030 | A | AAT | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+818_130+819dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712030 | |||||||
| chrX:123712136 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+714C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712136 | |||||||
| chrX:123712198 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130+652G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712198 | |||||||
| chrX:123712229 | C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+621G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712229 | |||||||
| chrX:123712831 | A | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+19T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712831 | |||||||
| chrX:123713000 | A | C | 2 | a0001c0001t0001g0112 a0001c0005t0001g0111 |
2 | HG01496.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.72-92T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713000 | |||||||
| chrX:123713251 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-343A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713251 | |||||||
| chrX:123713283 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-375C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713283 | |||||||
| chrX:123713411 | G | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
24 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.72-503C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713411 | |||||||
| chrX:123713432 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-524C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713432 | |||||||
| chrX:123713476 | C | CA | 16 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0081 others(13): Show |
16 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-569dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713476 | |||||||
| chrX:123713563 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72-655A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713563 | |||||||
| chrX:123713841 | G | GA | 10 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0120 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-934dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713841 | |||||||
| chrX:123714206 | G | GTAA | 7 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | NA18945.hp1 NA18970.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-1301_72-1299dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714206 | |||||||
| chrX:123714597 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0248 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-1689C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714597 | |||||||
| chrX:123715019 | C | CT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.72-2112dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | |||||||
| chrX:123715019 | C | CTT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(56): Show |
59 | HG00438.hp2 HG00621.hp1 HG01934.hp1 others(56): Show |
intron_variant | MODIFIER | c.72-2113_72-2112dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | |||||||
| chrX:123715019 | CT | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0001g0138 others(5): Show |
8 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-2112delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | |||||||
| chrX:123715760 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-2852C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715760 | |||||||
| chrX:123715784 | C | CA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(44): Show |
47 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.72-2877dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715784 | |||||||
| chrX:123715924 | A | G | 10 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(7): Show |
10 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-3016T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715924 | |||||||
| chrX:123716277 | C | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-3369G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716277 | |||||||
| chrX:123716375 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3467A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716375 | |||||||
| chrX:123716453 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.72-3545G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716453 | |||||||
| chrX:123716590 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0225 |
2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.72-3682C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716590 | |||||||
| chrX:123716728 | C | CA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0082 others(4): Show |
7 | HG02630.hp2 HG02717.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-3821dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716728 | |||||||
| chrX:123716728 | CA | C | 12 | a0001c0001t0001g0076 a0001c0001t0001g0117 a0001c0001t0001g0118 others(9): Show |
12 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-3821delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716728 | |||||||
| chrX:123716748 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-3840T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716748 | |||||||
| chrX:123716825 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01256.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.72-3917C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716825 | |||||||
| chrX:123717001 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.72-4093A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717001 | |||||||
| chrX:123717344 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.72-4436G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717344 | |||||||
| chrX:123717429 | A | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-4521T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717429 | |||||||
| chrX:123717693 | C | CA | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
235 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.72-4786dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717693 | |||||||
| chrX:123717693 | C | CAA | 8 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG01261.hp1 HG02738.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-4787_72-4786dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717693 | |||||||
| chrX:123717728 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01167.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72-4820G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717728 | |||||||
| chrX:123717892 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.72-4984G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717892 | |||||||
| chrX:123718000 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0140 |
2 | HG02109.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.72-5092C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718000 | |||||||
| chrX:123718262 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.72-5354G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718262 | |||||||
| chrX:123718288 | A | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.72-5380T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718288 | |||||||
| chrX:123718500 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.72-5592G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718500 | |||||||
| chrX:123718615 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0182 |
2 | HG01168.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.72-5707G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718615 | |||||||
| chrX:123718669 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 |
3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.72-5761C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718669 | |||||||
| chrX:123718816 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72-5908G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718816 | |||||||
| chrX:123719126 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-6218T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719126 | |||||||
| chrX:123719172 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.72-6264G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719172 | |||||||
| chrX:123719179 | C | CA | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0140 others(2): Show |
5 | HG01109.hp1 HG01496.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-6272dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719179 | |||||||
| chrX:123719253 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-6345T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719253 | |||||||
| chrX:123719297 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72-6389A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719297 | |||||||
| chrX:123719366 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-6458A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719366 | |||||||
| chrX:123719580 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-6672C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719580 | |||||||
| chrX:123719635 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6727A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719635 | |||||||
| chrX:123719636 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6728T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719636 | |||||||
| chrX:123719672 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.72-6764G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719672 | |||||||
| chrX:123719770 | C | CA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01891.hp1 NA18971.hp1 NA19007.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-6863dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719770 | |||||||
| chrX:123719773 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-6865T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719773 | |||||||
| chrX:123719783 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.72-6875T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719783 | |||||||
| chrX:123719824 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0247 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.72-6916C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719824 | |||||||
| chrX:123720004 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72-7096G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720004 | |||||||
| chrX:123720389 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72-7481C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720389 | |||||||
| chrX:123720429 | C | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(37): Show |
40 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.72-7521G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720429 | |||||||
| chrX:123720637 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(36): Show |
39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-7729T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720637 | |||||||
| chrX:123720825 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.72-7917G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720825 | |||||||
| chrX:123720892 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-7984A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720892 | |||||||
| chrX:123721015 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01167.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72-8107A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721015 | |||||||
| chrX:123721147 | G | GT | 11 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG00323.hp2 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-8240dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721147 | |||||||
| chrX:123721509 | C | CG | 10 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(7): Show |
10 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-8602dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721509 | |||||||
| chrX:123721701 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.72-8793C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721701 | |||||||
| chrX:123721936 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.72-9028A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721936 | |||||||
| chrX:123722100 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9192G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722100 | |||||||
| chrX:123722504 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.72-9596A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722504 | |||||||
| chrX:123722632 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9724G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722632 | |||||||
| chrX:123722732 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9824T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722732 | |||||||
| chrX:123723370 | C | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+9582G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723370 | |||||||
| chrX:123723411 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+9541C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723411 | |||||||
| chrX:123723519 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+9433G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723519 | |||||||
| chrX:123723602 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71+9350A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723602 | |||||||
| chrX:123723690 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+9262T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723690 | |||||||
| chrX:123723822 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.71+9130C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723822 | |||||||
| chrX:123723903 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71+9049G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723903 | |||||||
| chrX:123723904 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
237 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.71+9048T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723904 | |||||||
| chrX:123724272 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.71+8680A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724272 | |||||||
| chrX:123724295 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71+8657C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724295 | |||||||
| chrX:123724346 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.71+8606T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724346 | |||||||
| chrX:123724634 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+8318T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724634 | |||||||
| chrX:123724973 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.71+7979C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724973 | |||||||
| chrX:123724995 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71+7957G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724995 | |||||||
| chrX:123725157 | T | TA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.71+7794dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725157 | |||||||
| chrX:123725297 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+7655C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725297 | |||||||
| chrX:123725428 | C | CA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+7523dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725428 | |||||||
| chrX:123725428 | C | CAA | 5 | a0001c0001t0001g0076 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01168.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+7522_71+7523dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725428 | |||||||
| chrX:123725616 | C | CA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
41 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.71+7335dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | |||||||
| chrX:123725616 | C | CAA | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.71+7334_71+7335dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | |||||||
| chrX:123725616 | C | CAAA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0078 others(21): Show |
24 | HG00621.hp1 HG01978.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.71+7333_71+7335dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | |||||||
| chrX:123725639 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71+7313G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725639 | |||||||
| chrX:123725735 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(8): Show |
11 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+7217G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725735 | |||||||
| chrX:123725896 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.71+7056C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725896 | |||||||
| chrX:123726512 | C | CA | 9 | a0001c0001t0001g0093 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01175.hp1 HG01192.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+6439dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123726512 | |||||||
| chrX:123727220 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71+5732T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727220 | |||||||
| chrX:123727412 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71+5540G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727412 | |||||||
| chrX:123727650 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 |
3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71+5302G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727650 | |||||||
| chrX:123727651 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71+5301C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727651 | |||||||
| chrX:123727707 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+5245C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727707 | |||||||
| chrX:123727853 | G | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.71+5099C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727853 | |||||||
| chrX:123728053 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.71+4899C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728053 | |||||||
| chrX:123728137 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.71+4815A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728137 | |||||||
| chrX:123728339 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.71+4613G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728339 | |||||||
| chrX:123728785 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+4167T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728785 | |||||||
| chrX:123728811 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.71+4141A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728811 | |||||||
| chrX:123729193 | C | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.71+3759G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123729193 | |||||||
| chrX:123729651 | AAG | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0096 others(11): Show |
14 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+3299_71+3300del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123729651 | |||||||
| chrX:123730068 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+2884C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730068 | |||||||
| chrX:123730182 | G | GT | 9 | a0001c0001t0001g0112 a0001c0001t0001g0165 a0001c0001t0001g0166 others(6): Show |
9 | HG01496.hp1 HG02056.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+2769dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730182 | |||||||
| chrX:123730182 | GT | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.71+2769delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730182 | |||||||
| chrX:123730248 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.71+2704G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730248 | |||||||
| chrX:123730397 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71+2555C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730397 | |||||||
| chrX:123730851 | G | C | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.71+2101C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730851 | |||||||
| chrX:123731135 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.71+1817G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731135 | |||||||
| chrX:123731189 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.71+1763G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731189 | |||||||
| chrX:123731671 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+1281A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731671 | |||||||
| chrX:123732007 | T | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(8): Show |
11 | HG02622.hp2 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+945A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732007 | |||||||
| chrX:123732144 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.71+808G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732144 | |||||||
| chrX:123732391 | G | C | 77 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(74): Show |
77 | HG00438.hp2 HG00741.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.71+561C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732391 | |||||||
| chrX:123732461 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71+491C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732461 | |||||||
| chrX:123732462 | G | T | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71+490C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732462 | |||||||
| chrX:123732586 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.71+366A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732586 | |||||||
| chrX:123732817 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.71+135C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732817 | |||||||
| chrX:123732853 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.71+99C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732853 | |||||||
| chrX:123732941 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71+11G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732941 |