Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9984 |
| ensemblid | ENSG00000079134.13 |
| hgncid | 19070 |
| symbol | THOC1 |
| name | THO complex subunit 1 |
| refseq_nuc | NM_005131.3 |
| refseq_prot | NP_005122.2 |
| ensembl_nuc | ENST00000261600.11 |
| ensembl_prot | ENSP00000261600.6 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 214520 |
| end | 268047 |
| strand | - |
| ver | v1.2 |
| region | chr18:214520-268047 |
| region5000 | chr18:209520-273047 |
| regionname0 | THOC1_chr18_214520_268047 |
| regionname5000 | THOC1_chr18_209520_273047 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1971 | 293 | 73 | 60 | 104 | 14 | 41 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0002 | 0/0 | 1971 | 55 | 0 | 5 | 50 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0003 | 1/0 | 1971 | 24 | 21 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0004 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0005 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0006 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 | ||
| a0001c0007 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | ATGTC others(1966): Show |
chr18 | 209520 | 273047 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2108 | 277 | 73 | 54 | 104 | 11 | 34 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| a0001c0001t0002 | 0/0 | 2111 | 16 | 0 | 6 | 0 | 3 | 7 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2106): Show |
chr18 | 209520 | 273047 |
| a0001c0002t0001 | 0/0 | 2108 | 55 | 0 | 5 | 50 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| a0001c0003t0001 | 1/0 | 2108 | 24 | 21 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| a0001c0004t0001 | 0/0 | 2108 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| a0001c0005t0002 | 0/0 | 2111 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2106): Show |
chr18 | 209520 | 273047 |
| a0001c0006t0001 | 0/0 | 2108 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| a0001c0007t0001 | 0/0 | 2108 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | GCAGT others(2103): Show |
chr18 | 209520 | 273047 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0003 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0005t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| a0001c0007t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0263 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0264 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01358 | hp1 | a0001 | c0005 | t0002 | g0048 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0268 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0296 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0273 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0255 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0262 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0276 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0265 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | CHB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18959 | hp2 | a0001 | c0007 | t0001 | g0114 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18984 | hp2 | a0001 | c0006 | t0001 | g0191 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0234 | REF | REF | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0267 | REF | REF | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:214842 | C | T | 1 | a0001c0006 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1758G>A | p.Lys586Lys | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 21/21 | 1786/2108 | 1758/1974 | 586/657 | chr18 | 214842 | |||
| chr18:224131 | G | A | 2 | a0001c0002 a0001c0006 |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
synonymous_variant | LOW | c.1257C>T | p.Pro419Pro | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/21 | 1285/2108 | 1257/1974 | 419/657 | chr18 | 224131 | |||
| chr18:225116 | A | G | 1 | a0001c0005 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1110T>C | p.Asp370Asp | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/21 | 1138/2108 | 1110/1974 | 370/657 | chr18 | 225116 | |||
| chr18:226830 | T | C | 1 | a0001c0007 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.990A>G | p.Gln330Gln | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/21 | 1018/2108 | 990/1974 | 330/657 | chr18 | 226830 | |||
| chr18:252559 | G | A | 6 | a0001c0001 a0001c0002 a0001c0004 others(3): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
synonymous_variant | LOW | c.657C>T | p.Asp219Asp | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/21 | 685/2108 | 657/1974 | 219/657 | chr18 | 252559 | |||
| chr18:254315 | A | T | 1 | a0001c0004 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.561T>A | p.Thr187Thr | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/21 | 589/2108 | 561/1974 | 187/657 | chr18 | 254315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:214930 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1679-9A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214930 | |||||||
| chr18:214950 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1679-29G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214950 | |||||||
| chr18:214951 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-30C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214951 | |||||||
| chr18:214959 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(30): Show |
40 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1679-38T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214959 | |||||||
| chr18:214983 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1679-62A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214983 | |||||||
| chr18:214991 | C | T | 47 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(44): Show |
56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1679-70G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214991 | |||||||
| chr18:215020 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1679-99T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215020 | |||||||
| chr18:215060 | G | A | 3 | a0001c0002t0001g0029 a0001c0002t0001g0169 a0001c0002t0001g0173 |
4 | NA18947.hp1 NA18968.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-139C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215060 | |||||||
| chr18:215156 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1679-235G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215156 | |||||||
| chr18:215299 | A | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
37 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1678+130T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215299 | |||||||
| chr18:215345 | G | C | 48 | a0001c0001t0001g0197 a0001c0002t0001g0007 a0001c0002t0001g0028 others(45): Show |
57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1678+84C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215345 | |||||||
| chr18:215384 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1678+45T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215384 | |||||||
| chr18:215732 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0104 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1603-228G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215732 | |||||||
| chr18:215808 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603-304G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215808 | |||||||
| chr18:215966 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-463_1603-462i others(29): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215966 | |||||||
| chr18:215974 | A | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(51): Show |
72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1603-470T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215974 | |||||||
| chr18:215985 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-481A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215985 | |||||||
| chr18:215993 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-489A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215993 | |||||||
| chr18:216023 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602+463C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216023 | |||||||
| chr18:216142 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1602+344G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216142 | |||||||
| chr18:216291 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0151 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1602+195A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216291 | |||||||
| chr18:216332 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1602+154T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216332 | |||||||
| chr18:216434 | T | G | 1 | a0001c0002t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1602+52A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216434 | |||||||
| chr18:216869 | T | TA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455-237dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 216869 | |||||||
| chr18:216958 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1455-325G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 216958 | |||||||
| chr18:217041 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1455-408A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217041 | |||||||
| chr18:217049 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1455-416C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217049 | |||||||
| chr18:217069 | G | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455-436C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217069 | |||||||
| chr18:217085 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1455-452A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217085 | |||||||
| chr18:217171 | C | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0131 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1455-538G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217171 | |||||||
| chr18:217379 | G | A | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
24 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1455-746C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217379 | |||||||
| chr18:217485 | C | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1455-852G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217485 | |||||||
| chr18:217488 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1455-855C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217488 | |||||||
| chr18:217494 | T | C | 3 | a0001c0001t0001g0284 a0001c0001t0001g0289 a0001c0001t0001g0292 |
3 | HG00741.hp1 HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1455-861A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217494 | |||||||
| chr18:217593 | T | TG | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-961dupC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217593 | |||||||
| chr18:217673 | ACCTTCTC others(22): Show |
A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1455-1069_1455-104 others(33): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217673 | |||||||
| chr18:217866 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(20): Show |
29 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1454+1020C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217866 | |||||||
| chr18:217952 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1454+934C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217952 | |||||||
| chr18:218042 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1454+844T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218042 | |||||||
| chr18:218226 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1454+660C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218226 | |||||||
| chr18:218242 | A | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+644T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218242 | |||||||
| chr18:218285 | A | G | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+601T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218285 | |||||||
| chr18:218366 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+520G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218366 | |||||||
| chr18:218418 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1454+468A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218418 | |||||||
| chr18:218695 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1454+191A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218695 | |||||||
| chr18:218753 | C | A | 46 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(43): Show |
55 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1454+133G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218753 | |||||||
| chr18:218980 | CA | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(3): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1371-12delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 218980 | |||||||
| chr18:218980 | CAAAAATA others(90): Show |
C | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1371-108_1371-12de others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 218980 | |||||||
| chr18:219008 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1371-39A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219008 | |||||||
| chr18:219008 | TTCTTAAT others(89): Show |
T | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1371-135_1371-40de others(97): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219008 | |||||||
| chr18:219029 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(182): Show |
229 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1371-60C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219029 | |||||||
| chr18:219072 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(181): Show |
228 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1371-103T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219072 | |||||||
| chr18:219076 | CA | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0068 others(6): Show |
11 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1371-108delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219076 | |||||||
| chr18:219077 | A | AAAAATAA others(88): Show |
1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1371-109_1371-108i others(97): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | |||||||
| chr18:219077 | A | AAAAATAA others(183): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1371-109_1371-108i others(192): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | |||||||
| chr18:219077 | AAAAATAA others(183): Show |
A | 1 | a0001c0001t0001g0036 | 2 | NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1371-298_1371-109d others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | |||||||
| chr18:219172 | C | CA | 14 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
17 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1371-204dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAAATA others(185): Show |
1 | a0001c0001t0001g0017 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1371-204_1371-203i others(194): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(184): Show |
1 | a0001c0001t0001g0216 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(89): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0090 others(4): Show |
8 | HG00438.hp2 HG02027.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1371-299_1371-204d others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(184): Show |
259 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1371-394_1371-204d others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(470): Show |
1 | a0001c0001t0001g0094 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(479): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(565): Show |
1 | a0001c0001t0001g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(574): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219172 | C | CAAAATAA others(184): Show |
1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1371-204_1371-203i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | |||||||
| chr18:219190 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1371-221A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219190 | |||||||
| chr18:219242 | G | GTGGGCAT others(184): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0194 others(3): Show |
7 | HG02109.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1371-274_1371-273i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219242 | |||||||
| chr18:219242 | G | GTGGGCAT others(184): Show |
1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1371-274_1371-273i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219242 | |||||||
| chr18:219265 | T | TACAAAAA others(89): Show |
1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1371-297_1371-296i others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219265 | |||||||
| chr18:219265 | T | TACAAAAT others(184): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1371-297_1371-296i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219265 | |||||||
| chr18:219267 | C | CA | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0127 |
3 | HG01168.hp2 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1371-299dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219267 | |||||||
| chr18:219294 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-325G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219294 | |||||||
| chr18:219452 | C | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
8 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1371-483G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219452 | |||||||
| chr18:219457 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1371-488G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219457 | |||||||
| chr18:220071 | T | C | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1371-1102A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220071 | |||||||
| chr18:220084 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1115G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220084 | |||||||
| chr18:220226 | G | A | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1371-1257C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220226 | |||||||
| chr18:220341 | C | A | 96 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0020 others(93): Show |
115 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.1371-1372G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220341 | |||||||
| chr18:220441 | AAC | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(43): Show |
55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1371-1474_1371-147 others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220441 | |||||||
| chr18:220458 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1489G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220458 | |||||||
| chr18:220658 | G | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1371-1689C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220658 | |||||||
| chr18:220706 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1737T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220706 | |||||||
| chr18:220757 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0179 |
3 | HG02015.hp2 HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1371-1788A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220757 | |||||||
| chr18:220903 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1371-1934G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220903 | |||||||
| chr18:221102 | G | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
37 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1371-2133C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221102 | |||||||
| chr18:221131 | G | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1371-2162C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221131 | |||||||
| chr18:221145 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1371-2176A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221145 | |||||||
| chr18:221175 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1371-2206A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221175 | |||||||
| chr18:221228 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+2212T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221228 | |||||||
| chr18:221350 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0135 |
2 | HG01109.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1370+2090T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221350 | |||||||
| chr18:221410 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1370+2030A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221410 | |||||||
| chr18:221606 | C | CT | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(94): Show |
123 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1370+1833dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | |||||||
| chr18:221606 | C | CTT | 6 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0091 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370+1832_1370+183 others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | |||||||
| chr18:221606 | CT | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 others(54): Show |
68 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1370+1833delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | |||||||
| chr18:221640 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1370+1800C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221640 | |||||||
| chr18:221643 | C | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG01099.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1370+1797G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221643 | |||||||
| chr18:221647 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1370+1793G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221647 | |||||||
| chr18:221654 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1370+1786C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221654 | |||||||
| chr18:221664 | A | C | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(1): Show |
4 | HG00099.hp1 HG01109.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370+1776T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221664 | |||||||
| chr18:221672 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1370+1768C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221672 | |||||||
| chr18:221675 | C | G | 1 | a0001c0002t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370+1765G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221675 | |||||||
| chr18:221702 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0071 others(6): Show |
11 | HG01192.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+1738T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221702 | |||||||
| chr18:221717 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370+1723A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221717 | |||||||
| chr18:221753 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1370+1687G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221753 | |||||||
| chr18:221757 | T | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0081 a0001c0001t0001g0082 others(10): Show |
15 | HG01081.hp2 HG01123.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1370+1683A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221757 | |||||||
| chr18:221766 | A | G | 3 | a0001c0002t0001g0160 a0001c0002t0001g0172 a0001c0002t0001g0180 |
3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1674T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221766 | |||||||
| chr18:221768 | T | C | 3 | a0001c0002t0001g0160 a0001c0002t0001g0172 a0001c0002t0001g0180 |
3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1672A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221768 | |||||||
| chr18:221769 | T | C | 3 | a0001c0002t0001g0160 a0001c0002t0001g0172 a0001c0002t0001g0180 |
3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1671A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221769 | |||||||
| chr18:221791 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1370+1649C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221791 | |||||||
| chr18:221820 | C | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0296 |
3 | HG02055.hp1 NA18966.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1370+1620G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221820 | |||||||
| chr18:221830 | T | C | 1 | a0001c0003t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1370+1610A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221830 | |||||||
| chr18:221887 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1370+1553A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221887 | |||||||
| chr18:221888 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1370+1552T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221888 | |||||||
| chr18:221898 | G | A | 44 | a0001c0001t0001g0036 a0001c0002t0001g0007 a0001c0002t0001g0028 others(41): Show |
53 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1370+1542C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221898 | |||||||
| chr18:221900 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1370+1540C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221900 | |||||||
| chr18:221903 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG02257.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1370+1537A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221903 | |||||||
| chr18:221951 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0201 others(4): Show |
10 | HG00544.hp2 HG02074.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370+1489C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221951 | |||||||
| chr18:221989 | T | G | 6 | a0001c0002t0001g0031 a0001c0002t0001g0175 a0001c0002t0001g0176 others(3): Show |
7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1370+1451A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221989 | |||||||
| chr18:222167 | T | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0122 others(13): Show |
18 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370+1273A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222167 | |||||||
| chr18:222227 | AAAT | A | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1370+1210_1370+121 others(7): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222227 | |||||||
| chr18:222229 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370+1211T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222229 | |||||||
| chr18:222266 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1370+1174T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222266 | |||||||
| chr18:222334 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1370+1106G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222334 | |||||||
| chr18:222467 | C | T | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1370+973G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222467 | |||||||
| chr18:222676 | AAT | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(52): Show |
73 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1370+762_1370+763d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222676 | |||||||
| chr18:222793 | T | A | 1 | a0001c0002t0001g0190 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1370+647A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222793 | |||||||
| chr18:222973 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+467A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222973 | |||||||
| chr18:223185 | G | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(43): Show |
55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1370+255C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223185 | |||||||
| chr18:223189 | C | T | 21 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(18): Show |
25 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1370+251G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223189 | |||||||
| chr18:223309 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+131C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223309 | |||||||
| chr18:223366 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1370+74T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223366 | |||||||
| chr18:223514 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0279 |
2 | HG01175.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1305-9A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223514 | |||||||
| chr18:223885 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1304+199C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223885 | |||||||
| chr18:223974 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1304+110C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223974 | |||||||
| chr18:224021 | A | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1304+63T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 224021 | |||||||
| chr18:224184 | C | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
splice_region_variant&intron_variant | LOW | c.1209-5G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224184 | |||||||
| chr18:224268 | T | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01109.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1209-89A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224268 | |||||||
| chr18:224304 | C | T | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1209-125G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224304 | |||||||
| chr18:224510 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1209-331G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224510 | |||||||
| chr18:224526 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG00735.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-347G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224526 | |||||||
| chr18:224578 | CA | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(179): Show |
226 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1208+345delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224578 | |||||||
| chr18:224668 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1208+256C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224668 | |||||||
| chr18:224684 | ATTC | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+237_1208+239d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224684 | |||||||
| chr18:224690 | C | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+234G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224690 | |||||||
| chr18:224854 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208+70G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224854 | |||||||
| chr18:225005 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-11G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225005 | |||||||
| chr18:225009 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-15C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225009 | |||||||
| chr18:225027 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1138-33C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225027 | |||||||
| chr18:225051 | C | T | 46 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(43): Show |
55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137+38G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225051 | |||||||
| chr18:225081 | A | T | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1137+8T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225081 | |||||||
| chr18:225237 | T | C | 1 | a0001c0002t0001g0166 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1087-98A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 13/20 | chr18 | 225237 | |||||||
| chr18:225608 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020-205T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225608 | |||||||
| chr18:225964 | A | G | 47 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(44): Show |
56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1020-561T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225964 | |||||||
| chr18:225985 | G | A | 48 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(45): Show |
57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1020-582C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225985 | |||||||
| chr18:226011 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0239 |
3 | HG03710.hp1 NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1020-608A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226011 | |||||||
| chr18:226055 | C | T | 2 | a0001c0002t0001g0165 a0001c0002t0001g0166 |
2 | NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1020-652G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226055 | |||||||
| chr18:226219 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1019+582A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226219 | |||||||
| chr18:226334 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+467C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226334 | |||||||
| chr18:226420 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1019+381T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226420 | |||||||
| chr18:226459 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0216 a0001c0001t0001g0298 |
3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1019+342A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226459 | |||||||
| chr18:226485 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(32): Show |
41 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.1019+316T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226485 | |||||||
| chr18:226490 | T | C | 1 | a0001c0002t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1019+311A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226490 | |||||||
| chr18:226509 | G | A | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1019+292C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226509 | |||||||
| chr18:226525 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1019+276C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226525 | |||||||
| chr18:226634 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1019+167G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226634 | |||||||
| chr18:226650 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+151A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226650 | |||||||
| chr18:226664 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1019+137T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226664 | |||||||
| chr18:226672 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1019+129C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226672 | |||||||
| chr18:226928 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-27G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 226928 | |||||||
| chr18:227116 | A | G | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.919-215T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227116 | |||||||
| chr18:227314 | T | TA | 11 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.919-414dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227314 | |||||||
| chr18:227325 | T | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0061 |
4 | HG01168.hp2 HG01169.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-424A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227325 | |||||||
| chr18:227466 | C | G | 1 | a0001c0003t0001g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.919-565G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227466 | |||||||
| chr18:227472 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.919-571T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227472 | |||||||
| chr18:227608 | G | GTTC | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(193): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.919-710_919-708dup others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227608 | |||||||
| chr18:227731 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-830A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227731 | |||||||
| chr18:227839 | T | G | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-938A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227839 | |||||||
| chr18:227946 | T | TA | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(63): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.919-1046dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227946 | |||||||
| chr18:228001 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.919-1100A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228001 | |||||||
| chr18:228015 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919-1114A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228015 | |||||||
| chr18:228092 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG00735.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-1191G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228092 | |||||||
| chr18:228147 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.919-1246C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228147 | |||||||
| chr18:228152 | G | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.919-1251C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228152 | |||||||
| chr18:228303 | A | G | 1 | a0001c0003t0001g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.919-1402T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228303 | |||||||
| chr18:228346 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-1445C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228346 | |||||||
| chr18:228388 | C | A | 1 | a0001c0001t0001g0294 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.919-1487G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228388 | |||||||
| chr18:228527 | G | GA | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(175): Show |
222 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.919-1627dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228527 | |||||||
| chr18:228537 | C | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.919-1636G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228537 | |||||||
| chr18:228640 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.919-1739G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228640 | |||||||
| chr18:228875 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0227 |
2 | NA18967.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.919-1974A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228875 | |||||||
| chr18:229038 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0083 others(1): Show |
6 | HG01256.hp1 HG01258.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-2137A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229038 | |||||||
| chr18:229074 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-2173G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229074 | |||||||
| chr18:229112 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-2211G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229112 | |||||||
| chr18:229255 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919-2354G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229255 | |||||||
| chr18:229402 | C | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-2501G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229402 | |||||||
| chr18:229453 | G | A | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-2552C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229453 | |||||||
| chr18:229494 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.919-2593T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229494 | |||||||
| chr18:229518 | TA | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(190): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.919-2618delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229518 | |||||||
| chr18:229616 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.919-2715C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229616 | |||||||
| chr18:229676 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.919-2775G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229676 | |||||||
| chr18:229710 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0058 others(10): Show |
16 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919-2809T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229710 | |||||||
| chr18:229844 | TCTC | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-2946_919-2944d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229844 | |||||||
| chr18:229853 | C | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(192): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.919-2952G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229853 | |||||||
| chr18:229887 | C | T | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-2986G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229887 | |||||||
| chr18:229888 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0058 others(10): Show |
16 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919-2987C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229888 | |||||||
| chr18:230444 | T | G | 1 | a0001c0005t0002g0048 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.919-3543A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230444 | |||||||
| chr18:230482 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-3581G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230482 | |||||||
| chr18:230634 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.919-3733G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230634 | |||||||
| chr18:230739 | T | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(29): Show |
38 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.919-3838A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230739 | |||||||
| chr18:230756 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.919-3855C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230756 | |||||||
| chr18:230821 | G | C | 1 | a0001c0002t0001g0030 | 2 | HG02129.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.919-3920C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230821 | |||||||
| chr18:230848 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-3947C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230848 | |||||||
| chr18:230924 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919-4023C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230924 | |||||||
| chr18:230960 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-4059C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230960 | |||||||
| chr18:231035 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919-4134C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231035 | |||||||
| chr18:231063 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.919-4162A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231063 | |||||||
| chr18:231079 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.919-4178T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231079 | |||||||
| chr18:231242 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-4341G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231242 | |||||||
| chr18:231323 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.919-4422A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231323 | |||||||
| chr18:231453 | CAT | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0007t0001g0114 |
3 | HG06807.hp1 NA18906.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.919-4554_919-4553d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231453 | |||||||
| chr18:231457 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.919-4556A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231457 | |||||||
| chr18:231503 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.919-4602G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231503 | |||||||
| chr18:231730 | C | G | 2 | a0001c0001t0001g0008 a0001c0007t0001g0114 |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-4829G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231730 | |||||||
| chr18:232114 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.919-5213C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232114 | |||||||
| chr18:232280 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-5379T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232280 | |||||||
| chr18:232337 | A | G | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-5436T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232337 | |||||||
| chr18:232340 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.919-5439G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232340 | |||||||
| chr18:232462 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919-5561T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232462 | |||||||
| chr18:232508 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-5607A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232508 | |||||||
| chr18:232791 | T | TGAA | 35 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(32): Show |
41 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.919-5891_919-5890i others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232791 | |||||||
| chr18:232961 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-6060A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232961 | |||||||
| chr18:232995 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0216 a0001c0001t0001g0298 |
3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919-6094G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232995 | |||||||
| chr18:233016 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.919-6115G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233016 | |||||||
| chr18:233217 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919-6316T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233217 | |||||||
| chr18:233329 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.919-6428C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233329 | |||||||
| chr18:233379 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.919-6478C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233379 | |||||||
| chr18:233443 | G | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0049 others(9): Show |
15 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.919-6542C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233443 | |||||||
| chr18:233486 | T | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.919-6585A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233486 | |||||||
| chr18:233542 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919-6641G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233542 | |||||||
| chr18:233547 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-6646G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233547 | |||||||
| chr18:233830 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919-6929A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233830 | |||||||
| chr18:234138 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.919-7237C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234138 | |||||||
| chr18:234313 | C | T | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.919-7412G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234313 | |||||||
| chr18:234418 | T | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG03098.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-7517A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234418 | |||||||
| chr18:234473 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.919-7572A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234473 | |||||||
| chr18:234502 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0002g0018 |
3 | HG00642.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.919-7601C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234502 | |||||||
| chr18:234554 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-7653C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234554 | |||||||
| chr18:234555 | T | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-7654A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234555 | |||||||
| chr18:234627 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-7726G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234627 | |||||||
| chr18:234630 | C | A | 1 | a0001c0001t0001g0284 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.919-7729G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234630 | |||||||
| chr18:234661 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.919-7760G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234661 | |||||||
| chr18:234679 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.919-7778C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234679 | |||||||
| chr18:234773 | T | TAAC | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.919-7873_919-7872i others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234773 | |||||||
| chr18:234790 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.919-7889A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234790 | |||||||
| chr18:235001 | T | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-8100A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235001 | |||||||
| chr18:235083 | C | CT | 6 | a0001c0002t0001g0031 a0001c0002t0001g0175 a0001c0002t0001g0176 others(3): Show |
7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-8183dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235083 | |||||||
| chr18:235085 | A | AT | 158 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(155): Show |
197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.919-8185dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | |||||||
| chr18:235085 | A | ATT | 19 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0042 others(16): Show |
21 | HG00423.hp2 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.919-8186_919-8185d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | |||||||
| chr18:235085 | A | T | 6 | a0001c0002t0001g0031 a0001c0002t0001g0175 a0001c0002t0001g0176 others(3): Show |
7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-8184T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | |||||||
| chr18:235085 | AT | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0233 a0001c0001t0001g0251 others(3): Show |
6 | HG01169.hp2 HG03041.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-8185delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | |||||||
| chr18:235086 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.919-8185A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235086 | |||||||
| chr18:235087 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.919-8186A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235087 | |||||||
| chr18:235146 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919-8245A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235146 | |||||||
| chr18:235256 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.919-8355A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235256 | |||||||
| chr18:235383 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-8482C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235383 | |||||||
| chr18:235420 | C | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0187 |
2 | NA18963.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.919-8519G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235420 | |||||||
| chr18:235420 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919-8519G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235420 | |||||||
| chr18:235774 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-8873G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235774 | |||||||
| chr18:235780 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.919-8879A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235780 | |||||||
| chr18:235928 | A | G | 13 | a0001c0001t0001g0145 a0001c0001t0002g0006 a0001c0001t0002g0045 others(10): Show |
16 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.919-9027T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235928 | |||||||
| chr18:236019 | A | G | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-9118T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236019 | |||||||
| chr18:236244 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-9343A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236244 | |||||||
| chr18:236350 | CT | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(116): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.919-9450delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | |||||||
| chr18:236350 | CTT | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(59): Show |
75 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-9451_919-9450d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | |||||||
| chr18:236350 | CTTT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(90): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.919-9452_919-9450d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | |||||||
| chr18:236350 | CTTTT | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
10 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.919-9453_919-9450d others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | |||||||
| chr18:236352 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919-9451A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236352 | |||||||
| chr18:236381 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-9480T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236381 | |||||||
| chr18:236437 | G | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-9536C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236437 | |||||||
| chr18:236451 | G | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-9550C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236451 | |||||||
| chr18:236463 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919-9562G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236463 | |||||||
| chr18:236471 | TCAGCCTC others(18): Show |
T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.919-9595_919-9571d others(27): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236471 | |||||||
| chr18:236491 | GA | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(175): Show |
221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.919-9591delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236491 | |||||||
| chr18:236508 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.919-9607A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236508 | |||||||
| chr18:236518 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919-9617C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236518 | |||||||
| chr18:236523 | A | AT | 55 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(52): Show |
65 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.919-9623dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236523 | |||||||
| chr18:236718 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.918+9606T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236718 | |||||||
| chr18:237017 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+9307G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237017 | |||||||
| chr18:237063 | G | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG01167.hp1 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.918+9261C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237063 | |||||||
| chr18:237157 | A | AT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0058 others(22): Show |
31 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.918+9166dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | |||||||
| chr18:237157 | AT | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(87): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.918+9166delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | |||||||
| chr18:237157 | ATT | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(36): Show |
45 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+9165_918+9166d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | |||||||
| chr18:237177 | T | G | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
23 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.918+9147A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237177 | |||||||
| chr18:237230 | G | C | 1 | a0001c0001t0001g0017 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918+9094C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237230 | |||||||
| chr18:237301 | TGC | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+9021_918+9022d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237301 | |||||||
| chr18:237607 | GA | G | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+8716delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237607 | |||||||
| chr18:237653 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.918+8671G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237653 | |||||||
| chr18:237663 | G | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(180): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.918+8661C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237663 | |||||||
| chr18:237838 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+8486T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237838 | |||||||
| chr18:237843 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0149 others(1): Show |
7 | HG01106.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+8481G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237843 | |||||||
| chr18:237915 | A | G | 1 | a0001c0002t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.918+8409T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237915 | |||||||
| chr18:238024 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+8300C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238024 | |||||||
| chr18:238064 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.918+8260G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238064 | |||||||
| chr18:238128 | G | T | 1 | a0001c0001t0001g0017 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918+8196C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238128 | |||||||
| chr18:238213 | T | TA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+8110dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238213 | |||||||
| chr18:238475 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.918+7849C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238475 | |||||||
| chr18:238554 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0087 others(2): Show |
7 | HG01175.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+7770C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238554 | |||||||
| chr18:238596 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.918+7728C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238596 | |||||||
| chr18:238702 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+7622G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238702 | |||||||
| chr18:238715 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+7609A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238715 | |||||||
| chr18:238883 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.918+7441C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238883 | |||||||
| chr18:238970 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0216 a0001c0001t0001g0298 |
3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.918+7354T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238970 | |||||||
| chr18:239019 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.918+7305T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239019 | |||||||
| chr18:239041 | CTAT | C | 6 | a0001c0002t0001g0031 a0001c0002t0001g0175 a0001c0002t0001g0176 others(3): Show |
7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+7280_918+7282d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239041 | |||||||
| chr18:239052 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.918+7272A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239052 | |||||||
| chr18:239062 | T | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+7262A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239062 | |||||||
| chr18:239289 | C | T | 47 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(44): Show |
56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+7035G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239289 | |||||||
| chr18:239405 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.918+6919G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239405 | |||||||
| chr18:239463 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.918+6861G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239463 | |||||||
| chr18:239672 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.918+6652G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239672 | |||||||
| chr18:239855 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+6469T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239855 | |||||||
| chr18:239990 | A | AT | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.918+6333_918+6334i others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239990 | |||||||
| chr18:240098 | A | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG02257.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.918+6226T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240098 | |||||||
| chr18:240366 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.918+5958G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240366 | |||||||
| chr18:240436 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+5888A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240436 | |||||||
| chr18:240552 | T | TTTGGCTA | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+5765_918+5771d others(9): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240552 | |||||||
| chr18:240616 | A | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(29): Show |
38 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.918+5708T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240616 | |||||||
| chr18:240675 | T | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
24 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.918+5649A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240675 | |||||||
| chr18:240927 | A | G | 46 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(43): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.918+5397T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240927 | |||||||
| chr18:241147 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.918+5177G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241147 | |||||||
| chr18:241268 | T | C | 1 | a0001c0002t0001g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.918+5056A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241268 | |||||||
| chr18:241347 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.918+4977C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241347 | |||||||
| chr18:241482 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+4842A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241482 | |||||||
| chr18:241680 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.918+4644T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241680 | |||||||
| chr18:241764 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.918+4560A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241764 | |||||||
| chr18:241874 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0203 a0001c0001t0001g0213 others(2): Show |
6 | HG00621.hp1 HG02027.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+4450G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241874 | |||||||
| chr18:241993 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.918+4331C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241993 | |||||||
| chr18:242201 | G | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+4123C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242201 | |||||||
| chr18:242202 | CGTGGTGG others(61): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.918+4054_918+4121d others(70): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242202 | |||||||
| chr18:242214 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+4110G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242214 | |||||||
| chr18:242215 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.918+4109C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242215 | |||||||
| chr18:242268 | C | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(176): Show |
220 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.918+4056G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242268 | |||||||
| chr18:242283 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.918+4041G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242283 | |||||||
| chr18:242350 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(31): Show |
40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.918+3974G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242350 | |||||||
| chr18:242369 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(31): Show |
40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.918+3955A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242369 | |||||||
| chr18:242442 | C | CA | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+3881dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242442 | |||||||
| chr18:242442 | CA | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(76): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.918+3881delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242442 | |||||||
| chr18:242489 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.918+3835C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242489 | |||||||
| chr18:242494 | A | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.918+3830T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242494 | |||||||
| chr18:242855 | AAACACCA others(3): Show |
A | 1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+3459_918+3468d others(12): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242855 | |||||||
| chr18:242912 | T | G | 1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+3412A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242912 | |||||||
| chr18:243126 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0205 others(10): Show |
19 | HG00438.hp1 HG02074.hp2 HG03710.hp1 others(16): Show |
intron_variant | MODIFIER | c.918+3198A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243126 | |||||||
| chr18:243219 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+3105A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243219 | |||||||
| chr18:243430 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.918+2894G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243430 | |||||||
| chr18:243468 | G | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+2856C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243468 | |||||||
| chr18:243499 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.918+2825A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243499 | |||||||
| chr18:243545 | A | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0040 others(24): Show |
32 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.918+2779T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243545 | |||||||
| chr18:243546 | AT | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+2777delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243546 | |||||||
| chr18:243547 | T | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(138): Show |
176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.918+2777A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243547 | |||||||
| chr18:243549 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0104 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.918+2775A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243549 | |||||||
| chr18:243754 | T | TCGGGGGG others(3): Show |
1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+2569_918+2570i others(12): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243754 | |||||||
| chr18:243820 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG01099.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.918+2504A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243820 | |||||||
| chr18:243943 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.918+2381A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243943 | |||||||
| chr18:244065 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0202 |
3 | HG02080.hp2 NA18994.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.918+2259A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244065 | |||||||
| chr18:244125 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.918+2199T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244125 | |||||||
| chr18:244378 | T | A | 1 | a0001c0002t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.918+1946A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244378 | |||||||
| chr18:244553 | T | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+1771A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244553 | |||||||
| chr18:244768 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+1556G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244768 | |||||||
| chr18:244872 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0149 others(1): Show |
7 | HG01106.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+1452A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244872 | |||||||
| chr18:244908 | CCTT | C | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+1413_918+1415d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244908 | |||||||
| chr18:245056 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.918+1268A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245056 | |||||||
| chr18:245087 | G | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0179 |
3 | HG02015.hp2 HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.918+1237C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245087 | |||||||
| chr18:245168 | A | AAT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0120 others(5): Show |
11 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+1154_918+1155d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245168 | |||||||
| chr18:245179 | A | C | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+1145T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245179 | |||||||
| chr18:245249 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.918+1075T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245249 | |||||||
| chr18:245284 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.918+1040A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245284 | |||||||
| chr18:245465 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.918+859C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245465 | |||||||
| chr18:245888 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.918+436C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245888 | |||||||
| chr18:245971 | C | G | 1 | a0001c0001t0001g0223 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.918+353G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245971 | |||||||
| chr18:246057 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.918+267A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246057 | |||||||
| chr18:246063 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.918+261A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246063 | |||||||
| chr18:246199 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.918+125A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246199 | |||||||
| chr18:246265 | A | T | 1 | a0001c0002t0001g0188 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.918+59T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246265 | |||||||
| chr18:246297 | T | G | 1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+27A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246297 | |||||||
| chr18:246537 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-82A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246537 | |||||||
| chr18:246549 | A | T | 1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787-94T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246549 | |||||||
| chr18:246550 | A | T | 1 | a0001c0002t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787-95T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246550 | |||||||
| chr18:246568 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.787-113T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246568 | |||||||
| chr18:246675 | C | T | 1 | a0001c0003t0001g0263 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.787-220G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246675 | |||||||
| chr18:246677 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.787-222T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246677 | |||||||
| chr18:246916 | C | CA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0042 others(11): Show |
20 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.787-462dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | |||||||
| chr18:246916 | C | CAA | 4 | a0001c0001t0001g0015 a0001c0001t0001g0214 a0001c0001t0001g0219 others(1): Show |
6 | HG00673.hp2 NA19002.hp2 NA19060.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-463_787-462dup others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | |||||||
| chr18:246916 | CA | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.787-462delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | |||||||
| chr18:246916 | CAA | C | 9 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0124 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-463_787-462del others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | |||||||
| chr18:246916 | CAAA | C | 35 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(32): Show |
43 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.787-464_787-462del others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | |||||||
| chr18:246930 | A | C | 2 | a0001c0001t0001g0125 a0001c0003t0001g0275 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.787-475T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246930 | |||||||
| chr18:246935 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.787-480T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246935 | |||||||
| chr18:246970 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.787-515C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246970 | |||||||
| chr18:247127 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.787-672G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247127 | |||||||
| chr18:247378 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.786+471A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247378 | |||||||
| chr18:247509 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+340C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247509 | |||||||
| chr18:247510 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+339T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247510 | |||||||
| chr18:247521 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+328C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247521 | |||||||
| chr18:247568 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786+281A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247568 | |||||||
| chr18:247722 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.786+127A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247722 | |||||||
| chr18:247834 | T | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(42): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.786+15A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247834 | |||||||
| chr18:247972 | G | A | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-15C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 247972 | |||||||
| chr18:248187 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.678-230T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248187 | |||||||
| chr18:248228 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.678-271G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248228 | |||||||
| chr18:248254 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.678-297T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248254 | |||||||
| chr18:248266 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-309T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248266 | |||||||
| chr18:248268 | C | G | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-311G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248268 | |||||||
| chr18:248279 | G | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(43): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.678-322C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248279 | |||||||
| chr18:248342 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.678-385A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248342 | |||||||
| chr18:248481 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.678-524A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248481 | |||||||
| chr18:248710 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.678-753G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248710 | |||||||
| chr18:248838 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.678-881G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248838 | |||||||
| chr18:248912 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.678-955C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248912 | |||||||
| chr18:248992 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.678-1035A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248992 | |||||||
| chr18:249228 | G | A | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-1271C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249228 | |||||||
| chr18:249359 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0252 |
3 | HG02027.hp1 HG02165.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.678-1402C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249359 | |||||||
| chr18:249372 | A | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0060 others(7): Show |
13 | HG00544.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.678-1415T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249372 | |||||||
| chr18:249468 | C | T | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG01109.hp1 HG01256.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.678-1511G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249468 | |||||||
| chr18:249472 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(175): Show |
215 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.678-1515T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249472 | |||||||
| chr18:249594 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.678-1637T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249594 | |||||||
| chr18:249606 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(41): Show |
56 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.678-1649C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249606 | |||||||
| chr18:249653 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.678-1696G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249653 | |||||||
| chr18:249668 | G | GA | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(60): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.678-1712dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249668 | |||||||
| chr18:249668 | G | GAA | 35 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(32): Show |
41 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.678-1713_678-1712d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249668 | |||||||
| chr18:249910 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.678-1953T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249910 | |||||||
| chr18:249939 | T | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.678-1982A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249939 | |||||||
| chr18:250018 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.678-2061G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250018 | |||||||
| chr18:250047 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.678-2090A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250047 | |||||||
| chr18:250058 | A | G | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.678-2101T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250058 | |||||||
| chr18:250073 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.678-2116A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250073 | |||||||
| chr18:250462 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.677+2077T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250462 | |||||||
| chr18:250539 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.677+2000G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250539 | |||||||
| chr18:250589 | A | C | 97 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0020 others(94): Show |
116 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(113): Show |
intron_variant | MODIFIER | c.677+1950T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250589 | |||||||
| chr18:250616 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.677+1923A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250616 | |||||||
| chr18:251017 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.677+1522A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251017 | |||||||
| chr18:251123 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.677+1416A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251123 | |||||||
| chr18:251558 | T | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(42): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.677+981A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251558 | |||||||
| chr18:251565 | G | GA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.677+973dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251565 | |||||||
| chr18:251728 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.677+811C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251728 | |||||||
| chr18:251765 | C | T | 50 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(47): Show |
60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.677+774G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251765 | |||||||
| chr18:251789 | C | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG00733.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+750G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251789 | |||||||
| chr18:251954 | G | C | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG00438.hp2 HG02027.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.677+585C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251954 | |||||||
| chr18:252038 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.677+501G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252038 | |||||||
| chr18:252043 | AT | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+495delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252043 | |||||||
| chr18:252082 | T | C | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+457A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252082 | |||||||
| chr18:252156 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.677+383C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252156 | |||||||
| chr18:252253 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677+286A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252253 | |||||||
| chr18:252268 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.677+271G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252268 | |||||||
| chr18:252436 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.677+103T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252436 | |||||||
| chr18:252769 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.604-157T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252769 | |||||||
| chr18:252769 | AT | A | 1 | a0001c0001t0001g0012 | 3 | HG00621.hp2 NA18950.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.604-158delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252769 | |||||||
| chr18:252795 | G | C | 48 | a0001c0001t0001g0139 a0001c0002t0001g0007 a0001c0002t0001g0028 others(45): Show |
57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.604-183C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252795 | |||||||
| chr18:252925 | A | C | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.604-313T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252925 | |||||||
| chr18:252998 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.604-386T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252998 | |||||||
| chr18:253216 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.604-604A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253216 | |||||||
| chr18:253305 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.604-693C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253305 | |||||||
| chr18:253321 | G | A | 1 | a0001c0002t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.604-709C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253321 | |||||||
| chr18:253336 | A | T | 3 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 |
3 | NA18954.hp2 NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.604-724T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253336 | |||||||
| chr18:253506 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+767A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253506 | |||||||
| chr18:253587 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.603+686C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253587 | |||||||
| chr18:253902 | A | AT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
80 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.603+370dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | |||||||
| chr18:253902 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.603+371T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | |||||||
| chr18:253902 | AT | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0017 others(83): Show |
105 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.603+370delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | |||||||
| chr18:254013 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.603+260G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 254013 | |||||||
| chr18:254172 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.603+101T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 254172 | |||||||
| chr18:254368 | C | CA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521-14dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254368 | |||||||
| chr18:254565 | CTT | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-212_521-211del others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254565 | |||||||
| chr18:254613 | A | G | 2 | a0001c0003t0001g0275 a0001c0003t0001g0276 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.521-258T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254613 | |||||||
| chr18:254640 | G | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-285C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254640 | |||||||
| chr18:254762 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.521-407G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254762 | |||||||
| chr18:254762 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.521-407G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254762 | |||||||
| chr18:254798 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.521-443T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254798 | |||||||
| chr18:254817 | A | AT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
8 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.521-463dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254817 | |||||||
| chr18:254962 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.521-607T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254962 | |||||||
| chr18:255101 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.521-746T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255101 | |||||||
| chr18:255143 | G | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-788C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255143 | |||||||
| chr18:255156 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0298 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.521-801T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255156 | |||||||
| chr18:255209 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0187 |
2 | NA18963.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.521-854C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255209 | |||||||
| chr18:255210 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.521-855T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255210 | |||||||
| chr18:255552 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(31): Show |
40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.521-1197C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255552 | |||||||
| chr18:255581 | T | A | 2 | a0001c0003t0001g0273 a0001c0003t0001g0274 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.521-1226A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255581 | |||||||
| chr18:255622 | G | A | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.521-1267C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255622 | |||||||
| chr18:255799 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.521-1444T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255799 | |||||||
| chr18:255875 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.521-1520T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255875 | |||||||
| chr18:256008 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.521-1653A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256008 | |||||||
| chr18:256043 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.521-1688T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256043 | |||||||
| chr18:256138 | A | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.521-1783T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256138 | |||||||
| chr18:256200 | A | AC | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.521-1846dupG | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256200 | |||||||
| chr18:256238 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.521-1883C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256238 | |||||||
| chr18:256314 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.521-1959A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256314 | |||||||
| chr18:256900 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.520+2280G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256900 | |||||||
| chr18:256976 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(42): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.520+2204C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256976 | |||||||
| chr18:257104 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0297 |
2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520+2076C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257104 | |||||||
| chr18:257377 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.520+1803T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257377 | |||||||
| chr18:257661 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520+1519T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257661 | |||||||
| chr18:257671 | G | A | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.520+1509C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257671 | |||||||
| chr18:257785 | TA | T | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.520+1394delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257785 | |||||||
| chr18:257968 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520+1212A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257968 | |||||||
| chr18:258284 | C | G | 95 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0020 others(92): Show |
114 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.520+896G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258284 | |||||||
| chr18:258294 | G | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.520+886C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258294 | |||||||
| chr18:258324 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.520+856T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258324 | |||||||
| chr18:258681 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.520+499T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258681 | |||||||
| chr18:258685 | G | A | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.520+495C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258685 | |||||||
| chr18:258778 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02055.hp2 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+402G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258778 | |||||||
| chr18:258809 | T | C | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.520+371A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258809 | |||||||
| chr18:259148 | G | A | 50 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(47): Show |
60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.520+32C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 259148 | |||||||
| chr18:259379 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.425-104T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 6/20 | chr18 | 259379 | |||||||
| chr18:259743 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376-13G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259743 | |||||||
| chr18:259758 | T | C | 2 | a0001c0003t0001g0275 a0001c0003t0001g0276 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.376-28A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259758 | |||||||
| chr18:259789 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376-59T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259789 | |||||||
| chr18:259800 | G | GA | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(31): Show |
40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.376-71dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259800 | |||||||
| chr18:259944 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0112 |
2 | HG00408.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.376-214T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259944 | |||||||
| chr18:260040 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.375+146C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260040 | |||||||
| chr18:260041 | AG | A | 50 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(47): Show |
60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.375+144delC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260041 | |||||||
| chr18:260051 | A | ATATAATT others(309): Show |
1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.375+134_375+135ins others(316): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260051 | |||||||
| chr18:260108 | TA | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.375+77delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260108 | |||||||
| chr18:260109 | A | T | 8 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
8 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+77T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260109 | |||||||
| chr18:260140 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.375+46A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260140 | |||||||
| chr18:260152 | T | G | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.375+34A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260152 | |||||||
| chr18:260473 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0214 a0001c0001t0001g0246 others(3): Show |
8 | HG00673.hp2 HG02015.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.257-169A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260473 | |||||||
| chr18:260504 | T | C | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.257-200A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260504 | |||||||
| chr18:260597 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(183): Show |
230 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.257-293A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260597 | |||||||
| chr18:260684 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.257-380A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260684 | |||||||
| chr18:260966 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.257-662C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260966 | |||||||
| chr18:261106 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.257-802A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261106 | |||||||
| chr18:261268 | A | G | 47 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(44): Show |
56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.257-964T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261268 | |||||||
| chr18:261278 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.257-974T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261278 | |||||||
| chr18:261279 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.257-975A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261279 | |||||||
| chr18:261279 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.257-975A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261279 | |||||||
| chr18:261346 | C | T | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.257-1042G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261346 | |||||||
| chr18:261387 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.257-1083T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261387 | |||||||
| chr18:261500 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.257-1196T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261500 | |||||||
| chr18:261536 | C | T | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.257-1232G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261536 | |||||||
| chr18:261610 | G | A | 3 | a0001c0002t0001g0033 a0001c0002t0001g0189 a0001c0002t0001g0190 |
4 | NA18939.hp1 NA19010.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.257-1306C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261610 | |||||||
| chr18:261733 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.257-1429G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261733 | |||||||
| chr18:261903 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.257-1599A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261903 | |||||||
| chr18:262000 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.257-1696G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262000 | |||||||
| chr18:262187 | C | T | 1 | a0001c0007t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.256+1839G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262187 | |||||||
| chr18:262259 | T | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.256+1767A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262259 | |||||||
| chr18:262456 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.256+1570G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262456 | |||||||
| chr18:262526 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.256+1500A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262526 | |||||||
| chr18:262589 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.256+1437C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262589 | |||||||
| chr18:262597 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.256+1429C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262597 | |||||||
| chr18:262599 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.256+1427G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262599 | |||||||
| chr18:262616 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.256+1410C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262616 | |||||||
| chr18:262850 | GAATT | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(42): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.256+1172_256+1175d others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262850 | |||||||
| chr18:263137 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+889C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263137 | |||||||
| chr18:263174 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0018 |
4 | HG00642.hp2 HG01175.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+852C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263174 | |||||||
| chr18:263198 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.256+828C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263198 | |||||||
| chr18:263227 | C | CA | 47 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.256+798_256+799ins others(1): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263227 | |||||||
| chr18:263368 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.256+658G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263368 | |||||||
| chr18:263375 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.256+651C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263375 | |||||||
| chr18:263399 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.256+627C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263399 | |||||||
| chr18:263514 | A | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.256+512T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263514 | |||||||
| chr18:263600 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.256+426A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263600 | |||||||
| chr18:263641 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.256+385C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263641 | |||||||
| chr18:263677 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.256+349T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263677 | |||||||
| chr18:263679 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.256+347G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263679 | |||||||
| chr18:263687 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.256+339A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263687 | |||||||
| chr18:263698 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.256+328G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263698 | |||||||
| chr18:263718 | T | C | 12 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0049 others(9): Show |
15 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.256+308A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263718 | |||||||
| chr18:264012 | G | A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
37 | HG00280.hp2 HG01099.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.256+14C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 264012 | |||||||
| chr18:264330 | A | G | 2 | a0001c0001t0001g0008 a0001c0007t0001g0114 |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-238T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264330 | |||||||
| chr18:264341 | T | C | 1 | a0001c0006t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.190-249A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264341 | |||||||
| chr18:264342 | A | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG01167.hp1 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.190-250T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264342 | |||||||
| chr18:264352 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-260C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264352 | |||||||
| chr18:264431 | T | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.190-339A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264431 | |||||||
| chr18:264882 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.189+421C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264882 | |||||||
| chr18:264904 | TGAG | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0124 others(3): Show |
7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+396_189+398del others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264904 | |||||||
| chr18:264954 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+349A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264954 | |||||||
| chr18:265147 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.189+156C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 265147 | |||||||
| chr18:265237 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.189+66G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 265237 | |||||||
| chr18:265370 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.129-7T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 2/20 | chr18 | 265370 | |||||||
| chr18:265406 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.129-43C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 2/20 | chr18 | 265406 | |||||||
| chr18:265677 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0213 |
2 | HG00621.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.55-147G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265677 | |||||||
| chr18:265714 | A | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0201 others(4): Show |
10 | HG00544.hp2 HG02074.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-184T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265714 | |||||||
| chr18:265808 | CA | C | 68 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
80 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.55-279delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265808 | |||||||
| chr18:265846 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-316C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265846 | |||||||
| chr18:266146 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-616A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266146 | |||||||
| chr18:266177 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.55-647A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266177 | |||||||
| chr18:266222 | T | C | 1 | a0001c0002t0001g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.55-692A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266222 | |||||||
| chr18:266251 | T | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.55-721A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266251 | |||||||
| chr18:266457 | A | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0038 others(31): Show |
40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.55-927T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266457 | |||||||
| chr18:266539 | A | AT | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(120): Show |
154 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.55-1010dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | |||||||
| chr18:266539 | A | ATT | 57 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
66 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.55-1011_55-1010dup others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | |||||||
| chr18:266539 | A | ATTT | 9 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0117 others(6): Show |
11 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1012_55-1010dup others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | |||||||
| chr18:266539 | A | T | 1 | a0001c0001t0001g0260 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.55-1009T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | |||||||
| chr18:266539 | AT | A | 6 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG01071.hp1 HG02698.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1010delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | |||||||
| chr18:266552 | T | A | 1 | a0001c0001t0001g0260 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.55-1022A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266552 | |||||||
| chr18:266568 | T | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.55-1038A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266568 | |||||||
| chr18:266627 | G | C | 1 | a0001c0002t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.55-1097C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266627 | |||||||
| chr18:266725 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.55-1195G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266725 | |||||||
| chr18:266828 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0299 |
2 | HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+1138G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266828 | |||||||
| chr18:266848 | C | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
26 | HG00280.hp2 HG01099.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.54+1118G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266848 | |||||||
| chr18:267008 | CGT | C | 46 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(43): Show |
54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.54+956_54+957delAC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267008 | |||||||
| chr18:267014 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+952A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267014 | |||||||
| chr18:267019 | G | GTA | 3 | a0001c0001t0001g0297 a0001c0003t0001g0295 a0001c0003t0001g0296 |
3 | HG02055.hp1 HG02602.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54+945_54+946dupTA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267019 | |||||||
| chr18:267019 | GTA | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.54+945_54+946delTA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267019 | |||||||
| chr18:267023 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.54+943T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267023 | |||||||
| chr18:267048 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.54+918G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267048 | |||||||
| chr18:267262 | C | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.54+704G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267262 | |||||||
| chr18:267303 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.54+663A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267303 | |||||||
| chr18:267367 | A | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(21): Show |
29 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.54+599T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267367 | |||||||
| chr18:267496 | G | C | 7 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+470C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267496 | |||||||
| chr18:267499 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.54+467A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267499 | |||||||
| chr18:267625 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+341G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267625 | |||||||
| chr18:267768 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+198G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267768 | |||||||
| chr18:267923 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.54+43G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267923 |