Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9267 |
| ensemblid | ENSG00000108669.18 |
| hgncid | 9501 |
| symbol | CYTH1 |
| name | cytohesin 1 |
| refseq_nuc | NM_004762.6 |
| refseq_prot | NP_004753.1 |
| ensembl_nuc | ENST00000446868.8 |
| ensembl_prot | ENSP00000389095.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 78674048 |
| end | 78782273 |
| strand | - |
| ver | v1.2 |
| region | chr17:78674048-78782273 |
| region5000 | chr17:78669048-78787273 |
| regionname0 | CYTH1_chr17_78674048_78782273 |
| regionname5000 | CYTH1_chr17_78669048_78787273 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1194 | 373 | 83 | 60 | 178 | 12 | 38 | CYTH1_chr17_78669048_78787273 | CYTH1 | ATGGA others(1189): Show |
chr17 | 78669048 | 78787273 | ||
| a0001c0002 | 0/0 | 1194 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | ATGGA others(1189): Show |
chr17 | 78669048 | 78787273 | ||
| a0001c0003 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | ATGGA others(1189): Show |
chr17 | 78669048 | 78787273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3290 | 90 | 30 | 13 | 39 | 2 | 5 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0002 | 0/0 | 3289 | 77 | 2 | 12 | 54 | 1 | 8 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0003 | 0/0 | 3289 | 55 | 22 | 2 | 31 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0004 | 0/0 | 3290 | 44 | 3 | 10 | 19 | 1 | 11 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0005 | 0/0 | 3289 | 28 | 1 | 0 | 20 | 0 | 7 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0006 | 0/0 | 3289 | 23 | 1 | 7 | 7 | 4 | 4 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0007 | 0/1 | 3290 | 11 | 3 | 6 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0008 | 0/0 | 3289 | 9 | 0 | 6 | 0 | 3 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0009 | 0/0 | 3289 | 8 | 8 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0011 | 0/0 | 3290 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0012 | 0/0 | 3289 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0013 | 0/0 | 3289 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0014 | 0/0 | 3289 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0015 | 0/0 | 3290 | 2 | 1 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0016 | 0/0 | 3290 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0018 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0019 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0020 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0021 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0022 | 0/0 | 3290 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0023 | 0/0 | 3290 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0024 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0025 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0026 | 0/0 | 3290 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0027 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0028 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0029 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0030 | 0/0 | 3290 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3285): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0031 | 0/0 | 3289 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0001t0032 | 0/0 | 3289 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0002t0010 | 0/0 | 3289 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| a0001c0003t0017 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | GCGGC others(3284): Show |
chr17 | 78669048 | 78787273 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0013g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0013g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0015g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0015g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0016g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0018g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0020g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0021g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0022g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0024g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0025g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0026g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0027g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0028g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0029g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0030g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0031g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0032g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0003t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0327 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0329 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0126 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0291 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0332 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0334 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0343 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0338 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0344 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0220 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0267 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0268 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0335 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0348 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0303 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0336 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01074 | hp1 | a0001 | c0001 | t0031 | g0273 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0206 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0207 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0326 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01168 | hp2 | a0001 | c0001 | t0023 | g0151 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0321 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0100 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0333 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0061 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0116 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0349 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0205 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0320 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0266 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0265 | EUR | IBS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0345 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0189 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0346 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0368 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0117 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0361 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0370 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0352 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0373 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0353 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0372 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0365 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0058 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0331 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0216 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0375 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0132 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0363 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0366 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0369 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02895 | hp2 | a0001 | c0001 | t0025 | g0051 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0362 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02897 | hp1 | a0001 | c0001 | t0019 | g0046 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0360 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0374 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0350 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0053 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0347 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03209 | hp2 | a0001 | c0002 | t0010 | g0358 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03225 | hp1 | a0001 | c0002 | t0010 | g0359 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0330 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03491 | hp1 | a0001 | c0001 | t0026 | g0102 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0044 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0367 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03579 | hp1 | a0001 | c0003 | t0017 | g0017 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0371 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0037 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03669 | hp2 | a0001 | c0001 | t0030 | g0006 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0033 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0272 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0032 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0341 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0230 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0215 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0217 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0364 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18747 | hp1 | a0001 | c0001 | t0021 | g0186 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0340 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18943 | hp2 | a0001 | c0001 | t0027 | g0164 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18946 | hp1 | a0001 | c0001 | t0020 | g0229 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0339 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0342 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18979 | hp2 | a0001 | c0001 | t0015 | g0042 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0241 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19043 | hp2 | a0001 | c0002 | t0010 | g0357 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19058 | hp2 | a0001 | c0001 | t0028 | g0180 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0030 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | ASW | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ASW | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0262 | EUR | TSI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0204 | EUR | TSI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0328 | SAS | GIH | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0240 | SAS | GIH | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0351 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02109 | hp2 | a0001 | c0002 | t0010 | g0356 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0376 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0354 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0325 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG06807 | hp2 | a0001 | c0001 | t0029 | g0115 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0049 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0377 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0231 | REF | REF | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0234 | REF | REF | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78701721 | T | C | 1 | a0001c0003 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.387A>G | p.Ala129Ala | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/14 | 437/3290 | 387/1197 | 129/398 | chr17 | 78701721 | |||
| chr17:78709713 | T | G | 1 | a0001c0002 | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.42A>C | p.Ala14Ala | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/14 | 92/3290 | 42/1197 | 14/398 | chr17 | 78709713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78674151 | C | G | 5 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0019 others(2): Show |
34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1940G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1940 | chr17 | 78674151 | ||||||
| chr17:78674179 | T | C | 1 | a0001c0001t0026 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1912A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1912 | chr17 | 78674179 | ||||||
| chr17:78674625 | C | T | 1 | a0001c0001t0027 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1466 | chr17 | 78674625 | ||||||
| chr17:78674656 | C | T | 1 | a0001c0001t0008 | 9 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1435G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1435 | chr17 | 78674656 | ||||||
| chr17:78674667 | A | G | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(15): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1424T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1424 | chr17 | 78674667 | ||||||
| chr17:78674684 | C | T | 1 | a0001c0001t0026 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1407 | chr17 | 78674684 | ||||||
| chr17:78674713 | G | A | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1378C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1378 | chr17 | 78674713 | ||||||
| chr17:78674729 | A | C | 11 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(8): Show |
101 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1362T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1362 | chr17 | 78674729 | ||||||
| chr17:78674880 | A | G | 6 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0014 others(3): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1211T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1211 | chr17 | 78674880 | ||||||
| chr17:78675053 | C | T | 2 | a0001c0001t0009 a0001c0003t0017 |
9 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1038G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1038 | chr17 | 78675053 | ||||||
| chr17:78675057 | G | A | 1 | a0001c0001t0028 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1034 | chr17 | 78675057 | ||||||
| chr17:78675060 | C | T | 1 | a0001c0001t0024 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1031G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1031 | chr17 | 78675060 | ||||||
| chr17:78675279 | C | T | 1 | a0001c0001t0031 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 812 | chr17 | 78675279 | ||||||
| chr17:78675331 | G | A | 1 | a0001c0001t0029 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 760 | chr17 | 78675331 | ||||||
| chr17:78675341 | G | A | 1 | a0001c0001t0014 | 2 | HG03130.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 750 | chr17 | 78675341 | ||||||
| chr17:78675387 | C | T | 1 | a0001c0001t0023 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*704G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 704 | chr17 | 78675387 | ||||||
| chr17:78675459 | C | T | 1 | a0001c0001t0013 | 2 | HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*632G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 632 | chr17 | 78675459 | ||||||
| chr17:78675477 | G | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 614 | chr17 | 78675477 | ||||||
| chr17:78675520 | C | T | 1 | a0001c0001t0011 | 3 | NA18939.hp2 NA18983.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*571G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 571 | chr17 | 78675520 | ||||||
| chr17:78675542 | T | C | 1 | a0001c0002t0010 | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 549 | chr17 | 78675542 | ||||||
| chr17:78675587 | C | T | 1 | a0001c0001t0022 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 504 | chr17 | 78675587 | ||||||
| chr17:78675631 | TA | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*459delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 459 | chr17 | 78675631 | ||||||
| chr17:78675633 | A | T | 2 | a0001c0001t0012 a0001c0001t0018 |
3 | HG01261.hp1 HG02055.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 458 | chr17 | 78675633 | ||||||
| chr17:78675751 | C | T | 1 | a0001c0003t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 340 | chr17 | 78675751 | ||||||
| chr17:78675775 | T | C | 1 | a0001c0001t0030 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 316 | chr17 | 78675775 | ||||||
| chr17:78675915 | A | G | 1 | a0001c0001t0007 | 10 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*176T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 176 | chr17 | 78675915 | ||||||
| chr17:78675920 | T | C | 4 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0031 others(1): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*171A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 171 | chr17 | 78675920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78676240 | A | T | 65 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1119-71T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676240 | |||||||
| chr17:78676308 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1119-139G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676308 | |||||||
| chr17:78676364 | G | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0311 a0001c0001t0002g0312 |
3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1119-195C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676364 | |||||||
| chr17:78676377 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1119-208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676377 | |||||||
| chr17:78676521 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1119-352A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676521 | |||||||
| chr17:78676555 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1119-386G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676555 | |||||||
| chr17:78676618 | T | A | 23 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1119-449A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676618 | |||||||
| chr17:78676688 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0003g0237 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1119-519G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676688 | |||||||
| chr17:78676741 | C | T | 5 | a0001c0001t0003g0350 a0001c0002t0010g0356 a0001c0002t0010g0357 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119-572G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676741 | |||||||
| chr17:78676811 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1119-642C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676811 | |||||||
| chr17:78676821 | G | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01496.hp2 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1119-652C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676821 | |||||||
| chr17:78676958 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119-789G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676958 | |||||||
| chr17:78677111 | A | G | 1 | a0001c0001t0004g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1119-942T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677111 | |||||||
| chr17:78677152 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119-983T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677152 | |||||||
| chr17:78677221 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1119-1052A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677221 | |||||||
| chr17:78677840 | T | C | 1 | a0001c0001t0006g0329 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1119-1671A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677840 | |||||||
| chr17:78677941 | G | A | 3 | a0001c0001t0006g0332 a0001c0001t0006g0334 a0001c0001t0006g0335 |
3 | HG00280.hp2 HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1119-1772C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677941 | |||||||
| chr17:78677963 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1119-1794C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677963 | |||||||
| chr17:78678175 | T | C | 221 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1119-2006A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678175 | |||||||
| chr17:78678178 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1119-2009A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678178 | |||||||
| chr17:78678245 | C | A | 43 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.1118+1945G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678245 | |||||||
| chr17:78678358 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+1832C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678358 | |||||||
| chr17:78678377 | G | T | 2 | a0001c0001t0011g0030 a0001c0001t0011g0167 |
2 | NA18939.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1118+1813C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678377 | |||||||
| chr17:78678384 | A | G | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.1118+1806T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678384 | |||||||
| chr17:78678405 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1118+1785C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678405 | |||||||
| chr17:78678453 | G | A | 30 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(27): Show |
30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.1118+1737C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678453 | |||||||
| chr17:78678595 | G | T | 1 | a0001c0001t0004g0211 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1118+1595C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678595 | |||||||
| chr17:78678612 | AAC | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+1576_1118+157 others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678612 | |||||||
| chr17:78678685 | A | G | 353 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(350): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1118+1505T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678685 | |||||||
| chr17:78678800 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1118+1390A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678800 | |||||||
| chr17:78678853 | G | C | 1 | a0001c0001t0018g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1118+1337C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678853 | |||||||
| chr17:78678951 | C | T | 1 | a0001c0001t0013g0353 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1118+1239G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678951 | |||||||
| chr17:78678968 | A | G | 1 | a0001c0001t0006g0333 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1118+1222T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678968 | |||||||
| chr17:78679023 | A | G | 1 | a0001c0001t0003g0367 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1118+1167T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679023 | |||||||
| chr17:78679145 | A | T | 1 | a0001c0001t0004g0216 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1118+1045T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679145 | |||||||
| chr17:78679146 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+1044G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679146 | |||||||
| chr17:78679176 | G | A | 1 | a0001c0001t0020g0229 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1118+1014C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679176 | |||||||
| chr17:78679276 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1118+914A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679276 | |||||||
| chr17:78679356 | GATCACTG others(64): Show |
G | 7 | a0001c0001t0001g0113 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00733.hp2 HG01099.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1118+763_1118+833d others(73): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679356 | |||||||
| chr17:78679427 | C | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+763G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679427 | |||||||
| chr17:78679520 | C | T | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+670G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679520 | |||||||
| chr17:78679577 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1118+613T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679577 | |||||||
| chr17:78679579 | G | C | 218 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1118+611C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679579 | |||||||
| chr17:78679711 | C | T | 1 | a0001c0001t0029g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1118+479G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679711 | |||||||
| chr17:78679721 | G | A | 140 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.1118+469C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679721 | |||||||
| chr17:78679927 | G | A | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0028 others(1): Show |
4 | NA18940.hp1 NA18947.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1118+263C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679927 | |||||||
| chr17:78679942 | C | T | 42 | a0001c0001t0001g0179 a0001c0001t0005g0002 a0001c0001t0005g0003 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.1118+248G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679942 | |||||||
| chr17:78680044 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+146C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78680044 | |||||||
| chr17:78680116 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1118+74G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78680116 | |||||||
| chr17:78680815 | C | T | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.963+156G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680815 | |||||||
| chr17:78680907 | A | T | 33 | a0001c0001t0002g0299 a0001c0001t0005g0002 a0001c0001t0005g0003 others(30): Show |
33 | HG00673.hp1 HG02080.hp2 HG02132.hp2 others(30): Show |
intron_variant | MODIFIER | c.963+64T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680907 | |||||||
| chr17:78680931 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.963+40G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680931 | |||||||
| chr17:78681221 | T | C | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-179A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681221 | |||||||
| chr17:78681300 | T | C | 27 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.892-258A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681300 | |||||||
| chr17:78681399 | A | G | 178 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.892-357T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681399 | |||||||
| chr17:78681428 | A | C | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.892-386T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681428 | |||||||
| chr17:78681484 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.892-442G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681484 | |||||||
| chr17:78681485 | T | C | 42 | a0001c0001t0001g0093 a0001c0001t0005g0002 a0001c0001t0005g0003 others(39): Show |
42 | HG00673.hp1 HG01074.hp2 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.892-443A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681485 | |||||||
| chr17:78681662 | C | T | 65 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.892-620G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681662 | |||||||
| chr17:78681679 | A | G | 66 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.892-637T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681679 | |||||||
| chr17:78681687 | GA | G | 4 | a0001c0001t0002g0251 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-646delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681687 | |||||||
| chr17:78681837 | C | CA | 9 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0276 others(6): Show |
9 | HG02486.hp1 HG02895.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-796dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | |||||||
| chr17:78681837 | C | CAA | 39 | a0001c0001t0003g0065 a0001c0001t0003g0073 a0001c0001t0003g0236 others(36): Show |
39 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.892-797_892-796dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | |||||||
| chr17:78681837 | C | CAAA | 30 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0067 others(27): Show |
30 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.892-798_892-796dup others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | |||||||
| chr17:78681847 | A | AC | 138 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.892-806_892-805ins others(1): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681847 | |||||||
| chr17:78681863 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.892-821C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681863 | |||||||
| chr17:78681968 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-926G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681968 | |||||||
| chr17:78682013 | G | A | 2 | a0001c0001t0012g0116 a0001c0001t0012g0117 |
2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.892-971C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682013 | |||||||
| chr17:78682014 | A | C | 2 | a0001c0001t0012g0116 a0001c0001t0012g0117 |
2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.892-972T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682014 | |||||||
| chr17:78682030 | T | C | 1 | a0001c0001t0027g0164 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.892-988A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682030 | |||||||
| chr17:78682098 | A | ATT | 31 | a0001c0001t0002g0280 a0001c0001t0003g0107 a0001c0001t0003g0350 others(28): Show |
31 | HG01123.hp2 HG01255.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.892-1057_892-1056i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682098 | |||||||
| chr17:78682128 | C | A | 87 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(84): Show |
87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.892-1086G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682128 | |||||||
| chr17:78682209 | C | A | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.892-1167G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682209 | |||||||
| chr17:78682513 | G | A | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-1471C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682513 | |||||||
| chr17:78682547 | C | T | 1 | a0001c0001t0004g0125 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.892-1505G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682547 | |||||||
| chr17:78682576 | GGT | G | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0154 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1536_892-1535d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682576 | |||||||
| chr17:78682716 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-1674G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682716 | |||||||
| chr17:78682858 | T | C | 23 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.892-1816A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682858 | |||||||
| chr17:78683158 | G | A | 74 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(71): Show |
74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.892-2116C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683158 | |||||||
| chr17:78683218 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.892-2176C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683218 | |||||||
| chr17:78683222 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.892-2180G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683222 | |||||||
| chr17:78683227 | C | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-2185G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683227 | |||||||
| chr17:78683240 | A | T | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.892-2198T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683240 | |||||||
| chr17:78683261 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-2219G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683261 | |||||||
| chr17:78683481 | C | T | 31 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.892-2439G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683481 | |||||||
| chr17:78683484 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-2442C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683484 | |||||||
| chr17:78683490 | C | T | 1 | a0001c0001t0004g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.892-2448G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683490 | |||||||
| chr17:78683567 | G | A | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-2525C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683567 | |||||||
| chr17:78683655 | A | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-2613T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683655 | |||||||
| chr17:78683698 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-2656A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683698 | |||||||
| chr17:78683877 | C | A | 2 | a0001c0002t0010g0357 a0001c0002t0010g0358 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.892-2835G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683877 | |||||||
| chr17:78683910 | G | A | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-2868C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683910 | |||||||
| chr17:78683992 | C | T | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892-2950G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683992 | |||||||
| chr17:78684004 | A | G | 22 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-2962T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684004 | |||||||
| chr17:78684178 | C | G | 141 | a0001c0001t0001g0157 a0001c0001t0002g0012 a0001c0001t0002g0013 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.892-3136G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684178 | |||||||
| chr17:78684179 | C | T | 141 | a0001c0001t0001g0157 a0001c0001t0002g0012 a0001c0001t0002g0013 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.892-3137G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684179 | |||||||
| chr17:78684249 | T | A | 1 | a0001c0001t0003g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.892-3207A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684249 | |||||||
| chr17:78684276 | C | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-3234G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684276 | |||||||
| chr17:78684381 | C | T | 2 | a0001c0001t0003g0073 a0001c0001t0003g0084 |
2 | NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.892-3339G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684381 | |||||||
| chr17:78684882 | T | C | 30 | a0001c0001t0004g0010 a0001c0001t0004g0063 a0001c0001t0004g0111 others(27): Show |
30 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.892-3840A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684882 | |||||||
| chr17:78684924 | G | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.892-3882C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684924 | |||||||
| chr17:78684939 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.892-3897C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684939 | |||||||
| chr17:78685055 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.892-4013G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685055 | |||||||
| chr17:78685202 | T | A | 4 | a0001c0001t0004g0005 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG00597.hp2 NA18975.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-4160A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685202 | |||||||
| chr17:78685203 | C | CA | 73 | a0001c0001t0001g0108 a0001c0001t0001g0140 a0001c0001t0001g0141 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.892-4162dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | |||||||
| chr17:78685203 | C | CAA | 16 | a0001c0001t0003g0362 a0001c0001t0003g0363 a0001c0001t0003g0364 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.892-4163_892-4162d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | |||||||
| chr17:78685203 | CA | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0114 others(12): Show |
15 | HG00423.hp2 HG00738.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-4162delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | |||||||
| chr17:78685203 | CAA | C | 29 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0067 others(26): Show |
29 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.892-4163_892-4162d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | |||||||
| chr17:78685331 | T | C | 1 | a0001c0001t0004g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4289A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685331 | |||||||
| chr17:78685351 | T | TATTG | 97 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.892-4310_892-4309i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685351 | |||||||
| chr17:78685380 | T | C | 1 | a0001c0001t0004g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4338A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685380 | |||||||
| chr17:78685424 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.892-4382A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685424 | |||||||
| chr17:78685468 | ATTTAAG | A | 24 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.892-4432_892-4427d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685468 | |||||||
| chr17:78685525 | C | T | 10 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0200 others(7): Show |
10 | HG01081.hp2 HG02155.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.892-4483G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685525 | |||||||
| chr17:78685700 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.892-4658C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685700 | |||||||
| chr17:78685744 | C | T | 65 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.892-4702G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685744 | |||||||
| chr17:78685768 | T | C | 1 | a0001c0001t0004g0216 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.892-4726A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685768 | |||||||
| chr17:78685777 | G | C | 1 | a0001c0001t0002g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.892-4735C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685777 | |||||||
| chr17:78685783 | G | A | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-4741C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685783 | |||||||
| chr17:78685814 | GGCT | G | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-4775_892-4773d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685814 | |||||||
| chr17:78685818 | G | A | 2 | a0001c0001t0006g0326 a0001c0001t0006g0330 |
2 | HG01168.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.892-4776C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685818 | |||||||
| chr17:78685976 | C | A | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-4934G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685976 | |||||||
| chr17:78686096 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.892-5054T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686096 | |||||||
| chr17:78686378 | C | T | 1 | a0001c0001t0003g0365 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.892-5336G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686378 | |||||||
| chr17:78686561 | G | C | 1 | a0001c0001t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.892-5519C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686561 | |||||||
| chr17:78686682 | C | G | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.892-5640G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686682 | |||||||
| chr17:78687067 | C | T | 2 | a0001c0001t0009g0052 a0001c0001t0009g0055 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.891+5350G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687067 | |||||||
| chr17:78687070 | C | T | 5 | a0001c0001t0005g0050 a0001c0001t0014g0049 a0001c0001t0014g0053 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5347G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687070 | |||||||
| chr17:78687071 | G | A | 1 | a0001c0001t0008g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.891+5346C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687071 | |||||||
| chr17:78687072 | C | T | 5 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(2): Show |
5 | HG03471.hp1 NA18971.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5345G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687072 | |||||||
| chr17:78687333 | G | A | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.891+5084C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687333 | |||||||
| chr17:78687394 | A | G | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.891+5023T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687394 | |||||||
| chr17:78687430 | G | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+4987C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687430 | |||||||
| chr17:78687433 | C | T | 23 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+4984G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687433 | |||||||
| chr17:78687490 | C | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+4927G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687490 | |||||||
| chr17:78687537 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.891+4880G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687537 | |||||||
| chr17:78687573 | C | T | 2 | a0001c0001t0009g0048 a0001c0001t0009g0054 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.891+4844G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687573 | |||||||
| chr17:78687976 | C | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+4441G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687976 | |||||||
| chr17:78688087 | T | C | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.891+4330A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688087 | |||||||
| chr17:78688108 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+4309T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688108 | |||||||
| chr17:78688226 | A | G | 1 | a0001c0001t0004g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.891+4191T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688226 | |||||||
| chr17:78688263 | G | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+4154C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688263 | |||||||
| chr17:78688543 | G | A | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.891+3874C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688543 | |||||||
| chr17:78688643 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.891+3774C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688643 | |||||||
| chr17:78688741 | G | A | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.891+3676C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688741 | |||||||
| chr17:78688888 | G | A | 214 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.891+3529C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688888 | |||||||
| chr17:78689024 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.891+3393T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689024 | |||||||
| chr17:78689325 | T | C | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.891+3092A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689325 | |||||||
| chr17:78689435 | C | T | 1 | a0001c0001t0007g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.891+2982G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689435 | |||||||
| chr17:78689449 | T | C | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.891+2968A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689449 | |||||||
| chr17:78689477 | C | T | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.891+2940G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689477 | |||||||
| chr17:78689480 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+2937G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689480 | |||||||
| chr17:78689566 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.891+2851G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689566 | |||||||
| chr17:78689571 | G | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.891+2846C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689571 | |||||||
| chr17:78689855 | C | T | 28 | a0001c0001t0001g0093 a0001c0001t0005g0003 a0001c0001t0005g0019 others(25): Show |
28 | HG01074.hp2 HG02135.hp1 HG03239.hp2 others(25): Show |
intron_variant | MODIFIER | c.891+2562G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689855 | |||||||
| chr17:78689880 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.891+2537C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689880 | |||||||
| chr17:78689911 | G | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+2506C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689911 | |||||||
| chr17:78689926 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.891+2491A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689926 | |||||||
| chr17:78689959 | G | A | 87 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(84): Show |
87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.891+2458C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689959 | |||||||
| chr17:78689967 | C | T | 2 | a0001c0001t0002g0280 a0001c0001t0018g0189 |
2 | HG01255.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.891+2450G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689967 | |||||||
| chr17:78689968 | G | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.891+2449C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689968 | |||||||
| chr17:78690014 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+2403G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690014 | |||||||
| chr17:78690155 | G | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+2262C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690155 | |||||||
| chr17:78690255 | C | T | 1 | a0001c0002t0010g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.891+2162G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690255 | |||||||
| chr17:78690266 | C | T | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.891+2151G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690266 | |||||||
| chr17:78690318 | C | T | 1 | a0001c0001t0004g0376 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.891+2099G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690318 | |||||||
| chr17:78690326 | G | A | 1 | a0001c0001t0031g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.891+2091C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690326 | |||||||
| chr17:78690380 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+2037G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690380 | |||||||
| chr17:78690389 | ATCTCAAA others(298): Show |
A | 1 | a0001c0001t0016g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.891+1723_891+2027d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690389 | |||||||
| chr17:78690393 | C | CA | 25 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0130 others(22): Show |
25 | HG00738.hp1 HG01257.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.891+2023dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAA | 15 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0175 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+2022_891+2023d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAA | 10 | a0001c0001t0002g0280 a0001c0001t0002g0292 a0001c0001t0003g0354 others(7): Show |
10 | HG00280.hp2 HG01255.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+2021_891+2023d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAA | 14 | a0001c0001t0002g0249 a0001c0001t0002g0305 a0001c0001t0002g0316 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.891+2020_891+2023d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAA | 24 | a0001c0001t0002g0243 a0001c0001t0002g0246 a0001c0001t0002g0250 others(21): Show |
24 | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.891+2019_891+2023d others(7): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAA | 32 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0020 others(29): Show |
32 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.891+2018_891+2023d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0254 others(8): Show |
11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+2017_891+2023d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0012 a0001c0001t0002g0253 a0001c0001t0002g0307 others(5): Show |
8 | HG00099.hp2 HG00408.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+2016_891+2023d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0255 a0001c0001t0002g0314 a0001c0001t0003g0360 others(4): Show |
7 | HG00423.hp1 HG00621.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+2014_891+2023d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0242 a0001c0001t0002g0277 a0001c0001t0003g0361 |
3 | HG02280.hp1 HG04199.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.891+2013_891+2023d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.891+2012_891+2023d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0263 a0001c0001t0003g0068 a0001c0001t0003g0069 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+2011_891+2023d others(15): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0003g0071 a0001c0001t0006g0346 |
2 | HG02080.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.891+2010_891+2023d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.891+2009_891+2023d others(17): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+2008_891+2023d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(11): Show |
5 | a0001c0001t0003g0073 a0001c0001t0003g0077 a0001c0001t0003g0079 others(2): Show |
5 | HG02027.hp1 NA18978.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+2006_891+2023d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.891+2005_891+2023d others(21): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0003g0090 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.891+1997_891+2023d others(29): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0003g0085 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.891+1996_891+2023d others(30): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0003g0371 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.891+1992_891+2023d others(34): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0003g0081 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.891+1989_891+2023d others(37): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CA | C | 14 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0108 others(11): Show |
14 | HG01074.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.891+2023delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAA | C | 13 | a0001c0001t0001g0105 a0001c0001t0001g0188 a0001c0001t0004g0112 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.891+2022_891+2023d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA | C | 11 | a0001c0001t0002g0248 a0001c0001t0002g0258 a0001c0001t0002g0296 others(8): Show |
11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+2017_891+2023d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0293 others(4): Show |
7 | HG00621.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+2014_891+2023d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0033 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.891+2013_891+2023d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0005g0029 a0001c0001t0005g0034 a0001c0001t0005g0036 |
3 | NA18940.hp1 NA18961.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.891+2012_891+2023d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(6): Show |
C | 24 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(21): Show |
24 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2011_891+2023d others(15): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0191 a0001c0001t0003g0086 a0001c0001t0003g0087 others(6): Show |
9 | HG03130.hp1 HG03209.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+2010_891+2023d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(8): Show |
C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0026 others(49): Show |
52 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.891+2009_891+2023d others(17): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0163 a0001c0001t0006g0339 a0001c0001t0023g0151 |
3 | HG01168.hp2 HG02683.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.891+2008_891+2023d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+2006_891+2023d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(12): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0094 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+2005_891+2023d others(21): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(13): Show |
C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+2004_891+2023d others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0006g0328 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.891+2000_891+2023d others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690393 | CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0004g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.891+1998_891+2023d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | |||||||
| chr17:78690532 | G | A | 2 | a0001c0001t0006g0332 a0001c0001t0006g0334 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.891+1885C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690532 | |||||||
| chr17:78690546 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.891+1871T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690546 | |||||||
| chr17:78690564 | C | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+1853G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690564 | |||||||
| chr17:78690620 | C | T | 1 | a0001c0001t0005g0038 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.891+1797G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690620 | |||||||
| chr17:78690885 | G | C | 1 | a0001c0001t0004g0210 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.891+1532C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690885 | |||||||
| chr17:78691099 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.891+1318C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691099 | |||||||
| chr17:78691123 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.891+1294T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691123 | |||||||
| chr17:78691130 | C | T | 1 | a0001c0001t0005g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.891+1287G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691130 | |||||||
| chr17:78691149 | C | A | 1 | a0001c0001t0005g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.891+1268G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691149 | |||||||
| chr17:78691357 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+1060G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691357 | |||||||
| chr17:78691412 | G | C | 77 | a0001c0001t0002g0305 a0001c0001t0002g0315 a0001c0001t0002g0322 others(74): Show |
77 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.891+1005C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691412 | |||||||
| chr17:78691729 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.891+688G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691729 | |||||||
| chr17:78692071 | A | G | 353 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(350): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.891+346T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692071 | |||||||
| chr17:78692211 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+206G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692211 | |||||||
| chr17:78692243 | G | A | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+174C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692243 | |||||||
| chr17:78692300 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0130 a0001c0001t0001g0174 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+117G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692300 | |||||||
| chr17:78692497 | C | A | 9 | a0001c0001t0003g0107 a0001c0001t0003g0362 a0001c0001t0003g0363 others(6): Show |
9 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.815-4G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692497 | |||||||
| chr17:78692595 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.815-102C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692595 | |||||||
| chr17:78692707 | G | A | 1 | a0001c0001t0005g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.815-214C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692707 | |||||||
| chr17:78692805 | GC | G | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-313delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692805 | |||||||
| chr17:78692811 | G | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.815-318C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692811 | |||||||
| chr17:78692895 | C | A | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-402G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692895 | |||||||
| chr17:78692928 | A | C | 2 | a0001c0001t0002g0258 a0001c0001t0002g0260 |
2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.815-435T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692928 | |||||||
| chr17:78693052 | G | A | 4 | a0001c0001t0004g0112 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-559C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693052 | |||||||
| chr17:78693377 | C | T | 4 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(1): Show |
4 | HG01106.hp1 HG01109.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-884G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693377 | |||||||
| chr17:78693585 | C | T | 5 | a0001c0001t0003g0350 a0001c0002t0010g0356 a0001c0002t0010g0357 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.815-1092G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693585 | |||||||
| chr17:78693608 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.815-1115C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693608 | |||||||
| chr17:78693620 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.815-1138_815-1128d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693620 | |||||||
| chr17:78693692 | T | A | 2 | a0001c0001t0006g0327 a0001c0001t0006g0337 |
2 | HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.815-1199A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693692 | |||||||
| chr17:78693696 | G | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.815-1203C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693696 | |||||||
| chr17:78693842 | A | G | 3 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 |
3 | HG00558.hp2 NA18747.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.815-1349T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693842 | |||||||
| chr17:78694103 | C | T | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-1610G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694103 | |||||||
| chr17:78694354 | C | T | 1 | a0001c0001t0002g0323 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.814+1653G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694354 | |||||||
| chr17:78694459 | A | G | 2 | a0001c0001t0004g0126 a0001c0001t0004g0176 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.814+1548T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694459 | |||||||
| chr17:78694588 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(7): Show |
11 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.814+1419G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694588 | |||||||
| chr17:78694625 | G | A | 1 | a0001c0001t0003g0371 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.814+1382C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694625 | |||||||
| chr17:78694702 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.814+1305A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694702 | |||||||
| chr17:78694703 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.814+1304T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694703 | |||||||
| chr17:78694712 | T | A | 11 | a0001c0001t0001g0113 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.814+1295A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694712 | |||||||
| chr17:78694772 | A | G | 1 | a0001c0001t0006g0337 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814+1235T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694772 | |||||||
| chr17:78694848 | C | T | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.814+1159G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694848 | |||||||
| chr17:78694893 | G | T | 1 | a0001c0001t0005g0039 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.814+1114C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694893 | |||||||
| chr17:78694922 | A | C | 1 | a0001c0001t0002g0269 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.814+1085T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694922 | |||||||
| chr17:78694938 | G | A | 2 | a0001c0001t0004g0126 a0001c0001t0004g0176 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.814+1069C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694938 | |||||||
| chr17:78694984 | C | T | 1 | a0001c0001t0003g0354 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.814+1023G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694984 | |||||||
| chr17:78695006 | C | T | 11 | a0001c0001t0001g0113 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.814+1001G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695006 | |||||||
| chr17:78695176 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.814+831A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695176 | |||||||
| chr17:78695346 | C | T | 4 | a0001c0001t0002g0251 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.814+661G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695346 | |||||||
| chr17:78695437 | T | A | 1 | a0001c0001t0004g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.814+570A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695437 | |||||||
| chr17:78695467 | T | C | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.814+540A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695467 | |||||||
| chr17:78695482 | T | C | 111 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.814+525A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695482 | |||||||
| chr17:78695495 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.814+512A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695495 | |||||||
| chr17:78695688 | G | A | 3 | a0001c0001t0005g0050 a0001c0001t0014g0049 a0001c0001t0014g0053 |
3 | HG03130.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.814+319C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695688 | |||||||
| chr17:78695758 | A | G | 23 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.814+249T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695758 | |||||||
| chr17:78696128 | C | A | 1 | a0001c0001t0004g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.812-119G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696128 | |||||||
| chr17:78696163 | A | G | 2 | a0001c0001t0002g0258 a0001c0001t0002g0260 |
2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.812-154T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696163 | |||||||
| chr17:78696216 | G | C | 106 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.812-207C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696216 | |||||||
| chr17:78696216 | G | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | NA18940.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.812-207C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696216 | |||||||
| chr17:78696316 | A | G | 2 | a0001c0001t0014g0049 a0001c0001t0014g0053 |
2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.812-307T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696316 | |||||||
| chr17:78696529 | G | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.812-520C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696529 | |||||||
| chr17:78696702 | G | A | 13 | a0001c0001t0003g0107 a0001c0001t0003g0354 a0001c0001t0003g0355 others(10): Show |
13 | HG01123.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.812-693C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696702 | |||||||
| chr17:78696715 | A | G | 1 | a0001c0001t0004g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.812-706T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696715 | |||||||
| chr17:78696742 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.812-733G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696742 | |||||||
| chr17:78696824 | G | A | 6 | a0001c0001t0009g0004 a0001c0001t0009g0052 a0001c0001t0009g0055 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.812-815C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696824 | |||||||
| chr17:78696906 | T | C | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.812-897A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696906 | |||||||
| chr17:78696968 | T | C | 3 | a0001c0001t0014g0049 a0001c0001t0019g0046 a0001c0001t0025g0051 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.812-959A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696968 | |||||||
| chr17:78696988 | A | G | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.812-979T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696988 | |||||||
| chr17:78697039 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.812-1030C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697039 | |||||||
| chr17:78697082 | A | C | 3 | a0001c0001t0002g0280 a0001c0001t0016g0132 a0001c0001t0018g0189 |
3 | HG01255.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.812-1073T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697082 | |||||||
| chr17:78697200 | T | G | 6 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0002t0010g0356 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.811+1069A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697200 | |||||||
| chr17:78697220 | A | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+1049T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697220 | |||||||
| chr17:78697256 | C | G | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.811+1013G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697256 | |||||||
| chr17:78697279 | A | G | 1 | a0001c0001t0015g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811+990T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697279 | |||||||
| chr17:78697325 | C | CA | 178 | a0001c0001t0001g0149 a0001c0001t0001g0192 a0001c0001t0002g0012 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.811+943dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | |||||||
| chr17:78697325 | C | CAA | 38 | a0001c0001t0002g0013 a0001c0001t0002g0257 a0001c0001t0002g0288 others(35): Show |
38 | HG00673.hp1 HG01106.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.811+942_811+943dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | |||||||
| chr17:78697325 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.811+934_811+943del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | |||||||
| chr17:78697341 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.811+928T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697341 | |||||||
| chr17:78697409 | T | G | 1 | a0001c0001t0002g0275 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.811+860A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697409 | |||||||
| chr17:78697469 | C | G | 110 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.811+800G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697469 | |||||||
| chr17:78697604 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.811+665T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697604 | |||||||
| chr17:78697613 | A | AG | 3 | a0001c0001t0002g0278 a0001c0001t0002g0323 a0001c0001t0008g0268 |
3 | HG00733.hp1 HG03654.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.811+655dupC | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697613 | |||||||
| chr17:78697614 | G | GA | 11 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 others(8): Show |
11 | HG01074.hp2 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.811+654dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697614 | |||||||
| chr17:78697615 | A | G | 108 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.811+654T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697615 | |||||||
| chr17:78697629 | A | G | 219 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0168 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.811+640T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697629 | |||||||
| chr17:78697957 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+312G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697957 | |||||||
| chr17:78698018 | C | T | 2 | a0001c0001t0002g0250 a0001c0001t0002g0281 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.811+251G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698018 | |||||||
| chr17:78698019 | G | A | 9 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0200 others(6): Show |
9 | HG01081.hp2 HG02155.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.811+250C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698019 | |||||||
| chr17:78698024 | T | C | 10 | a0001c0001t0003g0107 a0001c0001t0003g0362 a0001c0001t0003g0363 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.811+245A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698024 | |||||||
| chr17:78698098 | T | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0040 |
2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.811+171A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698098 | |||||||
| chr17:78698128 | C | T | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.811+141G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698128 | |||||||
| chr17:78698143 | G | A | 1 | a0001c0001t0007g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.811+126C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698143 | |||||||
| chr17:78698144 | C | G | 7 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.811+125G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698144 | |||||||
| chr17:78698147 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+122C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698147 | |||||||
| chr17:78698149 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.811+120C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698149 | |||||||
| chr17:78698187 | A | G | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.811+82T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698187 | |||||||
| chr17:78698211 | A | G | 45 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(42): Show |
45 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(42): Show |
intron_variant | MODIFIER | c.811+58T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698211 | |||||||
| chr17:78698564 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.700-184G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698564 | |||||||
| chr17:78698700 | AC | A | 31 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.699+119delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698700 | |||||||
| chr17:78698712 | A | C | 1 | a0001c0001t0003g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.699+108T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698712 | |||||||
| chr17:78699084 | C | T | 1 | a0001c0001t0005g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.551-116G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699084 | |||||||
| chr17:78699274 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.551-306C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699274 | |||||||
| chr17:78699375 | A | C | 1 | a0001c0001t0016g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-407T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699375 | |||||||
| chr17:78699394 | G | T | 1 | a0001c0001t0004g0216 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.551-426C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699394 | |||||||
| chr17:78699416 | C | A | 1 | a0001c0001t0021g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.551-448G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699416 | |||||||
| chr17:78699468 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.551-500A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699468 | |||||||
| chr17:78700117 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0311 a0001c0001t0002g0312 |
3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.550+214A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700117 | |||||||
| chr17:78700213 | T | C | 1 | a0001c0001t0006g0333 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.550+118A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700213 | |||||||
| chr17:78700295 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550+36G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700295 | |||||||
| chr17:78700484 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.438-41G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700484 | |||||||
| chr17:78700529 | T | C | 2 | a0001c0001t0006g0328 a0001c0001t0006g0329 |
2 | HG00140.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.438-86A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700529 | |||||||
| chr17:78700532 | T | C | 3 | a0001c0001t0004g0111 a0001c0001t0004g0215 a0001c0001t0004g0230 |
3 | HG02735.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.438-89A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700532 | |||||||
| chr17:78700788 | G | T | 1 | a0001c0001t0002g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.438-345C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700788 | |||||||
| chr17:78700904 | G | A | 122 | a0001c0001t0001g0193 a0001c0001t0002g0012 a0001c0001t0002g0013 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.438-461C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700904 | |||||||
| chr17:78700947 | T | C | 1 | a0001c0001t0004g0211 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.438-504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700947 | |||||||
| chr17:78700970 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438-527C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700970 | |||||||
| chr17:78701030 | C | T | 31 | a0001c0001t0001g0140 a0001c0001t0005g0002 a0001c0001t0005g0003 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.438-587G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701030 | |||||||
| chr17:78701109 | T | C | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+562A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701109 | |||||||
| chr17:78701134 | G | A | 11 | a0001c0001t0001g0239 a0001c0001t0003g0351 a0001c0001t0003g0362 others(8): Show |
11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.437+537C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701134 | |||||||
| chr17:78701170 | G | GACAGGTT others(1): Show |
4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+493_437+500dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701170 | |||||||
| chr17:78701441 | C | T | 2 | a0001c0001t0004g0126 a0001c0001t0004g0176 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.437+230G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701441 | |||||||
| chr17:78701495 | T | G | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.437+176A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701495 | |||||||
| chr17:78701497 | G | A | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+174C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701497 | |||||||
| chr17:78701775 | G | T | 1 | a0001c0001t0003g0362 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.357-24C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78701775 | |||||||
| chr17:78701903 | G | A | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.357-152C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78701903 | |||||||
| chr17:78702064 | T | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.356+58A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78702064 | |||||||
| chr17:78702074 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.356+48C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78702074 | |||||||
| chr17:78702294 | A | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.238-54T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702294 | |||||||
| chr17:78702310 | C | G | 2 | a0001c0001t0002g0288 a0001c0001t0002g0313 |
2 | HG02056.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.238-70G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702310 | |||||||
| chr17:78702376 | G | A | 1 | a0001c0001t0016g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-136C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702376 | |||||||
| chr17:78702793 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.171-189A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702793 | |||||||
| chr17:78702868 | C | A | 125 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.171-264G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702868 | |||||||
| chr17:78702892 | G | C | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.171-288C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702892 | |||||||
| chr17:78703111 | T | A | 1 | a0001c0001t0002g0281 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.171-507A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703111 | |||||||
| chr17:78703149 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.171-545G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703149 | |||||||
| chr17:78703176 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.171-572C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703176 | |||||||
| chr17:78703182 | G | A | 2 | a0001c0001t0006g0336 a0001c0001t0006g0348 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.171-578C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703182 | |||||||
| chr17:78703411 | C | CA | 34 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0097 others(31): Show |
34 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.171-808dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703411 | |||||||
| chr17:78703411 | CA | C | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0016 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.171-808delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703411 | |||||||
| chr17:78703498 | A | G | 1 | a0001c0001t0006g0327 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.171-894T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703498 | |||||||
| chr17:78703505 | C | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0096 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.171-901G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703505 | |||||||
| chr17:78703514 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-910C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703514 | |||||||
| chr17:78703944 | C | G | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.171-1340G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703944 | |||||||
| chr17:78703971 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171-1367G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703971 | |||||||
| chr17:78703981 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.171-1377C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703981 | |||||||
| chr17:78704326 | G | A | 28 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(25): Show |
28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.171-1722C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704326 | |||||||
| chr17:78704413 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.171-1809C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704413 | |||||||
| chr17:78704474 | T | C | 28 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(25): Show |
28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.171-1870A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704474 | |||||||
| chr17:78704735 | T | G | 1 | a0001c0001t0002g0277 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171-2131A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704735 | |||||||
| chr17:78704812 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.171-2208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704812 | |||||||
| chr17:78705094 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.171-2490A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705094 | |||||||
| chr17:78705104 | T | C | 2 | a0001c0001t0009g0052 a0001c0001t0009g0055 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.171-2500A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705104 | |||||||
| chr17:78705122 | G | A | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.171-2518C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705122 | |||||||
| chr17:78705462 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.170+2735C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705462 | |||||||
| chr17:78705556 | T | C | 3 | a0001c0001t0002g0280 a0001c0001t0016g0132 a0001c0001t0018g0189 |
3 | HG01255.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.170+2641A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705556 | |||||||
| chr17:78705876 | C | T | 3 | a0001c0001t0003g0351 a0001c0001t0013g0352 a0001c0001t0013g0353 |
3 | HG02109.hp1 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.170+2321G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705876 | |||||||
| chr17:78706066 | C | G | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.170+2131G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706066 | |||||||
| chr17:78706298 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.170+1899T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706298 | |||||||
| chr17:78706408 | CCA | C | 5 | a0001c0001t0003g0350 a0001c0002t0010g0356 a0001c0002t0010g0357 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.170+1787_170+1788d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706408 | |||||||
| chr17:78706710 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0173 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.170+1487C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706710 | |||||||
| chr17:78706739 | T | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0097 others(10): Show |
13 | HG00544.hp2 HG02004.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.170+1458A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706739 | |||||||
| chr17:78706860 | T | C | 1 | a0001c0001t0004g0227 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.170+1337A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706860 | |||||||
| chr17:78707021 | C | T | 43 | a0001c0001t0001g0143 a0001c0001t0005g0002 a0001c0001t0005g0003 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.170+1176G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707021 | |||||||
| chr17:78707118 | A | T | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.170+1079T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707118 | |||||||
| chr17:78707434 | G | T | 22 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.170+763C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707434 | |||||||
| chr17:78707533 | C | T | 1 | a0001c0001t0004g0200 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.170+664G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707533 | |||||||
| chr17:78707595 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.170+602G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707595 | |||||||
| chr17:78707615 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.170+582C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707615 | |||||||
| chr17:78707663 | T | C | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.170+534A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707663 | |||||||
| chr17:78707672 | C | T | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.170+525G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707672 | |||||||
| chr17:78707682 | A | AT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0002g0254 others(3): Show |
6 | HG00408.hp2 HG01168.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+514dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | |||||||
| chr17:78707682 | A | ATTT | 29 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0003g0068 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.170+512_170+514dup others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | |||||||
| chr17:78707682 | AT | A | 11 | a0001c0001t0001g0185 a0001c0001t0002g0250 a0001c0001t0002g0279 others(8): Show |
11 | HG00140.hp1 HG02280.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.170+514delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | |||||||
| chr17:78707684 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.170+513A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707684 | |||||||
| chr17:78707704 | C | T | 28 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(25): Show |
28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.170+493G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707704 | |||||||
| chr17:78707773 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.170+424G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707773 | |||||||
| chr17:78707802 | T | A | 1 | a0001c0001t0016g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.170+395A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707802 | |||||||
| chr17:78707808 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0311 a0001c0001t0002g0312 |
3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170+389C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707808 | |||||||
| chr17:78707968 | C | T | 43 | a0001c0001t0001g0143 a0001c0001t0005g0002 a0001c0001t0005g0003 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.170+229G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707968 | |||||||
| chr17:78707983 | G | A | 11 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+214C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707983 | |||||||
| chr17:78708058 | T | C | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.170+139A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78708058 | |||||||
| chr17:78708075 | G | C | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.170+122C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78708075 | |||||||
| chr17:78708491 | C | G | 2 | a0001c0001t0006g0344 a0001c0001t0006g0345 |
2 | HG00621.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.106-230G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708491 | |||||||
| chr17:78708640 | C | A | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.106-379G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708640 | |||||||
| chr17:78708746 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106-485C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708746 | |||||||
| chr17:78708944 | G | C | 1 | a0001c0001t0006g0344 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106-683C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708944 | |||||||
| chr17:78709057 | T | G | 1 | a0001c0001t0003g0361 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+593A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709057 | |||||||
| chr17:78709070 | G | A | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.105+580C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709070 | |||||||
| chr17:78709201 | T | A | 1 | a0001c0001t0002g0294 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.105+449A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709201 | |||||||
| chr17:78709274 | AGAGCCAG others(16): Show |
A | 89 | a0001c0001t0001g0194 a0001c0001t0001g0276 a0001c0001t0002g0012 others(86): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.105+353_105+375del others(23): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709274 | |||||||
| chr17:78709291 | G | C | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.105+359C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709291 | |||||||
| chr17:78709416 | C | T | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.105+234G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709416 | |||||||
| chr17:78709630 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.105+20G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709630 | |||||||
| chr17:78709889 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.23-157T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78709889 | |||||||
| chr17:78710114 | A | G | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-382T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710114 | |||||||
| chr17:78710194 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.23-462G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710194 | |||||||
| chr17:78710595 | A | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-863T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710595 | |||||||
| chr17:78710634 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.23-902A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710634 | |||||||
| chr17:78710824 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.23-1092A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710824 | |||||||
| chr17:78710931 | A | G | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-1199T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710931 | |||||||
| chr17:78710979 | G | A | 1 | a0001c0001t0005g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.23-1247C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710979 | |||||||
| chr17:78710987 | G | C | 1 | a0001c0001t0005g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.23-1255C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710987 | |||||||
| chr17:78711122 | C | T | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-1390G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711122 | |||||||
| chr17:78711153 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.23-1421A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711153 | |||||||
| chr17:78711206 | G | A | 1 | a0001c0001t0009g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.23-1474C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711206 | |||||||
| chr17:78711226 | C | T | 1 | a0001c0001t0002g0269 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.23-1494G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711226 | |||||||
| chr17:78711261 | C | CAAAT | 26 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
27 | HG01069.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-1533_23-1530dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | |||||||
| chr17:78711261 | CAAAT | C | 6 | a0001c0001t0001g0143 a0001c0001t0003g0236 a0001c0001t0003g0237 others(3): Show |
6 | HG01106.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-1533_23-1530del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | |||||||
| chr17:78711261 | CAAATAAA others(1): Show |
C | 4 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(1): Show |
4 | NA18971.hp1 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-1537_23-1530del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | |||||||
| chr17:78711261 | CAAATAAA others(5): Show |
C | 27 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0071 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-1541_23-1530del others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | |||||||
| chr17:78711290 | AAATAAAT others(7): Show |
A | 4 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0006g0331 others(1): Show |
4 | HG00140.hp1 HG01257.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1572_23-1559del others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711290 | |||||||
| chr17:78711291 | AATAAATA others(3): Show |
A | 1 | a0001c0001t0003g0064 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-1569_23-1560del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711291 | |||||||
| chr17:78711298 | AAATAAT | A | 3 | a0001c0001t0006g0335 a0001c0001t0006g0337 a0001c0001t0013g0352 |
3 | HG00735.hp2 HG01361.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.23-1572_23-1567del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711298 | |||||||
| chr17:78711302 | A | AAATAAT | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0004g0010 |
3 | HG00639.hp1 HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.23-1571_23-1570ins others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | |||||||
| chr17:78711302 | A | T | 1 | a0001c0001t0003g0064 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-1570T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | |||||||
| chr17:78711302 | AAT | A | 104 | a0001c0001t0001g0276 a0001c0001t0002g0013 a0001c0001t0002g0014 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.23-1572_23-1571del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | |||||||
| chr17:78711303 | A | AAT | 15 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0002g0249 others(12): Show |
15 | HG00099.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-1572_23-1571ins others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711303 | |||||||
| chr17:78711304 | T | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0002g0249 others(36): Show |
39 | HG00099.hp1 HG00673.hp1 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.23-1572A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711304 | |||||||
| chr17:78711305 | A | T | 22 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(19): Show |
22 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.23-1573T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711305 | |||||||
| chr17:78711306 | T | A | 22 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(19): Show |
22 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.23-1574A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711306 | |||||||
| chr17:78711310 | T | C | 2 | a0001c0001t0003g0064 a0001c0003t0017g0017 |
2 | HG03579.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.23-1578A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711310 | |||||||
| chr17:78711312 | T | C | 48 | a0001c0001t0001g0093 a0001c0001t0002g0258 a0001c0001t0002g0260 others(45): Show |
48 | HG00423.hp2 HG00558.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.23-1580A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | |||||||
| chr17:78711312 | T | TAC | 6 | a0001c0001t0001g0113 a0001c0001t0001g0131 a0001c0001t0001g0137 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-1581_23-1580ins others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | |||||||
| chr17:78711312 | TATAC | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0031 a0001c0001t0005g0041 others(1): Show |
4 | HG03490.hp1 HG03927.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1581del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | |||||||
| chr17:78711312 | TATACAC | T | 13 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0048 others(10): Show |
13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-1586_23-1581del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | |||||||
| chr17:78711314 | T | C | 177 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0113 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.23-1582A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | |||||||
| chr17:78711314 | T | TAC | 4 | a0001c0001t0001g0149 a0001c0001t0001g0239 a0001c0001t0004g0126 others(1): Show |
4 | HG00140.hp2 HG01255.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1583dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | |||||||
| chr17:78711314 | TAC | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0142 others(1): Show |
4 | HG00408.hp1 NA18984.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1583del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | |||||||
| chr17:78711316 | C | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0005g0002 others(22): Show |
25 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-1584G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711316 | |||||||
| chr17:78711318 | C | T | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.23-1586G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711318 | |||||||
| chr17:78711706 | CT | C | 11 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0159 others(8): Show |
11 | HG01099.hp1 HG02109.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.23-1975delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711706 | |||||||
| chr17:78711872 | T | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(5): Show |
8 | HG00544.hp2 HG02083.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-2140A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711872 | |||||||
| chr17:78711906 | T | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-2174A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711906 | |||||||
| chr17:78712076 | A | AGAAAGAA others(1): Show |
30 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(27): Show |
30 | HG00423.hp2 HG00558.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.23-2352_23-2345dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712076 | |||||||
| chr17:78712076 | AGAAAGAA others(1): Show |
A | 27 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(24): Show |
27 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-2352_23-2345del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712076 | |||||||
| chr17:78712096 | A | G | 1 | a0001c0001t0005g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.23-2364T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712096 | |||||||
| chr17:78712104 | G | A | 3 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0075 |
3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2372C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712104 | |||||||
| chr17:78712106 | AAGGAAGG others(1): Show |
A | 3 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0075 |
3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2382_23-2375del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712106 | |||||||
| chr17:78712126 | G | A | 3 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0075 |
3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2394C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712126 | |||||||
| chr17:78712128 | G | A | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.23-2396C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712128 | |||||||
| chr17:78712129 | G | C | 1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.23-2397C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712129 | |||||||
| chr17:78712134 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-2402T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712134 | |||||||
| chr17:78712138 | AAGGGAAG others(13): Show |
A | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.23-2426_23-2407del others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712138 | |||||||
| chr17:78712154 | AAGGG | A | 194 | a0001c0001t0001g0149 a0001c0001t0001g0276 a0001c0001t0002g0012 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.23-2426_23-2423del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712154 | |||||||
| chr17:78712163 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.23-2431T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712163 | |||||||
| chr17:78712178 | GAGGT | G | 12 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-2450_23-2447del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712178 | |||||||
| chr17:78712466 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.23-2734T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712466 | |||||||
| chr17:78712558 | A | T | 1 | a0001c0001t0002g0285 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.23-2826T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712558 | |||||||
| chr17:78712684 | A | C | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-2952T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712684 | |||||||
| chr17:78712684 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.23-2952T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712684 | |||||||
| chr17:78713026 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-3294G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713026 | |||||||
| chr17:78713081 | T | TAA | 10 | a0001c0001t0005g0018 a0001c0001t0005g0021 a0001c0001t0005g0022 others(7): Show |
10 | HG02080.hp2 HG02135.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-3351_23-3350dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713081 | |||||||
| chr17:78713086 | A | AAT | 37 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(34): Show |
37 | HG00673.hp1 HG01106.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.23-3356_23-3355dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713086 | |||||||
| chr17:78713086 | AAT | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0246 a0001c0001t0002g0252 others(5): Show |
8 | HG02004.hp1 HG02280.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-3356_23-3355del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713086 | |||||||
| chr17:78713088 | T | A | 22 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-3356A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713088 | |||||||
| chr17:78713128 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-3396G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713128 | |||||||
| chr17:78713183 | A | G | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-3451T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713183 | |||||||
| chr17:78713196 | G | A | 1 | a0001c0001t0015g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.23-3464C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713196 | |||||||
| chr17:78713233 | C | T | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-3501G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713233 | |||||||
| chr17:78713285 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.23-3553T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713285 | |||||||
| chr17:78713392 | C | A | 1 | a0001c0001t0003g0365 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.23-3660G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713392 | |||||||
| chr17:78713480 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0032g0272 |
2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.23-3748C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713480 | |||||||
| chr17:78713546 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.23-3814A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | |||||||
| chr17:78713546 | T | TCCTATCT others(223): Show |
1 | a0001c0001t0018g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.23-4044_23-3815dup others(230): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | |||||||
| chr17:78713546 | TCCTATCT others(223): Show |
T | 10 | a0001c0001t0003g0351 a0001c0001t0003g0362 a0001c0001t0003g0363 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-4044_23-3815del | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | |||||||
| chr17:78713624 | T | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-3892A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713624 | |||||||
| chr17:78713805 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.23-4073C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713805 | |||||||
| chr17:78713956 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-4224G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713956 | |||||||
| chr17:78714027 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-4295G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714027 | |||||||
| chr17:78714095 | G | A | 43 | a0001c0001t0002g0306 a0001c0001t0005g0002 a0001c0001t0005g0003 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-4363C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714095 | |||||||
| chr17:78714118 | C | G | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-4386G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714118 | |||||||
| chr17:78714155 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.23-4423G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714155 | |||||||
| chr17:78714163 | AC | A | 123 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.23-4432delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714163 | |||||||
| chr17:78714249 | C | T | 1 | a0001c0001t0004g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.23-4517G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714249 | |||||||
| chr17:78714345 | T | G | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.23-4613A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714345 | |||||||
| chr17:78714428 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.23-4696G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714428 | |||||||
| chr17:78714691 | G | A | 13 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0048 others(10): Show |
13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-4959C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714691 | |||||||
| chr17:78714859 | G | A | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23-5127C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714859 | |||||||
| chr17:78714872 | G | GA | 39 | a0001c0001t0001g0155 a0001c0001t0002g0318 a0001c0001t0003g0064 others(36): Show |
39 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.23-5141dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714872 | |||||||
| chr17:78714875 | A | G | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.23-5143T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714875 | |||||||
| chr17:78714919 | T | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-5187A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714919 | |||||||
| chr17:78715108 | G | C | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.23-5376C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715108 | |||||||
| chr17:78715119 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-5387T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715119 | |||||||
| chr17:78715120 | T | C | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-5388A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715120 | |||||||
| chr17:78715230 | A | G | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-5498T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715230 | |||||||
| chr17:78715252 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-5520A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715252 | |||||||
| chr17:78715536 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23-5804T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715536 | |||||||
| chr17:78715552 | C | T | 4 | a0001c0001t0004g0005 a0001c0001t0004g0121 a0001c0001t0004g0123 others(1): Show |
4 | HG00597.hp2 NA18975.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-5820G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715552 | |||||||
| chr17:78715605 | G | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-5873C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715605 | |||||||
| chr17:78715739 | G | GCT | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-6009_23-6008dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715739 | |||||||
| chr17:78716099 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.23-6367T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716099 | |||||||
| chr17:78716200 | G | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-6468C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716200 | |||||||
| chr17:78716435 | C | T | 2 | a0001c0001t0007g0201 a0001c0001t0007g0203 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.23-6703G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716435 | |||||||
| chr17:78716486 | A | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-6754T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716486 | |||||||
| chr17:78716750 | G | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-7018C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716750 | |||||||
| chr17:78716831 | G | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-7099C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716831 | |||||||
| chr17:78716963 | C | T | 1 | a0001c0001t0004g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.23-7231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716963 | |||||||
| chr17:78717061 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.23-7329G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717061 | |||||||
| chr17:78717117 | A | G | 1 | a0001c0001t0002g0315 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.23-7385T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717117 | |||||||
| chr17:78717217 | A | G | 43 | a0001c0001t0001g0239 a0001c0001t0003g0364 a0001c0001t0005g0002 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-7485T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717217 | |||||||
| chr17:78717234 | G | T | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-7502C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717234 | |||||||
| chr17:78717263 | G | A | 1 | a0001c0001t0004g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.23-7531C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717263 | |||||||
| chr17:78717440 | T | C | 2 | a0001c0001t0003g0362 a0001c0001t0003g0367 |
2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.23-7708A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717440 | |||||||
| chr17:78717483 | C | T | 1 | a0001c0001t0004g0200 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.23-7751G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717483 | |||||||
| chr17:78717620 | C | T | 3 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0020g0229 |
3 | HG02523.hp2 NA18946.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.23-7888G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717620 | |||||||
| chr17:78717667 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0315 |
2 | NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.23-7935G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717667 | |||||||
| chr17:78717668 | G | A | 43 | a0001c0001t0004g0010 a0001c0001t0004g0062 a0001c0001t0004g0111 others(40): Show |
43 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.23-7936C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717668 | |||||||
| chr17:78717841 | G | A | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-8109C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717841 | |||||||
| chr17:78717904 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-8172G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717904 | |||||||
| chr17:78718140 | G | A | 1 | a0001c0001t0008g0320 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.23-8408C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718140 | |||||||
| chr17:78718153 | C | T | 1 | a0001c0001t0004g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.23-8421G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718153 | |||||||
| chr17:78718218 | T | TAC | 31 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 others(28): Show |
31 | HG01074.hp2 HG02040.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.23-8488_23-8487dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACAC | 16 | a0001c0001t0001g0133 a0001c0001t0003g0064 a0001c0001t0003g0066 others(13): Show |
16 | HG00099.hp2 HG02135.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.23-8490_23-8487dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACAC | 15 | a0001c0001t0003g0067 a0001c0001t0003g0071 a0001c0001t0003g0072 others(12): Show |
15 | HG00558.hp1 HG01106.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-8492_23-8487dup others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(1): Show |
8 | a0001c0001t0003g0065 a0001c0001t0003g0078 a0001c0001t0003g0079 others(5): Show |
8 | HG00423.hp2 HG02165.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-8494_23-8487dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(3): Show |
11 | a0001c0001t0001g0174 a0001c0001t0003g0069 a0001c0001t0003g0073 others(8): Show |
11 | HG01081.hp2 HG02071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.23-8496_23-8487dup others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0169 a0001c0001t0003g0068 a0001c0001t0003g0084 |
3 | NA18978.hp1 NA18980.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.23-8498_23-8487dup others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(7): Show |
3 | a0001c0001t0003g0070 a0001c0001t0003g0354 a0001c0001t0026g0102 |
3 | HG02559.hp2 HG03491.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.23-8500_23-8487dup others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(9): Show |
3 | a0001c0001t0003g0089 a0001c0001t0003g0355 a0001c0001t0003g0368 |
3 | HG01123.hp2 HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.23-8502_23-8487dup others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(13): Show |
1 | a0001c0001t0003g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.23-8506_23-8487dup others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TACACACA others(17): Show |
1 | a0001c0001t0003g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.23-8510_23-8487dup others(24): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | T | TCACACAC others(12): Show |
1 | a0001c0001t0003g0087 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.23-8487_23-8486ins others(19): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TAC | T | 58 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(55): Show |
58 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.23-8488_23-8487del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACAC | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0094 others(45): Show |
49 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.23-8490_23-8487del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACAC | T | 68 | a0001c0001t0001g0152 a0001c0001t0001g0194 a0001c0001t0001g0276 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.23-8492_23-8487del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACACA others(1): Show |
T | 6 | a0001c0001t0004g0374 a0001c0001t0006g0326 a0001c0001t0008g0268 others(3): Show |
6 | HG00733.hp1 HG01168.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-8494_23-8487del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACACA others(3): Show |
T | 19 | a0001c0001t0001g0026 a0001c0001t0002g0244 a0001c0001t0002g0245 others(16): Show |
19 | HG00597.hp2 HG00735.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.23-8496_23-8487del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACACA others(5): Show |
T | 5 | a0001c0001t0002g0247 a0001c0001t0002g0306 a0001c0001t0002g0307 others(2): Show |
5 | HG00408.hp2 NA18969.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-8498_23-8487del others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACACA others(9): Show |
T | 2 | a0001c0001t0002g0016 a0001c0001t0004g0176 |
2 | HG02683.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.23-8502_23-8487del others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718218 | TACACACA others(15): Show |
T | 1 | a0001c0001t0008g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.23-8508_23-8487del others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | |||||||
| chr17:78718220 | C | T | 14 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0050 others(11): Show |
14 | HG00673.hp1 HG02080.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-8488G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718220 | |||||||
| chr17:78718222 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.23-8490G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718222 | |||||||
| chr17:78718224 | C | T | 19 | a0001c0001t0005g0003 a0001c0001t0005g0019 a0001c0001t0005g0022 others(16): Show |
19 | HG02135.hp1 HG03239.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.23-8492G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718224 | |||||||
| chr17:78718226 | C | T | 4 | a0001c0001t0005g0021 a0001c0001t0005g0035 a0001c0001t0005g0036 others(1): Show |
4 | NA18612.hp1 NA18961.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-8494G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718226 | |||||||
| chr17:78718344 | C | T | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-8612G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718344 | |||||||
| chr17:78718391 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.23-8659A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718391 | |||||||
| chr17:78718403 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.23-8671C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718403 | |||||||
| chr17:78718421 | C | T | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.23-8689G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718421 | |||||||
| chr17:78718522 | T | C | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-8790A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718522 | |||||||
| chr17:78718900 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.23-9168A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718900 | |||||||
| chr17:78718922 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-9190A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718922 | |||||||
| chr17:78718935 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.23-9203A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718935 | |||||||
| chr17:78719184 | G | C | 3 | a0001c0001t0003g0073 a0001c0001t0003g0084 a0001c0001t0003g0090 |
3 | NA18978.hp1 NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.23-9452C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719184 | |||||||
| chr17:78719479 | T | C | 43 | a0001c0001t0001g0199 a0001c0001t0005g0002 a0001c0001t0005g0003 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-9747A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719479 | |||||||
| chr17:78719588 | A | G | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.23-9856T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719588 | |||||||
| chr17:78719602 | G | A | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-9870C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719602 | |||||||
| chr17:78719650 | G | A | 4 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0028 others(1): Show |
4 | NA18940.hp1 NA18947.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-9918C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719650 | |||||||
| chr17:78719726 | A | C | 1 | a0001c0001t0008g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.23-9994T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719726 | |||||||
| chr17:78719747 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.23-10015C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719747 | |||||||
| chr17:78719765 | G | A | 1 | a0001c0001t0027g0164 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.23-10033C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719765 | |||||||
| chr17:78719963 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.23-10231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719963 | |||||||
| chr17:78719982 | T | C | 1 | a0001c0001t0004g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.23-10250A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719982 | |||||||
| chr17:78720248 | T | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-10516A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720248 | |||||||
| chr17:78720447 | T | C | 1 | a0001c0001t0013g0352 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.23-10715A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720447 | |||||||
| chr17:78720468 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-10736C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720468 | |||||||
| chr17:78720517 | C | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-10785G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720517 | |||||||
| chr17:78720593 | A | G | 4 | a0001c0001t0002g0251 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-10861T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720593 | |||||||
| chr17:78720832 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.23-11100G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720832 | |||||||
| chr17:78720854 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.23-11122C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720854 | |||||||
| chr17:78720949 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.23-11217A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720949 | |||||||
| chr17:78720982 | G | C | 1 | a0001c0001t0004g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-11250C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720982 | |||||||
| chr17:78721109 | C | T | 7 | a0001c0001t0003g0350 a0001c0001t0003g0360 a0001c0001t0003g0361 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-11377G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721109 | |||||||
| chr17:78721164 | T | C | 1 | a0001c0001t0005g0018 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.23-11432A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721164 | |||||||
| chr17:78721216 | G | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-11484C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721216 | |||||||
| chr17:78721265 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-11533C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721265 | |||||||
| chr17:78721437 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-11705G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721437 | |||||||
| chr17:78721461 | T | C | 2 | a0001c0001t0004g0210 a0001c0001t0004g0218 |
2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.23-11729A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721461 | |||||||
| chr17:78721604 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.23-11872G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721604 | |||||||
| chr17:78721775 | G | A | 73 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(70): Show |
73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-12043C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721775 | |||||||
| chr17:78721990 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-12258G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721990 | |||||||
| chr17:78722472 | A | T | 74 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(71): Show |
74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.23-12740T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722472 | |||||||
| chr17:78722583 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.23-12851C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722583 | |||||||
| chr17:78722708 | A | G | 1 | a0001c0001t0002g0323 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.23-12976T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722708 | |||||||
| chr17:78722760 | C | T | 189 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.23-13028G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722760 | |||||||
| chr17:78722762 | C | T | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-13030G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722762 | |||||||
| chr17:78722763 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.23-13031C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722763 | |||||||
| chr17:78722766 | G | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-13034C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722766 | |||||||
| chr17:78722865 | C | T | 1 | a0001c0001t0002g0324 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.23-13133G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722865 | |||||||
| chr17:78722911 | T | C | 50 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(47): Show |
50 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(47): Show |
intron_variant | MODIFIER | c.23-13179A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722911 | |||||||
| chr17:78722954 | G | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-13222C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722954 | |||||||
| chr17:78722958 | T | C | 4 | a0001c0001t0003g0369 a0001c0001t0003g0371 a0001c0001t0003g0372 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-13226A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722958 | |||||||
| chr17:78723009 | T | A | 2 | a0001c0001t0008g0267 a0001c0001t0008g0303 |
2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.23-13277A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723009 | |||||||
| chr17:78723186 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23-13454A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723186 | |||||||
| chr17:78723258 | C | A | 1 | a0001c0001t0003g0084 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.23-13526G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723258 | |||||||
| chr17:78723261 | G | T | 4 | a0001c0001t0003g0369 a0001c0001t0003g0371 a0001c0001t0003g0372 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-13529C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723261 | |||||||
| chr17:78723275 | A | G | 2 | a0001c0001t0008g0266 a0001c0001t0008g0320 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.23-13543T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723275 | |||||||
| chr17:78723434 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.23-13702C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723434 | |||||||
| chr17:78723517 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.23-13785C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723517 | |||||||
| chr17:78723649 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.23-13917C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723649 | |||||||
| chr17:78723840 | G | A | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-14108C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723840 | |||||||
| chr17:78724242 | G | A | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-14510C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724242 | |||||||
| chr17:78724289 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.23-14557C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724289 | |||||||
| chr17:78724385 | A | G | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-14653T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724385 | |||||||
| chr17:78724413 | G | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0193 others(1): Show |
4 | HG02257.hp2 HG03669.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-14681C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724413 | |||||||
| chr17:78724451 | A | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-14719T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724451 | |||||||
| chr17:78724512 | C | A | 1 | a0001c0001t0004g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.23-14780G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724512 | |||||||
| chr17:78724512 | C | T | 6 | a0001c0001t0003g0362 a0001c0001t0003g0363 a0001c0001t0003g0364 others(3): Show |
6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-14780G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724512 | |||||||
| chr17:78724631 | T | C | 215 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.23-14899A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724631 | |||||||
| chr17:78724686 | A | G | 1 | a0001c0001t0009g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.23-14954T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724686 | |||||||
| chr17:78724727 | G | T | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-14995C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724727 | |||||||
| chr17:78724754 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-15022G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724754 | |||||||
| chr17:78724945 | C | T | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-15213G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724945 | |||||||
| chr17:78725031 | A | AAC | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-15301_23-15300d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725031 | |||||||
| chr17:78725174 | G | C | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-15442C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725174 | |||||||
| chr17:78725187 | A | G | 73 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(70): Show |
73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-15455T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725187 | |||||||
| chr17:78725269 | A | G | 7 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-15537T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725269 | |||||||
| chr17:78725275 | C | T | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-15543G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725275 | |||||||
| chr17:78725482 | G | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-15750C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725482 | |||||||
| chr17:78725499 | T | A | 2 | a0001c0001t0002g0242 a0001c0001t0002g0314 |
2 | NA18952.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.23-15767A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725499 | |||||||
| chr17:78725535 | C | T | 1 | a0001c0001t0009g0054 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.23-15803G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725535 | |||||||
| chr17:78725666 | G | T | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.23-15934C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725666 | |||||||
| chr17:78725668 | C | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-15936G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725668 | |||||||
| chr17:78725856 | A | G | 212 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.23-16124T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725856 | |||||||
| chr17:78725963 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.23-16231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725963 | |||||||
| chr17:78726042 | C | CT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0095 others(52): Show |
56 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.23-16311dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726042 | |||||||
| chr17:78726105 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.23-16373C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726105 | |||||||
| chr17:78726178 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.23-16446C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726178 | |||||||
| chr17:78726195 | T | C | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-16463A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726195 | |||||||
| chr17:78726376 | CGAGGCCC others(19): Show |
C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-16670_23-16645d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726376 | |||||||
| chr17:78726380 | G | A | 112 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.23-16648C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726380 | |||||||
| chr17:78726408 | C | T | 1 | a0001c0001t0006g0341 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.23-16676G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726408 | |||||||
| chr17:78726443 | A | G | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-16711T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726443 | |||||||
| chr17:78726662 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.23-16930C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726662 | |||||||
| chr17:78726751 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-17019C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726751 | |||||||
| chr17:78727104 | T | C | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-17372A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727104 | |||||||
| chr17:78727312 | G | T | 8 | a0001c0001t0006g0338 a0001c0001t0006g0339 a0001c0001t0006g0340 others(5): Show |
8 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-17580C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727312 | |||||||
| chr17:78727479 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-17747A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727479 | |||||||
| chr17:78727511 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-17779G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727511 | |||||||
| chr17:78727618 | G | A | 1 | a0001c0001t0004g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.23-17886C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727618 | |||||||
| chr17:78727620 | G | A | 4 | a0001c0001t0002g0299 a0001c0001t0003g0236 a0001c0001t0003g0237 others(1): Show |
4 | HG01106.hp2 HG02132.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-17888C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727620 | |||||||
| chr17:78728026 | G | A | 1 | a0001c0001t0003g0124 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.23-18294C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728026 | |||||||
| chr17:78728095 | A | G | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-18363T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728095 | |||||||
| chr17:78728130 | C | T | 1 | a0001c0001t0002g0012 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.23-18398G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728130 | |||||||
| chr17:78728220 | C | G | 1 | a0001c0001t0003g0090 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.23-18488G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728220 | |||||||
| chr17:78728230 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.23-18498C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728230 | |||||||
| chr17:78728312 | G | A | 1 | a0001c0001t0031g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.23-18580C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728312 | |||||||
| chr17:78728450 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.23-18718A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728450 | |||||||
| chr17:78728661 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-18929T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728661 | |||||||
| chr17:78728804 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.23-19072T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728804 | |||||||
| chr17:78728830 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-19098C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728830 | |||||||
| chr17:78729102 | T | A | 1 | a0001c0001t0003g0367 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.23-19370A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729102 | |||||||
| chr17:78729165 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-19433A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729165 | |||||||
| chr17:78729169 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-19437C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729169 | |||||||
| chr17:78729227 | C | A | 11 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.23-19495G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729227 | |||||||
| chr17:78729236 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.23-19504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729236 | |||||||
| chr17:78729665 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-19933G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729665 | |||||||
| chr17:78729858 | T | C | 10 | a0001c0001t0009g0004 a0001c0001t0009g0048 a0001c0001t0009g0052 others(7): Show |
10 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-20126A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729858 | |||||||
| chr17:78730236 | A | T | 1 | a0001c0001t0004g0197 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.23-20504T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730236 | |||||||
| chr17:78730248 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-20516C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730248 | |||||||
| chr17:78730254 | G | A | 13 | a0001c0001t0003g0351 a0001c0001t0003g0354 a0001c0001t0003g0355 others(10): Show |
13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.23-20522C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730254 | |||||||
| chr17:78730268 | T | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.23-20536A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730268 | |||||||
| chr17:78730341 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0003g0120 a0001c0001t0003g0122 others(14): Show |
17 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-20609G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730341 | |||||||
| chr17:78730369 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.23-20638dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | |||||||
| chr17:78730369 | C | CAA | 64 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0001c0001t0001g0140 others(61): Show |
64 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.23-20639_23-20638d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | |||||||
| chr17:78730369 | C | CAAA | 17 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(14): Show |
17 | HG00408.hp2 HG02027.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-20640_23-20638d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | |||||||
| chr17:78730433 | G | A | 137 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.23-20701C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730433 | |||||||
| chr17:78730468 | G | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-20736C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730468 | |||||||
| chr17:78730532 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.23-20800C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730532 | |||||||
| chr17:78730654 | G | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-20922C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730654 | |||||||
| chr17:78730814 | G | A | 3 | a0001c0001t0004g0374 a0001c0001t0004g0376 a0001c0001t0024g0375 |
3 | HG02559.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.23-21082C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730814 | |||||||
| chr17:78730910 | T | C | 12 | a0001c0001t0006g0326 a0001c0001t0006g0328 a0001c0001t0006g0329 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-21178A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730910 | |||||||
| chr17:78730943 | T | C | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-21211A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730943 | |||||||
| chr17:78730995 | T | G | 1 | a0001c0001t0005g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.23-21263A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730995 | |||||||
| chr17:78731373 | C | T | 22 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0249 others(19): Show |
22 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-21641G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731373 | |||||||
| chr17:78731547 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.23-21815G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731547 | |||||||
| chr17:78731566 | T | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-21834A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731566 | |||||||
| chr17:78731755 | C | CA | 75 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0095 others(72): Show |
75 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.23-22024dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | |||||||
| chr17:78731755 | C | CAA | 6 | a0001c0001t0001g0110 a0001c0001t0001g0169 a0001c0001t0005g0028 others(3): Show |
6 | HG00642.hp1 HG03927.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-22025_23-22024d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | |||||||
| chr17:78731755 | CA | C | 6 | a0001c0001t0002g0012 a0001c0001t0002g0245 a0001c0001t0002g0270 others(3): Show |
6 | HG03209.hp1 NA18940.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-22024delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | |||||||
| chr17:78731766 | A | C | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-22034T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731766 | |||||||
| chr17:78731767 | A | C | 1 | a0001c0001t0004g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-22035T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731767 | |||||||
| chr17:78731772 | C | A | 43 | a0001c0001t0001g0130 a0001c0001t0003g0363 a0001c0001t0005g0002 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-22040G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731772 | |||||||
| chr17:78731841 | C | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-22109G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731841 | |||||||
| chr17:78732033 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-22301C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732033 | |||||||
| chr17:78732147 | G | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.23-22415C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732147 | |||||||
| chr17:78732586 | C | T | 111 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-22854G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732586 | |||||||
| chr17:78732638 | C | T | 371 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(368): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.23-22906G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732638 | |||||||
| chr17:78732842 | A | T | 1 | a0001c0001t0004g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.23-23110T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732842 | |||||||
| chr17:78732943 | C | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-23211G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732943 | |||||||
| chr17:78732979 | C | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0200 others(4): Show |
7 | HG02155.hp2 NA18954.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.23-23247G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732979 | |||||||
| chr17:78733011 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-23279G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733011 | |||||||
| chr17:78733012 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0184 others(2): Show |
5 | HG02056.hp1 NA18955.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-23280C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733012 | |||||||
| chr17:78733070 | C | T | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-23338G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733070 | |||||||
| chr17:78733076 | C | CAAAAAA | 14 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(11): Show |
14 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-23350_23-23345d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733076 | C | CAAAAAAA | 10 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(7): Show |
10 | HG02135.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-23351_23-23345d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733076 | CA | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.23-23345delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733076 | CAA | C | 35 | a0001c0001t0001g0093 a0001c0001t0001g0104 a0001c0001t0001g0165 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.23-23346_23-23345d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733076 | CAAA | C | 34 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(31): Show |
34 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(31): Show |
intron_variant | MODIFIER | c.23-23347_23-23345d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733076 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0377 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.23-23355_23-23345d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | |||||||
| chr17:78733132 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-23400C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733132 | |||||||
| chr17:78733632 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.23-23900C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733632 | |||||||
| chr17:78733675 | C | A | 112 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.23-23943G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733675 | |||||||
| chr17:78733702 | A | G | 211 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-23970T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733702 | |||||||
| chr17:78733957 | A | T | 111 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-24225T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733957 | |||||||
| chr17:78734199 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.23-24467T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734199 | |||||||
| chr17:78734241 | C | CA | 33 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.23-24510dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734241 | |||||||
| chr17:78734241 | CA | C | 40 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(37): Show |
40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.23-24510delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734241 | |||||||
| chr17:78734395 | TATGTACC others(1): Show |
T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(341): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.23-24671_23-24664d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734395 | |||||||
| chr17:78734423 | A | T | 1 | a0001c0001t0005g0033 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.23-24691T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734423 | |||||||
| chr17:78734432 | C | CT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0141 others(26): Show |
29 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-24701dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | |||||||
| chr17:78734432 | CTT | C | 33 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0108 others(30): Show |
33 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.23-24702_23-24701d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | |||||||
| chr17:78734432 | CTTT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.23-24703_23-24701d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | |||||||
| chr17:78734432 | CTTTT | C | 62 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0002g0315 others(59): Show |
62 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.23-24704_23-24701d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | |||||||
| chr17:78734432 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0005g0018 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.23-24716_23-24701d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | |||||||
| chr17:78734435 | T | G | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-24703A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734435 | |||||||
| chr17:78734477 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-24745C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734477 | |||||||
| chr17:78734482 | C | A | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-24750G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734482 | |||||||
| chr17:78734676 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-24944C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734676 | |||||||
| chr17:78734717 | A | G | 211 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-24985T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734717 | |||||||
| chr17:78734907 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0152 |
2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.23-25175G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734907 | |||||||
| chr17:78734959 | T | A | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-25227A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734959 | |||||||
| chr17:78735237 | C | T | 211 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-25505G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735237 | |||||||
| chr17:78735803 | C | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-26071G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735803 | |||||||
| chr17:78735838 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.23-26106G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735838 | |||||||
| chr17:78735858 | A | G | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.23-26126T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735858 | |||||||
| chr17:78735867 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.23-26135A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735867 | |||||||
| chr17:78736166 | C | A | 1 | a0001c0001t0006g0345 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.23-26434G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736166 | |||||||
| chr17:78736166 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.23-26434G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736166 | |||||||
| chr17:78736175 | C | T | 5 | a0001c0001t0003g0350 a0001c0002t0010g0356 a0001c0002t0010g0357 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-26443G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736175 | |||||||
| chr17:78736256 | T | C | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-26524A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736256 | |||||||
| chr17:78736332 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.23-26600G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736332 | |||||||
| chr17:78736410 | TTC | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-26680_23-26679d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736410 | |||||||
| chr17:78736598 | G | A | 2 | a0001c0001t0003g0363 a0001c0001t0003g0366 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.23-26866C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736598 | |||||||
| chr17:78736976 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.23-27244G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736976 | |||||||
| chr17:78737079 | A | G | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27347T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737079 | |||||||
| chr17:78737099 | C | T | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27367G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737099 | |||||||
| chr17:78737380 | C | T | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-27648G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737380 | |||||||
| chr17:78737602 | C | CA | 34 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0002g0323 others(31): Show |
34 | HG00423.hp2 HG00558.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.23-27871dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737602 | |||||||
| chr17:78737602 | CA | C | 41 | a0001c0001t0001g0114 a0001c0001t0005g0002 a0001c0001t0005g0003 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27871delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737602 | |||||||
| chr17:78737678 | C | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(4): Show |
8 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-27946G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737678 | |||||||
| chr17:78737844 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.23-28112T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737844 | |||||||
| chr17:78737870 | T | C | 1 | a0001c0001t0015g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.23-28138A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737870 | |||||||
| chr17:78737874 | T | TAC | 176 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(173): Show |
176 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.23-28144_23-28143d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737874 | T | TACAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(7): Show |
11 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.23-28146_23-28143d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737874 | TAC | T | 46 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0360 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-28144_23-28143d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737874 | TACACACA others(1): Show |
T | 28 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.23-28150_23-28143d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737874 | TACACACA others(3): Show |
T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-28152_23-28143d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737874 | TACACACA others(5): Show |
T | 90 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(87): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.23-28154_23-28143d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | |||||||
| chr17:78737891 | A | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-28159T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737891 | |||||||
| chr17:78738081 | A | G | 1 | a0001c0001t0004g0376 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.23-28349T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738081 | |||||||
| chr17:78738089 | C | T | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-28357G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738089 | |||||||
| chr17:78738386 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0147 others(1): Show |
4 | HG02922.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-28654G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738386 | |||||||
| chr17:78738415 | A | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-28683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738415 | |||||||
| chr17:78738480 | T | C | 4 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0227 others(1): Show |
4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-28748A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738480 | |||||||
| chr17:78738501 | C | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-28769G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738501 | |||||||
| chr17:78738547 | A | G | 73 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(70): Show |
73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-28815T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738547 | |||||||
| chr17:78738626 | T | TA | 6 | a0001c0001t0001g0143 a0001c0001t0002g0269 a0001c0001t0002g0280 others(3): Show |
6 | HG01106.hp2 HG01255.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-28895dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | |||||||
| chr17:78738626 | TA | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0307 a0001c0001t0002g0309 others(16): Show |
19 | HG00408.hp2 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.23-28895delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | |||||||
| chr17:78738626 | TAA | T | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-28896_23-28895d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | |||||||
| chr17:78738935 | A | G | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-29203T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738935 | |||||||
| chr17:78739096 | A | G | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-29364T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739096 | |||||||
| chr17:78739276 | T | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-29544A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739276 | |||||||
| chr17:78739598 | C | T | 1 | a0001c0001t0004g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-29866G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739598 | |||||||
| chr17:78739639 | G | A | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23-29907C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739639 | |||||||
| chr17:78739730 | G | A | 17 | a0001c0001t0001g0026 a0001c0001t0003g0120 a0001c0001t0003g0122 others(14): Show |
17 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-29998C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739730 | |||||||
| chr17:78739759 | T | A | 2 | a0001c0001t0002g0288 a0001c0001t0002g0313 |
2 | HG02056.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.23-30027A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739759 | |||||||
| chr17:78739934 | A | ATCT | 372 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(369): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.23-30205_23-30203d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739934 | |||||||
| chr17:78740414 | T | C | 4 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0006g0331 others(1): Show |
4 | HG00140.hp1 HG01257.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-30682A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740414 | |||||||
| chr17:78740457 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.23-30725C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740457 | |||||||
| chr17:78740478 | T | C | 1 | a0001c0001t0004g0200 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.23-30746A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740478 | |||||||
| chr17:78740552 | CCTGGCTC others(9): Show |
C | 1 | a0001c0001t0006g0349 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.23-30836_23-30821d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740552 | |||||||
| chr17:78740651 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.23-30919G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740651 | |||||||
| chr17:78740772 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.23-31040G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740772 | |||||||
| chr17:78740815 | T | C | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-31083A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740815 | |||||||
| chr17:78741036 | A | G | 23 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-31304T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741036 | |||||||
| chr17:78741108 | C | G | 212 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.23-31376G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741108 | |||||||
| chr17:78741390 | A | G | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-31658T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741390 | |||||||
| chr17:78741462 | A | G | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-31730T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741462 | |||||||
| chr17:78741623 | A | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-31891T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741623 | |||||||
| chr17:78741765 | T | C | 211 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-32033A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741765 | |||||||
| chr17:78741811 | C | G | 1 | a0001c0001t0004g0118 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.23-32079G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741811 | |||||||
| chr17:78741840 | G | C | 1 | a0001c0001t0006g0335 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.23-32108C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741840 | |||||||
| chr17:78741978 | T | C | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-32246A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741978 | |||||||
| chr17:78742304 | A | G | 211 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-32572T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742304 | |||||||
| chr17:78742525 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.23-32793C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742525 | |||||||
| chr17:78742574 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-32842G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742574 | |||||||
| chr17:78742577 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.23-32845C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742577 | |||||||
| chr17:78742708 | C | G | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-32976G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742708 | |||||||
| chr17:78742726 | G | A | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.23-32994C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742726 | |||||||
| chr17:78742828 | C | T | 40 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(37): Show |
40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.23-33096G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742828 | |||||||
| chr17:78742847 | T | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-33115A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742847 | |||||||
| chr17:78742848 | C | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-33116G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742848 | |||||||
| chr17:78742885 | T | C | 13 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0048 others(10): Show |
13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-33153A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742885 | |||||||
| chr17:78742988 | G | T | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-33256C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742988 | |||||||
| chr17:78743053 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.23-33321A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743053 | |||||||
| chr17:78743059 | G | A | 111 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-33327C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743059 | |||||||
| chr17:78743282 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-33550G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743282 | |||||||
| chr17:78743373 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0025g0051 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.23-33641G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743373 | |||||||
| chr17:78743505 | T | C | 25 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0354 others(22): Show |
25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.23-33773A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743505 | |||||||
| chr17:78743768 | C | T | 137 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.23-34036G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743768 | |||||||
| chr17:78744504 | C | T | 1 | a0001c0001t0005g0047 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.23-34772G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744504 | |||||||
| chr17:78744508 | C | G | 22 | a0001c0001t0006g0326 a0001c0001t0006g0327 a0001c0001t0006g0328 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-34776G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744508 | |||||||
| chr17:78744535 | G | A | 1 | a0001c0001t0006g0337 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.23-34803C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744535 | |||||||
| chr17:78744575 | G | A | 13 | a0001c0001t0003g0351 a0001c0001t0003g0354 a0001c0001t0003g0355 others(10): Show |
13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.23-34843C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744575 | |||||||
| chr17:78744677 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-34945A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744677 | |||||||
| chr17:78744686 | A | T | 1 | a0001c0001t0002g0283 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.23-34954T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744686 | |||||||
| chr17:78744785 | A | G | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-35053T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744785 | |||||||
| chr17:78744845 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.23-35114dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | |||||||
| chr17:78744845 | CA | C | 12 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0003g0067 others(9): Show |
12 | HG01106.hp2 HG02165.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-35114delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | |||||||
| chr17:78744845 | CAAA | C | 41 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-35116_23-35114d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | |||||||
| chr17:78745095 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.23-35363C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745095 | |||||||
| chr17:78745211 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-35479A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745211 | |||||||
| chr17:78745499 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-35767A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745499 | |||||||
| chr17:78745565 | T | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-35833A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745565 | |||||||
| chr17:78745576 | T | C | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-35844A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745576 | |||||||
| chr17:78745899 | G | GA | 44 | a0001c0001t0002g0263 a0001c0001t0003g0084 a0001c0001t0005g0002 others(41): Show |
44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.23-36168dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745899 | |||||||
| chr17:78745926 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.23-36194G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745926 | |||||||
| chr17:78745940 | G | A | 1 | a0001c0001t0007g0204 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.23-36208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745940 | |||||||
| chr17:78745982 | T | C | 42 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.22+36220A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745982 | |||||||
| chr17:78746098 | T | A | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+36104A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746098 | |||||||
| chr17:78746102 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+36100G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746102 | |||||||
| chr17:78746176 | G | A | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+36026C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746176 | |||||||
| chr17:78746211 | G | T | 1 | a0001c0001t0001g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.22+35991C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746211 | |||||||
| chr17:78746299 | C | CA | 71 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(68): Show |
71 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.22+35902dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746299 | |||||||
| chr17:78746523 | TA | T | 70 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(67): Show |
70 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.22+35678delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746523 | |||||||
| chr17:78746661 | G | T | 1 | a0001c0001t0006g0334 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.22+35541C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746661 | |||||||
| chr17:78746723 | C | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0142 |
3 | HG00408.hp1 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.22+35479G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746723 | |||||||
| chr17:78746923 | GAC | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+35277_22+35278d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746923 | |||||||
| chr17:78746967 | A | G | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+35235T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746967 | |||||||
| chr17:78747145 | C | CA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0094 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.22+35056dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | |||||||
| chr17:78747145 | C | CAA | 21 | a0001c0001t0002g0252 a0001c0001t0002g0264 a0001c0001t0002g0270 others(18): Show |
21 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+35055_22+35056d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | |||||||
| chr17:78747145 | CA | C | 7 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0003g0072 others(4): Show |
7 | HG00558.hp1 HG03098.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+35056delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | |||||||
| chr17:78747145 | CAA | C | 37 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(34): Show |
37 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(34): Show |
intron_variant | MODIFIER | c.22+35055_22+35056d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | |||||||
| chr17:78747145 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+35046_22+35056d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | |||||||
| chr17:78747164 | A | G | 27 | a0001c0001t0005g0002 a0001c0001t0005g0003 a0001c0001t0005g0018 others(24): Show |
27 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+35038T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747164 | |||||||
| chr17:78747179 | T | G | 1 | a0001c0001t0008g0266 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.22+35023A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747179 | |||||||
| chr17:78747212 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.22+34990G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747212 | |||||||
| chr17:78747383 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+34819C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747383 | |||||||
| chr17:78747762 | G | T | 7 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0124 others(4): Show |
7 | HG00597.hp2 NA18941.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+34440C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747762 | |||||||
| chr17:78747865 | T | C | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+34337A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747865 | |||||||
| chr17:78748044 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+34158A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748044 | |||||||
| chr17:78748291 | G | A | 11 | a0001c0001t0003g0351 a0001c0001t0003g0362 a0001c0001t0003g0363 others(8): Show |
11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+33911C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748291 | |||||||
| chr17:78748473 | C | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0093 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.22+33729G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748473 | |||||||
| chr17:78748576 | G | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+33626C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748576 | |||||||
| chr17:78748764 | G | A | 5 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(2): Show |
5 | HG02165.hp2 NA18971.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+33438C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748764 | |||||||
| chr17:78748949 | C | T | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+33253G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748949 | |||||||
| chr17:78748999 | G | T | 10 | a0001c0001t0003g0351 a0001c0001t0003g0362 a0001c0001t0003g0363 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+33203C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748999 | |||||||
| chr17:78749278 | G | T | 1 | a0001c0001t0006g0327 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+32924C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749278 | |||||||
| chr17:78749287 | C | T | 1 | a0001c0001t0006g0327 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+32915G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749287 | |||||||
| chr17:78749289 | G | A | 1 | a0001c0001t0007g0204 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.22+32913C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749289 | |||||||
| chr17:78749305 | T | C | 1 | a0001c0001t0006g0337 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.22+32897A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749305 | |||||||
| chr17:78749353 | G | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+32849C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749353 | |||||||
| chr17:78749457 | C | T | 20 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0354 others(17): Show |
20 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+32745G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749457 | |||||||
| chr17:78749537 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+32665C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749537 | |||||||
| chr17:78749587 | GCCATTAT others(3): Show |
G | 1 | a0001c0001t0005g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.22+32605_22+32614d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749587 | |||||||
| chr17:78749665 | T | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+32537A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749665 | |||||||
| chr17:78749665 | T | TA | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+32536dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749665 | |||||||
| chr17:78749694 | T | C | 1 | a0001c0001t0002g0296 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.22+32508A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749694 | |||||||
| chr17:78750052 | G | T | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+32150C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750052 | |||||||
| chr17:78750130 | G | A | 12 | a0001c0001t0003g0350 a0001c0001t0003g0360 a0001c0001t0003g0361 others(9): Show |
12 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+32072C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750130 | |||||||
| chr17:78750243 | G | A | 213 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.22+31959C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750243 | |||||||
| chr17:78750442 | C | A | 1 | a0001c0001t0005g0021 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.22+31760G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750442 | |||||||
| chr17:78750450 | T | C | 1 | a0001c0001t0006g0333 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.22+31752A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750450 | |||||||
| chr17:78750538 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.22+31664C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750538 | |||||||
| chr17:78750590 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.22+31612G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750590 | |||||||
| chr17:78750669 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.22+31533C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750669 | |||||||
| chr17:78750672 | G | C | 4 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0002g0318 others(1): Show |
4 | NA18948.hp2 NA18993.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+31530C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750672 | |||||||
| chr17:78750727 | G | A | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.22+31475C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750727 | |||||||
| chr17:78750780 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.22+31422G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750780 | |||||||
| chr17:78750791 | G | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+31411C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750791 | |||||||
| chr17:78750801 | C | CA | 15 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0124 others(12): Show |
15 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+31400dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750801 | |||||||
| chr17:78750801 | CA | C | 187 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.22+31400delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750801 | |||||||
| chr17:78750813 | A | C | 2 | a0001c0001t0006g0336 a0001c0001t0006g0348 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.22+31389T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750813 | |||||||
| chr17:78750814 | A | C | 1 | a0001c0001t0005g0022 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.22+31388T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750814 | |||||||
| chr17:78750859 | G | A | 6 | a0001c0001t0003g0362 a0001c0001t0003g0363 a0001c0001t0003g0364 others(3): Show |
6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+31343C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750859 | |||||||
| chr17:78751064 | A | ACCTCTAC others(3): Show |
6 | a0001c0001t0004g0112 a0001c0001t0004g0118 a0001c0001t0004g0127 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+31128_22+31137d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751064 | |||||||
| chr17:78751126 | G | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0154 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+31076C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751126 | |||||||
| chr17:78751263 | G | A | 44 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(41): Show |
44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+30939C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751263 | |||||||
| chr17:78751264 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+30938G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751264 | |||||||
| chr17:78751265 | C | A | 30 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(27): Show |
30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+30937G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751265 | |||||||
| chr17:78751315 | A | G | 1 | a0001c0001t0006g0329 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.22+30887T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751315 | |||||||
| chr17:78751441 | A | G | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+30761T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751441 | |||||||
| chr17:78751474 | C | CA | 143 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.22+30727dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | |||||||
| chr17:78751474 | C | CAA | 20 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0003g0067 others(17): Show |
20 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+30726_22+30727d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | |||||||
| chr17:78751474 | C | CAAA | 12 | a0001c0001t0002g0280 a0001c0001t0003g0064 a0001c0001t0003g0066 others(9): Show |
12 | HG00423.hp2 HG01255.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+30725_22+30727d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | |||||||
| chr17:78751474 | C | CAAAA | 42 | a0001c0001t0001g0026 a0001c0001t0003g0065 a0001c0001t0003g0080 others(39): Show |
42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.22+30724_22+30727d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | |||||||
| chr17:78751514 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+30688C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751514 | |||||||
| chr17:78751569 | G | A | 1 | a0001c0001t0021g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.22+30633C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751569 | |||||||
| chr17:78751664 | C | T | 30 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(27): Show |
30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+30538G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751664 | |||||||
| chr17:78751895 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+30307C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751895 | |||||||
| chr17:78752168 | C | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+30034G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752168 | |||||||
| chr17:78752203 | T | C | 3 | a0001c0001t0005g0033 a0001c0001t0005g0040 a0001c0001t0005g0041 |
3 | HG03239.hp2 HG03490.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.22+29999A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752203 | |||||||
| chr17:78752456 | A | G | 214 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.22+29746T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752456 | |||||||
| chr17:78752506 | C | T | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+29696G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752506 | |||||||
| chr17:78752519 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+29683C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752519 | |||||||
| chr17:78752542 | T | C | 214 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.22+29660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752542 | |||||||
| chr17:78752623 | G | A | 43 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(40): Show |
43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.22+29579C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752623 | |||||||
| chr17:78752724 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.22+29478A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752724 | |||||||
| chr17:78752883 | A | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+29319T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752883 | |||||||
| chr17:78753143 | C | G | 1 | a0001c0001t0003g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.22+29059G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753143 | |||||||
| chr17:78753186 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+29016C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753186 | |||||||
| chr17:78753225 | T | G | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+28977A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753225 | |||||||
| chr17:78753239 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.22+28963A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753239 | |||||||
| chr17:78753302 | T | A | 6 | a0001c0001t0003g0362 a0001c0001t0003g0363 a0001c0001t0003g0364 others(3): Show |
6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+28900A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753302 | |||||||
| chr17:78753499 | T | TAATA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0095 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.22+28699_22+28702d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | |||||||
| chr17:78753499 | TAATA | T | 8 | a0001c0001t0001g0144 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG00544.hp2 HG02004.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+28699_22+28702d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | |||||||
| chr17:78753499 | TAATAAAT others(1): Show |
T | 118 | a0001c0001t0001g0097 a0001c0001t0001g0145 a0001c0001t0001g0146 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.22+28695_22+28702d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | |||||||
| chr17:78753529 | A | ATAAATAA others(9): Show |
1 | a0001c0001t0005g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.22+28672_22+28673i others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | |||||||
| chr17:78753529 | A | ATAAATAA others(5): Show |
38 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(35): Show |
38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+28672_22+28673i others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | |||||||
| chr17:78753529 | A | ATAAATAA others(1): Show |
3 | a0001c0001t0005g0032 a0001c0001t0005g0043 a0001c0001t0009g0048 |
3 | HG02976.hp1 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.22+28672_22+28673i others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | |||||||
| chr17:78753616 | A | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0227 others(1): Show |
4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+28586T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753616 | |||||||
| chr17:78753707 | C | T | 1 | a0001c0001t0005g0018 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.22+28495G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753707 | |||||||
| chr17:78753991 | C | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+28211G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753991 | |||||||
| chr17:78754015 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0093 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.22+28187C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754015 | |||||||
| chr17:78754245 | C | T | 2 | a0001c0001t0004g0126 a0001c0001t0004g0176 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.22+27957G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754245 | |||||||
| chr17:78754343 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+27859A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754343 | |||||||
| chr17:78754458 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+27744G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754458 | |||||||
| chr17:78754739 | A | AGTTT | 44 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(41): Show |
44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+27462_22+27463i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754739 | |||||||
| chr17:78754834 | T | C | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+27368A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754834 | |||||||
| chr17:78754906 | C | T | 29 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(26): Show |
29 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+27296G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754906 | |||||||
| chr17:78755044 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+27158A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755044 | |||||||
| chr17:78755152 | A | G | 15 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0124 others(12): Show |
15 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+27050T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755152 | |||||||
| chr17:78755413 | G | A | 38 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(35): Show |
38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+26789C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755413 | |||||||
| chr17:78755424 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+26778G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755424 | |||||||
| chr17:78755491 | T | TAAAAA | 12 | a0001c0001t0002g0282 a0001c0001t0002g0292 a0001c0001t0002g0297 others(9): Show |
12 | HG01070.hp1 HG02109.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+26706_22+26710d others(7): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | |||||||
| chr17:78755491 | T | TAAAAAA | 161 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0098 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.22+26705_22+26710d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | |||||||
| chr17:78755491 | T | TAAAAAAA | 191 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(188): Show |
192 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.22+26704_22+26710d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | |||||||
| chr17:78755491 | T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0003g0369 others(4): Show |
7 | HG00544.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+26703_22+26710d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | |||||||
| chr17:78755596 | CA | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | NA18948.hp1 NA18965.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+26605delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755596 | |||||||
| chr17:78755805 | G | A | 1 | a0001c0001t0004g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+26397C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755805 | |||||||
| chr17:78755910 | C | CA | 36 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0198 others(33): Show |
36 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.22+26291dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755910 | |||||||
| chr17:78755936 | A | G | 1 | a0001c0001t0005g0003 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.22+26266T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755936 | |||||||
| chr17:78756029 | C | T | 210 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.22+26173G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756029 | |||||||
| chr17:78756070 | TTTA | T | 3 | a0001c0001t0002g0305 a0001c0001t0002g0315 a0001c0001t0002g0322 |
3 | HG00597.hp1 NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.22+26129_22+26131d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756070 | |||||||
| chr17:78756073 | A | T | 2 | a0001c0001t0012g0116 a0001c0001t0012g0117 |
2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+26129T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756073 | |||||||
| chr17:78756075 | T | A | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+26127A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756075 | |||||||
| chr17:78756077 | T | A | 1 | a0001c0001t0004g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.22+26125A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756077 | |||||||
| chr17:78756078 | T | A | 3 | a0001c0001t0002g0305 a0001c0001t0002g0315 a0001c0001t0002g0322 |
3 | HG00597.hp1 NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.22+26124A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756078 | |||||||
| chr17:78756079 | A | AT | 161 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0276 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.22+26122dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | |||||||
| chr17:78756079 | A | ATT | 8 | a0001c0001t0002g0278 a0001c0001t0002g0280 a0001c0001t0005g0033 others(5): Show |
8 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+26121_22+26122d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | |||||||
| chr17:78756079 | A | T | 4 | a0001c0001t0002g0305 a0001c0001t0002g0315 a0001c0001t0002g0322 others(1): Show |
4 | HG00597.hp1 HG02155.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+26123T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | |||||||
| chr17:78756080 | T | A | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+26122A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756080 | |||||||
| chr17:78756082 | T | TA | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.22+26119_22+26120i others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756082 | |||||||
| chr17:78756170 | G | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+26032C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756170 | |||||||
| chr17:78756278 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.22+25924C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756278 | |||||||
| chr17:78756322 | C | A | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+25880G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756322 | |||||||
| chr17:78756467 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+25735C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756467 | |||||||
| chr17:78756632 | C | A | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+25570G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756632 | |||||||
| chr17:78756716 | G | C | 1 | a0001c0001t0003g0351 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.22+25486C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756716 | |||||||
| chr17:78756876 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25326C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756876 | |||||||
| chr17:78756903 | C | T | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+25299G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756903 | |||||||
| chr17:78756919 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25283G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756919 | |||||||
| chr17:78756921 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25281A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756921 | |||||||
| chr17:78756923 | G | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25279C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756923 | |||||||
| chr17:78756926 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25276T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756926 | |||||||
| chr17:78756927 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25275T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756927 | |||||||
| chr17:78756928 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25274T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756928 | |||||||
| chr17:78756929 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25273T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756929 | |||||||
| chr17:78756932 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25270T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756932 | |||||||
| chr17:78756933 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25269C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756933 | |||||||
| chr17:78756937 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25265T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756937 | |||||||
| chr17:78756938 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25264T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756938 | |||||||
| chr17:78756940 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25262T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756940 | |||||||
| chr17:78756943 | A | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25259T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756943 | |||||||
| chr17:78756944 | T | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25258A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756944 | |||||||
| chr17:78756946 | C | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25256G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756946 | |||||||
| chr17:78756949 | A | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25253T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756949 | |||||||
| chr17:78756950 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25252T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756950 | |||||||
| chr17:78756951 | G | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25251C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756951 | |||||||
| chr17:78756952 | G | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25250C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756952 | |||||||
| chr17:78756954 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25248C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756954 | |||||||
| chr17:78756956 | A | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25246T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756956 | |||||||
| chr17:78756961 | C | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25241G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756961 | |||||||
| chr17:78756962 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25240T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756962 | |||||||
| chr17:78756967 | T | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25235A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756967 | |||||||
| chr17:78756969 | G | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25233C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756969 | |||||||
| chr17:78756971 | A | T | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25231T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756971 | |||||||
| chr17:78756972 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25230A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756972 | |||||||
| chr17:78756973 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25229A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756973 | |||||||
| chr17:78756975 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25227A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756975 | |||||||
| chr17:78756976 | T | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25226A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756976 | |||||||
| chr17:78756977 | TTC | T | 6 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(3): Show |
6 | HG02165.hp2 NA18945.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+25223_22+25224d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756977 | |||||||
| chr17:78756978 | TC | T | 21 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0071 others(18): Show |
21 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+25223delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756978 | |||||||
| chr17:78756979 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25223G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756979 | |||||||
| chr17:78756980 | T | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25222A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756980 | |||||||
| chr17:78756983 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25219A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756983 | |||||||
| chr17:78756984 | T | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25218A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756984 | |||||||
| chr17:78756985 | T | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25217A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756985 | |||||||
| chr17:78756986 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25216A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756986 | |||||||
| chr17:78756986 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25216A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756986 | |||||||
| chr17:78756987 | T | C | 26 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0067 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+25215A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756987 | |||||||
| chr17:78756987 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25215A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756987 | |||||||
| chr17:78756988 | C | CT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0150 a0001c0001t0003g0236 others(8): Show |
11 | HG00597.hp2 HG01106.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+25213dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756988 | |||||||
| chr17:78756988 | C | T | 27 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+25214G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756988 | |||||||
| chr17:78756991 | T | A | 1 | a0001c0001t0002g0281 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.22+25211A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756991 | |||||||
| chr17:78756992 | T | C | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+25210A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756992 | |||||||
| chr17:78757009 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25193C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757009 | |||||||
| chr17:78757013 | G | C | 1 | a0001c0001t0004g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.22+25189C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757013 | |||||||
| chr17:78757020 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.22+25182C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757020 | |||||||
| chr17:78757028 | G | C | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25174C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757028 | |||||||
| chr17:78757031 | C | G | 1 | a0001c0001t0003g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25171G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757031 | |||||||
| chr17:78757049 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.22+25153C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757049 | |||||||
| chr17:78757062 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+25140G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757062 | |||||||
| chr17:78757092 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.22+25110G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757092 | |||||||
| chr17:78757216 | G | A | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+24986C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757216 | |||||||
| chr17:78757222 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.22+24980T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757222 | |||||||
| chr17:78757500 | G | C | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+24702C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757500 | |||||||
| chr17:78757702 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | NA18940.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24500C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757702 | |||||||
| chr17:78757718 | G | A | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+24484C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757718 | |||||||
| chr17:78757793 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.22+24409C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757793 | |||||||
| chr17:78757816 | G | A | 4 | a0001c0001t0002g0251 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24386C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757816 | |||||||
| chr17:78757985 | T | G | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24217A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757985 | |||||||
| chr17:78758027 | A | G | 1 | a0001c0001t0005g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+24175T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758027 | |||||||
| chr17:78758186 | A | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.22+24016T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758186 | |||||||
| chr17:78758254 | G | A | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+23948C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758254 | |||||||
| chr17:78758324 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0029g0115 |
2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.22+23878G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758324 | |||||||
| chr17:78758462 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.22+23740A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758462 | |||||||
| chr17:78758493 | T | A | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+23709A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758493 | |||||||
| chr17:78758542 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+23660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758542 | |||||||
| chr17:78758568 | G | A | 1 | a0001c0001t0004g0376 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.22+23634C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758568 | |||||||
| chr17:78758635 | C | T | 1 | a0001c0001t0004g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+23567G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758635 | |||||||
| chr17:78758655 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+23547G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758655 | |||||||
| chr17:78759303 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+22899G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759303 | |||||||
| chr17:78759371 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.22+22831T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759371 | |||||||
| chr17:78759664 | G | A | 1 | a0001c0001t0008g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.22+22538C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759664 | |||||||
| chr17:78759908 | C | A | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.22+22294G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759908 | |||||||
| chr17:78759987 | T | G | 1 | a0001c0001t0006g0334 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.22+22215A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759987 | |||||||
| chr17:78760022 | C | T | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+22180G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760022 | |||||||
| chr17:78760090 | C | T | 38 | a0001c0001t0001g0026 a0001c0001t0005g0002 a0001c0001t0005g0003 others(35): Show |
38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+22112G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760090 | |||||||
| chr17:78760187 | C | A | 1 | a0001c0001t0021g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.22+22015G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760187 | |||||||
| chr17:78760269 | C | T | 1 | a0001c0001t0007g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.22+21933G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760269 | |||||||
| chr17:78760305 | C | G | 2 | a0001c0001t0007g0219 a0001c0001t0007g0220 |
2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.22+21897G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760305 | |||||||
| chr17:78760353 | GT | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0264 a0001c0001t0003g0377 others(1): Show |
4 | HG02738.hp2 NA18940.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21848delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760353 | |||||||
| chr17:78760355 | TTATATA | T | 11 | a0001c0001t0003g0236 a0001c0001t0006g0326 a0001c0001t0006g0328 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+21841_22+21846d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760355 | |||||||
| chr17:78760361 | ATATATAT others(117): Show |
A | 2 | a0001c0001t0003g0080 a0001c0001t0003g0083 |
2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21717_22+21840d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760361 | |||||||
| chr17:78760363 | ATATATAT others(187): Show |
A | 1 | a0001c0001t0002g0256 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.22+21645_22+21838d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760363 | |||||||
| chr17:78760372 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+21830A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760372 | |||||||
| chr17:78760372 | TATATATA others(11): Show |
T | 24 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.22+21812_22+21829d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760372 | |||||||
| chr17:78760374 | TATATATA others(9): Show |
T | 3 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0088 |
3 | NA19003.hp2 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.22+21812_22+21827d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760374 | |||||||
| chr17:78760375 | ATATATAT others(103): Show |
A | 1 | a0001c0001t0002g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.22+21717_22+21826d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760375 | |||||||
| chr17:78760376 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.22+21826A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | |||||||
| chr17:78760376 | TATATATA others(3): Show |
T | 1 | a0001c0001t0006g0341 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.22+21816_22+21825d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | |||||||
| chr17:78760376 | TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0258 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.22+21814_22+21825d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | |||||||
| chr17:78760377 | ATATATAT others(123): Show |
A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0013 a0001c0001t0002g0014 others(17): Show |
20 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+21695_22+21824d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760377 | |||||||
| chr17:78760378 | T | C | 11 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0054 others(8): Show |
11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+21824A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | |||||||
| chr17:78760378 | TATATATA others(1): Show |
T | 3 | a0001c0001t0009g0048 a0001c0001t0009g0052 a0001c0001t0014g0053 |
3 | HG02976.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.22+21816_22+21823d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | |||||||
| chr17:78760378 | TATATATA others(3): Show |
T | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+21814_22+21823d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | |||||||
| chr17:78760378 | TATATATA others(47): Show |
T | 1 | a0001c0001t0005g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.22+21770_22+21823d others(56): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | |||||||
| chr17:78760378 | TATATATA others(113): Show |
T | 1 | a0001c0001t0031g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.22+21704_22+21823d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | |||||||
| chr17:78760379 | ATATATAC others(121): Show |
A | 18 | a0001c0001t0002g0020 a0001c0001t0002g0244 a0001c0001t0002g0245 others(15): Show |
18 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.22+21695_22+21822d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760379 | |||||||
| chr17:78760379 | ATATATAC others(159): Show |
A | 1 | a0001c0001t0005g0033 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.22+21657_22+21822d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760379 | |||||||
| chr17:78760380 | TATATACA others(45): Show |
T | 1 | a0001c0001t0011g0030 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.22+21770_22+21821d others(54): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760380 | |||||||
| chr17:78760380 | TATATACA others(149): Show |
T | 2 | a0001c0001t0005g0039 a0001c0001t0005g0043 |
2 | HG03927.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.22+21666_22+21821d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760380 | |||||||
| chr17:78760381 | ATATACAC others(119): Show |
A | 18 | a0001c0001t0001g0276 a0001c0001t0002g0259 a0001c0001t0002g0274 others(15): Show |
18 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.22+21695_22+21820d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760381 | |||||||
| chr17:78760381 | ATATACAC others(129): Show |
A | 5 | a0001c0001t0002g0251 a0001c0001t0002g0282 a0001c0001t0002g0284 others(2): Show |
5 | HG02109.hp1 HG02165.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+21685_22+21820d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760381 | |||||||
| chr17:78760382 | T | C | 13 | a0001c0001t0001g0177 a0001c0001t0001g0192 a0001c0001t0005g0050 others(10): Show |
13 | HG00544.hp1 HG01243.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+21820A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | |||||||
| chr17:78760382 | TATACACA others(7): Show |
T | 1 | a0001c0001t0003g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.22+21806_22+21819d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | |||||||
| chr17:78760382 | TATACACA others(43): Show |
T | 2 | a0001c0001t0001g0026 a0001c0001t0005g0034 |
2 | NA18939.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.22+21770_22+21819d others(52): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | |||||||
| chr17:78760382 | TATACACA others(147): Show |
T | 1 | a0001c0001t0005g0036 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.22+21666_22+21819d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | |||||||
| chr17:78760383 | ATACACAC others(19): Show |
A | 2 | a0001c0001t0003g0363 a0001c0001t0003g0366 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.22+21793_22+21818d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | |||||||
| chr17:78760383 | ATACACAC others(117): Show |
A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0269 a0001c0001t0002g0298 others(9): Show |
12 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+21695_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | |||||||
| chr17:78760383 | ATACACAC others(127): Show |
A | 8 | a0001c0001t0002g0283 a0001c0001t0002g0311 a0001c0001t0002g0312 others(5): Show |
8 | HG00673.hp2 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+21685_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | |||||||
| chr17:78760383 | ATACACAC others(155): Show |
A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0035 |
2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.22+21657_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | |||||||
| chr17:78760384 | T | C | 84 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0059 others(81): Show |
84 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.22+21818A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | T | TAC | 49 | a0001c0001t0001g0009 a0001c0001t0001g0095 a0001c0001t0001g0096 others(46): Show |
49 | HG00738.hp1 HG01081.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.22+21816_22+21817d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | T | TATAC | 4 | a0001c0001t0001g0170 a0001c0001t0004g0005 a0001c0001t0004g0010 others(1): Show |
4 | HG00597.hp2 HG01123.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21817_22+21818i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | T | TATATATA others(3): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
6 | HG00639.hp1 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21817_22+21818i others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.22+21817_22+21818i others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACAC | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0003g0360 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21814_22+21817d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACACACA others(37): Show |
T | 2 | a0001c0001t0005g0031 a0001c0001t0005g0047 |
2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.22+21774_22+21817d others(46): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACACACA others(41): Show |
T | 2 | a0001c0001t0005g0003 a0001c0001t0005g0045 |
2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.22+21770_22+21817d others(50): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACACACA others(107): Show |
T | 1 | a0001c0001t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.22+21704_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACACACA others(145): Show |
T | 1 | a0001c0001t0005g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+21666_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760384 | TACACACA others(179): Show |
T | 11 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0054 others(8): Show |
11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+21632_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | |||||||
| chr17:78760385 | ACACACAC others(17): Show |
A | 2 | a0001c0001t0002g0304 a0001c0003t0017g0017 |
2 | HG03579.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.22+21793_22+21816d others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | |||||||
| chr17:78760385 | ACACACAC others(51): Show |
A | 1 | a0001c0001t0005g0018 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.22+21759_22+21816d others(60): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | |||||||
| chr17:78760385 | ACACACAC others(115): Show |
A | 6 | a0001c0001t0002g0247 a0001c0001t0002g0264 a0001c0001t0002g0290 others(3): Show |
6 | HG02738.hp2 HG04204.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21695_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | |||||||
| chr17:78760385 | ACACACAC others(125): Show |
A | 34 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0242 others(31): Show |
34 | HG00621.hp1 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+21685_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | |||||||
| chr17:78760385 | ACACACAC others(153): Show |
A | 9 | a0001c0001t0005g0002 a0001c0001t0005g0021 a0001c0001t0005g0022 others(6): Show |
9 | HG00673.hp1 HG03239.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21657_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | |||||||
| chr17:78760386 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.22+21816G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760386 | |||||||
| chr17:78760388 | C | CACACATA others(29): Show |
1 | a0001c0001t0001g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.22+21813_22+21814i others(38): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760388 | |||||||
| chr17:78760388 | C | T | 4 | a0001c0001t0003g0236 a0001c0001t0003g0238 a0001c0001t0003g0368 others(1): Show |
4 | HG01106.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21814G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760388 | |||||||
| chr17:78760390 | C | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0005g0032 others(4): Show |
7 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21812G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760390 | |||||||
| chr17:78760394 | T | C | 2 | a0001c0001t0007g0219 a0001c0001t0007g0220 |
2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.22+21808A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760394 | |||||||
| chr17:78760396 | CAT | C | 15 | a0001c0001t0002g0258 a0001c0001t0005g0044 a0001c0001t0006g0326 others(12): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+21804_22+21805d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760396 | |||||||
| chr17:78760405 | ATG | A | 23 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+21795_22+21796d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760405 | |||||||
| chr17:78760407 | G | A | 8 | a0001c0001t0003g0237 a0001c0001t0005g0032 a0001c0001t0005g0037 others(5): Show |
8 | HG00642.hp1 HG01192.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+21795C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760407 | |||||||
| chr17:78760409 | G | A | 5 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0075 others(2): Show |
5 | HG02965.hp1 NA18946.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21793C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | |||||||
| chr17:78760409 | G | GTA | 3 | a0001c0001t0001g0106 a0001c0001t0001g0190 a0001c0001t0001g0239 |
3 | HG03041.hp2 HG03486.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.22+21791_22+21792d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | |||||||
| chr17:78760409 | GTA | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0148 a0001c0001t0001g0150 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21791_22+21792d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | |||||||
| chr17:78760411 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(8): Show |
12 | HG00639.hp1 HG00642.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+21791T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760411 | |||||||
| chr17:78760411 | ATATATAT others(167): Show |
A | 5 | a0001c0001t0005g0032 a0001c0001t0005g0037 a0001c0001t0009g0048 others(2): Show |
5 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21617_22+21790d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760411 | |||||||
| chr17:78760422 | T | C | 3 | a0001c0001t0003g0237 a0001c0001t0003g0363 a0001c0001t0003g0366 |
3 | HG02818.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.22+21780A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760422 | |||||||
| chr17:78760426 | C | T | 29 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0003g0064 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+21776G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760426 | |||||||
| chr17:78760432 | C | T | 2 | a0001c0001t0005g0031 a0001c0001t0005g0047 |
2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.22+21770G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760432 | |||||||
| chr17:78760432 | CAT | C | 24 | a0001c0001t0002g0258 a0001c0001t0003g0236 a0001c0001t0003g0238 others(21): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.22+21768_22+21769d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760432 | |||||||
| chr17:78760439 | A | G | 2 | a0001c0001t0004g0126 a0001c0003t0017g0017 |
2 | HG00140.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.22+21763T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760439 | |||||||
| chr17:78760441 | A | G | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+21761T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760441 | |||||||
| chr17:78760443 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0005g0003 a0001c0001t0005g0027 others(5): Show |
8 | NA18939.hp1 NA18942.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+21759C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760443 | |||||||
| chr17:78760445 | A | G | 6 | a0001c0001t0003g0237 a0001c0001t0003g0363 a0001c0001t0003g0366 others(3): Show |
6 | HG01261.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+21757T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | |||||||
| chr17:78760445 | ATATATAT others(65): Show |
A | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+21685_22+21756d others(74): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | |||||||
| chr17:78760445 | ATATATAT others(133): Show |
A | 23 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0002g0258 others(20): Show |
23 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+21617_22+21756d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | |||||||
| chr17:78760447 | ATATATAT others(131): Show |
A | 26 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+21617_22+21754d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760447 | |||||||
| chr17:78760449 | ATATATAC others(101): Show |
A | 3 | a0001c0001t0003g0237 a0001c0001t0003g0363 a0001c0001t0003g0366 |
3 | HG02818.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.22+21645_22+21752d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760449 | |||||||
| chr17:78760453 | ATACATAC others(57): Show |
A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21685_22+21748d others(66): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760453 | |||||||
| chr17:78760453 | ATACATAC others(97): Show |
A | 1 | a0001c0001t0003g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.22+21645_22+21748d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760453 | |||||||
| chr17:78760454 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0152 |
2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.22+21748A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760454 | |||||||
| chr17:78760454 | T | TAC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21746_22+21747d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760454 | |||||||
| chr17:78760456 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21746G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760456 | |||||||
| chr17:78760458 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21744A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760458 | |||||||
| chr17:78760460 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21742G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760460 | |||||||
| chr17:78760460 | CAT | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0190 a0001c0001t0003g0122 others(2): Show |
5 | HG03225.hp2 NA18747.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21740_22+21741d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760460 | |||||||
| chr17:78760462 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0003g0120 |
2 | HG03486.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.22+21740A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760462 | |||||||
| chr17:78760464 | T | C | 9 | a0001c0001t0001g0026 a0001c0001t0005g0003 a0001c0001t0005g0018 others(6): Show |
9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21738A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760464 | |||||||
| chr17:78760468 | T | C | 9 | a0001c0001t0001g0026 a0001c0001t0005g0003 a0001c0001t0005g0018 others(6): Show |
9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21734A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760468 | |||||||
| chr17:78760471 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0005g0003 a0001c0001t0005g0018 others(6): Show |
9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21731C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760471 | |||||||
| chr17:78760485 | GTATATAT others(95): Show |
G | 9 | a0001c0001t0001g0026 a0001c0001t0005g0003 a0001c0001t0005g0018 others(6): Show |
9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21615_22+21716d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760485 | |||||||
| chr17:78760494 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0171 others(1): Show |
4 | HG00544.hp2 NA18969.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21708A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760494 | |||||||
| chr17:78760494 | T | TAC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21707_22+21708i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760494 | |||||||
| chr17:78760498 | C | T | 1 | a0001c0001t0002g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.22+21704G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760498 | |||||||
| chr17:78760502 | T | C | 2 | a0001c0001t0003g0080 a0001c0001t0003g0083 |
2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21700A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760502 | |||||||
| chr17:78760507 | G | A | 5 | a0001c0001t0002g0249 a0001c0001t0002g0310 a0001c0001t0003g0080 others(2): Show |
5 | HG00099.hp1 HG01074.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21695C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760507 | |||||||
| chr17:78760507 | GTA | G | 7 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21693_22+21694d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760507 | |||||||
| chr17:78760508 | T | TATATATG others(19): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.22+21693_22+21694i others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760508 | |||||||
| chr17:78760510 | T | TATATGTA others(17): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0130 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.22+21691_22+21692i others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760510 | |||||||
| chr17:78760513 | A | G | 2 | a0001c0001t0003g0080 a0001c0001t0003g0083 |
2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21689T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760513 | |||||||
| chr17:78760517 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.22+21685C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | |||||||
| chr17:78760517 | G | GTA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0060 others(13): Show |
16 | HG00408.hp1 NA18747.hp1 NA18948.hp1 others(13): Show |
intron_variant | MODIFIER | c.22+21683_22+21684d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | |||||||
| chr17:78760517 | GTA | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0143 others(7): Show |
10 | HG02572.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+21683_22+21684d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | |||||||
| chr17:78760519 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(9): Show |
13 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+21683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760519 | |||||||
| chr17:78760526 | T | C | 7 | a0001c0001t0003g0350 a0001c0001t0003g0362 a0001c0001t0003g0364 others(4): Show |
7 | HG02647.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+21676A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760526 | |||||||
| chr17:78760527 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.22+21675T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760527 | |||||||
| chr17:78760528 | T | C | 8 | a0001c0001t0006g0327 a0001c0001t0006g0337 a0001c0001t0006g0342 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+21674A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760528 | |||||||
| chr17:78760530 | T | C | 117 | a0001c0001t0001g0097 a0001c0001t0001g0148 a0001c0001t0001g0150 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.22+21672A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760530 | |||||||
| chr17:78760532 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0003g0370 a0001c0001t0003g0371 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21670G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760532 | |||||||
| chr17:78760534 | TAC | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0168 others(1): Show |
4 | NA18964.hp2 NA18968.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21666_22+21667d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760534 | |||||||
| chr17:78760536 | C | CATATATA others(15): Show |
1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+21644_22+21665d others(24): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760536 | |||||||
| chr17:78760538 | T | C | 10 | a0001c0001t0001g0173 a0001c0001t0003g0351 a0001c0001t0003g0354 others(7): Show |
10 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+21664A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760538 | |||||||
| chr17:78760540 | T | C | 6 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21662A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760540 | |||||||
| chr17:78760541 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22+21661T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760541 | |||||||
| chr17:78760541 | ATATG | A | 7 | a0001c0001t0003g0350 a0001c0001t0003g0362 a0001c0001t0003g0364 others(4): Show |
7 | HG02647.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21657_22+21660d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760541 | |||||||
| chr17:78760542 | T | C | 10 | a0001c0001t0001g0173 a0001c0001t0003g0351 a0001c0001t0003g0354 others(7): Show |
10 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+21660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760542 | |||||||
| chr17:78760544 | T | C | 5 | a0001c0001t0003g0370 a0001c0001t0003g0371 a0001c0001t0003g0373 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21658A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760544 | |||||||
| chr17:78760545 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0003g0080 a0001c0001t0003g0083 others(18): Show |
21 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+21657C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760545 | |||||||
| chr17:78760545 | GTA | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0169 a0001c0001t0026g0102 others(1): Show |
4 | HG01074.hp2 HG03491.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21655_22+21656d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760545 | |||||||
| chr17:78760546 | T | C | 1 | a0001c0001t0003g0372 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.22+21656A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760546 | |||||||
| chr17:78760547 | A | G | 104 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.22+21655T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760547 | |||||||
| chr17:78760549 | A | G | 2 | a0001c0001t0002g0016 a0001c0003t0017g0017 |
2 | HG03579.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.22+21653T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760549 | |||||||
| chr17:78760551 | A | G | 10 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0362 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+21651T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760551 | |||||||
| chr17:78760551 | ATATATG | A | 102 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.22+21645_22+21650d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760551 | |||||||
| chr17:78760553 | A | G | 16 | a0001c0001t0001g0173 a0001c0001t0003g0350 a0001c0001t0003g0351 others(13): Show |
16 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.22+21649T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760553 | |||||||
| chr17:78760555 | A | G | 11 | a0001c0001t0001g0173 a0001c0001t0003g0354 a0001c0001t0003g0355 others(8): Show |
11 | HG01123.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+21647T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760555 | |||||||
| chr17:78760557 | G | A | 34 | a0001c0001t0001g0173 a0001c0001t0003g0080 a0001c0001t0003g0083 others(31): Show |
34 | HG00673.hp1 HG01123.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+21645C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760557 | |||||||
| chr17:78760559 | A | G | 1 | a0001c0001t0003g0372 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.22+21643T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760559 | |||||||
| chr17:78760559 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0005g0019 a0001c0001t0005g0038 |
2 | NA19080.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.22+21617_22+21642d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760559 | |||||||
| chr17:78760564 | T | C | 13 | a0001c0001t0005g0002 a0001c0001t0005g0021 a0001c0001t0005g0022 others(10): Show |
13 | HG00673.hp1 HG02135.hp1 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+21638A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760564 | |||||||
| chr17:78760566 | T | C | 4 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 others(1): Show |
4 | NA18973.hp1 NA18989.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21636A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760566 | |||||||
| chr17:78760568 | T | C | 16 | a0001c0001t0004g0214 a0001c0001t0005g0002 a0001c0001t0005g0021 others(13): Show |
16 | HG00673.hp1 HG02135.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.22+21634A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760568 | |||||||
| chr17:78760568 | TAC | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21632_22+21633d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760568 | |||||||
| chr17:78760570 | C | T | 20 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(17): Show |
20 | HG00673.hp1 HG02135.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.22+21632G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760570 | |||||||
| chr17:78760572 | C | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 |
3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21630G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760572 | |||||||
| chr17:78760576 | C | T | 30 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 others(27): Show |
30 | HG00673.hp1 HG02135.hp1 HG02647.hp2 others(27): Show |
intron_variant | MODIFIER | c.22+21626G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760576 | |||||||
| chr17:78760576 | CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0154 |
2 | HG01255.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.22+21616_22+21625d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760576 | |||||||
| chr17:78760581 | A | G | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 |
3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21621T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760581 | |||||||
| chr17:78760585 | G | A | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 |
3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21617C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760585 | |||||||
| chr17:78760585 | G | GTA | 188 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.22+21615_22+21616d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760585 | |||||||
| chr17:78760587 | A | ATG | 27 | a0001c0001t0005g0002 a0001c0001t0005g0021 a0001c0001t0005g0022 others(24): Show |
27 | HG00673.hp1 HG02135.hp1 HG02647.hp2 others(24): Show |
intron_variant | MODIFIER | c.22+21614_22+21615i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760587 | |||||||
| chr17:78760587 | A | G | 7 | a0001c0001t0005g0019 a0001c0001t0005g0032 a0001c0001t0005g0037 others(4): Show |
7 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21615T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760587 | |||||||
| chr17:78760591 | A | G | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+21611T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760591 | |||||||
| chr17:78760593 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.22+21609T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760593 | |||||||
| chr17:78760658 | A | G | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21544T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760658 | |||||||
| chr17:78760997 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21205C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760997 | |||||||
| chr17:78761045 | A | T | 31 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0003g0064 others(28): Show |
31 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+21157T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761045 | |||||||
| chr17:78761065 | AC | A | 10 | a0001c0001t0007g0061 a0001c0001t0007g0201 a0001c0001t0007g0202 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+21136delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761065 | |||||||
| chr17:78761134 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21068G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761134 | |||||||
| chr17:78761214 | C | A | 130 | a0001c0001t0001g0173 a0001c0001t0001g0276 a0001c0001t0002g0012 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.22+20988G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761214 | |||||||
| chr17:78761395 | G | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+20807C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761395 | |||||||
| chr17:78761523 | G | C | 3 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0075 |
3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.22+20679C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761523 | |||||||
| chr17:78761542 | G | T | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+20660C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761542 | |||||||
| chr17:78761566 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+20636C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761566 | |||||||
| chr17:78761607 | G | A | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+20595C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761607 | |||||||
| chr17:78761616 | T | G | 1 | a0001c0001t0013g0353 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.22+20586A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761616 | |||||||
| chr17:78761663 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+20539C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761663 | |||||||
| chr17:78761685 | A | C | 218 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.22+20517T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761685 | |||||||
| chr17:78761716 | G | C | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+20486C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761716 | |||||||
| chr17:78761810 | C | G | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+20392G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761810 | |||||||
| chr17:78762021 | G | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0029 |
2 | NA18940.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.22+20181C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762021 | |||||||
| chr17:78762149 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.22+20053C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762149 | |||||||
| chr17:78762160 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.22+20042A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762160 | |||||||
| chr17:78762169 | A | G | 96 | a0001c0001t0001g0148 a0001c0001t0001g0276 a0001c0001t0002g0012 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.22+20033T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762169 | |||||||
| chr17:78762181 | C | T | 4 | a0001c0002t0010g0356 a0001c0002t0010g0357 a0001c0002t0010g0358 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+20021G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762181 | |||||||
| chr17:78762226 | T | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19976A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762226 | |||||||
| chr17:78762240 | G | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19962C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762240 | |||||||
| chr17:78762293 | C | T | 1 | a0001c0001t0007g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+19909G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762293 | |||||||
| chr17:78762334 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.22+19868C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762334 | |||||||
| chr17:78762363 | G | A | 20 | a0001c0001t0002g0289 a0001c0001t0002g0314 a0001c0001t0003g0064 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.22+19839C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762363 | |||||||
| chr17:78762509 | G | C | 7 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+19693C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762509 | |||||||
| chr17:78762509 | G | T | 1 | a0001c0001t0029g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.22+19693C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762509 | |||||||
| chr17:78762662 | A | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19540T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762662 | |||||||
| chr17:78762674 | G | A | 1 | a0001c0001t0006g0328 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.22+19528C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762674 | |||||||
| chr17:78762928 | G | A | 69 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0064 others(66): Show |
69 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.22+19274C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762928 | |||||||
| chr17:78763163 | G | A | 11 | a0001c0001t0001g0026 a0001c0001t0005g0018 a0001c0001t0005g0021 others(8): Show |
11 | HG02080.hp2 HG02135.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+19039C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763163 | |||||||
| chr17:78763257 | C | T | 28 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.22+18945G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763257 | |||||||
| chr17:78763302 | C | CA | 6 | a0001c0001t0001g0141 a0001c0001t0001g0175 a0001c0001t0003g0361 others(3): Show |
6 | HG02145.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+18899dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763302 | |||||||
| chr17:78763473 | C | T | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+18729G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763473 | |||||||
| chr17:78763481 | C | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+18721G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763481 | |||||||
| chr17:78763601 | TAATA | T | 31 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+18597_22+18600d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763601 | |||||||
| chr17:78763999 | T | G | 14 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0018 others(11): Show |
14 | HG02080.hp2 HG02135.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+18203A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763999 | |||||||
| chr17:78764198 | C | CT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0141 others(43): Show |
46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+18003dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764198 | |||||||
| chr17:78764198 | CT | C | 31 | a0001c0001t0001g0194 a0001c0001t0003g0064 a0001c0001t0003g0065 others(28): Show |
31 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+18003delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764198 | |||||||
| chr17:78764283 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0193 |
2 | HG02257.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.22+17919C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764283 | |||||||
| chr17:78764328 | C | A | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+17874G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764328 | |||||||
| chr17:78764342 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.22+17860C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764342 | |||||||
| chr17:78764422 | G | A | 3 | a0001c0001t0007g0205 a0001c0001t0007g0206 a0001c0001t0007g0207 |
3 | HG01106.hp1 HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.22+17780C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764422 | |||||||
| chr17:78764453 | G | A | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+17749C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764453 | |||||||
| chr17:78764689 | G | A | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+17513C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764689 | |||||||
| chr17:78764837 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.22+17365C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764837 | |||||||
| chr17:78764859 | G | A | 41 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+17343C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764859 | |||||||
| chr17:78764920 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+17282G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764920 | |||||||
| chr17:78765009 | T | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+17193A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765009 | |||||||
| chr17:78765042 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+17160C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765042 | |||||||
| chr17:78765160 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+17042C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765160 | |||||||
| chr17:78765230 | G | A | 1 | a0001c0002t0010g0359 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.22+16972C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765230 | |||||||
| chr17:78765428 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+16774A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765428 | |||||||
| chr17:78765456 | T | C | 32 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.22+16746A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765456 | |||||||
| chr17:78765574 | A | G | 1 | a0001c0001t0006g0327 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+16628T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765574 | |||||||
| chr17:78765634 | G | T | 1 | a0001c0001t0004g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.22+16568C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765634 | |||||||
| chr17:78765711 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.22+16491C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765711 | |||||||
| chr17:78765957 | G | A | 113 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.22+16245C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765957 | |||||||
| chr17:78766015 | G | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG00408.hp1 HG00544.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+16187C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766015 | |||||||
| chr17:78766024 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.22+16178C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766024 | |||||||
| chr17:78766087 | G | GA | 95 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0095 others(92): Show |
95 | HG00558.hp1 HG00673.hp1 HG01106.hp2 others(92): Show |
intron_variant | MODIFIER | c.22+16114dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | |||||||
| chr17:78766087 | G | GAA | 34 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0003g0077 others(31): Show |
34 | HG00423.hp2 HG01070.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.22+16113_22+16114d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | |||||||
| chr17:78766087 | G | GAAA | 102 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.22+16112_22+16114d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | |||||||
| chr17:78766087 | G | GAAAA | 14 | a0001c0001t0002g0015 a0001c0001t0002g0244 a0001c0001t0002g0252 others(11): Show |
14 | HG00735.hp2 HG01175.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+16111_22+16114d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | |||||||
| chr17:78766299 | T | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+15903A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766299 | |||||||
| chr17:78766559 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.22+15643A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766559 | |||||||
| chr17:78766679 | C | T | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+15523G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766679 | |||||||
| chr17:78766761 | A | C | 1 | a0001c0001t0002g0313 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.22+15441T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766761 | |||||||
| chr17:78766779 | A | C | 13 | a0001c0001t0005g0050 a0001c0001t0009g0004 a0001c0001t0009g0048 others(10): Show |
13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+15423T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766779 | |||||||
| chr17:78766867 | G | C | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.22+15335C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766867 | |||||||
| chr17:78766985 | A | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0147 |
3 | HG02922.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.22+15217T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766985 | |||||||
| chr17:78767231 | T | C | 46 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0236 others(43): Show |
46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+14971A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767231 | |||||||
| chr17:78767283 | C | T | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.22+14919G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767283 | |||||||
| chr17:78767458 | A | G | 1 | a0001c0001t0005g0021 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.22+14744T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767458 | |||||||
| chr17:78767532 | CGGATGAA others(13): Show |
C | 6 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(3): Show |
6 | HG02523.hp2 NA18612.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+14650_22+14669d others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767532 | |||||||
| chr17:78767596 | C | T | 2 | a0001c0001t0002g0263 a0001c0001t0002g0264 |
2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.22+14606G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767596 | |||||||
| chr17:78767736 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.22+14466C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767736 | |||||||
| chr17:78767738 | G | T | 1 | a0001c0001t0002g0269 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.22+14464C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767738 | |||||||
| chr17:78768023 | C | T | 2 | a0001c0001t0013g0352 a0001c0001t0013g0353 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.22+14179G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768023 | |||||||
| chr17:78768028 | C | T | 1 | a0001c0001t0002g0315 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.22+14174G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768028 | |||||||
| chr17:78768063 | T | C | 219 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0103 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.22+14139A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768063 | |||||||
| chr17:78768472 | C | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+13730G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768472 | |||||||
| chr17:78768687 | C | T | 1 | a0001c0001t0006g0337 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.22+13515G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768687 | |||||||
| chr17:78769007 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+13195C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769007 | |||||||
| chr17:78769053 | C | G | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+13149G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769053 | |||||||
| chr17:78769145 | CA | C | 184 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(181): Show |
184 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.22+13056delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769145 | |||||||
| chr17:78769589 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+12613G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769589 | |||||||
| chr17:78769738 | C | T | 13 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0001t0002g0264 others(10): Show |
13 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+12464G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769738 | |||||||
| chr17:78769836 | G | C | 2 | a0001c0001t0003g0354 a0001c0001t0003g0355 |
2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+12366C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769836 | |||||||
| chr17:78769889 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+12313A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769889 | |||||||
| chr17:78769901 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+12301G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769901 | |||||||
| chr17:78769994 | A | G | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+12208T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769994 | |||||||
| chr17:78770197 | G | T | 1 | a0001c0001t0008g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.22+12005C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770197 | |||||||
| chr17:78770248 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.22+11954C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770248 | |||||||
| chr17:78770272 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0142 |
3 | HG00408.hp1 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.22+11930C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770272 | |||||||
| chr17:78770287 | C | T | 10 | a0001c0001t0003g0351 a0001c0001t0003g0362 a0001c0001t0003g0363 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+11915G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770287 | |||||||
| chr17:78770301 | C | A | 1 | a0001c0002t0010g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.22+11901G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770301 | |||||||
| chr17:78770325 | C | CA | 70 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0059 others(67): Show |
70 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.22+11876dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770325 | |||||||
| chr17:78770355 | GA | G | 179 | a0001c0001t0001g0026 a0001c0001t0001g0060 a0001c0001t0001g0103 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.22+11846delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770355 | |||||||
| chr17:78770361 | A | G | 1 | a0001c0001t0016g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+11841T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770361 | |||||||
| chr17:78770372 | A | G | 1 | a0001c0001t0005g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.22+11830T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770372 | |||||||
| chr17:78770405 | T | G | 3 | a0001c0001t0005g0018 a0001c0001t0006g0336 a0001c0001t0006g0348 |
3 | HG01069.hp1 HG01071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.22+11797A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770405 | |||||||
| chr17:78770541 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11661G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770541 | |||||||
| chr17:78770546 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11656C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770546 | |||||||
| chr17:78770547 | T | G | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11655A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770547 | |||||||
| chr17:78770660 | G | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+11542C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770660 | |||||||
| chr17:78770691 | C | T | 4 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(1): Show |
4 | NA18971.hp1 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+11511G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770691 | |||||||
| chr17:78770800 | C | T | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+11402G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770800 | |||||||
| chr17:78770817 | C | G | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.22+11385G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770817 | |||||||
| chr17:78770930 | C | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+11272G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770930 | |||||||
| chr17:78770931 | C | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+11271G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770931 | |||||||
| chr17:78771069 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02083.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.22+11133G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771069 | |||||||
| chr17:78771080 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+11122A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771080 | |||||||
| chr17:78771089 | C | T | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+11113G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771089 | |||||||
| chr17:78771161 | G | C | 31 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+11041C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771161 | |||||||
| chr17:78771162 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.22+11040G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771162 | |||||||
| chr17:78771499 | G | A | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+10703C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771499 | |||||||
| chr17:78771506 | G | A | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.22+10696C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771506 | |||||||
| chr17:78771662 | T | G | 2 | a0001c0001t0012g0116 a0001c0001t0012g0117 |
2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+10540A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771662 | |||||||
| chr17:78771698 | T | C | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+10504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771698 | |||||||
| chr17:78771721 | T | C | 215 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.22+10481A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771721 | |||||||
| chr17:78771729 | TA | T | 13 | a0001c0001t0001g0144 a0001c0001t0001g0178 a0001c0001t0002g0246 others(10): Show |
13 | HG00323.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+10472delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771729 | |||||||
| chr17:78771909 | T | C | 91 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(88): Show |
91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.22+10293A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771909 | |||||||
| chr17:78772187 | AGAG | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+10012_22+10014d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772187 | |||||||
| chr17:78772248 | G | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+9954C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772248 | |||||||
| chr17:78772496 | G | A | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | NA18984.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.22+9706C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772496 | |||||||
| chr17:78772519 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.22+9683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772519 | |||||||
| chr17:78772601 | G | A | 9 | a0001c0001t0005g0050 a0001c0001t0009g0048 a0001c0001t0009g0052 others(6): Show |
9 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+9601C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772601 | |||||||
| chr17:78772607 | G | A | 30 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(27): Show |
30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+9595C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772607 | |||||||
| chr17:78772741 | T | G | 1 | a0001c0001t0005g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+9461A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772741 | |||||||
| chr17:78772751 | T | A | 2 | a0001c0001t0006g0336 a0001c0001t0006g0348 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.22+9451A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772751 | |||||||
| chr17:78772758 | G | A | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+9444C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772758 | |||||||
| chr17:78772760 | T | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0197 a0001c0001t0004g0227 others(1): Show |
4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+9442A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772760 | |||||||
| chr17:78772806 | G | T | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.22+9396C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772806 | |||||||
| chr17:78772933 | G | A | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+9269C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772933 | |||||||
| chr17:78772991 | G | A | 1 | a0001c0001t0018g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.22+9211C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772991 | |||||||
| chr17:78773045 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+9157G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773045 | |||||||
| chr17:78773053 | G | A | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+9149C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773053 | |||||||
| chr17:78773098 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.22+9104C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773098 | |||||||
| chr17:78773143 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0005g0018 a0001c0001t0005g0021 others(8): Show |
11 | HG02080.hp2 HG02135.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+9059G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773143 | |||||||
| chr17:78773167 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.22+9035T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773167 | |||||||
| chr17:78773194 | G | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+9008C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773194 | |||||||
| chr17:78773352 | A | G | 224 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.22+8850T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773352 | |||||||
| chr17:78773405 | G | A | 11 | a0001c0001t0006g0327 a0001c0001t0006g0337 a0001c0001t0006g0338 others(8): Show |
11 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+8797C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773405 | |||||||
| chr17:78773419 | C | T | 1 | a0001c0001t0004g0200 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.22+8783G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773419 | |||||||
| chr17:78773488 | G | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0095 others(49): Show |
52 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.22+8714C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773488 | |||||||
| chr17:78773514 | C | CA | 44 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(41): Show |
44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+8687_22+8688ins others(1): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773514 | |||||||
| chr17:78773523 | G | A | 216 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.22+8679C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773523 | |||||||
| chr17:78773535 | A | C | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+8667T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773535 | |||||||
| chr17:78773578 | G | A | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.22+8624C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773578 | |||||||
| chr17:78773628 | C | CA | 47 | a0001c0001t0001g0026 a0001c0001t0001g0174 a0001c0001t0001g0175 others(44): Show |
47 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(44): Show |
intron_variant | MODIFIER | c.22+8573dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773628 | |||||||
| chr17:78773628 | CA | C | 15 | a0001c0001t0001g0060 a0001c0001t0002g0301 a0001c0001t0003g0086 others(12): Show |
15 | HG00099.hp2 HG00597.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+8573delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773628 | |||||||
| chr17:78773702 | A | C | 31 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(28): Show |
31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+8500T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773702 | |||||||
| chr17:78773784 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.22+8418G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773784 | |||||||
| chr17:78773979 | T | G | 9 | a0001c0001t0002g0248 a0001c0001t0002g0253 a0001c0001t0002g0292 others(6): Show |
9 | HG00621.hp1 NA18944.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+8223A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773979 | |||||||
| chr17:78773981 | T | G | 1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.22+8221A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773981 | |||||||
| chr17:78774063 | T | TA | 47 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0236 others(44): Show |
47 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(44): Show |
intron_variant | MODIFIER | c.22+8138dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774063 | |||||||
| chr17:78774065 | A | T | 1 | a0001c0001t0002g0323 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+8137T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774065 | |||||||
| chr17:78774084 | T | C | 1 | a0001c0001t0026g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+8118A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774084 | |||||||
| chr17:78774133 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+8069A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774133 | |||||||
| chr17:78774156 | T | C | 1 | a0001c0001t0004g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.22+8046A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774156 | |||||||
| chr17:78774213 | T | C | 1 | a0001c0001t0002g0324 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.22+7989A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774213 | |||||||
| chr17:78774327 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+7875A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774327 | |||||||
| chr17:78774334 | C | A | 2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+7868G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774334 | |||||||
| chr17:78774466 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.22+7736A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774466 | |||||||
| chr17:78774593 | T | C | 6 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+7609A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774593 | |||||||
| chr17:78774599 | T | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+7603A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774599 | |||||||
| chr17:78774640 | G | T | 1 | a0001c0001t0004g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+7562C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774640 | |||||||
| chr17:78774664 | G | A | 40 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0248 others(37): Show |
40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.22+7538C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774664 | |||||||
| chr17:78774708 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.22+7494C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774708 | |||||||
| chr17:78774713 | A | T | 1 | a0001c0001t0002g0323 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+7489T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774713 | |||||||
| chr17:78774727 | C | G | 1 | a0001c0001t0003g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.22+7475G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774727 | |||||||
| chr17:78774892 | A | G | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.22+7310T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774892 | |||||||
| chr17:78774927 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.22+7275G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774927 | |||||||
| chr17:78774938 | A | C | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.22+7264T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774938 | |||||||
| chr17:78774999 | C | T | 1 | a0001c0001t0004g0118 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.22+7203G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774999 | |||||||
| chr17:78775136 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.22+7066A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775136 | |||||||
| chr17:78775231 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.22+6971A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775231 | |||||||
| chr17:78775234 | G | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0003t0017g0017 |
3 | HG03486.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.22+6968C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775234 | |||||||
| chr17:78775435 | T | C | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+6767A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775435 | |||||||
| chr17:78775798 | A | G | 1 | a0001c0001t0002g0314 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.22+6404T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775798 | |||||||
| chr17:78775841 | T | C | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+6361A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775841 | |||||||
| chr17:78775957 | T | C | 217 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.22+6245A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775957 | |||||||
| chr17:78776091 | G | A | 3 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+6111C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776091 | |||||||
| chr17:78776206 | C | T | 138 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.22+5996G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776206 | |||||||
| chr17:78776427 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+5775G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776427 | |||||||
| chr17:78776428 | G | A | 4 | a0001c0001t0009g0048 a0001c0001t0009g0054 a0001c0001t0009g0055 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+5774C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776428 | |||||||
| chr17:78776433 | G | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0301 |
2 | NA18994.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.22+5769C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776433 | |||||||
| chr17:78776483 | C | A | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+5719G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776483 | |||||||
| chr17:78776658 | C | CA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0188 others(4): Show |
7 | HG02965.hp1 HG03098.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5543dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | |||||||
| chr17:78776658 | C | CAAAA | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+5540_22+5543dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | |||||||
| chr17:78776658 | CA | C | 118 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.22+5543delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | |||||||
| chr17:78776781 | TTGTC | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+5417_22+5420del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776781 | |||||||
| chr17:78776813 | GT | G | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0194 others(4): Show |
7 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5388delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776813 | |||||||
| chr17:78776826 | T | A | 2 | a0001c0001t0002g0305 a0001c0001t0003g0350 |
2 | HG03098.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.22+5376A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776826 | |||||||
| chr17:78776827 | A | T | 50 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(47): Show |
50 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(47): Show |
intron_variant | MODIFIER | c.22+5375T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776827 | |||||||
| chr17:78776828 | A | T | 40 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(37): Show |
40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.22+5374T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776828 | |||||||
| chr17:78776829 | A | T | 1 | a0001c0001t0014g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+5373T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776829 | |||||||
| chr17:78776962 | G | A | 25 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0354 others(22): Show |
25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.22+5240C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776962 | |||||||
| chr17:78776984 | G | A | 6 | a0001c0001t0002g0247 a0001c0001t0002g0306 a0001c0001t0002g0307 others(3): Show |
6 | HG00408.hp2 HG02027.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+5218C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776984 | |||||||
| chr17:78777109 | G | C | 41 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+5093C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777109 | |||||||
| chr17:78777186 | G | GAGGCCA | 46 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(43): Show |
46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+5015_22+5016ins others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777186 | |||||||
| chr17:78777379 | C | T | 2 | a0001c0001t0012g0116 a0001c0001t0012g0117 |
2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+4823G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777379 | |||||||
| chr17:78777556 | T | C | 139 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.22+4646A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777556 | |||||||
| chr17:78777609 | T | C | 1 | a0001c0001t0015g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.22+4593A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777609 | |||||||
| chr17:78777827 | A | G | 1 | a0001c0001t0002g0323 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+4375T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777827 | |||||||
| chr17:78777830 | C | CA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0108 others(18): Show |
21 | HG01175.hp1 HG02056.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+4371dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777830 | |||||||
| chr17:78777830 | C | CAA | 13 | a0001c0001t0003g0351 a0001c0001t0003g0354 a0001c0001t0003g0355 others(10): Show |
13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+4370_22+4371dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777830 | |||||||
| chr17:78777845 | A | G | 1 | a0001c0001t0009g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.22+4357T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777845 | |||||||
| chr17:78777894 | C | T | 1 | a0001c0001t0005g0047 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.22+4308G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777894 | |||||||
| chr17:78777935 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0009g0004 a0001c0001t0009g0056 others(2): Show |
5 | HG01074.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+4267C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777935 | |||||||
| chr17:78778221 | A | G | 1 | a0001c0002t0010g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.22+3981T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778221 | |||||||
| chr17:78778297 | C | CA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0190 others(11): Show |
14 | HG01069.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.22+3904dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778297 | |||||||
| chr17:78778317 | AAAAG | A | 83 | a0001c0001t0001g0276 a0001c0001t0002g0013 a0001c0001t0002g0014 others(80): Show |
83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.22+3881_22+3884del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778317 | |||||||
| chr17:78778318 | AAAG | A | 54 | a0001c0001t0002g0012 a0001c0001t0002g0289 a0001c0001t0003g0072 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.22+3881_22+3883del others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778318 | |||||||
| chr17:78778319 | AAG | A | 64 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0064 others(61): Show |
64 | HG00423.hp2 HG00673.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.22+3881_22+3882del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778319 | |||||||
| chr17:78778320 | AG | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0098 others(19): Show |
23 | HG00323.hp2 HG00639.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+3881delC | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778320 | |||||||
| chr17:78778321 | G | A | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
147 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.22+3881C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778321 | |||||||
| chr17:78778323 | G | A | 1 | a0001c0001t0003g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.22+3879C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778323 | |||||||
| chr17:78778347 | T | G | 1 | a0001c0001t0003g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.22+3855A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778347 | |||||||
| chr17:78778363 | C | T | 29 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+3839G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778363 | |||||||
| chr17:78778431 | A | G | 1 | a0001c0001t0015g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+3771T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778431 | |||||||
| chr17:78778494 | C | A | 5 | a0001c0001t0003g0350 a0001c0002t0010g0356 a0001c0002t0010g0357 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+3708G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778494 | |||||||
| chr17:78778545 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.22+3657C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778545 | |||||||
| chr17:78778637 | C | CA | 43 | a0001c0001t0001g0026 a0001c0001t0001g0198 a0001c0001t0001g0199 others(40): Show |
43 | HG02135.hp1 HG02723.hp1 HG02895.hp2 others(40): Show |
intron_variant | MODIFIER | c.22+3564dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | |||||||
| chr17:78778637 | CA | C | 128 | a0001c0001t0001g0094 a0001c0001t0001g0105 a0001c0001t0001g0110 others(125): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.22+3564delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | |||||||
| chr17:78778637 | CAA | C | 9 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 others(6): Show |
9 | HG00099.hp1 HG01943.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+3563_22+3564del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | |||||||
| chr17:78778676 | A | C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+3526T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778676 | |||||||
| chr17:78778772 | A | T | 43 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0236 others(40): Show |
43 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.22+3430T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778772 | |||||||
| chr17:78778904 | C | G | 1 | a0001c0001t0005g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.22+3298G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778904 | |||||||
| chr17:78779110 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.22+3092T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779110 | |||||||
| chr17:78779400 | CA | C | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0059 others(108): Show |
111 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.22+2801delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | |||||||
| chr17:78779400 | CAA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0094 others(105): Show |
109 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.22+2800_22+2801del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | |||||||
| chr17:78779400 | CAAA | C | 112 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0002g0020 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.22+2799_22+2801del others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | |||||||
| chr17:78779495 | A | T | 373 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(370): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.22+2707T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779495 | |||||||
| chr17:78779591 | G | T | 210 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.22+2611C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779591 | |||||||
| chr17:78780326 | A | C | 1 | a0001c0001t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.22+1876T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780326 | |||||||
| chr17:78780587 | T | C | 2 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
2 | NA18945.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.22+1615A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780587 | |||||||
| chr17:78780793 | G | C | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+1409C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780793 | |||||||
| chr17:78780835 | T | C | 215 | a0001c0001t0001g0026 a0001c0001t0001g0276 a0001c0001t0002g0012 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.22+1367A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780835 | |||||||
| chr17:78780858 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+1344A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780858 | |||||||
| chr17:78780931 | A | G | 74 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0003g0064 others(71): Show |
74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.22+1271T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780931 | |||||||
| chr17:78780941 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.22+1261G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780941 | |||||||
| chr17:78781061 | T | G | 1 | a0001c0001t0004g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+1141A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781061 | |||||||
| chr17:78781112 | T | C | 1 | a0001c0001t0011g0241 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.22+1090A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781112 | |||||||
| chr17:78781170 | TA | T | 9 | a0001c0001t0001g0060 a0001c0001t0002g0246 a0001c0001t0002g0247 others(6): Show |
9 | HG00099.hp2 HG01069.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+1031delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781170 | |||||||
| chr17:78781181 | A | AAAAAAG | 15 | a0001c0001t0005g0047 a0001c0001t0005g0050 a0001c0001t0009g0004 others(12): Show |
15 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+1015_22+1020dup others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781181 | |||||||
| chr17:78781181 | A | AAAAAG | 30 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(27): Show |
30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+1020_22+1021ins others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781181 | |||||||
| chr17:78781405 | C | T | 89 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.22+797G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781405 | |||||||
| chr17:78781420 | C | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0242 a0001c0001t0002g0243 others(2): Show |
5 | NA18940.hp2 NA18945.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+782G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781420 | |||||||
| chr17:78781433 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.22+769G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781433 | |||||||
| chr17:78781448 | C | T | 45 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(42): Show |
45 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(42): Show |
intron_variant | MODIFIER | c.22+754G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781448 | |||||||
| chr17:78781492 | C | T | 89 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.22+710G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781492 | |||||||
| chr17:78781505 | G | A | 41 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+697C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781505 | |||||||
| chr17:78781507 | G | A | 1 | a0001c0001t0003g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+695C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781507 | |||||||
| chr17:78781511 | C | T | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+691G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781511 | |||||||
| chr17:78781530 | G | C | 5 | a0001c0001t0003g0369 a0001c0001t0003g0370 a0001c0001t0003g0371 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+672C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781530 | |||||||
| chr17:78781609 | C | T | 1 | a0001c0003t0017g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+593G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781609 | |||||||
| chr17:78781612 | C | A | 113 | a0001c0001t0001g0276 a0001c0001t0002g0012 a0001c0001t0002g0013 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.22+590G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781612 | |||||||
| chr17:78781614 | C | T | 1 | a0001c0001t0003g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+588G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781614 | |||||||
| chr17:78781693 | G | A | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.22+509C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781693 | |||||||
| chr17:78781756 | G | A | 25 | a0001c0001t0003g0350 a0001c0001t0003g0351 a0001c0001t0003g0354 others(22): Show |
25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.22+446C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781756 | |||||||
| chr17:78781957 | A | G | 41 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0005g0002 others(38): Show |
41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+245T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781957 | |||||||
| chr17:78781995 | C | T | 1 | a0001c0001t0002g0016 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.22+207G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781995 | |||||||
| chr17:78782028 | A | AC | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(11): Show |
14 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+173dupG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782028 | |||||||
| chr17:78782057 | G | C | 3 | a0001c0001t0004g0374 a0001c0001t0004g0376 a0001c0001t0024g0375 |
3 | HG02559.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.22+145C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782057 | |||||||
| chr17:78782186 | G | A | 1 | a0001c0001t0003g0377 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.22+16C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782186 |