Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51444 |
| ensemblid | ENSG00000134758.14 |
| hgncid | 17765 |
| symbol | RNF138 |
| name | ring finger protein 138 |
| refseq_nuc | NM_016271.5 |
| refseq_prot | NP_057355.2 |
| ensembl_nuc | ENST00000261593.8 |
| ensembl_prot | ENSP00000261593.3 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 32091874 |
| end | 32131561 |
| strand | + |
| ver | v1.2 |
| region | chr18:32091874-32131561 |
| region5000 | chr18:32086874-32136561 |
| regionname0 | RNF138_chr18_32091874_32131561 |
| regionname5000 | RNF138_chr18_32086874_32136561 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 245 | 351 | 75 | 62 | 160 | 14 | 38 | 120 | RNF138_chr18_32086874_32136561 | RNF138 | MAEDL others(240): Show |
chr18 | 32086874 | 32136561 |
| a0002 | 0/0 | 245 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | MADDL others(240): Show |
chr18 | 32086874 | 32136561 |
| a0003 | 0/0 | 245 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | MAEDL others(240): Show |
chr18 | 32086874 | 32136561 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 735 | 344 | 75 | 61 | 154 | 14 | 38 | RNF138_chr18_32086874_32136561 | RNF138 | ATGGC others(730): Show |
chr18 | 32086874 | 32136561 | ||
| a0001c0003 | 0/0 | 735 | 6 | 0 | 0 | 6 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | ATGGC others(730): Show |
chr18 | 32086874 | 32136561 | ||
| a0001c0005 | 0/0 | 735 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | ATGGC others(730): Show |
chr18 | 32086874 | 32136561 | ||
| a0002c0002 | 0/0 | 735 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | ATGGC others(730): Show |
chr18 | 32086874 | 32136561 | ||
| a0003c0004 | 0/0 | 735 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | ATGGC others(730): Show |
chr18 | 32086874 | 32136561 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3507 | 133 | 16 | 27 | 74 | 8 | 8 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0002 | 1/0 | 3551 | 86 | 11 | 17 | 38 | 3 | 16 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0003 | 0/1 | 3507 | 38 | 15 | 6 | 8 | 2 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0004 | 0/0 | 3505 | 27 | 2 | 4 | 15 | 0 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3500): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0005 | 0/0 | 3507 | 14 | 13 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0007 | 0/0 | 3507 | 8 | 0 | 0 | 8 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0008 | 0/0 | 3550 | 7 | 7 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3545): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0009 | 0/0 | 3473 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3468): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0010 | 0/0 | 3549 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3544): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0011 | 0/0 | 3503 | 3 | 2 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3498): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0012 | 0/0 | 3507 | 3 | 2 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0013 | 0/0 | 3551 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0015 | 0/0 | 3551 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0016 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0017 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0018 | 0/0 | 3551 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0019 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0020 | 0/0 | 3551 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0021 | 0/0 | 3551 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0022 | 0/0 | 3555 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3550): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0023 | 0/0 | 3459 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3454): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0024 | 0/0 | 3505 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3500): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0025 | 0/0 | 3507 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0026 | 0/0 | 3507 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0027 | 0/0 | 3551 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0028 | 0/0 | 3551 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0001t0029 | 0/0 | 3507 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0003t0002 | 0/0 | 3551 | 5 | 0 | 0 | 5 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3546): Show |
chr18 | 32086874 | 32136561 |
| a0001c0003t0003 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0001c0005t0004 | 0/0 | 3505 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3500): Show |
chr18 | 32086874 | 32136561 |
| a0002c0002t0006 | 0/0 | 3507 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| a0003c0004t0014 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | GCCGT others(3502): Show |
chr18 | 32086874 | 32136561 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0006 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0019 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0009g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0010g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0011g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0012g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0013g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0013g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0015g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0016g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0017g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0020g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0021g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0022g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0023g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0024g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0025g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0026g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0027g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0028g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0001t0029g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0001c0005t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0002c0002t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| a0003c0004t0014g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0273 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0036 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00639 | hp1 | a0001 | c0005 | t0004 | g0168 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00735 | hp2 | a0001 | c0001 | t0013 | g0054 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01109 | hp2 | a0001 | c0001 | t0029 | g0226 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01167 | hp1 | a0002 | c0002 | t0006 | g0193 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01169 | hp2 | a0002 | c0002 | t0006 | g0190 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01243 | hp1 | a0001 | c0001 | t0026 | g0207 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01346 | hp1 | a0001 | c0001 | t0013 | g0057 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0042 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01891 | hp2 | a0002 | c0002 | t0006 | g0192 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0089 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02145 | hp2 | a0002 | c0002 | t0006 | g0195 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02723 | hp1 | a0003 | c0004 | t0014 | g0027 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0179 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02738 | hp2 | a0001 | c0001 | t0028 | g0084 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02895 | hp1 | a0003 | c0004 | t0014 | g0027 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0022 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03098 | hp2 | a0002 | c0002 | t0006 | g0194 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0191 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0045 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03453 | hp1 | a0002 | c0002 | t0006 | g0035 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0259 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0158 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0106 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0181 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG04199 | hp2 | a0001 | c0001 | t0020 | g0059 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18747 | hp2 | a0001 | c0001 | t0016 | g0246 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18940 | hp1 | a0001 | c0001 | t0019 | g0241 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18948 | hp1 | a0001 | c0001 | t0021 | g0017 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0127 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18984 | hp1 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18988 | hp1 | a0001 | c0001 | t0024 | g0161 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18991 | hp1 | a0001 | c0001 | t0022 | g0251 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18992 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18997 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19005 | hp1 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19012 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19030 | hp2 | a0002 | c0002 | t0006 | g0035 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19078 | hp2 | a0001 | c0003 | t0002 | g0122 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19089 | hp2 | a0001 | c0001 | t0018 | g0105 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0043 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0090 | AFR | ASW | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | ASW | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20752 | hp2 | a0001 | c0001 | t0023 | g0003 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01123 | hp1 | a0001 | c0001 | t0025 | g0233 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG01123 | hp2 | a0001 | c0001 | t0012 | g0157 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18955 | hp1 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | USA | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | USA | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0197 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| NA21309 | hp2 | a0001 | c0001 | t0027 | g0093 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0271 | REF | REF | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0019 | REF | REF | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32092785 | G | C | 1 | a0002 | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
missense_variant | MODERATE | c.9G>C | p.Glu3Asp | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 448/3551 | 9/738 | 3/245 | chr18 | 32092785 | |||
| chr18:32111885 | A | G | 1 | a0003 | 2 | HG02723.hp1 HG02895.hp1 |
missense_variant | MODERATE | c.242A>G | p.Lys81Arg | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/8 | 681/3551 | 242/738 | 81/245 | chr18 | 32111885 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32092872 | G | C | 1 | a0001c0003 | 6 | NA18955.hp1 NA18974.hp2 NA18984.hp1 others(3): Show |
synonymous_variant | LOW | c.96G>C | p.Thr32Thr | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 535/3551 | 96/738 | 32/245 | chr18 | 32092872 | |||
| chr18:32092872 | G | T | 1 | a0001c0005 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.96G>T | p.Thr32Thr | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 535/3551 | 96/738 | 32/245 | chr18 | 32092872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32091891 | A | G | 1 | a0001c0001t0029 | 1 | HG01109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-422A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091891 | |||||||
| chr18:32091904 | T | C | 1 | a0001c0001t0016 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-409T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 873 | chr18 | 32091904 | ||||||
| chr18:32091910 | C | T | 1 | a0001c0001t0001 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 867 | chr18 | 32091910 | ||||||
| chr18:32091923 | C | T | 1 | a0001c0001t0012 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-390C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091923 | |||||||
| chr18:32091942 | G | A | 1 | a0002c0002t0006 | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-371G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 835 | chr18 | 32091942 | ||||||
| chr18:32091953 | CGGCGCTC others(27): Show |
C | 1 | a0001c0001t0009 | 4 | HG00423.hp2 NA18952.hp1 NA19012.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-358_-325delGCGCTC others(28): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 789 | INFO_REALIGN_3_PRIME | chr18 | 32091953 | |||||
| chr18:32091974 | C | T | 1 | a0001c0001t0001 | 2 | NA18989.hp2 NA19084.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-339C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091974 | |||||||
| chr18:32092060 | C | G | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-253C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32092060 | |||||||
| chr18:32092072 | G | A | 1 | a0001c0001t0013 | 2 | HG00735.hp2 HG01346.hp1 |
5_prime_UTR_variant | MODIFIER | c.-241G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 705 | chr18 | 32092072 | ||||||
| chr18:32092154 | T | C | 1 | a0001c0001t0005 | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-159T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 623 | chr18 | 32092154 | ||||||
| chr18:32092155 | C | T | 1 | a0001c0001t0007 | 8 | NA18972.hp2 NA18991.hp2 NA18992.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32092155 | |||||||
| chr18:32092206 | C | A | 1 | a0001c0001t0017 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 571 | chr18 | 32092206 | ||||||
| chr18:32092713 | G | T | 1 | a0001c0001t0015 | 2 | HG02145.hp1 NA20129.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | chr18 | 32092713 | |||||||
| chr18:32092769 | C | T | 1 | a0001c0001t0027 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 8 | chr18 | 32092769 | ||||||
| chr18:32129197 | A | G | 1 | a0001c0001t0026 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 10 | chr18 | 32129197 | ||||||
| chr18:32129212 | TG | T | 1 | a0001c0001t0008 | 7 | HG01891.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*26delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 26 | chr18 | 32129212 | ||||||
| chr18:32129306 | T | A | 1 | a0001c0001t0018 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 119 | chr18 | 32129306 | ||||||
| chr18:32129307 | A | G | 1 | a0001c0001t0018 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 120 | chr18 | 32129307 | ||||||
| chr18:32129477 | T | A | 1 | a0001c0001t0019 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 290 | chr18 | 32129477 | ||||||
| chr18:32129482 | CATT | C | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(5): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*301_*303delTAT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 301 | INFO_REALIGN_3_PRIME | chr18 | 32129482 | |||||
| chr18:32129485 | T | C | 1 | a0001c0001t0019 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 298 | chr18 | 32129485 | ||||||
| chr18:32129569 | C | T | 1 | a0001c0001t0025 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 382 | chr18 | 32129569 | ||||||
| chr18:32129712 | T | C | 1 | a0003c0004t0014 | 2 | HG02723.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 525 | chr18 | 32129712 | ||||||
| chr18:32129800 | T | C | 1 | a0001c0001t0020 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 613 | chr18 | 32129800 | ||||||
| chr18:32129853 | A | G | 1 | a0001c0001t0024 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*666A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 666 | chr18 | 32129853 | ||||||
| chr18:32129875 | CTT | C | 1 | a0001c0001t0010 | 3 | HG01884.hp2 HG02818.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690_*691delTT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 690 | INFO_REALIGN_3_PRIME | chr18 | 32129875 | |||||
| chr18:32130076 | A | G | 1 | a0001c0001t0026 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 889 | chr18 | 32130076 | ||||||
| chr18:32130917 | A | AAG | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1732_*1733dupGA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1734 | INFO_REALIGN_3_PRIME | chr18 | 32130917 | |||||
| chr18:32130972 | TCAAAGTT others(41): Show |
T | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1929delCAAA others(44): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1882 | INFO_REALIGN_3_PRIME | chr18 | 32130972 | |||||
| chr18:32130972 | TCAAAGTT others(89): Show |
T | 1 | a0001c0001t0023 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1834_*1929delCAAA others(92): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1834 | INFO_REALIGN_3_PRIME | chr18 | 32130972 | |||||
| chr18:32131012 | TGGGATTT others(42): Show |
T | 1 | a0001c0001t0022 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828_*1876delGATT others(45): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1828 | INFO_REALIGN_3_PRIME | chr18 | 32131012 | |||||
| chr18:32131039 | A | G | 1 | a0001c0001t0021 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1852A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1852 | chr18 | 32131039 | ||||||
| chr18:32131298 | A | C | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(6): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*2111A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2111 | chr18 | 32131298 | ||||||
| chr18:32131304 | CCT | C | 3 | a0001c0001t0004 a0001c0001t0024 a0001c0005t0004 |
29 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2120_*2121delCT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2120 | INFO_REALIGN_3_PRIME | chr18 | 32131304 | |||||
| chr18:32131376 | G | GTT | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*2191_*2192dupTT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2193 | INFO_REALIGN_3_PRIME | chr18 | 32131376 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32092365 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
8 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+130A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092365 | |||||||
| chr18:32092417 | C | G | 4 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0001t0005g0288 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+182C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092417 | |||||||
| chr18:32092529 | C | T | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-171C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092529 | |||||||
| chr18:32092596 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-77-104A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092596 | |||||||
| chr18:32092629 | AG | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
39 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-77-68delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 32092629 | ||||||
| chr18:32092904 | C | A | 1 | a0001c0001t0002g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.110+18C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32092904 | |||||||
| chr18:32092944 | GGCCCGGG others(13): Show |
G | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+62_110+81delCG others(18): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32092944 | ||||||
| chr18:32092978 | C | A | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+92C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32092978 | |||||||
| chr18:32093105 | G | GCTCCCGC others(1): Show |
19 | a0001c0001t0001g0028 a0001c0001t0001g0199 a0001c0001t0001g0200 others(16): Show |
23 | HG00280.hp2 HG00423.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.110+257_110+264dup others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | ||||||
| chr18:32093105 | G | GCTCCCGC others(9): Show |
7 | a0001c0001t0001g0189 a0001c0001t0005g0010 a0001c0001t0005g0026 others(4): Show |
10 | HG01109.hp1 HG02055.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+249_110+264dup others(16): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | ||||||
| chr18:32093105 | G | GCTCCCGC others(17): Show |
1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+241_110+264dup others(24): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | ||||||
| chr18:32093105 | GCTCCCGC others(1): Show |
G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
99 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.110+257_110+264del others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | ||||||
| chr18:32093105 | GCTCCCGC others(9): Show |
G | 8 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
10 | HG00408.hp2 HG02109.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+249_110+264del others(16): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | ||||||
| chr18:32093393 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.110+507C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093393 | |||||||
| chr18:32093498 | G | A | 1 | a0001c0001t0005g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.110+612G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093498 | |||||||
| chr18:32093502 | T | A | 1 | a0001c0001t0004g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.110+616T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093502 | |||||||
| chr18:32093548 | G | A | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0159 |
3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.110+662G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093548 | |||||||
| chr18:32093592 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
54 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+706C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093592 | |||||||
| chr18:32093680 | G | T | 2 | a0001c0001t0009g0015 a0001c0001t0009g0043 |
3 | HG00423.hp2 NA19012.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.110+794G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093680 | |||||||
| chr18:32093770 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.110+884C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093770 | |||||||
| chr18:32093989 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+1103C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093989 | |||||||
| chr18:32094043 | G | A | 1 | a0001c0001t0008g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.110+1157G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094043 | |||||||
| chr18:32094208 | C | CT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.110+1332dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32094208 | ||||||
| chr18:32094328 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+1442C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094328 | |||||||
| chr18:32094437 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.110+1551A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094437 | |||||||
| chr18:32094458 | T | A | 1 | a0001c0001t0004g0160 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.110+1572T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094458 | |||||||
| chr18:32094559 | T | C | 1 | a0001c0001t0005g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+1673T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094559 | |||||||
| chr18:32094606 | A | G | 51 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(48): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.110+1720A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094606 | |||||||
| chr18:32094609 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+1723A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094609 | |||||||
| chr18:32094642 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.110+1756A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094642 | |||||||
| chr18:32094780 | C | CTA | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
40 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.110+1909_110+1910d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32094780 | ||||||
| chr18:32094851 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.110+1965A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094851 | |||||||
| chr18:32094879 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+1993C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094879 | |||||||
| chr18:32094965 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.110+2079C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094965 | |||||||
| chr18:32095023 | T | C | 1 | a0001c0001t0010g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.110+2137T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095023 | |||||||
| chr18:32095029 | G | A | 51 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(48): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.110+2143G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095029 | |||||||
| chr18:32095044 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2158T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095044 | |||||||
| chr18:32095047 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.110+2161A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095047 | |||||||
| chr18:32095073 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+2187G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095073 | |||||||
| chr18:32095178 | G | GT | 8 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0104 others(5): Show |
8 | HG01891.hp1 HG02132.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+2301dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32095178 | ||||||
| chr18:32095180 | T | TA | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.110+2294_110+2295i others(3): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095180 | |||||||
| chr18:32095194 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2308T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095194 | |||||||
| chr18:32095264 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+2378C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095264 | |||||||
| chr18:32095284 | C | T | 1 | a0001c0001t0007g0149 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.110+2398C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095284 | |||||||
| chr18:32095445 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(13): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.110+2559G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095445 | |||||||
| chr18:32095706 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110+2820G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095706 | |||||||
| chr18:32095830 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.110+2944C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095830 | |||||||
| chr18:32095863 | A | G | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110+2977A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095863 | |||||||
| chr18:32095883 | T | C | 1 | a0001c0001t0024g0161 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.110+2997T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095883 | |||||||
| chr18:32095956 | G | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA19057.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.110+3070G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095956 | |||||||
| chr18:32096171 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110+3285T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096171 | |||||||
| chr18:32096185 | C | T | 1 | a0001c0001t0004g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+3299C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096185 | |||||||
| chr18:32096224 | A | G | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+3338A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096224 | |||||||
| chr18:32096252 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110+3366A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096252 | |||||||
| chr18:32096437 | C | T | 1 | a0001c0001t0005g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+3551C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096437 | |||||||
| chr18:32096459 | T | C | 1 | a0001c0001t0008g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110+3573T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096459 | |||||||
| chr18:32096658 | A | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+3772A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096658 | |||||||
| chr18:32096701 | A | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+3815A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096701 | |||||||
| chr18:32096853 | A | G | 23 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(20): Show |
28 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+3967A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096853 | |||||||
| chr18:32096907 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.110+4021T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096907 | |||||||
| chr18:32096914 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.110+4028G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096914 | |||||||
| chr18:32096971 | G | A | 1 | a0001c0001t0004g0176 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.110+4085G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096971 | |||||||
| chr18:32097064 | AT | A | 5 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(2): Show |
5 | HG00741.hp1 HG01167.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4180delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097064 | ||||||
| chr18:32097071 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+4185T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097071 | |||||||
| chr18:32097272 | A | G | 6 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0272 others(3): Show |
8 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+4386A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097272 | |||||||
| chr18:32097387 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.110+4501A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097387 | |||||||
| chr18:32097534 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.110+4648A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097534 | |||||||
| chr18:32097557 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(290): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.110+4671T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097557 | |||||||
| chr18:32097559 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110+4673C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097559 | |||||||
| chr18:32097600 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.110+4714C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097600 | |||||||
| chr18:32097617 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+4731G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097617 | |||||||
| chr18:32097648 | C | G | 2 | a0001c0001t0008g0099 a0001c0001t0008g0106 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110+4762C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097648 | |||||||
| chr18:32097734 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.110+4848G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097734 | |||||||
| chr18:32097743 | G | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+4857G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097743 | |||||||
| chr18:32097781 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110+4895C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097781 | |||||||
| chr18:32097818 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110+4932C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097818 | |||||||
| chr18:32097876 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+4990G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097876 | |||||||
| chr18:32097878 | ATATATGT others(5): Show |
A | 1 | a0001c0003t0002g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.110+5008_110+5019d others(14): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097878 | ||||||
| chr18:32097902 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(196): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.110+5016G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097902 | |||||||
| chr18:32097944 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.110+5058A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097944 | |||||||
| chr18:32097944 | ATG | A | 49 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0016 others(46): Show |
56 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.110+5090_110+5091d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | ||||||
| chr18:32097944 | ATGTG | A | 11 | a0001c0001t0002g0041 a0001c0001t0002g0086 a0001c0001t0002g0087 others(8): Show |
11 | HG00733.hp2 HG01168.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.110+5088_110+5091d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | ||||||
| chr18:32097944 | ATGTGTG | A | 27 | a0001c0001t0002g0007 a0001c0001t0002g0094 a0001c0001t0002g0095 others(24): Show |
33 | HG01106.hp1 HG01243.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+5086_110+5091d others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | ||||||
| chr18:32097946 | G | A | 1 | a0001c0001t0013g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110+5060G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097946 | |||||||
| chr18:32097966 | GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0001g0290 a0001c0001t0005g0186 |
2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.110+5082_110+5092d others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097966 | ||||||
| chr18:32097968 | GTGTGTGT others(2): Show |
G | 15 | a0001c0001t0001g0151 a0001c0001t0001g0232 a0001c0001t0001g0258 others(12): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+5084_110+5092d others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097968 | ||||||
| chr18:32097970 | GTGTGTGT | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.110+5086_110+5092d others(9): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097970 | ||||||
| chr18:32097972 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.110+5086G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097972 | |||||||
| chr18:32097972 | GTGTGT | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(12): Show |
16 | HG00140.hp2 HG00597.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.110+5088_110+5092d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097972 | ||||||
| chr18:32097974 | GTGT | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
66 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.110+5090_110+5092d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097974 | ||||||
| chr18:32097976 | GT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0206 a0001c0001t0003g0036 others(3): Show |
6 | HG00558.hp1 HG00733.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+5092delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097976 | ||||||
| chr18:32097977 | T | TG | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(3): Show |
8 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(3): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097977 | T | TGTG | 4 | a0001c0001t0003g0003 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
4 | HG01099.hp2 NA18612.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097977 | T | TGTGTG | 8 | a0001c0001t0003g0003 a0001c0001t0003g0260 a0001c0001t0003g0263 others(5): Show |
8 | HG01070.hp1 HG01361.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097977 | T | TGTGTGTG | 3 | a0001c0001t0003g0003 a0001c0001t0003g0265 a0001c0001t0017g0197 |
4 | HG03490.hp1 HG03492.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(9): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097977 | T | TGTGTGTG others(2): Show |
4 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0272 others(1): Show |
5 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097977 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0003g0274 a0001c0001t0003g0275 |
2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.110+5091_110+5092i others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | |||||||
| chr18:32097979 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.110+5093A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097979 | |||||||
| chr18:32097979 | A | T | 2 | a0001c0001t0001g0253 a0001c0001t0004g0183 |
2 | HG00408.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.110+5093A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097979 | |||||||
| chr18:32097981 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0004g0183 |
2 | HG00408.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.110+5095T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097981 | |||||||
| chr18:32098008 | G | A | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+5122G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098008 | |||||||
| chr18:32098209 | A | G | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+5323A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098209 | |||||||
| chr18:32098298 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.110+5412G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098298 | |||||||
| chr18:32098488 | G | A | 1 | a0001c0001t0012g0157 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.110+5602G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098488 | |||||||
| chr18:32098677 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.110+5791C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098677 | |||||||
| chr18:32098688 | T | TA | 2 | a0001c0001t0001g0031 a0001c0001t0001g0213 |
3 | HG00099.hp1 HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.110+5807dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098688 | ||||||
| chr18:32098760 | G | A | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110+5874G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098760 | |||||||
| chr18:32098780 | G | A | 31 | a0001c0001t0002g0178 a0001c0001t0003g0024 a0001c0001t0003g0169 others(28): Show |
36 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.110+5894G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098780 | |||||||
| chr18:32098827 | C | T | 6 | a0002c0002t0006g0190 a0002c0002t0006g0191 a0002c0002t0006g0192 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+5941C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098827 | |||||||
| chr18:32098914 | A | AT | 8 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(5): Show |
9 | HG00741.hp1 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.110+6042dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | ||||||
| chr18:32098914 | AT | A | 28 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0199 others(25): Show |
32 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.110+6042delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | ||||||
| chr18:32098914 | ATT | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
52 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.110+6041_110+6042d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | ||||||
| chr18:32099034 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110+6148T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099034 | |||||||
| chr18:32099068 | A | G | 2 | a0001c0001t0007g0147 a0001c0001t0007g0148 |
2 | NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.110+6182A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099068 | |||||||
| chr18:32099096 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.110+6210T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099096 | |||||||
| chr18:32099161 | T | C | 1 | a0001c0001t0017g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+6275T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099161 | |||||||
| chr18:32099282 | T | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6396T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099282 | |||||||
| chr18:32099366 | AG | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6482delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32099366 | ||||||
| chr18:32099406 | A | G | 26 | a0001c0001t0002g0007 a0001c0001t0002g0094 a0001c0001t0002g0095 others(23): Show |
31 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.110+6520A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099406 | |||||||
| chr18:32099433 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.110+6547C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099433 | |||||||
| chr18:32099533 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+6647G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099533 | |||||||
| chr18:32099552 | A | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6666A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099552 | |||||||
| chr18:32099597 | G | A | 51 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(48): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.110+6711G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099597 | |||||||
| chr18:32099606 | T | C | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+6720T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099606 | |||||||
| chr18:32099844 | C | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+6958C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099844 | |||||||
| chr18:32099853 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+6967C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099853 | |||||||
| chr18:32099944 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+7058C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099944 | |||||||
| chr18:32099959 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(240): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.110+7073A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099959 | |||||||
| chr18:32099970 | A | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0015g0090 |
3 | HG01168.hp1 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110+7084A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099970 | |||||||
| chr18:32100201 | G | GAT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0113 a0001c0001t0001g0208 others(20): Show |
26 | HG00280.hp1 HG01106.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+7335_110+7336d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | ||||||
| chr18:32100201 | G | GATAT | 2 | a0001c0001t0001g0030 a0001c0001t0002g0083 |
3 | HG02602.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.110+7333_110+7336d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | ||||||
| chr18:32100201 | G | GATATAT | 2 | a0001c0001t0003g0038 a0001c0001t0003g0284 |
3 | HG02572.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.110+7331_110+7336d others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | ||||||
| chr18:32100201 | G | GATATATA others(3): Show |
1 | a0001c0001t0003g0285 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.110+7327_110+7336d others(12): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | ||||||
| chr18:32100201 | GAT | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
62 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.110+7335_110+7336d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | ||||||
| chr18:32100331 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.110+7445G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100331 | |||||||
| chr18:32100462 | A | G | 1 | a0001c0001t0005g0289 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110+7576A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100462 | |||||||
| chr18:32100468 | C | CT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(110): Show |
145 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.110+7606dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | ||||||
| chr18:32100468 | C | CTT | 25 | a0001c0001t0001g0114 a0001c0001t0001g0249 a0001c0001t0001g0250 others(22): Show |
30 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.110+7605_110+7606d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | ||||||
| chr18:32100468 | C | CTTT | 27 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0169 others(24): Show |
33 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+7604_110+7606d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | ||||||
| chr18:32100468 | CT | C | 6 | a0001c0001t0002g0041 a0001c0001t0002g0049 a0001c0001t0002g0055 others(3): Show |
6 | HG01167.hp2 HG02922.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+7606delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | ||||||
| chr18:32100498 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.110+7612G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100498 | |||||||
| chr18:32100498 | G | T | 1 | a0001c0001t0003g0263 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.110+7612G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100498 | |||||||
| chr18:32100500 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.110+7614A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100500 | |||||||
| chr18:32100512 | G | C | 1 | a0001c0001t0026g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110+7626G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100512 | |||||||
| chr18:32100516 | G | C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+7630G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100516 | |||||||
| chr18:32100538 | C | T | 1 | a0001c0001t0004g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110+7652C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100538 | |||||||
| chr18:32100561 | C | T | 5 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG01928.hp1 HG01981.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+7675C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100561 | |||||||
| chr18:32100588 | G | A | 1 | a0001c0001t0012g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.110+7702G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100588 | |||||||
| chr18:32100624 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+7738C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100624 | |||||||
| chr18:32100668 | G | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0001c0001t0026g0207 |
3 | HG01243.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+7782G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100668 | |||||||
| chr18:32100771 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+7885C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100771 | |||||||
| chr18:32100813 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(15): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.110+7927C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100813 | |||||||
| chr18:32100843 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
8 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+7957G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100843 | |||||||
| chr18:32100862 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.110+7976C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100862 | |||||||
| chr18:32100921 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.110+8035T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100921 | |||||||
| chr18:32100930 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(126): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.110+8044T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100930 | |||||||
| chr18:32101090 | C | T | 1 | a0001c0001t0003g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.110+8204C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101090 | |||||||
| chr18:32101214 | C | CT | 69 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0135 others(66): Show |
80 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.110+8344dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101214 | ||||||
| chr18:32101214 | C | CTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0128 others(4): Show |
13 | HG00423.hp1 HG00558.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+8343_110+8344d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101214 | ||||||
| chr18:32101230 | TC | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0291 others(1): Show |
4 | HG01070.hp1 HG01256.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+8345delC | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101230 | |||||||
| chr18:32101231 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(221): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.110+8345C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101231 | |||||||
| chr18:32101232 | A | T | 1 | a0001c0001t0004g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.110+8346A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101232 | |||||||
| chr18:32101283 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(288): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.110+8397G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101283 | |||||||
| chr18:32101295 | T | G | 1 | a0001c0001t0002g0061 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.110+8409T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101295 | |||||||
| chr18:32101323 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+8437A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101323 | |||||||
| chr18:32101393 | G | GTA | 6 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0001c0001t0001g0292 others(3): Show |
7 | HG01884.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+8519_110+8520d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101393 | ||||||
| chr18:32101468 | A | G | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8582A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101468 | |||||||
| chr18:32101573 | T | A | 1 | a0001c0001t0003g0023 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.110+8687T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101573 | |||||||
| chr18:32101631 | C | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0215 a0001c0001t0001g0242 others(14): Show |
18 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+8745C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101631 | |||||||
| chr18:32101646 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+8760C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101646 | |||||||
| chr18:32101745 | A | T | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.110+8859A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101745 | |||||||
| chr18:32101804 | C | T | 1 | a0001c0001t0004g0025 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.110+8918C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101804 | |||||||
| chr18:32101812 | T | G | 1 | a0001c0001t0001g0032 | 2 | HG00140.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.110+8926T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101812 | |||||||
| chr18:32102043 | A | AT | 39 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
49 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.110+9172dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102043 | ||||||
| chr18:32102079 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0003g0196 |
2 | HG02155.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.110+9193C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102079 | |||||||
| chr18:32102097 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+9211G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102097 | |||||||
| chr18:32102195 | C | CT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
63 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.110+9333dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | ||||||
| chr18:32102195 | C | CTT | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0005g0186 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+9332_110+9333d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | ||||||
| chr18:32102195 | CT | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+9333delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | ||||||
| chr18:32102195 | CTT | C | 7 | a0001c0001t0001g0109 a0001c0001t0001g0211 a0001c0001t0001g0214 others(4): Show |
7 | HG00639.hp2 HG01169.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+9332_110+9333d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | ||||||
| chr18:32102195 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0282 a0001c0001t0003g0285 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.110+9321_110+9333d others(15): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | ||||||
| chr18:32102307 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+9421T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102307 | |||||||
| chr18:32102350 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.111-9404C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102350 | |||||||
| chr18:32102359 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.111-9395G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102359 | |||||||
| chr18:32102405 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.111-9349G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102405 | |||||||
| chr18:32102490 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(195): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.111-9264T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102490 | |||||||
| chr18:32102538 | A | G | 21 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(18): Show |
26 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-9216A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102538 | |||||||
| chr18:32102640 | C | CT | 12 | a0001c0001t0002g0080 a0001c0001t0005g0010 a0001c0001t0005g0026 others(9): Show |
15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.111-9104dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102640 | ||||||
| chr18:32102669 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.111-9085G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102669 | |||||||
| chr18:32102681 | G | A | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-9073G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102681 | |||||||
| chr18:32102709 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.111-9045T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102709 | |||||||
| chr18:32102746 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-9008C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102746 | |||||||
| chr18:32102789 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111-8965C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102789 | |||||||
| chr18:32102791 | C | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA19005.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.111-8963C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102791 | |||||||
| chr18:32102861 | C | T | 1 | a0001c0001t0026g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.111-8893C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102861 | |||||||
| chr18:32103532 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.111-8222T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103532 | |||||||
| chr18:32103573 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.111-8181A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103573 | |||||||
| chr18:32103658 | T | G | 1 | a0001c0001t0002g0104 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.111-8096T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103658 | |||||||
| chr18:32103729 | C | T | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-8025C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103729 | |||||||
| chr18:32103824 | G | C | 1 | a0001c0001t0003g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-7930G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103824 | |||||||
| chr18:32103906 | A | C | 1 | a0001c0001t0011g0074 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7848A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103906 | |||||||
| chr18:32103921 | C | T | 1 | a0001c0001t0012g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111-7833C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103921 | |||||||
| chr18:32103955 | A | G | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-7799A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103955 | |||||||
| chr18:32103977 | G | A | 1 | a0001c0001t0011g0074 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7777G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103977 | |||||||
| chr18:32103978 | A | G | 1 | a0001c0001t0011g0074 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7776A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103978 | |||||||
| chr18:32103985 | C | G | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7769C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103985 | |||||||
| chr18:32104013 | C | CT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0113 others(15): Show |
20 | HG00408.hp1 HG02056.hp2 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-7724dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | ||||||
| chr18:32104013 | C | CTT | 48 | a0001c0001t0003g0003 a0001c0001t0003g0023 a0001c0001t0003g0024 others(45): Show |
59 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.111-7725_111-7724d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | ||||||
| chr18:32104013 | C | CTTT | 8 | a0001c0001t0002g0178 a0001c0001t0003g0266 a0001c0001t0003g0267 others(5): Show |
8 | HG02027.hp1 HG02056.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-7726_111-7724d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | ||||||
| chr18:32104013 | CT | C | 10 | a0001c0001t0001g0220 a0001c0001t0002g0086 a0002c0002t0006g0035 others(7): Show |
11 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.111-7724delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | ||||||
| chr18:32104013 | CTTT | C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-7726_111-7724d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | ||||||
| chr18:32104052 | C | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-7702C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104052 | |||||||
| chr18:32104089 | C | G | 1 | a0001c0001t0001g0033 | 2 | NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.111-7665C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104089 | |||||||
| chr18:32104252 | A | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0146 |
2 | HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.111-7502A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104252 | |||||||
| chr18:32104267 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.111-7487C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104267 | |||||||
| chr18:32104284 | A | C | 1 | a0001c0001t0005g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.111-7470A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104284 | |||||||
| chr18:32104295 | A | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-7459A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104295 | |||||||
| chr18:32104322 | A | T | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7432A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104322 | |||||||
| chr18:32104556 | GAAAC | G | 3 | a0001c0001t0004g0176 a0001c0001t0004g0177 a0001c0001t0004g0183 |
3 | HG00408.hp2 HG02056.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.111-7195_111-7192d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104556 | ||||||
| chr18:32104557 | A | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-7197A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104557 | |||||||
| chr18:32104635 | A | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7119A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104635 | |||||||
| chr18:32104707 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.111-7047A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104707 | |||||||
| chr18:32104933 | A | G | 1 | a0002c0002t0006g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.111-6821A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104933 | |||||||
| chr18:32104955 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.111-6799C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104955 | |||||||
| chr18:32104991 | A | T | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.111-6763A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104991 | |||||||
| chr18:32105283 | G | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.111-6471G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105283 | |||||||
| chr18:32105327 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0221 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.111-6427T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105327 | |||||||
| chr18:32105394 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.111-6360C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105394 | |||||||
| chr18:32105480 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.111-6274C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105480 | |||||||
| chr18:32105531 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.111-6223G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105531 | |||||||
| chr18:32105592 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.111-6162A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105592 | |||||||
| chr18:32105751 | C | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-6003C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105751 | |||||||
| chr18:32105840 | C | T | 1 | a0001c0001t0007g0148 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.111-5914C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105840 | |||||||
| chr18:32105853 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.111-5901A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105853 | |||||||
| chr18:32105920 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(196): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.111-5834C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105920 | |||||||
| chr18:32106063 | A | G | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-5691A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106063 | |||||||
| chr18:32106173 | G | A | 22 | a0001c0001t0002g0007 a0001c0001t0002g0094 a0001c0001t0002g0095 others(19): Show |
27 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-5581G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106173 | |||||||
| chr18:32106185 | G | C | 21 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(18): Show |
26 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-5569G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106185 | |||||||
| chr18:32106215 | G | A | 1 | a0001c0001t0008g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.111-5539G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106215 | |||||||
| chr18:32106235 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.111-5519C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106235 | |||||||
| chr18:32106356 | G | A | 1 | a0001c0001t0004g0160 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.111-5398G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106356 | |||||||
| chr18:32106523 | A | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0291 |
4 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-5231A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106523 | |||||||
| chr18:32106524 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.111-5230G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106524 | |||||||
| chr18:32106547 | AT | A | 8 | a0001c0001t0002g0178 a0001c0001t0004g0025 a0001c0001t0004g0177 others(5): Show |
9 | HG00408.hp2 HG02056.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-5203delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106547 | ||||||
| chr18:32106548 | T | TTTTA | 41 | a0001c0001t0003g0003 a0001c0001t0003g0023 a0001c0001t0003g0024 others(38): Show |
51 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.111-5182_111-5179d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | ||||||
| chr18:32106548 | T | TTTTATTT others(1): Show |
6 | a0001c0001t0003g0196 a0001c0001t0003g0269 a0001c0001t0004g0165 others(3): Show |
6 | HG01123.hp2 HG02080.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-5186_111-5179d others(10): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | ||||||
| chr18:32106548 | TTTTA | T | 9 | a0001c0001t0001g0111 a0001c0001t0002g0098 a0001c0001t0005g0010 others(6): Show |
12 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-5182_111-5179d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | ||||||
| chr18:32106595 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-5159C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106595 | |||||||
| chr18:32106702 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0209 |
3 | HG02895.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.111-5052C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106702 | |||||||
| chr18:32106710 | G | A | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5044G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106710 | |||||||
| chr18:32106713 | C | T | 1 | a0001c0001t0017g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-5041C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106713 | |||||||
| chr18:32106747 | G | C | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-5007G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106747 | |||||||
| chr18:32106808 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.111-4946C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106808 | |||||||
| chr18:32106855 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | NA18947.hp2 NA18951.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-4899C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106855 | |||||||
| chr18:32107051 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(126): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.111-4703C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107051 | |||||||
| chr18:32107116 | C | CT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(126): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.111-4617dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | ||||||
| chr18:32107116 | C | CTT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0138 a0001c0001t0001g0139 others(20): Show |
27 | HG00597.hp1 HG00642.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-4618_111-4617d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | ||||||
| chr18:32107116 | C | CTTT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0199 others(3): Show |
9 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-4619_111-4617d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | ||||||
| chr18:32107116 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.111-4638C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107116 | |||||||
| chr18:32107116 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0094 a0001c0001t0002g0119 others(1): Show |
6 | HG00733.hp2 HG01346.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-4627_111-4617d others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | ||||||
| chr18:32107176 | A | G | 1 | a0001c0001t0028g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.111-4578A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107176 | |||||||
| chr18:32107349 | C | CCTG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(196): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.111-4405_111-4404i others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107349 | |||||||
| chr18:32107479 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.111-4275A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107479 | |||||||
| chr18:32107510 | TTTTGTTT others(1): Show |
T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-4224_111-4217d others(10): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107510 | ||||||
| chr18:32107637 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.111-4117C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107637 | |||||||
| chr18:32107638 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.111-4116A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107638 | |||||||
| chr18:32107719 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111-4035A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107719 | |||||||
| chr18:32107738 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.111-4016C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107738 | |||||||
| chr18:32107768 | C | G | 4 | a0001c0001t0008g0014 a0001c0001t0008g0042 a0001c0001t0008g0099 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-3986C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107768 | |||||||
| chr18:32107811 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.111-3943C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107811 | |||||||
| chr18:32107819 | TTTAA | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-3931_111-3928d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107819 | ||||||
| chr18:32107859 | T | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-3895T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107859 | |||||||
| chr18:32107918 | G | A | 1 | a0001c0005t0004g0168 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111-3836G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107918 | |||||||
| chr18:32107941 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(195): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.111-3813A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107941 | |||||||
| chr18:32107953 | C | T | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-3801C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107953 | |||||||
| chr18:32108107 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.111-3647G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108107 | |||||||
| chr18:32108134 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.111-3620C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108134 | |||||||
| chr18:32108247 | A | G | 1 | a0001c0001t0004g0160 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.111-3507A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108247 | |||||||
| chr18:32108375 | C | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-3379C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108375 | |||||||
| chr18:32108409 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-3345T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108409 | |||||||
| chr18:32108824 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.111-2930G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108824 | |||||||
| chr18:32108970 | A | G | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-2784A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108970 | |||||||
| chr18:32108986 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0278 a0001c0001t0001g0280 |
4 | HG00099.hp1 HG00642.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-2768T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108986 | |||||||
| chr18:32108988 | G | A | 1 | a0001c0001t0005g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.111-2766G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108988 | |||||||
| chr18:32109023 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0278 a0001c0001t0001g0280 |
4 | HG00099.hp1 HG00642.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-2731T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109023 | |||||||
| chr18:32109157 | C | CT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.111-2582dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32109157 | ||||||
| chr18:32109161 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.111-2593T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109161 | |||||||
| chr18:32109193 | G | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-2561G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109193 | |||||||
| chr18:32109365 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.111-2389T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109365 | |||||||
| chr18:32109744 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(3): Show |
8 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.111-2010G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109744 | |||||||
| chr18:32109872 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-1882C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109872 | |||||||
| chr18:32109879 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.111-1875C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109879 | |||||||
| chr18:32109895 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-1859A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109895 | |||||||
| chr18:32109896 | A | G | 1 | a0001c0001t0027g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-1858A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109896 | |||||||
| chr18:32109990 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.111-1764T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109990 | |||||||
| chr18:32110197 | T | G | 1 | a0001c0001t0024g0161 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.111-1557T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110197 | |||||||
| chr18:32110230 | C | G | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111-1524C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110230 | |||||||
| chr18:32110369 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.111-1385C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110369 | |||||||
| chr18:32110398 | T | G | 1 | a0001c0001t0003g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.111-1356T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110398 | |||||||
| chr18:32110463 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.111-1291A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110463 | |||||||
| chr18:32110525 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.111-1229A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110525 | |||||||
| chr18:32110548 | TG | T | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 |
3 | HG02257.hp1 HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.111-1205delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110548 | |||||||
| chr18:32110623 | T | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-1131T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110623 | |||||||
| chr18:32110655 | G | C | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-1099G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110655 | |||||||
| chr18:32110659 | T | C | 33 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(30): Show |
39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.111-1095T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110659 | |||||||
| chr18:32110785 | C | CT | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-956dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32110785 | ||||||
| chr18:32110803 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-951C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110803 | |||||||
| chr18:32110912 | C | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0206 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.111-842C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110912 | |||||||
| chr18:32110926 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.111-828G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110926 | |||||||
| chr18:32110970 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-784C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110970 | |||||||
| chr18:32111034 | C | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-720C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111034 | |||||||
| chr18:32111069 | C | T | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-685C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111069 | |||||||
| chr18:32111122 | T | C | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0159 |
3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.111-632T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111122 | |||||||
| chr18:32111152 | C | T | 6 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(3): Show |
7 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-602C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111152 | |||||||
| chr18:32111200 | C | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-554C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111200 | |||||||
| chr18:32111250 | C | T | 2 | a0001c0001t0003g0267 a0001c0003t0003g0127 |
2 | NA18956.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.111-504C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111250 | |||||||
| chr18:32111314 | C | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0182 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.111-440C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111314 | |||||||
| chr18:32111401 | A | G | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-353A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111401 | |||||||
| chr18:32111578 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-176A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111578 | |||||||
| chr18:32111610 | A | G | 2 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.111-144A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111610 | |||||||
| chr18:32111644 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.111-110C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111644 | |||||||
| chr18:32111715 | AT | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-31delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32111715 | ||||||
| chr18:32111733 | G | A | 6 | a0002c0002t0006g0190 a0002c0002t0006g0191 a0002c0002t0006g0192 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-21G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111733 | |||||||
| chr18:32111736 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.111-18T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111736 | |||||||
| chr18:32111999 | G | GT | 12 | a0001c0001t0001g0136 a0001c0001t0005g0010 a0001c0001t0005g0026 others(9): Show |
16 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.276+94dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32111999 | ||||||
| chr18:32112116 | GA | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0185 others(3): Show |
9 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+206delA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32112116 | ||||||
| chr18:32112358 | C | G | 1 | a0001c0001t0003g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.276+439C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112358 | |||||||
| chr18:32112396 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.276+477T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112396 | |||||||
| chr18:32112443 | T | C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+524T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112443 | |||||||
| chr18:32112444 | G | A | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.276+525G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112444 | |||||||
| chr18:32112473 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.276+554G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112473 | |||||||
| chr18:32112488 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.276+569C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112488 | |||||||
| chr18:32112519 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.276+600C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112519 | |||||||
| chr18:32112598 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+679T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112598 | |||||||
| chr18:32112663 | CAA | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+745_276+746del others(2): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112663 | |||||||
| chr18:32112670 | G | A | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.276+751G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112670 | |||||||
| chr18:32112688 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.276+769A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112688 | |||||||
| chr18:32112872 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.277-873C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112872 | |||||||
| chr18:32112911 | G | A | 32 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(29): Show |
38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.277-834G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112911 | |||||||
| chr18:32113142 | G | A | 2 | a0001c0001t0003g0266 a0001c0001t0003g0268 |
2 | NA18943.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.277-603G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113142 | |||||||
| chr18:32113208 | A | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-537A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113208 | |||||||
| chr18:32113267 | A | G | 5 | a0001c0001t0002g0007 a0001c0001t0002g0094 a0001c0001t0002g0119 others(2): Show |
7 | HG00733.hp2 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-478A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113267 | |||||||
| chr18:32113367 | AT | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.277-369delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32113367 | ||||||
| chr18:32113559 | A | C | 19 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(16): Show |
24 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.277-186A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113559 | |||||||
| chr18:32113961 | A | T | 1 | a0001c0001t0028g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.392+101A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32113961 | |||||||
| chr18:32114155 | T | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.392+295T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114155 | |||||||
| chr18:32114180 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392+320A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114180 | |||||||
| chr18:32114461 | C | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+601C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114461 | |||||||
| chr18:32114627 | T | C | 1 | a0001c0001t0003g0267 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.392+767T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114627 | |||||||
| chr18:32114666 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+806A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114666 | |||||||
| chr18:32114876 | T | TG | 33 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(30): Show |
39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.392+1018dupG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32114876 | ||||||
| chr18:32114966 | G | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.392+1106G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114966 | |||||||
| chr18:32115013 | G | GT | 56 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(53): Show |
67 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.392+1162dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32115013 | ||||||
| chr18:32115048 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.392+1188A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115048 | |||||||
| chr18:32115148 | G | C | 57 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(54): Show |
68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.392+1288G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115148 | |||||||
| chr18:32115295 | A | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+1435A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115295 | |||||||
| chr18:32115473 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.392+1613G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115473 | |||||||
| chr18:32115677 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+1817G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115677 | |||||||
| chr18:32115736 | C | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+1876C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115736 | |||||||
| chr18:32115769 | G | A | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.392+1909G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115769 | |||||||
| chr18:32115782 | C | T | 1 | a0001c0001t0003g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.392+1922C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115782 | |||||||
| chr18:32115793 | T | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | HG02300.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.392+1933T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115793 | |||||||
| chr18:32115865 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.392+2005C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115865 | |||||||
| chr18:32115993 | C | G | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.392+2133C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115993 | |||||||
| chr18:32116034 | A | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+2174A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116034 | |||||||
| chr18:32116071 | A | G | 4 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 others(1): Show |
4 | HG02559.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+2211A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116071 | |||||||
| chr18:32116129 | T | A | 4 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
4 | NA18612.hp1 NA18966.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+2269T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116129 | |||||||
| chr18:32116515 | CT | C | 7 | a0001c0001t0001g0110 a0001c0001t0001g0227 a0001c0001t0002g0062 others(4): Show |
7 | HG00323.hp2 HG00558.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+2671delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32116515 | ||||||
| chr18:32116518 | T | C | 1 | a0001c0001t0001g0033 | 2 | NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.392+2658T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116518 | |||||||
| chr18:32116531 | T | A | 1 | a0001c0001t0003g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.392+2671T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116531 | |||||||
| chr18:32116613 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.392+2753G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116613 | |||||||
| chr18:32116696 | C | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+2836C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116696 | |||||||
| chr18:32116732 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.392+2872T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116732 | |||||||
| chr18:32116737 | T | TG | 28 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(25): Show |
35 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.392+2884dupG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32116737 | ||||||
| chr18:32116762 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.392+2902C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116762 | |||||||
| chr18:32116851 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.392+2991C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116851 | |||||||
| chr18:32116911 | T | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+3051T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116911 | |||||||
| chr18:32116937 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.392+3077C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116937 | |||||||
| chr18:32116987 | G | A | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0159 |
3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+3127G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116987 | |||||||
| chr18:32116993 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(26): Show |
36 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.392+3133C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116993 | |||||||
| chr18:32117154 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.392+3294G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117154 | |||||||
| chr18:32117172 | GATTACAG others(2): Show |
G | 6 | a0002c0002t0006g0190 a0002c0002t0006g0191 a0002c0002t0006g0192 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+3315_392+3323d others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32117172 | ||||||
| chr18:32117194 | C | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0056 a0001c0001t0002g0065 others(2): Show |
6 | HG02080.hp1 HG02083.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392+3334C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117194 | |||||||
| chr18:32117505 | G | GA | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+3654dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32117505 | ||||||
| chr18:32117591 | C | T | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0159 |
3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+3731C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117591 | |||||||
| chr18:32117701 | C | G | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.392+3841C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117701 | |||||||
| chr18:32117705 | T | C | 1 | a0001c0001t0003g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.392+3845T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117705 | |||||||
| chr18:32118230 | T | C | 55 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(52): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.392+4370T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118230 | |||||||
| chr18:32118248 | T | C | 2 | a0001c0001t0003g0267 a0001c0003t0003g0127 |
2 | NA18956.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.392+4388T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118248 | |||||||
| chr18:32118418 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.392+4558C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118418 | |||||||
| chr18:32118563 | G | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+4703G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118563 | |||||||
| chr18:32118564 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+4704C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118564 | |||||||
| chr18:32118664 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.392+4804C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118664 | |||||||
| chr18:32118690 | G | T | 1 | a0001c0001t0022g0251 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.393-4828G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118690 | |||||||
| chr18:32118702 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.393-4816G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118702 | |||||||
| chr18:32118753 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0032 others(10): Show |
18 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.393-4765C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118753 | |||||||
| chr18:32118798 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.393-4720C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118798 | |||||||
| chr18:32118982 | A | G | 5 | a0001c0001t0005g0184 a0001c0001t0005g0286 a0001c0001t0005g0287 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-4536A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118982 | |||||||
| chr18:32119129 | T | TTGAGGAG others(23): Show |
3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0018g0105 |
3 | NA18984.hp2 NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.393-4387_393-4358d others(32): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32119129 | ||||||
| chr18:32119192 | C | A | 1 | a0001c0001t0002g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.393-4326C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119192 | |||||||
| chr18:32119296 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.393-4222C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119296 | |||||||
| chr18:32119313 | C | A | 1 | a0001c0001t0002g0050 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393-4205C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119313 | |||||||
| chr18:32119358 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0286 a0001c0001t0005g0287 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-4160C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119358 | |||||||
| chr18:32119378 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.393-4140G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119378 | |||||||
| chr18:32119892 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.393-3626A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119892 | |||||||
| chr18:32120031 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.393-3487T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120031 | |||||||
| chr18:32120036 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.393-3482T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120036 | |||||||
| chr18:32120162 | G | A | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-3356G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120162 | |||||||
| chr18:32120296 | A | G | 1 | a0001c0001t0003g0262 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.393-3222A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120296 | |||||||
| chr18:32120323 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.393-3195C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120323 | |||||||
| chr18:32120335 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.393-3183T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120335 | |||||||
| chr18:32120363 | A | T | 1 | a0001c0001t0016g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.393-3155A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120363 | |||||||
| chr18:32120382 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393-3136A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120382 | |||||||
| chr18:32120587 | T | C | 33 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0094 others(30): Show |
39 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.393-2931T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120587 | |||||||
| chr18:32120829 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.393-2689A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120829 | |||||||
| chr18:32120879 | C | T | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.393-2639C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120879 | |||||||
| chr18:32120892 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-2626C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120892 | |||||||
| chr18:32120981 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393-2537C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120981 | |||||||
| chr18:32121033 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-2485G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121033 | |||||||
| chr18:32121090 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-2428G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121090 | |||||||
| chr18:32121095 | G | A | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393-2423G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121095 | |||||||
| chr18:32121133 | C | CA | 8 | a0001c0001t0001g0155 a0001c0001t0007g0132 a0002c0002t0006g0190 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-2376dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32121133 | ||||||
| chr18:32121137 | A | G | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-2381A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121137 | |||||||
| chr18:32121138 | A | C | 1 | a0001c0001t0020g0059 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393-2380A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121138 | |||||||
| chr18:32121142 | AC | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(147): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.393-2375delC | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121142 | |||||||
| chr18:32121143 | C | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
94 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.393-2375C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121143 | |||||||
| chr18:32121144 | A | C | 2 | a0002c0002t0006g0035 a0002c0002t0006g0259 |
3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.393-2374A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121144 | |||||||
| chr18:32121443 | C | T | 1 | a0001c0001t0011g0022 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.393-2075C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121443 | |||||||
| chr18:32121758 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393-1760C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121758 | |||||||
| chr18:32121899 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.393-1619G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121899 | |||||||
| chr18:32121996 | G | A | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0159 |
3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.393-1522G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121996 | |||||||
| chr18:32122014 | G | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-1504G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122014 | |||||||
| chr18:32122017 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-1501C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122017 | |||||||
| chr18:32122124 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(196): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.393-1394T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122124 | |||||||
| chr18:32122234 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393-1284T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122234 | |||||||
| chr18:32122237 | C | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-1281C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122237 | |||||||
| chr18:32122262 | T | C | 33 | a0001c0001t0002g0178 a0001c0001t0003g0023 a0001c0001t0003g0024 others(30): Show |
39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.393-1256T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122262 | |||||||
| chr18:32122329 | A | G | 1 | a0001c0001t0005g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.393-1189A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122329 | |||||||
| chr18:32122387 | A | T | 55 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0023 others(52): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.393-1131A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122387 | |||||||
| chr18:32122401 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.393-1117T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122401 | |||||||
| chr18:32122426 | A | G | 1 | a0001c0001t0007g0134 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.393-1092A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122426 | |||||||
| chr18:32122473 | ACTTAT | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.393-1039_393-1035d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32122473 | ||||||
| chr18:32122550 | G | A | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-968G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122550 | |||||||
| chr18:32122606 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(195): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.393-912T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122606 | |||||||
| chr18:32122657 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.393-861C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122657 | |||||||
| chr18:32122802 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.393-716C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122802 | |||||||
| chr18:32122845 | A | C | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-673A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122845 | |||||||
| chr18:32122864 | T | C | 3 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0268 |
3 | NA18943.hp1 NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.393-654T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122864 | |||||||
| chr18:32122982 | A | T | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-536A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122982 | |||||||
| chr18:32123112 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.393-406C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123112 | |||||||
| chr18:32123139 | T | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-379T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123139 | |||||||
| chr18:32123159 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.393-359C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123159 | |||||||
| chr18:32123390 | G | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(13): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.393-128G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123390 | |||||||
| chr18:32123652 | C | CT | 18 | a0001c0001t0001g0135 a0001c0001t0001g0145 a0001c0001t0001g0232 others(15): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.449+95dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123652 | ||||||
| chr18:32123694 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.449+120C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123694 | |||||||
| chr18:32123776 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.449+202C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123776 | |||||||
| chr18:32123860 | C | T | 1 | a0001c0001t0027g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.449+286C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123860 | |||||||
| chr18:32123965 | T | TA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.449+407dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | ||||||
| chr18:32123965 | T | TAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
49 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.449+406_449+407dup others(2): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | ||||||
| chr18:32123965 | TA | T | 7 | a0001c0001t0002g0067 a0001c0001t0002g0108 a0001c0001t0005g0010 others(4): Show |
10 | HG01109.hp1 HG02055.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.449+407delA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | ||||||
| chr18:32124161 | T | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0283 |
3 | HG02723.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450-573T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124161 | |||||||
| chr18:32124163 | C | A | 1 | a0001c0001t0002g0050 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450-571C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124163 | |||||||
| chr18:32124170 | A | G | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.450-564A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124170 | |||||||
| chr18:32124296 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.450-438A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124296 | |||||||
| chr18:32124301 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.450-433C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124301 | |||||||
| chr18:32124390 | A | G | 2 | a0002c0002t0006g0190 a0002c0002t0006g0193 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.450-344A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124390 | |||||||
| chr18:32124398 | A | T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.450-336A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124398 | |||||||
| chr18:32124558 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450-176G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124558 | |||||||
| chr18:32124631 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.450-103T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124631 | |||||||
| chr18:32124679 | C | T | 1 | a0001c0001t0009g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.450-55C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124679 | |||||||
| chr18:32124689 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.450-45G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124689 | |||||||
| chr18:32125121 | A | G | 1 | a0001c0001t0002g0020 | 2 | HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.561+276A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125121 | |||||||
| chr18:32125129 | G | A | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+284G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125129 | |||||||
| chr18:32125630 | T | C | 1 | a0001c0001t0005g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.561+785T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125630 | |||||||
| chr18:32125688 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561+843T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125688 | |||||||
| chr18:32125722 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.561+877A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125722 | |||||||
| chr18:32125746 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.561+901A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125746 | |||||||
| chr18:32125761 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.561+916G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125761 | |||||||
| chr18:32125876 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.562-817G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125876 | |||||||
| chr18:32125929 | C | T | 2 | a0001c0001t0002g0116 a0001c0001t0002g0118 |
2 | HG02735.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.562-764C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125929 | |||||||
| chr18:32126028 | T | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.562-665T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126028 | |||||||
| chr18:32126131 | A | T | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.562-562A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126131 | |||||||
| chr18:32126242 | G | T | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.562-451G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126242 | |||||||
| chr18:32126352 | T | C | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.562-341T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126352 | |||||||
| chr18:32126387 | GCCAGTTA others(4): Show |
G | 1 | a0001c0001t0018g0105 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.562-305_562-295del others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126387 | |||||||
| chr18:32126500 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0208 others(2): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-193C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126500 | |||||||
| chr18:32126587 | C | G | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.562-106C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126587 | |||||||
| chr18:32126589 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.562-104T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126589 | |||||||
| chr18:32126594 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.562-99A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126594 | |||||||
| chr18:32126651 | T | C | 1 | a0001c0001t0004g0166 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.562-42T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126651 | |||||||
| chr18:32127322 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.669+522A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127322 | |||||||
| chr18:32127631 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0143 |
4 | HG00423.hp1 HG00558.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+831G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127631 | |||||||
| chr18:32127904 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.669+1104C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127904 | |||||||
| chr18:32127936 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+1136C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127936 | |||||||
| chr18:32127985 | C | A | 8 | a0002c0002t0006g0035 a0002c0002t0006g0190 a0002c0002t0006g0191 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-1134C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127985 | |||||||
| chr18:32128003 | C | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(4): Show |
10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-1116C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128003 | |||||||
| chr18:32128005 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670-1114G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128005 | |||||||
| chr18:32128034 | C | A | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670-1085C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128034 | |||||||
| chr18:32128081 | A | AAAAAG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(190): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.670-1032_670-1028d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32128081 | ||||||
| chr18:32128232 | G | A | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-887G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128232 | |||||||
| chr18:32128311 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.670-808G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128311 | |||||||
| chr18:32128336 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(126): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.670-783A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128336 | |||||||
| chr18:32128422 | T | C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0026 a0001c0001t0005g0184 others(8): Show |
14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-697T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128422 | |||||||
| chr18:32128468 | G | A | 1 | a0001c0001t0003g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-651G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128468 | |||||||
| chr18:32128479 | A | C | 17 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.670-640A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128479 | |||||||
| chr18:32128663 | A | C | 1 | a0001c0001t0004g0176 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.670-456A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128663 | |||||||
| chr18:32128885 | CTGTT | C | 17 | a0001c0001t0003g0003 a0001c0001t0003g0036 a0001c0001t0003g0037 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.670-225_670-222del others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32128885 | ||||||
| chr18:32128957 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.670-162G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128957 | |||||||
| chr18:32129005 | GTGTGTAA others(12): Show |
G | 1 | a0003c0004t0014g0027 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.670-101_670-83delG others(18): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32129005 | ||||||
| chr18:32129018 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(287): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.670-101G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32129018 |