Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 95681 |
| ensemblid | ENSG00000106477.20 |
| hgncid | 12370 |
| symbol | CEP41 |
| name | centrosomal protein 41 |
| refseq_nuc | NM_018718.3 |
| refseq_prot | NP_061188.1 |
| ensembl_nuc | ENST00000223208.10 |
| ensembl_prot | ENSP00000223208.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 130393771 |
| end | 130441016 |
| strand | - |
| ver | v1.2 |
| region | chr7:130393771-130441016 |
| region5000 | chr7:130388771-130446016 |
| regionname0 | CEP41_chr7_130393771_130441016 |
| regionname5000 | CEP41_chr7_130388771_130446016 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 373 | 343 | 82 | 69 | 138 | 14 | 38 | 106 | CEP41_chr7_130388771_130446016 | CEP41 | MSLRR others(368): Show |
chr7 | 130388771 | 130446016 |
| a0002 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | MSLRR others(368): Show |
chr7 | 130388771 | 130446016 |
| a0003 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | MSLRR others(368): Show |
chr7 | 130388771 | 130446016 |
| a0004 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | MSLRR others(368): Show |
chr7 | 130388771 | 130446016 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1119 | 342 | 82 | 69 | 137 | 14 | 38 | CEP41_chr7_130388771_130446016 | CEP41 | ATGTC others(1114): Show |
chr7 | 130388771 | 130446016 | ||
| a0001c0005 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | ATGTC others(1114): Show |
chr7 | 130388771 | 130446016 | ||
| a0002c0002 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | ATGTC others(1114): Show |
chr7 | 130388771 | 130446016 | ||
| a0003c0003 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | ATGTC others(1114): Show |
chr7 | 130388771 | 130446016 | ||
| a0004c0004 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | ATGTC others(1114): Show |
chr7 | 130388771 | 130446016 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6292 | 45 | 2 | 15 | 23 | 1 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0002 | 0/0 | 6294 | 39 | 11 | 10 | 15 | 1 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0003 | 1/0 | 6292 | 25 | 12 | 3 | 4 | 3 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0004 | 0/0 | 6292 | 19 | 0 | 3 | 10 | 0 | 6 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0005 | 0/0 | 6293 | 11 | 0 | 1 | 10 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0006 | 0/0 | 6293 | 11 | 10 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0007 | 0/0 | 6293 | 11 | 1 | 2 | 4 | 0 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0008 | 0/0 | 6294 | 11 | 3 | 3 | 3 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0009 | 0/0 | 6293 | 10 | 0 | 3 | 0 | 4 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0010 | 0/0 | 6292 | 10 | 0 | 2 | 7 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0011 | 0/0 | 6293 | 8 | 0 | 3 | 3 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0012 | 0/0 | 6293 | 7 | 3 | 2 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0013 | 0/0 | 6289 | 6 | 0 | 1 | 5 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6284): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0014 | 0/0 | 6293 | 6 | 0 | 0 | 6 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0015 | 0/0 | 6295 | 5 | 1 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0016 | 0/0 | 6294 | 5 | 2 | 3 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0017 | 0/0 | 6292 | 5 | 0 | 2 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0018 | 0/0 | 6293 | 5 | 0 | 1 | 1 | 0 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0019 | 0/0 | 6292 | 4 | 4 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0020 | 0/0 | 6292 | 4 | 0 | 0 | 4 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0021 | 0/0 | 6295 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0022 | 0/0 | 6293 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0023 | 0/0 | 6294 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0024 | 0/0 | 6292 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0025 | 0/0 | 6291 | 3 | 1 | 0 | 1 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0026 | 0/0 | 6293 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0027 | 0/0 | 6292 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0028 | 0/0 | 6292 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0029 | 0/0 | 6292 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0030 | 0/0 | 6294 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0031 | 0/0 | 6291 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0032 | 0/0 | 6293 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0033 | 0/0 | 6294 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0034 | 0/0 | 6294 | 2 | 1 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0035 | 0/0 | 6293 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0036 | 0/0 | 6293 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0037 | 0/0 | 6293 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0038 | 0/0 | 6292 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0039 | 0/0 | 6293 | 2 | 0 | 0 | 1 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0040 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0041 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0042 | 0/0 | 6294 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0043 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0044 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0045 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0046 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0047 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0048 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0049 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0050 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0051 | 0/0 | 6291 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0052 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0053 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0054 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0055 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0056 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0057 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0058 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0059 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0060 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0061 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0062 | 0/0 | 6282 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6277): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0063 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0064 | 0/1 | 6292 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0065 | 0/0 | 6291 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0066 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0068 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0069 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0070 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0071 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0072 | 0/0 | 6292 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0073 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0074 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0075 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0076 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0077 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0078 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0079 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0080 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0082 | 0/0 | 6291 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0083 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0084 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0085 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6289): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0086 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0087 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0088 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0001c0001t0089 | 0/0 | 6335 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6330): Show |
chr7 | 130388771 | 130446016 |
| a0001c0005t0001 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6287): Show |
chr7 | 130388771 | 130446016 |
| a0002c0002t0005 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6288): Show |
chr7 | 130388771 | 130446016 |
| a0003c0003t0067 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6290): Show |
chr7 | 130388771 | 130446016 |
| a0004c0004t0081 | 0/0 | 6291 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | AGAGG others(6286): Show |
chr7 | 130388771 | 130446016 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0016 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0010g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0013g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0014g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0015g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0017g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0017g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0017g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0018g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0018g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0018g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0019g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0019g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0020g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0021g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0021g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0021g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0022g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0022g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0023g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0023g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0024g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0025g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0025g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0025g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0026g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0026g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0026g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0027g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0027g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0027g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0028g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0028g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0029g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0029g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0030g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0030g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0031g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0032g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0032g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0033g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0033g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0034g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0034g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0035g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0035g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0036g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0036g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0037g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0038g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0038g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0039g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0039g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0040g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0041g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0042g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0043g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0044g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0045g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0046g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0047g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0048g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0049g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0050g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0051g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0052g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0053g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0054g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0055g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0056g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0057g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0058g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0059g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0060g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0061g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0062g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0063g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0064g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0065g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0066g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0068g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0069g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0070g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0071g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0072g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0073g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0074g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0075g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0076g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0077g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0078g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0079g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0080g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0082g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0083g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0084g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0085g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0086g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0087g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0088g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0001t0089g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0001c0005t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0003c0003t0067g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| a0004c0004t0081g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0071 | g0295 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0112 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0092 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00280 | hp1 | a0001 | c0001 | t0059 | g0089 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0110 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00323 | hp2 | a0001 | c0001 | t0058 | g0111 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00408 | hp1 | a0001 | c0001 | t0089 | g0305 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00438 | hp1 | a0001 | c0001 | t0079 | g0254 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0276 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00558 | hp1 | a0001 | c0001 | t0021 | g0022 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00558 | hp2 | a0001 | c0001 | t0013 | g0031 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00597 | hp1 | a0001 | c0001 | t0011 | g0135 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00621 | hp1 | a0001 | c0001 | t0035 | g0255 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0131 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0128 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00733 | hp1 | a0001 | c0001 | t0033 | g0209 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01070 | hp1 | a0001 | c0001 | t0017 | g0021 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01071 | hp1 | a0001 | c0001 | t0017 | g0021 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0087 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01081 | hp2 | a0001 | c0001 | t0009 | g0088 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0279 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0259 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0264 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0178 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01175 | hp1 | a0001 | c0001 | t0042 | g0157 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01192 | hp1 | a0001 | c0001 | t0072 | g0240 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01192 | hp2 | a0001 | c0001 | t0016 | g0116 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0107 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0090 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01256 | hp2 | a0001 | c0001 | t0021 | g0205 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01257 | hp1 | a0001 | c0001 | t0065 | g0283 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0210 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0148 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01346 | hp2 | a0001 | c0001 | t0062 | g0099 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01358 | hp1 | a0001 | c0001 | t0084 | g0238 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01361 | hp1 | a0001 | c0001 | t0030 | g0136 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01361 | hp2 | a0001 | c0001 | t0018 | g0186 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0014 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0154 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0014 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01517 | hp2 | a0001 | c0001 | t0025 | g0278 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01884 | hp1 | a0001 | c0001 | t0031 | g0151 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0171 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01891 | hp1 | a0001 | c0001 | t0024 | g0012 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01891 | hp2 | a0001 | c0001 | t0068 | g0289 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0032 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01943 | hp1 | a0001 | c0001 | t0024 | g0012 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0119 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01978 | hp2 | a0001 | c0001 | t0063 | g0093 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0204 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01993 | hp2 | a0001 | c0001 | t0026 | g0300 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02004 | hp1 | a0001 | c0001 | t0033 | g0179 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02004 | hp2 | a0002 | c0002 | t0005 | g0074 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02055 | hp2 | a0003 | c0003 | t0067 | g0304 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0047 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02056 | hp2 | a0001 | c0001 | t0030 | g0133 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02074 | hp2 | a0001 | c0001 | t0040 | g0156 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02080 | hp2 | a0001 | c0001 | t0039 | g0202 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0213 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02135 | hp2 | a0001 | c0001 | t0011 | g0137 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0075 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02148 | hp2 | a0001 | c0001 | t0015 | g0043 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02165 | hp2 | a0001 | c0001 | t0013 | g0033 | EAS | CDX | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0100 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02273 | hp2 | a0001 | c0001 | t0035 | g0236 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02572 | hp1 | a0001 | c0001 | t0056 | g0029 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0072 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02615 | hp1 | a0001 | c0001 | t0044 | g0121 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02615 | hp2 | a0001 | c0001 | t0034 | g0299 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0302 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0256 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0109 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02717 | hp1 | a0001 | c0001 | t0048 | g0030 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02738 | hp2 | a0001 | c0001 | t0018 | g0277 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02809 | hp2 | a0001 | c0001 | t0023 | g0177 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02818 | hp2 | a0001 | c0001 | t0019 | g0159 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02886 | hp1 | a0001 | c0001 | t0026 | g0298 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0085 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02896 | hp2 | a0001 | c0001 | t0031 | g0066 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02897 | hp1 | a0001 | c0001 | t0023 | g0084 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02922 | hp1 | a0001 | c0001 | t0060 | g0028 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02965 | hp2 | a0001 | c0001 | t0026 | g0303 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02970 | hp2 | a0001 | c0001 | t0036 | g0291 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02976 | hp2 | a0001 | c0001 | t0045 | g0061 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0253 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03041 | hp2 | a0001 | c0001 | t0055 | g0027 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0172 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03098 | hp2 | a0001 | c0001 | t0066 | g0287 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0294 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0095 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03195 | hp2 | a0001 | c0001 | t0036 | g0290 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03209 | hp1 | a0001 | c0001 | t0050 | g0025 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0301 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03225 | hp1 | a0001 | c0001 | t0076 | g0285 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03490 | hp1 | a0001 | c0001 | t0037 | g0023 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0007 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03491 | hp2 | a0001 | c0001 | t0057 | g0132 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0007 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03492 | hp2 | a0001 | c0001 | t0037 | g0023 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03516 | hp2 | a0001 | c0001 | t0029 | g0167 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03540 | hp2 | a0001 | c0001 | t0024 | g0067 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0114 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0035 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03688 | hp2 | a0001 | c0001 | t0038 | g0250 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0108 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03710 | hp1 | a0001 | c0001 | t0034 | g0269 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03710 | hp2 | a0001 | c0001 | t0046 | g0081 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0199 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0118 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03834 | hp2 | a0001 | c0001 | t0082 | g0233 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03927 | hp2 | a0001 | c0001 | t0018 | g0197 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0243 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0296 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04184 | hp2 | a0001 | c0001 | t0039 | g0203 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0270 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04199 | hp2 | a0001 | c0001 | t0075 | g0267 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0117 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0208 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18522 | hp2 | a0001 | c0001 | t0054 | g0026 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18747 | hp1 | a0001 | c0001 | t0020 | g0015 | EAS | CHB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18747 | hp2 | a0001 | c0001 | t0061 | g0134 | EAS | CHB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18943 | hp1 | a0001 | c0001 | t0078 | g0274 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18943 | hp2 | a0001 | c0005 | t0001 | g0281 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18944 | hp1 | a0001 | c0001 | t0021 | g0022 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18944 | hp2 | a0001 | c0001 | t0014 | g0184 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18945 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18949 | hp1 | a0001 | c0001 | t0012 | g0124 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18949 | hp2 | a0001 | c0001 | t0032 | g0127 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18950 | hp1 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18950 | hp2 | a0001 | c0001 | t0017 | g0241 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18954 | hp2 | a0001 | c0001 | t0047 | g0052 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18959 | hp1 | a0001 | c0001 | t0025 | g0246 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18962 | hp1 | a0001 | c0001 | t0080 | g0211 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18962 | hp2 | a0001 | c0001 | t0027 | g0273 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18964 | hp2 | a0001 | c0001 | t0014 | g0185 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18969 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18972 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18972 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18978 | hp2 | a0001 | c0001 | t0049 | g0055 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18982 | hp1 | a0001 | c0001 | t0027 | g0272 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18982 | hp2 | a0001 | c0001 | t0020 | g0122 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18983 | hp2 | a0001 | c0001 | t0013 | g0168 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18984 | hp2 | a0001 | c0001 | t0074 | g0215 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18986 | hp2 | a0001 | c0001 | t0032 | g0036 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18987 | hp1 | a0001 | c0001 | t0041 | g0146 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18987 | hp2 | a0001 | c0001 | t0014 | g0230 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18990 | hp1 | a0001 | c0001 | t0083 | g0198 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18994 | hp2 | a0001 | c0001 | t0020 | g0015 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18999 | hp1 | a0001 | c0001 | t0014 | g0225 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA18999 | hp2 | a0001 | c0001 | t0086 | g0280 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19000 | hp1 | a0001 | c0001 | t0014 | g0282 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19000 | hp2 | a0001 | c0001 | t0053 | g0165 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19003 | hp1 | a0001 | c0001 | t0017 | g0227 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19003 | hp2 | a0001 | c0001 | t0052 | g0050 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19004 | hp2 | a0001 | c0001 | t0017 | g0226 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19009 | hp1 | a0001 | c0001 | t0027 | g0275 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19009 | hp2 | a0001 | c0001 | t0077 | g0262 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19030 | hp2 | a0001 | c0001 | t0043 | g0060 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19043 | hp1 | a0004 | c0004 | t0081 | g0293 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19043 | hp2 | a0001 | c0001 | t0022 | g0170 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19060 | hp1 | a0001 | c0001 | t0069 | g0206 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19062 | hp1 | a0001 | c0001 | t0028 | g0020 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19064 | hp1 | a0001 | c0001 | t0028 | g0020 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19064 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19065 | hp1 | a0001 | c0001 | t0021 | g0207 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19068 | hp2 | a0001 | c0001 | t0088 | g0235 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19072 | hp2 | a0001 | c0001 | t0070 | g0187 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19074 | hp1 | a0001 | c0001 | t0014 | g0245 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19078 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19079 | hp2 | a0001 | c0001 | t0085 | g0232 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19080 | hp2 | a0001 | c0001 | t0018 | g0189 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19082 | hp1 | a0001 | c0001 | t0028 | g0194 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19090 | hp1 | a0001 | c0001 | t0015 | g0057 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19090 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | ASW | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA20129 | hp2 | a0001 | c0001 | t0087 | g0292 | AFR | ASW | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | TSI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01123 | hp1 | a0001 | c0001 | t0016 | g0037 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02486 | hp1 | a0001 | c0001 | t0073 | g0286 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0164 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02559 | hp1 | a0001 | c0001 | t0051 | g0176 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0180 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | USA | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | USA | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0147 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| NA21309 | hp2 | a0001 | c0001 | t0029 | g0166 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0064 | g0271 | REF | REF | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0016 | REF | REF | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130398948 | G | C | 1 | a0004 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1065C>G | p.Ser355Arg | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1115/6292 | 1065/1122 | 355/373 | chr7 | 130398948 | |||
| chr7:130400746 | A | C | 1 | a0003 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.718T>G | p.Cys240Gly | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/11 | 768/6292 | 718/1122 | 240/373 | chr7 | 130400746 | |||
| chr7:130404579 | C | T | 1 | a0002 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.407G>A | p.Arg136His | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/11 | 457/6292 | 407/1122 | 136/373 | chr7 | 130404579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130412181 | G | A | 1 | a0001c0005 | 1 | NA18943.hp2 | splice_region_variant&synonymous_variant | LOW | c.205C>T | p.Leu69Leu | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/11 | 255/6292 | 205/1122 | 69/373 | chr7 | 130412181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130393789 | C | T | 59 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(56): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*5102G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5102 | chr7 | 130393789 | ||||||
| chr7:130393826 | C | CT | 2 | a0001c0001t0013 a0001c0001t0066 |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5064dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5064 | chr7 | 130393826 | ||||||
| chr7:130393833 | C | A | 1 | a0001c0001t0056 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5058G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5058 | chr7 | 130393833 | ||||||
| chr7:130393897 | A | G | 1 | a0001c0001t0075 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4994T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4994 | chr7 | 130393897 | ||||||
| chr7:130394296 | C | T | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4595G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4595 | chr7 | 130394296 | ||||||
| chr7:130394297 | G | A | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4594C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4594 | chr7 | 130394297 | ||||||
| chr7:130394577 | A | G | 1 | a0001c0001t0022 | 3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4314T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4314 | chr7 | 130394577 | ||||||
| chr7:130394596 | C | G | 33 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(30): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4295G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4295 | chr7 | 130394596 | ||||||
| chr7:130394645 | A | G | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4246T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4246 | chr7 | 130394645 | ||||||
| chr7:130394675 | G | A | 1 | a0001c0001t0042 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4216C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4216 | chr7 | 130394675 | ||||||
| chr7:130394700 | G | C | 1 | a0001c0001t0048 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4191C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4191 | chr7 | 130394700 | ||||||
| chr7:130394776 | T | C | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4115A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4115 | chr7 | 130394776 | ||||||
| chr7:130394854 | T | C | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(14): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4037A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4037 | chr7 | 130394854 | ||||||
| chr7:130394963 | G | A | 2 | a0001c0001t0073 a0001c0001t0076 |
2 | HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3928C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3928 | chr7 | 130394963 | ||||||
| chr7:130394981 | G | C | 1 | a0001c0001t0049 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3910C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3910 | chr7 | 130394981 | ||||||
| chr7:130394983 | G | A | 1 | a0001c0001t0077 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3908C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3908 | chr7 | 130394983 | ||||||
| chr7:130395004 | G | C | 12 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0018 others(9): Show |
49 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3887C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3887 | chr7 | 130395004 | ||||||
| chr7:130395108 | A | G | 1 | a0001c0001t0033 | 2 | HG00733.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3783T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3783 | chr7 | 130395108 | ||||||
| chr7:130395126 | C | A | 2 | a0001c0001t0037 a0001c0001t0071 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3765G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3765 | chr7 | 130395126 | ||||||
| chr7:130395140 | C | T | 1 | a0001c0001t0074 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3751G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3751 | chr7 | 130395140 | ||||||
| chr7:130395350 | C | T | 1 | a0001c0001t0073 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3541G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3541 | chr7 | 130395350 | ||||||
| chr7:130395364 | G | GA | 38 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(35): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*3526dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3526 | chr7 | 130395364 | ||||||
| chr7:130395384 | G | A | 2 | a0001c0001t0037 a0001c0001t0071 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3507C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3507 | chr7 | 130395384 | ||||||
| chr7:130395447 | G | T | 1 | a0001c0001t0024 | 3 | HG01891.hp1 HG01943.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3444C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3444 | chr7 | 130395447 | ||||||
| chr7:130395698 | G | A | 1 | a0001c0001t0028 | 3 | NA19062.hp1 NA19064.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3193C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3193 | chr7 | 130395698 | ||||||
| chr7:130395880 | T | TA | 8 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0018 others(5): Show |
44 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3010dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3010 | chr7 | 130395880 | ||||||
| chr7:130395880 | TA | T | 6 | a0001c0001t0025 a0001c0001t0031 a0001c0001t0051 others(3): Show |
9 | HG00323.hp2 HG01517.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3010delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3010 | chr7 | 130395880 | ||||||
| chr7:130395995 | C | T | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2896 | chr7 | 130395995 | ||||||
| chr7:130396012 | T | C | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2879A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2879 | chr7 | 130396012 | ||||||
| chr7:130396079 | C | T | 1 | a0001c0001t0066 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2812G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2812 | chr7 | 130396079 | ||||||
| chr7:130396409 | T | A | 5 | a0001c0001t0035 a0001c0001t0053 a0001c0001t0079 others(2): Show |
6 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2482A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2482 | chr7 | 130396409 | ||||||
| chr7:130396410 | A | T | 1 | a0001c0001t0038 | 2 | HG03688.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2481T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2481 | chr7 | 130396410 | ||||||
| chr7:130396477 | C | T | 1 | a0001c0001t0047 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2414G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2414 | chr7 | 130396477 | ||||||
| chr7:130396527 | C | T | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2364 | chr7 | 130396527 | ||||||
| chr7:130396665 | C | T | 1 | a0001c0001t0054 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2226G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2226 | chr7 | 130396665 | ||||||
| chr7:130396775 | A | G | 1 | a0001c0001t0045 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2116 | chr7 | 130396775 | ||||||
| chr7:130396850 | C | T | 22 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(19): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2041 | chr7 | 130396850 | ||||||
| chr7:130396868 | T | C | 1 | a0001c0001t0080 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2023 | chr7 | 130396868 | ||||||
| chr7:130396960 | G | A | 14 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(11): Show |
48 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1931C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1931 | chr7 | 130396960 | ||||||
| chr7:130396991 | C | T | 1 | a0001c0001t0072 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1900G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1900 | chr7 | 130396991 | ||||||
| chr7:130397032 | C | A | 19 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(16): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1859 | chr7 | 130397032 | ||||||
| chr7:130397245 | C | T | 1 | a0001c0001t0069 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1646G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1646 | chr7 | 130397245 | ||||||
| chr7:130397247 | T | C | 1 | a0001c0001t0043 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1644A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1644 | chr7 | 130397247 | ||||||
| chr7:130397324 | T | G | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1567A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1567 | chr7 | 130397324 | ||||||
| chr7:130397351 | T | C | 1 | a0001c0001t0044 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1540A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1540 | chr7 | 130397351 | ||||||
| chr7:130397357 | A | G | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1534T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1534 | chr7 | 130397357 | ||||||
| chr7:130397379 | G | A | 2 | a0001c0001t0036 a0001c0001t0068 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1512C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1512 | chr7 | 130397379 | ||||||
| chr7:130397506 | A | AT | 25 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(22): Show |
117 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1384dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | ||||||
| chr7:130397506 | A | ATT | 10 | a0001c0001t0015 a0001c0001t0021 a0001c0001t0041 others(7): Show |
17 | HG00558.hp1 HG01175.hp1 HG01256.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1383_*1384dupAA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | ||||||
| chr7:130397506 | A | C | 1 | a0001c0001t0071 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1385T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1385 | chr7 | 130397506 | ||||||
| chr7:130397506 | AT | A | 10 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0027 others(7): Show |
41 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1384delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | ||||||
| chr7:130397506 | ATTTT | A | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1381_*1384delAAAA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1381 | chr7 | 130397506 | ||||||
| chr7:130397506 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0062 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374_*1384delAAAA others(7): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1374 | chr7 | 130397506 | ||||||
| chr7:130397702 | G | A | 1 | a0001c0001t0084 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1189 | chr7 | 130397702 | ||||||
| chr7:130397964 | A | G | 1 | a0001c0001t0065 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*927T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 927 | chr7 | 130397964 | ||||||
| chr7:130397972 | G | A | 1 | a0001c0001t0063 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*919C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 919 | chr7 | 130397972 | ||||||
| chr7:130398086 | T | C | 3 | a0001c0001t0020 a0001c0001t0085 a0001c0001t0086 |
6 | NA18747.hp1 NA18982.hp2 NA18994.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*805A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 805 | chr7 | 130398086 | ||||||
| chr7:130398115 | C | T | 1 | a0001c0001t0040 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 776 | chr7 | 130398115 | ||||||
| chr7:130398236 | G | A | 2 | a0001c0001t0013 a0001c0001t0029 |
8 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*655C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 655 | chr7 | 130398236 | ||||||
| chr7:130398508 | G | A | 1 | a0001c0001t0087 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 383 | chr7 | 130398508 | ||||||
| chr7:130398748 | G | C | 1 | a0001c0001t0088 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 143 | chr7 | 130398748 | ||||||
| chr7:130398806 | G | T | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*85C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 85 | chr7 | 130398806 | ||||||
| chr7:130440971 | T | G | 45 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(42): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
5_prime_UTR_variant | MODIFIER | c.-5A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/11 | 5 | chr7 | 130440971 | ||||||
| chr7:130440986 | G | GTTCGGGG others(36): Show |
1 | a0001c0001t0089 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63_-21dupGGAAGCTA others(35): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/11 | 21 | chr7 | 130440986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130399187 | G | GGCCT | 36 | a0001c0001t0004g0004 a0001c0001t0004g0019 a0001c0001t0004g0182 others(33): Show |
45 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.974-152_974-149dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399187 | |||||||
| chr7:130399426 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-387G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399426 | |||||||
| chr7:130399544 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0016g0119 |
2 | HG01978.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.973+495C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399544 | |||||||
| chr7:130399654 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.973+385G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399654 | |||||||
| chr7:130399734 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.973+305G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399734 | |||||||
| chr7:130399819 | C | CA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(167): Show |
198 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.973+219dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | |||||||
| chr7:130399819 | C | CAA | 115 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(112): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.973+218_973+219dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | |||||||
| chr7:130399819 | C | CAAA | 6 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0036g0290 others(3): Show |
6 | HG01346.hp2 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+217_973+219dup others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | |||||||
| chr7:130399833 | G | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.973+206C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399833 | |||||||
| chr7:130399835 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.973+204G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399835 | |||||||
| chr7:130400408 | A | T | 1 | a0001c0001t0003g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.758-154T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400408 | |||||||
| chr7:130400510 | A | C | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.757+197T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400510 | |||||||
| chr7:130400604 | T | C | 1 | a0001c0001t0032g0036 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.757+103A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400604 | |||||||
| chr7:130400987 | T | G | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-166A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130400987 | |||||||
| chr7:130401119 | T | A | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.643-298A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401119 | |||||||
| chr7:130401325 | G | A | 7 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(4): Show |
8 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-504C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401325 | |||||||
| chr7:130401325 | G | C | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-504C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401325 | |||||||
| chr7:130401365 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.642+516A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401365 | |||||||
| chr7:130401467 | TATAAG | T | 119 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(116): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.642+409_642+413del others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401467 | |||||||
| chr7:130401656 | T | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+225A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401656 | |||||||
| chr7:130401797 | T | C | 7 | a0001c0001t0005g0098 a0001c0001t0014g0225 a0001c0001t0014g0230 others(4): Show |
7 | HG01243.hp1 NA18950.hp2 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+84A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401797 | |||||||
| chr7:130402251 | T | C | 1 | a0001c0001t0039g0203 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.575-303A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402251 | |||||||
| chr7:130402335 | G | C | 1 | a0001c0001t0043g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+313C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402335 | |||||||
| chr7:130402343 | C | CA | 44 | a0001c0001t0002g0040 a0001c0001t0005g0130 a0001c0001t0005g0158 others(41): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.574+304dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402343 | |||||||
| chr7:130402343 | C | CAA | 12 | a0001c0001t0003g0078 a0001c0001t0006g0103 a0001c0001t0009g0107 others(9): Show |
14 | HG00099.hp1 HG00558.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.574+303_574+304dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402343 | |||||||
| chr7:130402345 | A | AC | 5 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0016g0116 others(2): Show |
5 | HG01192.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+302_574+303ins others(1): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402345 | |||||||
| chr7:130402353 | AC | A | 47 | a0001c0001t0002g0038 a0001c0001t0002g0046 a0001c0001t0002g0048 others(44): Show |
55 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.574+294delG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402353 | |||||||
| chr7:130402354 | C | A | 142 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(139): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.574+294G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402354 | |||||||
| chr7:130402379 | A | G | 1 | a0001c0001t0031g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574+269T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402379 | |||||||
| chr7:130402418 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0046 a0001c0001t0002g0048 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.574+230C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402418 | |||||||
| chr7:130402606 | T | C | 1 | a0001c0001t0014g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+42A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402606 | |||||||
| chr7:130402607 | G | T | 1 | a0001c0001t0014g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+41C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402607 | |||||||
| chr7:130402833 | T | C | 1 | a0001c0001t0008g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.423-34A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402833 | |||||||
| chr7:130402856 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-57G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402856 | |||||||
| chr7:130402906 | G | A | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.423-107C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402906 | |||||||
| chr7:130402910 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-111C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402910 | |||||||
| chr7:130402934 | C | T | 6 | a0001c0001t0002g0139 a0001c0001t0013g0008 a0001c0001t0013g0031 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-135G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402934 | |||||||
| chr7:130403043 | C | T | 1 | a0001c0001t0014g0185 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.423-244G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403043 | |||||||
| chr7:130403048 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.423-249G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403048 | |||||||
| chr7:130403139 | G | A | 56 | a0001c0001t0003g0078 a0001c0001t0005g0130 a0001c0001t0006g0013 others(53): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.423-340C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403139 | |||||||
| chr7:130403258 | C | T | 5 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0065g0283 others(2): Show |
5 | HG01257.hp1 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423-459G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403258 | |||||||
| chr7:130403299 | C | T | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-500G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403299 | |||||||
| chr7:130403301 | T | G | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-502A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403301 | |||||||
| chr7:130403303 | C | G | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-504G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403303 | |||||||
| chr7:130403304 | A | T | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-505T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403304 | |||||||
| chr7:130403305 | T | A | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-506A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403305 | |||||||
| chr7:130403350 | T | A | 1 | a0001c0001t0038g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.423-551A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403350 | |||||||
| chr7:130403360 | T | G | 1 | a0001c0001t0051g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.423-561A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403360 | |||||||
| chr7:130403550 | C | T | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.423-751G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403550 | |||||||
| chr7:130403671 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-872C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403671 | |||||||
| chr7:130403724 | A | G | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.422+840T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403724 | |||||||
| chr7:130403770 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.422+794C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403770 | |||||||
| chr7:130403772 | A | T | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+792T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403772 | |||||||
| chr7:130403773 | A | G | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+791T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403773 | |||||||
| chr7:130403774 | C | T | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+790G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403774 | |||||||
| chr7:130403776 | G | C | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+788C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403776 | |||||||
| chr7:130403837 | G | A | 1 | a0001c0001t0005g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.422+727C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403837 | |||||||
| chr7:130404089 | A | G | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422+475T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404089 | |||||||
| chr7:130404196 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+368C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404196 | |||||||
| chr7:130404322 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.422+242G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404322 | |||||||
| chr7:130404810 | A | G | 2 | a0001c0001t0009g0088 a0001c0001t0009g0090 |
2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.278-102T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130404810 | |||||||
| chr7:130405194 | G | A | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-486C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405194 | |||||||
| chr7:130405221 | G | A | 2 | a0001c0001t0073g0286 a0001c0001t0076g0285 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.278-513C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405221 | |||||||
| chr7:130405229 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-521G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405229 | |||||||
| chr7:130405836 | A | G | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-1128T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405836 | |||||||
| chr7:130405842 | G | A | 193 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(190): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.278-1134C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405842 | |||||||
| chr7:130405922 | G | A | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.278-1214C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405922 | |||||||
| chr7:130406110 | TAATA | T | 105 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(102): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.278-1406_278-1403d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406110 | |||||||
| chr7:130406278 | G | GT | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1571dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406278 | |||||||
| chr7:130406285 | T | A | 3 | a0001c0001t0023g0084 a0001c0001t0023g0085 a0001c0001t0034g0299 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.278-1577A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406285 | |||||||
| chr7:130406305 | C | T | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.278-1597G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406305 | |||||||
| chr7:130406417 | C | T | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.278-1709G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406417 | |||||||
| chr7:130406514 | G | A | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.278-1806C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406514 | |||||||
| chr7:130406824 | T | TG | 8 | a0001c0001t0001g0263 a0001c0001t0002g0056 a0001c0001t0002g0086 others(5): Show |
8 | HG00140.hp2 HG01261.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-2117dupC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406824 | |||||||
| chr7:130406829 | G | GA | 6 | a0001c0001t0002g0051 a0001c0001t0002g0174 a0001c0001t0006g0115 others(3): Show |
6 | HG02258.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2122_278-2121i others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406829 | |||||||
| chr7:130406832 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2124G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406832 | |||||||
| chr7:130406928 | G | C | 194 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(191): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.278-2220C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406928 | |||||||
| chr7:130406964 | A | G | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2256T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406964 | |||||||
| chr7:130406989 | T | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2281A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406989 | |||||||
| chr7:130407206 | G | A | 67 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(64): Show |
78 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.278-2498C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407206 | |||||||
| chr7:130407219 | A | T | 1 | a0001c0001t0018g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.278-2511T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407219 | |||||||
| chr7:130407253 | A | AAC | 23 | a0001c0001t0001g0251 a0001c0001t0003g0153 a0001c0001t0005g0130 others(20): Show |
23 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.278-2547_278-2546d others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | A | AACAC | 7 | a0001c0001t0001g0216 a0001c0001t0035g0236 a0001c0001t0035g0255 others(4): Show |
7 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-2549_278-2546d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | A | AACACAC | 4 | a0001c0001t0016g0114 a0001c0001t0016g0119 a0001c0001t0022g0172 others(1): Show |
4 | HG01978.hp1 HG01978.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2551_278-2546d others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | AAC | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(160): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.278-2547_278-2546d others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | AACAC | A | 26 | a0001c0001t0001g0224 a0001c0001t0001g0284 a0001c0001t0001g0297 others(23): Show |
26 | HG00733.hp1 HG00738.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.278-2549_278-2546d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | AACACAC | A | 13 | a0001c0001t0001g0221 a0001c0001t0001g0266 a0001c0001t0002g0048 others(10): Show |
14 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-2551_278-2546d others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | AACACACA others(1): Show |
A | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-2553_278-2546d others(10): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407253 | AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0049 a0004c0004t0081g0293 |
2 | HG02523.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.278-2555_278-2546d others(12): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | |||||||
| chr7:130407255 | C | CAA | 3 | a0001c0001t0002g0086 a0001c0001t0026g0298 a0001c0001t0034g0269 |
3 | HG02280.hp1 HG02886.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.278-2548_278-2547i others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407255 | |||||||
| chr7:130407257 | C | A | 6 | a0001c0001t0002g0173 a0001c0001t0008g0302 a0001c0001t0010g0128 others(3): Show |
6 | HG00639.hp1 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2549G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407257 | |||||||
| chr7:130407259 | C | A | 40 | a0001c0001t0002g0018 a0001c0001t0002g0094 a0001c0001t0002g0096 others(37): Show |
50 | HG01070.hp2 HG01099.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.278-2551G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407259 | |||||||
| chr7:130407261 | C | A | 4 | a0001c0001t0004g0195 a0001c0001t0023g0084 a0001c0001t0023g0085 others(1): Show |
4 | HG00738.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2553G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407261 | |||||||
| chr7:130407263 | C | A | 1 | a0001c0001t0023g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.278-2555G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407263 | |||||||
| chr7:130407567 | T | C | 54 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(51): Show |
64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.278-2859A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407567 | |||||||
| chr7:130407825 | C | T | 67 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(64): Show |
78 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.278-3117G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407825 | |||||||
| chr7:130407991 | A | T | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.277+3131T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407991 | |||||||
| chr7:130408097 | T | G | 4 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0066g0287 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+3025A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408097 | |||||||
| chr7:130408134 | G | A | 3 | a0001c0001t0002g0094 a0001c0001t0008g0270 a0001c0001t0034g0269 |
3 | HG01070.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.277+2988C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408134 | |||||||
| chr7:130408211 | C | A | 1 | a0001c0001t0058g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.277+2911G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408211 | |||||||
| chr7:130408309 | A | G | 1 | a0001c0001t0013g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.277+2813T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408309 | |||||||
| chr7:130408322 | T | A | 20 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(17): Show |
21 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.277+2800A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408322 | |||||||
| chr7:130408349 | G | A | 1 | a0001c0001t0044g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277+2773C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408349 | |||||||
| chr7:130408387 | A | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+2735T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408387 | |||||||
| chr7:130408806 | G | GA | 7 | a0001c0001t0009g0014 a0001c0001t0009g0109 a0001c0001t0009g0110 others(4): Show |
8 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+2315dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408806 | |||||||
| chr7:130408943 | G | A | 1 | a0001c0001t0013g0031 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.277+2179C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408943 | |||||||
| chr7:130409009 | T | C | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277+2113A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409009 | |||||||
| chr7:130409236 | G | A | 1 | a0001c0001t0017g0227 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+1886C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409236 | |||||||
| chr7:130409237 | C | A | 1 | a0001c0001t0017g0227 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+1885G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409237 | |||||||
| chr7:130409608 | T | G | 1 | a0001c0001t0006g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277+1514A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409608 | |||||||
| chr7:130409765 | T | C | 2 | a0001c0001t0003g0079 a0001c0001t0012g0076 |
2 | NA18950.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.277+1357A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409765 | |||||||
| chr7:130409930 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.277+1192G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409930 | |||||||
| chr7:130409979 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.277+1143G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409979 | |||||||
| chr7:130410024 | G | GTCTTCTT others(8): Show |
1 | a0001c0001t0004g0201 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.277+1083_277+1097d others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410024 | |||||||
| chr7:130410026 | C | CTTCTTTT others(6): Show |
5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+1083_277+1095d others(15): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | |||||||
| chr7:130410026 | C | CTTCTTTT others(7): Show |
3 | a0001c0001t0023g0085 a0001c0001t0027g0273 a0001c0001t0087g0292 |
3 | HG02896.hp1 NA18962.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.277+1082_277+1095d others(16): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | |||||||
| chr7:130410026 | C | CTTCTTTT others(8): Show |
160 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(157): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.277+1081_277+1095d others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | |||||||
| chr7:130410029 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0037g0023 a0001c0001t0048g0030 |
3 | HG02717.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.277+1092_277+1093i others(18): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410029 | |||||||
| chr7:130410029 | C | CTTTTTTT others(10): Show |
1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277+1092_277+1093i others(19): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410029 | |||||||
| chr7:130410030 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0071g0295 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.277+1091_277+1092i others(16): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410030 | |||||||
| chr7:130410041 | T | G | 1 | a0001c0001t0014g0282 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.277+1081A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410041 | |||||||
| chr7:130410048 | C | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0041 others(7): Show |
13 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+1074G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410048 | |||||||
| chr7:130410060 | G | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0051 others(2): Show |
7 | HG02015.hp2 HG02074.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+1062C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410060 | |||||||
| chr7:130410087 | G | A | 1 | a0001c0001t0008g0301 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.277+1035C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410087 | |||||||
| chr7:130410129 | A | G | 173 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(170): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.277+993T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410129 | |||||||
| chr7:130410197 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.277+925A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410197 | |||||||
| chr7:130410262 | C | T | 1 | a0001c0001t0004g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.277+860G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410262 | |||||||
| chr7:130410274 | G | A | 1 | a0001c0001t0042g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.277+848C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410274 | |||||||
| chr7:130410279 | G | T | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277+843C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410279 | |||||||
| chr7:130410331 | G | A | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277+791C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410331 | |||||||
| chr7:130410526 | T | C | 105 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(102): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.277+596A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410526 | |||||||
| chr7:130410692 | C | T | 6 | a0001c0001t0011g0131 a0001c0001t0011g0135 a0001c0001t0011g0137 others(3): Show |
6 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+430G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410692 | |||||||
| chr7:130410720 | T | A | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277+402A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410720 | |||||||
| chr7:130411196 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.208-5A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411196 | |||||||
| chr7:130411229 | T | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.208-38A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411229 | |||||||
| chr7:130411364 | A | G | 3 | a0001c0001t0003g0129 a0001c0001t0037g0023 a0001c0001t0071g0295 |
4 | HG00099.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-173T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411364 | |||||||
| chr7:130411383 | T | C | 2 | a0001c0001t0006g0104 a0001c0001t0006g0105 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.208-192A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411383 | |||||||
| chr7:130411480 | T | G | 1 | a0001c0001t0026g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-289A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411480 | |||||||
| chr7:130411568 | C | T | 4 | a0001c0001t0023g0084 a0001c0001t0023g0085 a0001c0001t0023g0177 others(1): Show |
4 | HG02615.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-377G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411568 | |||||||
| chr7:130411601 | C | T | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-410G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411601 | |||||||
| chr7:130411640 | T | C | 53 | a0001c0001t0003g0129 a0001c0001t0005g0130 a0001c0001t0006g0013 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.208-449A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411640 | |||||||
| chr7:130411781 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0065 a0001c0001t0003g0069 others(2): Show |
5 | HG01167.hp2 HG02129.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+398G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411781 | |||||||
| chr7:130412053 | G | A | 1 | a0001c0001t0004g0191 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.207+126C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130412053 | |||||||
| chr7:130412394 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-154T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412394 | |||||||
| chr7:130412395 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-155C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412395 | |||||||
| chr7:130412396 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-156C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412396 | |||||||
| chr7:130412397 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-157A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412397 | |||||||
| chr7:130412398 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-158T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412398 | |||||||
| chr7:130412399 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-159C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412399 | |||||||
| chr7:130412404 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-164T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412404 | |||||||
| chr7:130412405 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-165A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412405 | |||||||
| chr7:130412406 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-166G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412406 | |||||||
| chr7:130412407 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-167T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412407 | |||||||
| chr7:130412409 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-169G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412409 | |||||||
| chr7:130412420 | G | T | 1 | a0001c0001t0008g0301 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.146-180C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412420 | |||||||
| chr7:130412448 | T | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-208A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412448 | |||||||
| chr7:130412546 | G | A | 1 | a0001c0001t0019g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-306C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412546 | |||||||
| chr7:130412563 | C | T | 68 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(65): Show |
79 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.146-323G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412563 | |||||||
| chr7:130413060 | C | T | 1 | a0001c0001t0046g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146-820G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413060 | |||||||
| chr7:130413155 | C | T | 3 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0068g0289 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.146-915G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413155 | |||||||
| chr7:130413270 | C | T | 1 | a0001c0001t0004g0196 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.146-1030G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413270 | |||||||
| chr7:130413282 | C | T | 48 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.146-1042G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413282 | |||||||
| chr7:130413367 | T | C | 175 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0002g0005 others(172): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.146-1127A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413367 | |||||||
| chr7:130413380 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.146-1140A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413380 | |||||||
| chr7:130413584 | A | C | 11 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(8): Show |
12 | HG00558.hp2 HG01257.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.146-1344T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413584 | |||||||
| chr7:130413590 | C | A | 2 | a0001c0001t0002g0045 a0001c0001t0072g0240 |
2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.146-1350G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413590 | |||||||
| chr7:130413590 | C | CA | 168 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0002g0005 others(165): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.146-1351dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413590 | |||||||
| chr7:130413814 | A | G | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1574T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413814 | |||||||
| chr7:130413859 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.146-1619G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413859 | |||||||
| chr7:130414227 | A | G | 6 | a0001c0001t0014g0225 a0001c0001t0014g0230 a0001c0001t0014g0282 others(3): Show |
6 | NA18950.hp2 NA18987.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1987T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414227 | |||||||
| chr7:130414298 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.146-2058G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414298 | |||||||
| chr7:130414483 | T | C | 1 | a0001c0001t0019g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146-2243A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414483 | |||||||
| chr7:130414611 | T | C | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.145+2308A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414611 | |||||||
| chr7:130414706 | G | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.145+2213C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414706 | |||||||
| chr7:130414802 | G | A | 1 | a0001c0001t0025g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.145+2117C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414802 | |||||||
| chr7:130414844 | G | A | 1 | a0001c0001t0010g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.145+2075C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414844 | |||||||
| chr7:130415271 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0001g0265 others(2): Show |
11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+1648A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415271 | |||||||
| chr7:130415443 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1476C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415443 | |||||||
| chr7:130415589 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145+1330G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415589 | |||||||
| chr7:130415637 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1282C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415637 | |||||||
| chr7:130415678 | G | T | 53 | a0001c0001t0003g0129 a0001c0001t0005g0130 a0001c0001t0006g0013 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+1241C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415678 | |||||||
| chr7:130415848 | A | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1071T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415848 | |||||||
| chr7:130415875 | T | C | 1 | a0001c0001t0011g0135 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.145+1044A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415875 | |||||||
| chr7:130415883 | G | A | 1 | a0001c0001t0073g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.145+1036C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415883 | |||||||
| chr7:130415889 | G | A | 1 | a0001c0001t0024g0012 | 2 | HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.145+1030C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415889 | |||||||
| chr7:130415922 | T | C | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.145+997A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415922 | |||||||
| chr7:130416041 | A | C | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145+878T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416041 | |||||||
| chr7:130416245 | C | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.145+674G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416245 | |||||||
| chr7:130416468 | C | T | 3 | a0001c0001t0003g0129 a0001c0001t0037g0023 a0001c0001t0071g0295 |
4 | HG00099.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+451G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416468 | |||||||
| chr7:130416481 | C | T | 1 | a0001c0001t0009g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.145+438G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416481 | |||||||
| chr7:130416520 | AG | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+398delC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416520 | |||||||
| chr7:130416532 | A | G | 54 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(51): Show |
64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.145+387T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416532 | |||||||
| chr7:130416547 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+372G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416547 | |||||||
| chr7:130416561 | T | C | 4 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0066g0287 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+358A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416561 | |||||||
| chr7:130416593 | T | C | 1 | a0001c0001t0005g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.145+326A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416593 | |||||||
| chr7:130416608 | T | G | 5 | a0001c0001t0050g0025 a0001c0001t0054g0026 a0001c0001t0055g0027 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+311A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416608 | |||||||
| chr7:130416623 | A | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+296T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416623 | |||||||
| chr7:130416642 | G | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+277C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416642 | |||||||
| chr7:130416861 | C | G | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.145+58G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416861 | |||||||
| chr7:130417036 | A | G | 1 | a0001c0001t0044g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98-70T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417036 | |||||||
| chr7:130417263 | A | G | 1 | a0001c0001t0016g0119 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.98-297T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417263 | |||||||
| chr7:130417320 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-354C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417320 | |||||||
| chr7:130417378 | G | A | 1 | a0001c0001t0035g0236 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.98-412C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417378 | |||||||
| chr7:130417414 | G | A | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98-448C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417414 | |||||||
| chr7:130417862 | C | G | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-896G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417862 | |||||||
| chr7:130418110 | T | G | 3 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0068g0289 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.98-1144A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418110 | |||||||
| chr7:130418259 | T | C | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.98-1293A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418259 | |||||||
| chr7:130418333 | C | CTCTG | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1368_98-1367ins others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418333 | |||||||
| chr7:130418334 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1368C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418334 | |||||||
| chr7:130418347 | A | G | 1 | a0002c0002t0005g0074 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.98-1381T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418347 | |||||||
| chr7:130418405 | A | G | 48 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.98-1439T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418405 | |||||||
| chr7:130418550 | T | A | 1 | a0001c0001t0045g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98-1584A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418550 | |||||||
| chr7:130418658 | C | G | 54 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(51): Show |
64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.98-1692G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418658 | |||||||
| chr7:130419254 | T | C | 1 | a0001c0001t0004g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.98-2288A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419254 | |||||||
| chr7:130419446 | T | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-2480A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419446 | |||||||
| chr7:130419467 | GA | G | 4 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0066g0287 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2502delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419467 | |||||||
| chr7:130419472 | C | T | 1 | a0001c0001t0045g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98-2506G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419472 | |||||||
| chr7:130419501 | T | C | 1 | a0001c0001t0019g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-2535A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419501 | |||||||
| chr7:130419535 | T | G | 54 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(51): Show |
64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.98-2569A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419535 | |||||||
| chr7:130419581 | T | A | 91 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(88): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.98-2615A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419581 | |||||||
| chr7:130419581 | T | TA | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-2616dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419581 | |||||||
| chr7:130419582 | A | T | 4 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0007g0259 others(1): Show |
4 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2616T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419582 | |||||||
| chr7:130419670 | C | T | 9 | a0001c0001t0003g0024 a0001c0001t0003g0068 a0001c0001t0003g0082 others(6): Show |
10 | HG01891.hp1 HG01943.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-2704G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419670 | |||||||
| chr7:130419950 | T | TAC | 34 | a0001c0001t0001g0237 a0001c0001t0004g0192 a0001c0001t0004g0200 others(31): Show |
37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.98-2986_98-2985dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419950 | |||||||
| chr7:130420124 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3158G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420124 | |||||||
| chr7:130420215 | A | G | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.98-3249T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420215 | |||||||
| chr7:130420240 | G | A | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-3274C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420240 | |||||||
| chr7:130420328 | C | CA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(72): Show |
91 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.98-3363dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | |||||||
| chr7:130420328 | C | CAA | 55 | a0001c0001t0001g0216 a0001c0001t0001g0251 a0001c0001t0001g0257 others(52): Show |
65 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.98-3364_98-3363dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | |||||||
| chr7:130420328 | CA | C | 94 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.98-3363delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | |||||||
| chr7:130420328 | CAA | C | 7 | a0001c0001t0005g0130 a0001c0001t0022g0172 a0001c0001t0030g0133 others(4): Show |
7 | HG02056.hp2 HG02080.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-3364_98-3363del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | |||||||
| chr7:130420328 | CAAA | C | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-3365_98-3363del others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | |||||||
| chr7:130420410 | G | A | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.98-3444C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420410 | |||||||
| chr7:130420412 | A | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3446T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420412 | |||||||
| chr7:130420539 | C | T | 5 | a0001c0001t0011g0131 a0001c0001t0011g0135 a0001c0001t0030g0133 others(2): Show |
5 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-3573G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420539 | |||||||
| chr7:130420600 | C | T | 2 | a0001c0001t0019g0159 a0001c0001t0019g0163 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.98-3634G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420600 | |||||||
| chr7:130420643 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3677C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420643 | |||||||
| chr7:130420687 | G | A | 1 | a0001c0001t0030g0136 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.98-3721C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420687 | |||||||
| chr7:130420728 | C | T | 1 | a0001c0001t0009g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98-3762G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420728 | |||||||
| chr7:130420759 | G | A | 5 | a0001c0001t0050g0025 a0001c0001t0054g0026 a0001c0001t0055g0027 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-3793C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420759 | |||||||
| chr7:130420782 | T | A | 43 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(40): Show |
49 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-3816A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420782 | |||||||
| chr7:130420843 | A | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3877T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420843 | |||||||
| chr7:130420931 | A | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-3965T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420931 | |||||||
| chr7:130420965 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.98-3999C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420965 | |||||||
| chr7:130421257 | G | C | 9 | a0001c0001t0006g0013 a0001c0001t0006g0101 a0001c0001t0006g0102 others(6): Show |
10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-4291C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421257 | |||||||
| chr7:130421737 | G | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-4771C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421737 | |||||||
| chr7:130421904 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.98-4938G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421904 | |||||||
| chr7:130421991 | A | G | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-5025T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421991 | |||||||
| chr7:130422026 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.98-5060T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422026 | |||||||
| chr7:130422237 | T | C | 2 | a0001c0001t0008g0210 a0001c0001t0021g0205 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.98-5271A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422237 | |||||||
| chr7:130422548 | C | T | 98 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(95): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.97+5407G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422548 | |||||||
| chr7:130422684 | C | T | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.97+5271G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422684 | |||||||
| chr7:130423037 | C | T | 1 | a0001c0001t0008g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+4918G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423037 | |||||||
| chr7:130423239 | C | T | 1 | a0001c0001t0008g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97+4716G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423239 | |||||||
| chr7:130423348 | A | G | 171 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(168): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.97+4607T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423348 | |||||||
| chr7:130423592 | T | C | 1 | a0001c0001t0063g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.97+4363A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423592 | |||||||
| chr7:130423882 | T | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+4073A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423882 | |||||||
| chr7:130423967 | A | G | 4 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0007g0259 others(1): Show |
4 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3988T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423967 | |||||||
| chr7:130424029 | G | A | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+3926C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424029 | |||||||
| chr7:130424194 | C | T | 3 | a0001c0001t0003g0063 a0001c0001t0003g0065 a0001c0001t0003g0071 |
3 | HG01167.hp2 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.97+3761G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424194 | |||||||
| chr7:130424399 | CA | C | 20 | a0001c0001t0001g0228 a0001c0001t0001g0234 a0001c0001t0001g0237 others(17): Show |
21 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.97+3555delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424399 | |||||||
| chr7:130424597 | T | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+3358A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424597 | |||||||
| chr7:130424646 | T | C | 53 | a0001c0001t0003g0129 a0001c0001t0005g0130 a0001c0001t0006g0013 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.97+3309A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424646 | |||||||
| chr7:130424698 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+3257G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424698 | |||||||
| chr7:130425155 | G | A | 2 | a0001c0001t0006g0104 a0001c0001t0006g0105 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.97+2800C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425155 | |||||||
| chr7:130425217 | A | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0041 others(7): Show |
13 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+2738T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425217 | |||||||
| chr7:130425238 | A | AC | 191 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(188): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.97+2716dupG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425238 | |||||||
| chr7:130425263 | A | C | 59 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(56): Show |
69 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.97+2692T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425263 | |||||||
| chr7:130425474 | T | C | 1 | a0001c0001t0016g0119 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.97+2481A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425474 | |||||||
| chr7:130425501 | C | A | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2454G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425501 | |||||||
| chr7:130425513 | A | G | 22 | a0001c0001t0003g0140 a0001c0001t0005g0017 a0001c0001t0005g0141 others(19): Show |
24 | HG01175.hp1 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+2442T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425513 | |||||||
| chr7:130425588 | T | C | 171 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(168): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.97+2367A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425588 | |||||||
| chr7:130425638 | T | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2317A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425638 | |||||||
| chr7:130425648 | G | C | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.97+2307C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425648 | |||||||
| chr7:130425699 | A | C | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+2256T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425699 | |||||||
| chr7:130425857 | A | G | 2 | a0001c0001t0004g0188 a0001c0001t0018g0186 |
2 | HG01361.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.97+2098T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425857 | |||||||
| chr7:130425890 | A | G | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2065T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425890 | |||||||
| chr7:130426186 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1769G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426186 | |||||||
| chr7:130426317 | A | G | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+1638T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426317 | |||||||
| chr7:130426367 | G | A | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+1588C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426367 | |||||||
| chr7:130426437 | GGAAA | G | 9 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(6): Show |
10 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+1514_97+1517del others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426437 | |||||||
| chr7:130426438 | GAAAGA | G | 59 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(56): Show |
69 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.97+1512_97+1516del others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426438 | |||||||
| chr7:130426445 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1510T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426445 | |||||||
| chr7:130426449 | A | ATCAGTAA others(10): Show |
1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1505_97+1506ins others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426449 | |||||||
| chr7:130426452 | A | C | 1 | a0001c0001t0005g0144 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.97+1503T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426452 | |||||||
| chr7:130426484 | A | G | 1 | a0001c0001t0006g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1471T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426484 | |||||||
| chr7:130426556 | C | T | 1 | a0001c0001t0045g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.97+1399G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426556 | |||||||
| chr7:130426558 | T | A | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1397A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426558 | |||||||
| chr7:130426979 | CG | C | 61 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(58): Show |
71 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.97+975delC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426979 | |||||||
| chr7:130427085 | G | A | 1 | a0001c0001t0004g0193 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.97+870C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427085 | |||||||
| chr7:130427099 | G | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+856C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427099 | |||||||
| chr7:130427241 | C | T | 61 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(58): Show |
71 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.97+714G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427241 | |||||||
| chr7:130427281 | A | C | 3 | a0001c0001t0022g0170 a0001c0001t0022g0171 a0001c0001t0022g0172 |
3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.97+674T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427281 | |||||||
| chr7:130427291 | A | C | 4 | a0001c0001t0003g0140 a0001c0001t0005g0155 a0001c0001t0005g0161 others(1): Show |
4 | NA18964.hp2 NA19060.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+664T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427291 | |||||||
| chr7:130427374 | G | A | 1 | a0001c0001t0007g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.97+581C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427374 | |||||||
| chr7:130427459 | T | C | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+496A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427459 | |||||||
| chr7:130427469 | T | C | 1 | a0001c0001t0011g0178 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97+486A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427469 | |||||||
| chr7:130427477 | C | A | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+478G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427477 | |||||||
| chr7:130427478 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+477A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427478 | |||||||
| chr7:130427481 | A | T | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+474T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427481 | |||||||
| chr7:130427525 | T | C | 3 | a0001c0001t0022g0170 a0001c0001t0022g0171 a0001c0001t0022g0172 |
3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.97+430A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427525 | |||||||
| chr7:130427532 | T | C | 2 | a0001c0001t0003g0064 a0001c0001t0003g0078 |
2 | HG02895.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+423A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427532 | |||||||
| chr7:130427827 | C | T | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.97+128G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427827 | |||||||
| chr7:130427878 | C | T | 1 | a0001c0001t0007g0259 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97+77G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427878 | |||||||
| chr7:130427912 | C | T | 1 | a0001c0001t0016g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97+43G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427912 | |||||||
| chr7:130428062 | A | T | 1 | a0001c0001t0043g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.34-44T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428062 | |||||||
| chr7:130428162 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.34-144C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428162 | |||||||
| chr7:130428163 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-145G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428163 | |||||||
| chr7:130428331 | G | A | 3 | a0001c0001t0029g0166 a0001c0001t0029g0167 a0001c0001t0065g0283 |
3 | HG01257.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-313C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428331 | |||||||
| chr7:130428425 | A | T | 1 | a0001c0001t0002g0039 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.34-407T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428425 | |||||||
| chr7:130428428 | C | CA | 99 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0002g0005 others(96): Show |
115 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.34-411dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | |||||||
| chr7:130428428 | C | CAA | 50 | a0001c0001t0002g0086 a0001c0001t0002g0173 a0001c0001t0003g0129 others(47): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.34-412_34-411dupTT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | |||||||
| chr7:130428428 | C | CAAA | 12 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0011g0118 others(9): Show |
12 | HG01192.hp2 HG01361.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.34-413_34-411dupTT others(1): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | |||||||
| chr7:130428428 | CA | C | 15 | a0001c0001t0001g0231 a0001c0001t0001g0258 a0001c0001t0003g0140 others(12): Show |
16 | HG02074.hp2 NA18944.hp2 NA18964.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-411delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | |||||||
| chr7:130428428 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-421_34-411delTT others(9): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | |||||||
| chr7:130428688 | T | C | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-670A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428688 | |||||||
| chr7:130428696 | AAGGTCAG others(1): Show |
A | 2 | a0001c0001t0004g0019 a0001c0001t0004g0214 |
3 | HG03490.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.34-686_34-679delCC others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428696 | |||||||
| chr7:130428718 | T | C | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-700A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428718 | |||||||
| chr7:130428792 | C | T | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-774G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428792 | |||||||
| chr7:130428857 | G | A | 1 | a0001c0001t0008g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.34-839C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428857 | |||||||
| chr7:130428914 | A | AAAAT | 12 | a0001c0001t0002g0056 a0001c0001t0003g0140 a0001c0001t0005g0155 others(9): Show |
12 | HG00621.hp2 HG01175.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-900_34-897dupAT others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428914 | |||||||
| chr7:130428918 | T | A | 63 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(60): Show |
73 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.34-900A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428918 | |||||||
| chr7:130428922 | T | A | 8 | a0001c0001t0004g0183 a0001c0001t0004g0195 a0001c0001t0023g0177 others(5): Show |
8 | HG00738.hp2 HG01257.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.34-904A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428922 | |||||||
| chr7:130428925 | A | AAT | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-908_34-907insAT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428925 | |||||||
| chr7:130428926 | T | A | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-908A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428926 | |||||||
| chr7:130428960 | G | T | 2 | a0001c0001t0003g0073 a0001c0001t0007g0229 |
2 | NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.34-942C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428960 | |||||||
| chr7:130429034 | A | G | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34-1016T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429034 | |||||||
| chr7:130429051 | G | T | 29 | a0001c0001t0005g0130 a0001c0001t0009g0014 a0001c0001t0009g0088 others(26): Show |
30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.34-1033C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429051 | |||||||
| chr7:130429329 | CAT | C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
7 | HG01099.hp1 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-1313_34-1312del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429329 | |||||||
| chr7:130429471 | T | C | 2 | a0001c0001t0003g0063 a0001c0001t0003g0071 |
2 | HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.34-1453A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429471 | |||||||
| chr7:130429508 | T | G | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-1490A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429508 | |||||||
| chr7:130429527 | A | G | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-1509T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429527 | |||||||
| chr7:130429540 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-1522C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429540 | |||||||
| chr7:130429569 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.34-1551G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429569 | |||||||
| chr7:130429624 | T | C | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-1606A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429624 | |||||||
| chr7:130429654 | T | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-1636A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429654 | |||||||
| chr7:130429724 | C | T | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-1706G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429724 | |||||||
| chr7:130429983 | C | T | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-1965G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429983 | |||||||
| chr7:130429984 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.34-1966C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429984 | |||||||
| chr7:130430054 | A | T | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-2036T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430054 | |||||||
| chr7:130430401 | C | T | 2 | a0001c0001t0005g0150 a0001c0001t0031g0151 |
2 | HG01884.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.34-2383G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430401 | |||||||
| chr7:130430412 | TTG | T | 60 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(57): Show |
70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.34-2396_34-2395del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430412 | |||||||
| chr7:130430427 | C | A | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-2409G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430427 | |||||||
| chr7:130430508 | T | C | 53 | a0001c0001t0003g0129 a0001c0001t0005g0130 a0001c0001t0006g0013 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.34-2490A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430508 | |||||||
| chr7:130430700 | C | T | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-2682G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430700 | |||||||
| chr7:130430729 | C | T | 2 | a0001c0001t0048g0030 a0003c0003t0067g0304 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-2711G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430729 | |||||||
| chr7:130430768 | G | A | 58 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(55): Show |
68 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.34-2750C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430768 | |||||||
| chr7:130430872 | G | C | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-2854C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430872 | |||||||
| chr7:130430995 | G | A | 1 | a0001c0001t0012g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.34-2977C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430995 | |||||||
| chr7:130431125 | T | TAAAA | 60 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(57): Show |
70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.34-3111_34-3108dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431125 | |||||||
| chr7:130431183 | CT | C | 170 | a0001c0001t0001g0257 a0001c0001t0002g0005 a0001c0001t0002g0006 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.34-3166delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431183 | |||||||
| chr7:130431192 | T | A | 1 | a0001c0001t0003g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.34-3174A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431192 | |||||||
| chr7:130431369 | T | C | 1 | a0001c0001t0043g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.34-3351A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431369 | |||||||
| chr7:130431391 | T | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-3373A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431391 | |||||||
| chr7:130431493 | G | A | 54 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(51): Show |
64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.34-3475C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431493 | |||||||
| chr7:130431681 | A | G | 66 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(63): Show |
77 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.34-3663T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431681 | |||||||
| chr7:130431738 | A | G | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-3720T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431738 | |||||||
| chr7:130431756 | G | A | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-3738C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431756 | |||||||
| chr7:130431780 | G | A | 6 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(3): Show |
7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-3762C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431780 | |||||||
| chr7:130431962 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.34-3944A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431962 | |||||||
| chr7:130431996 | C | G | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-3978G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431996 | |||||||
| chr7:130432063 | C | G | 1 | a0001c0001t0005g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.34-4045G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432063 | |||||||
| chr7:130432069 | T | C | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34-4051A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432069 | |||||||
| chr7:130432171 | AT | A | 66 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(63): Show |
77 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.34-4154delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432171 | |||||||
| chr7:130432390 | G | C | 1 | a0001c0001t0006g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.34-4372C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432390 | |||||||
| chr7:130432423 | G | A | 5 | a0001c0001t0050g0025 a0001c0001t0054g0026 a0001c0001t0055g0027 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.34-4405C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432423 | |||||||
| chr7:130432554 | C | T | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-4536G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432554 | |||||||
| chr7:130432588 | C | CA | 50 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(47): Show |
52 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.34-4571dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | C | CAA | 8 | a0001c0001t0002g0139 a0001c0001t0005g0161 a0001c0001t0013g0008 others(5): Show |
9 | HG01891.hp2 HG01934.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.34-4572_34-4571dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | C | CAAA | 8 | a0001c0001t0013g0031 a0001c0001t0027g0272 a0001c0001t0036g0290 others(5): Show |
8 | HG00558.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-4573_34-4571dup others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | C | CAAAA | 38 | a0001c0001t0002g0018 a0001c0001t0002g0094 a0001c0001t0002g0096 others(35): Show |
45 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.34-4574_34-4571dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | C | CAAAAA | 14 | a0001c0001t0002g0086 a0001c0001t0002g0097 a0001c0001t0002g0174 others(11): Show |
17 | HG01106.hp1 HG01123.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.34-4575_34-4571dup others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | CA | C | 10 | a0001c0001t0003g0024 a0001c0001t0009g0108 a0001c0001t0014g0225 others(7): Show |
10 | HG02630.hp1 HG02922.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.34-4571delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432588 | CAAAAAAA | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-4577_34-4571del others(7): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | |||||||
| chr7:130432656 | G | C | 1 | a0001c0001t0045g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.34-4638C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432656 | |||||||
| chr7:130432657 | A | G | 67 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(64): Show |
78 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.34-4639T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432657 | |||||||
| chr7:130432777 | C | T | 1 | a0001c0001t0011g0087 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.34-4759G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432777 | |||||||
| chr7:130432937 | A | C | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-4919T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432937 | |||||||
| chr7:130432961 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-4943C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432961 | |||||||
| chr7:130433064 | G | C | 1 | a0001c0001t0046g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.34-5046C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433064 | |||||||
| chr7:130433082 | G | A | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-5064C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433082 | |||||||
| chr7:130433254 | A | G | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-5236T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433254 | |||||||
| chr7:130433960 | G | A | 1 | a0001c0001t0065g0283 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.34-5942C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433960 | |||||||
| chr7:130434000 | T | G | 1 | a0001c0001t0041g0146 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.34-5982A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434000 | |||||||
| chr7:130434217 | A | G | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-6199T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434217 | |||||||
| chr7:130434258 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-6240G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434258 | |||||||
| chr7:130434259 | C | T | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-6241G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434259 | |||||||
| chr7:130434293 | T | C | 25 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(22): Show |
27 | HG00558.hp2 HG01167.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.34-6275A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434293 | |||||||
| chr7:130434356 | T | A | 62 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(59): Show |
72 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.34-6338A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434356 | |||||||
| chr7:130434357 | A | T | 6 | a0001c0001t0009g0107 a0001c0001t0013g0008 a0001c0001t0013g0031 others(3): Show |
7 | HG00558.hp2 HG01255.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-6339T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434357 | |||||||
| chr7:130434372 | T | G | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-6354A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434372 | |||||||
| chr7:130434389 | G | T | 166 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(163): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.34-6371C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434389 | |||||||
| chr7:130434403 | G | C | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-6385C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434403 | |||||||
| chr7:130434501 | A | G | 4 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0066g0287 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+6433T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434501 | |||||||
| chr7:130435156 | C | A | 1 | a0001c0001t0008g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.33+5778G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435156 | |||||||
| chr7:130435442 | G | T | 9 | a0001c0001t0006g0013 a0001c0001t0006g0101 a0001c0001t0006g0102 others(6): Show |
10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+5492C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435442 | |||||||
| chr7:130435482 | C | T | 3 | a0001c0001t0003g0149 a0001c0001t0012g0148 a0001c0001t0025g0278 |
3 | HG01261.hp1 HG01496.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.33+5452G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435482 | |||||||
| chr7:130435529 | C | T | 48 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.33+5405G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435529 | |||||||
| chr7:130435667 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.33+5267C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435667 | |||||||
| chr7:130435680 | G | A | 1 | a0001c0001t0004g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.33+5254C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435680 | |||||||
| chr7:130435737 | C | T | 1 | a0003c0003t0067g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33+5197G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435737 | |||||||
| chr7:130435771 | A | G | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+5163T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435771 | |||||||
| chr7:130435893 | G | A | 1 | a0001c0001t0015g0062 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.33+5041C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435893 | |||||||
| chr7:130436041 | C | T | 1 | a0001c0001t0019g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33+4893G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436041 | |||||||
| chr7:130436062 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33+4872C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436062 | |||||||
| chr7:130436082 | C | T | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4852G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436082 | |||||||
| chr7:130436113 | C | T | 1 | a0001c0001t0041g0146 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.33+4821G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436113 | |||||||
| chr7:130436191 | C | T | 9 | a0001c0001t0006g0013 a0001c0001t0006g0101 a0001c0001t0006g0102 others(6): Show |
10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+4743G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436191 | |||||||
| chr7:130436266 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.33+4668G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436266 | |||||||
| chr7:130436285 | GA | G | 15 | a0001c0001t0003g0024 a0001c0001t0003g0063 a0001c0001t0003g0065 others(12): Show |
16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.33+4648delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436285 | |||||||
| chr7:130436304 | C | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+4630G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436304 | |||||||
| chr7:130436342 | A | T | 171 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(168): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.33+4592T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436342 | |||||||
| chr7:130436407 | T | C | 1 | a0001c0001t0089g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.33+4527A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436407 | |||||||
| chr7:130436578 | TGTACTCA others(19): Show |
T | 50 | a0001c0001t0005g0130 a0001c0001t0006g0013 a0001c0001t0006g0101 others(47): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.33+4330_33+4355del others(26): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436578 | |||||||
| chr7:130436605 | G | A | 50 | a0001c0001t0005g0130 a0001c0001t0006g0013 a0001c0001t0006g0101 others(47): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.33+4329C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436605 | |||||||
| chr7:130436641 | CTA | C | 9 | a0001c0001t0002g0173 a0001c0001t0004g0019 a0001c0001t0004g0214 others(6): Show |
10 | HG01257.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+4291_33+4292del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436641 | |||||||
| chr7:130436642 | TA | T | 52 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(49): Show |
61 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.33+4291delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436642 | |||||||
| chr7:130436643 | A | T | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4291T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | |||||||
| chr7:130436643 | AT | A | 50 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
57 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.33+4290delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | |||||||
| chr7:130436643 | ATT | A | 57 | a0001c0001t0002g0038 a0001c0001t0002g0046 a0001c0001t0002g0048 others(54): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.33+4289_33+4290del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | |||||||
| chr7:130436655 | T | C | 1 | a0001c0001t0013g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.33+4279A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436655 | |||||||
| chr7:130436762 | A | G | 63 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(60): Show |
73 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.33+4172T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436762 | |||||||
| chr7:130436765 | G | A | 104 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(101): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.33+4169C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436765 | |||||||
| chr7:130436821 | G | T | 2 | a0001c0001t0005g0144 a0001c0001t0005g0162 |
2 | NA19011.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.33+4113C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436821 | |||||||
| chr7:130436844 | C | G | 1 | a0001c0001t0087g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4090G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436844 | |||||||
| chr7:130436940 | G | A | 48 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.33+3994C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436940 | |||||||
| chr7:130437012 | C | G | 63 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(60): Show |
73 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.33+3922G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437012 | |||||||
| chr7:130437055 | C | A | 63 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(60): Show |
73 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.33+3879G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437055 | |||||||
| chr7:130437173 | G | A | 5 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0032 others(2): Show |
6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+3761C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437173 | |||||||
| chr7:130437365 | C | CA | 165 | a0001c0001t0001g0266 a0001c0001t0002g0005 a0001c0001t0002g0006 others(162): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.33+3568dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437365 | |||||||
| chr7:130437412 | A | G | 167 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(164): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.33+3522T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437412 | |||||||
| chr7:130437581 | G | A | 1 | a0001c0001t0005g0162 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.33+3353C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437581 | |||||||
| chr7:130437595 | A | AC | 103 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(100): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.33+3338dupG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437595 | |||||||
| chr7:130437759 | T | A | 3 | a0001c0001t0036g0290 a0001c0001t0036g0291 a0001c0001t0068g0289 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.33+3175A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437759 | |||||||
| chr7:130437764 | C | CA | 9 | a0001c0001t0001g0268 a0001c0001t0001g0297 a0001c0001t0003g0082 others(6): Show |
9 | HG00597.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.33+3169dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | |||||||
| chr7:130437764 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0013g0008 a0001c0001t0013g0031 a0001c0001t0013g0168 |
4 | HG00558.hp2 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+3153_33+3169dup others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | |||||||
| chr7:130437764 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0013g0032 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33+3152_33+3169dup others(18): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | |||||||
| chr7:130437764 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0013g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.33+3147_33+3169dup others(23): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | |||||||
| chr7:130437764 | CA | C | 6 | a0001c0001t0001g0216 a0001c0001t0003g0063 a0001c0001t0003g0064 others(3): Show |
6 | HG01167.hp2 HG01934.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+3169delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | |||||||
| chr7:130437774 | AAAAAAAA others(14): Show |
A | 1 | a0004c0004t0081g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.33+3139_33+3159del others(21): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437774 | |||||||
| chr7:130437775 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33+3139_33+3158del others(20): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437775 | |||||||
| chr7:130437777 | A | AAAG | 36 | a0001c0001t0004g0004 a0001c0001t0004g0019 a0001c0001t0004g0182 others(33): Show |
45 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.33+3156_33+3157ins others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437777 | |||||||
| chr7:130437777 | A | AAG | 19 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(16): Show |
20 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.33+3156_33+3157ins others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437777 | |||||||
| chr7:130437784 | AAAAAGAA others(4): Show |
A | 3 | a0001c0001t0008g0301 a0001c0001t0016g0114 a0001c0001t0026g0303 |
3 | HG02965.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.33+3139_33+3149del others(11): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437784 | |||||||
| chr7:130437785 | AAAAGAAA others(3): Show |
A | 38 | a0001c0001t0003g0129 a0001c0001t0005g0130 a0001c0001t0006g0013 others(35): Show |
40 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.33+3139_33+3148del others(10): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437785 | |||||||
| chr7:130437786 | AAAGAAAA others(2): Show |
A | 44 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(41): Show |
47 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.33+3139_33+3147del others(9): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437786 | |||||||
| chr7:130437787 | AAGAAAAA others(1): Show |
A | 15 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0040 others(12): Show |
16 | HG02015.hp2 HG02074.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.33+3139_33+3146del others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437787 | |||||||
| chr7:130437789 | G | A | 1 | a0001c0001t0029g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.33+3145C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437789 | |||||||
| chr7:130437795 | G | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+3139C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437795 | |||||||
| chr7:130438112 | G | A | 1 | a0001c0001t0004g0201 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.33+2822C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438112 | |||||||
| chr7:130438312 | C | T | 1 | a0001c0001t0018g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.33+2622G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438312 | |||||||
| chr7:130438332 | C | T | 62 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(59): Show |
72 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.33+2602G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438332 | |||||||
| chr7:130438401 | C | A | 165 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(162): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.33+2533G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438401 | |||||||
| chr7:130438450 | C | T | 170 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.33+2484G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438450 | |||||||
| chr7:130438455 | A | C | 1 | a0001c0001t0003g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.33+2479T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438455 | |||||||
| chr7:130438473 | T | C | 29 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0094 others(26): Show |
30 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.33+2461A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438473 | |||||||
| chr7:130438610 | C | T | 1 | a0001c0001t0012g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.33+2324G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438610 | |||||||
| chr7:130438771 | A | C | 4 | a0001c0001t0020g0015 a0001c0001t0020g0122 a0001c0001t0020g0123 others(1): Show |
5 | NA18747.hp1 NA18982.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+2163T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438771 | |||||||
| chr7:130438860 | T | C | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+2074A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438860 | |||||||
| chr7:130438869 | T | A | 5 | a0001c0001t0008g0276 a0001c0001t0027g0272 a0001c0001t0027g0273 others(2): Show |
5 | HG00438.hp2 NA18943.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+2065A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438869 | |||||||
| chr7:130438998 | T | C | 1 | a0001c0001t0005g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33+1936A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438998 | |||||||
| chr7:130439009 | A | G | 1 | a0001c0001t0048g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.33+1925T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439009 | |||||||
| chr7:130439023 | T | C | 2 | a0001c0001t0002g0086 a0001c0001t0008g0302 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.33+1911A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439023 | |||||||
| chr7:130439078 | C | T | 2 | a0001c0001t0066g0287 a0001c0001t0087g0292 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33+1856G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439078 | |||||||
| chr7:130439084 | C | T | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+1850G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439084 | |||||||
| chr7:130439149 | T | G | 2 | a0001c0001t0002g0086 a0001c0001t0008g0302 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.33+1785A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439149 | |||||||
| chr7:130439171 | C | G | 1 | a0001c0001t0066g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+1763G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439171 | |||||||
| chr7:130439251 | G | C | 7 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0173 others(4): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+1683C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439251 | |||||||
| chr7:130439298 | G | A | 38 | a0001c0001t0002g0086 a0001c0001t0002g0120 a0001c0001t0006g0013 others(35): Show |
40 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.33+1636C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439298 | |||||||
| chr7:130439349 | G | GT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(246): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.33+1584dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439349 | |||||||
| chr7:130439468 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(200): Show |
238 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.33+1466G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439468 | |||||||
| chr7:130439554 | G | A | 1 | a0001c0001t0023g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33+1380C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439554 | |||||||
| chr7:130439573 | C | T | 4 | a0001c0001t0004g0182 a0001c0001t0004g0183 a0001c0001t0014g0184 others(1): Show |
4 | NA18944.hp2 NA18964.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+1361G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439573 | |||||||
| chr7:130439641 | C | T | 5 | a0001c0001t0050g0025 a0001c0001t0054g0026 a0001c0001t0055g0027 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+1293G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439641 | |||||||
| chr7:130439675 | C | T | 1 | a0001c0001t0071g0295 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.33+1259G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439675 | |||||||
| chr7:130439715 | A | G | 5 | a0001c0001t0050g0025 a0001c0001t0054g0026 a0001c0001t0055g0027 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+1219T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439715 | |||||||
| chr7:130439862 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.33+1072G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439862 | |||||||
| chr7:130439993 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(128): Show |
154 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.33+941G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439993 | |||||||
| chr7:130440006 | C | T | 1 | a0001c0001t0025g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.33+928G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440006 | |||||||
| chr7:130440050 | G | A | 10 | a0001c0001t0001g0297 a0001c0001t0004g0296 a0001c0001t0008g0301 others(7): Show |
11 | HG00099.hp1 HG01993.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.33+884C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440050 | |||||||
| chr7:130440056 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(131): Show |
157 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.33+878T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440056 | |||||||
| chr7:130440107 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0181 others(132): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.33+827A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440107 | |||||||
| chr7:130440136 | C | T | 3 | a0001c0001t0001g0284 a0001c0001t0073g0286 a0001c0001t0076g0285 |
3 | HG02486.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+798G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440136 | |||||||
| chr7:130440144 | C | A | 1 | a0001c0001t0019g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.33+790G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440144 | |||||||
| chr7:130440188 | T | C | 1 | a0001c0001t0053g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.33+746A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440188 | |||||||
| chr7:130440314 | G | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+620C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440314 | |||||||
| chr7:130440363 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+571T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440363 | |||||||
| chr7:130440699 | T | C | 22 | a0001c0001t0001g0284 a0001c0001t0001g0297 a0001c0001t0004g0296 others(19): Show |
23 | HG00099.hp1 HG01891.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.33+235A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440699 | |||||||
| chr7:130440782 | G | GCCCGC | 11 | a0001c0001t0002g0018 a0001c0001t0002g0173 a0001c0001t0002g0174 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.33+147_33+151dupGC others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440782 | |||||||
| chr7:130440793 | C | T | 1 | a0001c0001t0033g0179 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.33+141G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440793 | |||||||
| chr7:130440890 | T | C | 1 | a0001c0001t0011g0178 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.33+44A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440890 |