Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8895 |
| ensemblid | ENSG00000085719.13 |
| hgncid | 2316 |
| symbol | CPNE3 |
| name | copine 3 |
| refseq_nuc | NM_003909.5 |
| refseq_prot | NP_003900.1 |
| ensembl_nuc | ENST00000517490.6 |
| ensembl_prot | ENSP00000477590.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 86514435 |
| end | 86561498 |
| strand | + |
| ver | v1.2 |
| region | chr8:86514435-86561498 |
| region5000 | chr8:86509435-86566498 |
| regionname0 | CPNE3_chr8_86514435_86561498 |
| regionname5000 | CPNE3_chr8_86509435_86566498 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 537 | 261 | 41 | 47 | 139 | 6 | 26 | 106 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0002 | 0/0 | 537 | 38 | 16 | 9 | 3 | 2 | 8 | 3 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0003 | 0/0 | 537 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0004 | 0/0 | 537 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0005 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0006 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0007 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(343): Show |
chr8 | 86509435 | 86566498 |
| a0008 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0009 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| a0010 | 0/0 | 173 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(168): Show |
chr8 | 86509435 | 86566498 |
| a0011 | 0/0 | 537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | MAAQC others(532): Show |
chr8 | 86509435 | 86566498 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1611 | 214 | 22 | 42 | 122 | 5 | 21 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0001c0002 | 0/0 | 1611 | 42 | 17 | 4 | 15 | 1 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0001c0008 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0001c0010 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0001c0017 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0002c0003 | 0/0 | 1611 | 26 | 9 | 5 | 3 | 2 | 7 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0002c0005 | 0/0 | 1611 | 12 | 7 | 4 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0003c0004 | 0/0 | 1611 | 21 | 19 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0004c0006 | 0/0 | 1611 | 9 | 8 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0004c0013 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0005c0007 | 0/0 | 1611 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0006c0009 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0007c0015 | 0/0 | 1568 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1563): Show |
chr8 | 86509435 | 86566498 | ||
| a0008c0012 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0009c0014 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0010c0011 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 | ||
| a0011c0016 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | ATGGC others(1606): Show |
chr8 | 86509435 | 86566498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4858 | 66 | 2 | 20 | 38 | 1 | 4 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0002 | 0/0 | 4858 | 50 | 2 | 17 | 23 | 2 | 6 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0003 | 1/0 | 4857 | 49 | 1 | 1 | 39 | 2 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0004 | 0/0 | 4858 | 26 | 7 | 3 | 14 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0006 | 0/0 | 4858 | 5 | 4 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0007 | 0/0 | 4860 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4855): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0008 | 0/0 | 4858 | 7 | 0 | 0 | 7 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0009 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0010 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0013 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0015 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0016 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0017 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0018 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0001t0020 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0001 | 0/0 | 4858 | 7 | 3 | 1 | 1 | 1 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0002 | 0/0 | 4858 | 15 | 0 | 2 | 13 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0003 | 0/0 | 4857 | 3 | 0 | 0 | 1 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0004 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0005 | 0/0 | 4858 | 2 | 0 | 0 | 0 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0006 | 0/0 | 4858 | 6 | 6 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0007 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4855): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0009 | 0/0 | 4858 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0010 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0014 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0002t0019 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0008t0002 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0008t0004 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0010t0001 | 0/0 | 4858 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0001c0017t0001 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0002c0003t0002 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0002c0003t0004 | 0/0 | 4858 | 5 | 0 | 1 | 0 | 1 | 3 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0002c0003t0005 | 0/0 | 4858 | 20 | 9 | 3 | 3 | 1 | 4 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0002c0005t0004 | 0/0 | 4858 | 3 | 1 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0002c0005t0005 | 0/0 | 4858 | 9 | 6 | 2 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0003c0004t0004 | 0/0 | 4858 | 8 | 7 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0003c0004t0006 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0003c0004t0007 | 0/0 | 4860 | 5 | 4 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4855): Show |
chr8 | 86509435 | 86566498 |
| a0003c0004t0009 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0003c0004t0012 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0004c0006t0002 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0004c0006t0005 | 0/0 | 4858 | 4 | 3 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0004c0006t0011 | 0/0 | 4858 | 4 | 4 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0004c0013t0005 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0005c0007t0010 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0006c0009t0002 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0007c0015t0001 | 0/0 | 4815 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4810): Show |
chr8 | 86509435 | 86566498 |
| a0008c0012t0005 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0009c0014t0003 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4852): Show |
chr8 | 86509435 | 86566498 |
| a0010c0011t0005 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| a0011c0016t0008 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | GCCAG others(4853): Show |
chr8 | 86509435 | 86566498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0015g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0018g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0001t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0009g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0002t0019g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0008t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0008t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0010t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0001c0017t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0002c0005t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0003c0004t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0006t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0004c0013t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0005c0007t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0005c0007t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0005c0007t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0006c0009t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0006c0009t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0007c0015t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0008c0012t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0009c0014t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0010c0011t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| a0011c0016t0008g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | GBR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0321 | EUR | GBR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00323 | hp1 | a0002 | c0003 | t0004 | g0119 | EUR | FIN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0200 | EUR | FIN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00544 | hp1 | a0001 | c0010 | t0001 | g0071 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00609 | hp2 | a0007 | c0015 | t0001 | g0070 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00642 | hp2 | a0002 | c0003 | t0005 | g0183 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00733 | hp1 | a0008 | c0012 | t0005 | g0314 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00738 | hp2 | a0009 | c0014 | t0003 | g0006 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0289 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01069 | hp2 | a0002 | c0005 | t0004 | g0287 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01070 | hp1 | a0001 | c0002 | t0009 | g0315 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01071 | hp2 | a0002 | c0005 | t0004 | g0288 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01074 | hp1 | a0002 | c0003 | t0005 | g0216 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01081 | hp1 | a0003 | c0004 | t0007 | g0173 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01099 | hp2 | a0002 | c0003 | t0005 | g0143 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0144 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0335 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01243 | hp1 | a0003 | c0004 | t0004 | g0180 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01255 | hp2 | a0010 | c0011 | t0005 | g0312 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01261 | hp1 | a0004 | c0006 | t0005 | g0171 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01433 | hp1 | a0002 | c0005 | t0005 | g0331 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01433 | hp2 | a0002 | c0005 | t0005 | g0291 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01884 | hp1 | a0003 | c0004 | t0004 | g0156 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01928 | hp1 | a0001 | c0017 | t0001 | g0045 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02004 | hp2 | a0002 | c0003 | t0004 | g0226 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02015 | hp1 | a0001 | c0001 | t0015 | g0265 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02055 | hp2 | a0003 | c0004 | t0004 | g0179 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0270 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02257 | hp1 | a0002 | c0005 | t0004 | g0333 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02257 | hp2 | a0003 | c0004 | t0007 | g0176 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02258 | hp1 | a0002 | c0005 | t0005 | g0320 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02258 | hp2 | a0003 | c0004 | t0007 | g0158 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0037 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02572 | hp1 | a0004 | c0006 | t0002 | g0163 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02572 | hp2 | a0003 | c0004 | t0009 | g0189 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02615 | hp1 | a0001 | c0001 | t0020 | g0007 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02615 | hp2 | a0004 | c0006 | t0005 | g0161 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02622 | hp1 | a0002 | c0003 | t0005 | g0092 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02622 | hp2 | a0006 | c0009 | t0002 | g0097 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02647 | hp1 | a0003 | c0004 | t0006 | g0177 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02647 | hp2 | a0003 | c0004 | t0012 | g0283 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0316 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02698 | hp2 | a0002 | c0003 | t0005 | g0142 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02723 | hp2 | a0003 | c0004 | t0004 | g0165 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0317 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02886 | hp1 | a0003 | c0004 | t0012 | g0282 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02895 | hp2 | a0002 | c0003 | t0005 | g0145 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02896 | hp1 | a0003 | c0004 | t0009 | g0187 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02897 | hp2 | a0003 | c0004 | t0009 | g0188 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02922 | hp1 | a0001 | c0002 | t0009 | g0295 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02922 | hp2 | a0001 | c0002 | t0006 | g0268 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02965 | hp1 | a0001 | c0002 | t0019 | g0294 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02965 | hp2 | a0002 | c0003 | t0005 | g0140 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0301 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02976 | hp2 | a0004 | c0013 | t0005 | g0164 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0324 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03017 | hp2 | a0002 | c0003 | t0005 | g0048 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0138 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03041 | hp2 | a0003 | c0004 | t0007 | g0168 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03098 | hp1 | a0001 | c0008 | t0004 | g0298 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03098 | hp2 | a0004 | c0006 | t0011 | g0155 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03130 | hp1 | a0002 | c0003 | t0005 | g0133 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0292 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03139 | hp1 | a0004 | c0006 | t0011 | g0172 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03139 | hp2 | a0002 | c0003 | t0005 | g0131 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03195 | hp1 | a0004 | c0006 | t0005 | g0175 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0269 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03209 | hp1 | a0003 | c0004 | t0004 | g0157 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03225 | hp1 | a0001 | c0002 | t0014 | g0296 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03225 | hp2 | a0002 | c0003 | t0005 | g0139 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03453 | hp1 | a0001 | c0008 | t0002 | g0297 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03453 | hp2 | a0001 | c0002 | t0010 | g0302 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03486 | hp1 | a0002 | c0003 | t0005 | g0026 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0029 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03490 | hp2 | a0002 | c0003 | t0004 | g0201 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03491 | hp1 | a0001 | c0001 | t0017 | g0214 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0325 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03492 | hp1 | a0002 | c0003 | t0004 | g0218 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0326 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03516 | hp1 | a0002 | c0003 | t0005 | g0109 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03516 | hp2 | a0005 | c0007 | t0010 | g0281 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03540 | hp1 | a0002 | c0005 | t0005 | g0186 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03540 | hp2 | a0003 | c0004 | t0007 | g0174 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03579 | hp1 | a0004 | c0006 | t0011 | g0154 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03669 | hp2 | a0002 | c0003 | t0005 | g0034 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0130 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03704 | hp1 | a0001 | c0001 | t0016 | g0082 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03927 | hp1 | a0002 | c0005 | t0005 | g0304 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04115 | hp2 | a0002 | c0003 | t0005 | g0233 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0334 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG04199 | hp2 | a0001 | c0001 | t0018 | g0047 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18522 | hp1 | a0002 | c0005 | t0005 | g0003 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18906 | hp1 | a0003 | c0004 | t0012 | g0284 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18906 | hp2 | a0005 | c0007 | t0010 | g0280 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18953 | hp1 | a0001 | c0010 | t0001 | g0104 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18980 | hp1 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18986 | hp1 | a0002 | c0003 | t0005 | g0028 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18992 | hp1 | a0002 | c0003 | t0005 | g0059 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0117 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19030 | hp1 | a0004 | c0006 | t0005 | g0159 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0178 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0271 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19072 | hp1 | a0002 | c0003 | t0005 | g0052 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19078 | hp2 | a0011 | c0016 | t0008 | g0115 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19240 | hp1 | a0003 | c0004 | t0006 | g0170 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0137 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20129 | hp1 | a0002 | c0005 | t0005 | g0003 | AFR | ASW | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20752 | hp2 | a0002 | c0003 | t0005 | g0217 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20905 | hp2 | a0002 | c0003 | t0004 | g0199 | SAS | GIH | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02109 | hp1 | a0006 | c0009 | t0002 | g0116 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02109 | hp2 | a0002 | c0005 | t0005 | g0327 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02486 | hp1 | a0004 | c0006 | t0011 | g0167 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02486 | hp2 | a0003 | c0004 | t0004 | g0162 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02559 | hp1 | a0001 | c0002 | t0006 | g0293 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG02559 | hp2 | a0002 | c0005 | t0005 | g0290 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG03471 | hp2 | a0003 | c0004 | t0004 | g0166 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG06807 | hp1 | a0001 | c0002 | t0004 | g0336 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20300 | hp1 | a0003 | c0004 | t0004 | g0169 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA21309 | hp1 | a0005 | c0007 | t0010 | g0279 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0182 | REF | REF | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0272 | REF | REF | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:86531228 | C | T | 1 | a0005 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
missense_variant&splice_region_variant | MODERATE | c.386C>T | p.Thr129Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/17 | 541/4857 | 386/1614 | 129/537 | chr8 | 86531228 | |||
| chr8:86537625 | G | A | 1 | a0010 | 1 | HG01255.hp2 | stop_gained | HIGH | c.522G>A | p.Trp174* | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/17 | 677/4857 | 522/1614 | 174/537 | chr8 | 86537625 | |||
| chr8:86544740 | G | A | 1 | a0009 | 1 | HG00738.hp2 | missense_variant&splice_region_variant | MODERATE | c.634G>A | p.Val212Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/17 | 789/4857 | 634/1614 | 212/537 | chr8 | 86544740 | |||
| chr8:86546618 | G | C | 2 | a0003 a0004 |
31 | HG01081.hp1 HG01243.hp1 HG01261.hp1 others(28): Show |
missense_variant | MODERATE | c.756G>C | p.Glu252Asp | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/17 | 911/4857 | 756/1614 | 252/537 | chr8 | 86546618 | |||
| chr8:86548326 | A | G | 1 | a0008 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.905A>G | p.Asn302Ser | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/17 | 1060/4857 | 905/1614 | 302/537 | chr8 | 86548326 | |||
| chr8:86548378 | TAATGAGT others(36): Show |
T | 1 | a0007 | 1 | HG00609.hp2 | frameshift_variant | HIGH | c.960_1002delTGAGTAT others(36): Show |
p.Asn320fs | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/17 | 1115/4857 | 960/1614 | 320/537 | INFO_REALIGN_3_PRIME | chr8 | 86548378 | ||
| chr8:86554878 | G | A | 1 | a0006 | 2 | HG02109.hp1 HG02622.hp2 |
missense_variant | MODERATE | c.1148G>A | p.Arg383Gln | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1303/4857 | 1148/1614 | 383/537 | chr8 | 86554878 | |||
| chr8:86554965 | C | T | 5 | a0002 a0004 a0006 others(2): Show |
52 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
missense_variant | MODERATE | c.1235C>T | p.Thr412Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1390/4857 | 1235/1614 | 412/537 | chr8 | 86554965 | |||
| chr8:86556265 | G | A | 1 | a0011 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/17 | 1573/4857 | 1418/1614 | 473/537 | chr8 | 86556265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:86528644 | G | A | 5 | a0001c0002 a0001c0008 a0002c0005 others(2): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
synonymous_variant | LOW | c.99G>A | p.Leu33Leu | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/17 | 254/4857 | 99/1614 | 33/537 | chr8 | 86528644 | |||
| chr8:86540292 | T | G | 1 | a0004c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.591T>G | p.Ser197Ser | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/17 | 746/4857 | 591/1614 | 197/537 | chr8 | 86540292 | |||
| chr8:86540310 | C | T | 1 | a0001c0017 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.609C>T | p.Tyr203Tyr | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/17 | 764/4857 | 609/1614 | 203/537 | chr8 | 86540310 | |||
| chr8:86544742 | G | A | 1 | a0001c0008 | 2 | HG03098.hp1 HG03453.hp1 |
splice_region_variant&synonymous_variant | LOW | c.636G>A | p.Val212Val | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/17 | 791/4857 | 636/1614 | 212/537 | chr8 | 86544742 | |||
| chr8:86554966 | G | A | 1 | a0001c0010 | 2 | HG00544.hp1 NA18953.hp1 |
synonymous_variant | LOW | c.1236G>A | p.Thr412Thr | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1391/4857 | 1236/1614 | 412/537 | chr8 | 86554966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:86514496 | A | C | 1 | a0003c0004t0012 | 3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-94A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/17 | 14050 | chr8 | 86514496 | ||||||
| chr8:86558437 | A | C | 14 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 others(11): Show |
112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*27A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 27 | chr8 | 86558437 | ||||||
| chr8:86558500 | C | T | 14 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 others(11): Show |
112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 90 | chr8 | 86558500 | ||||||
| chr8:86558821 | A | G | 14 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 others(11): Show |
112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 411 | chr8 | 86558821 | ||||||
| chr8:86559016 | G | A | 1 | a0001c0001t0013 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*606G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 606 | chr8 | 86559016 | ||||||
| chr8:86559024 | A | G | 12 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(9): Show |
92 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*614A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 614 | chr8 | 86559024 | ||||||
| chr8:86559130 | T | TAA | 3 | a0001c0001t0007 a0001c0002t0007 a0003c0004t0007 |
9 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*723dupAA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 724 | INFO_REALIGN_3_PRIME | chr8 | 86559130 | |||||
| chr8:86559306 | G | A | 8 | a0001c0001t0007 a0001c0001t0010 a0001c0002t0007 others(5): Show |
18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 896 | chr8 | 86559306 | ||||||
| chr8:86559410 | T | A | 8 | a0001c0001t0007 a0001c0001t0010 a0001c0002t0007 others(5): Show |
18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1000 | chr8 | 86559410 | ||||||
| chr8:86559594 | A | G | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0020 others(7): Show |
90 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1184 | chr8 | 86559594 | ||||||
| chr8:86559689 | G | A | 1 | a0001c0002t0019 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1279 | chr8 | 86559689 | ||||||
| chr8:86559921 | G | A | 1 | a0001c0001t0020 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1511G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1511 | chr8 | 86559921 | ||||||
| chr8:86560238 | C | A | 1 | a0001c0001t0015 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1828 | chr8 | 86560238 | ||||||
| chr8:86560332 | C | T | 1 | a0001c0001t0018 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1922 | chr8 | 86560332 | ||||||
| chr8:86560435 | C | T | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(14): Show |
137 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2025C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2025 | chr8 | 86560435 | ||||||
| chr8:86560437 | A | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
281 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*2027A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2027 | chr8 | 86560437 | ||||||
| chr8:86560473 | G | A | 1 | a0001c0001t0016 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2063 | chr8 | 86560473 | ||||||
| chr8:86560606 | T | TA | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
281 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*2200dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2201 | INFO_REALIGN_3_PRIME | chr8 | 86560606 | |||||
| chr8:86560675 | A | G | 2 | a0001c0001t0008 a0011c0016t0008 |
8 | NA18980.hp1 NA18987.hp2 NA18990.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2265A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2265 | chr8 | 86560675 | ||||||
| chr8:86560771 | C | T | 10 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 others(7): Show |
23 | HG01070.hp1 HG01081.hp1 HG02257.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2361 | chr8 | 86560771 | ||||||
| chr8:86560840 | G | A | 1 | a0001c0001t0017 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2430 | chr8 | 86560840 | ||||||
| chr8:86560892 | C | T | 7 | a0001c0002t0005 a0002c0003t0005 a0002c0005t0005 others(4): Show |
38 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2482C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2482 | chr8 | 86560892 | ||||||
| chr8:86561416 | G | C | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(23): Show |
144 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3006G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 3006 | chr8 | 86561416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:86514562 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
127 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49+21G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514562 | |||||||
| chr8:86514595 | C | G | 53 | a0001c0001t0002g0286 a0001c0002t0001g0303 a0001c0002t0001g0310 others(50): Show |
54 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-49+54C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514595 | |||||||
| chr8:86514740 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+199G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514740 | |||||||
| chr8:86514820 | C | T | 1 | a0001c0001t0013g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-49+279C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514820 | |||||||
| chr8:86514850 | G | T | 1 | a0001c0002t0002g0337 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-49+309G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514850 | |||||||
| chr8:86514952 | G | A | 15 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49+411G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514952 | |||||||
| chr8:86515176 | C | T | 3 | a0003c0004t0012g0282 a0003c0004t0012g0283 a0003c0004t0012g0284 |
3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-48-286C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86515176 | |||||||
| chr8:86515335 | G | T | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-48-127G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86515335 | |||||||
| chr8:86515571 | A | G | 1 | a0004c0006t0005g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-11+72A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515571 | |||||||
| chr8:86515605 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+106C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515605 | |||||||
| chr8:86515785 | G | A | 7 | a0001c0001t0001g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(4): Show |
7 | HG00558.hp1 NA18950.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+286G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515785 | |||||||
| chr8:86515833 | A | G | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+334A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515833 | |||||||
| chr8:86516190 | C | T | 38 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(35): Show |
39 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-11+691C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516190 | |||||||
| chr8:86516192 | G | T | 1 | a0001c0002t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+693G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516192 | |||||||
| chr8:86516207 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-11+708A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516207 | |||||||
| chr8:86516216 | G | T | 3 | a0001c0001t0001g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 |
3 | NA19007.hp1 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-11+717G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516216 | |||||||
| chr8:86516279 | G | T | 4 | a0001c0001t0002g0275 a0001c0001t0004g0002 a0001c0001t0004g0273 others(1): Show |
5 | NA18965.hp1 NA18984.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+780G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516279 | |||||||
| chr8:86516282 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-11+783C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516282 | |||||||
| chr8:86516479 | G | C | 1 | a0001c0002t0004g0300 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+980G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516479 | |||||||
| chr8:86516521 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-11+1022G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516521 | |||||||
| chr8:86516630 | T | A | 135 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(132): Show |
137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-11+1131T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516630 | |||||||
| chr8:86516915 | G | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+1416G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516915 | |||||||
| chr8:86517069 | A | C | 150 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(147): Show |
152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-11+1570A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517069 | |||||||
| chr8:86517080 | T | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1581T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517080 | |||||||
| chr8:86517127 | G | A | 327 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(324): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.-11+1628G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517127 | |||||||
| chr8:86517269 | A | C | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1770A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517269 | |||||||
| chr8:86517284 | A | T | 34 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0027 others(31): Show |
34 | HG00597.hp2 HG00673.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+1785A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517284 | |||||||
| chr8:86517288 | A | G | 1 | a0002c0003t0004g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11+1789A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517288 | |||||||
| chr8:86517304 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-11+1805T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517304 | |||||||
| chr8:86517431 | C | A | 4 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+1932C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517431 | |||||||
| chr8:86517435 | C | G | 1 | a0001c0001t0002g0267 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-11+1936C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517435 | |||||||
| chr8:86517828 | A | G | 94 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(91): Show |
96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-11+2329A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517828 | |||||||
| chr8:86517843 | G | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2344G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517843 | |||||||
| chr8:86517972 | A | G | 3 | a0003c0004t0009g0187 a0003c0004t0009g0188 a0003c0004t0009g0189 |
3 | HG02572.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+2473A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517972 | |||||||
| chr8:86518137 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-11+2638C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518137 | |||||||
| chr8:86518201 | G | A | 2 | a0004c0006t0011g0154 a0004c0006t0011g0155 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-11+2702G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518201 | |||||||
| chr8:86518242 | G | A | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2743G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518242 | |||||||
| chr8:86518256 | C | T | 1 | a0002c0003t0005g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+2757C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518256 | |||||||
| chr8:86518257 | A | G | 208 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0206 others(205): Show |
211 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.-11+2758A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518257 | |||||||
| chr8:86518433 | T | C | 2 | a0003c0004t0004g0156 a0003c0004t0004g0157 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-11+2934T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518433 | |||||||
| chr8:86518518 | G | A | 2 | a0001c0001t0002g0005 a0009c0014t0003g0006 |
2 | HG00738.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-11+3019G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518518 | |||||||
| chr8:86518563 | G | T | 53 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(50): Show |
54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+3064G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518563 | |||||||
| chr8:86518565 | T | C | 53 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(50): Show |
54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+3066T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518565 | |||||||
| chr8:86518732 | A | G | 1 | a0002c0003t0002g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+3233A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518732 | |||||||
| chr8:86518762 | T | A | 2 | a0002c0003t0005g0131 a0002c0003t0005g0145 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+3263T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518762 | |||||||
| chr8:86518762 | TA | T | 54 | a0001c0001t0008g0117 a0001c0002t0001g0303 a0001c0002t0001g0310 others(51): Show |
55 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.-11+3272delA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86518762 | ||||||
| chr8:86518763 | A | T | 10 | a0001c0001t0001g0058 a0001c0001t0002g0207 a0001c0001t0003g0046 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+3264A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518763 | |||||||
| chr8:86519052 | G | A | 1 | a0001c0002t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+3553G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519052 | |||||||
| chr8:86519119 | A | G | 15 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+3620A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519119 | |||||||
| chr8:86519322 | T | C | 4 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+3823T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519322 | |||||||
| chr8:86519504 | T | G | 1 | a0001c0001t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+4005T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519504 | |||||||
| chr8:86519637 | G | C | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+4138G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519637 | |||||||
| chr8:86519691 | G | C | 1 | a0001c0001t0020g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11+4192G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519691 | |||||||
| chr8:86519779 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-11+4280T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519779 | |||||||
| chr8:86519799 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0015g0265 |
2 | HG02015.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-11+4300C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519799 | |||||||
| chr8:86519816 | C | T | 53 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(50): Show |
54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+4317C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519816 | |||||||
| chr8:86519991 | C | T | 1 | a0006c0009t0002g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11+4492C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519991 | |||||||
| chr8:86520001 | C | T | 1 | a0011c0016t0008g0115 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-11+4502C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520001 | |||||||
| chr8:86520002 | G | A | 53 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(50): Show |
54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+4503G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520002 | |||||||
| chr8:86520060 | T | C | 40 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(37): Show |
41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+4561T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520060 | |||||||
| chr8:86520140 | C | CCACTTCC others(197): Show |
5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+4644_-11+4847d others(206): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520140 | ||||||
| chr8:86520270 | C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-11+4771C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520270 | |||||||
| chr8:86520331 | G | A | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+4832G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520331 | |||||||
| chr8:86520398 | A | T | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+4899A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520398 | |||||||
| chr8:86520487 | G | A | 1 | a0001c0002t0004g0301 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+4988G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520487 | |||||||
| chr8:86520504 | C | G | 40 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(37): Show |
41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+5005C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520504 | |||||||
| chr8:86520532 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+5033C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520532 | |||||||
| chr8:86520554 | C | CAA | 39 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(36): Show |
40 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-11+5066_-11+5067d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520554 | ||||||
| chr8:86520593 | C | T | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5094C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520593 | |||||||
| chr8:86520608 | G | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+5109G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520608 | |||||||
| chr8:86520662 | C | CT | 191 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(188): Show |
194 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-11+5178dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520662 | ||||||
| chr8:86520662 | C | CTT | 13 | a0001c0001t0001g0184 a0001c0001t0001g0263 a0001c0001t0001g0276 others(10): Show |
13 | HG00642.hp2 HG01109.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+5177_-11+5178d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520662 | ||||||
| chr8:86520959 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0002g0004 a0001c0001t0002g0147 others(6): Show |
9 | HG00438.hp2 HG00558.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+5460G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520959 | |||||||
| chr8:86521165 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11+5666C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521165 | |||||||
| chr8:86521289 | T | C | 1 | a0001c0001t0003g0009 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-11+5790T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521289 | |||||||
| chr8:86521537 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-11+6038G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521537 | |||||||
| chr8:86521875 | G | A | 1 | a0001c0002t0006g0292 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-11+6376G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521875 | |||||||
| chr8:86521973 | T | TA | 7 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0002g0195 others(4): Show |
7 | HG00642.hp1 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+6483dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86521973 | ||||||
| chr8:86521982 | A | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+6483A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521982 | |||||||
| chr8:86522123 | C | T | 53 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(50): Show |
54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-10-6413C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522123 | |||||||
| chr8:86522201 | T | G | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-6335T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522201 | |||||||
| chr8:86522274 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10-6262G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522274 | |||||||
| chr8:86522302 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-10-6234T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522302 | |||||||
| chr8:86522306 | C | T | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6230C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522306 | |||||||
| chr8:86522442 | T | C | 1 | a0002c0003t0004g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-10-6094T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522442 | |||||||
| chr8:86522462 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-10-6074A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522462 | |||||||
| chr8:86522500 | G | A | 1 | a0001c0002t0004g0300 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-6036G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522500 | |||||||
| chr8:86522516 | G | GGATTTAC | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-6019_-10-6013d others(9): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522516 | ||||||
| chr8:86522543 | C | T | 3 | a0001c0001t0002g0262 a0001c0001t0003g0260 a0001c0001t0003g0261 |
3 | NA18953.hp2 NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-10-5993C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522543 | |||||||
| chr8:86522544 | G | A | 1 | a0003c0004t0007g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10-5992G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522544 | |||||||
| chr8:86522548 | C | CT | 45 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00673.hp1 HG00735.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.-10-5959dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | C | CTTTT | 30 | a0001c0002t0001g0310 a0001c0002t0001g0319 a0001c0002t0001g0321 others(27): Show |
31 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-10-5962_-10-5959d others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | C | CTTTTT | 10 | a0001c0002t0002g0299 a0001c0002t0002g0330 a0001c0002t0002g0332 others(7): Show |
10 | HG01175.hp2 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-5963_-10-5959d others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-5968_-10-5959d others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | C | CTTTTTTT others(4): Show |
1 | a0002c0005t0005g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-10-5969_-10-5959d others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | C | CTTTTTTT others(6): Show |
1 | a0002c0005t0005g0291 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10-5971_-10-5959d others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | CT | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(8): Show |
11 | HG01167.hp2 HG01192.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-5959delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0259 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-5968_-10-5959d others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | CTTTTTTT others(4): Show |
C | 91 | a0001c0001t0001g0190 a0001c0001t0001g0206 a0001c0001t0001g0209 others(88): Show |
93 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-10-5969_-10-5959d others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522548 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0146 a0001c0001t0003g0200 a0002c0003t0004g0201 |
3 | HG00323.hp2 HG03490.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-10-5970_-10-5959d others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | ||||||
| chr8:86522641 | T | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-10-5895T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522641 | |||||||
| chr8:86522762 | A | G | 1 | a0001c0001t0002g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-10-5774A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522762 | |||||||
| chr8:86523018 | G | A | 60 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(57): Show |
61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10-5518G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523018 | |||||||
| chr8:86523105 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-10-5431A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523105 | |||||||
| chr8:86523157 | C | T | 54 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0002g0141 others(51): Show |
54 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10-5379C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523157 | |||||||
| chr8:86523345 | G | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-10-5191G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523345 | |||||||
| chr8:86523349 | A | T | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5187A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523349 | |||||||
| chr8:86523493 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-10-5043A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523493 | |||||||
| chr8:86523589 | G | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-4947G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523589 | |||||||
| chr8:86523641 | A | C | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-4895A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523641 | |||||||
| chr8:86523688 | T | C | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-10-4848T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523688 | |||||||
| chr8:86523710 | C | T | 4 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4826C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523710 | |||||||
| chr8:86524383 | T | A | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-4153T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524383 | |||||||
| chr8:86524410 | T | G | 60 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(57): Show |
61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10-4126T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524410 | |||||||
| chr8:86524656 | G | A | 1 | a0004c0006t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-3880G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524656 | |||||||
| chr8:86524674 | C | T | 16 | a0001c0001t0001g0244 a0001c0001t0001g0250 a0001c0001t0002g0253 others(13): Show |
16 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-3862C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524674 | |||||||
| chr8:86524681 | A | AT | 63 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(60): Show |
63 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10-3835dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | ||||||
| chr8:86524681 | A | ATT | 49 | a0001c0001t0001g0088 a0001c0001t0001g0184 a0001c0001t0001g0276 others(46): Show |
50 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-3836_-10-3835d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | ||||||
| chr8:86524681 | A | ATTT | 9 | a0001c0001t0002g0194 a0001c0001t0010g0178 a0001c0002t0002g0289 others(6): Show |
9 | HG00741.hp1 HG01167.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-3837_-10-3835d others(5): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | ||||||
| chr8:86524681 | A | ATTTTT | 74 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0211 others(71): Show |
76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-10-3839_-10-3835d others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | ||||||
| chr8:86524681 | A | ATTTTTT | 17 | a0001c0001t0001g0190 a0001c0001t0001g0237 a0001c0001t0001g0263 others(14): Show |
17 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-3840_-10-3835d others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | ||||||
| chr8:86524742 | G | A | 149 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(146): Show |
151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-10-3794G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524742 | |||||||
| chr8:86524848 | T | TTTTCTTT others(1): Show |
143 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(140): Show |
145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.-10-3672_-10-3665d others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(5): Show |
8 | a0001c0001t0001g0266 a0001c0001t0003g0200 a0001c0001t0004g0202 others(5): Show |
8 | HG00323.hp2 HG02015.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-3676_-10-3665d others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(21): Show |
4 | a0001c0002t0002g0328 a0001c0002t0003g0334 a0001c0008t0004g0298 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(30): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(25): Show |
13 | a0001c0002t0001g0319 a0001c0002t0001g0321 a0001c0002t0001g0322 others(10): Show |
14 | HG00099.hp2 HG01175.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(34): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(29): Show |
17 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0002g0309 others(14): Show |
17 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(38): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(33): Show |
5 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0006g0270 others(2): Show |
5 | HG01433.hp1 HG02083.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(42): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(37): Show |
6 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0293 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(46): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(41): Show |
3 | a0001c0002t0004g0300 a0001c0002t0004g0336 a0001c0002t0006g0292 |
3 | HG02055.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(50): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524848 | T | TTTTCTTT others(45): Show |
2 | a0001c0002t0010g0302 a0001c0008t0002g0297 |
2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(54): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | ||||||
| chr8:86524853 | T | TTTCTTTC others(82): Show |
1 | a0002c0005t0004g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-10-3664_-10-3663i others(91): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | ||||||
| chr8:86524853 | T | TTTCTTTC others(73): Show |
2 | a0002c0005t0005g0290 a0002c0005t0005g0291 |
2 | HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-10-3662_-10-3661i others(82): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | ||||||
| chr8:86524853 | T | TTTCTTTC others(81): Show |
1 | a0002c0005t0004g0288 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10-3662_-10-3661i others(90): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | ||||||
| chr8:86524853 | T | TTTCTTTC others(85): Show |
1 | a0001c0002t0002g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-3662_-10-3661i others(94): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | ||||||
| chr8:86524869 | T | TTTCTTTC others(31): Show |
1 | a0001c0002t0002g0305 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-10-3665_-10-3664i others(40): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524869 | ||||||
| chr8:86524870 | T | TTCTTTCT others(31): Show |
1 | a0001c0002t0002g0330 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-10-3665_-10-3664i others(40): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524870 | ||||||
| chr8:86524894 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
6 | HG01192.hp1 HG01496.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3642C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524894 | |||||||
| chr8:86525044 | G | A | 260 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0027 others(257): Show |
263 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.-10-3492G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525044 | |||||||
| chr8:86525128 | T | C | 4 | a0001c0001t0001g0244 a0001c0001t0003g0241 a0001c0001t0003g0242 others(1): Show |
4 | HG00673.hp2 HG02027.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3408T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525128 | |||||||
| chr8:86525147 | G | A | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-3389G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525147 | |||||||
| chr8:86525228 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-10-3308C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525228 | |||||||
| chr8:86525351 | A | T | 3 | a0001c0001t0001g0126 a0001c0001t0003g0125 a0001c0001t0003g0127 |
3 | HG02056.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-10-3185A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525351 | |||||||
| chr8:86525363 | A | G | 5 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3173A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525363 | |||||||
| chr8:86525445 | G | A | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3091G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525445 | |||||||
| chr8:86525480 | A | T | 95 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(92): Show |
97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-3056A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525480 | |||||||
| chr8:86525659 | T | C | 1 | a0003c0004t0006g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-2877T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525659 | |||||||
| chr8:86525753 | G | A | 2 | a0003c0004t0004g0162 a0004c0006t0005g0161 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-10-2783G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525753 | |||||||
| chr8:86525778 | T | C | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-2758T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525778 | |||||||
| chr8:86526184 | C | T | 95 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(92): Show |
97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-2352C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526184 | |||||||
| chr8:86526227 | C | CA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0089 a0001c0001t0002g0121 others(3): Show |
6 | HG04199.hp2 NA19010.hp1 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2296dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86526227 | ||||||
| chr8:86526241 | T | C | 2 | a0001c0001t0002g0049 a0002c0003t0005g0048 |
2 | HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-10-2295T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526241 | |||||||
| chr8:86526503 | TTTTG | T | 39 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0003g0185 others(36): Show |
39 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10-2021_-10-2018d others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86526503 | ||||||
| chr8:86526718 | A | T | 9 | a0003c0004t0004g0180 a0003c0004t0007g0158 a0003c0004t0007g0173 others(6): Show |
9 | HG01081.hp1 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-1818A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526718 | |||||||
| chr8:86526764 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0003g0050 a0001c0001t0003g0051 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1772G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526764 | |||||||
| chr8:86526827 | C | T | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-1709C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526827 | |||||||
| chr8:86526904 | T | A | 15 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-1632T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526904 | |||||||
| chr8:86527100 | A | C | 3 | a0001c0001t0003g0046 a0002c0003t0005g0109 a0006c0009t0002g0116 |
3 | HG02109.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-1436A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527100 | |||||||
| chr8:86527162 | G | C | 1 | a0001c0001t0008g0020 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-10-1374G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527162 | |||||||
| chr8:86527217 | G | C | 1 | a0001c0001t0002g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10-1319G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527217 | |||||||
| chr8:86527242 | C | T | 2 | a0003c0004t0007g0158 a0003c0004t0007g0176 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-10-1294C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527242 | |||||||
| chr8:86527472 | G | A | 2 | a0001c0001t0003g0203 a0001c0001t0003g0204 |
2 | HG00544.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-10-1064G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527472 | |||||||
| chr8:86527524 | A | G | 33 | a0001c0001t0004g0160 a0001c0001t0010g0178 a0003c0004t0004g0156 others(30): Show |
33 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-10-1012A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527524 | |||||||
| chr8:86527604 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10-932T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527604 | |||||||
| chr8:86527639 | T | C | 95 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(92): Show |
97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-897T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527639 | |||||||
| chr8:86527711 | A | G | 14 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(11): Show |
14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10-825A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527711 | |||||||
| chr8:86527798 | A | T | 94 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(91): Show |
96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-10-738A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527798 | |||||||
| chr8:86527831 | A | C | 1 | a0001c0001t0001g0228 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-10-705A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527831 | |||||||
| chr8:86527891 | A | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-645A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527891 | |||||||
| chr8:86527946 | A | AT | 19 | a0001c0001t0001g0087 a0001c0001t0001g0105 a0001c0001t0002g0081 others(16): Show |
19 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-565dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATT | 9 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0003g0185 others(6): Show |
9 | HG00642.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-566_-10-565dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(2): Show |
42 | a0001c0001t0001g0146 a0001c0001t0001g0206 a0001c0001t0001g0209 others(39): Show |
43 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-10-573_-10-565dup others(9): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(3): Show |
27 | a0001c0001t0001g0190 a0001c0001t0001g0219 a0001c0001t0001g0228 others(24): Show |
28 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-10-574_-10-565dup others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(4): Show |
17 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(14): Show |
17 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-575_-10-565dup others(11): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0244 a0001c0001t0002g0238 a0001c0001t0003g0153 others(4): Show |
7 | HG00438.hp1 HG00741.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-576_-10-565dup others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(6): Show |
6 | a0001c0001t0004g0135 a0001c0001t0004g0136 a0001c0001t0004g0240 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-577_-10-565dup others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0004g0132 a0001c0001t0007g0138 a0002c0003t0005g0131 others(1): Show |
4 | HG01099.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-578_-10-565dup others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(8): Show |
2 | a0002c0003t0005g0139 a0002c0003t0005g0140 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-579_-10-565dup others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0002g0141 a0002c0003t0002g0144 |
2 | HG01109.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-580_-10-565dup others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(10): Show |
1 | a0002c0003t0005g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10-581_-10-565dup others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(13): Show |
3 | a0003c0004t0004g0156 a0003c0004t0012g0283 a0004c0013t0005g0164 |
3 | HG01884.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-10-584_-10-565dup others(20): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(14): Show |
6 | a0003c0004t0004g0157 a0003c0004t0004g0165 a0003c0004t0004g0180 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-585_-10-565dup others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(15): Show |
3 | a0003c0004t0004g0162 a0003c0004t0004g0179 a0004c0006t0005g0161 |
3 | HG02055.hp2 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-10-586_-10-565dup others(22): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-587_-10-565dup others(23): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(17): Show |
1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-588_-10-565dup others(24): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(19): Show |
2 | a0003c0004t0007g0168 a0004c0006t0011g0167 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(26): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(20): Show |
2 | a0003c0004t0004g0169 a0004c0006t0011g0154 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(27): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(21): Show |
4 | a0003c0004t0006g0170 a0004c0006t0005g0171 a0004c0006t0011g0155 others(1): Show |
4 | HG01261.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(28): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | A | ATTTTTTT others(22): Show |
1 | a0004c0006t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-565_-10-564ins others(29): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | AT | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0022 others(47): Show |
50 | HG00323.hp1 HG00597.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10-565delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527946 | ATT | A | 6 | a0001c0001t0002g0024 a0001c0001t0003g0023 a0001c0001t0006g0012 others(3): Show |
6 | HG01167.hp2 HG02615.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-566_-10-565del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | ||||||
| chr8:86527974 | A | G | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-562A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527974 | |||||||
| chr8:86528186 | G | A | 1 | a0001c0001t0004g0054 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-10-350G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86528186 | |||||||
| chr8:86528210 | A | G | 1 | a0001c0002t0003g0334 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-10-326A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86528210 | |||||||
| chr8:86528745 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+68A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/16 | chr8 | 86528745 | |||||||
| chr8:86528918 | C | T | 5 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0042 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-27C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/16 | chr8 | 86528918 | |||||||
| chr8:86529225 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.312+101C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529225 | |||||||
| chr8:86529274 | C | T | 3 | a0001c0001t0002g0121 a0001c0001t0003g0120 a0001c0001t0003g0124 |
3 | NA19062.hp2 NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.312+150C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529274 | |||||||
| chr8:86529415 | C | T | 4 | a0001c0001t0002g0275 a0001c0001t0004g0002 a0001c0001t0004g0273 others(1): Show |
5 | NA18965.hp1 NA18984.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+291C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529415 | |||||||
| chr8:86529618 | G | C | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.312+494G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529618 | |||||||
| chr8:86529847 | A | G | 2 | a0001c0001t0001g0008 a0001c0010t0001g0104 |
2 | NA18946.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.312+723A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529847 | |||||||
| chr8:86529930 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.312+806T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529930 | |||||||
| chr8:86529955 | A | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.312+831A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529955 | |||||||
| chr8:86530058 | C | T | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.312+934C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530058 | |||||||
| chr8:86530089 | A | G | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.312+965A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530089 | |||||||
| chr8:86530170 | CT | C | 205 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0001g0184 others(202): Show |
208 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.313-968delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530170 | ||||||
| chr8:86530690 | ATT | A | 149 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(146): Show |
151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.313-448_313-447del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530690 | ||||||
| chr8:86530690 | ATTT | A | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-449_313-447del others(3): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530690 | ||||||
| chr8:86530736 | G | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0003g0185 others(3): Show |
6 | HG00642.hp2 NA18960.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-419G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530736 | |||||||
| chr8:86530740 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.313-415G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530740 | |||||||
| chr8:86530796 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.313-359A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530796 | |||||||
| chr8:86530938 | C | T | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.313-217C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530938 | |||||||
| chr8:86530991 | T | C | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.313-164T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530991 | |||||||
| chr8:86531031 | G | GAATGTTT others(8): Show |
2 | a0001c0001t0001g0184 a0001c0001t0003g0185 |
2 | NA18960.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.313-119_313-105dup others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86531031 | ||||||
| chr8:86531052 | C | T | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-103C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86531052 | |||||||
| chr8:86531279 | A | T | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.387+50A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531279 | |||||||
| chr8:86531551 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.387+322G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531551 | |||||||
| chr8:86531643 | T | C | 1 | a0001c0001t0006g0012 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.387+414T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531643 | |||||||
| chr8:86531645 | GTCAATGA others(19): Show |
G | 48 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(45): Show |
49 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.387+420_387+445del others(26): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr8 | 86531645 | ||||||
| chr8:86531946 | G | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.388-563G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531946 | |||||||
| chr8:86531962 | G | A | 333 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(330): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.388-547G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531962 | |||||||
| chr8:86532012 | G | A | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-497G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86532012 | |||||||
| chr8:86532240 | C | T | 6 | a0001c0001t0001g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | NA18950.hp2 NA18964.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-269C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86532240 | |||||||
| chr8:86532604 | A | G | 52 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(49): Show |
53 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.459+24A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532604 | |||||||
| chr8:86532798 | T | TAAGAGAG others(339): Show |
2 | a0001c0002t0005g0325 a0001c0002t0005g0326 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.459+232_459+233ins others(346): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86532798 | ||||||
| chr8:86532814 | T | C | 1 | a0002c0005t0005g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459+234T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532814 | |||||||
| chr8:86532842 | A | T | 1 | a0001c0001t0015g0265 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.459+262A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532842 | |||||||
| chr8:86532870 | G | A | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.459+290G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532870 | |||||||
| chr8:86532931 | A | C | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+351A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532931 | |||||||
| chr8:86533024 | T | TTATC | 104 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(101): Show |
104 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.459+486_459+489dup others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533024 | T | TTATCTAT others(1): Show |
48 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.459+482_459+489dup others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533024 | T | TTATCTAT others(5): Show |
5 | a0001c0002t0002g0328 a0001c0002t0003g0308 a0001c0010t0001g0104 others(2): Show |
6 | HG02258.hp1 NA18522.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+478_459+489dup others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533024 | TTATC | T | 12 | a0001c0001t0001g0209 a0001c0001t0002g0122 a0001c0001t0002g0123 others(9): Show |
12 | HG00099.hp1 HG01496.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+486_459+489del others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533024 | TTATCTAT others(5): Show |
T | 13 | a0001c0001t0001g0190 a0001c0001t0001g0211 a0001c0001t0001g0212 others(10): Show |
13 | HG00558.hp2 HG00609.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+478_459+489del others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533024 | TTATCTAT others(9): Show |
T | 12 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0275 others(9): Show |
14 | HG01975.hp2 HG02300.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.459+474_459+489del others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | ||||||
| chr8:86533054 | A | ATCTC | 6 | a0003c0004t0004g0169 a0003c0004t0007g0168 a0004c0006t0011g0154 others(3): Show |
6 | HG02486.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+477_459+478ins others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533054 | ||||||
| chr8:86533308 | C | T | 3 | a0003c0004t0012g0282 a0003c0004t0012g0283 a0003c0004t0012g0284 |
3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.459+728C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533308 | |||||||
| chr8:86533324 | C | T | 1 | a0002c0003t0005g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.459+744C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533324 | |||||||
| chr8:86533501 | T | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+921T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533501 | |||||||
| chr8:86533825 | C | T | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+1245C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533825 | |||||||
| chr8:86533878 | CTCCCTCC others(2): Show |
C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0027 others(40): Show |
43 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.459+1302_459+1310d others(11): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533878 | ||||||
| chr8:86533884 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+1304C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533884 | |||||||
| chr8:86533970 | C | A | 1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459+1390C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533970 | |||||||
| chr8:86534089 | C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.459+1509C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534089 | |||||||
| chr8:86534152 | G | A | 14 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(11): Show |
14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+1572G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534152 | |||||||
| chr8:86534323 | A | T | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.459+1743A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534323 | |||||||
| chr8:86534633 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.459+2053C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534633 | |||||||
| chr8:86534784 | G | A | 1 | a0001c0001t0013g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.459+2204G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534784 | |||||||
| chr8:86534800 | T | C | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.459+2220T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534800 | |||||||
| chr8:86534806 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0003g0251 a0001c0001t0003g0252 |
3 | NA18941.hp2 NA18987.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.459+2226A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534806 | |||||||
| chr8:86534823 | C | A | 95 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(92): Show |
97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+2243C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534823 | |||||||
| chr8:86534900 | TTG | T | 5 | a0001c0001t0004g0132 a0001c0001t0004g0135 a0001c0001t0004g0136 others(2): Show |
5 | HG02965.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+2326_459+2327d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86534900 | ||||||
| chr8:86535045 | A | G | 60 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(57): Show |
61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.459+2465A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535045 | |||||||
| chr8:86535073 | T | TC | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-2489dupC | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86535073 | ||||||
| chr8:86535320 | C | CT | 95 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(92): Show |
97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.460-2229dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86535320 | ||||||
| chr8:86535396 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0077 |
2 | NA18943.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.460-2167G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535396 | |||||||
| chr8:86535597 | G | C | 3 | a0001c0002t0002g0305 a0001c0002t0002g0309 a0001c0002t0002g0330 |
3 | NA18941.hp1 NA19067.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.460-1966G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535597 | |||||||
| chr8:86535607 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-1956A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535607 | |||||||
| chr8:86535674 | A | T | 1 | a0004c0006t0005g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.460-1889A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535674 | |||||||
| chr8:86535680 | A | T | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-1883A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535680 | |||||||
| chr8:86536029 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.460-1534A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536029 | |||||||
| chr8:86536341 | A | T | 3 | a0001c0001t0001g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 |
3 | NA19007.hp1 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.460-1222A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536341 | |||||||
| chr8:86536565 | T | A | 39 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0003g0185 others(36): Show |
39 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.460-998T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536565 | |||||||
| chr8:86536709 | A | G | 1 | a0001c0001t0003g0208 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.460-854A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536709 | |||||||
| chr8:86536725 | C | G | 60 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(57): Show |
61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.460-838C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536725 | |||||||
| chr8:86536761 | T | C | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.460-802T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536761 | |||||||
| chr8:86536781 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.460-782T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536781 | |||||||
| chr8:86536825 | T | C | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-738T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536825 | |||||||
| chr8:86536933 | G | C | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-630G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536933 | |||||||
| chr8:86537183 | A | C | 5 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-380A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537183 | |||||||
| chr8:86537215 | A | G | 14 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(11): Show |
14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-348A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537215 | |||||||
| chr8:86537226 | C | T | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-337C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537226 | |||||||
| chr8:86537369 | A | G | 1 | a0001c0001t0009g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460-194A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537369 | |||||||
| chr8:86537400 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.460-163C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537400 | |||||||
| chr8:86537738 | A | G | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+92A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537738 | |||||||
| chr8:86537966 | G | C | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+320G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537966 | |||||||
| chr8:86537966 | GTC | G | 36 | a0001c0001t0001g0285 a0001c0001t0004g0160 a0001c0002t0004g0300 others(33): Show |
36 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.543+341_543+342del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537966 | ||||||
| chr8:86537966 | GTCTC | G | 9 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0093 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+339_543+342del others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537966 | ||||||
| chr8:86537980 | C | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+334C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537980 | |||||||
| chr8:86537985 | T | A | 4 | a0001c0002t0004g0300 a0001c0002t0007g0317 a0001c0002t0010g0302 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+339T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537985 | |||||||
| chr8:86537985 | T | TCA | 41 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(38): Show |
42 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.543+340_543+341ins others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537985 | ||||||
| chr8:86537987 | T | A | 58 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0001g0285 others(55): Show |
59 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.543+341T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537987 | |||||||
| chr8:86537987 | T | TCA | 107 | a0001c0001t0001g0058 a0001c0001t0001g0101 a0001c0001t0001g0146 others(104): Show |
109 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.543+361_543+362dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537987 | ||||||
| chr8:86537987 | T | TCTCA | 11 | a0001c0001t0001g0250 a0001c0001t0002g0253 a0001c0001t0003g0245 others(8): Show |
11 | HG00597.hp1 HG02056.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+342_543+343ins others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537987 | ||||||
| chr8:86538699 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0003g0125 a0001c0001t0003g0127 |
3 | HG02056.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.543+1053C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538699 | |||||||
| chr8:86538769 | A | G | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+1123A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538769 | |||||||
| chr8:86538827 | C | G | 1 | a0004c0013t0005g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+1181C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538827 | |||||||
| chr8:86538861 | G | C | 14 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(11): Show |
14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+1215G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538861 | |||||||
| chr8:86539163 | T | C | 32 | a0001c0001t0004g0160 a0003c0004t0004g0156 a0003c0004t0004g0157 others(29): Show |
32 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-1082T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539163 | |||||||
| chr8:86539196 | G | A | 4 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0235 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-1049G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539196 | |||||||
| chr8:86539227 | C | A | 1 | a0001c0001t0017g0214 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.544-1018C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539227 | |||||||
| chr8:86539336 | T | C | 2 | a0001c0001t0001g0086 a0011c0016t0008g0115 |
2 | HG01109.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.544-909T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539336 | |||||||
| chr8:86539358 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.544-887G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539358 | |||||||
| chr8:86539467 | A | G | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-778A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539467 | |||||||
| chr8:86539547 | T | A | 1 | a0001c0001t0004g0273 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.544-698T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539547 | |||||||
| chr8:86539656 | C | T | 40 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(37): Show |
41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.544-589C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539656 | |||||||
| chr8:86539660 | G | GT | 27 | a0001c0001t0001g0078 a0001c0001t0001g0099 a0001c0001t0001g0112 others(24): Show |
27 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.544-565dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | ||||||
| chr8:86539660 | G | GTT | 120 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(117): Show |
122 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.544-566_544-565dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | ||||||
| chr8:86539660 | G | GTTT | 29 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0002g0148 others(26): Show |
29 | HG00438.hp1 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.544-567_544-565dup others(3): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | ||||||
| chr8:86539688 | T | C | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-557T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539688 | |||||||
| chr8:86539890 | C | G | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.544-355C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539890 | |||||||
| chr8:86539912 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.544-333G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539912 | |||||||
| chr8:86539916 | C | T | 1 | a0002c0003t0005g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-329C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539916 | |||||||
| chr8:86539956 | C | T | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544-289C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539956 | |||||||
| chr8:86539958 | C | A | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-287C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539958 | |||||||
| chr8:86539984 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-261T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539984 | |||||||
| chr8:86540198 | T | C | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.544-47T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86540198 | |||||||
| chr8:86540205 | G | A | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.544-40G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86540205 | |||||||
| chr8:86540567 | G | A | 5 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+233G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540567 | |||||||
| chr8:86540767 | G | C | 4 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+433G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540767 | |||||||
| chr8:86540784 | T | C | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.633+450T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540784 | |||||||
| chr8:86540859 | T | A | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633+525T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540859 | |||||||
| chr8:86540972 | A | G | 1 | a0002c0003t0005g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.633+638A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540972 | |||||||
| chr8:86541011 | TG | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0112 |
3 | NA18966.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.633+678delG | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541011 | |||||||
| chr8:86541069 | T | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.633+735T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541069 | |||||||
| chr8:86541120 | A | G | 333 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(330): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.633+786A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541120 | |||||||
| chr8:86541425 | C | T | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+1091C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541425 | |||||||
| chr8:86541465 | A | C | 1 | a0001c0001t0001g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.633+1131A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541465 | |||||||
| chr8:86541506 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.633+1172C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541506 | |||||||
| chr8:86541652 | C | T | 2 | a0001c0008t0002g0297 a0001c0008t0004g0298 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.633+1318C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541652 | |||||||
| chr8:86541705 | T | TA | 35 | a0001c0001t0001g0010 a0001c0001t0001g0083 a0001c0001t0001g0110 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.633+1390dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr8 | 86541705 | ||||||
| chr8:86541721 | A | C | 2 | a0001c0001t0003g0073 a0002c0003t0004g0119 |
2 | HG00323.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.633+1387A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541721 | |||||||
| chr8:86541945 | G | C | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.633+1611G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541945 | |||||||
| chr8:86542203 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633+1869C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542203 | |||||||
| chr8:86542222 | A | G | 1 | a0003c0004t0004g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.633+1888A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542222 | |||||||
| chr8:86542328 | A | G | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.633+1994A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542328 | |||||||
| chr8:86542422 | G | A | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.633+2088G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542422 | |||||||
| chr8:86542496 | G | T | 4 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+2162G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542496 | |||||||
| chr8:86542683 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.634-2057G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542683 | |||||||
| chr8:86542729 | C | A | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634-2011C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542729 | |||||||
| chr8:86542741 | C | T | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.634-1999C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542741 | |||||||
| chr8:86542742 | G | A | 40 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(37): Show |
41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.634-1998G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542742 | |||||||
| chr8:86542815 | A | G | 55 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0002g0141 others(52): Show |
55 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.634-1925A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542815 | |||||||
| chr8:86543614 | G | A | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634-1126G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543614 | |||||||
| chr8:86543633 | G | A | 2 | a0001c0002t0001g0303 a0001c0002t0002g0311 |
2 | HG02132.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.634-1107G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543633 | |||||||
| chr8:86543706 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.634-1034G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543706 | |||||||
| chr8:86543812 | G | A | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-928G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543812 | |||||||
| chr8:86543826 | A | G | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.634-914A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543826 | |||||||
| chr8:86543836 | T | C | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-904T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543836 | |||||||
| chr8:86544120 | G | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.634-620G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544120 | |||||||
| chr8:86544154 | T | G | 2 | a0001c0001t0001g0008 a0001c0010t0001g0104 |
2 | NA18946.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.634-586T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544154 | |||||||
| chr8:86544204 | T | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-536T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544204 | |||||||
| chr8:86544437 | T | G | 1 | a0001c0001t0004g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-303T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544437 | |||||||
| chr8:86544463 | G | A | 94 | a0001c0001t0001g0146 a0001c0001t0001g0190 a0001c0001t0001g0206 others(91): Show |
96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.634-277G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544463 | |||||||
| chr8:86544535 | C | T | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.634-205C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544535 | |||||||
| chr8:86544567 | A | G | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-173A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544567 | |||||||
| chr8:86544676 | G | A | 1 | a0002c0003t0002g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.634-64G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544676 | |||||||
| chr8:86544693 | A | C | 1 | a0001c0001t0004g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-47A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544693 | |||||||
| chr8:86544726 | A | G | 1 | a0001c0001t0003g0124 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.634-14A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544726 | |||||||
| chr8:86544925 | C | T | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+87C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86544925 | |||||||
| chr8:86544964 | G | A | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.732+126G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86544964 | |||||||
| chr8:86545123 | T | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+285T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545123 | |||||||
| chr8:86545129 | T | G | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+291T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545129 | |||||||
| chr8:86545154 | T | G | 2 | a0001c0001t0008g0080 a0002c0003t0005g0059 |
2 | NA18980.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.732+316T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545154 | |||||||
| chr8:86545206 | A | C | 4 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0009g0295 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+368A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545206 | |||||||
| chr8:86545313 | C | G | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+475C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545313 | |||||||
| chr8:86545561 | C | T | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.732+723C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545561 | |||||||
| chr8:86545636 | G | A | 3 | a0001c0001t0004g0202 a0001c0001t0004g0210 a0001c0001t0004g0234 |
3 | NA18939.hp1 NA18960.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.732+798G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545636 | |||||||
| chr8:86545714 | C | G | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.732+876C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545714 | |||||||
| chr8:86545742 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.733-853G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545742 | |||||||
| chr8:86545910 | A | G | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-685A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545910 | |||||||
| chr8:86545914 | T | G | 149 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(146): Show |
151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.733-681T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545914 | |||||||
| chr8:86545982 | G | T | 55 | a0001c0001t0001g0184 a0001c0001t0001g0276 a0001c0001t0002g0141 others(52): Show |
55 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.733-613G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545982 | |||||||
| chr8:86546055 | C | A | 149 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(146): Show |
151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.733-540C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546055 | |||||||
| chr8:86546118 | C | T | 15 | a0001c0001t0002g0141 a0001c0001t0004g0132 a0001c0001t0004g0135 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.733-477C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546118 | |||||||
| chr8:86546176 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.733-419T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546176 | |||||||
| chr8:86546197 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.733-398G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546197 | |||||||
| chr8:86546427 | T | C | 1 | a0001c0001t0010g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733-168T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546427 | |||||||
| chr8:86546862 | C | A | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+181C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86546862 | |||||||
| chr8:86546926 | G | C | 5 | a0003c0004t0007g0158 a0003c0004t0007g0173 a0003c0004t0007g0174 others(2): Show |
5 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+245G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86546926 | |||||||
| chr8:86547004 | C | T | 2 | a0001c0008t0002g0297 a0001c0008t0004g0298 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.819+323C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547004 | |||||||
| chr8:86547214 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820-497A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547214 | |||||||
| chr8:86547513 | A | G | 1 | a0002c0003t0005g0028 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.820-198A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547513 | |||||||
| chr8:86547553 | TA | T | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.820-157delA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547553 | |||||||
| chr8:86547573 | A | G | 1 | a0001c0002t0002g0335 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.820-138A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547573 | |||||||
| chr8:86547651 | GT | G | 33 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0039 others(30): Show |
33 | HG00597.hp2 HG00673.hp1 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.820-54delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr8 | 86547651 | ||||||
| chr8:86547923 | T | C | 40 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(37): Show |
41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.879+153T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86547923 | |||||||
| chr8:86547952 | C | T | 2 | a0001c0002t0005g0325 a0001c0002t0005g0326 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.879+182C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86547952 | |||||||
| chr8:86548080 | A | G | 4 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-221A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86548080 | |||||||
| chr8:86548083 | A | G | 57 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(54): Show |
58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.880-218A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86548083 | |||||||
| chr8:86548481 | C | T | 2 | a0003c0004t0004g0162 a0004c0006t0005g0161 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1013+47C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548481 | |||||||
| chr8:86548625 | T | G | 60 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(57): Show |
61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1013+191T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548625 | |||||||
| chr8:86548986 | A | G | 1 | a0001c0017t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1013+552A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548986 | |||||||
| chr8:86549131 | C | G | 1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1013+697C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549131 | |||||||
| chr8:86549156 | T | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013+722T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549156 | |||||||
| chr8:86549171 | G | A | 2 | a0001c0008t0002g0297 a0001c0008t0004g0298 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1013+737G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549171 | |||||||
| chr8:86549172 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1013+738G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549172 | |||||||
| chr8:86549223 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1013+789A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549223 | |||||||
| chr8:86549514 | T | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1013+1080T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549514 | |||||||
| chr8:86549750 | G | C | 37 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(34): Show |
38 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014-1296G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549750 | |||||||
| chr8:86549879 | C | G | 1 | a0001c0001t0002g0192 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1014-1167C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549879 | |||||||
| chr8:86550052 | G | A | 209 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0190 others(206): Show |
212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1014-994G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550052 | |||||||
| chr8:86550102 | T | C | 37 | a0001c0002t0001g0303 a0001c0002t0001g0310 a0001c0002t0001g0319 others(34): Show |
38 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014-944T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550102 | |||||||
| chr8:86550291 | C | G | 4 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-755C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550291 | |||||||
| chr8:86550492 | C | T | 1 | a0004c0006t0005g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1014-554C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550492 | |||||||
| chr8:86550494 | G | C | 8 | a0001c0001t0001g0222 a0001c0001t0002g0192 a0001c0001t0003g0203 others(5): Show |
8 | HG00544.hp2 HG02071.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-552G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550494 | |||||||
| chr8:86550540 | A | C | 5 | a0001c0002t0002g0289 a0002c0005t0004g0287 a0002c0005t0004g0288 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-506A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550540 | |||||||
| chr8:86550558 | T | C | 212 | a0001c0001t0001g0088 a0001c0001t0001g0146 a0001c0001t0001g0184 others(209): Show |
215 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1014-488T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550558 | |||||||
| chr8:86550575 | G | A | 3 | a0005c0007t0010g0279 a0005c0007t0010g0280 a0005c0007t0010g0281 |
3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1014-471G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550575 | |||||||
| chr8:86550867 | A | C | 3 | a0001c0001t0004g0160 a0002c0003t0002g0144 a0004c0006t0002g0163 |
3 | HG01069.hp1 HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1014-179A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550867 | |||||||
| chr8:86550970 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014-76G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550970 | |||||||
| chr8:86551403 | G | T | 1 | a0001c0001t0003g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1120+169G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551403 | |||||||
| chr8:86551439 | C | T | 18 | a0001c0001t0004g0160 a0001c0001t0010g0178 a0001c0001t0013g0130 others(15): Show |
18 | HG01069.hp1 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1120+205C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551439 | |||||||
| chr8:86551517 | T | C | 4 | a0001c0001t0009g0029 a0003c0004t0009g0187 a0003c0004t0009g0188 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+283T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551517 | |||||||
| chr8:86551650 | G | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0088 others(86): Show |
91 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1120+416G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551650 | |||||||
| chr8:86551691 | T | C | 3 | a0001c0001t0004g0132 a0001c0002t0004g0300 a0002c0003t0005g0139 |
3 | HG02055.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1120+457T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551691 | |||||||
| chr8:86551770 | C | T | 2 | a0001c0001t0002g0005 a0001c0002t0002g0289 |
2 | HG00741.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1120+536C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551770 | |||||||
| chr8:86552085 | T | C | 88 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(85): Show |
90 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1120+851T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552085 | |||||||
| chr8:86552100 | T | G | 1 | a0001c0010t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+866T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552100 | |||||||
| chr8:86552101 | A | G | 1 | a0001c0010t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+867A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552101 | |||||||
| chr8:86552104 | T | TGGGAGGG others(12): Show |
1 | a0001c0010t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+871_1120+872i others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552104 | ||||||
| chr8:86552269 | C | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(200): Show |
204 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1120+1035C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552269 | |||||||
| chr8:86552358 | T | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1120+1124T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552358 | |||||||
| chr8:86552407 | T | C | 1 | a0001c0001t0004g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1120+1173T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552407 | |||||||
| chr8:86552418 | T | A | 1 | a0003c0004t0004g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1120+1184T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552418 | |||||||
| chr8:86552463 | TAATTAGC others(14): Show |
T | 1 | a0001c0001t0001g0190 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1120+1233_1120+125 others(25): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552463 | ||||||
| chr8:86552549 | G | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(63): Show |
66 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1120+1315G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552549 | |||||||
| chr8:86552564 | G | C | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1120+1330G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552564 | |||||||
| chr8:86552574 | C | T | 1 | a0001c0001t0003g0277 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1120+1340C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552574 | |||||||
| chr8:86552576 | A | G | 2 | a0001c0001t0001g0129 a0001c0002t0001g0321 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1120+1342A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552576 | |||||||
| chr8:86552837 | A | AT | 72 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0024 others(69): Show |
72 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1120+1621dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552837 | ||||||
| chr8:86552837 | AT | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0093 a0001c0001t0001g0129 others(5): Show |
8 | HG01975.hp1 HG02897.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+1621delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552837 | ||||||
| chr8:86552856 | C | T | 2 | a0001c0001t0002g0005 a0001c0002t0002g0289 |
2 | HG00741.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1120+1622C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552856 | |||||||
| chr8:86552862 | G | A | 65 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(62): Show |
65 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1120+1628G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552862 | |||||||
| chr8:86552908 | T | C | 257 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(254): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1120+1674T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552908 | |||||||
| chr8:86552930 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1120+1696C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552930 | |||||||
| chr8:86552932 | C | T | 5 | a0001c0001t0006g0012 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01167.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+1698C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552932 | |||||||
| chr8:86552958 | G | GCAGCCCC others(57): Show |
1 | a0001c0001t0001g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1120+1725_1120+172 others(68): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552958 | ||||||
| chr8:86552962 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1120+1728G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552962 | |||||||
| chr8:86552962 | G | GCACCCCC others(6): Show |
1 | a0001c0001t0001g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1120+1729_1120+173 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCC | 29 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(26): Show |
29 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+1742_1120+174 others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCACCC others(51): Show |
1 | a0007c0015t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1120+1731_1120+173 others(62): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCC | 27 | a0001c0001t0002g0036 a0001c0001t0002g0064 a0001c0001t0002g0079 others(24): Show |
27 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1120+1741_1120+174 others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(4): Show |
1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1120+1736_1120+173 others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(6): Show |
4 | a0001c0001t0001g0224 a0001c0002t0001g0319 a0001c0002t0001g0322 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1736_1120+173 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(3): Show |
4 | a0001c0001t0001g0084 a0001c0001t0004g0056 a0001c0001t0006g0098 others(1): Show |
4 | HG02886.hp2 HG03490.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1735_1120+174 others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(4): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0106 a0001c0001t0001g0110 others(1): Show |
4 | HG00735.hp1 NA19009.hp2 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+1734_1120+174 others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(5): Show |
8 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0075 others(5): Show |
8 | HG00558.hp2 HG01975.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+1733_1120+174 others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(6): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0095 a0001c0001t0001g0108 others(3): Show |
6 | HG01255.hp1 HG01358.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+1732_1120+174 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(7): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0074 others(4): Show |
7 | HG01106.hp1 HG01192.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+1731_1120+174 others(18): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(8): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(3): Show |
6 | HG02083.hp2 HG02129.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+1730_1120+174 others(19): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(9): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(5): Show |
8 | HG01496.hp1 HG01496.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+1729_1120+174 others(20): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(10): Show |
9 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0099 others(6): Show |
9 | HG00609.hp1 HG01928.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(11): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0244 |
2 | HG01109.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(22): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(12): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0276 a0001c0002t0001g0310 others(1): Show |
4 | HG00735.hp2 HG01978.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(23): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(13): Show |
1 | a0001c0010t0001g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(24): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552962 | G | GCCCCCCC others(17): Show |
1 | a0001c0001t0006g0012 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(28): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | ||||||
| chr8:86552970 | C | CCCG | 29 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0113 others(26): Show |
29 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+1738_1120+173 others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552970 | ||||||
| chr8:86552970 | C | CCG | 30 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0088 others(27): Show |
30 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1120+1737_1120+173 others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552970 | ||||||
| chr8:86552970 | C | G | 1 | a0001c0001t0003g0225 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1120+1736C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552970 | |||||||
| chr8:86552972 | C | CCCCCCA | 22 | a0002c0003t0004g0201 a0002c0003t0005g0026 a0002c0003t0005g0048 others(19): Show |
22 | HG00733.hp1 HG01255.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1120+1743_1120+174 others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552972 | ||||||
| chr8:86552972 | C | CCCCCCCC others(3): Show |
1 | a0002c0003t0005g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552972 | ||||||
| chr8:86552973 | C | CT | 26 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0054 others(23): Show |
28 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120+1739_1120+174 others(5): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552973 | |||||||
| chr8:86552973 | C | T | 12 | a0001c0001t0004g0025 a0001c0001t0004g0132 a0001c0001t0007g0137 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120+1739C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552973 | |||||||
| chr8:86552979 | G | A | 130 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1120+1745G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552979 | |||||||
| chr8:86552979 | G | C | 9 | a0001c0001t0002g0141 a0001c0001t0008g0021 a0001c0002t0006g0268 others(6): Show |
9 | HG02145.hp1 HG02647.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120+1745G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552979 | |||||||
| chr8:86552980 | C | CCCCCCCC others(8): Show |
1 | a0001c0001t0008g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1120+1748_1120+174 others(19): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552980 | ||||||
| chr8:86553098 | T | C | 257 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(254): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1121-1753T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553098 | |||||||
| chr8:86553277 | A | T | 12 | a0001c0001t0004g0056 a0001c0001t0004g0076 a0001c0001t0004g0160 others(9): Show |
12 | HG01069.hp1 HG01070.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-1574A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553277 | |||||||
| chr8:86553366 | C | G | 1 | a0001c0001t0003g0009 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1121-1485C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553366 | |||||||
| chr8:86553483 | A | T | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1121-1368A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553483 | |||||||
| chr8:86553484 | A | C | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1121-1367A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553484 | |||||||
| chr8:86553509 | A | G | 1 | a0003c0004t0004g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1121-1342A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553509 | |||||||
| chr8:86553529 | G | A | 17 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(14): Show |
17 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1121-1322G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553529 | |||||||
| chr8:86553703 | C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1121-1148C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553703 | |||||||
| chr8:86553749 | G | GT | 53 | a0001c0001t0001g0060 a0001c0001t0001g0263 a0001c0001t0002g0005 others(50): Show |
54 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1121-1085dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | ||||||
| chr8:86553749 | G | GTT | 67 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1121-1086_1121-108 others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | ||||||
| chr8:86553749 | GT | G | 20 | a0001c0001t0001g0022 a0001c0001t0001g0285 a0001c0001t0002g0255 others(17): Show |
20 | HG01070.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1121-1085delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | ||||||
| chr8:86553828 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0113 |
2 | NA18956.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1121-1023T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553828 | |||||||
| chr8:86553930 | A | G | 142 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(139): Show |
143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1121-921A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553930 | |||||||
| chr8:86553931 | G | A | 257 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(254): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1121-920G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553931 | |||||||
| chr8:86554215 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1121-636A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554215 | |||||||
| chr8:86554304 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1121-547C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554304 | |||||||
| chr8:86554352 | A | C | 2 | a0004c0006t0005g0159 a0004c0006t0005g0175 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1121-499A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554352 | |||||||
| chr8:86554537 | A | G | 1 | a0001c0002t0006g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1121-314A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554537 | |||||||
| chr8:86554595 | G | T | 2 | a0003c0004t0004g0156 a0003c0004t0004g0157 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1121-256G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554595 | |||||||
| chr8:86554596 | T | A | 2 | a0003c0004t0004g0156 a0003c0004t0004g0157 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1121-255T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554596 | |||||||
| chr8:86554645 | G | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1121-206G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554645 | |||||||
| chr8:86554687 | T | C | 6 | a0001c0001t0006g0012 a0001c0001t0006g0040 a0001c0001t0006g0041 others(3): Show |
6 | HG01167.hp2 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-164T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554687 | |||||||
| chr8:86554803 | G | A | 142 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(139): Show |
143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1121-48G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554803 | |||||||
| chr8:86554848 | T | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0077 |
2 | NA18943.hp2 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.1121-3T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554848 | |||||||
| chr8:86555077 | A | C | 142 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(139): Show |
143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1254+93A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555077 | |||||||
| chr8:86555156 | A | C | 9 | a0001c0001t0004g0025 a0001c0001t0004g0132 a0001c0002t0004g0300 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+172A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555156 | |||||||
| chr8:86555199 | T | C | 1 | a0003c0004t0004g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1254+215T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555199 | |||||||
| chr8:86555234 | C | CA | 25 | a0001c0001t0001g0075 a0001c0001t0004g0025 a0001c0001t0004g0132 others(22): Show |
25 | HG01081.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1254+263dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555234 | ||||||
| chr8:86555234 | C | CAA | 15 | a0001c0001t0009g0029 a0001c0001t0010g0178 a0001c0002t0004g0336 others(12): Show |
15 | HG01070.hp1 HG02572.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+262_1254+263d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555234 | ||||||
| chr8:86555300 | G | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(62): Show |
65 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1254+316G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555300 | |||||||
| chr8:86555418 | G | A | 41 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0014 others(38): Show |
43 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1254+434G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555418 | |||||||
| chr8:86555478 | A | G | 142 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(139): Show |
143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1254+494A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555478 | |||||||
| chr8:86555549 | A | T | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1255-553A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555549 | |||||||
| chr8:86555620 | A | C | 73 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(70): Show |
73 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1255-482A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555620 | |||||||
| chr8:86555686 | C | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0049 a0001c0001t0002g0064 others(5): Show |
8 | HG00639.hp2 HG00642.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-416C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555686 | |||||||
| chr8:86555709 | TATTCTA | T | 13 | a0002c0003t0005g0048 a0002c0003t0005g0142 a0002c0003t0005g0143 others(10): Show |
13 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-384_1255-379d others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555709 | ||||||
| chr8:86555746 | T | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1255-356T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555746 | |||||||
| chr8:86555770 | C | T | 9 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(6): Show |
9 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-332C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555770 | |||||||
| chr8:86555906 | G | A | 115 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0067 others(112): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1255-196G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555906 | |||||||
| chr8:86556365 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1491+27C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556365 | |||||||
| chr8:86556416 | T | G | 142 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(139): Show |
143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1491+78T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556416 | |||||||
| chr8:86556943 | T | C | 1 | a0002c0003t0005g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1491+605T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556943 | |||||||
| chr8:86557120 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0114 a0001c0002t0002g0289 |
3 | HG00741.hp1 HG03579.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1491+782G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557120 | |||||||
| chr8:86557196 | C | T | 53 | a0001c0002t0005g0325 a0001c0002t0005g0326 a0002c0003t0002g0144 others(50): Show |
54 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1491+858C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557196 | |||||||
| chr8:86557217 | T | G | 141 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(138): Show |
142 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1491+879T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557217 | |||||||
| chr8:86557249 | T | C | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1491+911T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557249 | |||||||
| chr8:86557261 | A | G | 248 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(245): Show |
251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1491+923A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557261 | |||||||
| chr8:86557297 | C | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0191 |
3 | HG00438.hp2 HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1491+959C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557297 | |||||||
| chr8:86557337 | C | T | 248 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(245): Show |
251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-951C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557337 | |||||||
| chr8:86557414 | C | G | 248 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(245): Show |
251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-874C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557414 | |||||||
| chr8:86557415 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1492-873C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557415 | |||||||
| chr8:86557425 | C | T | 58 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0014 others(55): Show |
60 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1492-863C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557425 | |||||||
| chr8:86557426 | G | T | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1492-862G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557426 | |||||||
| chr8:86557482 | A | G | 66 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(63): Show |
66 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1492-806A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557482 | |||||||
| chr8:86557516 | T | C | 9 | a0001c0001t0004g0025 a0001c0001t0004g0132 a0001c0002t0004g0300 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1492-772T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557516 | |||||||
| chr8:86557624 | T | C | 2 | a0001c0001t0008g0020 a0001c0001t0008g0021 |
2 | NA19010.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1492-664T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557624 | |||||||
| chr8:86557755 | T | TAC | 3 | a0001c0001t0004g0056 a0001c0001t0004g0076 a0001c0001t0004g0160 |
3 | HG01069.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1492-515_1492-514d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr8 | 86557755 | ||||||
| chr8:86557884 | T | G | 18 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(15): Show |
18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1492-404T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557884 | |||||||
| chr8:86557898 | T | G | 18 | a0001c0001t0007g0134 a0001c0001t0007g0137 a0001c0001t0007g0138 others(15): Show |
18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1492-390T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557898 | |||||||
| chr8:86557909 | T | C | 248 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(245): Show |
251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-379T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557909 | |||||||
| chr8:86557976 | A | C | 57 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0032 others(54): Show |
57 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1492-312A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557976 | |||||||
| chr8:86558019 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1492-269T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558019 | |||||||
| chr8:86558028 | A | T | 1 | a0001c0001t0004g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492-260A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558028 | |||||||
| chr8:86558150 | C | T | 5 | a0001c0002t0006g0268 a0001c0002t0006g0269 a0001c0002t0006g0270 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1492-138C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558150 | |||||||
| chr8:86558166 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(7): Show |
10 | HG01192.hp1 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492-122G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558166 | |||||||
| chr8:86558213 | T | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1492-75T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558213 |