Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6674 |
| ensemblid | ENSG00000104450.13 |
| hgncid | 11212 |
| symbol | SPAG1 |
| name | sperm associated antigen 1 |
| refseq_nuc | NM_003114.5 |
| refseq_prot | NP_003105.2 |
| ensembl_nuc | ENST00000388798.7 |
| ensembl_prot | ENSP00000373450.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 100158587 |
| end | 100241904 |
| strand | + |
| ver | v1.2 |
| region | chr8:100158587-100241904 |
| region5000 | chr8:100153587-100246904 |
| regionname0 | SPAG1_chr8_100158587_100241904 |
| regionname5000 | SPAG1_chr8_100153587_100246904 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 926 | 160 | 47 | 33 | 59 | 6 | 14 | 42 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0002 | 1/0 | 926 | 130 | 27 | 17 | 67 | 1 | 17 | 53 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0003 | 0/0 | 927 | 56 | 5 | 16 | 19 | 7 | 9 | 17 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(922): Show |
chr8 | 100153587 | 100246904 |
| a0004 | 0/0 | 926 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0005 | 0/0 | 926 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0006 | 0/0 | 926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0007 | 0/0 | 926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0008 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(922): Show |
chr8 | 100153587 | 100246904 |
| a0009 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0010 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0011 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0012 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| a0013 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(922): Show |
chr8 | 100153587 | 100246904 |
| a0014 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | MTTKD others(921): Show |
chr8 | 100153587 | 100246904 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 2778 | 91 | 1 | 22 | 52 | 4 | 11 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0003 | 0/0 | 2778 | 37 | 30 | 7 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0008 | 0/0 | 2778 | 14 | 14 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0009 | 0/0 | 2778 | 11 | 1 | 4 | 2 | 1 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0012 | 0/0 | 2778 | 2 | 1 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0015 | 0/0 | 2778 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0016 | 0/0 | 2778 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0001c0021 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0002c0001 | 1/0 | 2778 | 93 | 17 | 14 | 51 | 1 | 9 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0002c0005 | 0/0 | 2778 | 22 | 0 | 2 | 16 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0002c0007 | 0/0 | 2778 | 15 | 10 | 1 | 0 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0003c0004 | 0/0 | 2781 | 35 | 5 | 15 | 0 | 7 | 8 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2776): Show |
chr8 | 100153587 | 100246904 | ||
| a0003c0006 | 0/0 | 2781 | 20 | 0 | 1 | 19 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2776): Show |
chr8 | 100153587 | 100246904 | ||
| a0003c0018 | 0/0 | 2781 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2776): Show |
chr8 | 100153587 | 100246904 | ||
| a0004c0010 | 0/0 | 2778 | 6 | 0 | 0 | 6 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0005c0011 | 0/0 | 2778 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0006c0013 | 0/0 | 2778 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0007c0014 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0008c0019 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2776): Show |
chr8 | 100153587 | 100246904 | ||
| a0009c0020 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0010c0024 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0011c0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0012c0025 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 | ||
| a0013c0017 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2776): Show |
chr8 | 100153587 | 100246904 | ||
| a0014c0022 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | ATGAC others(2773): Show |
chr8 | 100153587 | 100246904 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3695 | 90 | 1 | 21 | 52 | 4 | 11 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0002t0007 | 0/0 | 3695 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0003t0001 | 0/0 | 3695 | 22 | 19 | 3 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0003t0003 | 0/0 | 3695 | 14 | 11 | 3 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0003t0005 | 0/0 | 3695 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0008t0002 | 0/0 | 3698 | 13 | 13 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0001c0008t0008 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0001c0009t0001 | 0/0 | 3695 | 11 | 1 | 4 | 2 | 1 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0012t0001 | 0/0 | 3695 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0012t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0001c0015t0001 | 0/0 | 3695 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0016t0001 | 0/0 | 3695 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0001c0021t0001 | 0/0 | 3695 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0001t0001 | 1/0 | 3695 | 88 | 15 | 13 | 49 | 1 | 9 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0001t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0002c0001t0004 | 0/0 | 3695 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0001t0006 | 0/0 | 3695 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0005t0001 | 0/0 | 3695 | 3 | 0 | 0 | 2 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0005t0002 | 0/0 | 3698 | 19 | 0 | 2 | 14 | 0 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0002c0007t0001 | 0/0 | 3695 | 13 | 10 | 1 | 0 | 0 | 2 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0002c0007t0002 | 0/0 | 3698 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0003c0004t0001 | 0/0 | 3698 | 34 | 4 | 15 | 0 | 7 | 8 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0003c0004t0005 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0003c0006t0001 | 0/0 | 3698 | 20 | 0 | 1 | 19 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0003c0018t0001 | 0/0 | 3698 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0004c0010t0001 | 0/0 | 3695 | 6 | 0 | 0 | 6 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0005c0011t0002 | 0/0 | 3698 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0006c0013t0001 | 0/0 | 3695 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0007c0014t0001 | 0/0 | 3695 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0008c0019t0001 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0009c0020t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0010c0024t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0011c0023t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0012c0025t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| a0013c0017t0001 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3693): Show |
chr8 | 100153587 | 100246904 |
| a0014c0022t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | GTTAG others(3690): Show |
chr8 | 100153587 | 100246904 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0012t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0015t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0015t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0016t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0016t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0021t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0006t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0018t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0011t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0011t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0006c0013t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0006c0013t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0007c0014t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0007c0014t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0008c0019t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0009c0020t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0010c0024t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0011c0023t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0012c0025t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0013c0017t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0014c0022t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0033 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0082 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0047 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0180 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0279 | EUR | FIN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0044 | EUR | FIN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0319 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00423 | hp1 | a0008 | c0019 | t0001 | g0049 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0336 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00438 | hp2 | a0003 | c0006 | t0001 | g0059 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0325 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0339 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0350 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00621 | hp2 | a0001 | c0021 | t0001 | g0153 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0332 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0270 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0099 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0080 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0101 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0271 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01071 | hp1 | a0003 | c0004 | t0001 | g0070 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0269 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01074 | hp1 | a0003 | c0004 | t0001 | g0068 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01081 | hp1 | a0002 | c0005 | t0002 | g0230 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0081 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01099 | hp2 | a0001 | c0003 | t0005 | g0289 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01167 | hp1 | a0002 | c0007 | t0001 | g0194 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01168 | hp1 | a0006 | c0013 | t0001 | g0131 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0341 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01169 | hp2 | a0006 | c0013 | t0001 | g0098 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01175 | hp1 | a0001 | c0002 | t0007 | g0177 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0093 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0247 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0112 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01255 | hp1 | a0003 | c0004 | t0001 | g0029 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01255 | hp2 | a0002 | c0001 | t0004 | g0273 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0266 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0026 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0062 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0301 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01346 | hp2 | a0003 | c0004 | t0001 | g0043 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0267 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01361 | hp1 | a0003 | c0004 | t0001 | g0045 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01496 | hp1 | a0001 | c0009 | t0001 | g0007 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01516 | hp1 | a0003 | c0004 | t0001 | g0072 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01516 | hp2 | a0001 | c0012 | t0001 | g0169 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01517 | hp1 | a0003 | c0004 | t0001 | g0071 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0349 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0213 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0261 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0198 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0218 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01934 | hp2 | a0003 | c0004 | t0001 | g0067 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01943 | hp1 | a0003 | c0006 | t0001 | g0041 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0291 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01978 | hp1 | a0001 | c0009 | t0001 | g0290 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0028 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0331 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02004 | hp2 | a0001 | c0009 | t0001 | g0285 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0304 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0322 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0308 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0012 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02056 | hp1 | a0003 | c0006 | t0001 | g0073 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0297 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0334 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02145 | hp1 | a0009 | c0020 | t0001 | g0248 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02148 | hp1 | a0002 | c0005 | t0002 | g0232 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0333 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0288 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02257 | hp1 | a0001 | c0008 | t0002 | g0240 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0287 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02258 | hp2 | a0002 | c0007 | t0001 | g0193 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02273 | hp1 | a0003 | c0004 | t0001 | g0030 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02280 | hp2 | a0005 | c0011 | t0002 | g0005 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0259 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02451 | hp2 | a0002 | c0007 | t0001 | g0132 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02572 | hp1 | a0002 | c0007 | t0001 | g0187 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02572 | hp2 | a0007 | c0014 | t0001 | g0253 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0109 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02630 | hp1 | a0010 | c0024 | t0002 | g0128 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0282 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02647 | hp1 | a0002 | c0007 | t0001 | g0199 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02647 | hp2 | a0001 | c0008 | t0002 | g0090 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02683 | hp1 | a0002 | c0007 | t0002 | g0175 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02683 | hp2 | a0003 | c0004 | t0001 | g0060 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0352 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0284 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02717 | hp1 | a0002 | c0001 | t0004 | g0278 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02717 | hp2 | a0011 | c0023 | t0001 | g0079 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0105 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0354 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02735 | hp1 | a0002 | c0005 | t0002 | g0229 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0353 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0355 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0100 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0272 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02818 | hp2 | a0002 | c0007 | t0001 | g0192 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0296 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0034 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02895 | hp1 | a0012 | c0025 | t0001 | g0260 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02895 | hp2 | a0001 | c0008 | t0002 | g0091 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02897 | hp1 | a0001 | c0008 | t0002 | g0089 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02897 | hp2 | a0005 | c0011 | t0002 | g0249 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0264 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02922 | hp2 | a0005 | c0011 | t0002 | g0005 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0356 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0108 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0076 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0286 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03017 | hp2 | a0003 | c0004 | t0001 | g0001 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03041 | hp1 | a0001 | c0008 | t0002 | g0214 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0009 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0102 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03130 | hp2 | a0002 | c0001 | t0001 | g0262 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03139 | hp1 | a0002 | c0007 | t0001 | g0189 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03139 | hp2 | a0013 | c0017 | t0001 | g0246 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03195 | hp1 | a0002 | c0007 | t0001 | g0190 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0107 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0197 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03209 | hp2 | a0002 | c0007 | t0001 | g0103 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03225 | hp1 | a0001 | c0008 | t0002 | g0242 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03225 | hp2 | a0001 | c0012 | t0002 | g0113 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03239 | hp1 | a0002 | c0005 | t0002 | g0237 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03239 | hp2 | a0002 | c0007 | t0001 | g0149 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03486 | hp2 | a0001 | c0008 | t0002 | g0244 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0283 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03491 | hp1 | a0003 | c0004 | t0001 | g0032 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0106 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03516 | hp2 | a0001 | c0008 | t0002 | g0216 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03540 | hp2 | a0014 | c0022 | t0001 | g0173 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0281 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03579 | hp2 | a0001 | c0008 | t0002 | g0238 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03654 | hp1 | a0003 | c0018 | t0001 | g0061 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0300 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03710 | hp2 | a0001 | c0009 | t0001 | g0276 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03831 | hp2 | a0003 | c0004 | t0001 | g0051 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03834 | hp2 | a0002 | c0005 | t0002 | g0217 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0294 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03927 | hp2 | a0002 | c0007 | t0002 | g0174 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03942 | hp1 | a0002 | c0005 | t0001 | g0234 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03942 | hp2 | a0003 | c0004 | t0001 | g0054 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0277 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04115 | hp2 | a0003 | c0004 | t0001 | g0042 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0219 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0024 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0337 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04228 | hp1 | a0002 | c0007 | t0001 | g0200 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04228 | hp2 | a0003 | c0004 | t0001 | g0052 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | CHB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | CHB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0110 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0255 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18943 | hp1 | a0003 | c0006 | t0001 | g0048 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18944 | hp2 | a0002 | c0005 | t0002 | g0235 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18946 | hp1 | a0004 | c0010 | t0001 | g0142 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18946 | hp2 | a0002 | c0005 | t0002 | g0245 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18947 | hp1 | a0001 | c0016 | t0001 | g0345 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0307 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0323 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18949 | hp2 | a0002 | c0005 | t0002 | g0088 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18951 | hp2 | a0003 | c0006 | t0001 | g0039 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18952 | hp2 | a0003 | c0006 | t0001 | g0066 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18953 | hp2 | a0004 | c0010 | t0001 | g0138 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18954 | hp2 | a0003 | c0006 | t0001 | g0038 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18957 | hp1 | a0001 | c0015 | t0001 | g0225 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18961 | hp1 | a0002 | c0001 | t0006 | g0094 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18961 | hp2 | a0004 | c0010 | t0001 | g0209 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18962 | hp2 | a0003 | c0006 | t0001 | g0035 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0298 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0329 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18965 | hp2 | a0002 | c0005 | t0002 | g0236 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18966 | hp2 | a0002 | c0005 | t0002 | g0220 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18968 | hp1 | a0002 | c0005 | t0001 | g0226 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0299 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18969 | hp2 | a0002 | c0005 | t0002 | g0228 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18971 | hp1 | a0001 | c0015 | t0001 | g0221 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18975 | hp1 | a0004 | c0010 | t0001 | g0143 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18975 | hp2 | a0002 | c0005 | t0002 | g0223 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0328 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0312 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0295 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0335 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18983 | hp2 | a0002 | c0005 | t0002 | g0231 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18985 | hp2 | a0002 | c0005 | t0002 | g0351 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18988 | hp1 | a0002 | c0005 | t0002 | g0250 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18992 | hp1 | a0003 | c0006 | t0001 | g0058 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18995 | hp2 | a0002 | c0005 | t0002 | g0239 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18997 | hp1 | a0003 | c0006 | t0001 | g0057 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18997 | hp2 | a0001 | c0009 | t0001 | g0309 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0330 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18999 | hp1 | a0003 | c0006 | t0001 | g0040 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19001 | hp1 | a0002 | c0005 | t0002 | g0227 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0321 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19002 | hp2 | a0003 | c0006 | t0001 | g0036 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0305 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19003 | hp2 | a0003 | c0006 | t0001 | g0037 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19007 | hp1 | a0001 | c0009 | t0001 | g0326 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0258 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19030 | hp1 | a0001 | c0008 | t0008 | g0243 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0263 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0111 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19043 | hp2 | a0001 | c0008 | t0002 | g0006 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19054 | hp1 | a0002 | c0005 | t0002 | g0224 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19054 | hp2 | a0004 | c0010 | t0001 | g0196 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0320 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19062 | hp2 | a0003 | c0006 | t0001 | g0056 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19063 | hp2 | a0003 | c0006 | t0001 | g0069 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0313 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19068 | hp2 | a0003 | c0006 | t0001 | g0065 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19070 | hp1 | a0003 | c0006 | t0001 | g0063 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19070 | hp2 | a0004 | c0010 | t0001 | g0152 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0357 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19076 | hp1 | a0002 | c0001 | t0001 | g0318 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0302 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19079 | hp1 | a0001 | c0016 | t0001 | g0347 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0316 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19085 | hp1 | a0002 | c0005 | t0002 | g0222 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0324 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19086 | hp1 | a0002 | c0005 | t0001 | g0233 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0314 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19088 | hp1 | a0003 | c0006 | t0001 | g0064 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19091 | hp1 | a0002 | c0001 | t0002 | g0338 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19091 | hp2 | a0003 | c0006 | t0001 | g0340 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20129 | hp1 | a0001 | c0008 | t0002 | g0215 | AFR | ASW | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0342 | AFR | ASW | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20752 | hp1 | a0001 | c0009 | t0001 | g0007 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0053 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20805 | hp2 | a0003 | c0004 | t0001 | g0055 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01123 | hp1 | a0001 | c0009 | t0001 | g0268 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02109 | hp1 | a0001 | c0008 | t0002 | g0006 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0046 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0188 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02486 | hp2 | a0007 | c0014 | t0001 | g0254 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03471 | hp2 | a0003 | c0004 | t0005 | g0251 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18955 | hp1 | a0003 | c0006 | t0001 | g0050 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20300 | hp1 | a0002 | c0007 | t0001 | g0191 | AFR | USA | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0031 | AFR | USA | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA21309 | hp1 | a0001 | c0008 | t0002 | g0241 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA21309 | hp2 | a0002 | c0001 | t0004 | g0275 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0186 | REF | REF | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0274 | REF | REF | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100177913 | G | A | 1 | a0013 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.398G>A | p.Gly133Asp | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/19 | 430/3695 | 398/2781 | 133/926 | chr8 | 100177913 | |||
| chr8:100183424 | C | T | 1 | a0012 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.476C>T | p.Ala159Val | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/19 | 508/3695 | 476/2781 | 159/926 | chr8 | 100183424 | |||
| chr8:100184027 | A | C | 1 | a0010 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.560A>C | p.His187Pro | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/19 | 592/3695 | 560/2781 | 187/926 | chr8 | 100184027 | |||
| chr8:100184628 | G | C | 1 | a0005 | 3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
missense_variant&splice_region_variant | MODERATE | c.596G>C | p.Gly199Ala | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/19 | 628/3695 | 596/2781 | 199/926 | chr8 | 100184628 | |||
| chr8:100191434 | C | T | 1 | a0007 | 2 | HG02486.hp2 HG02572.hp2 |
missense_variant | MODERATE | c.877C>T | p.Arg293Trp | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/19 | 909/3695 | 877/2781 | 293/926 | chr8 | 100191434 | |||
| chr8:100194163 | G | A | 3 | a0003 a0008 a0013 |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
missense_variant | MODERATE | c.991G>A | p.Glu331Lys | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1023/3695 | 991/2781 | 331/926 | chr8 | 100194163 | |||
| chr8:100194229 | A | G | 1 | a0008 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1057A>G | p.Lys353Glu | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1089/3695 | 1057/2781 | 353/926 | chr8 | 100194229 | |||
| chr8:100194231 | A | AGAC | 3 | a0003 a0008 a0013 |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
conservative_inframe_insertion | MODERATE | c.1059_1060insGAC | p.Lys353_Ser354insAs others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1092/3695 | 1060/2781 | 354/926 | chr8 | 100194231 | |||
| chr8:100213219 | C | G | 1 | a0011 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1226C>G | p.Thr409Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/19 | 1258/3695 | 1226/2781 | 409/926 | chr8 | 100213219 | |||
| chr8:100220329 | T | C | 2 | a0009 a0011 |
2 | HG02145.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1586T>C | p.Met529Thr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/19 | 1618/3695 | 1586/2781 | 529/926 | chr8 | 100220329 | |||
| chr8:100225243 | C | T | 1 | a0004 | 6 | NA18946.hp1 NA18953.hp2 NA18961.hp2 others(3): Show |
missense_variant | MODERATE | c.1759C>T | p.Pro587Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/19 | 1791/3695 | 1759/2781 | 587/926 | chr8 | 100225243 | |||
| chr8:100240452 | T | C | 11 | a0001 a0003 a0004 others(8): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
missense_variant | MODERATE | c.2330T>C | p.Met777Thr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2362/3695 | 2330/2781 | 777/926 | chr8 | 100240452 | |||
| chr8:100240601 | C | T | 1 | a0014 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2479C>T | p.His827Tyr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2511/3695 | 2479/2781 | 827/926 | chr8 | 100240601 | |||
| chr8:100240958 | A | G | 1 | a0006 | 2 | HG01168.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.2717A>G | p.Asp906Gly | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 2749/3695 | 2717/2781 | 906/926 | chr8 | 100240958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100183422 | C | T | 1 | a0001c0016 | 2 | NA18947.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.474C>T | p.Tyr158Tyr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/19 | 506/3695 | 474/2781 | 158/926 | chr8 | 100183422 | |||
| chr8:100184701 | A | G | 3 | a0001c0008 a0001c0015 a0002c0005 |
38 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(35): Show |
synonymous_variant | LOW | c.669A>G | p.Gly223Gly | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/19 | 701/3695 | 669/2781 | 223/926 | chr8 | 100184701 | |||
| chr8:100213331 | C | G | 9 | a0001c0002 a0001c0012 a0001c0016 others(6): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
synonymous_variant | LOW | c.1338C>G | p.Ala446Ala | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/19 | 1370/3695 | 1338/2781 | 446/926 | chr8 | 100213331 | |||
| chr8:100240579 | G | A | 1 | a0001c0021 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.2457G>A | p.Arg819Arg | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2489/3695 | 2457/2781 | 819/926 | chr8 | 100240579 | |||
| chr8:100240956 | G | A | 7 | a0001c0002 a0001c0009 a0001c0015 others(4): Show |
113 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(110): Show |
synonymous_variant | LOW | c.2715G>A | p.Ser905Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 2747/3695 | 2715/2781 | 905/926 | chr8 | 100240956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100158594 | G | T | 1 | a0001c0008t0008 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/19 | chr8 | 100158594 | |||||||
| chr8:100158601 | G | C | 1 | a0002c0001t0006 | 1 | NA18961.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/19 | 3680 | chr8 | 100158601 | ||||||
| chr8:100241146 | C | G | 1 | a0002c0001t0004 | 3 | HG01255.hp2 HG02717.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 124 | chr8 | 100241146 | ||||||
| chr8:100241241 | T | C | 1 | a0001c0003t0003 | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 219 | chr8 | 100241241 | ||||||
| chr8:100241314 | G | T | 2 | a0001c0003t0005 a0003c0004t0005 |
2 | HG01099.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 292 | chr8 | 100241314 | ||||||
| chr8:100241772 | T | TCCC | 8 | a0001c0008t0002 a0001c0008t0008 a0001c0012t0002 others(5): Show |
41 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*755dupCCC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 756 | INFO_REALIGN_3_PRIME | chr8 | 100241772 | |||||
| chr8:100241796 | C | G | 1 | a0001c0002t0007 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 774 | chr8 | 100241796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100158692 | T | C | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+76T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158692 | |||||||
| chr8:100158754 | G | T | 1 | a0002c0001t0001g0357 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-3+138G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158754 | |||||||
| chr8:100158828 | A | G | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-3+212A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158828 | |||||||
| chr8:100158971 | C | CA | 14 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(11): Show |
15 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+371dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | ||||||
| chr8:100158971 | C | CAA | 62 | a0001c0003t0001g0074 a0001c0003t0001g0075 a0001c0003t0001g0076 others(59): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-3+370_-3+371dupAA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | ||||||
| chr8:100158971 | C | CAAA | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+369_-3+371dupAA others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | ||||||
| chr8:100158971 | CA | C | 11 | a0001c0002t0001g0343 a0001c0002t0001g0344 a0001c0002t0001g0346 others(8): Show |
11 | HG00609.hp1 HG01517.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+371delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | ||||||
| chr8:100159010 | T | C | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-3+394T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100159010 | |||||||
| chr8:100159781 | T | C | 4 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0007c0014t0001g0253 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1165T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100159781 | |||||||
| chr8:100160027 | G | A | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-3+1411G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160027 | |||||||
| chr8:100160041 | G | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1425G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160041 | |||||||
| chr8:100160166 | C | G | 1 | a0003c0004t0005g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+1550C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160166 | |||||||
| chr8:100160203 | G | C | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1587G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160203 | |||||||
| chr8:100160626 | C | CA | 177 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(174): Show |
181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-2-1636dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100160626 | ||||||
| chr8:100160674 | A | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1605A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160674 | |||||||
| chr8:100160715 | G | C | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2-1564G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160715 | |||||||
| chr8:100161023 | C | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1256C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161023 | |||||||
| chr8:100161150 | G | A | 3 | a0001c0008t0002g0214 a0001c0008t0002g0215 a0001c0008t0002g0216 |
3 | HG03041.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-1129G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161150 | |||||||
| chr8:100161214 | C | T | 9 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0001c0002t0001g0203 others(6): Show |
9 | HG00639.hp2 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-1065C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161214 | |||||||
| chr8:100161232 | T | C | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1047T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161232 | |||||||
| chr8:100161480 | C | T | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-799C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161480 | |||||||
| chr8:100161568 | A | G | 1 | a0001c0009t0001g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-711A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161568 | |||||||
| chr8:100161646 | A | G | 2 | a0002c0001t0001g0008 a0002c0001t0001g0341 |
3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-2-633A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161646 | |||||||
| chr8:100161678 | C | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-601C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161678 | |||||||
| chr8:100161686 | A | G | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-593A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161686 | |||||||
| chr8:100161861 | T | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-2-418T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161861 | |||||||
| chr8:100161903 | T | G | 1 | a0002c0001t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2-376T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161903 | |||||||
| chr8:100161958 | A | C | 246 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-2-321A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161958 | |||||||
| chr8:100162115 | G | T | 1 | a0001c0003t0003g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-164G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162115 | |||||||
| chr8:100162131 | C | A | 1 | a0002c0001t0001g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-148C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162131 | |||||||
| chr8:100162160 | C | T | 39 | a0001c0009t0001g0309 a0001c0009t0001g0326 a0002c0001t0001g0258 others(36): Show |
39 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2-119C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162160 | |||||||
| chr8:100162198 | G | A | 103 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(100): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-2-81G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162198 | |||||||
| chr8:100162243 | A | G | 1 | a0002c0001t0001g0339 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-2-36A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162243 | |||||||
| chr8:100162629 | G | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+209G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162629 | |||||||
| chr8:100162715 | C | T | 62 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(59): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.140+295C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162715 | |||||||
| chr8:100162869 | T | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+449T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162869 | |||||||
| chr8:100162975 | TA | T | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+563delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 100162975 | ||||||
| chr8:100162985 | A | T | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140+565A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162985 | |||||||
| chr8:100163075 | C | T | 1 | a0003c0004t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140+655C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163075 | |||||||
| chr8:100163160 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.140+740G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163160 | |||||||
| chr8:100163202 | G | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+782G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163202 | |||||||
| chr8:100163407 | CT | C | 7 | a0001c0002t0001g0082 a0001c0002t0001g0096 a0001c0002t0001g0097 others(4): Show |
7 | HG00099.hp2 HG01169.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+1002delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 100163407 | ||||||
| chr8:100163573 | G | A | 4 | a0001c0003t0001g0263 a0002c0001t0001g0261 a0002c0001t0001g0262 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+1153G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163573 | |||||||
| chr8:100163637 | C | G | 1 | a0001c0003t0003g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140+1217C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163637 | |||||||
| chr8:100163669 | C | T | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1249C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163669 | |||||||
| chr8:100163990 | T | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1570T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163990 | |||||||
| chr8:100164003 | A | G | 134 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(131): Show |
136 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.140+1583A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164003 | |||||||
| chr8:100164012 | A | T | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1592A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164012 | |||||||
| chr8:100164051 | T | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1631T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164051 | |||||||
| chr8:100164078 | C | G | 1 | a0001c0003t0003g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.140+1658C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164078 | |||||||
| chr8:100164321 | A | T | 1 | a0004c0010t0001g0196 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141-1493A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164321 | |||||||
| chr8:100164356 | T | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1458T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164356 | |||||||
| chr8:100164421 | T | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1393T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164421 | |||||||
| chr8:100164477 | T | C | 4 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1337T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164477 | |||||||
| chr8:100164956 | T | C | 3 | a0002c0001t0001g0218 a0005c0011t0002g0005 a0005c0011t0002g0249 |
4 | HG01891.hp2 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-858T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164956 | |||||||
| chr8:100165220 | A | G | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-594A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165220 | |||||||
| chr8:100165368 | T | C | 1 | a0002c0007t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141-446T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165368 | |||||||
| chr8:100165486 | G | T | 1 | a0001c0002t0001g0350 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.141-328G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165486 | |||||||
| chr8:100165529 | C | A | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.141-285C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165529 | |||||||
| chr8:100165538 | C | T | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.141-276C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165538 | |||||||
| chr8:100165766 | G | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.141-48G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165766 | |||||||
| chr8:100166152 | G | A | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+179G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166152 | |||||||
| chr8:100166174 | A | G | 1 | a0001c0002t0001g0195 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.300+201A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166174 | |||||||
| chr8:100166175 | T | C | 4 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0011 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+202T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166175 | |||||||
| chr8:100166177 | A | G | 141 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.300+204A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166177 | |||||||
| chr8:100166284 | A | G | 6 | a0002c0001t0001g0013 a0002c0001t0001g0014 a0002c0001t0001g0015 others(3): Show |
6 | NA18612.hp2 NA18950.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+311A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166284 | |||||||
| chr8:100166487 | C | T | 8 | a0002c0007t0001g0187 a0002c0007t0001g0188 a0002c0007t0001g0189 others(5): Show |
8 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+514C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166487 | |||||||
| chr8:100166568 | T | A | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.300+595T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166568 | |||||||
| chr8:100166645 | C | T | 1 | a0002c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+672C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166645 | |||||||
| chr8:100166665 | T | C | 16 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(13): Show |
16 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.300+692T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166665 | |||||||
| chr8:100166787 | A | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.300+814A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166787 | |||||||
| chr8:100166936 | A | C | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+963A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166936 | |||||||
| chr8:100167182 | A | G | 1 | a0002c0005t0002g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.300+1209A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100167182 | |||||||
| chr8:100167495 | T | C | 1 | a0002c0005t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.300+1522T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100167495 | |||||||
| chr8:100168020 | A | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.300+2047A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168020 | |||||||
| chr8:100168040 | A | C | 65 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(62): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.300+2067A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168040 | |||||||
| chr8:100168115 | T | C | 1 | a0002c0001t0001g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.300+2142T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168115 | |||||||
| chr8:100168360 | G | A | 1 | a0001c0012t0002g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300+2387G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168360 | |||||||
| chr8:100168362 | TA | T | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+2398delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168362 | ||||||
| chr8:100168422 | G | A | 62 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(59): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.300+2449G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168422 | |||||||
| chr8:100168430 | T | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2457T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168430 | |||||||
| chr8:100168559 | A | AT | 19 | a0001c0003t0001g0263 a0001c0009t0001g0294 a0002c0001t0001g0002 others(16): Show |
20 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.300+2599dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168559 | ||||||
| chr8:100168559 | AT | A | 17 | a0001c0002t0001g0003 a0001c0002t0001g0083 a0001c0002t0001g0114 others(14): Show |
18 | HG02055.hp1 HG02080.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+2599delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168559 | ||||||
| chr8:100168610 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2637G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168610 | |||||||
| chr8:100168647 | A | AAGT | 65 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(62): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.300+2676_300+2678d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168647 | ||||||
| chr8:100168687 | C | CTTTTTTT others(7): Show |
5 | a0001c0002t0001g0096 a0001c0002t0001g0124 a0001c0002t0001g0125 others(2): Show |
5 | HG01168.hp2 HG01943.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(8): Show |
95 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(92): Show |
97 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(17): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(9): Show |
31 | a0001c0002t0001g0095 a0001c0002t0001g0121 a0001c0002t0001g0122 others(28): Show |
31 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(10): Show |
5 | a0001c0002t0001g0185 a0001c0003t0003g0101 a0001c0003t0003g0102 others(2): Show |
5 | HG00738.hp2 HG01243.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(19): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(11): Show |
3 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0003g0197 |
3 | HG02559.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(14): Show |
18 | a0001c0008t0002g0214 a0001c0015t0001g0221 a0001c0015t0001g0225 others(15): Show |
19 | HG01081.hp1 HG02280.hp2 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(23): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(15): Show |
9 | a0001c0008t0002g0215 a0001c0008t0002g0238 a0002c0005t0001g0233 others(6): Show |
9 | HG02148.hp1 HG03239.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(16): Show |
27 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(24): Show |
28 | HG00099.hp1 HG01081.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(25): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(17): Show |
17 | a0001c0008t0002g0091 a0001c0008t0002g0216 a0001c0008t0002g0244 others(14): Show |
19 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(18): Show |
14 | a0003c0004t0001g0051 a0003c0004t0001g0052 a0003c0004t0001g0053 others(11): Show |
14 | HG00438.hp2 HG01261.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(27): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(20): Show |
1 | a0003c0004t0001g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(29): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(21): Show |
2 | a0003c0006t0001g0063 a0009c0020t0001g0248 |
2 | HG02145.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(22): Show |
7 | a0001c0003t0001g0257 a0002c0001t0001g0009 a0002c0001t0001g0010 others(4): Show |
7 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(31): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(23): Show |
3 | a0003c0004t0001g0067 a0003c0004t0001g0068 a0003c0006t0001g0069 |
3 | HG01074.hp1 HG01934.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(32): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(24): Show |
2 | a0002c0001t0001g0012 a0003c0004t0001g0070 |
2 | HG01071.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(33): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(27): Show |
1 | a0003c0004t0001g0071 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(36): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168687 | C | CTTTTTTT others(28): Show |
1 | a0003c0004t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(37): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | ||||||
| chr8:100168696 | T | G | 7 | a0001c0009t0001g0268 a0002c0001t0001g0259 a0002c0001t0001g0266 others(4): Show |
7 | HG01071.hp2 HG01123.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2723T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168696 | |||||||
| chr8:100168698 | TG | T | 9 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+2726delG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168698 | |||||||
| chr8:100168699 | G | T | 265 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.300+2726G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168699 | |||||||
| chr8:100168805 | A | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2832A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168805 | |||||||
| chr8:100168837 | G | A | 1 | a0001c0009t0001g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.300+2864G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168837 | |||||||
| chr8:100168876 | A | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2903A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168876 | |||||||
| chr8:100168906 | C | G | 3 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0293 |
3 | HG01952.hp2 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.300+2933C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168906 | |||||||
| chr8:100168925 | G | A | 1 | a0002c0001t0001g0307 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.300+2952G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168925 | |||||||
| chr8:100168958 | A | G | 1 | a0002c0001t0001g0353 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.300+2985A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168958 | |||||||
| chr8:100169194 | C | T | 1 | a0001c0009t0001g0290 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.300+3221C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169194 | |||||||
| chr8:100169234 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300+3261A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169234 | |||||||
| chr8:100169273 | G | T | 114 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(111): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.300+3300G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169273 | |||||||
| chr8:100169285 | G | C | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+3312G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169285 | |||||||
| chr8:100169477 | C | T | 1 | a0001c0003t0005g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.300+3504C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169477 | |||||||
| chr8:100169478 | G | A | 1 | a0002c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+3505G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169478 | |||||||
| chr8:100169480 | C | T | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(132): Show |
137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.300+3507C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169480 | |||||||
| chr8:100169768 | GT | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+3796delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169768 | |||||||
| chr8:100169832 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+3859G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169832 | |||||||
| chr8:100169984 | G | GA | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.300+4021dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100169984 | ||||||
| chr8:100170094 | T | C | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+4121T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170094 | |||||||
| chr8:100170098 | T | A | 14 | a0003c0004t0001g0026 a0003c0004t0001g0028 a0003c0004t0001g0029 others(11): Show |
14 | HG01071.hp1 HG01074.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+4125T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170098 | |||||||
| chr8:100170126 | T | C | 1 | a0003c0004t0005g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.300+4153T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170126 | |||||||
| chr8:100170305 | A | G | 4 | a0001c0003t0001g0263 a0002c0001t0001g0261 a0002c0001t0001g0262 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+4332A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170305 | |||||||
| chr8:100170432 | G | A | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0006c0013t0001g0131 |
3 | HG00639.hp1 HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300+4459G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170432 | |||||||
| chr8:100170563 | A | G | 1 | a0006c0013t0001g0131 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.300+4590A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170563 | |||||||
| chr8:100170637 | G | A | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300+4664G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170637 | |||||||
| chr8:100170641 | G | A | 1 | a0003c0004t0001g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300+4668G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170641 | |||||||
| chr8:100170776 | A | T | 1 | a0001c0002t0001g0127 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.300+4803A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170776 | |||||||
| chr8:100170800 | C | CATTT | 22 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0001g0074 others(19): Show |
22 | HG01891.hp2 HG02040.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.300+4876_300+4879d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | C | CATTTATT others(1): Show |
4 | a0001c0003t0001g0018 a0001c0015t0001g0221 a0002c0005t0002g0222 others(1): Show |
4 | HG02148.hp1 HG02280.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+4872_300+4879d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTT | C | 204 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(201): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.300+4876_300+4879d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTTATT others(1): Show |
C | 46 | a0001c0003t0001g0255 a0001c0003t0001g0263 a0001c0003t0005g0289 others(43): Show |
48 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.300+4872_300+4879d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTTATT others(5): Show |
C | 12 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(9): Show |
14 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+4868_300+4879d others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTTATT others(9): Show |
C | 1 | a0003c0006t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.300+4864_300+4879d others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTTATT others(17): Show |
C | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.300+4856_300+4879d others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170800 | CATTTATT others(21): Show |
C | 1 | a0002c0001t0001g0288 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.300+4852_300+4879d others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | ||||||
| chr8:100170829 | A | T | 1 | a0001c0002t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+4856A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170829 | |||||||
| chr8:100170837 | A | T | 110 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(107): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.300+4864A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170837 | |||||||
| chr8:100170845 | A | ATTTATTT others(1): Show |
5 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0101 others(2): Show |
5 | HG00733.hp2 HG00738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+4875_300+4882d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170845 | ||||||
| chr8:100170845 | A | ATTTT | 13 | a0001c0003t0001g0354 a0001c0003t0003g0100 a0001c0003t0003g0102 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+4875_300+4876i others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170845 | ||||||
| chr8:100170845 | A | T | 120 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.300+4872A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170845 | |||||||
| chr8:100170966 | T | C | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+4993T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170966 | |||||||
| chr8:100170972 | G | A | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300+4999G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170972 | |||||||
| chr8:100171307 | C | T | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.300+5334C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171307 | |||||||
| chr8:100171331 | G | A | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.300+5358G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171331 | |||||||
| chr8:100171525 | A | G | 2 | a0002c0005t0002g0230 a0002c0005t0002g0232 |
2 | HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.300+5552A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171525 | |||||||
| chr8:100171564 | G | A | 1 | a0002c0001t0001g0323 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.300+5591G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171564 | |||||||
| chr8:100171617 | C | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+5644C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171617 | |||||||
| chr8:100171668 | C | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.300+5695C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171668 | |||||||
| chr8:100171881 | A | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.300+5908A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171881 | |||||||
| chr8:100171935 | C | G | 3 | a0002c0007t0001g0188 a0002c0007t0001g0189 a0002c0007t0001g0190 |
3 | HG02486.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.301-5881C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171935 | |||||||
| chr8:100171937 | C | T | 1 | a0001c0008t0002g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-5879C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171937 | |||||||
| chr8:100171938 | G | A | 120 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.301-5878G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171938 | |||||||
| chr8:100171939 | G | C | 2 | a0001c0003t0001g0075 a0001c0003t0001g0076 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.301-5877G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171939 | |||||||
| chr8:100172034 | A | G | 1 | a0002c0005t0002g0228 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.301-5782A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172034 | |||||||
| chr8:100172055 | C | T | 40 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(37): Show |
42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301-5761C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172055 | |||||||
| chr8:100172166 | G | A | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.301-5650G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172166 | |||||||
| chr8:100172490 | C | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5326C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172490 | |||||||
| chr8:100172494 | C | T | 2 | a0001c0009t0001g0007 a0001c0009t0001g0285 |
3 | HG01496.hp1 HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.301-5322C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172494 | |||||||
| chr8:100172512 | T | C | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.301-5304T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172512 | |||||||
| chr8:100172528 | G | A | 1 | a0002c0001t0001g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.301-5288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172528 | |||||||
| chr8:100172534 | C | T | 1 | a0002c0001t0004g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.301-5282C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172534 | |||||||
| chr8:100172634 | A | ATG | 43 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(40): Show |
44 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-5150_301-5149d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | A | ATGTG | 6 | a0001c0003t0001g0257 a0001c0008t0002g0090 a0001c0008t0008g0243 others(3): Show |
7 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-5152_301-5149d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | A | ATGTGTG | 19 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(16): Show |
19 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.301-5154_301-5149d others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | A | ATGTGTGT others(1): Show |
35 | a0001c0003t0001g0075 a0001c0003t0001g0076 a0001c0003t0001g0077 others(32): Show |
37 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.301-5156_301-5149d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | A | ATGTGTGT others(3): Show |
24 | a0001c0003t0001g0019 a0001c0003t0001g0021 a0001c0003t0001g0022 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-5158_301-5149d others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | A | ATGTGTGT others(5): Show |
3 | a0001c0003t0001g0018 a0001c0003t0001g0020 a0003c0004t0001g0024 |
3 | HG02145.hp2 HG02280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.301-5160_301-5149d others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | ATG | A | 21 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0123 others(18): Show |
21 | HG00544.hp1 HG00639.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.301-5150_301-5149d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172634 | ATGTG | A | 106 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(103): Show |
108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.301-5152_301-5149d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | ||||||
| chr8:100172640 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5176G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172640 | |||||||
| chr8:100172664 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5152G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172664 | |||||||
| chr8:100172666 | GTA | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5148_301-5147d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172666 | ||||||
| chr8:100172727 | G | T | 121 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(118): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.301-5089G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172727 | |||||||
| chr8:100172759 | T | C | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.301-5057T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172759 | |||||||
| chr8:100172860 | A | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.301-4956A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172860 | |||||||
| chr8:100172908 | A | G | 1 | a0002c0001t0001g0016 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.301-4908A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172908 | |||||||
| chr8:100173033 | C | CT | 62 | a0001c0003t0001g0022 a0001c0003t0001g0252 a0001c0003t0001g0257 others(59): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.301-4756dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173033 | C | CTT | 16 | a0001c0003t0001g0255 a0002c0001t0001g0092 a0002c0001t0001g0093 others(13): Show |
16 | HG00738.hp1 HG01175.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.301-4757_301-4756d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173033 | CT | C | 21 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0104 others(18): Show |
21 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.301-4756delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173033 | CTT | C | 50 | a0001c0002t0001g0134 a0001c0002t0001g0172 a0001c0002t0001g0182 others(47): Show |
52 | HG00438.hp1 HG01081.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.301-4757_301-4756d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173033 | CTTT | C | 93 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(90): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.301-4758_301-4756d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173033 | CTTTT | C | 14 | a0001c0002t0001g0087 a0001c0002t0001g0122 a0001c0002t0001g0125 others(11): Show |
14 | HG00140.hp2 HG01167.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301-4759_301-4756d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | ||||||
| chr8:100173184 | A | T | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.301-4632A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173184 | |||||||
| chr8:100173268 | A | G | 3 | a0003c0006t0001g0058 a0003c0006t0001g0059 a0003c0006t0001g0340 |
3 | HG00438.hp2 NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.301-4548A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173268 | |||||||
| chr8:100173733 | A | G | 1 | a0001c0008t0002g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-4083A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173733 | |||||||
| chr8:100174097 | G | A | 40 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(37): Show |
42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301-3719G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174097 | |||||||
| chr8:100174202 | G | T | 4 | a0002c0007t0001g0187 a0002c0007t0001g0188 a0002c0007t0001g0189 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-3614G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174202 | |||||||
| chr8:100174365 | C | T | 3 | a0003c0004t0001g0247 a0003c0004t0005g0251 a0013c0017t0001g0246 |
3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.301-3451C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174365 | |||||||
| chr8:100174366 | C | T | 1 | a0002c0001t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301-3450C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174366 | |||||||
| chr8:100174548 | C | T | 164 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(161): Show |
168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.301-3268C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174548 | |||||||
| chr8:100174631 | T | G | 4 | a0002c0001t0001g0008 a0002c0001t0001g0256 a0002c0001t0001g0265 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-3185T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174631 | |||||||
| chr8:100174790 | G | A | 1 | a0002c0001t0001g0266 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.301-3026G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174790 | |||||||
| chr8:100174902 | G | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.301-2914G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174902 | |||||||
| chr8:100174970 | CT | C | 11 | a0001c0002t0001g0167 a0001c0003t0001g0252 a0001c0003t0001g0255 others(8): Show |
11 | HG00323.hp1 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-2830delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100174970 | ||||||
| chr8:100174970 | CTT | C | 241 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(238): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.301-2831_301-2830d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100174970 | ||||||
| chr8:100175071 | T | C | 2 | a0002c0001t0001g0305 a0002c0001t0001g0308 |
2 | HG02040.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.301-2745T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175071 | |||||||
| chr8:100175096 | C | T | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301-2720C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175096 | |||||||
| chr8:100175284 | C | CT | 50 | a0002c0001t0001g0286 a0003c0004t0001g0001 a0003c0004t0001g0024 others(47): Show |
52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.301-2514dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100175284 | ||||||
| chr8:100175284 | CT | C | 7 | a0002c0001t0001g0011 a0002c0001t0001g0310 a0002c0005t0002g0217 others(4): Show |
7 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-2514delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100175284 | ||||||
| chr8:100175522 | G | A | 1 | a0003c0004t0001g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-2294G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175522 | |||||||
| chr8:100175647 | G | A | 1 | a0001c0003t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.301-2169G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175647 | |||||||
| chr8:100175885 | A | G | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.301-1931A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175885 | |||||||
| chr8:100175897 | C | G | 2 | a0002c0005t0001g0234 a0002c0005t0002g0237 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.301-1919C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175897 | |||||||
| chr8:100176136 | C | T | 1 | a0003c0004t0001g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-1680C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176136 | |||||||
| chr8:100176439 | C | T | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1377C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176439 | |||||||
| chr8:100176611 | C | T | 1 | a0006c0013t0001g0131 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.301-1205C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176611 | |||||||
| chr8:100176807 | C | CCCTCT | 61 | a0001c0002t0001g0171 a0001c0003t0001g0018 a0001c0003t0001g0019 others(58): Show |
63 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.301-978_301-974dup others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100176807 | C | CCCTCTCC others(3): Show |
49 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(46): Show |
49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.301-983_301-974dup others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100176807 | C | CCCTCTCC others(8): Show |
77 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(74): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.301-988_301-974dup others(15): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100176807 | C | CCCTCTCC others(13): Show |
6 | a0001c0002t0001g0119 a0001c0002t0001g0185 a0001c0008t0008g0243 others(3): Show |
6 | HG02647.hp1 HG02683.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-993_301-974dup others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100176807 | CCCTCT | C | 57 | a0001c0003t0001g0255 a0001c0008t0002g0241 a0001c0009t0001g0342 others(54): Show |
59 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.301-978_301-974del others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100176807 | CCCTCTCC others(3): Show |
C | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.301-983_301-974del others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | ||||||
| chr8:100177000 | T | G | 3 | a0003c0006t0001g0058 a0003c0006t0001g0059 a0003c0006t0001g0340 |
3 | HG00438.hp2 NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.301-816T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177000 | |||||||
| chr8:100177024 | T | C | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.301-792T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177024 | |||||||
| chr8:100177534 | T | C | 1 | a0002c0001t0001g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.301-282T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177534 | |||||||
| chr8:100177601 | A | G | 7 | a0001c0002t0001g0097 a0001c0002t0001g0127 a0001c0002t0001g0164 others(4): Show |
7 | HG00673.hp1 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-215A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177601 | |||||||
| chr8:100178458 | C | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.426+517C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178458 | |||||||
| chr8:100178528 | T | C | 2 | a0002c0001t0001g0352 a0002c0001t0001g0353 |
2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.426+587T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178528 | |||||||
| chr8:100178562 | G | C | 3 | a0001c0002t0001g0127 a0001c0002t0001g0164 a0001c0002t0001g0212 |
3 | NA18962.hp1 NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.426+621G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178562 | |||||||
| chr8:100178669 | G | A | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.426+728G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178669 | |||||||
| chr8:100179006 | A | G | 1 | a0002c0005t0002g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.426+1065A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179006 | |||||||
| chr8:100179063 | C | CA | 64 | a0001c0002t0001g0121 a0001c0002t0001g0124 a0001c0002t0001g0133 others(61): Show |
66 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.426+1138dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179063 | ||||||
| chr8:100179063 | C | CAA | 7 | a0003c0004t0001g0028 a0003c0004t0001g0029 a0003c0004t0001g0042 others(4): Show |
7 | HG01071.hp1 HG01255.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+1137_426+1138d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179063 | ||||||
| chr8:100179085 | AAAAC | A | 31 | a0001c0008t0002g0006 a0001c0008t0002g0240 a0001c0008t0002g0241 others(28): Show |
32 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.426+1152_426+1155d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179085 | ||||||
| chr8:100179520 | G | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.426+1579G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179520 | |||||||
| chr8:100179607 | C | T | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.426+1666C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179607 | |||||||
| chr8:100179934 | T | C | 1 | a0002c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.426+1993T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179934 | |||||||
| chr8:100180296 | T | C | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.426+2355T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180296 | |||||||
| chr8:100180394 | A | G | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.426+2453A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180394 | |||||||
| chr8:100180789 | T | C | 1 | a0003c0018t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.427-2586T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180789 | |||||||
| chr8:100180878 | T | C | 1 | a0002c0005t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.427-2497T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180878 | |||||||
| chr8:100181135 | A | G | 1 | a0001c0002t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.427-2240A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181135 | |||||||
| chr8:100181221 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.427-2154T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181221 | |||||||
| chr8:100181307 | G | C | 6 | a0002c0001t0001g0324 a0002c0001t0001g0327 a0002c0001t0001g0328 others(3): Show |
6 | HG00609.hp2 NA18965.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-2068G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181307 | |||||||
| chr8:100181393 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.427-1982G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181393 | |||||||
| chr8:100181459 | T | G | 1 | a0001c0003t0005g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.427-1916T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181459 | |||||||
| chr8:100181847 | A | C | 3 | a0003c0004t0001g0024 a0003c0004t0001g0080 a0003c0004t0001g0081 |
3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.427-1528A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181847 | |||||||
| chr8:100182170 | T | C | 1 | a0001c0002t0001g0195 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.427-1205T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182170 | |||||||
| chr8:100182236 | T | C | 1 | a0002c0001t0001g0311 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.427-1139T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182236 | |||||||
| chr8:100182250 | T | C | 1 | a0001c0009t0001g0268 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.427-1125T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182250 | |||||||
| chr8:100182298 | C | T | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.427-1077C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182298 | |||||||
| chr8:100183003 | T | G | 1 | a0001c0002t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.427-372T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183003 | |||||||
| chr8:100183076 | C | A | 3 | a0002c0001t0001g0013 a0002c0001t0001g0014 a0002c0001t0001g0017 |
3 | NA18612.hp2 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.427-299C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183076 | |||||||
| chr8:100183078 | A | G | 17 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.427-297A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183078 | |||||||
| chr8:100183170 | A | G | 1 | a0002c0001t0001g0322 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.427-205A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183170 | |||||||
| chr8:100183359 | G | T | 17 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.427-16G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183359 | |||||||
| chr8:100183470 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.488+34A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183470 | |||||||
| chr8:100183475 | A | G | 3 | a0001c0008t0002g0089 a0001c0008t0002g0090 a0001c0008t0002g0091 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.488+39A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183475 | |||||||
| chr8:100183541 | A | G | 1 | a0001c0003t0003g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.488+105A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183541 | |||||||
| chr8:100183645 | G | A | 1 | a0002c0001t0001g0262 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.488+209G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183645 | |||||||
| chr8:100183850 | A | G | 2 | a0002c0001t0001g0008 a0002c0001t0001g0341 |
3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-106A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183850 | |||||||
| chr8:100183851 | A | T | 2 | a0002c0001t0001g0008 a0002c0001t0001g0341 |
3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-105A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183851 | |||||||
| chr8:100183852 | TATGTATC others(6): Show |
T | 2 | a0002c0001t0001g0008 a0002c0001t0001g0341 |
3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-103_489-91delA others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183852 | |||||||
| chr8:100184592 | A | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.596-36A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/18 | chr8 | 100184592 | |||||||
| chr8:100184596 | G | A | 164 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(161): Show |
168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.596-32G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/18 | chr8 | 100184596 | |||||||
| chr8:100184818 | G | A | 1 | a0014c0022t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701+85G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100184818 | |||||||
| chr8:100184881 | C | G | 1 | a0002c0005t0002g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.701+148C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100184881 | |||||||
| chr8:100185026 | T | C | 1 | a0002c0007t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.701+293T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185026 | |||||||
| chr8:100185129 | T | C | 1 | a0001c0003t0005g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.701+396T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185129 | |||||||
| chr8:100185199 | G | A | 1 | a0003c0006t0001g0037 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.701+466G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185199 | |||||||
| chr8:100185493 | C | A | 1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.701+760C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185493 | |||||||
| chr8:100185648 | A | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.701+915A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185648 | |||||||
| chr8:100185726 | C | A | 2 | a0003c0006t0001g0058 a0003c0006t0001g0340 |
2 | NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.701+993C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185726 | |||||||
| chr8:100185998 | A | G | 1 | a0001c0003t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-1122A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185998 | |||||||
| chr8:100186060 | C | CT | 188 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(185): Show |
192 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.702-1037dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | ||||||
| chr8:100186060 | C | CTT | 58 | a0001c0002t0001g0117 a0001c0002t0001g0119 a0001c0002t0001g0134 others(55): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.702-1038_702-1037d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | ||||||
| chr8:100186060 | C | CTTT | 11 | a0001c0003t0001g0257 a0001c0008t0002g0244 a0003c0004t0001g0024 others(8): Show |
11 | HG00438.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.702-1039_702-1037d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | ||||||
| chr8:100186140 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.702-980G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186140 | |||||||
| chr8:100186341 | G | C | 220 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(217): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.702-779G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186341 | |||||||
| chr8:100186443 | G | A | 1 | a0002c0001t0001g0267 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.702-677G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186443 | |||||||
| chr8:100186642 | G | T | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.702-478G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186642 | |||||||
| chr8:100186697 | G | A | 2 | a0005c0011t0002g0005 a0005c0011t0002g0249 |
3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.702-423G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186697 | |||||||
| chr8:100186801 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.702-319G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186801 | |||||||
| chr8:100186810 | C | A | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-310C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186810 | |||||||
| chr8:100186811 | A | G | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-309A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186811 | |||||||
| chr8:100186812 | G | T | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-308G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186812 | |||||||
| chr8:100187025 | G | C | 1 | a0002c0001t0001g0315 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.702-95G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100187025 | |||||||
| chr8:100187290 | A | C | 1 | a0003c0004t0005g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+40A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187290 | |||||||
| chr8:100187487 | A | C | 2 | a0001c0009t0001g0276 a0002c0001t0001g0277 |
2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.832+237A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187487 | |||||||
| chr8:100187566 | C | T | 1 | a0001c0021t0001g0153 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.832+316C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187566 | |||||||
| chr8:100187691 | T | G | 1 | a0002c0001t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.832+441T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187691 | |||||||
| chr8:100187821 | C | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.832+571C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187821 | |||||||
| chr8:100187998 | G | A | 1 | a0002c0001t0001g0325 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.832+748G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187998 | |||||||
| chr8:100188306 | C | T | 2 | a0002c0001t0001g0092 a0002c0001t0001g0093 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.832+1056C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188306 | |||||||
| chr8:100188355 | G | A | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.832+1105G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188355 | |||||||
| chr8:100188884 | T | G | 4 | a0001c0009t0001g0007 a0001c0009t0001g0285 a0001c0009t0001g0290 others(1): Show |
5 | HG01496.hp1 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+1634T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188884 | |||||||
| chr8:100189040 | C | A | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.832+1790C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189040 | |||||||
| chr8:100189050 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.832+1800G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189050 | |||||||
| chr8:100189054 | A | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.832+1804A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189054 | |||||||
| chr8:100189176 | TA | T | 87 | a0001c0002t0001g0133 a0001c0003t0001g0018 a0001c0003t0001g0019 others(84): Show |
89 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.832+1942delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100189176 | ||||||
| chr8:100189371 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-2019G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189371 | |||||||
| chr8:100189446 | C | T | 1 | a0003c0018t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.833-1944C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189446 | |||||||
| chr8:100189498 | T | A | 40 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(37): Show |
42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.833-1892T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189498 | |||||||
| chr8:100189641 | A | C | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1749A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189641 | |||||||
| chr8:100189760 | G | T | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1630G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189760 | |||||||
| chr8:100189775 | A | C | 1 | a0002c0001t0004g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.833-1615A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189775 | |||||||
| chr8:100189827 | C | T | 1 | a0002c0001t0001g0337 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-1563C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189827 | |||||||
| chr8:100189829 | T | C | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1561T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189829 | |||||||
| chr8:100189876 | G | A | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.833-1514G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189876 | |||||||
| chr8:100190009 | G | A | 1 | a0001c0003t0001g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.833-1381G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190009 | |||||||
| chr8:100190037 | G | C | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-1353G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190037 | |||||||
| chr8:100190107 | G | A | 1 | a0002c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-1283G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190107 | |||||||
| chr8:100190176 | G | T | 6 | a0001c0015t0001g0221 a0001c0015t0001g0225 a0002c0005t0001g0233 others(3): Show |
6 | NA18946.hp2 NA18957.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-1214G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190176 | |||||||
| chr8:100190211 | A | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.833-1179A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190211 | |||||||
| chr8:100190241 | A | G | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-1149A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190241 | |||||||
| chr8:100190298 | G | C | 1 | a0002c0001t0001g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.833-1092G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190298 | |||||||
| chr8:100190312 | C | CA | 17 | a0001c0002t0001g0083 a0001c0002t0001g0119 a0001c0002t0001g0137 others(14): Show |
17 | HG00408.hp1 HG01993.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.833-1059dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190312 | ||||||
| chr8:100190312 | CA | C | 28 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0021 others(25): Show |
28 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.833-1059delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190312 | ||||||
| chr8:100190332 | T | A | 3 | a0002c0001t0001g0015 a0002c0001t0001g0016 a0002c0001t0001g0027 |
3 | NA18954.hp1 NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.833-1058T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190332 | |||||||
| chr8:100190404 | A | G | 1 | a0004c0010t0001g0152 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.833-986A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190404 | |||||||
| chr8:100190520 | T | TG | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-869dupG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190520 | ||||||
| chr8:100190663 | C | CT | 155 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(152): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.833-709dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190663 | ||||||
| chr8:100190663 | C | CTT | 10 | a0001c0002t0001g0086 a0001c0002t0001g0133 a0001c0002t0001g0135 others(7): Show |
10 | HG00621.hp2 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-710_833-709dup others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190663 | ||||||
| chr8:100190668 | T | C | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.833-722T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190668 | |||||||
| chr8:100190670 | T | TC | 3 | a0001c0015t0001g0221 a0001c0015t0001g0225 a0002c0005t0001g0233 |
3 | NA18957.hp1 NA18971.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.833-720_833-719ins others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190670 | |||||||
| chr8:100191043 | A | G | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-347A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191043 | |||||||
| chr8:100191044 | G | T | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-346G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191044 | |||||||
| chr8:100191314 | C | A | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.833-76C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191314 | |||||||
| chr8:100191370 | T | C | 1 | a0013c0017t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.833-20T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191370 | |||||||
| chr8:100191375 | T | A | 1 | a0002c0001t0006g0094 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.833-15T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191375 | |||||||
| chr8:100191509 | T | C | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.939+13T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191509 | |||||||
| chr8:100191826 | T | C | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.939+330T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191826 | |||||||
| chr8:100191882 | A | G | 1 | a0002c0001t0006g0094 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.939+386A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191882 | |||||||
| chr8:100191909 | T | C | 2 | a0005c0011t0002g0005 a0005c0011t0002g0249 |
3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.939+413T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191909 | |||||||
| chr8:100191981 | T | C | 3 | a0002c0001t0001g0298 a0002c0001t0001g0299 a0002c0001t0001g0303 |
3 | NA18964.hp1 NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.939+485T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191981 | |||||||
| chr8:100192109 | T | C | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.939+613T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192109 | |||||||
| chr8:100192131 | GCA | G | 13 | a0002c0005t0002g0088 a0002c0005t0002g0220 a0002c0005t0002g0222 others(10): Show |
13 | HG01081.hp1 HG02148.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+639_939+640del others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100192131 | ||||||
| chr8:100192180 | A | C | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.939+684A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192180 | |||||||
| chr8:100192401 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.939+905G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192401 | |||||||
| chr8:100192424 | A | G | 104 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(101): Show |
106 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.939+928A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192424 | |||||||
| chr8:100192519 | A | G | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.939+1023A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192519 | |||||||
| chr8:100192773 | A | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.939+1277A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192773 | |||||||
| chr8:100192785 | T | G | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.939+1289T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192785 | |||||||
| chr8:100193356 | G | C | 32 | a0001c0002t0001g0084 a0001c0002t0001g0086 a0001c0002t0001g0096 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.940-756G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193356 | |||||||
| chr8:100193386 | G | A | 4 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0007c0014t0001g0253 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-726G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193386 | |||||||
| chr8:100193477 | A | C | 117 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(114): Show |
119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.940-635A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193477 | |||||||
| chr8:100193479 | A | C | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.940-633A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193479 | |||||||
| chr8:100193481 | C | A | 1 | a0001c0002t0001g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.940-631C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193481 | |||||||
| chr8:100193552 | A | G | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.940-560A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193552 | |||||||
| chr8:100193709 | C | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.940-403C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193709 | |||||||
| chr8:100193761 | TAAAC | T | 105 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.940-345_940-342del others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100193761 | ||||||
| chr8:100193927 | C | T | 4 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0007c0014t0001g0253 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-185C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193927 | |||||||
| chr8:100193947 | T | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.940-165T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193947 | |||||||
| chr8:100193990 | C | CA | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.940-114dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100193990 | ||||||
| chr8:100194303 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+35G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194303 | |||||||
| chr8:100194343 | C | T | 2 | a0005c0011t0002g0005 a0005c0011t0002g0249 |
3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096+75C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194343 | |||||||
| chr8:100194540 | A | G | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+272A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194540 | |||||||
| chr8:100194582 | A | G | 1 | a0002c0001t0001g0304 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1096+314A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194582 | |||||||
| chr8:100194610 | A | G | 2 | a0001c0008t0002g0214 a0001c0008t0002g0215 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1096+342A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194610 | |||||||
| chr8:100194687 | G | A | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1096+419G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194687 | |||||||
| chr8:100194809 | C | T | 3 | a0001c0008t0002g0089 a0001c0008t0002g0090 a0001c0008t0002g0091 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1096+541C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194809 | |||||||
| chr8:100194836 | G | A | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1096+568G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194836 | |||||||
| chr8:100194882 | G | A | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1096+614G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194882 | |||||||
| chr8:100194970 | G | A | 43 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(40): Show |
45 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096+702G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194970 | |||||||
| chr8:100194981 | A | G | 1 | a0002c0001t0001g0288 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1096+713A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194981 | |||||||
| chr8:100195089 | C | T | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+821C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195089 | |||||||
| chr8:100195164 | C | CA | 194 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(191): Show |
198 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1096+909dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100195164 | ||||||
| chr8:100195178 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1096+910G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195178 | |||||||
| chr8:100195297 | T | C | 1 | a0002c0001t0001g0269 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1096+1029T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195297 | |||||||
| chr8:100195308 | T | C | 1 | a0001c0009t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1096+1040T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195308 | |||||||
| chr8:100195856 | A | G | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1096+1588A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195856 | |||||||
| chr8:100196113 | T | A | 30 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(27): Show |
30 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1096+1845T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196113 | |||||||
| chr8:100196115 | C | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1096+1847C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196115 | |||||||
| chr8:100196432 | G | T | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+2164G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196432 | |||||||
| chr8:100196516 | G | A | 1 | a0002c0007t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1096+2248G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196516 | |||||||
| chr8:100196522 | C | G | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+2254C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196522 | |||||||
| chr8:100196555 | G | T | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1096+2287G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196555 | |||||||
| chr8:100196606 | G | A | 1 | a0001c0003t0003g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1096+2338G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196606 | |||||||
| chr8:100196610 | A | G | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+2342A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196610 | |||||||
| chr8:100196894 | G | A | 1 | a0002c0001t0001g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1096+2626G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196894 | |||||||
| chr8:100196945 | G | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+2677G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196945 | |||||||
| chr8:100197031 | G | A | 1 | a0001c0002t0001g0127 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1096+2763G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197031 | |||||||
| chr8:100197273 | C | T | 1 | a0001c0003t0001g0354 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1096+3005C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197273 | |||||||
| chr8:100197349 | C | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+3081C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197349 | |||||||
| chr8:100197575 | G | A | 1 | a0002c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096+3307G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197575 | |||||||
| chr8:100197642 | G | A | 4 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+3374G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197642 | |||||||
| chr8:100198243 | A | G | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+3975A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198243 | |||||||
| chr8:100198269 | TCAAA | T | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+4005_1096+400 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100198269 | ||||||
| chr8:100198340 | G | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+4072G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198340 | |||||||
| chr8:100198422 | C | T | 10 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4154C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198422 | |||||||
| chr8:100198698 | T | C | 1 | a0002c0001t0001g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1096+4430T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198698 | |||||||
| chr8:100198770 | A | C | 4 | a0001c0002t0001g0124 a0001c0002t0001g0160 a0001c0002t0001g0168 others(1): Show |
4 | HG00597.hp1 NA18972.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096+4502A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198770 | |||||||
| chr8:100198959 | C | A | 1 | a0014c0022t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1096+4691C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198959 | |||||||
| chr8:100199109 | T | C | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1096+4841T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199109 | |||||||
| chr8:100199136 | T | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1096+4868T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199136 | |||||||
| chr8:100199145 | A | G | 1 | a0001c0009t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1096+4877A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199145 | |||||||
| chr8:100199146 | T | C | 1 | a0001c0002t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1096+4878T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199146 | |||||||
| chr8:100199217 | A | G | 1 | a0002c0001t0001g0336 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1096+4949A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199217 | |||||||
| chr8:100199241 | G | A | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1096+4973G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199241 | |||||||
| chr8:100199442 | C | T | 1 | a0002c0001t0001g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1096+5174C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199442 | |||||||
| chr8:100199481 | T | C | 2 | a0001c0009t0001g0309 a0002c0001t0001g0315 |
2 | NA18969.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1096+5213T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199481 | |||||||
| chr8:100199571 | A | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1096+5303A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199571 | |||||||
| chr8:100199594 | C | T | 4 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0007c0014t0001g0253 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5326C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199594 | |||||||
| chr8:100199670 | C | T | 1 | a0003c0004t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1096+5402C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199670 | |||||||
| chr8:100199960 | T | A | 2 | a0001c0009t0001g0326 a0011c0023t0001g0079 |
2 | HG02717.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1096+5692T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199960 | |||||||
| chr8:100200342 | A | G | 1 | a0001c0008t0002g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1096+6074A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200342 | |||||||
| chr8:100200349 | A | T | 5 | a0003c0004t0001g0067 a0003c0004t0001g0068 a0003c0004t0001g0070 others(2): Show |
5 | HG01071.hp1 HG01074.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096+6081A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200349 | |||||||
| chr8:100200582 | A | G | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1096+6314A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200582 | |||||||
| chr8:100200717 | A | G | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1096+6449A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200717 | |||||||
| chr8:100200791 | GTTGT | G | 117 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(114): Show |
119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1096+6530_1096+653 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100200791 | ||||||
| chr8:100200870 | GC | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1096+6603delC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200870 | |||||||
| chr8:100200998 | T | A | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1096+6730T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200998 | |||||||
| chr8:100201037 | A | G | 1 | a0003c0004t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1096+6769A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201037 | |||||||
| chr8:100201296 | T | A | 3 | a0003c0004t0001g0247 a0003c0004t0005g0251 a0013c0017t0001g0246 |
3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1096+7028T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201296 | |||||||
| chr8:100201605 | G | A | 275 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1096+7337G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201605 | |||||||
| chr8:100201672 | A | T | 1 | a0002c0001t0001g0266 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1096+7404A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201672 | |||||||
| chr8:100201741 | C | G | 5 | a0002c0007t0001g0187 a0002c0007t0001g0188 a0002c0007t0001g0189 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096+7473C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201741 | |||||||
| chr8:100201788 | A | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0141 |
2 | HG00735.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1096+7520A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201788 | |||||||
| chr8:100201961 | A | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1096+7693A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201961 | |||||||
| chr8:100202013 | C | T | 1 | a0002c0001t0001g0335 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1096+7745C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202013 | |||||||
| chr8:100202342 | T | TA | 95 | a0001c0002t0001g0144 a0001c0003t0001g0018 a0001c0003t0001g0019 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1096+8085dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202342 | ||||||
| chr8:100202432 | C | T | 29 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(26): Show |
29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1096+8164C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202432 | |||||||
| chr8:100202437 | G | A | 30 | a0001c0008t0002g0006 a0001c0008t0002g0240 a0001c0008t0002g0241 others(27): Show |
31 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(28): Show |
intron_variant | MODIFIER | c.1096+8169G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202437 | |||||||
| chr8:100202448 | T | G | 29 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(26): Show |
29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1096+8180T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202448 | |||||||
| chr8:100202506 | C | T | 161 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(158): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1096+8238C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202506 | |||||||
| chr8:100202567 | G | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+8299G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202567 | |||||||
| chr8:100202583 | G | A | 30 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(27): Show |
30 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1096+8315G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202583 | |||||||
| chr8:100202591 | T | C | 114 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(111): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1096+8323T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202591 | |||||||
| chr8:100202649 | G | C | 10 | a0001c0009t0001g0326 a0002c0001t0001g0219 a0002c0001t0001g0317 others(7): Show |
10 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096+8381G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202649 | |||||||
| chr8:100202666 | C | T | 40 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(37): Show |
42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1096+8398C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202666 | |||||||
| chr8:100202709 | C | CA | 61 | a0001c0002t0001g0117 a0001c0002t0001g0122 a0001c0002t0001g0123 others(58): Show |
62 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1096+8470dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | C | CAA | 9 | a0001c0003t0001g0257 a0001c0008t0002g0216 a0001c0008t0008g0243 others(6): Show |
9 | HG02055.hp2 HG02738.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8469_1096+847 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | C | CAAA | 5 | a0001c0008t0002g0006 a0001c0008t0002g0240 a0001c0008t0002g0241 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096+8468_1096+847 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | CA | C | 9 | a0001c0002t0001g0096 a0001c0002t0001g0162 a0002c0001t0001g0010 others(6): Show |
9 | HG01943.hp2 HG03041.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8470delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | CAA | C | 52 | a0002c0001t0001g0012 a0003c0004t0001g0001 a0003c0004t0001g0024 others(49): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1096+8469_1096+847 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | CAAAAAAA others(3): Show |
C | 1 | a0012c0025t0001g0260 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1096+8461_1096+847 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202709 | CAAAAAAA others(5): Show |
C | 3 | a0002c0007t0001g0191 a0002c0007t0001g0192 a0002c0007t0001g0193 |
3 | HG02258.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1096+8459_1096+847 others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | ||||||
| chr8:100202927 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1096+8659G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202927 | |||||||
| chr8:100203238 | C | T | 1 | a0002c0001t0001g0280 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1096+8970C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203238 | |||||||
| chr8:100203295 | C | T | 1 | a0001c0003t0003g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096+9027C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203295 | |||||||
| chr8:100203329 | A | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1096+9061A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203329 | |||||||
| chr8:100203418 | G | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+9150G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203418 | |||||||
| chr8:100203979 | A | G | 1 | a0002c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097-9111A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203979 | |||||||
| chr8:100204067 | G | C | 1 | a0014c0022t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1097-9023G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204067 | |||||||
| chr8:100204267 | A | G | 2 | a0001c0002t0001g0167 a0001c0002t0007g0177 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1097-8823A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204267 | |||||||
| chr8:100204389 | A | T | 1 | a0001c0002t0001g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1097-8701A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204389 | |||||||
| chr8:100204403 | T | A | 1 | a0001c0002t0001g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1097-8687T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204403 | |||||||
| chr8:100204512 | TA | T | 172 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(169): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1097-8566delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100204512 | ||||||
| chr8:100204652 | T | C | 1 | a0001c0009t0001g0268 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1097-8438T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204652 | |||||||
| chr8:100204816 | G | T | 1 | a0002c0001t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1097-8274G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204816 | |||||||
| chr8:100204872 | C | T | 1 | a0002c0007t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1097-8218C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204872 | |||||||
| chr8:100204935 | T | C | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-8155T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204935 | |||||||
| chr8:100205172 | C | A | 117 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(114): Show |
119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1097-7918C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205172 | |||||||
| chr8:100205481 | C | T | 1 | a0002c0001t0001g0295 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1097-7609C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205481 | |||||||
| chr8:100205482 | G | A | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1097-7608G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205482 | |||||||
| chr8:100205730 | G | A | 4 | a0001c0008t0002g0214 a0001c0008t0002g0215 a0001c0008t0002g0216 others(1): Show |
4 | HG03041.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-7360G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205730 | |||||||
| chr8:100205754 | T | C | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1097-7336T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205754 | |||||||
| chr8:100205755 | G | A | 1 | a0001c0003t0001g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1097-7335G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205755 | |||||||
| chr8:100205768 | G | A | 43 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(40): Show |
45 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1097-7322G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205768 | |||||||
| chr8:100205788 | G | A | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1097-7302G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205788 | |||||||
| chr8:100205798 | C | T | 1 | a0003c0004t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1097-7292C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205798 | |||||||
| chr8:100206017 | C | CA | 42 | a0001c0003t0001g0263 a0001c0003t0001g0291 a0001c0003t0001g0292 others(39): Show |
43 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1097-7035dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | C | CAA | 19 | a0001c0003t0001g0104 a0001c0003t0003g0101 a0001c0003t0003g0102 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1097-7036_1097-703 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CA | C | 7 | a0001c0003t0005g0289 a0001c0009t0001g0294 a0002c0001t0001g0002 others(4): Show |
8 | HG01099.hp2 HG01346.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097-7035delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(1): Show |
C | 54 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(51): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1097-7042_1097-703 others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(3): Show |
C | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-7044_1097-703 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(6): Show |
C | 2 | a0001c0003t0001g0020 a0002c0001t0001g0296 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1097-7047_1097-703 others(17): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(7): Show |
C | 11 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0021 others(8): Show |
11 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1097-7048_1097-703 others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(12): Show |
C | 8 | a0001c0009t0001g0326 a0002c0001t0001g0317 a0002c0001t0001g0318 others(5): Show |
8 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-7053_1097-703 others(23): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(13): Show |
C | 2 | a0001c0002t0001g0127 a0001c0002t0001g0164 |
2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1097-7054_1097-703 others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(14): Show |
C | 155 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(152): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1097-7055_1097-703 others(25): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206017 | CAAAAAAA others(15): Show |
C | 4 | a0002c0005t0002g0227 a0002c0005t0002g0229 a0002c0005t0002g0250 others(1): Show |
4 | HG02630.hp1 HG02735.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-7056_1097-703 others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | ||||||
| chr8:100206052 | A | G | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1097-7038A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206052 | |||||||
| chr8:100206052 | A | T | 2 | a0002c0001t0001g0015 a0002c0001t0001g0027 |
2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1097-7038A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206052 | |||||||
| chr8:100206083 | C | T | 38 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(35): Show |
39 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1097-7007C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206083 | |||||||
| chr8:100206097 | A | G | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1097-6993A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206097 | |||||||
| chr8:100206126 | G | A | 161 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(158): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1097-6964G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206126 | |||||||
| chr8:100206178 | C | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1097-6912C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206178 | |||||||
| chr8:100206248 | G | A | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1097-6842G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206248 | |||||||
| chr8:100206261 | G | C | 2 | a0001c0002t0001g0127 a0001c0002t0001g0164 |
2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1097-6829G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206261 | |||||||
| chr8:100206409 | A | G | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-6681A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206409 | |||||||
| chr8:100206464 | T | G | 53 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1097-6626T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206464 | |||||||
| chr8:100206614 | T | C | 1 | a0002c0001t0001g0265 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1097-6476T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206614 | |||||||
| chr8:100206648 | CAAGATAT others(17): Show |
C | 1 | a0002c0001t0001g0288 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1097-6417_1097-639 others(28): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206648 | ||||||
| chr8:100206767 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-6323G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206767 | |||||||
| chr8:100206863 | G | A | 1 | a0011c0023t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1097-6227G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206863 | |||||||
| chr8:100207217 | C | T | 1 | a0002c0007t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1097-5873C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207217 | |||||||
| chr8:100207289 | A | G | 8 | a0003c0006t0001g0035 a0003c0006t0001g0037 a0003c0006t0001g0038 others(5): Show |
8 | HG01943.hp1 NA18951.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-5801A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207289 | |||||||
| chr8:100207353 | T | G | 1 | a0001c0003t0001g0255 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-5737T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207353 | |||||||
| chr8:100207359 | G | A | 1 | a0002c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097-5731G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207359 | |||||||
| chr8:100207438 | C | T | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1097-5652C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207438 | |||||||
| chr8:100207461 | G | A | 1 | a0001c0003t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1097-5629G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207461 | |||||||
| chr8:100207666 | C | T | 6 | a0003c0004t0001g0001 a0003c0004t0001g0026 a0003c0004t0001g0053 others(3): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097-5424C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207666 | |||||||
| chr8:100207739 | C | T | 1 | a0002c0001t0001g0299 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1097-5351C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207739 | |||||||
| chr8:100207782 | G | A | 37 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(34): Show |
38 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(35): Show |
intron_variant | MODIFIER | c.1097-5308G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207782 | |||||||
| chr8:100207875 | C | T | 1 | a0001c0008t0002g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1097-5215C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207875 | |||||||
| chr8:100207914 | A | T | 1 | a0002c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1097-5176A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207914 | |||||||
| chr8:100207950 | G | A | 4 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0007c0014t0001g0253 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-5140G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207950 | |||||||
| chr8:100208536 | A | G | 1 | a0002c0001t0001g0337 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1097-4554A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208536 | |||||||
| chr8:100208549 | A | G | 1 | a0003c0004t0001g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1097-4541A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208549 | |||||||
| chr8:100208577 | C | T | 1 | a0001c0009t0001g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1097-4513C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208577 | |||||||
| chr8:100208941 | G | C | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-4149G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208941 | |||||||
| chr8:100208985 | G | C | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-4105G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208985 | |||||||
| chr8:100208999 | A | G | 1 | a0001c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1097-4091A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208999 | |||||||
| chr8:100209025 | C | G | 1 | a0003c0006t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1097-4065C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209025 | |||||||
| chr8:100209080 | C | T | 1 | a0008c0019t0001g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1097-4010C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209080 | |||||||
| chr8:100209224 | G | A | 1 | a0013c0017t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-3866G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209224 | |||||||
| chr8:100209248 | A | T | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1097-3842A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209248 | |||||||
| chr8:100209303 | C | CAT | 57 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(54): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1097-3772_1097-377 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100209303 | ||||||
| chr8:100209305 | T | C | 1 | a0001c0003t0001g0293 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1097-3785T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209305 | |||||||
| chr8:100209560 | T | C | 17 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1097-3530T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209560 | |||||||
| chr8:100209626 | TAA | T | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-3463_1097-346 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209626 | |||||||
| chr8:100209633 | T | C | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-3457T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209633 | |||||||
| chr8:100209917 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1097-3173A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209917 | |||||||
| chr8:100210191 | GT | G | 57 | a0001c0003t0001g0252 a0002c0001t0001g0265 a0002c0001t0001g0320 others(54): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1097-2885delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100210191 | ||||||
| chr8:100210192 | T | G | 1 | a0002c0001t0004g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1097-2898T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210192 | |||||||
| chr8:100210257 | G | A | 1 | a0002c0001t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1097-2833G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210257 | |||||||
| chr8:100210271 | A | G | 191 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1097-2819A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210271 | |||||||
| chr8:100210404 | C | T | 4 | a0001c0003t0001g0263 a0002c0001t0001g0261 a0002c0001t0001g0262 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-2686C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210404 | |||||||
| chr8:100210639 | T | C | 1 | a0001c0008t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1097-2451T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210639 | |||||||
| chr8:100210656 | C | T | 40 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(37): Show |
42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1097-2434C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210656 | |||||||
| chr8:100210866 | C | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1097-2224C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210866 | |||||||
| chr8:100210920 | C | T | 5 | a0001c0008t0002g0006 a0001c0008t0002g0240 a0001c0008t0002g0241 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-2170C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210920 | |||||||
| chr8:100211080 | C | T | 29 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(26): Show |
29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1097-2010C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211080 | |||||||
| chr8:100211195 | T | C | 1 | a0002c0007t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1097-1895T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211195 | |||||||
| chr8:100211410 | C | A | 1 | a0002c0001t0001g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1097-1680C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211410 | |||||||
| chr8:100211550 | G | A | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1097-1540G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211550 | |||||||
| chr8:100211587 | G | A | 1 | a0002c0001t0001g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1097-1503G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211587 | |||||||
| chr8:100211784 | T | C | 1 | a0001c0002t0001g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1097-1306T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211784 | |||||||
| chr8:100211846 | G | C | 1 | a0001c0003t0005g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1097-1244G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211846 | |||||||
| chr8:100211874 | T | C | 1 | a0002c0001t0001g0288 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1097-1216T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211874 | |||||||
| chr8:100212103 | G | A | 2 | a0002c0001t0001g0008 a0002c0001t0001g0341 |
3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1097-987G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212103 | |||||||
| chr8:100212269 | A | C | 2 | a0002c0005t0002g0227 a0002c0005t0002g0245 |
2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1097-821A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212269 | |||||||
| chr8:100212436 | T | C | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1097-654T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212436 | |||||||
| chr8:100212535 | G | T | 3 | a0001c0002t0001g0204 a0001c0002t0001g0205 a0001c0002t0001g0206 |
3 | HG00639.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1097-555G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212535 | |||||||
| chr8:100212652 | T | C | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1097-438T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212652 | |||||||
| chr8:100212784 | G | T | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1097-306G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212784 | |||||||
| chr8:100212851 | G | C | 7 | a0001c0002t0001g0097 a0001c0002t0001g0127 a0001c0002t0001g0164 others(4): Show |
7 | HG00673.hp1 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097-239G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212851 | |||||||
| chr8:100212893 | AG | A | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1097-192delG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100212893 | ||||||
| chr8:100212923 | C | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-167C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212923 | |||||||
| chr8:100212989 | A | G | 1 | a0001c0003t0001g0255 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-101A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212989 | |||||||
| chr8:100213013 | C | CCCGCGGC others(2): Show |
237 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1097-60_1097-52dup others(9): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | ||||||
| chr8:100213013 | C | CCCGCGGC others(11): Show |
5 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097-69_1097-52dup others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | ||||||
| chr8:100213013 | C | CCCGCGGC others(20): Show |
1 | a0001c0003t0003g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-52_1097-51ins others(27): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | ||||||
| chr8:100213013 | CCCGCGGC others(2): Show |
C | 10 | a0001c0003t0001g0252 a0001c0003t0001g0255 a0003c0004t0001g0001 others(7): Show |
12 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-60_1097-52del others(9): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | ||||||
| chr8:100213070 | C | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1097-20C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100213070 | |||||||
| chr8:100213444 | C | T | 3 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 |
3 | HG02145.hp2 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1435+16C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213444 | |||||||
| chr8:100213480 | C | A | 57 | a0001c0009t0001g0007 a0001c0009t0001g0268 a0001c0009t0001g0276 others(54): Show |
58 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1435+52C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213480 | |||||||
| chr8:100213537 | G | A | 1 | a0002c0007t0002g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1435+109G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213537 | |||||||
| chr8:100213610 | C | G | 253 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(250): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1435+182C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213610 | |||||||
| chr8:100213666 | G | A | 56 | a0003c0004t0001g0001 a0003c0004t0001g0024 a0003c0004t0001g0025 others(53): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1436-153G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213666 | |||||||
| chr8:100213782 | T | A | 2 | a0007c0014t0001g0253 a0007c0014t0001g0254 |
2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1436-37T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213782 | |||||||
| chr8:100214130 | A | AC | 3 | a0001c0003t0001g0257 a0002c0007t0001g0188 a0008c0019t0001g0049 |
3 | HG00423.hp1 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1535+214dupC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214130 | ||||||
| chr8:100214143 | G | A | 5 | a0003c0006t0001g0035 a0003c0006t0001g0037 a0003c0006t0001g0038 others(2): Show |
5 | HG01943.hp1 NA18954.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1535+225G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214143 | |||||||
| chr8:100214206 | G | A | 17 | a0001c0003t0001g0104 a0001c0003t0003g0099 a0001c0003t0003g0100 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1535+288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214206 | |||||||
| chr8:100214215 | A | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1535+297A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214215 | |||||||
| chr8:100214485 | A | G | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1535+567A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214485 | |||||||
| chr8:100214566 | C | A | 2 | a0007c0014t0001g0253 a0007c0014t0001g0254 |
2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1535+648C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214566 | |||||||
| chr8:100214679 | G | A | 1 | a0002c0001t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1535+761G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214679 | |||||||
| chr8:100214796 | A | T | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1535+878A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214796 | |||||||
| chr8:100214810 | T | C | 11 | a0001c0009t0001g0294 a0002c0001t0001g0002 a0002c0001t0001g0092 others(8): Show |
12 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535+892T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214810 | |||||||
| chr8:100214885 | C | G | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1535+967C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214885 | |||||||
| chr8:100214924 | G | A | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1535+1006G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214924 | |||||||
| chr8:100214966 | A | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1535+1048A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214966 | |||||||
| chr8:100214988 | C | CAT | 3 | a0002c0001t0001g0267 a0002c0001t0001g0333 a0002c0001t0006g0094 |
3 | HG01358.hp1 HG02155.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1535+1131_1535+113 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CAT | C | 3 | a0001c0002t0001g0207 a0002c0001t0001g0322 a0002c0001t0001g0353 |
3 | HG02027.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1535+1131_1535+113 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATAT | C | 19 | a0001c0002t0001g0124 a0001c0002t0001g0158 a0001c0002t0001g0163 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1535+1129_1535+113 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATAT | C | 20 | a0001c0002t0001g0086 a0001c0002t0001g0096 a0001c0002t0001g0119 others(17): Show |
20 | HG00438.hp1 HG00544.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535+1127_1535+113 others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(1): Show |
C | 21 | a0001c0002t0001g0082 a0001c0002t0001g0123 a0001c0002t0001g0126 others(18): Show |
21 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1535+1125_1535+113 others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(3): Show |
C | 26 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0115 others(23): Show |
26 | HG00609.hp1 HG01175.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.1535+1123_1535+113 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(5): Show |
C | 7 | a0001c0002t0001g0095 a0001c0002t0001g0122 a0001c0002t0001g0166 others(4): Show |
7 | HG00673.hp2 HG01109.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535+1121_1535+113 others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(9): Show |
C | 47 | a0001c0002t0001g0125 a0001c0002t0001g0127 a0001c0002t0001g0135 others(44): Show |
49 | HG00597.hp2 HG00741.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1535+1117_1535+113 others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(11): Show |
C | 23 | a0001c0002t0001g0141 a0001c0002t0001g0144 a0001c0002t0001g0154 others(20): Show |
23 | HG00735.hp1 HG01255.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1535+1115_1535+113 others(22): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(13): Show |
C | 8 | a0001c0002t0001g0097 a0001c0002t0001g0165 a0001c0002t0001g0179 others(5): Show |
8 | HG00673.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535+1113_1535+113 others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(15): Show |
C | 3 | a0001c0003t0003g0099 a0002c0001t0001g0334 a0002c0001t0002g0338 |
3 | HG00733.hp2 HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1535+1111_1535+113 others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(17): Show |
C | 3 | a0001c0003t0001g0257 a0002c0001t0001g0314 a0002c0001t0001g0352 |
3 | HG02055.hp2 HG02698.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1535+1109_1535+113 others(28): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(19): Show |
C | 1 | a0001c0003t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1535+1107_1535+113 others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(23): Show |
C | 2 | a0001c0002t0001g0211 a0002c0001t0001g0014 |
2 | NA18950.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1535+1103_1535+113 others(34): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(25): Show |
C | 1 | a0003c0006t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1535+1101_1535+113 others(36): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(27): Show |
C | 7 | a0002c0001t0001g0008 a0002c0001t0001g0341 a0003c0004t0001g0032 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535+1099_1535+113 others(38): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(29): Show |
C | 49 | a0001c0003t0003g0213 a0002c0001t0001g0288 a0002c0001t0001g0297 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1535+1097_1535+113 others(40): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(31): Show |
C | 6 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535+1095_1535+113 others(42): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(33): Show |
C | 1 | a0002c0005t0001g0226 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1535+1093_1535+113 others(44): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(35): Show |
C | 39 | a0001c0003t0003g0105 a0001c0008t0002g0006 a0001c0008t0002g0089 others(36): Show |
41 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1535+1091_1535+113 others(46): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100214988 | CATATATA others(39): Show |
C | 1 | a0003c0004t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1535+1087_1535+113 others(50): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | ||||||
| chr8:100215104 | G | C | 1 | a0014c0022t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1535+1186G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215104 | |||||||
| chr8:100215194 | T | G | 180 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(177): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1535+1276T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215194 | |||||||
| chr8:100215620 | G | A | 2 | a0002c0001t0001g0281 a0002c0001t0001g0282 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1535+1702G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215620 | |||||||
| chr8:100215686 | G | A | 39 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(36): Show |
41 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1535+1768G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215686 | |||||||
| chr8:100215816 | G | A | 1 | a0001c0021t0001g0153 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1535+1898G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215816 | |||||||
| chr8:100215854 | T | A | 121 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(118): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1535+1936T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215854 | |||||||
| chr8:100216140 | T | C | 1 | a0002c0007t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1535+2222T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216140 | |||||||
| chr8:100216220 | C | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1535+2302C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216220 | |||||||
| chr8:100216253 | A | T | 1 | a0002c0007t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1535+2335A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216253 | |||||||
| chr8:100216255 | C | G | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1535+2337C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216255 | |||||||
| chr8:100216302 | C | T | 251 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1535+2384C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216302 | |||||||
| chr8:100216495 | G | C | 1 | a0002c0007t0001g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1535+2577G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216495 | |||||||
| chr8:100216563 | C | T | 61 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0002c0001t0001g0009 others(58): Show |
63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1535+2645C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216563 | |||||||
| chr8:100216931 | CT | C | 22 | a0001c0002t0001g0127 a0001c0002t0001g0133 a0001c0002t0001g0183 others(19): Show |
22 | HG00438.hp2 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1535+3036delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | ||||||
| chr8:100216931 | CTT | C | 185 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1535+3035_1535+303 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | ||||||
| chr8:100216931 | CTTT | C | 43 | a0001c0002t0001g0117 a0001c0002t0001g0122 a0001c0003t0001g0356 others(40): Show |
45 | HG00323.hp2 HG01081.hp1 HG01516.hp2 others(42): Show |
intron_variant | MODIFIER | c.1535+3034_1535+303 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | ||||||
| chr8:100217225 | G | A | 59 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1536-3054G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217225 | |||||||
| chr8:100217351 | A | G | 253 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(250): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1536-2928A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217351 | |||||||
| chr8:100217366 | A | G | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1536-2913A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217366 | |||||||
| chr8:100217399 | G | A | 36 | a0001c0008t0002g0089 a0001c0008t0002g0090 a0001c0008t0002g0091 others(33): Show |
37 | HG01081.hp1 HG02148.hp1 HG02280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536-2880G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217399 | |||||||
| chr8:100217661 | A | G | 44 | a0001c0002t0001g0127 a0001c0002t0001g0133 a0001c0002t0001g0164 others(41): Show |
46 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1536-2618A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217661 | |||||||
| chr8:100217689 | C | T | 13 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1536-2590C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217689 | |||||||
| chr8:100217814 | A | G | 1 | a0001c0002t0001g0148 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1536-2465A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217814 | |||||||
| chr8:100217828 | G | A | 1 | a0002c0007t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1536-2451G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217828 | |||||||
| chr8:100217891 | T | G | 1 | a0001c0008t0002g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1536-2388T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217891 | |||||||
| chr8:100218035 | A | G | 106 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(103): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1536-2244A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218035 | |||||||
| chr8:100218242 | T | C | 1 | a0003c0004t0001g0060 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1536-2037T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218242 | |||||||
| chr8:100218247 | C | A | 2 | a0003c0004t0001g0068 a0003c0004t0001g0070 |
2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1536-2032C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218247 | |||||||
| chr8:100218295 | A | G | 241 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(238): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1536-1984A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218295 | |||||||
| chr8:100218306 | T | A | 241 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(238): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1536-1973T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218306 | |||||||
| chr8:100218867 | G | T | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1536-1412G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218867 | |||||||
| chr8:100219091 | A | G | 1 | a0001c0003t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1536-1188A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219091 | |||||||
| chr8:100219290 | T | A | 352 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(349): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1536-989T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219290 | |||||||
| chr8:100219295 | T | C | 4 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-984T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219295 | |||||||
| chr8:100219460 | T | C | 1 | a0001c0012t0002g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1536-819T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219460 | |||||||
| chr8:100219539 | T | G | 1 | a0004c0010t0001g0143 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1536-740T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219539 | |||||||
| chr8:100219579 | G | A | 1 | a0001c0003t0005g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1536-700G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219579 | |||||||
| chr8:100220162 | C | T | 2 | a0001c0002t0001g0127 a0001c0002t0001g0164 |
2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1536-117C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220162 | |||||||
| chr8:100220171 | G | A | 4 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-108G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220171 | |||||||
| chr8:100220193 | TCAGTACT others(1): Show |
T | 31 | a0001c0003t0001g0104 a0001c0003t0001g0252 a0001c0003t0001g0255 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1536-80_1536-73del others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100220193 | ||||||
| chr8:100220199 | C | G | 1 | a0003c0004t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1536-80C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220199 | |||||||
| chr8:100220201 | G | T | 1 | a0003c0004t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1536-78G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220201 | |||||||
| chr8:100220270 | C | G | 4 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-9C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220270 | |||||||
| chr8:100220473 | T | C | 242 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(239): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1688+42T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220473 | |||||||
| chr8:100220549 | G | A | 6 | a0003c0004t0001g0001 a0003c0004t0001g0026 a0003c0004t0001g0053 others(3): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+118G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220549 | |||||||
| chr8:100220550 | ATTGCCT | A | 6 | a0003c0004t0001g0001 a0003c0004t0001g0026 a0003c0004t0001g0053 others(3): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+121_1688+126d others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 100220550 | ||||||
| chr8:100220559 | T | A | 6 | a0003c0004t0001g0001 a0003c0004t0001g0026 a0003c0004t0001g0053 others(3): Show |
8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+128T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220559 | |||||||
| chr8:100220588 | C | T | 1 | a0002c0001t0001g0307 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1688+157C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220588 | |||||||
| chr8:100220780 | T | C | 235 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(232): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1688+349T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220780 | |||||||
| chr8:100220844 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1688+413G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220844 | |||||||
| chr8:100220870 | C | T | 1 | a0002c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1688+439C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220870 | |||||||
| chr8:100220945 | C | T | 1 | a0002c0001t0006g0094 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1688+514C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220945 | |||||||
| chr8:100221014 | G | A | 2 | a0002c0001t0001g0305 a0002c0001t0001g0308 |
2 | HG02040.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1688+583G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221014 | |||||||
| chr8:100221055 | G | A | 1 | a0002c0001t0001g0301 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1688+624G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221055 | |||||||
| chr8:100221069 | A | T | 242 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(239): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1688+638A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221069 | |||||||
| chr8:100221072 | C | CAA | 4 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688+641_1688+642i others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221072 | |||||||
| chr8:100221073 | C | A | 242 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(239): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1688+642C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221073 | |||||||
| chr8:100221178 | T | C | 3 | a0001c0008t0002g0089 a0001c0008t0002g0090 a0001c0008t0002g0091 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1688+747T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221178 | |||||||
| chr8:100221383 | C | T | 1 | a0013c0017t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1688+952C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221383 | |||||||
| chr8:100221430 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1688+999C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221430 | |||||||
| chr8:100221668 | T | C | 242 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(239): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1688+1237T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221668 | |||||||
| chr8:100221898 | A | G | 245 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(242): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1688+1467A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221898 | |||||||
| chr8:100222256 | C | T | 1 | a0003c0004t0001g0029 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1688+1825C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222256 | |||||||
| chr8:100222261 | C | G | 4 | a0001c0008t0002g0214 a0001c0008t0002g0215 a0001c0008t0002g0216 others(1): Show |
4 | HG03041.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1688+1830C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222261 | |||||||
| chr8:100222333 | A | C | 1 | a0005c0011t0002g0249 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1688+1902A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222333 | |||||||
| chr8:100222357 | C | T | 40 | a0002c0001t0001g0002 a0002c0001t0001g0009 a0002c0001t0001g0010 others(37): Show |
41 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1688+1926C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222357 | |||||||
| chr8:100222915 | G | A | 1 | a0002c0007t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1689-2258G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222915 | |||||||
| chr8:100223074 | C | A | 1 | a0001c0002t0001g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1689-2099C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223074 | |||||||
| chr8:100223238 | A | G | 1 | a0002c0001t0001g0219 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1689-1935A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223238 | |||||||
| chr8:100223363 | G | T | 1 | a0001c0002t0001g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1689-1810G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223363 | |||||||
| chr8:100223580 | CT | C | 126 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(123): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1689-1579delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 100223580 | ||||||
| chr8:100223804 | C | T | 1 | a0002c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1689-1369C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223804 | |||||||
| chr8:100223836 | A | T | 1 | a0002c0001t0001g0325 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1689-1337A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223836 | |||||||
| chr8:100223943 | T | G | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689-1230T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223943 | |||||||
| chr8:100224075 | C | T | 1 | a0002c0001t0001g0306 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1689-1098C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224075 | |||||||
| chr8:100224219 | C | A | 1 | a0002c0001t0001g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1689-954C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224219 | |||||||
| chr8:100224283 | C | G | 1 | a0001c0002t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1689-890C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224283 | |||||||
| chr8:100224411 | G | A | 37 | a0001c0003t0001g0257 a0001c0003t0003g0099 a0001c0003t0003g0100 others(34): Show |
39 | HG00733.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1689-762G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224411 | |||||||
| chr8:100224528 | T | C | 45 | a0001c0002t0001g0133 a0001c0008t0002g0006 a0001c0008t0002g0089 others(42): Show |
47 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1689-645T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224528 | |||||||
| chr8:100224579 | A | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1689-594A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224579 | |||||||
| chr8:100224884 | T | G | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689-289T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224884 | |||||||
| chr8:100224979 | G | A | 1 | a0014c0022t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1689-194G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224979 | |||||||
| chr8:100225442 | C | T | 1 | a0002c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1855+103C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225442 | |||||||
| chr8:100225516 | C | T | 5 | a0003c0004t0001g0024 a0003c0004t0001g0032 a0003c0004t0001g0033 others(2): Show |
5 | HG00099.hp1 HG00735.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+177C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225516 | |||||||
| chr8:100225573 | C | T | 1 | a0001c0002t0001g0195 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1855+234C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225573 | |||||||
| chr8:100225635 | G | T | 3 | a0001c0002t0001g0150 a0001c0002t0001g0210 a0001c0003t0001g0018 |
3 | HG02280.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1855+296G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225635 | |||||||
| chr8:100225636 | T | G | 28 | a0001c0002t0001g0133 a0001c0015t0001g0221 a0001c0015t0001g0225 others(25): Show |
28 | HG01081.hp1 HG02148.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.1855+297T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225636 | |||||||
| chr8:100225689 | G | T | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0020 others(16): Show |
21 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1855+350G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225689 | |||||||
| chr8:100225714 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1855+375A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225714 | |||||||
| chr8:100225801 | T | C | 1 | a0002c0001t0001g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1855+462T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225801 | |||||||
| chr8:100225829 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1855+490G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225829 | |||||||
| chr8:100225881 | G | A | 1 | a0001c0002t0001g0004 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1855+542G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225881 | |||||||
| chr8:100225882 | G | A | 1 | a0005c0011t0002g0005 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1855+543G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225882 | |||||||
| chr8:100225892 | G | T | 200 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1855+553G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225892 | |||||||
| chr8:100225902 | G | A | 17 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(14): Show |
19 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1855+563G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225902 | |||||||
| chr8:100225936 | A | G | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+597A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225936 | |||||||
| chr8:100225998 | G | GT | 14 | a0001c0002t0001g0095 a0001c0002t0001g0157 a0001c0002t0001g0161 others(11): Show |
14 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+677dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100225998 | ||||||
| chr8:100225998 | GT | G | 6 | a0002c0001t0001g0110 a0002c0007t0001g0187 a0002c0007t0001g0188 others(3): Show |
6 | HG01167.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855+677delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100225998 | ||||||
| chr8:100226278 | T | C | 1 | a0001c0002t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1855+939T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226278 | |||||||
| chr8:100226363 | T | C | 1 | a0002c0001t0001g0269 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1855+1024T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226363 | |||||||
| chr8:100226912 | T | C | 1 | a0001c0008t0008g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1855+1573T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226912 | |||||||
| chr8:100227360 | A | G | 6 | a0001c0003t0001g0257 a0001c0003t0001g0354 a0001c0003t0001g0355 others(3): Show |
6 | HG01099.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1855+2021A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227360 | |||||||
| chr8:100227662 | G | C | 37 | a0001c0003t0001g0257 a0001c0003t0001g0354 a0001c0003t0001g0355 others(34): Show |
39 | HG00733.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1855+2323G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227662 | |||||||
| chr8:100227841 | A | AT | 37 | a0001c0002t0001g0084 a0001c0002t0001g0096 a0001c0002t0001g0122 others(34): Show |
37 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1855+2525dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | ||||||
| chr8:100227841 | A | ATT | 140 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1855+2524_1855+252 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | ||||||
| chr8:100227841 | A | ATTT | 68 | a0001c0002t0001g0085 a0001c0002t0001g0133 a0001c0002t0001g0147 others(65): Show |
70 | HG00140.hp2 HG00544.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.1855+2523_1855+252 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | ||||||
| chr8:100227872 | G | T | 2 | a0001c0009t0001g0276 a0002c0001t0001g0277 |
2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1855+2533G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227872 | |||||||
| chr8:100227980 | G | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1855+2641G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227980 | |||||||
| chr8:100228063 | C | T | 1 | a0001c0003t0003g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1855+2724C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100228063 | |||||||
| chr8:100228159 | A | G | 1 | a0001c0009t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1855+2820A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100228159 | |||||||
| chr8:100228410 | C | CA | 49 | a0001c0002t0001g0117 a0001c0003t0001g0257 a0001c0003t0001g0354 others(46): Show |
51 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1856-2728dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100228410 | ||||||
| chr8:100228410 | C | CAA | 196 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1856-2729_1856-272 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100228410 | ||||||
| chr8:100229063 | C | T | 1 | a0002c0001t0001g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1856-2093C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229063 | |||||||
| chr8:100229174 | G | A | 2 | a0002c0007t0001g0188 a0002c0007t0001g0189 |
2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1856-1982G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229174 | |||||||
| chr8:100229387 | G | A | 1 | a0002c0001t0001g0314 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1856-1769G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229387 | |||||||
| chr8:100229403 | G | A | 14 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(11): Show |
15 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1856-1753G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229403 | |||||||
| chr8:100229418 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1856-1738C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229418 | |||||||
| chr8:100229445 | C | A | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1856-1711C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229445 | |||||||
| chr8:100229445 | C | CA | 13 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(10): Show |
13 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1856-1702dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100229445 | ||||||
| chr8:100229497 | T | A | 1 | a0011c0023t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1856-1659T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229497 | |||||||
| chr8:100229670 | T | C | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1856-1486T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229670 | |||||||
| chr8:100229684 | A | G | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856-1472A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229684 | |||||||
| chr8:100229940 | T | C | 59 | a0001c0002t0001g0133 a0001c0003t0003g0099 a0001c0003t0003g0100 others(56): Show |
61 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1856-1216T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229940 | |||||||
| chr8:100230385 | C | T | 32 | a0001c0003t0001g0104 a0001c0003t0001g0252 a0001c0003t0001g0255 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1856-771C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230385 | |||||||
| chr8:100230529 | C | G | 172 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(169): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1856-627C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230529 | |||||||
| chr8:100230598 | A | G | 1 | a0013c0017t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1856-558A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230598 | |||||||
| chr8:100230748 | C | T | 1 | a0002c0001t0001g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1856-408C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230748 | |||||||
| chr8:100230863 | C | T | 2 | a0003c0004t0001g0247 a0013c0017t0001g0246 |
2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1856-293C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230863 | |||||||
| chr8:100230868 | G | A | 1 | a0001c0009t0001g0326 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1856-288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230868 | |||||||
| chr8:100230910 | T | C | 1 | a0002c0001t0001g0307 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1856-246T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230910 | |||||||
| chr8:100231038 | C | T | 4 | a0001c0009t0001g0007 a0001c0009t0001g0285 a0001c0009t0001g0290 others(1): Show |
5 | HG01496.hp1 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856-118C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100231038 | |||||||
| chr8:100231119 | A | G | 65 | a0001c0002t0001g0133 a0001c0003t0001g0257 a0001c0003t0001g0354 others(62): Show |
67 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1856-37A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100231119 | |||||||
| chr8:100231350 | TAA | T | 45 | a0001c0002t0001g0133 a0001c0008t0002g0006 a0001c0008t0002g0089 others(42): Show |
47 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(44): Show |
intron_variant | MODIFIER | c.1988+63_1988+64del others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231350 | |||||||
| chr8:100231465 | G | A | 45 | a0001c0002t0001g0133 a0001c0008t0002g0006 a0001c0008t0002g0089 others(42): Show |
47 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(44): Show |
intron_variant | MODIFIER | c.1988+177G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231465 | |||||||
| chr8:100231497 | C | T | 4 | a0001c0002t0001g0202 a0001c0002t0001g0203 a0001c0002t0001g0207 others(1): Show |
4 | HG02738.hp2 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1988+209C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231497 | |||||||
| chr8:100231509 | T | C | 1 | a0001c0009t0001g0342 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1988+221T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231509 | |||||||
| chr8:100231726 | G | A | 1 | a0001c0003t0003g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1988+438G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231726 | |||||||
| chr8:100231833 | G | C | 2 | a0001c0002t0001g0127 a0001c0002t0001g0164 |
2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1988+545G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231833 | |||||||
| chr8:100231961 | C | CA | 45 | a0001c0002t0001g0114 a0001c0003t0001g0104 a0001c0003t0001g0252 others(42): Show |
45 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1988+688dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 100231961 | ||||||
| chr8:100231976 | A | AAAT | 44 | a0001c0002t0001g0133 a0001c0008t0002g0006 a0001c0008t0002g0089 others(41): Show |
46 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(43): Show |
intron_variant | MODIFIER | c.1988+688_1988+689i others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231976 | |||||||
| chr8:100231976 | A | AAT | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1988+688_1988+689i others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231976 | |||||||
| chr8:100231977 | T | A | 59 | a0001c0002t0001g0133 a0001c0003t0003g0099 a0001c0003t0003g0100 others(56): Show |
61 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1988+689T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231977 | |||||||
| chr8:100231987 | G | T | 240 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(237): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1988+699G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231987 | |||||||
| chr8:100232043 | G | C | 1 | a0003c0004t0005g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1988+755G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232043 | |||||||
| chr8:100232225 | T | C | 1 | a0001c0002t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1988+937T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232225 | |||||||
| chr8:100232307 | A | T | 1 | a0002c0001t0001g0219 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1988+1019A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232307 | |||||||
| chr8:100232660 | A | G | 1 | a0002c0007t0001g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1989-751A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232660 | |||||||
| chr8:100232670 | T | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1989-741T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232670 | |||||||
| chr8:100232748 | C | T | 3 | a0003c0004t0001g0024 a0003c0004t0001g0080 a0003c0004t0001g0081 |
3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1989-663C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232748 | |||||||
| chr8:100232844 | T | C | 1 | a0011c0023t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1989-567T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232844 | |||||||
| chr8:100233014 | G | A | 35 | a0002c0001t0001g0002 a0002c0001t0001g0092 a0002c0001t0001g0093 others(32): Show |
36 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1989-397G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233014 | |||||||
| chr8:100233171 | G | T | 1 | a0002c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1989-240G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233171 | |||||||
| chr8:100233210 | C | G | 3 | a0001c0008t0002g0089 a0001c0008t0002g0090 a0001c0008t0002g0091 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1989-201C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233210 | |||||||
| chr8:100233776 | G | T | 1 | a0009c0020t0001g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2115+239G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100233776 | |||||||
| chr8:100234010 | A | G | 1 | a0002c0001t0001g0283 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2115+473A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234010 | |||||||
| chr8:100234359 | T | TA | 199 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(196): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2115+831dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100234359 | ||||||
| chr8:100234603 | G | A | 1 | a0002c0001t0001g0324 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2115+1066G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234603 | |||||||
| chr8:100234707 | T | C | 7 | a0001c0008t0002g0006 a0001c0008t0002g0240 a0001c0008t0002g0241 others(4): Show |
8 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2115+1170T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234707 | |||||||
| chr8:100234709 | T | G | 1 | a0002c0007t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2115+1172T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234709 | |||||||
| chr8:100235092 | T | C | 244 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2115+1555T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235092 | |||||||
| chr8:100235123 | G | C | 1 | a0002c0005t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2115+1586G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235123 | |||||||
| chr8:100235258 | G | A | 1 | a0002c0007t0001g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2115+1721G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235258 | |||||||
| chr8:100235373 | C | A | 1 | a0001c0003t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2115+1836C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235373 | |||||||
| chr8:100235594 | G | A | 1 | a0003c0004t0001g0029 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2115+2057G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235594 | |||||||
| chr8:100235741 | T | A | 1 | a0002c0001t0001g0322 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2115+2204T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235741 | |||||||
| chr8:100235761 | C | T | 117 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(114): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2115+2224C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235761 | |||||||
| chr8:100235782 | G | A | 2 | a0002c0001t0001g0258 a0002c0001t0001g0321 |
2 | NA19002.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2115+2245G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235782 | |||||||
| chr8:100235888 | C | T | 25 | a0001c0003t0001g0104 a0003c0004t0001g0024 a0003c0004t0001g0025 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2115+2351C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235888 | |||||||
| chr8:100235954 | T | C | 1 | a0003c0004t0001g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2115+2417T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235954 | |||||||
| chr8:100235965 | G | A | 3 | a0001c0008t0002g0214 a0001c0008t0002g0215 a0001c0008t0002g0216 |
3 | HG03041.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2115+2428G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235965 | |||||||
| chr8:100236054 | C | T | 3 | a0001c0003t0001g0354 a0001c0003t0001g0355 a0001c0003t0001g0356 |
3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2115+2517C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236054 | |||||||
| chr8:100236090 | A | C | 6 | a0001c0003t0001g0257 a0001c0003t0001g0354 a0001c0003t0001g0355 others(3): Show |
6 | HG01099.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+2553A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236090 | |||||||
| chr8:100236135 | T | G | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2115+2598T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236135 | |||||||
| chr8:100236210 | G | C | 1 | a0002c0001t0001g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2115+2673G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236210 | |||||||
| chr8:100236283 | G | A | 1 | a0002c0005t0002g0237 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2115+2746G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236283 | |||||||
| chr8:100236298 | A | G | 42 | a0001c0008t0002g0006 a0001c0008t0002g0089 a0001c0008t0002g0090 others(39): Show |
44 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(41): Show |
intron_variant | MODIFIER | c.2115+2761A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236298 | |||||||
| chr8:100236542 | C | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-2698C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236542 | |||||||
| chr8:100236712 | T | C | 2 | a0001c0003t0001g0292 a0001c0003t0001g0293 |
2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2116-2528T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236712 | |||||||
| chr8:100237269 | C | T | 14 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2116-1971C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237269 | |||||||
| chr8:100237346 | G | C | 1 | a0001c0003t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2116-1894G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237346 | |||||||
| chr8:100237534 | G | T | 202 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2116-1706G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237534 | |||||||
| chr8:100237543 | T | C | 4 | a0002c0001t0001g0011 a0002c0007t0001g0191 a0002c0007t0001g0192 others(1): Show |
4 | HG01109.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-1697T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237543 | |||||||
| chr8:100237679 | C | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-1561C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237679 | |||||||
| chr8:100238007 | A | G | 1 | a0002c0001t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2116-1233A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238007 | |||||||
| chr8:100238012 | A | G | 1 | a0003c0006t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2116-1228A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238012 | |||||||
| chr8:100238190 | C | T | 1 | a0001c0009t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2116-1050C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238190 | |||||||
| chr8:100238288 | TC | T | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-949delC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100238288 | ||||||
| chr8:100238379 | A | G | 1 | a0003c0004t0005g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2116-861A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238379 | |||||||
| chr8:100238517 | T | C | 2 | a0002c0001t0001g0261 a0002c0001t0001g0262 |
2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2116-723T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238517 | |||||||
| chr8:100238623 | A | G | 56 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(53): Show |
58 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.2116-617A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238623 | |||||||
| chr8:100238679 | C | T | 165 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2116-561C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238679 | |||||||
| chr8:100238741 | A | G | 1 | a0001c0003t0001g0356 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-499A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238741 | |||||||
| chr8:100238750 | T | C | 1 | a0001c0002t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2116-490T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238750 | |||||||
| chr8:100238765 | CTTA | C | 165 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2116-469_2116-467d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100238765 | ||||||
| chr8:100238857 | C | G | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-383C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238857 | |||||||
| chr8:100239068 | G | A | 1 | a0001c0002t0001g0004 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2116-172G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239068 | |||||||
| chr8:100239137 | G | GC | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-102dupC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100239137 | ||||||
| chr8:100239138 | C | A | 3 | a0001c0002t0001g0204 a0001c0002t0001g0205 a0001c0002t0001g0206 |
3 | HG00639.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2116-102C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239138 | |||||||
| chr8:100239196 | C | T | 3 | a0001c0012t0002g0113 a0005c0011t0002g0005 a0005c0011t0002g0249 |
4 | HG02280.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-44C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239196 | |||||||
| chr8:100239479 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2280+75A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239479 | |||||||
| chr8:100239707 | G | A | 2 | a0001c0003t0001g0075 a0001c0003t0001g0076 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2280+303G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239707 | |||||||
| chr8:100239715 | G | C | 3 | a0002c0001t0001g0009 a0002c0001t0001g0010 a0002c0001t0001g0012 |
3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2280+311G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239715 | |||||||
| chr8:100240234 | C | T | 205 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0082 others(202): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2281-169C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100240234 | |||||||
| chr8:100240864 | G | GT | 10 | a0001c0003t0001g0022 a0001c0003t0001g0255 a0001c0003t0001g0257 others(7): Show |
11 | HG00438.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2650-12dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 100240864 | ||||||
| chr8:100240864 | G | T | 1 | a0002c0001t0001g0318 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2650-27G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | chr8 | 100240864 | |||||||
| chr8:100240871 | T | G | 1 | a0001c0002t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2650-20T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | chr8 | 100240871 |