Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9043 |
| ensemblid | ENSG00000008294.22 |
| hgncid | 14524 |
| symbol | SPAG9 |
| name | sperm associated antigen 9 |
| refseq_nuc | NM_001130528.3 |
| refseq_prot | NP_001124000.1 |
| ensembl_nuc | ENST00000262013.12 |
| ensembl_prot | ENSP00000262013.7 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 50962174 |
| end | 51120868 |
| strand | - |
| ver | v1.2 |
| region | chr17:50962174-51120868 |
| region5000 | chr17:50957174-51125868 |
| regionname0 | SPAG9_chr17_50962174_51120868 |
| regionname5000 | SPAG9_chr17_50957174_51125868 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1321 | 260 | 64 | 62 | 92 | 14 | 26 | 69 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| a0002 | 0/0 | 1321 | 28 | 24 | 2 | 0 | 0 | 2 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| a0003 | 0/0 | 1321 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| a0004 | 0/0 | 1321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| a0005 | 0/0 | 1321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| a0006 | 0/0 | 1321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | MELED others(1316): Show |
chr17 | 50957174 | 51125868 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3963 | 229 | 46 | 54 | 87 | 14 | 26 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0001c0002 | 0/0 | 3963 | 21 | 16 | 5 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0001c0005 | 0/0 | 3963 | 8 | 1 | 3 | 4 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0001c0007 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0001c0008 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0002c0003 | 0/0 | 3963 | 18 | 18 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0002c0004 | 0/0 | 3963 | 10 | 6 | 2 | 0 | 0 | 2 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0003c0009 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0004c0006 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0005c0010 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 | ||
| a0006c0011 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | ATGGA others(3958): Show |
chr17 | 50957174 | 51125868 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8277 | 87 | 20 | 23 | 24 | 6 | 13 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0002 | 1/0 | 8276 | 70 | 16 | 10 | 32 | 6 | 5 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0003 | 0/0 | 8278 | 36 | 4 | 6 | 23 | 0 | 3 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0004 | 0/0 | 8278 | 12 | 2 | 7 | 0 | 2 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0006 | 0/0 | 8276 | 7 | 0 | 4 | 0 | 0 | 3 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0008 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0009 | 0/0 | 8277 | 4 | 1 | 0 | 3 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0012 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0013 | 0/0 | 8278 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0014 | 0/0 | 8276 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0017 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0019 | 0/0 | 8276 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0020 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0022 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0025 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0026 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0001c0001t0027 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0002t0001 | 0/0 | 8277 | 18 | 13 | 5 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0002t0004 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0002t0023 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0002t0024 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0005t0001 | 0/0 | 8277 | 7 | 1 | 3 | 3 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0005t0004 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0001c0007t0001 | 0/0 | 8277 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0001c0008t0002 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8274): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0007 | 0/0 | 8278 | 6 | 6 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0008 | 0/0 | 8278 | 4 | 4 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0010 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0011 | 0/0 | 8278 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0018 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0002c0003t0021 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0002c0004t0005 | 0/0 | 8279 | 7 | 4 | 1 | 0 | 0 | 2 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8274): Show |
chr17 | 50957174 | 51125868 |
| a0002c0004t0007 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| a0002c0004t0015 | 0/0 | 8279 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8274): Show |
chr17 | 50957174 | 51125868 |
| a0002c0004t0016 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8274): Show |
chr17 | 50957174 | 51125868 |
| a0003c0009t0002 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0004c0006t0001 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8272): Show |
chr17 | 50957174 | 51125868 |
| a0005c0010t0002 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8271): Show |
chr17 | 50957174 | 51125868 |
| a0006c0011t0003 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | GGCAG others(8273): Show |
chr17 | 50957174 | 51125868 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0013g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0014g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0020g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0022g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0025g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0026g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0001t0027g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0002t0024g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0005t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0001c0008t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0018g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0003t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0002c0004t0016g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0003c0009t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0004c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0005c0010t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| a0006c0011t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | GBR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0185 | EUR | GBR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0093 | EUR | FIN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00558 | hp1 | a0001 | c0005 | t0004 | g0246 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00558 | hp2 | a0003 | c0009 | t0002 | g0095 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0212 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0188 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0184 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0180 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01168 | hp2 | a0002 | c0004 | t0015 | g0008 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01243 | hp2 | a0002 | c0004 | t0005 | g0004 | AMR | PUR | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0124 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0115 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0060 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01884 | hp2 | a0002 | c0003 | t0008 | g0292 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01891 | hp1 | a0001 | c0001 | t0022 | g0070 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0252 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0119 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02055 | hp1 | a0002 | c0004 | t0005 | g0001 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0162 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02083 | hp2 | a0001 | c0001 | t0012 | g0032 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0183 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0101 | EAS | CDX | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CDX | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02258 | hp1 | a0001 | c0001 | t0026 | g0147 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02258 | hp2 | a0002 | c0004 | t0016 | g0002 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02273 | hp1 | a0001 | c0001 | t0014 | g0106 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02300 | hp2 | a0001 | c0005 | t0001 | g0238 | AMR | PEL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02451 | hp2 | a0002 | c0004 | t0005 | g0005 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02572 | hp2 | a0001 | c0002 | t0024 | g0286 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02615 | hp1 | a0002 | c0003 | t0018 | g0200 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02622 | hp2 | a0002 | c0003 | t0008 | g0287 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02683 | hp1 | a0002 | c0004 | t0005 | g0007 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0160 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02717 | hp1 | a0002 | c0003 | t0007 | g0114 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02723 | hp1 | a0001 | c0002 | t0023 | g0284 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02809 | hp2 | a0002 | c0004 | t0007 | g0009 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02895 | hp1 | a0002 | c0003 | t0010 | g0198 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02896 | hp1 | a0002 | c0003 | t0010 | g0199 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02897 | hp2 | a0002 | c0003 | t0010 | g0197 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02965 | hp1 | a0002 | c0003 | t0007 | g0077 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02970 | hp2 | a0002 | c0004 | t0005 | g0010 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03041 | hp1 | a0002 | c0003 | t0011 | g0195 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03041 | hp2 | a0002 | c0003 | t0007 | g0096 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03130 | hp2 | a0001 | c0008 | t0002 | g0080 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03195 | hp1 | a0002 | c0003 | t0008 | g0173 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03195 | hp2 | a0002 | c0004 | t0005 | g0003 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03486 | hp2 | a0002 | c0003 | t0008 | g0260 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03516 | hp2 | a0002 | c0003 | t0005 | g0094 | AFR | ESN | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03540 | hp1 | a0002 | c0003 | t0021 | g0067 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03540 | hp2 | a0005 | c0010 | t0002 | g0140 | AFR | GWD | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0280 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03579 | hp2 | a0002 | c0003 | t0007 | g0129 | AFR | MSL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0107 | SAS | PJL | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0131 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04199 | hp2 | a0002 | c0004 | t0005 | g0006 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04228 | hp1 | a0001 | c0001 | t0019 | g0090 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | STU | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18522 | hp2 | a0001 | c0001 | t0027 | g0098 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18747 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | CHB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18906 | hp1 | a0002 | c0003 | t0007 | g0102 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18952 | hp2 | a0006 | c0011 | t0003 | g0040 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18982 | hp1 | a0001 | c0005 | t0001 | g0211 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18984 | hp2 | a0001 | c0005 | t0001 | g0258 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18989 | hp2 | a0001 | c0001 | t0009 | g0189 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0291 | AFR | LWK | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19030 | hp2 | a0002 | c0003 | t0007 | g0168 | AFR | LWK | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19063 | hp1 | a0001 | c0001 | t0017 | g0084 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19064 | hp1 | a0001 | c0001 | t0025 | g0156 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19085 | hp2 | a0001 | c0007 | t0001 | g0250 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ASW | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ASW | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0181 | EUR | TSI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | TSI | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | GIH | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18955 | hp1 | a0001 | c0005 | t0001 | g0267 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0244 | AFR | USA | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | USA | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA21309 | hp1 | a0002 | c0003 | t0011 | g0196 | AFR | LWK | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0110 | REF | REF | SPAG9_chr17_50957174_51125868 | SPAG9 | chr17 | 50957174 | 51125868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50966279 | T | C | 1 | a0002 | 28 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(25): Show |
missense_variant | MODERATE | c.3959A>G | p.Asn1320Ser | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 4171/8276 | 3959/3966 | 1320/1321 | chr17 | 50966279 | |||
| chr17:50987163 | T | A | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2888A>T | p.Gln963Leu | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/30 | 3100/8276 | 2888/3966 | 963/1321 | chr17 | 50987163 | |||
| chr17:50996680 | A | G | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1853T>C | p.Leu618Ser | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/30 | 2065/8276 | 1853/3966 | 618/1321 | chr17 | 50996680 | |||
| chr17:50998522 | G | A | 1 | a0005 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1760C>T | p.Pro587Leu | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/30 | 1972/8276 | 1760/3966 | 587/1321 | chr17 | 50998522 | |||
| chr17:51021229 | G | A | 1 | a0006 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.920C>T | p.Ala307Val | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 7/30 | 1132/8276 | 920/3966 | 307/1321 | chr17 | 51021229 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50979786 | T | C | 1 | a0001c0008 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.3369A>G | p.Leu1123Leu | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/30 | 3581/8276 | 3369/3966 | 1123/1321 | chr17 | 50979786 | |||
| chr17:50979825 | A | T | 1 | a0001c0007 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.3330T>A | p.Ser1110Ser | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/30 | 3542/8276 | 3330/3966 | 1110/1321 | chr17 | 50979825 | |||
| chr17:50999678 | C | T | 1 | a0001c0005 | 8 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(5): Show |
synonymous_variant | LOW | c.1647G>A | p.Arg549Arg | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/30 | 1859/8276 | 1647/3966 | 549/1321 | chr17 | 50999678 | |||
| chr17:51006167 | G | A | 1 | a0001c0002 | 21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
synonymous_variant | LOW | c.1342C>T | p.Leu448Leu | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 11/30 | 1554/8276 | 1342/3966 | 448/1321 | chr17 | 51006167 | |||
| chr17:51120522 | C | T | 1 | a0002c0004 | 10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
synonymous_variant | LOW | c.135G>A | p.Glu45Glu | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/30 | 347/8276 | 135/3966 | 45/1321 | chr17 | 51120522 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50962479 | A | T | 2 | a0001c0002t0023 a0001c0002t0024 |
2 | HG02572.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3793T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 3793 | chr17 | 50962479 | ||||||
| chr17:50962501 | G | C | 1 | a0001c0001t0019 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3771C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 3771 | chr17 | 50962501 | ||||||
| chr17:50962722 | T | C | 7 | a0002c0003t0005 a0002c0003t0007 a0002c0003t0021 others(4): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3550A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 3550 | chr17 | 50962722 | ||||||
| chr17:50962879 | A | G | 3 | a0001c0001t0022 a0002c0003t0010 a0002c0003t0018 |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3393T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 3393 | chr17 | 50962879 | ||||||
| chr17:50962920 | T | C | 1 | a0001c0001t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3352A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 3352 | chr17 | 50962920 | ||||||
| chr17:50963418 | A | G | 1 | a0001c0001t0017 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 2854 | chr17 | 50963418 | ||||||
| chr17:50964150 | G | GA | 10 | a0001c0001t0008 a0002c0003t0005 a0002c0003t0007 others(7): Show |
25 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2121dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 2121 | chr17 | 50964150 | ||||||
| chr17:50964248 | T | C | 7 | a0002c0003t0005 a0002c0003t0007 a0002c0003t0021 others(4): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2024A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 2024 | chr17 | 50964248 | ||||||
| chr17:50964250 | A | G | 1 | a0001c0001t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2022T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 2022 | chr17 | 50964250 | ||||||
| chr17:50964556 | C | T | 1 | a0001c0001t0013 | 2 | HG01109.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1716 | chr17 | 50964556 | ||||||
| chr17:50964587 | C | CA | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(13): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1684dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1684 | chr17 | 50964587 | ||||||
| chr17:50964587 | C | CAA | 10 | a0001c0001t0004 a0001c0001t0013 a0001c0002t0004 others(7): Show |
30 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684dupTT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1684 | chr17 | 50964587 | ||||||
| chr17:50964646 | A | C | 1 | a0002c0004t0016 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1626T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1626 | chr17 | 50964646 | ||||||
| chr17:50964744 | T | C | 1 | a0001c0001t0012 | 2 | HG02083.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1528A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1528 | chr17 | 50964744 | ||||||
| chr17:50964928 | G | GT | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(1): Show |
43 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1343dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1343 | chr17 | 50964928 | ||||||
| chr17:50964928 | G | T | 1 | a0002c0004t0015 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1344 | chr17 | 50964928 | ||||||
| chr17:50964957 | C | T | 1 | a0001c0001t0014 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1315G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1315 | chr17 | 50964957 | ||||||
| chr17:50965120 | T | C | 1 | a0001c0001t0025 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 1152 | chr17 | 50965120 | ||||||
| chr17:50965440 | C | T | 1 | a0002c0003t0011 | 2 | HG03041.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*832G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 832 | chr17 | 50965440 | ||||||
| chr17:50965968 | T | C | 1 | a0001c0001t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 304 | chr17 | 50965968 | ||||||
| chr17:50965987 | C | T | 1 | a0001c0001t0006 | 7 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 285 | chr17 | 50965987 | ||||||
| chr17:50966047 | G | T | 1 | a0002c0003t0011 | 2 | HG03041.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 225 | chr17 | 50966047 | ||||||
| chr17:50966174 | G | A | 1 | a0001c0001t0027 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 30/30 | 98 | chr17 | 50966174 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50966426 | A | G | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3851-39T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966426 | |||||||
| chr17:50966432 | T | C | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.3851-45A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966432 | |||||||
| chr17:50966496 | G | C | 1 | a0001c0001t0002g0088 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3851-109C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966496 | |||||||
| chr17:50966523 | T | C | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.3851-136A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966523 | |||||||
| chr17:50966537 | A | T | 24 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(21): Show |
24 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.3851-150T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966537 | |||||||
| chr17:50966857 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0161 |
2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3851-470A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966857 | |||||||
| chr17:50966950 | A | G | 10 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0002c0003t0005g0094 others(7): Show |
10 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3851-563T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50966950 | |||||||
| chr17:50967113 | G | A | 10 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0141 others(7): Show |
10 | HG02280.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3851-726C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50967113 | |||||||
| chr17:50967177 | T | G | 2 | a0001c0001t0004g0152 a0001c0001t0004g0191 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3851-790A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50967177 | |||||||
| chr17:50967986 | A | G | 1 | a0001c0001t0003g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3851-1599T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50967986 | |||||||
| chr17:50968217 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3851-1830A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50968217 | |||||||
| chr17:50968294 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3851-1907A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50968294 | |||||||
| chr17:50968392 | T | G | 1 | a0001c0001t0003g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3851-2005A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50968392 | |||||||
| chr17:50968604 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3850+2103C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50968604 | |||||||
| chr17:50968969 | G | A | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0170 |
3 | HG02451.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3850+1738C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50968969 | |||||||
| chr17:50969025 | C | T | 1 | a0001c0001t0006g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3850+1682G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50969025 | |||||||
| chr17:50969905 | C | T | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3850+802G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50969905 | |||||||
| chr17:50970164 | C | T | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0213 others(12): Show |
15 | HG01074.hp1 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3850+543G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970164 | |||||||
| chr17:50970254 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3850+453C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970254 | |||||||
| chr17:50970505 | G | T | 24 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(21): Show |
24 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.3850+202C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970505 | |||||||
| chr17:50970512 | C | CA | 30 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0001g0158 others(27): Show |
30 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.3850+194dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970512 | |||||||
| chr17:50970582 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0002g0116 a0001c0001t0009g0162 |
3 | HG00140.hp1 HG00323.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3850+125G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970582 | |||||||
| chr17:50970607 | C | T | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3850+100G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970607 | |||||||
| chr17:50970703 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01257.hp1 HG01952.hp1 |
splice_region_variant&intron_variant | LOW | c.3850+4T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 29/29 | chr17 | 50970703 | |||||||
| chr17:50970867 | C | T | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3701-11G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50970867 | |||||||
| chr17:50970925 | T | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0049 |
2 | NA18994.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.3701-69A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50970925 | |||||||
| chr17:50970945 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3701-89G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50970945 | |||||||
| chr17:50971144 | C | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3701-288G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971144 | |||||||
| chr17:50971279 | C | T | 1 | a0002c0004t0015g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3701-423G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971279 | |||||||
| chr17:50971309 | AAAAC | A | 176 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0075 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.3701-457_3701-454d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971309 | |||||||
| chr17:50971309 | AAAACAAA others(1): Show |
A | 22 | a0001c0001t0004g0192 a0001c0002t0001g0270 a0001c0002t0001g0271 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.3701-461_3701-454d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971309 | |||||||
| chr17:50971434 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3701-578C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971434 | |||||||
| chr17:50971456 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3701-600A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971456 | |||||||
| chr17:50971459 | C | CT | 34 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(31): Show |
34 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.3701-604dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971459 | |||||||
| chr17:50971459 | CT | C | 76 | a0001c0001t0001g0151 a0001c0001t0001g0172 a0001c0001t0001g0203 others(73): Show |
76 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.3701-604delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971459 | |||||||
| chr17:50971459 | CTT | C | 7 | a0001c0001t0001g0222 a0001c0001t0003g0232 a0001c0001t0003g0268 others(4): Show |
7 | HG01168.hp1 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3701-605_3701-604d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971459 | |||||||
| chr17:50971459 | CTTT | C | 14 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(11): Show |
14 | HG01168.hp2 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3701-606_3701-604d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971459 | |||||||
| chr17:50971561 | G | A | 19 | a0001c0001t0027g0098 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.3701-705C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50971561 | |||||||
| chr17:50972363 | C | A | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3701-1507G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50972363 | |||||||
| chr17:50972811 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3701-1955C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50972811 | |||||||
| chr17:50972877 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0057 |
2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.3700+1894T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50972877 | |||||||
| chr17:50972898 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3700+1873G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50972898 | |||||||
| chr17:50972899 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3700+1872C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50972899 | |||||||
| chr17:50973111 | G | C | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.3700+1660C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973111 | |||||||
| chr17:50973195 | C | T | 3 | a0001c0001t0006g0108 a0001c0001t0006g0124 a0001c0001t0006g0159 |
3 | HG01257.hp2 HG01258.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.3700+1576G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973195 | |||||||
| chr17:50973198 | C | T | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0213 others(12): Show |
15 | HG01074.hp1 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3700+1573G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973198 | |||||||
| chr17:50973224 | C | T | 24 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(21): Show |
24 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.3700+1547G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973224 | |||||||
| chr17:50973311 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3700+1460C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973311 | |||||||
| chr17:50973452 | A | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700+1319T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973452 | |||||||
| chr17:50973727 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3700+1044A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973727 | |||||||
| chr17:50973749 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3700+1022A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973749 | |||||||
| chr17:50973918 | T | C | 53 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.3700+853A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973918 | |||||||
| chr17:50973957 | C | T | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3700+814G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50973957 | |||||||
| chr17:50974027 | A | G | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3700+744T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50974027 | |||||||
| chr17:50974490 | T | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.3700+281A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50974490 | |||||||
| chr17:50974682 | C | T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3700+89G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 28/29 | chr17 | 50974682 | |||||||
| chr17:50975029 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3524-82T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975029 | |||||||
| chr17:50975113 | A | C | 1 | a0003c0009t0002g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3524-166T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975113 | |||||||
| chr17:50975164 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3524-217G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975164 | |||||||
| chr17:50975311 | A | C | 1 | a0001c0001t0003g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3524-364T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975311 | |||||||
| chr17:50975554 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0178 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3524-607G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975554 | |||||||
| chr17:50975570 | C | T | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3524-623G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50975570 | |||||||
| chr17:50976126 | G | GT | 6 | a0001c0001t0001g0221 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
6 | HG01192.hp2 HG02280.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.3523+981dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50976126 | |||||||
| chr17:50976225 | T | C | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3523+883A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50976225 | |||||||
| chr17:50976336 | A | C | 1 | a0001c0001t0003g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3523+772T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50976336 | |||||||
| chr17:50976533 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3523+575A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50976533 | |||||||
| chr17:50976935 | G | A | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3523+173C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50976935 | |||||||
| chr17:50977078 | T | C | 105 | a0001c0001t0001g0177 a0001c0001t0001g0194 a0001c0001t0001g0203 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.3523+30A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 27/29 | chr17 | 50977078 | |||||||
| chr17:50977236 | G | A | 1 | a0001c0002t0001g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3410-15C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50977236 | |||||||
| chr17:50977248 | T | C | 1 | a0006c0011t0003g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3410-27A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50977248 | |||||||
| chr17:50977488 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3410-267A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50977488 | |||||||
| chr17:50977714 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3410-493G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50977714 | |||||||
| chr17:50977800 | C | G | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3410-579G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50977800 | |||||||
| chr17:50978083 | C | T | 197 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(194): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.3410-862G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978083 | |||||||
| chr17:50978178 | C | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-957G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978178 | |||||||
| chr17:50978213 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3410-992A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978213 | |||||||
| chr17:50978306 | C | A | 1 | a0001c0001t0014g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3410-1085G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978306 | |||||||
| chr17:50978469 | A | G | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3410-1248T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978469 | |||||||
| chr17:50978780 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3409+966G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978780 | |||||||
| chr17:50978899 | A | G | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3409+847T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978899 | |||||||
| chr17:50978957 | G | C | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.3409+789C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50978957 | |||||||
| chr17:50979297 | A | G | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3409+449T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50979297 | |||||||
| chr17:50979380 | GA | G | 19 | a0001c0001t0001g0222 a0001c0001t0001g0228 a0001c0001t0001g0229 others(16): Show |
19 | HG01070.hp1 HG01168.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3409+365delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50979380 | |||||||
| chr17:50979441 | G | GTTCACTA others(91): Show |
1 | a0001c0001t0002g0145 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3409+207_3409+304d others(100): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50979441 | |||||||
| chr17:50979687 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3409+59C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 26/29 | chr17 | 50979687 | |||||||
| chr17:50980158 | G | A | 2 | a0001c0001t0004g0152 a0001c0001t0004g0191 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3238-241C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980158 | |||||||
| chr17:50980169 | A | G | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238-252T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980169 | |||||||
| chr17:50980180 | C | T | 156 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(153): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.3238-263G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980180 | |||||||
| chr17:50980495 | G | A | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3238-578C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980495 | |||||||
| chr17:50980637 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0263 |
3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3238-720C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980637 | |||||||
| chr17:50980696 | C | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3238-779G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980696 | |||||||
| chr17:50980778 | ATTTGAGC others(7): Show |
A | 25 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(22): Show |
25 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.3238-875_3238-862d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980778 | |||||||
| chr17:50980952 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3238-1035A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980952 | |||||||
| chr17:50980958 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01891.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3238-1041G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980958 | |||||||
| chr17:50980959 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0002g0214 |
2 | NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3238-1042C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50980959 | |||||||
| chr17:50981064 | T | C | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3238-1147A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981064 | |||||||
| chr17:50981071 | G | C | 1 | a0002c0003t0007g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3238-1154C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981071 | |||||||
| chr17:50981150 | ATGATACC others(11): Show |
A | 57 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.3238-1251_3238-123 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981150 | |||||||
| chr17:50981230 | T | A | 3 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0025g0156 |
3 | HG02257.hp2 HG03017.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3237+1294A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981230 | |||||||
| chr17:50981390 | G | GTGGA | 33 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.3237+1130_3237+113 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981390 | |||||||
| chr17:50981390 | G | GTGGATGG others(1): Show |
14 | a0001c0001t0001g0053 a0001c0001t0001g0261 a0001c0001t0001g0269 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3237+1126_3237+113 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981390 | |||||||
| chr17:50981390 | G | GTGGATGG others(5): Show |
4 | a0002c0003t0007g0168 a0002c0004t0005g0004 a0002c0004t0005g0005 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3237+1122_3237+113 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981390 | |||||||
| chr17:50981390 | G | GTGGATGG others(9): Show |
1 | a0002c0004t0005g0003 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3237+1118_3237+113 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981390 | |||||||
| chr17:50981390 | GTGGATGG others(5): Show |
G | 1 | a0001c0001t0003g0021 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3237+1122_3237+113 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981390 | |||||||
| chr17:50981462 | A | G | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3237+1062T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981462 | |||||||
| chr17:50981483 | A | AAGAT | 45 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0053 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.3237+1037_3237+104 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | A | AAGATAGA others(1): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0064 others(6): Show |
9 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.3237+1033_3237+104 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | A | AAGATAGA others(5): Show |
1 | a0001c0001t0002g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3237+1029_3237+104 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | AAGAT | A | 51 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0085 others(48): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.3237+1037_3237+104 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | AAGATAGA others(1): Show |
A | 39 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(36): Show |
39 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.3237+1033_3237+104 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | AAGATAGA others(5): Show |
A | 43 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0215 others(40): Show |
43 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3237+1029_3237+104 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | AAGATAGA others(9): Show |
A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01243.hp2 HG01257.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3237+1025_3237+104 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981483 | AAGATAGA others(13): Show |
A | 1 | a0001c0001t0003g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3237+1021_3237+104 others(24): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981483 | |||||||
| chr17:50981527 | T | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0240 a0001c0001t0001g0248 |
3 | HG01109.hp1 HG01934.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3237+997A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981527 | |||||||
| chr17:50981527 | T | TAGAA | 5 | a0001c0001t0002g0143 a0002c0003t0008g0173 a0002c0003t0008g0287 others(2): Show |
5 | HG01884.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3237+993_3237+996d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981527 | |||||||
| chr17:50981541 | G | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3237+983C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981541 | |||||||
| chr17:50981561 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3237+963T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981561 | |||||||
| chr17:50981632 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3237+892C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981632 | |||||||
| chr17:50981637 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3237+887A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981637 | |||||||
| chr17:50981645 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3237+879C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981645 | |||||||
| chr17:50981710 | T | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.3237+814A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981710 | |||||||
| chr17:50981716 | C | CA | 12 | a0001c0001t0001g0062 a0001c0001t0001g0091 a0001c0001t0001g0126 others(9): Show |
12 | HG00609.hp2 HG00738.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.3237+807dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981716 | |||||||
| chr17:50981716 | CA | C | 91 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(88): Show |
91 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3237+807delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981716 | |||||||
| chr17:50981733 | C | T | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3237+791G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981733 | |||||||
| chr17:50981988 | A | G | 196 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(193): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.3237+536T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50981988 | |||||||
| chr17:50982111 | C | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3237+413G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50982111 | |||||||
| chr17:50982178 | G | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3237+346C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 25/29 | chr17 | 50982178 | |||||||
| chr17:50982746 | T | G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.3089-74A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50982746 | |||||||
| chr17:50982986 | G | C | 1 | a0001c0001t0003g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3089-314C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50982986 | |||||||
| chr17:50983349 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3089-677A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50983349 | |||||||
| chr17:50983524 | C | T | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3089-852G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50983524 | |||||||
| chr17:50984075 | A | T | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3088+848T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984075 | |||||||
| chr17:50984114 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3088+809C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984114 | |||||||
| chr17:50984257 | T | G | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3088+666A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984257 | |||||||
| chr17:50984297 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3088+626T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984297 | |||||||
| chr17:50984320 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3088+603T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984320 | |||||||
| chr17:50984424 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.3088+499G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984424 | |||||||
| chr17:50984610 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0124 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3088+313G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984610 | |||||||
| chr17:50984639 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3088+284A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984639 | |||||||
| chr17:50984718 | TG | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3088+204delC | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984718 | |||||||
| chr17:50984724 | T | A | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3088+199A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 24/29 | chr17 | 50984724 | |||||||
| chr17:50985176 | G | C | 1 | a0001c0001t0004g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3021-186C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 23/29 | chr17 | 50985176 | |||||||
| chr17:50985406 | A | G | 1 | a0001c0002t0001g0281 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3020+292T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 23/29 | chr17 | 50985406 | |||||||
| chr17:50985499 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3020+199T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 23/29 | chr17 | 50985499 | |||||||
| chr17:50985542 | CA | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0002g0093 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3020+155delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 23/29 | chr17 | 50985542 | |||||||
| chr17:50985873 | A | G | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.2940-95T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50985873 | |||||||
| chr17:50985889 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2940-111A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50985889 | |||||||
| chr17:50986077 | C | A | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2940-299G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986077 | |||||||
| chr17:50986233 | T | G | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2940-455A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986233 | |||||||
| chr17:50986234 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2940-456C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986234 | |||||||
| chr17:50986289 | A | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2940-511T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986289 | |||||||
| chr17:50986520 | A | G | 7 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0143 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2939+592T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986520 | |||||||
| chr17:50986579 | T | C | 2 | a0001c0001t0013g0180 a0001c0001t0013g0183 |
2 | HG01109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2939+533A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986579 | |||||||
| chr17:50986609 | C | T | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2939+503G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986609 | |||||||
| chr17:50986637 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2939+475G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 22/29 | chr17 | 50986637 | |||||||
| chr17:50987350 | A | AT | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2814-114dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50987350 | |||||||
| chr17:50987471 | C | T | 2 | a0002c0003t0007g0114 a0002c0003t0007g0168 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2814-234G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50987471 | |||||||
| chr17:50987505 | C | T | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2814-268G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50987505 | |||||||
| chr17:50987646 | T | C | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2814-409A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50987646 | |||||||
| chr17:50987953 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2814-716G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50987953 | |||||||
| chr17:50988027 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2814-790G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50988027 | |||||||
| chr17:50988148 | G | A | 1 | a0001c0001t0004g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2814-911C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50988148 | |||||||
| chr17:50988694 | T | C | 88 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2813+983A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50988694 | |||||||
| chr17:50989228 | C | T | 2 | a0001c0001t0006g0131 a0001c0001t0006g0160 |
2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2813+449G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50989228 | |||||||
| chr17:50989334 | T | C | 40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.2813+343A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50989334 | |||||||
| chr17:50989399 | C | T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2813+278G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 21/29 | chr17 | 50989399 | |||||||
| chr17:50989921 | A | G | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2618-49T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50989921 | |||||||
| chr17:50989948 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2618-76A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50989948 | |||||||
| chr17:50990128 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2618-256G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50990128 | |||||||
| chr17:50990174 | C | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0243 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2617+276G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50990174 | |||||||
| chr17:50990276 | C | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2617+174G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50990276 | |||||||
| chr17:50990283 | C | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2617+167G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50990283 | |||||||
| chr17:50990402 | T | C | 158 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(155): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2617+48A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 20/29 | chr17 | 50990402 | |||||||
| chr17:50990820 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2399-152A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50990820 | |||||||
| chr17:50990907 | C | CT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0257 a0001c0001t0001g0264 others(3): Show |
6 | HG01175.hp1 HG01175.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2399-240dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50990907 | |||||||
| chr17:50991064 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2399-396C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991064 | |||||||
| chr17:50991140 | C | T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2399-472G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991140 | |||||||
| chr17:50991145 | G | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2399-477C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991145 | |||||||
| chr17:50991272 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2399-604G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991272 | |||||||
| chr17:50991323 | T | C | 2 | a0001c0001t0002g0134 a0001c0001t0002g0165 |
2 | NA18979.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2399-655A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991323 | |||||||
| chr17:50991567 | T | C | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2399-899A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991567 | |||||||
| chr17:50991627 | A | AT | 22 | a0001c0001t0001g0058 a0001c0002t0001g0270 a0001c0002t0001g0271 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2399-960dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991627 | |||||||
| chr17:50991910 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2399-1242G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991910 | |||||||
| chr17:50991923 | C | CT | 71 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0158 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2399-1256dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991923 | |||||||
| chr17:50991923 | C | CTT | 17 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0227 others(14): Show |
17 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2399-1257_2399-125 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991923 | |||||||
| chr17:50991923 | CT | C | 17 | a0001c0001t0002g0093 a0001c0001t0002g0097 a0001c0001t0002g0109 others(14): Show |
17 | HG00323.hp1 HG01943.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2399-1256delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991923 | |||||||
| chr17:50991929 | T | G | 1 | a0002c0004t0015g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2399-1261A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991929 | |||||||
| chr17:50991951 | TTA | T | 20 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0004g0152 others(17): Show |
20 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2399-1285_2399-128 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991951 | |||||||
| chr17:50991952 | TA | T | 43 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0069 others(40): Show |
43 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2399-1285delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991952 | |||||||
| chr17:50991953 | A | T | 131 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0052 others(128): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2399-1285T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991953 | |||||||
| chr17:50991961 | G | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2399-1293C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50991961 | |||||||
| chr17:50992033 | A | G | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2399-1365T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992033 | |||||||
| chr17:50992056 | T | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2399-1388A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992056 | |||||||
| chr17:50992148 | A | C | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2399-1480T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992148 | |||||||
| chr17:50992210 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2399-1542G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992210 | |||||||
| chr17:50992373 | G | A | 64 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.2398+1391C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992373 | |||||||
| chr17:50992543 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0003g0121 |
2 | NA18952.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2398+1221G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992543 | |||||||
| chr17:50992610 | G | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2398+1154C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992610 | |||||||
| chr17:50992818 | C | T | 1 | a0002c0004t0015g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2398+946G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992818 | |||||||
| chr17:50992904 | T | C | 13 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(10): Show |
13 | HG01106.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2398+860A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992904 | |||||||
| chr17:50992967 | G | C | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.2398+797C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50992967 | |||||||
| chr17:50993056 | A | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0002g0122 |
3 | HG00738.hp1 HG01256.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2398+708T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993056 | |||||||
| chr17:50993095 | C | CA | 25 | a0001c0001t0001g0104 a0001c0001t0002g0029 a0001c0001t0002g0109 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2398+668dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993095 | |||||||
| chr17:50993095 | CA | C | 69 | a0001c0001t0001g0150 a0001c0001t0001g0203 a0001c0001t0001g0205 others(66): Show |
69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2398+668delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993095 | |||||||
| chr17:50993315 | C | CA | 6 | a0001c0001t0001g0126 a0001c0001t0002g0157 a0001c0001t0004g0193 others(3): Show |
6 | HG01106.hp1 HG01109.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2398+448dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993315 | |||||||
| chr17:50993315 | CA | C | 149 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0052 others(146): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2398+448delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993315 | |||||||
| chr17:50993342 | A | T | 197 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(194): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2398+422T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 19/29 | chr17 | 50993342 | |||||||
| chr17:50994431 | C | A | 1 | a0001c0001t0002g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2227-496G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50994431 | |||||||
| chr17:50994594 | A | C | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2226+463T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50994594 | |||||||
| chr17:50994836 | C | T | 1 | a0004c0006t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2226+221G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50994836 | |||||||
| chr17:50994838 | CAT | C | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2226+217_2226+218d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50994838 | |||||||
| chr17:50994970 | A | G | 11 | a0001c0001t0001g0158 a0001c0001t0001g0172 a0001c0001t0001g0176 others(8): Show |
11 | HG00558.hp2 HG00609.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2226+87T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50994970 | |||||||
| chr17:50995029 | C | G | 7 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2226+28G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50995029 | |||||||
| chr17:50995046 | C | T | 8 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(5): Show |
8 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2226+11G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50995046 | |||||||
| chr17:50995048 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2226+9G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 18/29 | chr17 | 50995048 | |||||||
| chr17:50995279 | T | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2059-55A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 17/29 | chr17 | 50995279 | |||||||
| chr17:50995710 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0002g0082 a0001c0001t0002g0089 others(3): Show |
6 | HG01070.hp2 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1969-177T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50995710 | |||||||
| chr17:50995935 | G | C | 18 | a0001c0001t0001g0028 a0001c0001t0002g0014 a0001c0001t0002g0029 others(15): Show |
18 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1969-402C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50995935 | |||||||
| chr17:50996101 | A | C | 16 | a0001c0001t0001g0177 a0001c0001t0001g0194 a0001c0001t0004g0152 others(13): Show |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1968+464T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996101 | |||||||
| chr17:50996126 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0231 a0001c0001t0001g0237 |
3 | HG00741.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1968+439G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996126 | |||||||
| chr17:50996170 | A | G | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1968+395T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996170 | |||||||
| chr17:50996256 | A | T | 1 | a0001c0001t0003g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1968+309T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996256 | |||||||
| chr17:50996358 | C | T | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1968+207G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996358 | |||||||
| chr17:50996359 | C | G | 3 | a0001c0001t0003g0048 a0001c0001t0004g0185 a0001c0001t0004g0193 |
3 | HG00140.hp2 HG01106.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1968+206G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996359 | |||||||
| chr17:50996456 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1968+109C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996456 | |||||||
| chr17:50996475 | G | A | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1968+90C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 16/29 | chr17 | 50996475 | |||||||
| chr17:50996791 | C | A | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1839-97G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50996791 | |||||||
| chr17:50996855 | A | T | 53 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1839-161T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50996855 | |||||||
| chr17:50996868 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1839-174C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50996868 | |||||||
| chr17:50996906 | G | A | 8 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(5): Show |
8 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1839-212C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50996906 | |||||||
| chr17:50996968 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1839-274G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50996968 | |||||||
| chr17:50997139 | AAAAC | A | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0030 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839-449_1839-446d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997139 | |||||||
| chr17:50997139 | AAAACAAA others(1): Show |
A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1839-453_1839-446d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997139 | |||||||
| chr17:50997393 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1839-699G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997393 | |||||||
| chr17:50997432 | T | C | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0263 |
3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1839-738A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997432 | |||||||
| chr17:50997625 | A | C | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838+819T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997625 | |||||||
| chr17:50997655 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1838+789G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997655 | |||||||
| chr17:50997677 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1838+767G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997677 | |||||||
| chr17:50997794 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0148 |
2 | HG01943.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1838+650G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997794 | |||||||
| chr17:50997801 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1838+643G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997801 | |||||||
| chr17:50997942 | T | C | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1838+502A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997942 | |||||||
| chr17:50997993 | T | TA | 6 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(3): Show |
6 | HG00639.hp2 HG01928.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1838+450dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50997993 | |||||||
| chr17:50998022 | A | AT | 66 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(63): Show |
66 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1838+421dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998022 | |||||||
| chr17:50998022 | A | ATT | 27 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0194 others(24): Show |
27 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1838+420_1838+421d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998022 | |||||||
| chr17:50998022 | AT | A | 10 | a0001c0001t0001g0113 a0001c0001t0001g0172 a0001c0001t0001g0207 others(7): Show |
10 | HG00323.hp2 HG01515.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1838+421delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998022 | |||||||
| chr17:50998022 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1838+410_1838+421d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998022 | |||||||
| chr17:50998022 | ATTTTTTT others(6): Show |
A | 8 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(5): Show |
8 | HG02717.hp1 HG02965.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1838+409_1838+421d others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998022 | |||||||
| chr17:50998052 | A | T | 1 | a0001c0001t0002g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1838+392T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998052 | |||||||
| chr17:50998117 | C | T | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1838+327G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998117 | |||||||
| chr17:50998134 | C | T | 2 | a0001c0002t0001g0275 a0001c0002t0001g0276 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1838+310G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998134 | |||||||
| chr17:50998180 | C | T | 2 | a0001c0001t0002g0115 a0001c0001t0002g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1838+264G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998180 | |||||||
| chr17:50998225 | T | A | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1838+219A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998225 | |||||||
| chr17:50998320 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0242 |
2 | HG00621.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1838+124C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998320 | |||||||
| chr17:50998328 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0148 |
2 | HG01943.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1838+116G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 15/29 | chr17 | 50998328 | |||||||
| chr17:50998690 | T | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1665-73A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/29 | chr17 | 50998690 | |||||||
| chr17:50998803 | A | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1665-186T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/29 | chr17 | 50998803 | |||||||
| chr17:50999408 | C | A | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1664+253G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/29 | chr17 | 50999408 | |||||||
| chr17:50999546 | T | TA | 38 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(35): Show |
38 | HG00544.hp1 HG00609.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.1664+114dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/29 | chr17 | 50999546 | |||||||
| chr17:50999546 | TA | T | 66 | a0001c0001t0001g0172 a0001c0001t0001g0203 a0001c0001t0001g0205 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1664+114delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 14/29 | chr17 | 50999546 | |||||||
| chr17:50999794 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1608-77T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 50999794 | |||||||
| chr17:50999923 | T | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1608-206A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 50999923 | |||||||
| chr17:50999979 | C | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1608-262G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 50999979 | |||||||
| chr17:51000010 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1608-293A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000010 | |||||||
| chr17:51000124 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608-407A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000124 | |||||||
| chr17:51000125 | G | A | 2 | a0002c0003t0008g0173 a0002c0003t0008g0287 |
2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1608-408C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000125 | |||||||
| chr17:51000218 | T | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1608-501A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000218 | |||||||
| chr17:51000361 | T | C | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1608-644A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000361 | |||||||
| chr17:51000634 | A | C | 195 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(192): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1608-917T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000634 | |||||||
| chr17:51000659 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0056 |
2 | NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1608-942C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000659 | |||||||
| chr17:51000669 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1608-952A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000669 | |||||||
| chr17:51000743 | CAATAAAT others(5): Show |
C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1607+960_1607+971d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000743 | |||||||
| chr17:51000747 | AAATG | A | 20 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(17): Show |
20 | HG00280.hp1 HG01358.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1607+964_1607+967d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000747 | |||||||
| chr17:51000751 | GAATGAAT others(1): Show |
G | 96 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0057 others(93): Show |
96 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1607+956_1607+963d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000751 | |||||||
| chr17:51000751 | GAATGAAT others(5): Show |
G | 6 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1607+952_1607+963d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000751 | |||||||
| chr17:51000751 | GAATGAAT others(9): Show |
G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1607+948_1607+963d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000751 | |||||||
| chr17:51000751 | GAATGAAT others(13): Show |
G | 2 | a0002c0004t0005g0006 a0002c0004t0005g0007 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1607+944_1607+963d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000751 | |||||||
| chr17:51000755 | G | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1607+960C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000755 | |||||||
| chr17:51000755 | GAATA | G | 86 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0104 others(83): Show |
86 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1607+956_1607+959d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000755 | |||||||
| chr17:51000755 | GAATAAAT others(1): Show |
G | 3 | a0001c0001t0001g0113 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG01106.hp2 HG02109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1607+952_1607+959d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000755 | |||||||
| chr17:51000835 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1607+880C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000835 | |||||||
| chr17:51000851 | T | C | 4 | a0001c0001t0003g0036 a0001c0001t0003g0043 a0001c0001t0003g0047 others(1): Show |
4 | NA18944.hp1 NA18994.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1607+864A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51000851 | |||||||
| chr17:51001106 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1607+609C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51001106 | |||||||
| chr17:51001393 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1607+322C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51001393 | |||||||
| chr17:51001508 | A | T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1607+207T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51001508 | |||||||
| chr17:51001528 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1607+187G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 13/29 | chr17 | 51001528 | |||||||
| chr17:51001855 | C | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1477-10G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51001855 | |||||||
| chr17:51001965 | C | A | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1477-120G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51001965 | |||||||
| chr17:51002016 | T | A | 23 | a0001c0001t0002g0081 a0001c0002t0001g0270 a0001c0002t0001g0271 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1477-171A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002016 | |||||||
| chr17:51002017 | A | T | 2 | a0001c0001t0001g0130 a0001c0001t0002g0071 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1477-172T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002017 | |||||||
| chr17:51002284 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1477-439A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002284 | |||||||
| chr17:51002576 | T | A | 48 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(45): Show |
48 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1477-731A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002576 | |||||||
| chr17:51002597 | T | C | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1477-752A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002597 | |||||||
| chr17:51002728 | A | C | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1477-883T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002728 | |||||||
| chr17:51002766 | A | AAAC | 21 | a0001c0001t0001g0177 a0001c0001t0001g0194 a0001c0001t0004g0152 others(18): Show |
21 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1477-924_1477-922d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002766 | |||||||
| chr17:51002810 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1477-965C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002810 | |||||||
| chr17:51002909 | C | T | 8 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(5): Show |
8 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1477-1064G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002909 | |||||||
| chr17:51002954 | C | G | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-1109G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002954 | |||||||
| chr17:51002988 | T | TA | 38 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(35): Show |
38 | HG00280.hp1 HG01168.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1477-1144dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002988 | |||||||
| chr17:51002988 | TA | T | 41 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(38): Show |
41 | HG00544.hp1 HG00609.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1477-1144delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51002988 | |||||||
| chr17:51003427 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1477-1582G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51003427 | |||||||
| chr17:51003608 | G | A | 67 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1476+1604C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51003608 | |||||||
| chr17:51003977 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1476+1235G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51003977 | |||||||
| chr17:51004194 | T | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1476+1018A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51004194 | |||||||
| chr17:51004286 | T | C | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1476+926A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51004286 | |||||||
| chr17:51004443 | A | G | 3 | a0001c0001t0006g0107 a0001c0001t0006g0131 a0001c0001t0006g0160 |
3 | HG02683.hp2 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1476+769T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51004443 | |||||||
| chr17:51004639 | A | G | 1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1476+573T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51004639 | |||||||
| chr17:51004969 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1476+243C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 12/29 | chr17 | 51004969 | |||||||
| chr17:51005603 | C | T | 4 | a0002c0004t0005g0003 a0002c0004t0005g0004 a0002c0004t0005g0005 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1425-340G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 11/29 | chr17 | 51005603 | |||||||
| chr17:51005839 | G | T | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0146 |
3 | HG01106.hp2 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1424+246C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 11/29 | chr17 | 51005839 | |||||||
| chr17:51005847 | G | A | 4 | a0001c0001t0019g0090 a0002c0003t0011g0195 a0002c0003t0011g0196 others(1): Show |
4 | HG02683.hp1 HG03041.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1424+238C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 11/29 | chr17 | 51005847 | |||||||
| chr17:51006258 | G | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-21C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51006258 | |||||||
| chr17:51006407 | G | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1272-170C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51006407 | |||||||
| chr17:51006523 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0145 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272-286G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51006523 | |||||||
| chr17:51006774 | A | G | 2 | a0002c0004t0005g0004 a0002c0004t0005g0010 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1271+495T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51006774 | |||||||
| chr17:51007014 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1271+255A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007014 | |||||||
| chr17:51007110 | G | GGT | 65 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0158 others(62): Show |
65 | HG00558.hp2 HG00609.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1271+157_1271+158d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007110 | |||||||
| chr17:51007110 | G | GGTGT | 4 | a0001c0002t0024g0286 a0002c0003t0021g0067 a0002c0004t0005g0004 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271+155_1271+158d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007110 | |||||||
| chr17:51007110 | G | GGTGTGT | 3 | a0001c0001t0004g0191 a0002c0003t0011g0195 a0002c0003t0011g0196 |
3 | HG02572.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1271+153_1271+158d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007110 | |||||||
| chr17:51007110 | GGTGT | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0230 a0001c0001t0006g0160 |
3 | HG02559.hp1 HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1271+155_1271+158d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007110 | |||||||
| chr17:51007110 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1271+147_1271+158d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 10/29 | chr17 | 51007110 | |||||||
| chr17:51007566 | C | T | 53 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1214-240G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51007566 | |||||||
| chr17:51007783 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1214-457G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51007783 | |||||||
| chr17:51007814 | C | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1214-488G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51007814 | |||||||
| chr17:51007907 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1214-581C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51007907 | |||||||
| chr17:51008395 | A | C | 3 | a0001c0002t0001g0270 a0001c0002t0001g0279 a0001c0002t0001g0288 |
3 | HG01167.hp2 HG01169.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1214-1069T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008395 | |||||||
| chr17:51008587 | T | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1214-1261A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008587 | |||||||
| chr17:51008628 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1214-1302G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008628 | |||||||
| chr17:51008844 | C | T | 53 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1214-1518G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008844 | |||||||
| chr17:51008896 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1214-1570G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008896 | |||||||
| chr17:51008935 | T | C | 40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1214-1609A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51008935 | |||||||
| chr17:51009099 | A | T | 20 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1214-1773T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51009099 | |||||||
| chr17:51009675 | A | G | 288 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(285): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1214-2349T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51009675 | |||||||
| chr17:51010341 | T | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214-3015A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010341 | |||||||
| chr17:51010371 | A | G | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1214-3045T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010371 | |||||||
| chr17:51010568 | G | GA | 29 | a0001c0001t0001g0194 a0001c0001t0002g0014 a0001c0001t0002g0029 others(26): Show |
29 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1214-3243dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010568 | |||||||
| chr17:51010568 | GA | G | 11 | a0001c0001t0001g0249 a0001c0001t0002g0072 a0001c0001t0002g0117 others(8): Show |
11 | HG01975.hp1 HG01981.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214-3243delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010568 | |||||||
| chr17:51010568 | GAAA | G | 53 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1214-3245_1214-324 others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010568 | |||||||
| chr17:51010568 | GAAAA | G | 8 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(5): Show |
8 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1214-3246_1214-324 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010568 | |||||||
| chr17:51010578 | A | AT | 11 | a0001c0001t0001g0062 a0001c0002t0001g0271 a0001c0002t0001g0272 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1214-3253_1214-325 others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010578 | |||||||
| chr17:51010578 | A | T | 3 | a0001c0001t0022g0070 a0001c0002t0004g0291 a0001c0002t0023g0284 |
3 | HG01891.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1214-3252T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010578 | |||||||
| chr17:51010580 | A | AT | 9 | a0001c0001t0004g0182 a0001c0002t0001g0270 a0001c0002t0001g0273 others(6): Show |
9 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1214-3255_1214-325 others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010580 | |||||||
| chr17:51010580 | A | T | 26 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0057 others(23): Show |
26 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1214-3254T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010580 | |||||||
| chr17:51010582 | A | AT | 10 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0002g0033 others(7): Show |
10 | HG00609.hp1 HG02015.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1214-3257_1214-325 others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010582 | |||||||
| chr17:51010582 | A | T | 103 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(100): Show |
103 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1214-3256T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010582 | |||||||
| chr17:51010582 | AAT | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-3258_1214-325 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010582 | |||||||
| chr17:51010584 | T | A | 11 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0002g0013 others(8): Show |
11 | HG00621.hp2 HG00738.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1214-3258A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010584 | |||||||
| chr17:51010586 | T | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG02809.hp1 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-3260A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010586 | |||||||
| chr17:51010600 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1214-3274A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010600 | |||||||
| chr17:51010600 | T | TAC | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214-3276_1214-327 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010600 | |||||||
| chr17:51010600 | T | TATAC | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1214-3275_1214-327 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010600 | |||||||
| chr17:51010711 | A | T | 1 | a0001c0001t0003g0024 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1214-3385T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010711 | |||||||
| chr17:51010756 | T | C | 2 | a0002c0003t0007g0114 a0002c0003t0007g0168 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1214-3430A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010756 | |||||||
| chr17:51010783 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1213+3449A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010783 | |||||||
| chr17:51010931 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1213+3301T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51010931 | |||||||
| chr17:51011117 | C | T | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213+3115G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51011117 | |||||||
| chr17:51011385 | C | CT | 18 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1213+2846dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51011385 | |||||||
| chr17:51011531 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1213+2701G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51011531 | |||||||
| chr17:51011653 | G | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1213+2579C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51011653 | |||||||
| chr17:51011947 | G | T | 1 | a0001c0001t0017g0084 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1213+2285C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51011947 | |||||||
| chr17:51012192 | C | T | 67 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1213+2040G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012192 | |||||||
| chr17:51012422 | T | C | 2 | a0001c0001t0002g0115 a0001c0001t0002g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1213+1810A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012422 | |||||||
| chr17:51012507 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1213+1725A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012507 | |||||||
| chr17:51012722 | C | CTTTA | 35 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0057 others(32): Show |
35 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1213+1506_1213+150 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012722 | |||||||
| chr17:51012722 | C | CTTTATTT others(1): Show |
40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1213+1502_1213+150 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012722 | |||||||
| chr17:51012722 | C | CTTTATTT others(5): Show |
4 | a0001c0001t0001g0062 a0001c0001t0002g0017 a0001c0001t0002g0033 others(1): Show |
4 | HG02015.hp1 HG02559.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213+1498_1213+150 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012722 | |||||||
| chr17:51012722 | CTTTATTT others(5): Show |
C | 67 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1213+1498_1213+150 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012722 | |||||||
| chr17:51012841 | G | A | 1 | a0002c0003t0005g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1213+1391C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012841 | |||||||
| chr17:51012894 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1213+1338T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51012894 | |||||||
| chr17:51013224 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0178 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1213+1008T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013224 | |||||||
| chr17:51013298 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1213+934C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013298 | |||||||
| chr17:51013344 | T | A | 7 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0239 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1213+888A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013344 | |||||||
| chr17:51013424 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1213+808A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013424 | |||||||
| chr17:51013487 | A | G | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1213+745T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013487 | |||||||
| chr17:51013709 | C | A | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213+523G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013709 | |||||||
| chr17:51013897 | CACAT | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1213+331_1213+334d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013897 | |||||||
| chr17:51013901 | T | TAC | 9 | a0001c0002t0001g0270 a0001c0002t0001g0278 a0001c0002t0001g0279 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1213+329_1213+330d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013901 | |||||||
| chr17:51013901 | TAC | T | 255 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0062 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1213+329_1213+330d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013901 | |||||||
| chr17:51013903 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1213+329G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013903 | |||||||
| chr17:51013907 | CACACACA others(5): Show |
C | 11 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1213+313_1213+324d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013907 | |||||||
| chr17:51013927 | CA | C | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0170 |
3 | HG02451.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1213+304delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 9/29 | chr17 | 51013927 | |||||||
| chr17:51014385 | CA | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-33delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014385 | |||||||
| chr17:51014408 | G | A | 4 | a0001c0001t0003g0036 a0001c0001t0003g0043 a0001c0001t0003g0047 others(1): Show |
4 | NA18944.hp1 NA18994.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-55C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014408 | |||||||
| chr17:51014646 | T | C | 2 | a0002c0003t0008g0173 a0002c0003t0008g0287 |
2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1092-293A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014646 | |||||||
| chr17:51014802 | G | GTATAGAG others(1): Show |
40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1092-450_1092-449i others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014802 | |||||||
| chr17:51014803 | G | T | 41 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(38): Show |
41 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1092-450C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014803 | |||||||
| chr17:51014807 | A | T | 41 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(38): Show |
41 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1092-454T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014807 | |||||||
| chr17:51014812 | A | T | 41 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(38): Show |
41 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1092-459T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014812 | |||||||
| chr17:51014813 | T | TTATA | 41 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(38): Show |
41 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1092-461_1092-460i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014813 | |||||||
| chr17:51014887 | A | G | 1 | a0001c0001t0019g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1092-534T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51014887 | |||||||
| chr17:51015038 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1092-685A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51015038 | |||||||
| chr17:51015406 | T | C | 15 | a0001c0001t0001g0194 a0001c0001t0004g0152 a0001c0001t0004g0179 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1092-1053A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51015406 | |||||||
| chr17:51015473 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1092-1120A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51015473 | |||||||
| chr17:51015648 | T | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1092-1295A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51015648 | |||||||
| chr17:51015734 | T | TA | 64 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1092-1382dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51015734 | |||||||
| chr17:51016026 | C | G | 1 | a0004c0006t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1092-1673G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51016026 | |||||||
| chr17:51016057 | A | G | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1092-1704T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51016057 | |||||||
| chr17:51016100 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-1747A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51016100 | |||||||
| chr17:51016533 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1092-2180T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51016533 | |||||||
| chr17:51016675 | G | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1092-2322C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51016675 | |||||||
| chr17:51017025 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1092-2672A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017025 | |||||||
| chr17:51017097 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1092-2744G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017097 | |||||||
| chr17:51017249 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1092-2896A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017249 | |||||||
| chr17:51017339 | A | G | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+2820T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017339 | |||||||
| chr17:51017394 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+2765A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017394 | |||||||
| chr17:51017519 | T | TGA | 7 | a0001c0001t0001g0194 a0001c0001t0002g0081 a0001c0001t0003g0050 others(4): Show |
7 | HG00741.hp2 HG01074.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1091+2638_1091+263 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017519 | |||||||
| chr17:51017519 | TGA | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+2638_1091+263 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017519 | |||||||
| chr17:51017519 | TGAGA | T | 58 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(55): Show |
58 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1091+2636_1091+263 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017519 | |||||||
| chr17:51017519 | TGAGAGAG others(1): Show |
T | 64 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1091+2632_1091+263 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017519 | |||||||
| chr17:51017519 | TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0001g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1091+2630_1091+263 others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017519 | |||||||
| chr17:51017655 | G | A | 1 | a0001c0001t0006g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1091+2504C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017655 | |||||||
| chr17:51017907 | C | T | 3 | a0001c0001t0002g0157 a0001c0001t0009g0189 a0001c0001t0014g0106 |
3 | HG02273.hp1 NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1091+2252G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51017907 | |||||||
| chr17:51018257 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1091+1902G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51018257 | |||||||
| chr17:51018267 | C | CG | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+1891dupC | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51018267 | |||||||
| chr17:51018295 | G | A | 1 | a0001c0005t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1091+1864C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51018295 | |||||||
| chr17:51018439 | G | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+1720C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51018439 | |||||||
| chr17:51019094 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1091+1065G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019094 | |||||||
| chr17:51019273 | A | G | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+886T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019273 | |||||||
| chr17:51019369 | A | G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1091+790T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019369 | |||||||
| chr17:51019370 | T | C | 19 | a0001c0002t0001g0270 a0001c0002t0001g0272 a0001c0002t0001g0273 others(16): Show |
19 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1091+789A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019370 | |||||||
| chr17:51019618 | C | T | 2 | a0001c0001t0002g0089 a0002c0004t0005g0006 |
2 | HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1091+541G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019618 | |||||||
| chr17:51019681 | C | T | 58 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1091+478G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019681 | |||||||
| chr17:51019784 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1091+375C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019784 | |||||||
| chr17:51019792 | C | T | 20 | a0001c0002t0001g0271 a0001c0002t0001g0290 a0002c0003t0005g0094 others(17): Show |
20 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1091+367G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019792 | |||||||
| chr17:51019896 | G | A | 1 | a0001c0005t0001g0267 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1091+263C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019896 | |||||||
| chr17:51019924 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1091+235G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51019924 | |||||||
| chr17:51020118 | T | TG | 10 | a0001c0002t0001g0271 a0001c0002t0001g0290 a0002c0003t0005g0094 others(7): Show |
10 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1091+40dupC | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51020118 | |||||||
| chr17:51020140 | C | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1091+19G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 8/29 | chr17 | 51020140 | |||||||
| chr17:51020593 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.992-335G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 7/29 | chr17 | 51020593 | |||||||
| chr17:51020613 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.992-355A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 7/29 | chr17 | 51020613 | |||||||
| chr17:51020649 | T | G | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.992-391A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 7/29 | chr17 | 51020649 | |||||||
| chr17:51020756 | A | G | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.991+402T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 7/29 | chr17 | 51020756 | |||||||
| chr17:51021663 | T | C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-298A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021663 | |||||||
| chr17:51021708 | C | A | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784-343G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021708 | |||||||
| chr17:51021747 | G | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01891.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.784-382C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021747 | |||||||
| chr17:51021767 | T | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0167 |
2 | HG02083.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.784-402A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021767 | |||||||
| chr17:51021790 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.784-425C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021790 | |||||||
| chr17:51021809 | T | C | 11 | a0001c0002t0001g0281 a0002c0004t0005g0001 a0002c0004t0005g0003 others(8): Show |
11 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.784-444A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021809 | |||||||
| chr17:51021816 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.784-451T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021816 | |||||||
| chr17:51021822 | TTTGAAGT others(2): Show |
T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-466_784-458del others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51021822 | |||||||
| chr17:51022028 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.784-663G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022028 | |||||||
| chr17:51022122 | C | CA | 29 | a0001c0001t0001g0061 a0001c0001t0001g0177 a0001c0001t0001g0259 others(26): Show |
29 | HG00609.hp1 HG01168.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.784-758dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022122 | |||||||
| chr17:51022122 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.784-757G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022122 | |||||||
| chr17:51022122 | CA | C | 8 | a0001c0001t0001g0207 a0001c0001t0001g0233 a0001c0001t0002g0066 others(5): Show |
8 | HG00323.hp2 HG02015.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-758delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022122 | |||||||
| chr17:51022167 | C | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-802G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022167 | |||||||
| chr17:51022189 | A | G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-824T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022189 | |||||||
| chr17:51022585 | G | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-1220C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022585 | |||||||
| chr17:51022631 | C | CTAA | 18 | a0001c0001t0001g0177 a0001c0001t0001g0194 a0001c0001t0001g0234 others(15): Show |
18 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.784-1269_784-1267d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022631 | |||||||
| chr17:51022631 | C | CTAATAA | 4 | a0001c0001t0004g0181 a0001c0001t0004g0184 a0002c0003t0007g0114 others(1): Show |
4 | HG01081.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1272_784-1267d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022631 | |||||||
| chr17:51022648 | A | G | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.784-1283T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022648 | |||||||
| chr17:51022693 | A | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-1328T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022693 | |||||||
| chr17:51022821 | A | G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-1456T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022821 | |||||||
| chr17:51022885 | G | T | 1 | a0001c0002t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.784-1520C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022885 | |||||||
| chr17:51022943 | A | AAAT | 29 | a0001c0001t0001g0062 a0001c0001t0001g0176 a0001c0001t0002g0078 others(26): Show |
29 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.784-1581_784-1579d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAAT | 7 | a0001c0001t0002g0120 a0001c0001t0004g0192 a0001c0002t0001g0271 others(4): Show |
7 | HG01167.hp1 HG02615.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-1584_784-1579d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(2): Show |
63 | a0001c0001t0001g0194 a0001c0001t0001g0203 a0001c0001t0001g0205 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.784-1587_784-1579d others(11): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(5): Show |
15 | a0001c0001t0001g0177 a0001c0001t0001g0209 a0001c0001t0001g0210 others(12): Show |
15 | HG00639.hp1 HG01884.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.784-1590_784-1579d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(8): Show |
8 | a0001c0001t0001g0208 a0001c0001t0001g0242 a0001c0001t0022g0070 others(5): Show |
8 | HG00621.hp1 HG01168.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1593_784-1579d others(17): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(11): Show |
16 | a0001c0001t0001g0265 a0001c0001t0004g0182 a0001c0002t0001g0281 others(13): Show |
16 | HG01099.hp2 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.784-1596_784-1579d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(14): Show |
3 | a0002c0004t0005g0004 a0002c0004t0007g0009 a0002c0004t0016g0002 |
3 | HG01243.hp2 HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.784-1599_784-1579d others(23): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51022943 | A | AAATAATA others(17): Show |
2 | a0001c0001t0013g0180 a0001c0001t0013g0183 |
2 | HG01109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.784-1602_784-1579d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51022943 | |||||||
| chr17:51023094 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.784-1729T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023094 | |||||||
| chr17:51023134 | T | A | 3 | a0002c0004t0005g0006 a0002c0004t0005g0007 a0002c0004t0015g0008 |
3 | HG01168.hp2 HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.784-1769A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023134 | |||||||
| chr17:51023175 | CTAT | C | 20 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.784-1813_784-1811d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023175 | |||||||
| chr17:51023232 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-1867A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023232 | |||||||
| chr17:51023237 | T | G | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-1872A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023237 | |||||||
| chr17:51023385 | C | T | 1 | a0001c0001t0019g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.784-2020G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023385 | |||||||
| chr17:51023513 | A | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0231 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.784-2148T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023513 | |||||||
| chr17:51023580 | G | A | 88 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.784-2215C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023580 | |||||||
| chr17:51023642 | G | A | 22 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.784-2277C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023642 | |||||||
| chr17:51023642 | G | T | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.784-2277C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023642 | |||||||
| chr17:51023655 | C | T | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.784-2290G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51023655 | |||||||
| chr17:51024124 | G | A | 2 | a0001c0002t0001g0271 a0001c0002t0001g0290 |
2 | HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.784-2759C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024124 | |||||||
| chr17:51024156 | G | C | 1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784-2791C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024156 | |||||||
| chr17:51024185 | G | A | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-2820C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024185 | |||||||
| chr17:51024247 | G | A | 1 | a0001c0002t0024g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.784-2882C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024247 | |||||||
| chr17:51024569 | C | T | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-3204G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024569 | |||||||
| chr17:51024659 | G | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.784-3294C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024659 | |||||||
| chr17:51024688 | G | C | 1 | a0001c0002t0001g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.784-3323C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024688 | |||||||
| chr17:51024713 | C | CA | 96 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(93): Show |
96 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.784-3349dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024713 | |||||||
| chr17:51024773 | A | C | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.784-3408T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024773 | |||||||
| chr17:51024792 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.784-3427C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024792 | |||||||
| chr17:51024975 | C | T | 20 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.784-3610G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51024975 | |||||||
| chr17:51025003 | A | G | 2 | a0001c0002t0001g0283 a0001c0002t0001g0289 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.784-3638T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025003 | |||||||
| chr17:51025018 | C | CA | 80 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(77): Show |
80 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.784-3654dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025018 | |||||||
| chr17:51025165 | A | G | 5 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-3800T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025165 | |||||||
| chr17:51025316 | C | CA | 38 | a0001c0001t0001g0104 a0001c0001t0001g0126 a0001c0001t0001g0130 others(35): Show |
38 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.784-3952dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CA | C | 48 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0127 others(45): Show |
48 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.784-3952delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CAA | C | 34 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0069 others(31): Show |
34 | HG00544.hp1 HG01069.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.784-3953_784-3952d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CAAAAAAA | C | 8 | a0001c0001t0001g0247 a0001c0001t0001g0254 a0001c0001t0001g0259 others(5): Show |
8 | HG01175.hp2 HG01928.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-3958_784-3952d others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CAAAAAAA others(1): Show |
C | 56 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.784-3959_784-3952d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0061 a0001c0001t0002g0066 |
2 | HG02015.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.784-3964_784-3952d others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025316 | CAAAAAAA others(7): Show |
C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.784-3965_784-3952d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025316 | |||||||
| chr17:51025469 | TA | T | 104 | a0001c0001t0001g0177 a0001c0001t0001g0194 a0001c0001t0001g0203 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.784-4105delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025469 | |||||||
| chr17:51025507 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784-4142T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025507 | |||||||
| chr17:51025577 | T | G | 1 | a0001c0001t0002g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.784-4212A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025577 | |||||||
| chr17:51025605 | T | C | 1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784-4240A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025605 | |||||||
| chr17:51025655 | T | C | 67 | a0001c0001t0001g0130 a0001c0001t0001g0203 a0001c0001t0001g0205 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-4290A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025655 | |||||||
| chr17:51025765 | G | A | 3 | a0001c0001t0006g0108 a0001c0001t0006g0124 a0001c0001t0006g0159 |
3 | HG01257.hp2 HG01258.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.784-4400C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025765 | |||||||
| chr17:51025864 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.784-4499A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51025864 | |||||||
| chr17:51026031 | T | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.784-4666A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026031 | |||||||
| chr17:51026226 | T | C | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784-4861A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026226 | |||||||
| chr17:51026320 | G | GA | 8 | a0001c0001t0002g0076 a0001c0001t0002g0097 a0001c0001t0002g0112 others(5): Show |
8 | HG01106.hp2 HG01943.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-4956dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026320 | |||||||
| chr17:51026320 | GA | G | 11 | a0001c0001t0002g0071 a0001c0001t0002g0093 a0001c0001t0002g0116 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.784-4956delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026320 | |||||||
| chr17:51026327 | A | T | 173 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(170): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.784-4962T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026327 | |||||||
| chr17:51026333 | A | T | 175 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(172): Show |
175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.784-4968T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026333 | |||||||
| chr17:51026403 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.784-5038G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026403 | |||||||
| chr17:51026674 | C | CT | 21 | a0001c0001t0001g0053 a0001c0001t0001g0177 a0001c0001t0001g0194 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.783+5006dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026674 | |||||||
| chr17:51026674 | CT | C | 73 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.783+5006delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026674 | |||||||
| chr17:51026674 | CTT | C | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.783+5005_783+5006d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026674 | |||||||
| chr17:51026680 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.783+5001A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026680 | |||||||
| chr17:51026681 | T | C | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783+5000A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026681 | |||||||
| chr17:51026825 | C | T | 1 | a0001c0001t0019g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.783+4856G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026825 | |||||||
| chr17:51026895 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.783+4786G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026895 | |||||||
| chr17:51026896 | G | A | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.783+4785C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026896 | |||||||
| chr17:51026975 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.783+4706G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026975 | |||||||
| chr17:51026998 | T | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.783+4683A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51026998 | |||||||
| chr17:51027073 | C | T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.783+4608G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027073 | |||||||
| chr17:51027082 | T | C | 196 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(193): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.783+4599A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027082 | |||||||
| chr17:51027085 | T | A | 1 | a0001c0001t0003g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.783+4596A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027085 | |||||||
| chr17:51027098 | C | T | 5 | a0001c0002t0001g0281 a0002c0004t0005g0003 a0002c0004t0005g0004 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+4583G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027098 | |||||||
| chr17:51027421 | C | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.783+4260G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027421 | |||||||
| chr17:51027434 | C | CA | 8 | a0001c0001t0001g0208 a0001c0001t0001g0226 a0001c0001t0001g0240 others(5): Show |
8 | HG01109.hp1 HG01175.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+4246dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027434 | |||||||
| chr17:51027490 | C | CAACAGTA others(12): Show |
4 | a0001c0001t0003g0036 a0001c0001t0003g0043 a0001c0001t0003g0047 others(1): Show |
4 | NA18944.hp1 NA18994.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+4172_783+4190d others(21): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027490 | |||||||
| chr17:51027697 | G | A | 64 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.783+3984C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027697 | |||||||
| chr17:51027709 | A | G | 20 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.783+3972T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027709 | |||||||
| chr17:51027718 | G | A | 195 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(192): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.783+3963C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027718 | |||||||
| chr17:51027775 | T | C | 1 | a0001c0001t0003g0268 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.783+3906A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51027775 | |||||||
| chr17:51028066 | C | CA | 22 | a0001c0001t0001g0208 a0001c0002t0001g0270 a0001c0002t0001g0271 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.783+3614dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028066 | |||||||
| chr17:51028081 | T | A | 132 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(129): Show |
132 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.783+3600A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028081 | |||||||
| chr17:51028082 | T | A | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.783+3599A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028082 | |||||||
| chr17:51028155 | T | G | 1 | a0001c0001t0003g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.783+3526A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028155 | |||||||
| chr17:51028432 | T | C | 1 | a0001c0001t0003g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.783+3249A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028432 | |||||||
| chr17:51028440 | T | A | 2 | a0001c0001t0001g0194 a0001c0001t0004g0202 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.783+3241A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028440 | |||||||
| chr17:51028693 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.783+2988G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51028693 | |||||||
| chr17:51029235 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.783+2446G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51029235 | |||||||
| chr17:51029390 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.783+2291T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51029390 | |||||||
| chr17:51030081 | A | G | 90 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(87): Show |
90 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.783+1600T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030081 | |||||||
| chr17:51030145 | C | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.783+1536G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030145 | |||||||
| chr17:51030164 | C | T | 90 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(87): Show |
90 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.783+1517G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030164 | |||||||
| chr17:51030589 | C | T | 2 | a0002c0003t0008g0173 a0002c0003t0008g0287 |
2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.783+1092G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030589 | |||||||
| chr17:51030625 | T | A | 7 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0239 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+1056A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030625 | |||||||
| chr17:51030817 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.783+864A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030817 | |||||||
| chr17:51030847 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.783+834A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030847 | |||||||
| chr17:51030913 | C | CT | 6 | a0001c0001t0001g0126 a0001c0001t0002g0066 a0001c0001t0003g0015 others(3): Show |
6 | HG02015.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+767dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030913 | |||||||
| chr17:51030913 | CT | C | 127 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(124): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.783+767delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030913 | |||||||
| chr17:51030913 | CTT | C | 6 | a0001c0001t0002g0253 a0002c0003t0008g0173 a0002c0003t0008g0260 others(3): Show |
6 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+766_783+767del others(2): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51030913 | |||||||
| chr17:51031096 | G | T | 3 | a0002c0003t0007g0096 a0002c0003t0007g0102 a0002c0003t0007g0129 |
3 | HG03041.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.783+585C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51031096 | |||||||
| chr17:51031300 | A | G | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.783+381T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51031300 | |||||||
| chr17:51031337 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.783+344T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 6/29 | chr17 | 51031337 | |||||||
| chr17:51031871 | T | C | 2 | a0001c0001t0004g0185 a0001c0001t0004g0193 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.742-149A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51031871 | |||||||
| chr17:51031944 | T | C | 19 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.742-222A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51031944 | |||||||
| chr17:51032199 | T | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0002g0093 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-477A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51032199 | |||||||
| chr17:51032283 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.742-561G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51032283 | |||||||
| chr17:51032688 | C | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.742-966G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51032688 | |||||||
| chr17:51032883 | G | A | 11 | a0001c0001t0001g0104 a0001c0001t0002g0012 a0001c0001t0002g0072 others(8): Show |
11 | HG01070.hp2 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.742-1161C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51032883 | |||||||
| chr17:51032953 | C | A | 1 | a0001c0001t0002g0134 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.742-1231G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51032953 | |||||||
| chr17:51033023 | GT | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(5): Show |
8 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-1302delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033023 | |||||||
| chr17:51033213 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.742-1491T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033213 | |||||||
| chr17:51033259 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.742-1537C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033259 | |||||||
| chr17:51033304 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742-1582A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033304 | |||||||
| chr17:51033310 | GA | G | 13 | a0001c0001t0001g0194 a0001c0001t0001g0261 a0001c0001t0002g0088 others(10): Show |
13 | HG01884.hp2 HG02258.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.742-1589delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033310 | |||||||
| chr17:51033310 | GAA | G | 23 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(20): Show |
23 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.742-1590_742-1589d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033310 | |||||||
| chr17:51033767 | A | G | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.742-2045T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033767 | |||||||
| chr17:51033858 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.742-2136A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51033858 | |||||||
| chr17:51034087 | T | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.742-2365A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51034087 | |||||||
| chr17:51034541 | A | C | 1 | a0001c0002t0023g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742-2819T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51034541 | |||||||
| chr17:51034662 | C | G | 1 | a0001c0005t0004g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.742-2940G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51034662 | |||||||
| chr17:51035160 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.742-3438A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51035160 | |||||||
| chr17:51035913 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.742-4191G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51035913 | |||||||
| chr17:51036156 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.742-4434G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51036156 | |||||||
| chr17:51036577 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.742-4855A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51036577 | |||||||
| chr17:51036809 | C | T | 3 | a0001c0001t0006g0108 a0001c0001t0006g0124 a0001c0001t0006g0159 |
3 | HG01257.hp2 HG01258.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.741+4692G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51036809 | |||||||
| chr17:51036932 | C | T | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.741+4569G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51036932 | |||||||
| chr17:51037144 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.741+4357G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037144 | |||||||
| chr17:51037235 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.741+4266G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037235 | |||||||
| chr17:51037248 | C | T | 43 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(40): Show |
43 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.741+4253G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037248 | |||||||
| chr17:51037449 | C | T | 1 | a0001c0005t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.741+4052G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037449 | |||||||
| chr17:51037486 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0003g0022 a0001c0001t0003g0026 others(2): Show |
5 | NA18948.hp1 NA18952.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+4015C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037486 | |||||||
| chr17:51037500 | C | G | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.741+4001G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037500 | |||||||
| chr17:51037505 | T | G | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.741+3996A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037505 | |||||||
| chr17:51037616 | TA | T | 25 | a0001c0001t0001g0177 a0001c0001t0026g0147 a0001c0002t0001g0281 others(22): Show |
25 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.741+3884delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037616 | |||||||
| chr17:51037663 | T | TTATATAT others(3): Show |
1 | a0002c0003t0007g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.741+3837_741+3838i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037663 | |||||||
| chr17:51037663 | T | TTATATAT others(5): Show |
2 | a0002c0003t0007g0102 a0002c0003t0007g0129 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.741+3837_741+3838i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037663 | |||||||
| chr17:51037663 | T | TTATATAT others(9): Show |
2 | a0002c0003t0005g0094 a0002c0003t0021g0067 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.741+3837_741+3838i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037663 | |||||||
| chr17:51037665 | T | A | 8 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(5): Show |
8 | HG02717.hp1 HG02965.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+3836A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TATATATA others(28): Show |
1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.741+3835_741+3836i others(37): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0004g0152 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.741+3828_741+3835d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(4): Show |
7 | HG01168.hp2 HG01891.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+3826_741+3835d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(5): Show |
3 | a0002c0003t0008g0292 a0002c0004t0005g0004 a0002c0004t0005g0005 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.741+3824_741+3835d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(9): Show |
2 | a0001c0001t0022g0070 a0002c0004t0005g0007 |
2 | HG01891.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.741+3820_741+3835d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(11): Show |
1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.741+3818_741+3835d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | T | TTATATAT others(17): Show |
2 | a0002c0004t0007g0009 a0002c0004t0016g0002 |
2 | HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.741+3835_741+3836i others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037665 | TTA | T | 98 | a0001c0001t0001g0028 a0001c0001t0001g0085 a0001c0001t0001g0104 others(95): Show |
98 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.741+3834_741+3835d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037665 | |||||||
| chr17:51037667 | A | T | 2 | a0001c0001t0001g0178 a0001c0001t0004g0191 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.741+3834T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037667 | |||||||
| chr17:51037683 | A | AGT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0127 a0001c0001t0002g0074 others(3): Show |
6 | HG01516.hp1 HG03017.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+3817_741+3818i others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037683 | |||||||
| chr17:51037683 | A | AGTGT | 4 | a0001c0001t0001g0035 a0001c0001t0002g0093 a0001c0001t0002g0116 others(1): Show |
4 | HG00140.hp1 HG00323.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+3817_741+3818i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037683 | |||||||
| chr17:51037683 | ATAGT | A | 3 | a0001c0001t0002g0088 a0001c0001t0003g0043 a0001c0001t0003g0201 |
3 | HG02132.hp1 NA18947.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.741+3814_741+3817d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037683 | |||||||
| chr17:51037684 | T | G | 29 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0091 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.741+3817A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037684 | |||||||
| chr17:51037685 | A | AGT | 11 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0062 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.741+3814_741+3815d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | AGTGT | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0056 others(8): Show |
11 | HG01884.hp1 HG01952.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.741+3812_741+3815d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATAGTG others(3): Show |
1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.741+3815_741+3816i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATAT | 7 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0228 others(4): Show |
7 | HG01109.hp1 HG01934.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+3815_741+3816i others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(3): Show |
10 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0181 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+3815_741+3816i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(5): Show |
2 | a0001c0001t0004g0185 a0001c0001t0004g0202 |
2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.741+3815_741+3816i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(5): Show |
2 | a0001c0001t0004g0179 a0001c0001t0004g0193 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.741+3815_741+3816i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(4): Show |
1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.741+3815_741+3816i others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(7): Show |
2 | a0002c0004t0005g0003 a0002c0004t0005g0010 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.741+3815_741+3816i others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0281 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.741+3815_741+3816i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(10): Show |
2 | a0002c0003t0008g0173 a0002c0003t0008g0287 |
2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.741+3815_741+3816i others(19): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(17): Show |
1 | a0002c0003t0011g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.741+3815_741+3816i others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | ATATATAT others(25): Show |
1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.741+3815_741+3816i others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | A | T | 29 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0091 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.741+3816T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037685 | AG | A | 48 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(45): Show |
48 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.741+3815delC | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037685 | |||||||
| chr17:51037686 | G | A | 15 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0228 others(12): Show |
15 | HG01109.hp1 HG01934.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.741+3815C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037686 | |||||||
| chr17:51037686 | G | T | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0226 others(8): Show |
11 | HG01884.hp2 HG02717.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.741+3815C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037686 | |||||||
| chr17:51037687 | T | A | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0226 others(7): Show |
10 | HG02717.hp1 HG02965.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+3814A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037687 | |||||||
| chr17:51037688 | G | A | 63 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.741+3813C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037688 | |||||||
| chr17:51037688 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.741+3813C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037688 | |||||||
| chr17:51037689 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.741+3812A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037689 | |||||||
| chr17:51037689 | T | TA | 4 | a0002c0003t0007g0096 a0002c0003t0008g0173 a0002c0003t0008g0260 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+3811_741+3812i others(3): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037689 | |||||||
| chr17:51037689 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.741+3811_741+3812i others(25): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037689 | |||||||
| chr17:51037689 | T | TATATATA others(24): Show |
1 | a0001c0001t0002g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.741+3811_741+3812i others(33): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037689 | |||||||
| chr17:51037690 | G | A | 56 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.741+3811C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037690 | |||||||
| chr17:51037690 | G | T | 3 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 |
3 | HG02622.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.741+3811C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037690 | |||||||
| chr17:51037691 | T | A | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.741+3810A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TA | 8 | a0001c0001t0001g0221 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG01975.hp2 HG02280.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+3809_741+3810i others(3): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(16): Show |
3 | a0001c0001t0001g0255 a0001c0001t0001g0259 a0001c0005t0004g0246 |
3 | HG00558.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.741+3809_741+3810i others(25): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(18): Show |
3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0002g0216 |
3 | HG00741.hp1 HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.741+3809_741+3810i others(27): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(20): Show |
12 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0208 others(9): Show |
12 | HG00323.hp2 HG00621.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.741+3809_741+3810i others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(22): Show |
10 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+3809_741+3810i others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(24): Show |
2 | a0001c0001t0001g0233 a0001c0005t0001g0238 |
2 | HG02300.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.741+3809_741+3810i others(33): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(26): Show |
2 | a0001c0001t0001g0262 a0001c0005t0001g0244 |
2 | NA18947.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.741+3809_741+3810i others(35): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(28): Show |
4 | a0001c0001t0001g0225 a0001c0001t0001g0266 a0001c0001t0002g0204 others(1): Show |
4 | HG01515.hp1 HG02071.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+3809_741+3810i others(37): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(30): Show |
3 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0257 |
3 | HG00280.hp2 HG01192.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.741+3809_741+3810i others(39): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037691 | T | TATATATA others(32): Show |
6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0249 others(3): Show |
6 | HG00639.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+3809_741+3810i others(41): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037691 | |||||||
| chr17:51037692 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0240 a0001c0001t0001g0248 |
3 | HG01109.hp1 HG01934.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.741+3809C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037692 | |||||||
| chr17:51037693 | T | TA | 3 | a0001c0001t0001g0213 a0001c0001t0001g0240 a0001c0001t0001g0248 |
3 | HG01109.hp1 HG01934.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.741+3807_741+3808i others(3): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037693 | |||||||
| chr17:51037722 | A | G | 20 | a0001c0002t0001g0281 a0001c0002t0023g0284 a0001c0002t0024g0286 others(17): Show |
20 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.741+3779T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51037722 | |||||||
| chr17:51038255 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.741+3246T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51038255 | |||||||
| chr17:51038414 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.741+3087C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51038414 | |||||||
| chr17:51038561 | G | C | 1 | a0001c0002t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.741+2940C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51038561 | |||||||
| chr17:51038752 | C | T | 1 | a0004c0006t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.741+2749G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51038752 | |||||||
| chr17:51039301 | G | A | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.741+2200C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51039301 | |||||||
| chr17:51039520 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01891.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.741+1981A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51039520 | |||||||
| chr17:51039944 | G | A | 2 | a0001c0001t0013g0180 a0001c0001t0013g0183 |
2 | HG01109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.741+1557C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51039944 | |||||||
| chr17:51040052 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.741+1449A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040052 | |||||||
| chr17:51040175 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0231 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.741+1326C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040175 | |||||||
| chr17:51040246 | C | CA | 22 | a0001c0001t0001g0062 a0001c0001t0001g0177 a0001c0001t0001g0178 others(19): Show |
22 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.741+1254dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040246 | |||||||
| chr17:51040272 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.741+1229G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040272 | |||||||
| chr17:51040506 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0002g0109 |
2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.741+995A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040506 | |||||||
| chr17:51040585 | T | G | 1 | a0001c0001t0019g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.741+916A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040585 | |||||||
| chr17:51040713 | A | G | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00609.hp2 HG01069.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.741+788T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040713 | |||||||
| chr17:51040856 | T | C | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.741+645A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040856 | |||||||
| chr17:51040867 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.741+634A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51040867 | |||||||
| chr17:51041125 | C | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0256 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.741+376G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51041125 | |||||||
| chr17:51041401 | A | G | 5 | a0001c0002t0001g0281 a0002c0004t0005g0003 a0002c0004t0005g0004 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+100T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 5/29 | chr17 | 51041401 | |||||||
| chr17:51041848 | C | T | 1 | a0002c0003t0007g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591-197G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51041848 | |||||||
| chr17:51042002 | T | G | 1 | a0002c0004t0015g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.591-351A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042002 | |||||||
| chr17:51042056 | G | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.591-405C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042056 | |||||||
| chr17:51042092 | T | A | 9 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.591-441A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042092 | |||||||
| chr17:51042265 | T | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.591-614A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042265 | |||||||
| chr17:51042311 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-660A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042311 | |||||||
| chr17:51042587 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.591-936C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042587 | |||||||
| chr17:51042588 | C | T | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.591-937G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042588 | |||||||
| chr17:51042701 | A | G | 2 | a0001c0001t0012g0025 a0001c0001t0012g0032 |
2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.591-1050T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042701 | |||||||
| chr17:51042758 | G | A | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.591-1107C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042758 | |||||||
| chr17:51042804 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.591-1153A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042804 | |||||||
| chr17:51042940 | A | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.591-1289T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042940 | |||||||
| chr17:51042989 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0025g0156 |
2 | HG03017.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.591-1338G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51042989 | |||||||
| chr17:51043040 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.591-1389G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043040 | |||||||
| chr17:51043126 | A | G | 242 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(239): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.591-1475T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043126 | |||||||
| chr17:51043471 | C | T | 1 | a0001c0001t0002g0013 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.591-1820G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043471 | |||||||
| chr17:51043630 | G | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.591-1979C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043630 | |||||||
| chr17:51043769 | T | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0047 a0001c0001t0003g0049 |
3 | NA18994.hp1 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.591-2118A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043769 | |||||||
| chr17:51043818 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.591-2167C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51043818 | |||||||
| chr17:51044187 | C | T | 2 | a0001c0002t0001g0282 a0001c0002t0004g0291 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.591-2536G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044187 | |||||||
| chr17:51044255 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.591-2604T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044255 | |||||||
| chr17:51044317 | A | C | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.591-2666T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044317 | |||||||
| chr17:51044341 | A | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.591-2690T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044341 | |||||||
| chr17:51044463 | T | C | 25 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(22): Show |
25 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.591-2812A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044463 | |||||||
| chr17:51044469 | T | C | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.591-2818A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044469 | |||||||
| chr17:51044817 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.590+2558G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044817 | |||||||
| chr17:51044849 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.590+2526G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044849 | |||||||
| chr17:51044859 | G | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.590+2516C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044859 | |||||||
| chr17:51044971 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.590+2404A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51044971 | |||||||
| chr17:51045074 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.590+2301C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045074 | |||||||
| chr17:51045139 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.590+2236C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045139 | |||||||
| chr17:51045257 | A | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590+2118T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045257 | |||||||
| chr17:51045307 | G | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.590+2068C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045307 | |||||||
| chr17:51045432 | A | G | 3 | a0001c0005t0001g0238 a0001c0005t0001g0244 a0001c0005t0001g0252 |
3 | HG01928.hp2 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.590+1943T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045432 | |||||||
| chr17:51045527 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.590+1848G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045527 | |||||||
| chr17:51045674 | A | G | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.590+1701T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045674 | |||||||
| chr17:51045698 | C | T | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590+1677G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045698 | |||||||
| chr17:51045837 | A | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.590+1538T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045837 | |||||||
| chr17:51045874 | C | T | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.590+1501G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51045874 | |||||||
| chr17:51046030 | C | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.590+1345G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046030 | |||||||
| chr17:51046123 | G | T | 7 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0143 others(4): Show |
7 | HG02280.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.590+1252C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046123 | |||||||
| chr17:51046201 | G | A | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.590+1174C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046201 | |||||||
| chr17:51046283 | T | C | 6 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(3): Show |
6 | HG00639.hp2 HG01928.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.590+1092A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046283 | |||||||
| chr17:51046370 | C | A | 1 | a0001c0001t0002g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.590+1005G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046370 | |||||||
| chr17:51046524 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.590+851C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046524 | |||||||
| chr17:51046526 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0264 |
3 | HG01168.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.590+849G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51046526 | |||||||
| chr17:51047112 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.590+263G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51047112 | |||||||
| chr17:51047250 | A | T | 1 | a0003c0009t0002g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.590+125T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 4/29 | chr17 | 51047250 | |||||||
| chr17:51047484 | G | GA | 195 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(192): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.496-16dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047484 | |||||||
| chr17:51047583 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.496-114G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047583 | |||||||
| chr17:51047665 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.496-196C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047665 | |||||||
| chr17:51047702 | C | CA | 85 | a0001c0001t0001g0028 a0001c0001t0001g0062 a0001c0001t0001g0130 others(82): Show |
85 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.496-234dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047702 | |||||||
| chr17:51047702 | CA | C | 7 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0089 others(4): Show |
7 | HG01070.hp2 HG01099.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.496-234delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047702 | |||||||
| chr17:51047719 | C | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.496-250G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047719 | |||||||
| chr17:51047732 | C | A | 4 | a0002c0004t0005g0003 a0002c0004t0005g0004 a0002c0004t0005g0005 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-263G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047732 | |||||||
| chr17:51047898 | A | C | 1 | a0001c0002t0001g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.496-429T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51047898 | |||||||
| chr17:51048172 | A | T | 156 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(153): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.496-703T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51048172 | |||||||
| chr17:51048327 | A | G | 1 | a0001c0002t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496-858T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51048327 | |||||||
| chr17:51048586 | G | A | 1 | a0001c0001t0002g0013 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.496-1117C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51048586 | |||||||
| chr17:51048743 | C | G | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-1274G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51048743 | |||||||
| chr17:51048877 | A | T | 2 | a0001c0001t0001g0130 a0001c0001t0002g0071 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.496-1408T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51048877 | |||||||
| chr17:51049236 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.496-1767T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049236 | |||||||
| chr17:51049239 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.496-1770G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049239 | |||||||
| chr17:51049308 | T | A | 173 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(170): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.496-1839A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049308 | |||||||
| chr17:51049325 | C | T | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-1856G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049325 | |||||||
| chr17:51049502 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.496-2033G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049502 | |||||||
| chr17:51049583 | G | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-2114C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049583 | |||||||
| chr17:51049617 | T | C | 1 | a0001c0001t0003g0046 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.496-2148A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049617 | |||||||
| chr17:51049629 | T | C | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.496-2160A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049629 | |||||||
| chr17:51049667 | G | A | 5 | a0001c0002t0001g0270 a0001c0002t0001g0278 a0001c0002t0001g0279 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-2198C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049667 | |||||||
| chr17:51049709 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.496-2240C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049709 | |||||||
| chr17:51049852 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-2383G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049852 | |||||||
| chr17:51049909 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.496-2440A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51049909 | |||||||
| chr17:51050022 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-2553A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050022 | |||||||
| chr17:51050028 | T | C | 48 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(45): Show |
48 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.496-2559A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050028 | |||||||
| chr17:51050663 | G | T | 16 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(13): Show |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.496-3194C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050663 | |||||||
| chr17:51050697 | T | C | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.496-3228A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050697 | |||||||
| chr17:51050837 | T | C | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.496-3368A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050837 | |||||||
| chr17:51050994 | GGAAA | G | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-3529_496-3526d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51050994 | |||||||
| chr17:51051033 | T | TA | 110 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(107): Show |
110 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.496-3565dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51051033 | |||||||
| chr17:51051033 | T | TAA | 19 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0179 others(16): Show |
19 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.496-3566_496-3565d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51051033 | |||||||
| chr17:51051061 | AAGGG | A | 23 | a0001c0001t0001g0055 a0002c0003t0005g0094 a0002c0003t0007g0077 others(20): Show |
23 | HG01168.hp2 HG01243.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.496-3596_496-3593d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51051061 | |||||||
| chr17:51051403 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.496-3934G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51051403 | |||||||
| chr17:51051706 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.496-4237G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51051706 | |||||||
| chr17:51052230 | G | C | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.495+4182C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052230 | |||||||
| chr17:51052232 | C | T | 2 | a0001c0001t0001g0172 a0003c0009t0002g0095 |
2 | HG00558.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.495+4180G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052232 | |||||||
| chr17:51052282 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.495+4130G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052282 | |||||||
| chr17:51052514 | G | A | 2 | a0001c0001t0013g0180 a0001c0001t0013g0183 |
2 | HG01109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.495+3898C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052514 | |||||||
| chr17:51052516 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01891.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.495+3896G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052516 | |||||||
| chr17:51052636 | C | CA | 21 | a0001c0002t0001g0281 a0002c0003t0005g0094 a0002c0003t0007g0077 others(18): Show |
21 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+3775dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052636 | |||||||
| chr17:51052810 | G | C | 16 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+3602C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51052810 | |||||||
| chr17:51053107 | A | C | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+3305T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053107 | |||||||
| chr17:51053225 | T | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+3187A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053225 | |||||||
| chr17:51053419 | G | A | 1 | a0002c0004t0005g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.495+2993C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053419 | |||||||
| chr17:51053447 | T | C | 2 | a0001c0002t0001g0281 a0001c0002t0001g0289 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.495+2965A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053447 | |||||||
| chr17:51053510 | C | A | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495+2902G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053510 | |||||||
| chr17:51053616 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495+2796G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053616 | |||||||
| chr17:51053622 | T | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.495+2790A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053622 | |||||||
| chr17:51053627 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.495+2785C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053627 | |||||||
| chr17:51053690 | A | C | 72 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0075 others(69): Show |
72 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.495+2722T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053690 | |||||||
| chr17:51053792 | T | A | 1 | a0001c0001t0002g0167 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.495+2620A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053792 | |||||||
| chr17:51053823 | G | C | 5 | a0001c0001t0001g0035 a0001c0001t0003g0022 a0001c0001t0003g0026 others(2): Show |
5 | NA18948.hp1 NA18952.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+2589C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053823 | |||||||
| chr17:51053843 | AAAAAAAA others(28): Show |
A | 5 | a0002c0004t0005g0004 a0002c0004t0005g0005 a0002c0004t0005g0006 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+2534_495+2568d others(37): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053843 | |||||||
| chr17:51053845 | AAAAAAAA others(28): Show |
A | 9 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0114 others(6): Show |
9 | HG01168.hp2 HG02055.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+2532_495+2566d others(37): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053845 | |||||||
| chr17:51053846 | AAAAAAAA others(25): Show |
A | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.495+2534_495+2565d others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053846 | |||||||
| chr17:51053847 | AAAAAAAA others(28): Show |
A | 4 | a0002c0003t0007g0096 a0002c0003t0007g0102 a0002c0003t0007g0129 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+2530_495+2564d others(37): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053847 | |||||||
| chr17:51053848 | AAAAAAAG others(25): Show |
A | 1 | a0002c0003t0011g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.495+2532_495+2563d others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053848 | |||||||
| chr17:51053849 | AAAAAAGT | A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+2556_495+2562d others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053849 | |||||||
| chr17:51053850 | AAAAAGTA others(5): Show |
A | 2 | a0002c0003t0008g0173 a0002c0003t0008g0260 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+2550_495+2561d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053850 | |||||||
| chr17:51053850 | AAAAAGTA others(11): Show |
A | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.495+2544_495+2561d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053850 | |||||||
| chr17:51053851 | A | T | 2 | a0001c0001t0002g0253 a0001c0001t0003g0268 |
2 | NA18959.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.495+2561T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053851 | |||||||
| chr17:51053852 | AAAGTATA others(7): Show |
A | 1 | a0002c0003t0008g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.495+2546_495+2559d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053852 | |||||||
| chr17:51053853 | A | T | 3 | a0001c0001t0001g0251 a0001c0001t0002g0204 a0001c0001t0003g0268 |
3 | NA18973.hp2 NA18999.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.495+2559T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGT | A | 22 | a0001c0001t0001g0208 a0001c0001t0001g0221 a0001c0001t0001g0225 others(19): Show |
22 | HG00558.hp1 HG00621.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.495+2556_495+2558d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTAT | A | 10 | a0001c0001t0001g0177 a0001c0001t0001g0215 a0001c0001t0001g0233 others(7): Show |
10 | HG00738.hp2 HG01934.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.495+2554_495+2558d others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTATAT | A | 6 | a0001c0005t0001g0211 a0001c0005t0001g0212 a0001c0005t0001g0238 others(3): Show |
6 | HG00639.hp2 HG01928.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+2552_495+2558d others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTATAT others(4): Show |
A | 2 | a0001c0001t0001g0059 a0001c0001t0006g0131 |
2 | HG02717.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.495+2548_495+2558d others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTATAT others(6): Show |
A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.495+2546_495+2558d others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTATAT others(8): Show |
A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0229 a0001c0002t0001g0277 |
3 | HG01891.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.495+2544_495+2558d others(17): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053853 | AAGTATAT others(22): Show |
A | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.495+2530_495+2558d others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053853 | |||||||
| chr17:51053854 | A | AAGTAT | 7 | a0001c0001t0001g0075 a0001c0001t0004g0181 a0001c0001t0004g0182 others(4): Show |
7 | HG01081.hp1 HG01099.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+2557_495+2558i others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | AAGTATAT others(4): Show |
3 | a0001c0001t0004g0187 a0001c0001t0004g0190 a0001c0001t0004g0202 |
3 | HG01070.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.495+2557_495+2558i others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | AAGTATAT others(6): Show |
2 | a0001c0001t0001g0151 a0001c0001t0013g0183 |
2 | HG02148.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.495+2557_495+2558i others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | AAGTATAT others(8): Show |
1 | a0001c0001t0001g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.495+2557_495+2558i others(17): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | AAGTATAT others(16): Show |
1 | a0001c0001t0009g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.495+2557_495+2558i others(25): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.495+2557_495+2558i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | A | T | 8 | a0001c0001t0001g0210 a0001c0001t0001g0226 a0001c0001t0001g0228 others(5): Show |
8 | HG02886.hp2 NA18944.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+2558T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | AG | A | 10 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0001g0230 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+2557delC | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053854 | AGTATATA others(7): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.495+2544_495+2557d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053854 | |||||||
| chr17:51053855 | G | A | 41 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(38): Show |
41 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.495+2557C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTA | 17 | a0001c0001t0001g0028 a0001c0001t0001g0085 a0001c0001t0002g0071 others(14): Show |
17 | HG00544.hp2 HG01433.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.495+2555_495+2556d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATA | 17 | a0001c0001t0002g0100 a0001c0001t0002g0111 a0001c0001t0002g0122 others(14): Show |
17 | HG00558.hp2 HG00621.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.495+2553_495+2556d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATA | 9 | a0001c0001t0001g0091 a0001c0001t0002g0088 a0001c0001t0002g0167 others(6): Show |
9 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+2551_495+2556d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(1): Show |
17 | a0001c0001t0002g0033 a0001c0001t0002g0081 a0001c0001t0002g0092 others(14): Show |
17 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.495+2549_495+2556d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(3): Show |
8 | a0001c0001t0001g0035 a0001c0001t0002g0093 a0001c0001t0002g0161 others(5): Show |
8 | HG00323.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+2547_495+2556d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0172 a0001c0001t0002g0073 a0001c0001t0002g0120 others(2): Show |
5 | HG00544.hp1 HG02735.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2545_495+2556d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(7): Show |
2 | a0001c0001t0002g0079 a0001c0001t0003g0015 |
2 | HG03831.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.495+2543_495+2556d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(9): Show |
2 | a0001c0001t0002g0014 a0001c0001t0002g0148 |
2 | NA18977.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.495+2541_495+2556d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0158 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.495+2539_495+2556d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTATATAT others(13): Show |
1 | a0001c0001t0003g0163 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.495+2537_495+2556d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0003g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.495+2556_495+2557i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTA | G | 8 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0002g0089 others(5): Show |
8 | HG00140.hp1 HG01099.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+2555_495+2556d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATA | G | 10 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0002g0072 others(7): Show |
10 | HG01070.hp2 HG01192.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+2551_495+2556d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0128 a0001c0001t0008g0119 |
3 | HG01934.hp2 HG02135.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.495+2549_495+2556d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0002g0029 a0001c0001t0002g0144 a0001c0001t0003g0020 |
3 | HG02615.hp2 HG02630.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.495+2547_495+2556d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(5): Show |
G | 5 | a0001c0001t0002g0083 a0001c0001t0002g0175 a0001c0001t0006g0107 others(2): Show |
5 | HG02683.hp2 HG03654.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+2545_495+2556d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(9): Show |
G | 2 | a0001c0001t0002g0017 a0001c0001t0002g0133 |
2 | HG02735.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.495+2541_495+2556d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(11): Show |
G | 2 | a0001c0001t0002g0074 a0001c0001t0002g0157 |
2 | NA19011.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.495+2539_495+2556d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.495+2537_495+2556d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.495+2533_495+2556d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053855 | GTATATAT others(23): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.495+2527_495+2556d others(32): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053855 | |||||||
| chr17:51053856 | T | A | 4 | a0001c0001t0001g0227 a0001c0001t0022g0070 a0001c0002t0001g0275 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2556A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053856 | |||||||
| chr17:51053857 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.495+2554_495+2555i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053857 | |||||||
| chr17:51053857 | A | G | 4 | a0001c0001t0002g0135 a0001c0001t0022g0070 a0001c0002t0001g0275 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2555T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053857 | |||||||
| chr17:51053858 | T | A | 14 | a0001c0001t0001g0208 a0001c0001t0001g0225 a0001c0001t0001g0242 others(11): Show |
14 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+2554A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053858 | |||||||
| chr17:51053859 | A | G | 9 | a0001c0002t0001g0270 a0001c0002t0001g0278 a0001c0002t0001g0279 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+2553T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053859 | |||||||
| chr17:51053860 | T | A | 10 | a0001c0001t0001g0177 a0001c0001t0001g0208 a0001c0001t0001g0215 others(7): Show |
10 | HG00738.hp2 HG02486.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.495+2552A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053860 | |||||||
| chr17:51053861 | A | G | 5 | a0001c0001t0001g0177 a0001c0002t0001g0271 a0001c0002t0001g0282 others(2): Show |
5 | HG02486.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2551T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053861 | |||||||
| chr17:51053862 | T | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0257 a0001c0001t0001g0266 others(2): Show |
5 | HG01928.hp2 HG04184.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2550A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053862 | |||||||
| chr17:51053864 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.495+2548A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053864 | |||||||
| chr17:51053866 | T | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0266 a0001c0001t0006g0131 |
3 | HG02717.hp2 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.495+2546A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053866 | |||||||
| chr17:51053867 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0006g0131 |
2 | HG02717.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.495+2545T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053867 | |||||||
| chr17:51053868 | T | A | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+2544A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053868 | |||||||
| chr17:51053869 | A | G | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+2543T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053869 | |||||||
| chr17:51053870 | T | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0155 a0001c0002t0001g0277 |
3 | HG01891.hp2 HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.495+2542A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053870 | |||||||
| chr17:51053871 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0155 a0001c0002t0001g0277 |
3 | HG01891.hp2 HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.495+2541T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053871 | |||||||
| chr17:51053886 | T | G | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495+2526A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053886 | |||||||
| chr17:51053898 | T | A | 5 | a0001c0001t0001g0177 a0001c0001t0002g0076 a0001c0001t0003g0020 others(2): Show |
5 | HG02615.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2514A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053898 | |||||||
| chr17:51053899 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0049 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.495+2512_495+2513i others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053899 | |||||||
| chr17:51053899 | A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.495+2512_495+2513i others(35): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51053899 | |||||||
| chr17:51054100 | C | A | 1 | a0001c0001t0012g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.495+2312G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054100 | |||||||
| chr17:51054116 | C | CT | 96 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(93): Show |
96 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.495+2295dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054116 | |||||||
| chr17:51054116 | C | CTT | 14 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0001g0247 others(11): Show |
14 | HG01243.hp1 HG02135.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.495+2294_495+2295d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054116 | |||||||
| chr17:51054116 | CT | C | 64 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0064 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.495+2295delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054116 | |||||||
| chr17:51054140 | G | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.495+2272C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054140 | |||||||
| chr17:51054162 | G | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+2250C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054162 | |||||||
| chr17:51054204 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0056 |
3 | NA18982.hp2 NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.495+2208G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054204 | |||||||
| chr17:51054311 | C | T | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2101G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054311 | |||||||
| chr17:51054442 | C | CT | 26 | a0001c0001t0001g0242 a0001c0001t0001g0249 a0001c0001t0001g0265 others(23): Show |
26 | HG00621.hp1 HG01168.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.495+1969dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054442 | |||||||
| chr17:51054460 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.495+1952C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054460 | |||||||
| chr17:51054513 | T | C | 1 | a0006c0011t0003g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.495+1899A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054513 | |||||||
| chr17:51054544 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.495+1868G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054544 | |||||||
| chr17:51054571 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.495+1841C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054571 | |||||||
| chr17:51054638 | G | A | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.495+1774C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054638 | |||||||
| chr17:51054718 | G | A | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.495+1694C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054718 | |||||||
| chr17:51054962 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.495+1450A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054962 | |||||||
| chr17:51054974 | T | C | 16 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(13): Show |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1438A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51054974 | |||||||
| chr17:51055049 | A | C | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.495+1363T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055049 | |||||||
| chr17:51055145 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.495+1267G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055145 | |||||||
| chr17:51055353 | T | TCA | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.495+1057_495+1058d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055353 | |||||||
| chr17:51055423 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.495+989C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055423 | |||||||
| chr17:51055524 | C | T | 5 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+888G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055524 | |||||||
| chr17:51055592 | G | GA | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.495+819dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055592 | |||||||
| chr17:51055633 | T | C | 48 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(45): Show |
48 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.495+779A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055633 | |||||||
| chr17:51055745 | A | C | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.495+667T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055745 | |||||||
| chr17:51055818 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.495+594C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055818 | |||||||
| chr17:51055822 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.495+590C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055822 | |||||||
| chr17:51055980 | A | G | 1 | a0001c0002t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+432T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51055980 | |||||||
| chr17:51056038 | A | G | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.495+374T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51056038 | |||||||
| chr17:51056367 | C | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+45G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 3/29 | chr17 | 51056367 | |||||||
| chr17:51056657 | T | A | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.425-175A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51056657 | |||||||
| chr17:51056721 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-239G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51056721 | |||||||
| chr17:51056816 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0027g0098 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.425-334T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51056816 | |||||||
| chr17:51056980 | G | C | 2 | a0001c0001t0002g0029 a0001c0001t0003g0018 |
2 | HG04228.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.425-498C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51056980 | |||||||
| chr17:51057085 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.425-603A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057085 | |||||||
| chr17:51057240 | G | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.425-758C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057240 | |||||||
| chr17:51057255 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.425-773C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057255 | |||||||
| chr17:51057279 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.425-797G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057279 | |||||||
| chr17:51057290 | C | T | 2 | a0002c0004t0005g0006 a0002c0004t0005g0007 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.425-808G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057290 | |||||||
| chr17:51057868 | A | C | 1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.425-1386T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51057868 | |||||||
| chr17:51058020 | G | T | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.425-1538C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058020 | |||||||
| chr17:51058047 | C | G | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0170 |
3 | HG02451.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.425-1565G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058047 | |||||||
| chr17:51058132 | G | C | 25 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0001g0158 others(22): Show |
25 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.425-1650C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058132 | |||||||
| chr17:51058442 | T | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.425-1960A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058442 | |||||||
| chr17:51058493 | G | T | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.425-2011C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058493 | |||||||
| chr17:51058557 | G | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2075C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058557 | |||||||
| chr17:51058800 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0002g0217 |
2 | HG02071.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.425-2318C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51058800 | |||||||
| chr17:51059112 | T | C | 1 | a0002c0004t0007g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.425-2630A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059112 | |||||||
| chr17:51059277 | G | A | 156 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(153): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.425-2795C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059277 | |||||||
| chr17:51059547 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.425-3065A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059547 | |||||||
| chr17:51059654 | A | G | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.425-3172T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059654 | |||||||
| chr17:51059725 | C | T | 25 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.425-3243G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059725 | |||||||
| chr17:51059771 | A | AAAAC | 10 | a0001c0001t0001g0035 a0001c0001t0003g0022 a0001c0001t0003g0026 others(7): Show |
10 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-3293_425-3290d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059771 | |||||||
| chr17:51059771 | AAAAC | A | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.425-3293_425-3290d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51059771 | |||||||
| chr17:51060146 | C | G | 2 | a0002c0004t0005g0004 a0002c0004t0005g0010 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.425-3664G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060146 | |||||||
| chr17:51060196 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.425-3714C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060196 | |||||||
| chr17:51060210 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.425-3728C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060210 | |||||||
| chr17:51060227 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.425-3745C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060227 | |||||||
| chr17:51060301 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.425-3819C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060301 | |||||||
| chr17:51060380 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-3898C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060380 | |||||||
| chr17:51060410 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-3928C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060410 | |||||||
| chr17:51060418 | G | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.425-3936C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060418 | |||||||
| chr17:51060500 | CT | C | 15 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0179 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.425-4019delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060500 | |||||||
| chr17:51060505 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.425-4023A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060505 | |||||||
| chr17:51060505 | T | TA | 6 | a0001c0001t0001g0127 a0001c0001t0001g0266 a0001c0005t0001g0211 others(3): Show |
6 | HG00639.hp2 HG01516.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-4024dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060505 | |||||||
| chr17:51060505 | TA | T | 116 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0052 others(113): Show |
116 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.425-4024delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060505 | |||||||
| chr17:51060505 | TAA | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-4025_425-4024d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060505 | |||||||
| chr17:51060506 | A | T | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.425-4024T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060506 | |||||||
| chr17:51060838 | G | GT | 11 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0150 others(8): Show |
11 | HG01175.hp1 HG01192.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-4357dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060838 | |||||||
| chr17:51060847 | G | GT | 25 | a0001c0001t0001g0054 a0001c0001t0001g0126 a0001c0001t0001g0176 others(22): Show |
25 | HG01168.hp2 HG01243.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.425-4366dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060847 | |||||||
| chr17:51060847 | G | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-4365C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060847 | |||||||
| chr17:51060862 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0239 a0001c0001t0001g0245 others(1): Show |
4 | HG01074.hp1 HG01243.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-4380G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51060862 | |||||||
| chr17:51061080 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-4598A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061080 | |||||||
| chr17:51061098 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.425-4616C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061098 | |||||||
| chr17:51061340 | C | T | 55 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0178 others(52): Show |
55 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.425-4858G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061340 | |||||||
| chr17:51061612 | C | CA | 66 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0091 others(63): Show |
66 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.425-5131dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CAA | 34 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(31): Show |
34 | HG00280.hp1 HG01167.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.425-5132_425-5131d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CAAA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0002g0138 others(5): Show |
8 | HG02630.hp1 HG02647.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-5133_425-5131d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CAAAA | 10 | a0001c0001t0002g0145 a0002c0003t0007g0077 a0002c0003t0007g0096 others(7): Show |
10 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-5134_425-5131d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CAAAAAAA others(5): Show |
2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.425-5142_425-5131d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CCAA | 38 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(35): Show |
38 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.425-5131_425-5130i others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CCAAA | 22 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0222 others(19): Show |
22 | HG00558.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.425-5131_425-5130i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061612 | C | CCAAAA | 3 | a0001c0001t0001g0218 a0001c0001t0001g0256 a0001c0001t0001g0264 |
3 | HG01175.hp2 HG01256.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.425-5131_425-5130i others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061612 | |||||||
| chr17:51061669 | T | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.425-5187A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061669 | |||||||
| chr17:51061674 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0264 |
3 | HG01168.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.425-5192A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061674 | |||||||
| chr17:51061716 | CCATTGTT | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-5241_425-5235d others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51061716 | |||||||
| chr17:51062008 | T | A | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-5526A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062008 | |||||||
| chr17:51062088 | G | A | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.425-5606C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062088 | |||||||
| chr17:51062299 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.425-5817T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062299 | |||||||
| chr17:51062477 | G | A | 1 | a0001c0001t0004g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-5995C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062477 | |||||||
| chr17:51062499 | C | G | 6 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-6017G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062499 | |||||||
| chr17:51062543 | G | T | 1 | a0001c0002t0001g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-6061C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062543 | |||||||
| chr17:51062595 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.425-6113A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062595 | |||||||
| chr17:51062764 | T | C | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.425-6282A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062764 | |||||||
| chr17:51062771 | G | A | 1 | a0001c0002t0001g0279 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.425-6289C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062771 | |||||||
| chr17:51062888 | C | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-6406G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51062888 | |||||||
| chr17:51063035 | T | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.425-6553A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063035 | |||||||
| chr17:51063118 | T | C | 5 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-6636A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063118 | |||||||
| chr17:51063272 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.425-6790G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063272 | |||||||
| chr17:51063302 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.425-6820G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063302 | |||||||
| chr17:51063375 | G | A | 1 | a0002c0003t0011g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.425-6893C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063375 | |||||||
| chr17:51063398 | C | T | 1 | a0001c0005t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.425-6916G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063398 | |||||||
| chr17:51063411 | C | CA | 12 | a0001c0001t0001g0264 a0001c0001t0002g0141 a0001c0001t0003g0037 others(9): Show |
12 | HG01175.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-6930dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063411 | |||||||
| chr17:51063411 | C | CAA | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-6931_425-6930d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063411 | |||||||
| chr17:51063411 | CA | C | 31 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0194 others(28): Show |
31 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-6930delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063411 | |||||||
| chr17:51063741 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.425-7259C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063741 | |||||||
| chr17:51063898 | ATAAG | A | 8 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
8 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-7420_425-7417d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063898 | |||||||
| chr17:51063902 | G | A | 41 | a0001c0001t0004g0187 a0001c0001t0004g0190 a0001c0002t0001g0270 others(38): Show |
41 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.425-7420C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51063902 | |||||||
| chr17:51064037 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.425-7555A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064037 | |||||||
| chr17:51064072 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.425-7590C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064072 | |||||||
| chr17:51064432 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0002g0166 |
2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.425-7950C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064432 | |||||||
| chr17:51064641 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.425-8159G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064641 | |||||||
| chr17:51064750 | A | G | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.425-8268T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064750 | |||||||
| chr17:51064762 | A | G | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0243 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-8280T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064762 | |||||||
| chr17:51064844 | G | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-8362C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51064844 | |||||||
| chr17:51065078 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.425-8596C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065078 | |||||||
| chr17:51065341 | A | G | 2 | a0002c0003t0008g0173 a0002c0003t0008g0287 |
2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.425-8859T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065341 | |||||||
| chr17:51065415 | G | A | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.425-8933C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065415 | |||||||
| chr17:51065474 | T | G | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.425-8992A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065474 | |||||||
| chr17:51065593 | C | A | 1 | a0001c0001t0004g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.425-9111G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065593 | |||||||
| chr17:51065618 | C | T | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-9136G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51065618 | |||||||
| chr17:51066018 | T | C | 1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.425-9536A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066018 | |||||||
| chr17:51066107 | C | T | 135 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.425-9625G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066107 | |||||||
| chr17:51066109 | CTTT | C | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.425-9630_425-9628d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066109 | |||||||
| chr17:51066261 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.425-9779G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066261 | |||||||
| chr17:51066294 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.425-9812T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066294 | |||||||
| chr17:51066417 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0002g0166 |
2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.425-9935T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066417 | |||||||
| chr17:51066558 | A | AAAAAAAA others(3): Show |
1 | a0002c0003t0008g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.425-10077_425-1007 others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066558 | |||||||
| chr17:51066567 | G | A | 6 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(3): Show |
6 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-10085C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066567 | |||||||
| chr17:51066567 | G | GAAAAAA | 36 | a0001c0001t0002g0073 a0001c0001t0003g0018 a0001c0001t0003g0201 others(33): Show |
36 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.425-10091_425-1008 others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066567 | |||||||
| chr17:51066567 | G | GAAAAAAA | 73 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(70): Show |
73 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.425-10092_425-1008 others(11): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066567 | |||||||
| chr17:51066567 | G | GAAAAAAA others(1): Show |
73 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(70): Show |
73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.425-10093_425-1008 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066567 | |||||||
| chr17:51066567 | G | GAAAAAAA others(2): Show |
8 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0209 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-10094_425-1008 others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066567 | |||||||
| chr17:51066613 | T | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-10131A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066613 | |||||||
| chr17:51066742 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.425-10260T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066742 | |||||||
| chr17:51066890 | C | CA | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-10409dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51066890 | |||||||
| chr17:51067217 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.425-10735A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51067217 | |||||||
| chr17:51067622 | C | A | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-11140G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51067622 | |||||||
| chr17:51068016 | C | T | 2 | a0002c0004t0005g0003 a0002c0004t0005g0005 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.425-11534G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51068016 | |||||||
| chr17:51068313 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.424+11271T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51068313 | |||||||
| chr17:51068382 | T | C | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.424+11202A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51068382 | |||||||
| chr17:51068507 | G | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+11077C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51068507 | |||||||
| chr17:51069224 | T | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0041 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.424+10360A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51069224 | |||||||
| chr17:51069239 | T | C | 1 | a0001c0005t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.424+10345A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51069239 | |||||||
| chr17:51069711 | A | G | 2 | a0001c0001t0002g0115 a0001c0001t0002g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424+9873T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51069711 | |||||||
| chr17:51069872 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0231 a0001c0001t0001g0237 |
3 | HG00741.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.424+9712C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51069872 | |||||||
| chr17:51069987 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.424+9597T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51069987 | |||||||
| chr17:51070049 | A | T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+9535T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070049 | |||||||
| chr17:51070071 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+9513A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070071 | |||||||
| chr17:51070072 | T | A | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+9512A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070072 | |||||||
| chr17:51070072 | T | TA | 69 | a0001c0001t0001g0130 a0001c0001t0001g0203 a0001c0001t0001g0205 others(66): Show |
69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.424+9511dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070072 | |||||||
| chr17:51070084 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.424+9500G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070084 | |||||||
| chr17:51070162 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424+9422T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070162 | |||||||
| chr17:51070325 | C | G | 67 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.424+9259G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070325 | |||||||
| chr17:51070391 | T | C | 2 | a0002c0004t0005g0006 a0002c0004t0005g0007 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.424+9193A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070391 | |||||||
| chr17:51070513 | A | G | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+9071T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070513 | |||||||
| chr17:51070801 | C | T | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.424+8783G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070801 | |||||||
| chr17:51070839 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.424+8745A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070839 | |||||||
| chr17:51070992 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+8592G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51070992 | |||||||
| chr17:51071276 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+8308A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071276 | |||||||
| chr17:51071299 | C | T | 3 | a0001c0001t0026g0147 a0002c0003t0011g0195 a0002c0003t0011g0196 |
3 | HG02258.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.424+8285G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071299 | |||||||
| chr17:51071378 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.424+8206T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071378 | |||||||
| chr17:51071446 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+8138G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071446 | |||||||
| chr17:51071609 | A | G | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7975T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071609 | |||||||
| chr17:51071663 | A | G | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.424+7921T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071663 | |||||||
| chr17:51071842 | T | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.424+7742A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071842 | |||||||
| chr17:51071906 | GA | G | 67 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.424+7677delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51071906 | |||||||
| chr17:51072112 | C | T | 16 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(13): Show |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+7472G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072112 | |||||||
| chr17:51072205 | GGGATTAC others(20): Show |
G | 32 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(29): Show |
32 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+7352_424+7378d others(29): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072205 | |||||||
| chr17:51072218 | T | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0167 |
2 | HG02083.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.424+7366A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072218 | |||||||
| chr17:51072553 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.424+7031G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072553 | |||||||
| chr17:51072558 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7026G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072558 | |||||||
| chr17:51072632 | C | T | 16 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(13): Show |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6952G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072632 | |||||||
| chr17:51072671 | G | A | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6913C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072671 | |||||||
| chr17:51072699 | A | G | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424+6885T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072699 | |||||||
| chr17:51072856 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.424+6728A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51072856 | |||||||
| chr17:51073032 | A | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6552T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073032 | |||||||
| chr17:51073115 | C | G | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6469G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073115 | |||||||
| chr17:51073260 | G | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.424+6324C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073260 | |||||||
| chr17:51073383 | G | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6201C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073383 | |||||||
| chr17:51073597 | A | T | 1 | a0001c0001t0002g0017 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.424+5987T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073597 | |||||||
| chr17:51073635 | G | A | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.424+5949C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073635 | |||||||
| chr17:51073792 | G | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5792C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073792 | |||||||
| chr17:51073869 | G | T | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424+5715C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51073869 | |||||||
| chr17:51074015 | T | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424+5569A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074015 | |||||||
| chr17:51074033 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.424+5551C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074033 | |||||||
| chr17:51074052 | C | T | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5532G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074052 | |||||||
| chr17:51074064 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5520C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074064 | |||||||
| chr17:51074122 | G | A | 15 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0179 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5462C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074122 | |||||||
| chr17:51074128 | C | T | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424+5456G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074128 | |||||||
| chr17:51074129 | G | A | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5455C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074129 | |||||||
| chr17:51074312 | C | G | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.424+5272G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074312 | |||||||
| chr17:51074393 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5191C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074393 | |||||||
| chr17:51074476 | C | T | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424+5108G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074476 | |||||||
| chr17:51074518 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+5066A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074518 | |||||||
| chr17:51074546 | A | C | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5038T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074546 | |||||||
| chr17:51074786 | C | T | 3 | a0002c0003t0007g0096 a0002c0003t0007g0102 a0002c0003t0007g0129 |
3 | HG03041.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.424+4798G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074786 | |||||||
| chr17:51074983 | G | T | 4 | a0002c0004t0005g0003 a0002c0004t0005g0004 a0002c0004t0005g0005 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+4601C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51074983 | |||||||
| chr17:51075024 | C | T | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+4560G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075024 | |||||||
| chr17:51075111 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.424+4473C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075111 | |||||||
| chr17:51075195 | C | CA | 79 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0001g0203 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+4388dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | C | CAA | 9 | a0001c0001t0001g0177 a0001c0001t0001g0240 a0001c0001t0001g0247 others(6): Show |
9 | HG00639.hp2 HG01109.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+4387_424+4388d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | C | CAAAAAAA others(3): Show |
1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.424+4379_424+4388d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | C | CAAAAAAA others(15): Show |
1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424+4367_424+4388d others(24): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | CA | C | 24 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0068 others(21): Show |
24 | HG01070.hp2 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+4388delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | CAAA | C | 10 | a0002c0003t0011g0195 a0002c0004t0005g0001 a0002c0004t0005g0003 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4386_424+4388d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | CAAAAAAA | C | 16 | a0001c0001t0002g0014 a0001c0001t0002g0029 a0001c0001t0002g0073 others(13): Show |
16 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+4382_424+4388d others(9): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075195 | CAAAAAAA others(5): Show |
C | 1 | a0001c0005t0001g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.424+4377_424+4388d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075195 | |||||||
| chr17:51075222 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4362C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075222 | |||||||
| chr17:51075239 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.424+4345C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075239 | |||||||
| chr17:51075944 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.424+3640T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075944 | |||||||
| chr17:51075958 | G | A | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+3626C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075958 | |||||||
| chr17:51075966 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+3618C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51075966 | |||||||
| chr17:51076168 | T | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+3416A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076168 | |||||||
| chr17:51076286 | G | C | 1 | a0001c0001t0002g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.424+3298C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076286 | |||||||
| chr17:51076412 | G | C | 2 | a0001c0005t0001g0267 a0001c0005t0004g0246 |
2 | HG00558.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.424+3172C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076412 | |||||||
| chr17:51076533 | C | T | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+3051G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076533 | |||||||
| chr17:51076684 | C | T | 53 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(50): Show |
53 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+2900G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076684 | |||||||
| chr17:51076717 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.424+2867A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076717 | |||||||
| chr17:51076735 | TA | T | 90 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(87): Show |
90 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.424+2848delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076735 | |||||||
| chr17:51076881 | C | T | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2703G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076881 | |||||||
| chr17:51076926 | A | C | 1 | a0001c0005t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.424+2658T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076926 | |||||||
| chr17:51076938 | C | T | 2 | a0002c0003t0005g0094 a0002c0003t0007g0077 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.424+2646G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076938 | |||||||
| chr17:51076982 | T | TTATCTAG others(29): Show |
8 | a0001c0001t0001g0158 a0001c0001t0002g0079 a0001c0001t0002g0092 others(5): Show |
8 | HG00558.hp2 HG00609.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+2566_424+2601d others(38): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076982 | T | TTATCTAG others(45): Show |
1 | a0001c0001t0002g0214 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.424+2601_424+2602i others(54): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076982 | TTATCTAG others(49): Show |
T | 5 | a0001c0001t0004g0182 a0001c0001t0004g0187 a0001c0001t0004g0190 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2546_424+2601d others(58): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076982 | TTATCTAG others(57): Show |
T | 3 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 |
3 | HG00639.hp1 HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.424+2538_424+2601d others(66): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076982 | TTATCTAG others(81): Show |
T | 2 | a0001c0001t0001g0178 a0001c0001t0004g0191 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.424+2514_424+2601d others(90): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076982 | TTATCTAG others(117): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.424+2478_424+2601d others(2): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076982 | |||||||
| chr17:51076985 | TCTAGCTA others(21): Show |
T | 1 | a0001c0001t0002g0013 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.424+2571_424+2598d others(30): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076985 | |||||||
| chr17:51076985 | TCTAGCTA others(109): Show |
T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.424+2483_424+2598d others(2): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076985 | |||||||
| chr17:51076989 | G | T | 5 | a0001c0001t0001g0194 a0001c0001t0004g0185 a0001c0001t0004g0192 others(2): Show |
5 | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2595C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076989 | |||||||
| chr17:51076993 | T | TCTAGCTA others(5): Show |
1 | a0002c0004t0015g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.424+2590_424+2591i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076993 | |||||||
| chr17:51076993 | T | TCTAGCTA others(101): Show |
2 | a0001c0001t0009g0189 a0001c0001t0014g0106 |
2 | HG02273.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.424+2483_424+2590d others(110): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076993 | |||||||
| chr17:51076993 | TCTAGCTA others(9): Show |
T | 15 | a0001c0001t0004g0193 a0002c0003t0005g0094 a0002c0003t0007g0077 others(12): Show |
15 | HG01106.hp1 HG01243.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.424+2575_424+2590d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076993 | |||||||
| chr17:51076993 | TCTAGCTA others(13): Show |
T | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.424+2571_424+2590d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076993 | |||||||
| chr17:51076997 | G | GCTAGCTA others(9): Show |
4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0004t0005g0001 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2586_424+2587i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51076997 | G | GCTAGCTA others(41): Show |
1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.424+2586_424+2587i others(50): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51076997 | GCTATCTA others(17): Show |
G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+2563_424+2586d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51076997 | GCTATCTA others(25): Show |
G | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.424+2555_424+2586d others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51076997 | GCTATCTA others(37): Show |
G | 2 | a0001c0001t0004g0185 a0001c0001t0004g0192 |
2 | HG00140.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.424+2543_424+2586d others(46): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51076997 | GCTATCTA others(93): Show |
G | 2 | a0001c0001t0001g0194 a0001c0001t0004g0202 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.424+2487_424+2586d others(102): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51076997 | |||||||
| chr17:51077001 | T | G | 1 | a0001c0001t0003g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.424+2583A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(113): Show |
1 | a0001c0001t0002g0216 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.424+2582_424+2583i others(122): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(133): Show |
1 | a0001c0001t0001g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+2582_424+2583i others(142): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(65): Show |
1 | a0001c0001t0001g0261 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.424+2582_424+2583i others(74): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(101): Show |
1 | a0001c0001t0001g0265 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.424+2582_424+2583i others(110): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(65): Show |
38 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(35): Show |
38 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+2582_424+2583i others(74): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(97): Show |
5 | a0001c0001t0001g0208 a0001c0001t0001g0242 a0001c0001t0001g0251 others(2): Show |
5 | HG00621.hp1 NA18947.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2582_424+2583i others(106): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(89): Show |
1 | a0001c0001t0002g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.424+2582_424+2583i others(98): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | T | TCTAGCTA others(101): Show |
1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.424+2582_424+2583i others(110): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | TCTAGCTA others(57): Show |
T | 1 | a0001c0001t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.424+2519_424+2582d others(66): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077001 | TCTAGCTA others(77): Show |
T | 1 | a0004c0006t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.424+2499_424+2582d others(86): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077001 | |||||||
| chr17:51077005 | G | GCTATCTA others(33): Show |
12 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0240 others(9): Show |
12 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+2578_424+2579i others(42): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077005 | |||||||
| chr17:51077005 | G | T | 4 | a0001c0001t0002g0125 a0001c0001t0026g0147 a0002c0003t0008g0292 others(1): Show |
4 | HG01168.hp2 HG01884.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2579C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077005 | |||||||
| chr17:51077005 | GCTAGCTA others(17): Show |
G | 1 | a0001c0005t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.424+2555_424+2578d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077005 | |||||||
| chr17:51077005 | GCTAGCTA others(49): Show |
G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0056 |
2 | NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.424+2523_424+2578d others(58): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077005 | |||||||
| chr17:51077005 | GCTAGCTA others(105): Show |
G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2467_424+2578d others(2): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077005 | |||||||
| chr17:51077009 | G | GCTAGCTA others(45): Show |
1 | a0005c0010t0002g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424+2574_424+2575i others(54): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077009 | G | GCTAGCTA others(25): Show |
1 | a0001c0001t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424+2543_424+2574d others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077009 | G | GCTAGCTA others(45): Show |
11 | a0001c0001t0001g0113 a0001c0001t0002g0136 a0001c0001t0002g0137 others(8): Show |
11 | HG01106.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+2523_424+2574d others(54): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077009 | G | T | 64 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.424+2575C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077009 | GCTAGCTA others(17): Show |
G | 9 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0150 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+2551_424+2574d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077009 | GCTAGCTA others(57): Show |
G | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.424+2511_424+2574d others(66): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077009 | |||||||
| chr17:51077013 | G | GCTAGCTA others(29): Show |
1 | a0001c0001t0001g0172 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.424+2570_424+2571i others(38): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | G | GCTAT | 22 | a0001c0001t0001g0028 a0001c0001t0002g0029 a0001c0001t0003g0018 others(19): Show |
22 | HG00609.hp2 HG01069.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+2570_424+2571i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | G | GCTATCTA others(5): Show |
2 | a0001c0001t0001g0035 a0001c0001t0003g0026 |
2 | NA18948.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.424+2570_424+2571i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | G | GCTATCTA others(77): Show |
1 | a0001c0001t0003g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.424+2570_424+2571i others(86): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | G | T | 17 | a0001c0001t0001g0213 a0001c0001t0001g0227 a0001c0001t0001g0229 others(14): Show |
17 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+2571C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | GCTAGCTA others(9): Show |
G | 1 | a0001c0001t0002g0017 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.424+2555_424+2570d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | GCTAGCTA others(13): Show |
G | 3 | a0001c0001t0002g0134 a0001c0002t0001g0278 a0001c0002t0001g0280 |
3 | HG03516.hp1 HG03579.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.424+2551_424+2570d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077013 | GCTAGCTA others(41): Show |
G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0073 a0001c0001t0003g0015 others(1): Show |
4 | HG00544.hp1 HG03831.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2523_424+2570d others(50): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077013 | |||||||
| chr17:51077017 | G | T | 62 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(59): Show |
62 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.424+2567C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077017 | |||||||
| chr17:51077017 | GCTATCTA others(5): Show |
G | 13 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+2555_424+2566d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077017 | |||||||
| chr17:51077021 | T | G | 93 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(90): Show |
93 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.424+2563A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077021 | |||||||
| chr17:51077021 | T | TCTAGCTA others(13): Show |
3 | a0001c0002t0001g0270 a0001c0002t0001g0279 a0001c0002t0001g0288 |
3 | HG01167.hp2 HG01169.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.424+2562_424+2563i others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077021 | |||||||
| chr17:51077021 | TCTAGCTA others(25): Show |
T | 1 | a0001c0002t0001g0281 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+2531_424+2562d others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077021 | |||||||
| chr17:51077025 | G | T | 14 | a0001c0001t0002g0033 a0001c0001t0003g0019 a0001c0001t0003g0020 others(11): Show |
14 | HG01433.hp2 HG01891.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+2559C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077025 | |||||||
| chr17:51077025 | GCTAT | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0154 a0001c0001t0003g0022 |
3 | HG03098.hp1 HG03225.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.424+2555_424+2558d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077025 | |||||||
| chr17:51077029 | T | G | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(19): Show |
22 | HG01106.hp1 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+2555A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077029 | |||||||
| chr17:51077029 | T | TCTAG | 24 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0029 others(21): Show |
24 | HG00609.hp2 HG01069.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.424+2554_424+2555i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077029 | |||||||
| chr17:51077029 | T | TCTATCTA others(33): Show |
1 | a0001c0001t0006g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.424+2515_424+2554d others(42): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077029 | |||||||
| chr17:51077029 | T | TCTATCTA others(73): Show |
1 | a0001c0001t0002g0145 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.424+2554_424+2555i others(82): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077029 | |||||||
| chr17:51077029 | TCTATCTA others(41): Show |
T | 1 | a0002c0003t0018g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424+2507_424+2554d others(50): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077029 | |||||||
| chr17:51077033 | T | G | 65 | a0001c0001t0001g0177 a0001c0001t0001g0203 a0001c0001t0001g0205 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.424+2551A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077033 | |||||||
| chr17:51077033 | T | TCTAGCTA others(45): Show |
1 | a0001c0001t0002g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+2499_424+2550d others(54): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077033 | |||||||
| chr17:51077033 | TCTAGCTA others(61): Show |
T | 2 | a0001c0001t0002g0111 a0001c0001t0003g0164 |
2 | HG03831.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.424+2483_424+2550d others(70): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077033 | |||||||
| chr17:51077041 | T | G | 5 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0009g0027 others(2): Show |
5 | HG01891.hp1 HG02135.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2543A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077041 | |||||||
| chr17:51077041 | T | TCTAGCTA others(5): Show |
2 | a0001c0001t0001g0240 a0001c0001t0001g0248 |
2 | HG01109.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.424+2531_424+2542d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077041 | |||||||
| chr17:51077041 | T | TCTAGCTA others(21): Show |
1 | a0001c0001t0001g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.424+2542_424+2543i others(30): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077041 | |||||||
| chr17:51077041 | TCTAGCTA others(5): Show |
G | 1 | a0001c0002t0023g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.424+2532_424+2543d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077041 | |||||||
| chr17:51077041 | TCTAGCTA others(5): Show |
T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0047 a0001c0001t0003g0049 others(1): Show |
4 | HG02572.hp2 NA18994.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2531_424+2542d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077041 | |||||||
| chr17:51077045 | G | T | 5 | a0001c0001t0004g0182 a0001c0001t0004g0187 a0001c0001t0004g0190 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2539C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077045 | |||||||
| chr17:51077045 | GCTAT | G | 4 | a0001c0005t0001g0252 a0002c0003t0008g0173 a0002c0003t0008g0260 others(1): Show |
4 | HG01928.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2535_424+2538d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077045 | |||||||
| chr17:51077049 | T | G | 25 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(22): Show |
25 | HG00609.hp2 HG01069.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+2535A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077049 | |||||||
| chr17:51077049 | T | TCTAG | 9 | a0001c0001t0001g0245 a0001c0001t0002g0033 a0001c0005t0001g0211 others(6): Show |
9 | HG00558.hp1 HG00639.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+2531_424+2534d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077049 | |||||||
| chr17:51077049 | TCTAG | T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG01891.hp2 HG02735.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+2531_424+2534d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077049 | |||||||
| chr17:51077053 | GCTAGCTA others(13): Show |
G | 1 | a0001c0001t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.424+2511_424+2530d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077053 | |||||||
| chr17:51077053 | GCTAGCTA others(57): Show |
G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2467_424+2530d others(66): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077053 | |||||||
| chr17:51077057 | G | GCTATCTA others(29): Show |
1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.424+2491_424+2526d others(38): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077057 | |||||||
| chr17:51077057 | G | T | 23 | a0001c0001t0001g0069 a0001c0001t0003g0046 a0002c0003t0005g0094 others(20): Show |
23 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+2527C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077057 | |||||||
| chr17:51077057 | GCTATCTA others(29): Show |
G | 3 | a0001c0001t0002g0105 a0001c0002t0001g0278 a0001c0002t0001g0280 |
3 | HG02300.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.424+2491_424+2526d others(38): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077057 | |||||||
| chr17:51077057 | GCTATCTA others(33): Show |
G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0030 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2487_424+2526d others(42): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077057 | |||||||
| chr17:51077061 | T | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0069 others(5): Show |
8 | NA18906.hp2 NA18952.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+2523A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077061 | |||||||
| chr17:51077065 | G | GCTAT | 13 | a0001c0001t0001g0035 a0001c0001t0002g0029 a0001c0001t0003g0018 others(10): Show |
13 | HG00609.hp2 HG02083.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+2518_424+2519i others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077065 | |||||||
| chr17:51077065 | G | T | 40 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0056 others(37): Show |
40 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.424+2519C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077065 | |||||||
| chr17:51077069 | G | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG01069.hp2 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+2515C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077069 | |||||||
| chr17:51077069 | GCTATCTA others(17): Show |
G | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424+2491_424+2514d others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077069 | |||||||
| chr17:51077073 | T | G | 18 | a0001c0001t0001g0028 a0001c0001t0001g0075 a0001c0001t0001g0150 others(15): Show |
18 | HG01069.hp2 HG01433.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.424+2511A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077073 | |||||||
| chr17:51077077 | G | T | 7 | a0001c0001t0001g0028 a0001c0001t0003g0021 a0001c0001t0003g0034 others(4): Show |
7 | HG01069.hp2 HG01433.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+2507C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077077 | |||||||
| chr17:51077081 | T | G | 33 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0052 others(30): Show |
33 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+2503A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077081 | |||||||
| chr17:51077085 | G | GCTATCTA others(9): Show |
1 | a0001c0001t0001g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+2498_424+2499i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077085 | |||||||
| chr17:51077085 | G | T | 10 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0182 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+2499C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077085 | |||||||
| chr17:51077085 | GCTAGCTA others(1): Show |
G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0047 a0001c0001t0003g0049 |
3 | NA18994.hp1 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.424+2491_424+2498d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077085 | |||||||
| chr17:51077089 | G | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0002g0014 others(3): Show |
6 | HG00544.hp1 HG03831.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+2495C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077089 | |||||||
| chr17:51077089 | GCTAT | G | 46 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0069 others(43): Show |
46 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.424+2491_424+2494d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077089 | |||||||
| chr17:51077093 | T | G | 32 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0054 others(29): Show |
32 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+2491A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(21): Show |
1 | a0001c0001t0002g0029 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.424+2490_424+2491i others(30): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(21): Show |
3 | a0001c0001t0003g0031 a0001c0001t0003g0050 a0001c0001t0009g0027 |
3 | HG02135.hp2 HG02165.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.424+2490_424+2491i others(30): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(21): Show |
8 | a0001c0001t0001g0035 a0001c0001t0003g0018 a0001c0001t0003g0026 others(5): Show |
8 | HG02083.hp2 HG02132.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+2490_424+2491i others(30): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(25): Show |
1 | a0001c0001t0001g0249 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.424+2490_424+2491i others(34): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(61): Show |
1 | a0001c0001t0003g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.424+2490_424+2491i others(70): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(57): Show |
1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424+2490_424+2491i others(66): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | T | TCTAGCTA others(9): Show |
1 | a0001c0001t0003g0024 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.424+2490_424+2491i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077093 | TCTATCTA others(5): Show |
T | 1 | a0001c0001t0002g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.424+2479_424+2490d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077093 | |||||||
| chr17:51077097 | T | G | 9 | a0001c0001t0001g0051 a0001c0001t0001g0178 a0001c0001t0001g0239 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2487A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077097 | |||||||
| chr17:51077097 | TCTAG | T | 23 | a0001c0001t0001g0054 a0001c0001t0001g0065 a0002c0003t0005g0094 others(20): Show |
23 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.424+2483_424+2486d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077097 | |||||||
| chr17:51077101 | G | T | 3 | a0001c0005t0001g0252 a0002c0003t0008g0292 a0004c0006t0001g0060 |
3 | HG01884.hp1 HG01884.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.424+2483C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077101 | |||||||
| chr17:51077105 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0191 others(1): Show |
4 | HG02572.hp1 HG03654.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2479C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077105 | |||||||
| chr17:51077109 | T | G | 14 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0063 others(11): Show |
14 | HG00544.hp1 HG02572.hp1 HG03654.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+2475A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077109 | |||||||
| chr17:51077117 | T | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0056 others(3): Show |
6 | HG01884.hp1 HG03017.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+2467A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077117 | |||||||
| chr17:51077121 | G | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2463C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077121 | |||||||
| chr17:51077129 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.424+2455A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077129 | |||||||
| chr17:51077186 | T | C | 13 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(10): Show |
13 | HG01106.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+2398A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077186 | |||||||
| chr17:51077215 | C | G | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.424+2369G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077215 | |||||||
| chr17:51077279 | A | G | 1 | a0001c0005t0004g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.424+2305T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077279 | |||||||
| chr17:51077447 | A | G | 1 | a0001c0005t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.424+2137T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077447 | |||||||
| chr17:51077568 | T | C | 23 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(20): Show |
23 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+2016A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077568 | |||||||
| chr17:51077585 | T | C | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.424+1999A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077585 | |||||||
| chr17:51077903 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+1681C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51077903 | |||||||
| chr17:51078156 | G | T | 1 | a0001c0001t0003g0128 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+1428C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51078156 | |||||||
| chr17:51078437 | T | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+1147A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51078437 | |||||||
| chr17:51078848 | T | A | 15 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0179 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+736A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51078848 | |||||||
| chr17:51079076 | T | A | 19 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+508A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51079076 | |||||||
| chr17:51079231 | CT | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+352delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51079231 | |||||||
| chr17:51079546 | A | G | 91 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(88): Show |
91 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.424+38T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51079546 | |||||||
| chr17:51079548 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+36G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 2/29 | chr17 | 51079548 | |||||||
| chr17:51079883 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.304-179A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51079883 | |||||||
| chr17:51079971 | C | T | 19 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.304-267G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51079971 | |||||||
| chr17:51080051 | G | C | 2 | a0001c0001t0002g0029 a0001c0001t0003g0018 |
2 | HG04228.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.304-347C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080051 | |||||||
| chr17:51080117 | A | C | 3 | a0001c0001t0026g0147 a0002c0003t0011g0195 a0002c0003t0011g0196 |
3 | HG02258.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-413T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080117 | |||||||
| chr17:51080138 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.304-434T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080138 | |||||||
| chr17:51080280 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.304-576G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080280 | |||||||
| chr17:51080294 | C | CT | 37 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0029 others(34): Show |
37 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.304-591dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080294 | |||||||
| chr17:51080294 | CT | C | 19 | a0001c0001t0001g0207 a0001c0001t0001g0245 a0001c0001t0001g0247 others(16): Show |
19 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-591delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080294 | |||||||
| chr17:51080794 | T | C | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.304-1090A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080794 | |||||||
| chr17:51080864 | G | A | 6 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-1160C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080864 | |||||||
| chr17:51080886 | C | CA | 47 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(44): Show |
47 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.304-1183dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51080886 | C | CAA | 20 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 others(17): Show |
20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1184_304-1183d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51080886 | C | CAAA | 40 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(37): Show |
40 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.304-1185_304-1183d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51080886 | C | CAAAA | 28 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(25): Show |
28 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.304-1186_304-1183d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51080886 | C | CAAAAA | 7 | a0001c0001t0002g0029 a0001c0001t0003g0024 a0001c0001t0003g0039 others(4): Show |
7 | HG00609.hp2 HG02293.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-1187_304-1183d others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51080886 | CAAAAAAA others(2): Show |
C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.304-1191_304-1183d others(11): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51080886 | |||||||
| chr17:51081354 | G | A | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.304-1650C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51081354 | |||||||
| chr17:51081418 | T | G | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.304-1714A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51081418 | |||||||
| chr17:51081468 | G | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-1764C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51081468 | |||||||
| chr17:51081515 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.304-1811C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51081515 | |||||||
| chr17:51081570 | C | T | 1 | a0001c0002t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.304-1866G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51081570 | |||||||
| chr17:51082166 | C | A | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.304-2462G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082166 | |||||||
| chr17:51082248 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.304-2544C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082248 | |||||||
| chr17:51082377 | C | CA | 30 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0058 others(27): Show |
30 | HG00280.hp1 HG01071.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.304-2674dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082377 | |||||||
| chr17:51082377 | C | CAA | 14 | a0001c0001t0001g0057 a0001c0001t0001g0240 a0001c0001t0001g0269 others(11): Show |
14 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-2675_304-2674d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082377 | |||||||
| chr17:51082377 | C | CAAA | 10 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 others(7): Show |
10 | HG01081.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-2676_304-2674d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082377 | |||||||
| chr17:51082377 | CA | C | 123 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(120): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.304-2674delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082377 | |||||||
| chr17:51082400 | A | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2696T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082400 | |||||||
| chr17:51082447 | T | C | 65 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.304-2743A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082447 | |||||||
| chr17:51082466 | T | C | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-2762A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082466 | |||||||
| chr17:51082635 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.304-2931A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082635 | |||||||
| chr17:51082834 | C | T | 22 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(19): Show |
22 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.304-3130G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51082834 | |||||||
| chr17:51083446 | G | A | 195 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(192): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.304-3742C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083446 | |||||||
| chr17:51083483 | C | T | 4 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0114 others(1): Show |
4 | HG02717.hp1 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-3779G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083483 | |||||||
| chr17:51083543 | T | TTTTA | 51 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0091 others(48): Show |
51 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.304-3843_304-3840d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | T | TTTTATTT others(1): Show |
63 | a0001c0001t0001g0126 a0001c0001t0001g0203 a0001c0001t0001g0205 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.304-3847_304-3840d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | T | TTTTATTT others(5): Show |
10 | a0001c0001t0001g0225 a0001c0001t0001g0235 a0001c0001t0002g0204 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-3851_304-3840d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | T | TTTTATTT others(9): Show |
3 | a0002c0004t0005g0003 a0002c0004t0005g0005 a0002c0004t0007g0009 |
3 | HG02451.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.304-3855_304-3840d others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | T | TTTTATTT others(13): Show |
1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.304-3859_304-3840d others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | TTTTA | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-3843_304-3840d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083543 | TTTTATTT others(1): Show |
T | 29 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(26): Show |
29 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.304-3847_304-3840d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083543 | |||||||
| chr17:51083932 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.304-4228G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51083932 | |||||||
| chr17:51084220 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-4516A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084220 | |||||||
| chr17:51084394 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.304-4690T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084394 | |||||||
| chr17:51084395 | A | T | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.304-4691T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084395 | |||||||
| chr17:51084447 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.304-4743C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084447 | |||||||
| chr17:51084521 | C | T | 2 | a0002c0004t0005g0006 a0002c0004t0005g0007 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.304-4817G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084521 | |||||||
| chr17:51084848 | TTTTA | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-5148_304-5145d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084848 | |||||||
| chr17:51084860 | A | T | 1 | a0001c0001t0003g0128 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-5156T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084860 | |||||||
| chr17:51084898 | T | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-5194A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51084898 | |||||||
| chr17:51085111 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0002g0214 |
2 | NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.304-5407C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085111 | |||||||
| chr17:51085240 | G | T | 1 | a0001c0001t0002g0013 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.304-5536C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085240 | |||||||
| chr17:51085370 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.304-5666C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085370 | |||||||
| chr17:51085479 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-5775G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085479 | |||||||
| chr17:51085958 | CA | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0230 a0001c0001t0002g0217 |
3 | HG02071.hp2 NA19060.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.304-6255delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085958 | |||||||
| chr17:51085959 | A | AT | 59 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(56): Show |
59 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.304-6256dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085959 | |||||||
| chr17:51085959 | A | ATT | 35 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0052 others(32): Show |
35 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.304-6257_304-6256d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085959 | |||||||
| chr17:51085959 | A | ATTT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0013g0183 others(4): Show |
7 | HG01358.hp2 HG02148.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-6258_304-6256d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085959 | |||||||
| chr17:51085959 | AT | A | 52 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.304-6256delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51085959 | |||||||
| chr17:51086008 | G | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0047 a0001c0001t0003g0049 |
3 | NA18994.hp1 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.304-6304C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086008 | |||||||
| chr17:51086276 | G | A | 1 | a0001c0001t0012g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.304-6572C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086276 | |||||||
| chr17:51086409 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.304-6705C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086409 | |||||||
| chr17:51086489 | T | TA | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0002g0071 others(3): Show |
6 | HG02698.hp1 HG03239.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-6786dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086489 | |||||||
| chr17:51086489 | TA | T | 20 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-6786delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086489 | |||||||
| chr17:51086685 | C | A | 1 | a0001c0001t0004g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.304-6981G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086685 | |||||||
| chr17:51086837 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.304-7133C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086837 | |||||||
| chr17:51086967 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.304-7263A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51086967 | |||||||
| chr17:51087028 | G | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-7324C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087028 | |||||||
| chr17:51087331 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.304-7627A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087331 | |||||||
| chr17:51087450 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.304-7746C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087450 | |||||||
| chr17:51087506 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.304-7802A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087506 | |||||||
| chr17:51087762 | T | C | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.304-8058A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087762 | |||||||
| chr17:51087777 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.304-8073G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087777 | |||||||
| chr17:51087999 | C | A | 2 | a0001c0001t0001g0176 a0001c0001t0002g0166 |
2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.304-8295G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51087999 | |||||||
| chr17:51088114 | C | T | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.304-8410G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51088114 | |||||||
| chr17:51088163 | G | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-8459C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51088163 | |||||||
| chr17:51088380 | C | G | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-8676G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51088380 | |||||||
| chr17:51088561 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-8857G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51088561 | |||||||
| chr17:51089122 | C | A | 6 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0002g0093 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-9418G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089122 | |||||||
| chr17:51089124 | A | C | 112 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0001g0203 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.304-9420T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089124 | |||||||
| chr17:51089298 | C | T | 7 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(4): Show |
7 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-9594G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089298 | |||||||
| chr17:51089352 | A | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-9648T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089352 | |||||||
| chr17:51089541 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.304-9837A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089541 | |||||||
| chr17:51089615 | TTATTTTA others(22): Show |
T | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-9940_304-9912d others(31): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089615 | |||||||
| chr17:51089618 | TTTTATAT others(5): Show |
T | 1 | a0002c0003t0011g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.304-9926_304-9915d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089618 | |||||||
| chr17:51089618 | TTTTATAT others(7): Show |
T | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.304-9928_304-9915d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089618 | |||||||
| chr17:51089620 | T | A | 2 | a0001c0001t0002g0137 a0001c0001t0003g0048 |
2 | HG02109.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.304-9916A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TATATATA others(6): Show |
1 | a0001c0001t0003g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.304-9917_304-9916i others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.304-9917_304-9916i others(17): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTA | 31 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0130 others(28): Show |
31 | HG00738.hp2 HG01074.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.304-9918_304-9917d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATA | 8 | a0001c0001t0001g0132 a0001c0001t0002g0078 a0001c0001t0002g0111 others(5): Show |
8 | HG02132.hp2 HG03654.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-9920_304-9917d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATATA | 14 | a0001c0001t0001g0113 a0001c0001t0001g0237 a0001c0001t0002g0066 others(11): Show |
14 | HG00544.hp2 HG00558.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-9922_304-9917d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATATAT others(1): Show |
8 | a0001c0001t0001g0172 a0001c0001t0002g0099 a0001c0001t0002g0100 others(5): Show |
8 | HG00609.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-9924_304-9917d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATATAT others(3): Show |
3 | a0001c0001t0002g0079 a0001c0001t0002g0125 a0001c0001t0002g0136 |
3 | HG01106.hp2 NA18959.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.304-9926_304-9917d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATATAT others(5): Show |
4 | a0001c0001t0001g0158 a0001c0001t0002g0097 a0001c0001t0003g0128 others(1): Show |
4 | HG01943.hp2 HG02135.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-9928_304-9917d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | T | TTATATAT others(7): Show |
2 | a0001c0001t0002g0120 a0001c0001t0002g0165 |
2 | HG02735.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.304-9930_304-9917d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | TTA | T | 22 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0150 others(19): Show |
22 | HG00140.hp1 HG00558.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.304-9918_304-9917d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | TTATA | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0117 a0001c0001t0006g0188 others(1): Show |
4 | HG00741.hp2 HG03486.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-9920_304-9917d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | TTATATA | T | 3 | a0001c0001t0001g0075 a0001c0001t0003g0169 a0001c0001t0004g0152 |
3 | HG01433.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.304-9922_304-9917d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089620 | TTATATAT others(5): Show |
T | 1 | a0001c0005t0001g0267 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.304-9928_304-9917d others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089620 | |||||||
| chr17:51089643 | TATATATA others(15): Show |
T | 1 | a0001c0001t0004g0184 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.304-9961_304-9940d others(24): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089643 | |||||||
| chr17:51089647 | TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.304-9961_304-9944d others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089647 | |||||||
| chr17:51089655 | TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0177 a0001c0001t0001g0259 |
3 | HG02698.hp2 HG03017.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.304-9961_304-9952d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089655 | |||||||
| chr17:51089657 | T | C | 9 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-9953A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089657 | |||||||
| chr17:51089657 | TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-9961_304-9954d others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089657 | |||||||
| chr17:51089659 | T | C | 11 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-9955A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089659 | |||||||
| chr17:51089659 | TATATAC | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0214 a0001c0001t0004g0187 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-9961_304-9956d others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089659 | |||||||
| chr17:51089661 | T | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0003g0015 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.304-9957A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATAC | 6 | a0001c0001t0003g0023 a0001c0001t0003g0034 a0001c0001t0003g0036 others(3): Show |
6 | HG01433.hp2 HG02040.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-9958_304-9957i others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(1): Show |
5 | a0001c0001t0002g0014 a0001c0001t0003g0016 a0001c0001t0003g0022 others(2): Show |
5 | HG00544.hp1 NA18951.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-9958_304-9957i others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(3): Show |
1 | a0001c0001t0003g0044 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.304-9958_304-9957i others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(5): Show |
8 | a0001c0001t0002g0073 a0001c0001t0003g0020 a0001c0001t0003g0021 others(5): Show |
8 | HG01069.hp2 HG01981.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-9958_304-9957i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(7): Show |
3 | a0001c0001t0003g0038 a0001c0001t0003g0042 a0001c0001t0003g0043 |
3 | HG02293.hp1 NA19064.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.304-9958_304-9957i others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(9): Show |
4 | a0001c0001t0002g0017 a0001c0001t0002g0029 a0001c0001t0002g0033 others(1): Show |
4 | HG02015.hp1 HG02083.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-9958_304-9957i others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(11): Show |
6 | a0001c0001t0003g0019 a0001c0001t0003g0030 a0001c0001t0003g0039 others(3): Show |
6 | HG00609.hp2 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-9958_304-9957i others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | T | TATATATA others(17): Show |
2 | a0001c0001t0003g0018 a0001c0001t0012g0025 |
2 | HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.304-9958_304-9957i others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089661 | TATAC | T | 17 | a0001c0001t0001g0062 a0001c0001t0001g0203 a0001c0001t0001g0205 others(14): Show |
17 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.304-9961_304-9958d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089661 | |||||||
| chr17:51089663 | T | C | 18 | a0001c0001t0001g0153 a0001c0002t0001g0271 a0001c0002t0001g0272 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-9959A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089663 | |||||||
| chr17:51089663 | T | TATATACA others(5): Show |
3 | a0001c0002t0001g0270 a0001c0002t0001g0279 a0001c0002t0001g0288 |
3 | HG01167.hp2 HG01169.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.304-9960_304-9959i others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089663 | |||||||
| chr17:51089663 | T | TATATATA others(7): Show |
3 | a0001c0002t0001g0277 a0001c0002t0001g0278 a0001c0002t0001g0280 |
3 | HG03139.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.304-9960_304-9959i others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089663 | |||||||
| chr17:51089663 | TAC | T | 29 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0207 others(26): Show |
29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.304-9961_304-9960d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089663 | |||||||
| chr17:51089665 | C | T | 45 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0055 others(42): Show |
45 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.304-9961G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089665 | |||||||
| chr17:51089669 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-9965A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089669 | |||||||
| chr17:51089790 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.304-10086G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089790 | |||||||
| chr17:51089833 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.304-10129A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089833 | |||||||
| chr17:51089866 | C | T | 5 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-10162G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089866 | |||||||
| chr17:51089956 | C | T | 3 | a0002c0003t0008g0173 a0002c0003t0008g0287 a0002c0003t0008g0292 |
3 | HG01884.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.304-10252G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51089956 | |||||||
| chr17:51090025 | A | G | 1 | a0001c0001t0006g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.304-10321T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51090025 | |||||||
| chr17:51090257 | C | T | 1 | a0002c0003t0011g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.304-10553G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51090257 | |||||||
| chr17:51090469 | C | T | 40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.304-10765G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51090469 | |||||||
| chr17:51090470 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-10766C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51090470 | |||||||
| chr17:51091140 | G | A | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-11436C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091140 | |||||||
| chr17:51091273 | C | CA | 19 | a0001c0001t0001g0054 a0001c0001t0001g0068 a0001c0001t0001g0069 others(16): Show |
19 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.304-11570dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091273 | |||||||
| chr17:51091275 | A | G | 1 | a0001c0001t0003g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.304-11571T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091275 | |||||||
| chr17:51091329 | A | T | 1 | a0001c0001t0003g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.304-11625T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091329 | |||||||
| chr17:51091366 | G | A | 1 | a0001c0001t0003g0206 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.304-11662C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091366 | |||||||
| chr17:51091495 | G | T | 49 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(46): Show |
49 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.304-11791C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091495 | |||||||
| chr17:51091510 | G | GTTT | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-11809_304-1180 others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091510 | |||||||
| chr17:51091510 | G | T | 190 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.304-11806C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091510 | |||||||
| chr17:51091780 | T | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-12076A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091780 | |||||||
| chr17:51091815 | T | TA | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.304-12112dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091815 | |||||||
| chr17:51091984 | TA | T | 142 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0053 others(139): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.304-12281delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091984 | |||||||
| chr17:51091984 | TAA | T | 36 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0075 others(33): Show |
36 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.304-12282_304-1228 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51091984 | |||||||
| chr17:51092279 | A | T | 2 | a0001c0001t0002g0115 a0001c0001t0002g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.304-12575T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51092279 | |||||||
| chr17:51092287 | A | G | 3 | a0001c0001t0026g0147 a0002c0003t0011g0195 a0002c0003t0011g0196 |
3 | HG02258.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-12583T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51092287 | |||||||
| chr17:51092696 | T | C | 32 | a0001c0001t0001g0194 a0001c0001t0002g0170 a0001c0001t0004g0179 others(29): Show |
32 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.304-12992A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51092696 | |||||||
| chr17:51092751 | CAAAAAAA others(3): Show |
C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.304-13057_304-1304 others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51092751 | |||||||
| chr17:51092946 | T | A | 1 | a0001c0001t0003g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.304-13242A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51092946 | |||||||
| chr17:51093069 | T | TA | 7 | a0001c0001t0001g0055 a0001c0001t0001g0155 a0001c0001t0002g0125 others(4): Show |
7 | HG01358.hp2 HG01891.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-13366dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093069 | |||||||
| chr17:51093069 | TA | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0218 a0001c0001t0001g0231 others(7): Show |
10 | HG01070.hp2 HG01081.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-13366delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093069 | |||||||
| chr17:51093254 | C | A | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-13550G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093254 | |||||||
| chr17:51093318 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.304-13614A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093318 | |||||||
| chr17:51093468 | T | C | 197 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(194): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.304-13764A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093468 | |||||||
| chr17:51093498 | C | A | 2 | a0001c0002t0001g0275 a0001c0002t0001g0276 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.304-13794G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093498 | |||||||
| chr17:51093694 | C | CA | 177 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.304-13991dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093694 | |||||||
| chr17:51093694 | C | CAA | 16 | a0001c0001t0001g0061 a0001c0001t0001g0227 a0001c0001t0001g0239 others(13): Show |
16 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.304-13992_304-1399 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093694 | |||||||
| chr17:51093694 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.304-14001_304-1399 others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51093694 | |||||||
| chr17:51094022 | A | C | 1 | a0002c0003t0008g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.304-14318T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51094022 | |||||||
| chr17:51094053 | T | C | 216 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.304-14349A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51094053 | |||||||
| chr17:51094122 | C | G | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-14418G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51094122 | |||||||
| chr17:51094470 | A | C | 18 | a0001c0001t0001g0028 a0001c0001t0002g0014 a0001c0001t0002g0029 others(15): Show |
18 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.304-14766T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51094470 | |||||||
| chr17:51095013 | A | G | 3 | a0001c0001t0006g0107 a0001c0001t0006g0131 a0001c0001t0006g0160 |
3 | HG02683.hp2 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.304-15309T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095013 | |||||||
| chr17:51095033 | C | T | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-15329G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095033 | |||||||
| chr17:51095245 | G | A | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.304-15541C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095245 | |||||||
| chr17:51095296 | T | TA | 13 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0243 others(10): Show |
13 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-15593dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095296 | |||||||
| chr17:51095296 | TA | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0127 a0001c0001t0002g0014 others(7): Show |
10 | HG01257.hp2 HG01516.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-15593delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095296 | |||||||
| chr17:51095296 | TAAAAAAA others(4): Show |
T | 60 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(57): Show |
60 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.304-15603_304-1559 others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095296 | |||||||
| chr17:51095296 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0002g0220 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.304-15604_304-1559 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095296 | |||||||
| chr17:51095357 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.304-15653G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095357 | |||||||
| chr17:51095522 | G | A | 1 | a0001c0001t0027g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.304-15818C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095522 | |||||||
| chr17:51095670 | GTA | G | 31 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(28): Show |
31 | HG01168.hp2 HG01243.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.304-15968_304-1596 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095670 | |||||||
| chr17:51095673 | TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0178 a0001c0001t0004g0191 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.304-15983_304-1597 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095673 | |||||||
| chr17:51095689 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.304-15997_304-1598 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095689 | |||||||
| chr17:51095693 | T | C | 1 | a0001c0001t0009g0027 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.304-15989A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095693 | |||||||
| chr17:51095705 | TATATAGT others(9): Show |
T | 2 | a0001c0001t0001g0127 a0001c0001t0003g0169 |
2 | HG01433.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.304-16017_304-1600 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095705 | |||||||
| chr17:51095765 | CATATAGT others(5): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.304-16073_304-1606 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095765 | |||||||
| chr17:51095791 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-16087G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095791 | |||||||
| chr17:51095823 | GAGAGATA others(1): Show |
G | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.304-16127_304-1612 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095823 | |||||||
| chr17:51095908 | T | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.304-16204A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095908 | |||||||
| chr17:51095926 | GAT | G | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-16224_304-1622 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095926 | |||||||
| chr17:51095930 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.304-16226A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095930 | |||||||
| chr17:51095945 | T | TTA | 90 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(87): Show |
90 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.304-16243_304-1624 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095945 | |||||||
| chr17:51095956 | G | T | 36 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(33): Show |
36 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.304-16252C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095956 | |||||||
| chr17:51095957 | T | A | 36 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(33): Show |
36 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.304-16253A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095957 | |||||||
| chr17:51095958 | GAT | G | 9 | a0001c0001t0001g0127 a0001c0001t0001g0210 a0001c0001t0001g0257 others(6): Show |
9 | HG01516.hp1 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-16256_304-1625 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095958 | |||||||
| chr17:51095958 | GATATATA others(11): Show |
G | 9 | a0001c0001t0001g0207 a0001c0001t0001g0218 a0001c0001t0001g0219 others(6): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-16272_304-1625 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095958 | |||||||
| chr17:51095959 | A | T | 36 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(33): Show |
36 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.304-16255T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095959 | |||||||
| chr17:51095960 | T | G | 36 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(33): Show |
36 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.304-16256A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095960 | |||||||
| chr17:51095960 | T | TATATATA others(5): Show |
1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.304-16257_304-1625 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095960 | |||||||
| chr17:51095960 | T | TATATATA others(21): Show |
1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-16257_304-1625 others(32): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095960 | |||||||
| chr17:51095970 | T | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-16266A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095970 | |||||||
| chr17:51095971 | A | T | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-16267T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095971 | |||||||
| chr17:51095973 | T | A | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-16269A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095973 | |||||||
| chr17:51095974 | G | T | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-16270C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095974 | |||||||
| chr17:51095974 | GAT | G | 99 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0051 others(96): Show |
99 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.304-16272_304-1627 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095974 | |||||||
| chr17:51095974 | GATAT | G | 59 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0208 others(56): Show |
59 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.304-16274_304-1627 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095974 | |||||||
| chr17:51095976 | T | TATATATA others(5): Show |
7 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(4): Show |
7 | HG01192.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-16273_304-1627 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095976 | |||||||
| chr17:51095976 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.304-16273_304-1627 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095976 | |||||||
| chr17:51095976 | TATATATA others(9): Show |
T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0259 |
2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.304-16288_304-1627 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095976 | |||||||
| chr17:51095978 | T | TATATATA others(109): Show |
2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-16275_304-1627 others(120): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095978 | |||||||
| chr17:51095978 | T | TATATATA others(5): Show |
2 | a0001c0001t0004g0184 a0002c0003t0010g0199 |
2 | HG01081.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.304-16275_304-1627 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095978 | |||||||
| chr17:51095986 | T | G | 9 | a0001c0001t0001g0230 a0001c0005t0001g0211 a0001c0005t0001g0212 others(6): Show |
9 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-16282A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095986 | |||||||
| chr17:51095987 | A | T | 9 | a0001c0001t0001g0230 a0001c0005t0001g0211 a0001c0005t0001g0212 others(6): Show |
9 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-16283T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095987 | |||||||
| chr17:51095988 | T | G | 20 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0150 others(17): Show |
20 | HG00558.hp1 HG00639.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.304-16284A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095988 | |||||||
| chr17:51095989 | A | T | 10 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0150 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-16285T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095989 | |||||||
| chr17:51095990 | G | T | 9 | a0001c0001t0001g0230 a0001c0005t0001g0211 a0001c0005t0001g0212 others(6): Show |
9 | HG00558.hp1 HG00639.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-16286C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095990 | |||||||
| chr17:51095991 | T | A | 19 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0150 others(16): Show |
19 | HG00558.hp1 HG00639.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-16287A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095991 | |||||||
| chr17:51095992 | G | GAT | 67 | a0001c0001t0001g0069 a0001c0001t0001g0203 a0001c0001t0001g0205 others(64): Show |
67 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.304-16290_304-1628 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095992 | |||||||
| chr17:51095992 | G | GATATATA others(9): Show |
1 | a0001c0001t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.304-16304_304-1628 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095992 | |||||||
| chr17:51095992 | G | GATATATA others(25): Show |
1 | a0001c0001t0002g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.304-16320_304-1628 others(36): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095992 | |||||||
| chr17:51095992 | G | T | 19 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0150 others(16): Show |
19 | HG00558.hp1 HG00639.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-16288C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095992 | |||||||
| chr17:51095992 | GATATATA others(25): Show |
G | 1 | a0001c0001t0006g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.304-16320_304-1628 others(36): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095992 | |||||||
| chr17:51095994 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0210 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304-16302_304-1629 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51095994 | |||||||
| chr17:51096006 | G | GAT | 6 | a0001c0001t0001g0209 a0001c0001t0001g0236 a0001c0001t0001g0247 others(3): Show |
6 | HG01106.hp1 NA18948.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-16304_304-1630 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096006 | |||||||
| chr17:51096006 | G | GATATATA others(25): Show |
15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0004g0179 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.304-16303_304-1630 others(36): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096006 | |||||||
| chr17:51096006 | G | GATATATA others(43): Show |
2 | a0001c0001t0001g0194 a0001c0001t0004g0202 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.304-16303_304-1630 others(54): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096006 | |||||||
| chr17:51096008 | TATATATA others(7): Show |
T | 1 | a0001c0001t0003g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.304-16318_304-1630 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096008 | |||||||
| chr17:51096018 | T | G | 2 | a0001c0001t0001g0233 a0001c0001t0003g0023 |
2 | HG02040.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.304-16314A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096018 | |||||||
| chr17:51096019 | A | T | 2 | a0001c0001t0001g0233 a0001c0001t0003g0023 |
2 | HG02040.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.304-16315T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096019 | |||||||
| chr17:51096021 | T | A | 2 | a0001c0001t0001g0233 a0001c0001t0003g0023 |
2 | HG02040.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.304-16317A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096021 | |||||||
| chr17:51096022 | G | GAT | 75 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0075 others(72): Show |
75 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.304-16320_304-1631 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096022 | |||||||
| chr17:51096022 | G | GATATATA others(9): Show |
70 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
70 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.304-16319_304-1631 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096022 | |||||||
| chr17:51096022 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0003g0023 |
2 | HG02040.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.304-16318C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096022 | |||||||
| chr17:51096026 | TATATATA others(5): Show |
T | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-16334_304-1632 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096026 | |||||||
| chr17:51096038 | G | GAT | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(17): Show |
20 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-16336_304-1633 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | G | GATAT | 18 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-16338_304-1633 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | G | GATATATA others(11): Show |
2 | a0001c0001t0004g0184 a0002c0003t0010g0199 |
2 | HG01081.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.304-16352_304-1633 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | G | GATATATA others(15): Show |
1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-16356_304-1633 others(26): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | G | GATATATA others(49): Show |
1 | a0002c0003t0008g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-16335_304-1633 others(60): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | G | GATATATA others(11): Show |
1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.304-16335_304-1633 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096038 | GAT | G | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-16336_304-1633 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096038 | |||||||
| chr17:51096054 | G | GATATATA others(17): Show |
1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.304-16351_304-1635 others(28): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096054 | |||||||
| chr17:51096056 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.304-16353_304-1635 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096056 | |||||||
| chr17:51096058 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.304-16354A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096058 | |||||||
| chr17:51096070 | T | A | 1 | a0001c0001t0003g0044 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.304-16366A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096070 | |||||||
| chr17:51096182 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.304-16478G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096182 | |||||||
| chr17:51096400 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.304-16696C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096400 | |||||||
| chr17:51096431 | T | C | 19 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(16): Show |
19 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.304-16727A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096431 | |||||||
| chr17:51096465 | G | C | 23 | a0001c0001t0002g0170 a0002c0003t0005g0094 a0002c0003t0007g0077 others(20): Show |
23 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.304-16761C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096465 | |||||||
| chr17:51096493 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.304-16789A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096493 | |||||||
| chr17:51096624 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.304-16920G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096624 | |||||||
| chr17:51096636 | T | G | 11 | a0001c0001t0002g0066 a0001c0001t0002g0103 a0001c0001t0002g0111 others(8): Show |
11 | HG02015.hp2 HG02083.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-16932A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096636 | |||||||
| chr17:51096713 | G | A | 5 | a0001c0002t0001g0270 a0001c0002t0001g0278 a0001c0002t0001g0279 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-17009C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096713 | |||||||
| chr17:51096734 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.304-17030T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096734 | |||||||
| chr17:51096804 | A | G | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.304-17100T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096804 | |||||||
| chr17:51096810 | T | C | 1 | a0002c0004t0005g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.304-17106A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51096810 | |||||||
| chr17:51097160 | G | A | 1 | a0002c0003t0008g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-17456C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51097160 | |||||||
| chr17:51097381 | T | A | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.304-17677A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51097381 | |||||||
| chr17:51097613 | G | A | 64 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.304-17909C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51097613 | |||||||
| chr17:51097717 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.304-18013C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51097717 | |||||||
| chr17:51098279 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.304-18575G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098279 | |||||||
| chr17:51098325 | GT | G | 88 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.304-18622delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098325 | |||||||
| chr17:51098406 | AT | A | 88 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.304-18703delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098406 | |||||||
| chr17:51098421 | C | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-18717G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098421 | |||||||
| chr17:51098425 | C | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-18721G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098425 | |||||||
| chr17:51098503 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.304-18799A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098503 | |||||||
| chr17:51098669 | T | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-18965A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098669 | |||||||
| chr17:51098917 | T | C | 1 | a0001c0001t0009g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.304-19213A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098917 | |||||||
| chr17:51098966 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.304-19262C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51098966 | |||||||
| chr17:51099099 | C | CA | 33 | a0001c0001t0001g0153 a0001c0001t0001g0257 a0001c0001t0002g0170 others(30): Show |
33 | HG00558.hp1 HG00639.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.304-19396dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099099 | |||||||
| chr17:51099099 | CA | C | 9 | a0001c0001t0001g0245 a0001c0001t0002g0079 a0001c0001t0002g0100 others(6): Show |
9 | HG01975.hp2 HG02273.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-19396delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099099 | |||||||
| chr17:51099230 | T | C | 4 | a0001c0002t0001g0271 a0001c0002t0001g0282 a0001c0002t0001g0290 others(1): Show |
4 | HG02486.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-19526A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099230 | |||||||
| chr17:51099233 | A | C | 1 | a0001c0001t0019g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.304-19529T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099233 | |||||||
| chr17:51099236 | C | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0262 a0001c0001t0003g0206 |
3 | NA18947.hp2 NA19057.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.304-19532G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099236 | |||||||
| chr17:51099298 | T | C | 1 | a0002c0003t0007g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.304-19594A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099298 | |||||||
| chr17:51099433 | C | CA | 80 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0130 others(77): Show |
80 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.304-19730dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099433 | |||||||
| chr17:51099664 | C | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0186 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.304-19960G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099664 | |||||||
| chr17:51099735 | G | A | 58 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.304-20031C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099735 | |||||||
| chr17:51099759 | T | TA | 66 | a0001c0001t0001g0113 a0001c0001t0001g0132 a0001c0001t0001g0153 others(63): Show |
66 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.304-20056dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099759 | |||||||
| chr17:51099759 | T | TAA | 28 | a0001c0001t0001g0063 a0001c0001t0001g0126 a0001c0001t0001g0158 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.304-20057_304-2005 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099759 | |||||||
| chr17:51099759 | TA | T | 34 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(31): Show |
34 | HG00280.hp1 HG01099.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.304-20056delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099759 | |||||||
| chr17:51099778 | A | C | 21 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(18): Show |
21 | HG01168.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.304-20074T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099778 | |||||||
| chr17:51099780 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.304-20076T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099780 | |||||||
| chr17:51099825 | C | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.304-20121G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51099825 | |||||||
| chr17:51100032 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303+20322C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100032 | |||||||
| chr17:51100071 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.303+20283C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100071 | |||||||
| chr17:51100076 | A | G | 1 | a0001c0005t0001g0212 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.303+20278T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100076 | |||||||
| chr17:51100161 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303+20193T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100161 | |||||||
| chr17:51100270 | T | C | 112 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(109): Show |
112 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.303+20084A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100270 | |||||||
| chr17:51100320 | T | TCTTTAGT others(4): Show |
20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(17): Show |
20 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+20033_303+2003 others(15): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100320 | |||||||
| chr17:51100322 | G | C | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(17): Show |
20 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+20032C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100322 | |||||||
| chr17:51100323 | G | T | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(17): Show |
20 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+20031C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100323 | |||||||
| chr17:51100461 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.303+19893A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100461 | |||||||
| chr17:51100735 | C | T | 1 | a0002c0003t0008g0287 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+19619G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51100735 | |||||||
| chr17:51101032 | T | C | 2 | a0001c0001t0002g0138 a0005c0010t0002g0140 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.303+19322A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101032 | |||||||
| chr17:51101041 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.303+19313C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101041 | |||||||
| chr17:51101233 | C | A | 1 | a0001c0001t0004g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.303+19121G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101233 | |||||||
| chr17:51101271 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.303+19083T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101271 | |||||||
| chr17:51101331 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+19023C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101331 | |||||||
| chr17:51101345 | C | CA | 44 | a0001c0001t0001g0028 a0001c0001t0001g0127 a0001c0001t0002g0017 others(41): Show |
44 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.303+19008dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101345 | |||||||
| chr17:51101345 | CA | C | 27 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0056 others(24): Show |
27 | HG00280.hp1 HG01070.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.303+19008delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101345 | |||||||
| chr17:51101345 | CAA | C | 36 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.303+19007_303+1900 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101345 | |||||||
| chr17:51101345 | CAAAAAAA others(1): Show |
C | 61 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.303+19001_303+1900 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101345 | |||||||
| chr17:51101573 | T | C | 4 | a0002c0003t0008g0173 a0002c0003t0008g0260 a0002c0003t0008g0287 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+18781A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101573 | |||||||
| chr17:51101635 | A | G | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+18719T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51101635 | |||||||
| chr17:51102057 | T | C | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+18297A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51102057 | |||||||
| chr17:51102211 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0003g0026 |
2 | NA18948.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.303+18143G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51102211 | |||||||
| chr17:51102404 | C | CA | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.303+17949dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51102404 | |||||||
| chr17:51102508 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.303+17846A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51102508 | |||||||
| chr17:51102720 | T | G | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+17634A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51102720 | |||||||
| chr17:51103077 | G | A | 21 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+17277C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51103077 | |||||||
| chr17:51103173 | T | A | 13 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0004g0179 others(10): Show |
13 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.303+17181A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51103173 | |||||||
| chr17:51103326 | A | G | 8 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(5): Show |
8 | HG02717.hp1 HG02965.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+17028T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51103326 | |||||||
| chr17:51103501 | G | A | 154 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(151): Show |
154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.303+16853C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51103501 | |||||||
| chr17:51103517 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+16837G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51103517 | |||||||
| chr17:51104308 | A | G | 90 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(87): Show |
90 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.303+16046T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104308 | |||||||
| chr17:51104397 | G | T | 3 | a0001c0001t0026g0147 a0002c0003t0011g0195 a0002c0003t0011g0196 |
3 | HG02258.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.303+15957C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104397 | |||||||
| chr17:51104613 | G | T | 3 | a0002c0003t0008g0173 a0002c0003t0008g0287 a0002c0003t0008g0292 |
3 | HG01884.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.303+15741C>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104613 | |||||||
| chr17:51104643 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.303+15711T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104643 | |||||||
| chr17:51104671 | C | A | 18 | a0002c0003t0005g0094 a0002c0003t0007g0077 a0002c0003t0007g0096 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+15683G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104671 | |||||||
| chr17:51104671 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.303+15683G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104671 | |||||||
| chr17:51104845 | A | C | 1 | a0001c0001t0002g0014 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.303+15509T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104845 | |||||||
| chr17:51104914 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.303+15440G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104914 | |||||||
| chr17:51104927 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.303+15427G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104927 | |||||||
| chr17:51104932 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.303+15408_303+1542 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.303+15421_303+1542 others(19): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(9): Show |
52 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0208 others(49): Show |
52 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.303+15421_303+1542 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(10): Show |
19 | a0001c0001t0001g0215 a0001c0001t0001g0224 a0001c0001t0001g0226 others(16): Show |
19 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.303+15421_303+1542 others(21): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(11): Show |
11 | a0001c0001t0001g0205 a0002c0003t0007g0077 a0002c0003t0007g0129 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+15421_303+1542 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(12): Show |
5 | a0002c0003t0005g0094 a0002c0004t0005g0001 a0002c0004t0005g0006 others(2): Show |
5 | HG01168.hp2 HG02055.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+15421_303+1542 others(23): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104932 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.303+15421_303+1542 others(21): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104932 | |||||||
| chr17:51104955 | G | GTGT | 69 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(66): Show |
69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.303+15396_303+1539 others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51104955 | |||||||
| chr17:51105012 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.303+15342A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105012 | |||||||
| chr17:51105044 | C | A | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+15310G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105044 | |||||||
| chr17:51105107 | G | GATAA | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+15243_303+1524 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105107 | |||||||
| chr17:51105107 | G | GATAAATA others(1): Show |
40 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0014 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.303+15239_303+1524 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105107 | |||||||
| chr17:51105219 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+15135C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105219 | |||||||
| chr17:51105552 | T | C | 1 | a0001c0001t0004g0184 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.303+14802A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105552 | |||||||
| chr17:51105651 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0148 |
2 | HG01943.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.303+14703G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105651 | |||||||
| chr17:51105665 | C | G | 1 | a0001c0001t0003g0018 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.303+14689G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105665 | |||||||
| chr17:51105878 | G | A | 89 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.303+14476C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51105878 | |||||||
| chr17:51106084 | C | T | 2 | a0001c0002t0023g0284 a0001c0002t0024g0286 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.303+14270G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106084 | |||||||
| chr17:51106102 | T | TAC | 15 | a0001c0001t0001g0132 a0001c0001t0001g0213 a0001c0001t0001g0233 others(12): Show |
15 | HG01167.hp2 HG01169.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.303+14250_303+1425 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACAC | 11 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0234 others(8): Show |
11 | HG00738.hp2 HG01257.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.303+14248_303+1425 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACAC | 26 | a0001c0001t0001g0153 a0001c0001t0001g0209 a0001c0001t0001g0210 others(23): Show |
26 | HG01074.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.303+14246_303+1425 others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0113 a0001c0001t0001g0203 a0001c0001t0001g0207 others(14): Show |
17 | HG00280.hp2 HG00323.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.303+14244_303+1425 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(3): Show |
10 | a0001c0001t0001g0150 a0001c0001t0001g0236 a0001c0001t0001g0241 others(7): Show |
10 | HG00621.hp1 HG01934.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+14242_303+1425 others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0208 others(1): Show |
4 | HG02897.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+14240_303+1425 others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(7): Show |
2 | a0001c0001t0001g0225 a0001c0001t0003g0206 |
2 | HG02071.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.303+14238_303+1425 others(18): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0226 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.303+14236_303+1425 others(20): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.303+14234_303+1425 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | T | TACACACA others(13): Show |
1 | a0001c0001t0001g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.303+14232_303+1425 others(24): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TAC | T | 57 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0057 others(54): Show |
57 | HG00558.hp1 HG00639.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.303+14250_303+1425 others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TACAC | T | 63 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0054 others(60): Show |
63 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.303+14248_303+1425 others(8): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TACACAC | T | 24 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0061 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.303+14246_303+1425 others(10): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TACACACA others(1): Show |
T | 19 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0002g0012 others(16): Show |
19 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.303+14244_303+1425 others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0237 a0001c0001t0006g0188 a0002c0003t0008g0173 others(4): Show |
7 | HG00741.hp1 HG00741.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+14242_303+1425 others(14): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106102 | TACACACA others(11): Show |
T | 2 | a0001c0002t0001g0281 a0001c0002t0001g0289 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.303+14234_303+1425 others(22): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106102 | |||||||
| chr17:51106158 | C | G | 1 | a0001c0001t0003g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.303+14196G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106158 | |||||||
| chr17:51106175 | C | A | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.303+14179G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106175 | |||||||
| chr17:51106201 | G | A | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.303+14153C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106201 | |||||||
| chr17:51106328 | A | T | 25 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+14026T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106328 | |||||||
| chr17:51106336 | T | G | 15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.303+14018A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106336 | |||||||
| chr17:51106442 | G | A | 2 | a0002c0003t0007g0114 a0002c0003t0007g0168 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+13912C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106442 | |||||||
| chr17:51106449 | T | C | 1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303+13905A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106449 | |||||||
| chr17:51106524 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.303+13830G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106524 | |||||||
| chr17:51106713 | C | G | 1 | a0001c0005t0001g0267 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.303+13641G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51106713 | |||||||
| chr17:51107086 | C | T | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.303+13268G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107086 | |||||||
| chr17:51107100 | C | CA | 7 | a0001c0001t0002g0017 a0001c0001t0002g0161 a0001c0001t0003g0049 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+13253dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107100 | |||||||
| chr17:51107100 | CA | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
11 | HG02896.hp2 HG02976.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.303+13253delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107100 | |||||||
| chr17:51107113 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.303+13241T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107113 | |||||||
| chr17:51107242 | A | C | 2 | a0001c0001t0004g0187 a0001c0001t0004g0190 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.303+13112T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107242 | |||||||
| chr17:51107364 | A | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0236 others(2): Show |
5 | NA18944.hp2 NA18948.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+12990T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107364 | |||||||
| chr17:51107405 | T | A | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.303+12949A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107405 | |||||||
| chr17:51107678 | A | G | 1 | a0001c0002t0001g0271 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.303+12676T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107678 | |||||||
| chr17:51107693 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.303+12661A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107693 | |||||||
| chr17:51107744 | TA | T | 75 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(72): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.303+12609delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107744 | |||||||
| chr17:51107814 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.303+12540G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51107814 | |||||||
| chr17:51108084 | G | GA | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
17 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.303+12269dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108084 | |||||||
| chr17:51108084 | GA | G | 8 | a0001c0001t0001g0178 a0001c0001t0001g0208 a0001c0001t0002g0076 others(5): Show |
8 | HG00558.hp1 HG01168.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+12269delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108084 | |||||||
| chr17:51108200 | A | C | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+12154T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108200 | |||||||
| chr17:51108373 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+11981G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108373 | |||||||
| chr17:51108386 | C | CA | 54 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0176 others(51): Show |
54 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+11967dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108386 | |||||||
| chr17:51108386 | CA | C | 43 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.303+11967delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108386 | |||||||
| chr17:51108386 | CAAA | C | 63 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.303+11965_303+1196 others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108386 | |||||||
| chr17:51108697 | A | G | 1 | a0001c0007t0001g0250 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.303+11657T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108697 | |||||||
| chr17:51108819 | T | C | 2 | a0001c0001t0004g0185 a0001c0001t0004g0193 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.303+11535A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108819 | |||||||
| chr17:51108837 | A | T | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+11517T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108837 | |||||||
| chr17:51108944 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+11410G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51108944 | |||||||
| chr17:51109174 | T | C | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+11180A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109174 | |||||||
| chr17:51109180 | C | A | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+11174G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109180 | |||||||
| chr17:51109308 | C | G | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+11046G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109308 | |||||||
| chr17:51109618 | T | A | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+10736A>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109618 | |||||||
| chr17:51109637 | TATA | T | 9 | a0001c0001t0001g0085 a0001c0001t0002g0078 a0001c0001t0002g0083 others(6): Show |
9 | HG00544.hp2 NA18947.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+10714_303+1071 others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109637 | |||||||
| chr17:51109732 | G | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+10622C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51109732 | |||||||
| chr17:51110049 | T | C | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.303+10305A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110049 | |||||||
| chr17:51110279 | G | A | 4 | a0002c0003t0010g0197 a0002c0003t0010g0198 a0002c0003t0010g0199 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+10075C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110279 | |||||||
| chr17:51110293 | A | C | 9 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+10061T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110293 | |||||||
| chr17:51110342 | C | T | 101 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(98): Show |
101 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.303+10012G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110342 | |||||||
| chr17:51110388 | C | CA | 22 | a0001c0001t0001g0065 a0001c0001t0001g0155 a0001c0001t0001g0230 others(19): Show |
22 | HG00621.hp2 HG00741.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.303+9965dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110388 | |||||||
| chr17:51110418 | T | C | 1 | a0001c0008t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.303+9936A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110418 | |||||||
| chr17:51110456 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.303+9898G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110456 | |||||||
| chr17:51110489 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.303+9865C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110489 | |||||||
| chr17:51110704 | T | C | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+9650A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110704 | |||||||
| chr17:51110886 | G | A | 1 | a0004c0006t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.303+9468C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110886 | |||||||
| chr17:51110902 | G | A | 35 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(32): Show |
35 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.303+9452C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110902 | |||||||
| chr17:51110960 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+9394G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51110960 | |||||||
| chr17:51111329 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.303+9025A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51111329 | |||||||
| chr17:51111366 | C | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0186 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.303+8988G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51111366 | |||||||
| chr17:51111593 | A | AT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.303+8760dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51111593 | |||||||
| chr17:51111703 | A | G | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+8651T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51111703 | |||||||
| chr17:51112042 | TA | T | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.303+8311delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112042 | |||||||
| chr17:51112047 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+8307T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112047 | |||||||
| chr17:51112051 | A | C | 22 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.303+8303T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112051 | |||||||
| chr17:51112095 | T | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.303+8259A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112095 | |||||||
| chr17:51112370 | C | CA | 23 | a0001c0001t0001g0178 a0001c0001t0001g0233 a0001c0001t0001g0234 others(20): Show |
23 | HG01243.hp2 HG01256.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+7983dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112370 | |||||||
| chr17:51112370 | C | CAA | 43 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(40): Show |
43 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+7982_303+7983d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112370 | |||||||
| chr17:51112370 | C | CAAA | 6 | a0001c0001t0001g0035 a0001c0001t0003g0036 a0001c0001t0003g0042 others(3): Show |
6 | HG02293.hp1 NA18944.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+7981_303+7983d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112370 | |||||||
| chr17:51112370 | CA | C | 6 | a0001c0001t0001g0052 a0001c0001t0022g0070 a0002c0003t0010g0197 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+7983delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112370 | |||||||
| chr17:51112431 | G | A | 22 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.303+7923C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112431 | |||||||
| chr17:51112543 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+7811G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112543 | |||||||
| chr17:51112647 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+7707G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112647 | |||||||
| chr17:51112671 | C | CA | 66 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(63): Show |
66 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.303+7682dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112671 | C | CAA | 23 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0062 others(20): Show |
23 | HG00140.hp2 HG01069.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.303+7681_303+7682d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112671 | C | CAAA | 32 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(29): Show |
32 | HG01433.hp2 HG01891.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.303+7680_303+7682d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112671 | C | CAAAA | 11 | a0001c0001t0003g0016 a0001c0001t0003g0037 a0001c0001t0003g0038 others(8): Show |
11 | HG00544.hp1 HG00609.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+7679_303+7682d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112671 | CA | C | 13 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0002g0079 others(10): Show |
13 | HG00323.hp2 HG00558.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.303+7682delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112671 | CAAAAAAA others(4): Show |
C | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+7672_303+7682d others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112671 | |||||||
| chr17:51112674 | A | C | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0146 |
3 | HG01106.hp2 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.303+7680T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112674 | |||||||
| chr17:51112738 | C | T | 2 | a0002c0004t0005g0006 a0002c0004t0005g0007 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.303+7616G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112738 | |||||||
| chr17:51112971 | G | GA | 78 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(75): Show |
78 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.303+7382dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112971 | |||||||
| chr17:51112975 | A | G | 1 | a0001c0001t0026g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.303+7379T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112975 | |||||||
| chr17:51112996 | GA | G | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+7357delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51112996 | |||||||
| chr17:51113026 | G | GA | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
17 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.303+7327dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113026 | |||||||
| chr17:51113353 | C | A | 1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303+7001G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113353 | |||||||
| chr17:51113353 | C | CA | 60 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+7000dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113353 | |||||||
| chr17:51113353 | CA | C | 77 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(74): Show |
77 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.303+7000delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113353 | |||||||
| chr17:51113353 | CAA | C | 25 | a0001c0001t0001g0251 a0001c0002t0001g0270 a0001c0002t0001g0271 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+6999_303+7000d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113353 | |||||||
| chr17:51113354 | A | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+7000T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113354 | |||||||
| chr17:51113368 | A | G | 3 | a0001c0001t0002g0078 a0001c0002t0001g0271 a0001c0002t0001g0290 |
3 | HG02970.hp1 NA19074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.303+6986T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113368 | |||||||
| chr17:51113388 | C | A | 144 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.303+6966G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113388 | |||||||
| chr17:51113486 | C | T | 5 | a0001c0002t0001g0270 a0001c0002t0001g0278 a0001c0002t0001g0279 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+6868G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113486 | |||||||
| chr17:51113510 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+6844A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113510 | |||||||
| chr17:51113679 | CA | C | 142 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(139): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.303+6674delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113679 | |||||||
| chr17:51113691 | A | C | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.303+6663T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113691 | |||||||
| chr17:51113926 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.303+6428G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51113926 | |||||||
| chr17:51114065 | C | T | 1 | a0001c0001t0003g0206 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.303+6289G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51114065 | |||||||
| chr17:51114709 | T | C | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+5645A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51114709 | |||||||
| chr17:51114809 | G | A | 11 | a0001c0001t0001g0194 a0001c0001t0004g0179 a0001c0001t0004g0181 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+5545C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51114809 | |||||||
| chr17:51114874 | C | T | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.303+5480G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51114874 | |||||||
| chr17:51114951 | C | CA | 23 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.303+5402dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51114951 | |||||||
| chr17:51115119 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0013 others(35): Show |
38 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.303+5235T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115119 | |||||||
| chr17:51115329 | C | T | 1 | a0001c0005t0001g0267 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.303+5025G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115329 | |||||||
| chr17:51115394 | G | A | 2 | a0002c0003t0011g0195 a0002c0003t0011g0196 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.303+4960C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115394 | |||||||
| chr17:51115416 | C | CT | 95 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(92): Show |
95 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.303+4937dupA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115416 | |||||||
| chr17:51115416 | CT | C | 40 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(37): Show |
40 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.303+4937delA | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115416 | |||||||
| chr17:51115491 | T | C | 47 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0068 others(44): Show |
47 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.303+4863A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115491 | |||||||
| chr17:51115601 | C | T | 1 | a0001c0001t0025g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.303+4753G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115601 | |||||||
| chr17:51115652 | GA | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0194 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+4701delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115652 | |||||||
| chr17:51115744 | T | G | 1 | a0001c0001t0022g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+4610A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115744 | |||||||
| chr17:51115753 | C | T | 5 | a0001c0001t0022g0070 a0002c0003t0010g0197 a0002c0003t0010g0198 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+4601G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115753 | |||||||
| chr17:51115833 | AAAAAG | A | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+4516_303+4520d others(7): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115833 | |||||||
| chr17:51115833 | AAAAAGAA others(3): Show |
A | 2 | a0001c0001t0002g0149 a0001c0007t0001g0250 |
2 | HG03239.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.303+4511_303+4520d others(12): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115833 | |||||||
| chr17:51115848 | GAAAAGAA others(4): Show |
G | 10 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
10 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+4495_303+4505d others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115848 | |||||||
| chr17:51115965 | A | C | 69 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(66): Show |
69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.303+4389T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51115965 | |||||||
| chr17:51116035 | GTTTCTTT others(4): Show |
G | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+4308_303+4318d others(13): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116035 | |||||||
| chr17:51116101 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.303+4253T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116101 | |||||||
| chr17:51116139 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+4215C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116139 | |||||||
| chr17:51116253 | C | T | 1 | a0002c0003t0007g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.303+4101G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116253 | |||||||
| chr17:51116642 | T | C | 1 | a0002c0004t0016g0002 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+3712A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116642 | |||||||
| chr17:51116974 | G | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+3380C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51116974 | |||||||
| chr17:51117206 | T | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+3148A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117206 | |||||||
| chr17:51117434 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+2920G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117434 | |||||||
| chr17:51117708 | C | CA | 44 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(41): Show |
44 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.303+2645dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117708 | |||||||
| chr17:51117708 | C | CAA | 25 | a0001c0001t0001g0194 a0001c0001t0004g0191 a0001c0001t0004g0192 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+2644_303+2645d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117708 | |||||||
| chr17:51117708 | C | CAAA | 10 | a0001c0002t0001g0290 a0001c0002t0004g0291 a0002c0004t0005g0001 others(7): Show |
10 | HG01168.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+2643_303+2645d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117708 | |||||||
| chr17:51117708 | CA | C | 60 | a0001c0001t0001g0075 a0001c0001t0001g0203 a0001c0001t0001g0205 others(57): Show |
60 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.303+2645delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117708 | |||||||
| chr17:51117708 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.303+2632_303+2645d others(16): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117708 | |||||||
| chr17:51117811 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.303+2543T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51117811 | |||||||
| chr17:51118041 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.303+2313C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118041 | |||||||
| chr17:51118133 | C | CAA | 9 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(6): Show |
9 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+2219_303+2220d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118133 | |||||||
| chr17:51118152 | A | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0003g0015 others(1): Show |
4 | HG00544.hp1 HG03831.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+2202T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118152 | |||||||
| chr17:51118255 | A | C | 1 | a0002c0003t0011g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.303+2099T>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118255 | |||||||
| chr17:51118287 | A | T | 1 | a0002c0003t0021g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.303+2067T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118287 | |||||||
| chr17:51118351 | C | G | 1 | a0002c0003t0008g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303+2003G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118351 | |||||||
| chr17:51118957 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.303+1397G>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51118957 | |||||||
| chr17:51119012 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.303+1342G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119012 | |||||||
| chr17:51119030 | T | G | 1 | a0001c0001t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.303+1324A>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119030 | |||||||
| chr17:51119033 | C | CA | 49 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(46): Show |
49 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.303+1320dupT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119033 | C | CAA | 7 | a0001c0001t0001g0203 a0002c0003t0010g0197 a0002c0003t0010g0198 others(4): Show |
7 | HG01516.hp2 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1319_303+1320d others(4): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119033 | C | CAAA | 60 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(57): Show |
60 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.303+1318_303+1320d others(5): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119033 | C | CAAAA | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG01175.hp2 HG01358.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+1317_303+1320d others(6): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119033 | CA | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00280.hp1 HG01175.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+1320delT | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119033 | CAAAAAAA others(2): Show |
C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0002g0013 others(35): Show |
38 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.303+1312_303+1320d others(11): Show |
SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119033 | |||||||
| chr17:51119049 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.303+1305T>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119049 | |||||||
| chr17:51119096 | T | C | 1 | a0001c0001t0003g0268 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.303+1258A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119096 | |||||||
| chr17:51119203 | A | T | 1 | a0002c0004t0005g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303+1151T>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119203 | |||||||
| chr17:51119509 | T | C | 66 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(63): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.303+845A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119509 | |||||||
| chr17:51119511 | G | C | 1 | a0001c0001t0004g0202 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.303+843C>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119511 | |||||||
| chr17:51119524 | C | G | 22 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.303+830G>C | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119524 | |||||||
| chr17:51119557 | T | C | 99 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0207 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.303+797A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119557 | |||||||
| chr17:51119743 | C | T | 10 | a0002c0004t0005g0001 a0002c0004t0005g0003 a0002c0004t0005g0004 others(7): Show |
10 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+611G>A | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119743 | |||||||
| chr17:51119816 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.303+538A>G | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51119816 | |||||||
| chr17:51120071 | G | A | 23 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+283C>T | SPAG9 | ENSG00000008294.22 | transcript | ENST00000262013.12 | protein_coding | 1/29 | chr17 | 51120071 |