Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6674 |
|---|---|
| ensemblid | ENSG00000104450.13 |
| hgncid | 11212 |
| symbol | SPAG1 |
| name | sperm associated antigen 1 |
| refseq_nuc | NM_003114.5 |
| refseq_prot | NP_003105.2 |
| ensembl_nuc | ENST00000388798.7 |
| ensembl_prot | ENSP00000373450.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 100158587 |
| end | 100241904 |
| strand | + |
| ver | v1.2 |
| region | chr8:100158587-100241904 |
| region5000 | chr8:100153587-100246904 |
| regionname0 | SPAG1_chr8_100158587_100241904 |
| regionname5000 | SPAG1_chr8_100153587_100246904 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 926 | 160 | 47 | 33 | 59 | 6 | 14 | 42 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002 | 1/0 | 926 | 130 | 27 | 17 | 67 | 1 | 17 | 53 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003 | 0/0 | 927 | 36 | 5 | 15 | 0 | 7 | 9 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0004 | 0/0 | 927 | 20 | 0 | 1 | 19 | 0 | 0 | 17 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0005 | 0/0 | 926 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0006 | 0/0 | 926 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0007 | 0/0 | 926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0008 | 0/0 | 926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0009 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0010 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0011 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0012 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0013 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0014 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0015 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2781 | 93 | 17 | 14 | 51 | 1 | 9 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0002 | 0/1 | 2781 | 91 | 1 | 22 | 52 | 4 | 11 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0003 | 0/0 | 2781 | 37 | 30 | 7 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0004 | 0/0 | 2784 | 35 | 5 | 15 | 0 | 7 | 8 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0005 | 0/0 | 2781 | 22 | 0 | 2 | 16 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0006 | 0/0 | 2784 | 20 | 0 | 1 | 19 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0007 | 0/0 | 2781 | 15 | 10 | 1 | 0 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0008 | 0/0 | 2781 | 14 | 14 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0009 | 0/0 | 2781 | 11 | 1 | 4 | 2 | 1 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0010 | 0/0 | 2781 | 6 | 0 | 0 | 6 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0011 | 0/0 | 2781 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0012 | 0/0 | 2781 | 2 | 1 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0013 | 0/0 | 2781 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0014 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0015 | 0/0 | 2781 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0016 | 0/0 | 2781 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0017 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0018 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0019 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0020 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0021 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0022 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0023 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0024 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| c0025 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 915 | 304 | 57 | 60 | 136 | 14 | 35 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0002 | 0/0 | 918 | 40 | 18 | 2 | 15 | 0 | 5 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0003 | 0/0 | 915 | 14 | 11 | 3 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0004 | 0/0 | 915 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0005 | 0/0 | 915 | 2 | 1 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0006 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0007 | 0/0 | 915 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| t0008 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 2781 | 91 | 1 | 22 | 52 | 4 | 11 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0003 | 0/0 | 2781 | 37 | 30 | 7 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0008 | 0/0 | 2781 | 14 | 14 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0009 | 0/0 | 2781 | 11 | 1 | 4 | 2 | 1 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0012 | 0/0 | 2781 | 2 | 1 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0015 | 0/0 | 2781 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0016 | 0/0 | 2781 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0021 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0001 | 1/0 | 2781 | 93 | 17 | 14 | 51 | 1 | 9 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0005 | 0/0 | 2781 | 22 | 0 | 2 | 16 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0007 | 0/0 | 2781 | 15 | 10 | 1 | 0 | 0 | 4 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003c0004 | 0/0 | 2784 | 35 | 5 | 15 | 0 | 7 | 8 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003c0018 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0004c0006 | 0/0 | 2784 | 20 | 0 | 1 | 19 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0005c0010 | 0/0 | 2781 | 6 | 0 | 0 | 6 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0006c0011 | 0/0 | 2781 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0007c0013 | 0/0 | 2781 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0008c0014 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0009c0017 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0010c0023 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0011c0022 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0012c0020 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0013c0019 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0014c0024 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0015c0025 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3695 | 90 | 1 | 21 | 52 | 4 | 11 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0002t0007 | 0/0 | 3695 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0003t0001 | 0/0 | 3695 | 22 | 19 | 3 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0003t0003 | 0/0 | 3695 | 14 | 11 | 3 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0003t0005 | 0/0 | 3695 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0008t0002 | 0/0 | 3698 | 13 | 13 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0008t0008 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0009t0001 | 0/0 | 3695 | 11 | 1 | 4 | 2 | 1 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0012t0001 | 0/0 | 3695 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0012t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0015t0001 | 0/0 | 3695 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0016t0001 | 0/0 | 3695 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0001c0021t0001 | 0/0 | 3695 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0001t0001 | 1/0 | 3695 | 88 | 15 | 13 | 49 | 1 | 9 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0001t0002 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0001t0004 | 0/0 | 3695 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0001t0006 | 0/0 | 3695 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0005t0001 | 0/0 | 3695 | 3 | 0 | 0 | 2 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0005t0002 | 0/0 | 3698 | 19 | 0 | 2 | 14 | 0 | 3 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0007t0001 | 0/0 | 3695 | 13 | 10 | 1 | 0 | 0 | 2 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0002c0007t0002 | 0/0 | 3698 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003c0004t0001 | 0/0 | 3698 | 34 | 4 | 15 | 0 | 7 | 8 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003c0004t0005 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0003c0018t0001 | 0/0 | 3698 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0004c0006t0001 | 0/0 | 3698 | 20 | 0 | 1 | 19 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0005c0010t0001 | 0/0 | 3695 | 6 | 0 | 0 | 6 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0006c0011t0002 | 0/0 | 3698 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0007c0013t0001 | 0/0 | 3695 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0008c0014t0001 | 0/0 | 3695 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0009c0017t0001 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0010c0023t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0011c0022t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0012c0020t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0013c0019t0001 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0014c0024t0002 | 0/0 | 3698 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| a0015c0025t0001 | 0/0 | 3695 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | copy fasta | chr8 | 100153587 | 100246904 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0002t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0003t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0008t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0009t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0012t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0012t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0015t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0015t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0016t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0016t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0001c0021t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0005t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0002c0007t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0004t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0003c0018t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0004c0006t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0005c0010t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0006c0011t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0006c0011t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0007c0013t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0007c0013t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0008c0014t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0008c0014t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0009c0017t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0010c0023t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0011c0022t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0012c0020t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0013c0019t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0014c0024t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| a0015c0025t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0031 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0045 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0178 | EUR | GBR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0282 | EUR | FIN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0042 | EUR | FIN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0321 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00423 | hp1 | a0013 | c0019 | t0001 | g0047 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0337 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00438 | hp2 | a0004 | c0006 | t0001 | g0060 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0328 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0342 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0330 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00621 | hp2 | a0001 | c0021 | t0001 | g0157 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0334 | EAS | CHS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0274 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0102 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0081 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0104 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0275 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01071 | hp1 | a0003 | c0004 | t0001 | g0071 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0272 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01074 | hp1 | a0003 | c0004 | t0001 | g0069 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01081 | hp1 | a0002 | c0005 | t0002 | g0233 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0082 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01099 | hp2 | a0001 | c0003 | t0005 | g0296 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01167 | hp1 | a0002 | c0007 | t0001 | g0197 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01168 | hp1 | a0007 | c0013 | t0001 | g0134 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0344 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01169 | hp2 | a0007 | c0013 | t0001 | g0101 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01175 | hp1 | a0001 | c0002 | t0007 | g0187 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0096 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0250 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0115 | AMR | PUR | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01255 | hp1 | a0003 | c0004 | t0001 | g0027 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01255 | hp2 | a0002 | c0001 | t0004 | g0276 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0269 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0050 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0049 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0024 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0063 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0299 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01346 | hp2 | a0003 | c0004 | t0001 | g0040 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0270 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01361 | hp1 | a0003 | c0004 | t0001 | g0043 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01496 | hp1 | a0001 | c0009 | t0001 | g0005 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01516 | hp1 | a0003 | c0004 | t0001 | g0073 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01516 | hp2 | a0001 | c0012 | t0001 | g0174 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01517 | hp1 | a0003 | c0004 | t0001 | g0072 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0352 | EUR | IBS | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0216 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0264 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0201 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0221 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01934 | hp2 | a0003 | c0004 | t0001 | g0068 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01943 | hp1 | a0004 | c0006 | t0001 | g0039 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01978 | hp1 | a0001 | c0009 | t0001 | g0291 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0026 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0333 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0349 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02004 | hp2 | a0001 | c0009 | t0001 | g0288 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0307 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0324 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02056 | hp1 | a0004 | c0006 | t0001 | g0074 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0305 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0340 | EAS | KHV | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02145 | hp1 | a0012 | c0020 | t0001 | g0251 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02148 | hp1 | a0002 | c0005 | t0002 | g0235 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0294 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0335 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0290 | EAS | CDX | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02257 | hp1 | a0001 | c0008 | t0002 | g0243 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0289 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02258 | hp2 | a0002 | c0007 | t0001 | g0196 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02273 | hp1 | a0003 | c0004 | t0001 | g0028 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02280 | hp2 | a0006 | c0011 | t0002 | g0003 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0262 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02451 | hp2 | a0002 | c0007 | t0001 | g0135 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02572 | hp1 | a0002 | c0007 | t0001 | g0190 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02572 | hp2 | a0008 | c0014 | t0001 | g0257 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0112 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0023 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02630 | hp1 | a0014 | c0024 | t0002 | g0131 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0285 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02647 | hp1 | a0002 | c0007 | t0001 | g0202 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02647 | hp2 | a0001 | c0008 | t0002 | g0091 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02683 | hp1 | a0002 | c0007 | t0002 | g0180 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02683 | hp2 | a0003 | c0004 | t0001 | g0061 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0355 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0287 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02717 | hp1 | a0002 | c0001 | t0004 | g0281 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02717 | hp2 | a0010 | c0023 | t0001 | g0080 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0108 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0357 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02735 | hp1 | a0002 | c0005 | t0002 | g0232 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0356 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0358 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0103 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0279 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02818 | hp2 | a0002 | c0007 | t0001 | g0195 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0300 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0032 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02895 | hp1 | a0015 | c0025 | t0001 | g0263 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02895 | hp2 | a0001 | c0008 | t0002 | g0092 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02897 | hp1 | a0001 | c0008 | t0002 | g0090 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02897 | hp2 | a0006 | c0011 | t0002 | g0252 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0267 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02922 | hp2 | a0006 | c0011 | t0002 | g0003 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0359 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0111 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0295 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03017 | hp2 | a0003 | c0004 | t0001 | g0051 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03041 | hp1 | a0001 | c0008 | t0002 | g0217 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0105 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03130 | hp2 | a0002 | c0001 | t0001 | g0265 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03139 | hp1 | a0002 | c0007 | t0001 | g0192 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03139 | hp2 | a0009 | c0017 | t0001 | g0249 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03195 | hp1 | a0002 | c0007 | t0001 | g0193 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0109 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0200 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03209 | hp2 | a0002 | c0007 | t0001 | g0106 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03225 | hp1 | a0001 | c0008 | t0002 | g0245 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03225 | hp2 | a0001 | c0012 | t0002 | g0116 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03239 | hp1 | a0002 | c0005 | t0002 | g0240 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03239 | hp2 | a0002 | c0007 | t0001 | g0150 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03486 | hp2 | a0001 | c0008 | t0002 | g0247 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0093 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0286 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03491 | hp1 | a0003 | c0004 | t0001 | g0030 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0094 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0110 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03516 | hp2 | a0001 | c0008 | t0002 | g0219 | AFR | ESN | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03540 | hp2 | a0011 | c0022 | t0001 | g0177 | AFR | GWD | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0284 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03579 | hp2 | a0001 | c0008 | t0002 | g0241 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03654 | hp1 | a0003 | c0018 | t0001 | g0062 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0303 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03710 | hp2 | a0001 | c0009 | t0001 | g0278 | SAS | PJL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0185 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03831 | hp2 | a0003 | c0004 | t0001 | g0053 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03834 | hp2 | a0002 | c0005 | t0002 | g0220 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0298 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03927 | hp2 | a0002 | c0007 | t0002 | g0179 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03942 | hp1 | a0002 | c0005 | t0001 | g0237 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03942 | hp2 | a0003 | c0004 | t0001 | g0055 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0280 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04115 | hp2 | a0003 | c0004 | t0001 | g0041 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0222 | SAS | BEB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0022 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0338 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04228 | hp1 | a0002 | c0007 | t0001 | g0206 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG04228 | hp2 | a0003 | c0004 | t0001 | g0052 | SAS | STU | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | CHB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | CHB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0113 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18943 | hp1 | a0004 | c0006 | t0001 | g0046 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0313 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18944 | hp2 | a0002 | c0005 | t0002 | g0238 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18946 | hp1 | a0005 | c0010 | t0001 | g0145 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18946 | hp2 | a0002 | c0005 | t0002 | g0248 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18947 | hp1 | a0001 | c0016 | t0001 | g0348 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0326 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18949 | hp2 | a0002 | c0005 | t0002 | g0089 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18951 | hp2 | a0004 | c0006 | t0001 | g0035 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18952 | hp2 | a0004 | c0006 | t0001 | g0067 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0268 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18953 | hp2 | a0005 | c0010 | t0001 | g0141 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18954 | hp2 | a0004 | c0006 | t0001 | g0038 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18957 | hp1 | a0001 | c0015 | t0001 | g0228 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18961 | hp1 | a0002 | c0001 | t0006 | g0097 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18961 | hp2 | a0005 | c0010 | t0001 | g0212 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18962 | hp2 | a0004 | c0006 | t0001 | g0033 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0332 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18965 | hp2 | a0002 | c0005 | t0002 | g0239 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18966 | hp2 | a0002 | c0005 | t0002 | g0223 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18968 | hp1 | a0002 | c0005 | t0001 | g0229 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0302 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0318 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18969 | hp2 | a0002 | c0005 | t0002 | g0231 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18971 | hp1 | a0001 | c0015 | t0001 | g0224 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0309 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18975 | hp1 | a0005 | c0010 | t0001 | g0146 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18975 | hp2 | a0002 | c0005 | t0002 | g0226 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0331 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0297 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0336 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18983 | hp2 | a0002 | c0005 | t0002 | g0234 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0320 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0346 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18985 | hp2 | a0002 | c0005 | t0002 | g0354 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18988 | hp1 | a0002 | c0005 | t0002 | g0253 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18992 | hp1 | a0004 | c0006 | t0001 | g0059 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18995 | hp2 | a0002 | c0005 | t0002 | g0242 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18997 | hp1 | a0004 | c0006 | t0001 | g0058 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18997 | hp2 | a0001 | c0009 | t0001 | g0312 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0339 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18999 | hp1 | a0004 | c0006 | t0001 | g0036 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19001 | hp1 | a0002 | c0005 | t0002 | g0230 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0323 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19002 | hp2 | a0004 | c0006 | t0001 | g0034 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0308 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19003 | hp2 | a0004 | c0006 | t0001 | g0037 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19007 | hp1 | a0001 | c0009 | t0001 | g0329 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0261 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19030 | hp1 | a0001 | c0008 | t0008 | g0246 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0114 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19043 | hp2 | a0001 | c0008 | t0002 | g0004 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19054 | hp1 | a0002 | c0005 | t0002 | g0227 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19054 | hp2 | a0005 | c0010 | t0001 | g0199 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0322 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19062 | hp2 | a0004 | c0006 | t0001 | g0057 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19063 | hp2 | a0004 | c0006 | t0001 | g0070 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0316 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19068 | hp2 | a0004 | c0006 | t0001 | g0066 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19070 | hp1 | a0004 | c0006 | t0001 | g0064 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19070 | hp2 | a0005 | c0010 | t0001 | g0156 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0360 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19076 | hp1 | a0002 | c0001 | t0001 | g0325 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0304 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19079 | hp1 | a0001 | c0016 | t0001 | g0350 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0314 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0319 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19085 | hp1 | a0002 | c0005 | t0002 | g0225 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19086 | hp1 | a0002 | c0005 | t0001 | g0236 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19088 | hp1 | a0004 | c0006 | t0001 | g0065 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19091 | hp1 | a0002 | c0001 | t0002 | g0341 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19091 | hp2 | a0004 | c0006 | t0001 | g0343 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | YRI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20129 | hp1 | a0001 | c0008 | t0002 | g0218 | AFR | ASW | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0345 | AFR | ASW | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20752 | hp1 | a0001 | c0009 | t0001 | g0005 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0054 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20805 | hp2 | a0003 | c0004 | t0001 | g0056 | EUR | TSI | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01123 | hp1 | a0001 | c0009 | t0001 | g0271 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02109 | hp1 | a0001 | c0008 | t0002 | g0004 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0044 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0191 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02486 | hp2 | a0008 | c0014 | t0001 | g0256 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| HG03471 | hp2 | a0003 | c0004 | t0005 | g0254 | AFR | MSL | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18955 | hp1 | a0004 | c0006 | t0001 | g0048 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20300 | hp1 | a0002 | c0007 | t0001 | g0194 | AFR | USA | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0029 | AFR | USA | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA21309 | hp1 | a0001 | c0008 | t0002 | g0244 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| NA21309 | hp2 | a0002 | c0001 | t0004 | g0277 | AFR | LWK | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0154 | REF | REF | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0273 | REF | REF | SPAG1_chr8_100153587_100246904 | SPAG1 | chr8 | 100153587 | 100246904 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100177913
|
G | A | 1 | a0009 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.398G>A | p.Gly133Asp | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/19 | 430/3695 | 398/2781 | 133/926 | chr8 | 100177913 | ||
| chr8:100183424
|
C | T | 1 | a0015 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.476C>T | p.Ala159Val | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/19 | 508/3695 | 476/2781 | 159/926 | chr8 | 100183424 | ||
| chr8:100184027
|
A | C | 1 | a0014 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.560A>C | p.His187Pro | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/19 | 592/3695 | 560/2781 | 187/926 | chr8 | 100184027 | ||
| chr8:100184628
|
G | C | 1 | a0006 | 3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
missense_variant&splice_region_variant | MODERATE | c.596G>C | p.Gly199Ala | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/19 | 628/3695 | 596/2781 | 199/926 | chr8 | 100184628 | ||
| chr8:100191434
|
C | T | 1 | a0008 | 2 | HG02486.hp2 HG02572.hp2 |
missense_variant | MODERATE | c.877C>T | p.Arg293Trp | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/19 | 909/3695 | 877/2781 | 293/926 | chr8 | 100191434 | ||
| chr8:100194163
|
G | A | 4 | a0003a0004a0009others(1): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
missense_variant | MODERATE | c.991G>A | p.Glu331Lys | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1023/3695 | 991/2781 | 331/926 | chr8 | 100194163 | ||
| chr8:100194229
|
A | G | 1 | a0013 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1057A>G | p.Lys353Glu | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1089/3695 | 1057/2781 | 353/926 | chr8 | 100194229 | ||
| chr8:100194231
|
A | AGAC | 4 | a0003a0004a0009others(1): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
conservative_inframe_insertion | MODERATE | c.1059_1060insGAC | p.Lys353_Ser354insAs others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/19 | 1092/3695 | 1060/2781 | 354/926 | chr8 | 100194231 | ||
| chr8:100213219
|
C | G | 1 | a0010 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1226C>G | p.Thr409Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/19 | 1258/3695 | 1226/2781 | 409/926 | chr8 | 100213219 | ||
| chr8:100220329
|
T | C | 2 | a0010a0012 | 2 | HG02145.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1586T>C | p.Met529Thr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/19 | 1618/3695 | 1586/2781 | 529/926 | chr8 | 100220329 | ||
| chr8:100225243
|
C | T | 1 | a0005 | 6 | NA18946.hp1 NA18953.hp2 NA18961.hp2 others(3): Show |
missense_variant | MODERATE | c.1759C>T | p.Pro587Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/19 | 1791/3695 | 1759/2781 | 587/926 | chr8 | 100225243 | ||
| chr8:100240452
|
T | C | 11 | a0001a0003a0005others(8): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
missense_variant | MODERATE | c.2330T>C | p.Met777Thr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2362/3695 | 2330/2781 | 777/926 | chr8 | 100240452 | ||
| chr8:100240601
|
C | T | 1 | a0011 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2479C>T | p.His827Tyr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2511/3695 | 2479/2781 | 827/926 | chr8 | 100240601 | ||
| chr8:100240958
|
A | G | 1 | a0007 | 2 | HG01168.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.2717A>G | p.Asp906Gly | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 2749/3695 | 2717/2781 | 906/926 | chr8 | 100240958 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100183422
|
C | T | 1 | a0001c0016 | 2 | NA18947.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.474C>T | p.Tyr158Tyr | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/19 | 506/3695 | 474/2781 | 158/926 | chr8 | 100183422 | ||
| chr8:100184701
|
A | G | 3 | a0001c0008a0001c0015a0002c0005 | 38 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(35): Show |
synonymous_variant | LOW | c.669A>G | p.Gly223Gly | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/19 | 701/3695 | 669/2781 | 223/926 | chr8 | 100184701 | ||
| chr8:100213331
|
C | G | 9 | a0001c0002a0001c0012a0001c0016others(6): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
synonymous_variant | LOW | c.1338C>G | p.Ala446Ala | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/19 | 1370/3695 | 1338/2781 | 446/926 | chr8 | 100213331 | ||
| chr8:100240579
|
G | A | 1 | a0001c0021 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.2457G>A | p.Arg819Arg | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/19 | 2489/3695 | 2457/2781 | 819/926 | chr8 | 100240579 | ||
| chr8:100240956
|
G | A | 7 | a0001c0002a0001c0009a0001c0015others(4): Show | 114 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(111): Show |
synonymous_variant | LOW | c.2715G>A | p.Ser905Ser | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 2747/3695 | 2715/2781 | 905/926 | chr8 | 100240956 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100158594
|
G | T | 1 | a0001c0008t0008 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/19 | chr8 | 100158594 | ||||||
| chr8:100158601
|
G | C | 1 | a0002c0001t0006 | 1 | NA18961.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/19 | 3680 | chr8 | 100158601 | |||||
| chr8:100241146
|
C | G | 1 | a0002c0001t0004 | 3 | HG01255.hp2 HG02717.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 124 | chr8 | 100241146 | |||||
| chr8:100241241
|
T | C | 1 | a0001c0003t0003 | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 219 | chr8 | 100241241 | |||||
| chr8:100241314
|
G | T | 2 | a0001c0003t0005a0003c0004t0005 | 2 | HG01099.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 292 | chr8 | 100241314 | |||||
| chr8:100241772
|
T | TCCC | 8 | a0001c0008t0002a0001c0008t0008a0001c0012t0002others(5): Show | 41 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*755dupCCC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 756 | INFO_REALIGN_3_PRIME | chr8 | 100241772 | ||||
| chr8:100241796
|
C | G | 1 | a0001c0002t0007 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 19/19 | 774 | chr8 | 100241796 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:100158692
|
T | C | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+76T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158692 | ||||||
| chr8:100158754
|
G | T | 1 | a0002c0001t0001g0360 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-3+138G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158754 | ||||||
| chr8:100158828
|
A | G | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-3+212A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100158828 | ||||||
| chr8:100158971
|
C | CA | 15 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(12): Show | 15 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+371dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | |||||
| chr8:100158971
|
C | CAA | 64 | a0001c0003t0001g0075a0001c0003t0001g0076a0001c0003t0001g0077others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-3+370_-3+371dupAA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | |||||
| chr8:100158971
|
C | CAAA | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+369_-3+371dupAA others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | |||||
| chr8:100158971
|
CA | C | 11 | a0001c0002t0001g0346a0001c0002t0001g0347a0001c0002t0001g0349others(8): Show | 11 | HG00609.hp1 HG01517.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+371delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100158971 | |||||
| chr8:100159010
|
T | C | 259 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-3+394T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100159010 | ||||||
| chr8:100159781
|
T | C | 4 | a0001c0003t0001g0255a0001c0003t0001g0258a0008c0014t0001g0256others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1165T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100159781 | ||||||
| chr8:100160027
|
G | A | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-3+1411G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160027 | ||||||
| chr8:100160041
|
G | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1425G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160041 | ||||||
| chr8:100160166
|
C | G | 1 | a0003c0004t0005g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+1550C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160166 | ||||||
| chr8:100160203
|
G | C | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1587G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160203 | ||||||
| chr8:100160626
|
C | CA | 178 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(175): Show | 182 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-2-1636dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 100160626 | |||||
| chr8:100160674
|
A | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1605A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160674 | ||||||
| chr8:100160715
|
G | C | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2-1564G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100160715 | ||||||
| chr8:100161023
|
C | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1256C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161023 | ||||||
| chr8:100161150
|
G | A | 3 | a0001c0008t0002g0217a0001c0008t0002g0218a0001c0008t0002g0219 | 3 | HG03041.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-1129G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161150 | ||||||
| chr8:100161214
|
C | T | 9 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0205others(6): Show | 9 | HG00639.hp2 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-1065C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161214 | ||||||
| chr8:100161232
|
T | C | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1047T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161232 | ||||||
| chr8:100161480
|
C | T | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-799C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161480 | ||||||
| chr8:100161568
|
A | G | 1 | a0001c0009t0001g0345 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-711A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161568 | ||||||
| chr8:100161646
|
A | G | 2 | a0002c0001t0001g0006a0002c0001t0001g0344 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-2-633A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161646 | ||||||
| chr8:100161678
|
C | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-601C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161678 | ||||||
| chr8:100161686
|
A | G | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-593A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161686 | ||||||
| chr8:100161861
|
T | G | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-2-418T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161861 | ||||||
| chr8:100161903
|
T | G | 1 | a0002c0001t0001g0261 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2-376T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161903 | ||||||
| chr8:100161958
|
A | C | 249 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-2-321A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100161958 | ||||||
| chr8:100162115
|
G | T | 1 | a0001c0003t0003g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-164G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162115 | ||||||
| chr8:100162131
|
C | A | 1 | a0002c0001t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-148C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162131 | ||||||
| chr8:100162160
|
C | T | 39 | a0001c0009t0001g0312a0001c0009t0001g0329a0002c0001t0001g0261others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2-119C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162160 | ||||||
| chr8:100162198
|
G | A | 105 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(102): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-2-81G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162198 | ||||||
| chr8:100162243
|
A | G | 1 | a0002c0001t0001g0342 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-2-36A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 1/18 | chr8 | 100162243 | ||||||
| chr8:100162629
|
G | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+209G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162629 | ||||||
| chr8:100162715
|
C | T | 64 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.140+295C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162715 | ||||||
| chr8:100162869
|
T | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+449T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162869 | ||||||
| chr8:100162975
|
TA | T | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+563delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 100162975 | |||||
| chr8:100162985
|
A | T | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140+565A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100162985 | ||||||
| chr8:100163075
|
C | T | 1 | a0003c0004t0001g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140+655C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163075 | ||||||
| chr8:100163160
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.140+740G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163160 | ||||||
| chr8:100163202
|
G | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+782G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163202 | ||||||
| chr8:100163407
|
CT | C | 7 | a0001c0002t0001g0083a0001c0002t0001g0099a0001c0002t0001g0100others(4): Show | 7 | HG00099.hp2 HG01169.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+1002delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 100163407 | |||||
| chr8:100163573
|
G | A | 4 | a0001c0003t0001g0266a0002c0001t0001g0264a0002c0001t0001g0265others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+1153G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163573 | ||||||
| chr8:100163637
|
C | G | 1 | a0001c0003t0003g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140+1217C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163637 | ||||||
| chr8:100163669
|
C | T | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1249C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163669 | ||||||
| chr8:100163990
|
T | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1570T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100163990 | ||||||
| chr8:100164003
|
A | G | 135 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(132): Show | 137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.140+1583A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164003 | ||||||
| chr8:100164012
|
A | T | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1592A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164012 | ||||||
| chr8:100164051
|
T | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1631T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164051 | ||||||
| chr8:100164078
|
C | G | 1 | a0001c0003t0003g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.140+1658C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164078 | ||||||
| chr8:100164321
|
A | T | 1 | a0005c0010t0001g0199 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141-1493A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164321 | ||||||
| chr8:100164356
|
T | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1458T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164356 | ||||||
| chr8:100164421
|
T | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1393T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164421 | ||||||
| chr8:100164477
|
T | C | 4 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1337T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164477 | ||||||
| chr8:100164956
|
T | C | 3 | a0002c0001t0001g0221a0006c0011t0002g0003a0006c0011t0002g0252 | 4 | HG01891.hp2 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-858T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100164956 | ||||||
| chr8:100165220
|
A | G | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-594A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165220 | ||||||
| chr8:100165368
|
T | C | 1 | a0002c0007t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141-446T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165368 | ||||||
| chr8:100165486
|
G | T | 1 | a0001c0002t0001g0353 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.141-328G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165486 | ||||||
| chr8:100165529
|
C | A | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.141-285C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165529 | ||||||
| chr8:100165538
|
C | T | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.141-276C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165538 | ||||||
| chr8:100165766
|
G | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.141-48G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 2/18 | chr8 | 100165766 | ||||||
| chr8:100166152
|
G | A | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+179G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166152 | ||||||
| chr8:100166174
|
A | G | 1 | a0001c0002t0001g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.300+201A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166174 | ||||||
| chr8:100166175
|
T | C | 4 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0009others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+202T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166175 | ||||||
| chr8:100166177
|
A | G | 142 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.300+204A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166177 | ||||||
| chr8:100166284
|
A | G | 6 | a0002c0001t0001g0011a0002c0001t0001g0012a0002c0001t0001g0013others(3): Show | 6 | NA18612.hp2 NA18950.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+311A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166284 | ||||||
| chr8:100166487
|
C | T | 8 | a0002c0007t0001g0190a0002c0007t0001g0191a0002c0007t0001g0192others(5): Show | 8 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+514C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166487 | ||||||
| chr8:100166568
|
T | A | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.300+595T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166568 | ||||||
| chr8:100166645
|
C | T | 1 | a0002c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+672C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166645 | ||||||
| chr8:100166665
|
T | C | 16 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(13): Show | 16 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.300+692T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166665 | ||||||
| chr8:100166787
|
A | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.300+814A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166787 | ||||||
| chr8:100166936
|
A | C | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+963A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100166936 | ||||||
| chr8:100167182
|
A | G | 1 | a0002c0005t0002g0248 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.300+1209A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100167182 | ||||||
| chr8:100167495
|
T | C | 1 | a0002c0005t0002g0223 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.300+1522T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100167495 | ||||||
| chr8:100168020
|
A | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.300+2047A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168020 | ||||||
| chr8:100168040
|
A | C | 67 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.300+2067A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168040 | ||||||
| chr8:100168115
|
T | C | 1 | a0002c0001t0001g0267 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.300+2142T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168115 | ||||||
| chr8:100168360
|
G | A | 1 | a0001c0012t0002g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300+2387G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168360 | ||||||
| chr8:100168362
|
TA | T | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+2398delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168362 | |||||
| chr8:100168422
|
G | A | 64 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.300+2449G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168422 | ||||||
| chr8:100168430
|
T | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2457T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168430 | ||||||
| chr8:100168559
|
A | AT | 20 | a0001c0003t0001g0266a0001c0009t0001g0298a0002c0001t0001g0093others(17): Show | 20 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.300+2599dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168559 | |||||
| chr8:100168559
|
AT | A | 17 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0117others(14): Show | 18 | HG02055.hp1 HG02080.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+2599delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168559 | |||||
| chr8:100168610
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2637G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168610 | ||||||
| chr8:100168647
|
A | AAGT | 67 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.300+2676_300+2678d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168647 | |||||
| chr8:100168687
|
C | CTTTTTTT others(7): Show |
5 | a0001c0002t0001g0099a0001c0002t0001g0127a0001c0002t0001g0128others(2): Show | 5 | HG01168.hp2 HG01943.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(8): Show |
96 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(93): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(17): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(9): Show |
31 | a0001c0002t0001g0098a0001c0002t0001g0124a0001c0002t0001g0125others(28): Show | 31 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(10): Show |
5 | a0001c0002t0001g0189a0001c0003t0003g0104a0001c0003t0003g0105others(2): Show | 5 | HG00738.hp2 HG01243.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(19): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(11): Show |
3 | a0001c0003t0001g0078a0001c0003t0001g0079a0001c0003t0003g0200 | 3 | HG02559.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(14): Show |
18 | a0001c0008t0002g0217a0001c0015t0001g0224a0001c0015t0001g0228others(15): Show | 19 | HG01081.hp1 HG02280.hp2 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(23): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(15): Show |
9 | a0001c0008t0002g0218a0001c0008t0002g0241a0002c0005t0001g0236others(6): Show | 9 | HG02148.hp1 HG03239.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(16): Show |
27 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(24): Show | 28 | HG00099.hp1 HG01081.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(25): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(17): Show |
19 | a0001c0008t0002g0092a0001c0008t0002g0219a0001c0008t0002g0247others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(18): Show |
14 | a0003c0004t0001g0052a0003c0004t0001g0053a0003c0004t0001g0054others(11): Show | 14 | HG00438.hp2 HG01261.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(27): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(20): Show |
1 | a0003c0004t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(29): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(21): Show |
2 | a0004c0006t0001g0064a0012c0020t0001g0251 | 2 | HG02145.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(22): Show |
7 | a0001c0003t0001g0260a0002c0001t0001g0007a0002c0001t0001g0008others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2725_300+2726i others(31): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(23): Show |
3 | a0003c0004t0001g0068a0003c0004t0001g0069a0004c0006t0001g0070 | 3 | HG01074.hp1 HG01934.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(32): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(24): Show |
2 | a0002c0001t0001g0010a0003c0004t0001g0071 | 2 | HG01071.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.300+2725_300+2726i others(33): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(27): Show |
1 | a0003c0004t0001g0072 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(36): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168687
|
C | CTTTTTTT others(28): Show |
1 | a0003c0004t0001g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.300+2725_300+2726i others(37): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100168687 | |||||
| chr8:100168696
|
T | G | 7 | a0001c0009t0001g0271a0002c0001t0001g0262a0002c0001t0001g0269others(4): Show | 7 | HG01071.hp2 HG01123.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2723T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168696 | ||||||
| chr8:100168698
|
TG | T | 9 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+2726delG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168698 | ||||||
| chr8:100168699
|
G | T | 269 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.300+2726G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168699 | ||||||
| chr8:100168805
|
A | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2832A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168805 | ||||||
| chr8:100168837
|
G | A | 1 | a0001c0009t0001g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.300+2864G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168837 | ||||||
| chr8:100168876
|
A | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+2903A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168876 | ||||||
| chr8:100168906
|
C | G | 3 | a0001c0003t0001g0292a0001c0003t0001g0293a0001c0003t0001g0294 | 3 | HG01952.hp2 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.300+2933C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168906 | ||||||
| chr8:100168925
|
G | A | 1 | a0002c0001t0001g0310 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.300+2952G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168925 | ||||||
| chr8:100168958
|
A | G | 1 | a0002c0001t0001g0356 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.300+2985A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100168958 | ||||||
| chr8:100169194
|
C | T | 1 | a0001c0009t0001g0291 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.300+3221C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169194 | ||||||
| chr8:100169234
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300+3261A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169234 | ||||||
| chr8:100169273
|
G | T | 115 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(112): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.300+3300G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169273 | ||||||
| chr8:100169285
|
G | C | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+3312G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169285 | ||||||
| chr8:100169477
|
C | T | 1 | a0001c0003t0005g0296 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.300+3504C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169477 | ||||||
| chr8:100169478
|
G | A | 1 | a0002c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+3505G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169478 | ||||||
| chr8:100169480
|
C | T | 136 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(133): Show | 138 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.300+3507C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169480 | ||||||
| chr8:100169768
|
GT | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+3796delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169768 | ||||||
| chr8:100169832
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+3859G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100169832 | ||||||
| chr8:100169984
|
G | GA | 138 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(135): Show | 140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.300+4021dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100169984 | |||||
| chr8:100170094
|
T | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+4121T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170094 | ||||||
| chr8:100170098
|
T | A | 14 | a0003c0004t0001g0024a0003c0004t0001g0026a0003c0004t0001g0027others(11): Show | 14 | HG01071.hp1 HG01074.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+4125T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170098 | ||||||
| chr8:100170126
|
T | C | 1 | a0003c0004t0005g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.300+4153T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170126 | ||||||
| chr8:100170305
|
A | G | 4 | a0001c0003t0001g0266a0002c0001t0001g0264a0002c0001t0001g0265others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+4332A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170305 | ||||||
| chr8:100170432
|
G | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0007c0013t0001g0134 | 3 | HG00639.hp1 HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300+4459G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170432 | ||||||
| chr8:100170563
|
A | G | 1 | a0007c0013t0001g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.300+4590A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170563 | ||||||
| chr8:100170637
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300+4664G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170637 | ||||||
| chr8:100170641
|
G | A | 1 | a0003c0004t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300+4668G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170641 | ||||||
| chr8:100170776
|
A | T | 1 | a0001c0002t0001g0130 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.300+4803A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170776 | ||||||
| chr8:100170800
|
C | CATTT | 22 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0075others(19): Show | 22 | HG01891.hp2 HG02040.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.300+4876_300+4879d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
C | CATTTATT others(1): Show |
4 | a0001c0003t0001g0016a0001c0015t0001g0224a0002c0005t0002g0225others(1): Show | 4 | HG02148.hp1 HG02280.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+4872_300+4879d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTT | C | 205 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.300+4876_300+4879d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTTATT others(1): Show |
C | 47 | a0001c0003t0001g0258a0001c0003t0001g0266a0001c0003t0005g0296others(44): Show | 48 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.300+4872_300+4879d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTTATT others(5): Show |
C | 14 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(11): Show | 14 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+4868_300+4879d others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTTATT others(9): Show |
C | 1 | a0004c0006t0001g0039 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.300+4864_300+4879d others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTTATT others(17): Show |
C | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.300+4856_300+4879d others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170800
|
CATTTATT others(21): Show |
C | 1 | a0002c0001t0001g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.300+4852_300+4879d others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170800 | |||||
| chr8:100170829
|
A | T | 1 | a0001c0002t0001g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+4856A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170829 | ||||||
| chr8:100170837
|
A | T | 111 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(108): Show | 113 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.300+4864A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170837 | ||||||
| chr8:100170845
|
A | ATTTATTT others(1): Show |
5 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0104others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+4875_300+4882d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170845 | |||||
| chr8:100170845
|
A | ATTTT | 13 | a0001c0003t0001g0357a0001c0003t0003g0103a0001c0003t0003g0105others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+4875_300+4876i others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100170845 | |||||
| chr8:100170845
|
A | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(118): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.300+4872A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170845 | ||||||
| chr8:100170966
|
T | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+4993T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170966 | ||||||
| chr8:100170972
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300+4999G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100170972 | ||||||
| chr8:100171307
|
C | T | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.300+5334C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171307 | ||||||
| chr8:100171331
|
G | A | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.300+5358G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171331 | ||||||
| chr8:100171525
|
A | G | 2 | a0002c0005t0002g0233a0002c0005t0002g0235 | 2 | HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.300+5552A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171525 | ||||||
| chr8:100171564
|
G | A | 1 | a0002c0001t0001g0326 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.300+5591G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171564 | ||||||
| chr8:100171617
|
C | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.300+5644C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171617 | ||||||
| chr8:100171668
|
C | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.300+5695C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171668 | ||||||
| chr8:100171881
|
A | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.300+5908A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171881 | ||||||
| chr8:100171935
|
C | G | 3 | a0002c0007t0001g0191a0002c0007t0001g0192a0002c0007t0001g0193 | 3 | HG02486.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.301-5881C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171935 | ||||||
| chr8:100171937
|
C | T | 1 | a0001c0008t0002g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-5879C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171937 | ||||||
| chr8:100171938
|
G | A | 121 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(118): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.301-5878G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171938 | ||||||
| chr8:100171939
|
G | C | 2 | a0001c0003t0001g0076a0001c0003t0001g0077 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.301-5877G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100171939 | ||||||
| chr8:100172034
|
A | G | 1 | a0002c0005t0002g0231 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.301-5782A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172034 | ||||||
| chr8:100172055
|
C | T | 40 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(37): Show | 42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301-5761C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172055 | ||||||
| chr8:100172166
|
G | A | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.301-5650G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172166 | ||||||
| chr8:100172490
|
C | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5326C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172490 | ||||||
| chr8:100172494
|
C | T | 2 | a0001c0009t0001g0005a0001c0009t0001g0288 | 3 | HG01496.hp1 HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.301-5322C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172494 | ||||||
| chr8:100172512
|
T | C | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.301-5304T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172512 | ||||||
| chr8:100172528
|
G | A | 1 | a0002c0001t0001g0313 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.301-5288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172528 | ||||||
| chr8:100172534
|
C | T | 1 | a0002c0001t0004g0281 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.301-5282C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172534 | ||||||
| chr8:100172634
|
A | ATG | 43 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(40): Show | 44 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-5150_301-5149d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
A | ATGTG | 6 | a0001c0003t0001g0260a0001c0008t0002g0091a0001c0008t0008g0246others(3): Show | 7 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-5152_301-5149d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
A | ATGTGTG | 19 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(16): Show | 19 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.301-5154_301-5149d others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
A | ATGTGTGT others(1): Show |
37 | a0001c0003t0001g0076a0001c0003t0001g0077a0001c0003t0001g0078others(34): Show | 37 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.301-5156_301-5149d others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
A | ATGTGTGT others(3): Show |
24 | a0001c0003t0001g0017a0001c0003t0001g0019a0001c0003t0001g0020others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-5158_301-5149d others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
A | ATGTGTGT others(5): Show |
3 | a0001c0003t0001g0016a0001c0003t0001g0018a0003c0004t0001g0022 | 3 | HG02145.hp2 HG02280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.301-5160_301-5149d others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
ATG | A | 21 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0126others(18): Show | 21 | HG00544.hp1 HG00639.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.301-5150_301-5149d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172634
|
ATGTG | A | 107 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.301-5152_301-5149d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172634 | |||||
| chr8:100172640
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5176G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172640 | ||||||
| chr8:100172664
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5152G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172664 | ||||||
| chr8:100172666
|
GTA | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.301-5148_301-5147d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100172666 | |||||
| chr8:100172727
|
G | T | 122 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.301-5089G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172727 | ||||||
| chr8:100172759
|
T | C | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.301-5057T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172759 | ||||||
| chr8:100172860
|
A | T | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.301-4956A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172860 | ||||||
| chr8:100172908
|
A | G | 1 | a0002c0001t0001g0014 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.301-4908A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100172908 | ||||||
| chr8:100173033
|
C | CT | 63 | a0001c0003t0001g0021a0001c0003t0001g0255a0001c0003t0001g0260others(60): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.301-4756dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173033
|
C | CTT | 16 | a0001c0003t0001g0258a0002c0001t0001g0095a0002c0001t0001g0096others(13): Show | 16 | HG00738.hp1 HG01175.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.301-4757_301-4756d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173033
|
CT | C | 21 | a0001c0003t0001g0078a0001c0003t0001g0079a0001c0003t0001g0107others(18): Show | 21 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.301-4756delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173033
|
CTT | C | 50 | a0001c0002t0001g0171a0001c0002t0001g0176a0001c0002t0001g0188others(47): Show | 52 | HG00438.hp1 HG01081.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.301-4757_301-4756d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173033
|
CTTT | C | 94 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(91): Show | 96 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.301-4758_301-4756d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173033
|
CTTTT | C | 14 | a0001c0002t0001g0088a0001c0002t0001g0124a0001c0002t0001g0127others(11): Show | 14 | HG00140.hp2 HG01167.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301-4759_301-4756d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100173033 | |||||
| chr8:100173184
|
A | T | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.301-4632A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173184 | ||||||
| chr8:100173268
|
A | G | 3 | a0004c0006t0001g0059a0004c0006t0001g0060a0004c0006t0001g0343 | 3 | HG00438.hp2 NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.301-4548A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173268 | ||||||
| chr8:100173733
|
A | G | 1 | a0001c0008t0002g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-4083A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100173733 | ||||||
| chr8:100174097
|
G | A | 40 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(37): Show | 42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301-3719G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174097 | ||||||
| chr8:100174202
|
G | T | 4 | a0002c0007t0001g0190a0002c0007t0001g0191a0002c0007t0001g0192others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-3614G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174202 | ||||||
| chr8:100174365
|
C | T | 3 | a0003c0004t0001g0250a0003c0004t0005g0254a0009c0017t0001g0249 | 3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.301-3451C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174365 | ||||||
| chr8:100174366
|
C | T | 1 | a0002c0001t0001g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301-3450C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174366 | ||||||
| chr8:100174548
|
C | T | 165 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(162): Show | 169 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.301-3268C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174548 | ||||||
| chr8:100174631
|
T | G | 4 | a0002c0001t0001g0006a0002c0001t0001g0259a0002c0001t0001g0268others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-3185T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174631 | ||||||
| chr8:100174790
|
G | A | 1 | a0002c0001t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.301-3026G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174790 | ||||||
| chr8:100174902
|
G | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.301-2914G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100174902 | ||||||
| chr8:100174970
|
CT | C | 11 | a0001c0002t0001g0170a0001c0003t0001g0255a0001c0003t0001g0258others(8): Show | 11 | HG00323.hp1 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-2830delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100174970 | |||||
| chr8:100174970
|
CTT | C | 244 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.301-2831_301-2830d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100174970 | |||||
| chr8:100175071
|
T | C | 2 | a0002c0001t0001g0308a0002c0001t0001g0311 | 2 | HG02040.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.301-2745T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175071 | ||||||
| chr8:100175096
|
C | T | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301-2720C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175096 | ||||||
| chr8:100175284
|
C | CT | 52 | a0002c0001t0001g0295a0003c0004t0001g0022a0003c0004t0001g0023others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.301-2514dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100175284 | |||||
| chr8:100175284
|
CT | C | 7 | a0002c0001t0001g0009a0002c0001t0001g0313a0002c0005t0002g0220others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-2514delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100175284 | |||||
| chr8:100175522
|
G | A | 1 | a0003c0004t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-2294G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175522 | ||||||
| chr8:100175647
|
G | A | 1 | a0001c0003t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.301-2169G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175647 | ||||||
| chr8:100175885
|
A | G | 2 | a0001c0003t0001g0078a0001c0003t0001g0079 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.301-1931A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175885 | ||||||
| chr8:100175897
|
C | G | 2 | a0002c0005t0001g0237a0002c0005t0002g0240 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.301-1919C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100175897 | ||||||
| chr8:100176136
|
C | T | 1 | a0003c0004t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-1680C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176136 | ||||||
| chr8:100176439
|
C | T | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1377C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176439 | ||||||
| chr8:100176611
|
C | T | 1 | a0007c0013t0001g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.301-1205C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176611 | ||||||
| chr8:100176807
|
C | CCCTCT | 61 | a0001c0002t0001g0175a0001c0003t0001g0016a0001c0003t0001g0017others(58): Show | 63 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.301-978_301-974dup others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176807
|
C | CCCTCTCC others(3): Show |
49 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087others(46): Show | 49 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.301-983_301-974dup others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176807
|
C | CCCTCTCC others(8): Show |
78 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(75): Show | 80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-988_301-974dup others(15): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176807
|
C | CCCTCTCC others(13): Show |
6 | a0001c0002t0001g0122a0001c0002t0001g0189a0001c0008t0008g0246others(3): Show | 6 | HG02647.hp1 HG02683.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-993_301-974dup others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176807
|
CCCTCT | C | 59 | a0001c0003t0001g0258a0001c0008t0002g0244a0001c0009t0001g0345others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.301-978_301-974del others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176807
|
CCCTCTCC others(3): Show |
C | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.301-983_301-974del others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 100176807 | |||||
| chr8:100176869
|
A | C | 359 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(356): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.301-947A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100176869 | ||||||
| chr8:100177000
|
T | G | 3 | a0004c0006t0001g0059a0004c0006t0001g0060a0004c0006t0001g0343 | 3 | HG00438.hp2 NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.301-816T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177000 | ||||||
| chr8:100177024
|
T | C | 259 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.301-792T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177024 | ||||||
| chr8:100177534
|
T | C | 1 | a0002c0001t0001g0300 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.301-282T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177534 | ||||||
| chr8:100177601
|
A | G | 7 | a0001c0002t0001g0100a0001c0002t0001g0130a0001c0002t0001g0167others(4): Show | 7 | HG00673.hp1 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-215A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 3/18 | chr8 | 100177601 | ||||||
| chr8:100178458
|
C | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.426+517C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178458 | ||||||
| chr8:100178528
|
T | C | 2 | a0002c0001t0001g0355a0002c0001t0001g0356 | 2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.426+587T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178528 | ||||||
| chr8:100178562
|
G | C | 3 | a0001c0002t0001g0130a0001c0002t0001g0167a0001c0002t0001g0214 | 3 | NA18962.hp1 NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.426+621G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178562 | ||||||
| chr8:100178669
|
G | A | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.426+728G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100178669 | ||||||
| chr8:100179006
|
A | G | 1 | a0002c0005t0002g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.426+1065A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179006 | ||||||
| chr8:100179063
|
C | CA | 66 | a0001c0002t0001g0125a0001c0002t0001g0128a0001c0002t0001g0137others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.426+1138dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179063 | |||||
| chr8:100179063
|
C | CAA | 7 | a0003c0004t0001g0026a0003c0004t0001g0027a0003c0004t0001g0041others(4): Show | 7 | HG01071.hp1 HG01255.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+1137_426+1138d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179063 | |||||
| chr8:100179085
|
AAAAC | A | 31 | a0001c0008t0002g0004a0001c0008t0002g0243a0001c0008t0002g0244others(28): Show | 32 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.426+1152_426+1155d others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 100179085 | |||||
| chr8:100179520
|
G | T | 2 | a0001c0003t0001g0078a0001c0003t0001g0079 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.426+1579G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179520 | ||||||
| chr8:100179607
|
C | T | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.426+1666C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179607 | ||||||
| chr8:100179934
|
T | C | 1 | a0002c0001t0001g0011 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.426+1993T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100179934 | ||||||
| chr8:100180296
|
T | C | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.426+2355T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180296 | ||||||
| chr8:100180394
|
A | G | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.426+2453A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180394 | ||||||
| chr8:100180789
|
T | C | 1 | a0003c0018t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.427-2586T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180789 | ||||||
| chr8:100180878
|
T | C | 1 | a0002c0005t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.427-2497T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100180878 | ||||||
| chr8:100181135
|
A | G | 1 | a0001c0002t0001g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.427-2240A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181135 | ||||||
| chr8:100181221
|
T | C | 1 | a0001c0002t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.427-2154T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181221 | ||||||
| chr8:100181307
|
G | C | 6 | a0002c0001t0001g0327a0002c0001t0001g0330a0002c0001t0001g0331others(3): Show | 6 | HG00609.hp2 NA18965.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-2068G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181307 | ||||||
| chr8:100181393
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.427-1982G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181393 | ||||||
| chr8:100181459
|
T | G | 1 | a0001c0003t0005g0296 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.427-1916T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181459 | ||||||
| chr8:100181847
|
A | C | 3 | a0003c0004t0001g0022a0003c0004t0001g0081a0003c0004t0001g0082 | 3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.427-1528A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100181847 | ||||||
| chr8:100182170
|
T | C | 1 | a0001c0002t0001g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.427-1205T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182170 | ||||||
| chr8:100182236
|
T | C | 1 | a0002c0001t0001g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.427-1139T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182236 | ||||||
| chr8:100182250
|
T | C | 1 | a0001c0009t0001g0271 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.427-1125T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182250 | ||||||
| chr8:100182298
|
C | T | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.427-1077C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100182298 | ||||||
| chr8:100183003
|
T | G | 1 | a0001c0002t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.427-372T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183003 | ||||||
| chr8:100183076
|
C | A | 3 | a0002c0001t0001g0011a0002c0001t0001g0012a0002c0001t0001g0015 | 3 | NA18612.hp2 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.427-299C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183076 | ||||||
| chr8:100183078
|
A | G | 17 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.427-297A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183078 | ||||||
| chr8:100183170
|
A | G | 1 | a0002c0001t0001g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.427-205A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183170 | ||||||
| chr8:100183359
|
G | T | 17 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.427-16G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 4/18 | chr8 | 100183359 | ||||||
| chr8:100183470
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.488+34A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183470 | ||||||
| chr8:100183475
|
A | G | 3 | a0001c0008t0002g0090a0001c0008t0002g0091a0001c0008t0002g0092 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.488+39A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183475 | ||||||
| chr8:100183541
|
A | G | 1 | a0001c0003t0003g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.488+105A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183541 | ||||||
| chr8:100183645
|
G | A | 1 | a0002c0001t0001g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.488+209G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183645 | ||||||
| chr8:100183850
|
A | G | 2 | a0002c0001t0001g0006a0002c0001t0001g0344 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-106A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183850 | ||||||
| chr8:100183851
|
A | T | 2 | a0002c0001t0001g0006a0002c0001t0001g0344 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-105A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183851 | ||||||
| chr8:100183852
|
TATGTATC others(6): Show |
T | 2 | a0002c0001t0001g0006a0002c0001t0001g0344 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.489-103_489-91delA others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 5/18 | chr8 | 100183852 | ||||||
| chr8:100184592
|
A | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.596-36A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/18 | chr8 | 100184592 | ||||||
| chr8:100184596
|
G | A | 165 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(162): Show | 169 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.596-32G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 6/18 | chr8 | 100184596 | ||||||
| chr8:100184818
|
G | A | 1 | a0011c0022t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701+85G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100184818 | ||||||
| chr8:100184881
|
C | G | 1 | a0002c0005t0002g0248 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.701+148C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100184881 | ||||||
| chr8:100185026
|
T | C | 1 | a0002c0007t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.701+293T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185026 | ||||||
| chr8:100185129
|
T | C | 1 | a0001c0003t0005g0296 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.701+396T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185129 | ||||||
| chr8:100185199
|
G | A | 1 | a0004c0006t0001g0037 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.701+466G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185199 | ||||||
| chr8:100185493
|
C | A | 1 | a0001c0002t0001g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.701+760C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185493 | ||||||
| chr8:100185648
|
A | G | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.701+915A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185648 | ||||||
| chr8:100185726
|
C | A | 2 | a0004c0006t0001g0059a0004c0006t0001g0343 | 2 | NA18992.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.701+993C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185726 | ||||||
| chr8:100185998
|
A | G | 1 | a0001c0003t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-1122A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100185998 | ||||||
| chr8:100186060
|
C | CT | 189 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(186): Show | 193 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.702-1037dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | |||||
| chr8:100186060
|
C | CTT | 60 | a0001c0002t0001g0120a0001c0002t0001g0122a0001c0002t0001g0158others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.702-1038_702-1037d others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | |||||
| chr8:100186060
|
C | CTTT | 11 | a0001c0003t0001g0260a0001c0008t0002g0247a0003c0004t0001g0022others(8): Show | 11 | HG00438.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.702-1039_702-1037d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 100186060 | |||||
| chr8:100186140
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.702-980G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186140 | ||||||
| chr8:100186341
|
G | C | 223 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.702-779G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186341 | ||||||
| chr8:100186443
|
G | A | 1 | a0002c0001t0001g0270 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.702-677G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186443 | ||||||
| chr8:100186642
|
G | T | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.702-478G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186642 | ||||||
| chr8:100186697
|
G | A | 2 | a0006c0011t0002g0003a0006c0011t0002g0252 | 3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.702-423G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186697 | ||||||
| chr8:100186801
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.702-319G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186801 | ||||||
| chr8:100186810
|
C | A | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-310C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186810 | ||||||
| chr8:100186811
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-309A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186811 | ||||||
| chr8:100186812
|
G | T | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-308G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100186812 | ||||||
| chr8:100187025
|
G | C | 1 | a0002c0001t0001g0318 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.702-95G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 7/18 | chr8 | 100187025 | ||||||
| chr8:100187290
|
A | C | 1 | a0003c0004t0005g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+40A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187290 | ||||||
| chr8:100187487
|
A | C | 2 | a0001c0009t0001g0278a0002c0001t0001g0280 | 2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.832+237A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187487 | ||||||
| chr8:100187566
|
C | T | 1 | a0001c0021t0001g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.832+316C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187566 | ||||||
| chr8:100187691
|
T | G | 1 | a0002c0001t0001g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.832+441T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187691 | ||||||
| chr8:100187821
|
C | G | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.832+571C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187821 | ||||||
| chr8:100187998
|
G | A | 1 | a0002c0001t0001g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.832+748G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100187998 | ||||||
| chr8:100188306
|
C | T | 2 | a0002c0001t0001g0095a0002c0001t0001g0096 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.832+1056C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188306 | ||||||
| chr8:100188355
|
G | A | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.832+1105G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188355 | ||||||
| chr8:100188884
|
T | G | 4 | a0001c0009t0001g0005a0001c0009t0001g0288a0001c0009t0001g0291others(1): Show | 5 | HG01496.hp1 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+1634T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100188884 | ||||||
| chr8:100189040
|
C | A | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.832+1790C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189040 | ||||||
| chr8:100189050
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.832+1800G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189050 | ||||||
| chr8:100189054
|
A | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.832+1804A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189054 | ||||||
| chr8:100189176
|
TA | T | 89 | a0001c0002t0001g0137a0001c0003t0001g0016a0001c0003t0001g0017others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.832+1942delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100189176 | |||||
| chr8:100189371
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-2019G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189371 | ||||||
| chr8:100189446
|
C | T | 1 | a0003c0018t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.833-1944C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189446 | ||||||
| chr8:100189498
|
T | A | 40 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(37): Show | 42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.833-1892T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189498 | ||||||
| chr8:100189641
|
A | C | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1749A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189641 | ||||||
| chr8:100189760
|
G | T | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1630G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189760 | ||||||
| chr8:100189775
|
A | C | 1 | a0002c0001t0004g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.833-1615A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189775 | ||||||
| chr8:100189827
|
C | T | 1 | a0002c0001t0001g0338 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-1563C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189827 | ||||||
| chr8:100189829
|
T | C | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-1561T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189829 | ||||||
| chr8:100189876
|
G | A | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.833-1514G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100189876 | ||||||
| chr8:100190009
|
G | A | 1 | a0001c0003t0001g0358 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.833-1381G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190009 | ||||||
| chr8:100190037
|
G | C | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-1353G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190037 | ||||||
| chr8:100190107
|
G | A | 1 | a0002c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-1283G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190107 | ||||||
| chr8:100190176
|
G | T | 6 | a0001c0015t0001g0224a0001c0015t0001g0228a0002c0005t0001g0236others(3): Show | 6 | NA18946.hp2 NA18957.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-1214G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190176 | ||||||
| chr8:100190211
|
A | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.833-1179A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190211 | ||||||
| chr8:100190241
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-1149A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190241 | ||||||
| chr8:100190298
|
G | C | 1 | a0002c0001t0001g0282 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.833-1092G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190298 | ||||||
| chr8:100190312
|
C | CA | 17 | a0001c0002t0001g0084a0001c0002t0001g0122a0001c0002t0001g0140others(14): Show | 17 | HG00408.hp1 HG01993.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.833-1059dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190312 | |||||
| chr8:100190312
|
CA | C | 28 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0019others(25): Show | 28 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.833-1059delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190312 | |||||
| chr8:100190332
|
T | A | 3 | a0002c0001t0001g0013a0002c0001t0001g0014a0002c0001t0001g0025 | 3 | NA18954.hp1 NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.833-1058T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190332 | ||||||
| chr8:100190404
|
A | G | 1 | a0005c0010t0001g0156 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.833-986A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190404 | ||||||
| chr8:100190520
|
T | TG | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.833-869dupG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190520 | |||||
| chr8:100190663
|
C | CT | 156 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(153): Show | 160 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.833-709dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190663 | |||||
| chr8:100190663
|
C | CTT | 10 | a0001c0002t0001g0087a0001c0002t0001g0137a0001c0002t0001g0138others(7): Show | 10 | HG00621.hp2 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-710_833-709dup others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 100190663 | |||||
| chr8:100190668
|
T | C | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.833-722T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190668 | ||||||
| chr8:100190670
|
T | TC | 3 | a0001c0015t0001g0224a0001c0015t0001g0228a0002c0005t0001g0236 | 3 | NA18957.hp1 NA18971.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.833-720_833-719ins others(1): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190670 | ||||||
| chr8:100190743
|
G | C | 359 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(356): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.833-647G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100190743 | ||||||
| chr8:100191043
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-347A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191043 | ||||||
| chr8:100191044
|
G | T | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.833-346G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191044 | ||||||
| chr8:100191314
|
C | A | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.833-76C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191314 | ||||||
| chr8:100191370
|
T | C | 1 | a0009c0017t0001g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.833-20T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191370 | ||||||
| chr8:100191375
|
T | A | 1 | a0002c0001t0006g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.833-15T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 8/18 | chr8 | 100191375 | ||||||
| chr8:100191509
|
T | C | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.939+13T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191509 | ||||||
| chr8:100191826
|
T | C | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.939+330T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191826 | ||||||
| chr8:100191882
|
A | G | 1 | a0002c0001t0006g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.939+386A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191882 | ||||||
| chr8:100191909
|
T | C | 2 | a0006c0011t0002g0003a0006c0011t0002g0252 | 3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.939+413T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191909 | ||||||
| chr8:100191981
|
T | C | 3 | a0002c0001t0001g0301a0002c0001t0001g0302a0002c0001t0001g0306 | 3 | NA18964.hp1 NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.939+485T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100191981 | ||||||
| chr8:100192109
|
T | C | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.939+613T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192109 | ||||||
| chr8:100192131
|
GCA | G | 13 | a0002c0005t0002g0089a0002c0005t0002g0223a0002c0005t0002g0225others(10): Show | 13 | HG01081.hp1 HG02148.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+639_939+640del others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100192131 | |||||
| chr8:100192180
|
A | C | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.939+684A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192180 | ||||||
| chr8:100192401
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.939+905G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192401 | ||||||
| chr8:100192424
|
A | G | 105 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(102): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.939+928A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192424 | ||||||
| chr8:100192519
|
A | G | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.939+1023A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192519 | ||||||
| chr8:100192773
|
A | G | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.939+1277A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192773 | ||||||
| chr8:100192785
|
T | G | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.939+1289T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100192785 | ||||||
| chr8:100193356
|
G | C | 32 | a0001c0002t0001g0085a0001c0002t0001g0087a0001c0002t0001g0099others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.940-756G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193356 | ||||||
| chr8:100193386
|
G | A | 4 | a0001c0003t0001g0255a0001c0003t0001g0258a0008c0014t0001g0256others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-726G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193386 | ||||||
| chr8:100193477
|
A | C | 118 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(115): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.940-635A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193477 | ||||||
| chr8:100193479
|
A | C | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.940-633A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193479 | ||||||
| chr8:100193481
|
C | A | 1 | a0001c0002t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.940-631C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193481 | ||||||
| chr8:100193552
|
A | G | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.940-560A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193552 | ||||||
| chr8:100193709
|
C | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.940-403C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193709 | ||||||
| chr8:100193761
|
TAAAC | T | 106 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(103): Show | 108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.940-345_940-342del others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100193761 | |||||
| chr8:100193927
|
C | T | 4 | a0001c0003t0001g0255a0001c0003t0001g0258a0008c0014t0001g0256others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-185C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193927 | ||||||
| chr8:100193947
|
T | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.940-165T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | chr8 | 100193947 | ||||||
| chr8:100193990
|
C | CA | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.940-114dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 100193990 | |||||
| chr8:100194303
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+35G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194303 | ||||||
| chr8:100194343
|
C | T | 2 | a0006c0011t0002g0003a0006c0011t0002g0252 | 3 | HG02280.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096+75C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194343 | ||||||
| chr8:100194540
|
A | G | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+272A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194540 | ||||||
| chr8:100194582
|
A | G | 1 | a0002c0001t0001g0307 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1096+314A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194582 | ||||||
| chr8:100194610
|
A | G | 2 | a0001c0008t0002g0217a0001c0008t0002g0218 | 2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1096+342A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194610 | ||||||
| chr8:100194687
|
G | A | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1096+419G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194687 | ||||||
| chr8:100194809
|
C | T | 3 | a0001c0008t0002g0090a0001c0008t0002g0091a0001c0008t0002g0092 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1096+541C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194809 | ||||||
| chr8:100194836
|
G | A | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1096+568G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194836 | ||||||
| chr8:100194882
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1096+614G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194882 | ||||||
| chr8:100194970
|
G | A | 43 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(40): Show | 45 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096+702G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194970 | ||||||
| chr8:100194981
|
A | G | 1 | a0002c0001t0001g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1096+713A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100194981 | ||||||
| chr8:100195089
|
C | T | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+821C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195089 | ||||||
| chr8:100195164
|
C | CA | 195 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(192): Show | 199 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1096+909dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100195164 | |||||
| chr8:100195178
|
G | A | 57 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1096+910G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195178 | ||||||
| chr8:100195297
|
T | C | 1 | a0002c0001t0001g0272 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1096+1029T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195297 | ||||||
| chr8:100195308
|
T | C | 1 | a0001c0009t0001g0278 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1096+1040T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195308 | ||||||
| chr8:100195856
|
A | G | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1096+1588A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100195856 | ||||||
| chr8:100196113
|
T | A | 30 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(27): Show | 30 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1096+1845T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196113 | ||||||
| chr8:100196115
|
C | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1096+1847C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196115 | ||||||
| chr8:100196432
|
G | T | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+2164G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196432 | ||||||
| chr8:100196516
|
G | A | 1 | a0002c0007t0001g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1096+2248G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196516 | ||||||
| chr8:100196522
|
C | G | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+2254C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196522 | ||||||
| chr8:100196555
|
G | T | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1096+2287G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196555 | ||||||
| chr8:100196606
|
G | A | 1 | a0001c0003t0003g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1096+2338G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196606 | ||||||
| chr8:100196610
|
A | G | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+2342A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196610 | ||||||
| chr8:100196894
|
G | A | 1 | a0002c0001t0001g0334 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1096+2626G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196894 | ||||||
| chr8:100196945
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+2677G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100196945 | ||||||
| chr8:100197031
|
G | A | 1 | a0001c0002t0001g0130 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1096+2763G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197031 | ||||||
| chr8:100197273
|
C | T | 1 | a0001c0003t0001g0357 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1096+3005C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197273 | ||||||
| chr8:100197349
|
C | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+3081C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197349 | ||||||
| chr8:100197575
|
G | A | 1 | a0002c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096+3307G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197575 | ||||||
| chr8:100197642
|
G | A | 4 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+3374G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100197642 | ||||||
| chr8:100198243
|
A | G | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+3975A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198243 | ||||||
| chr8:100198269
|
TCAAA | T | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+4005_1096+400 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100198269 | |||||
| chr8:100198340
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+4072G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198340 | ||||||
| chr8:100198422
|
C | T | 10 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4154C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198422 | ||||||
| chr8:100198698
|
T | C | 1 | a0002c0001t0001g0267 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1096+4430T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198698 | ||||||
| chr8:100198770
|
A | C | 4 | a0001c0002t0001g0128a0001c0002t0001g0163a0001c0002t0001g0172others(1): Show | 4 | HG00597.hp1 NA18972.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096+4502A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198770 | ||||||
| chr8:100198959
|
C | A | 1 | a0011c0022t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1096+4691C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100198959 | ||||||
| chr8:100199109
|
T | C | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1096+4841T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199109 | ||||||
| chr8:100199136
|
T | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1096+4868T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199136 | ||||||
| chr8:100199145
|
A | G | 1 | a0001c0009t0001g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1096+4877A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199145 | ||||||
| chr8:100199146
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1096+4878T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199146 | ||||||
| chr8:100199217
|
A | G | 1 | a0002c0001t0001g0337 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1096+4949A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199217 | ||||||
| chr8:100199241
|
G | A | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1096+4973G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199241 | ||||||
| chr8:100199442
|
C | T | 1 | a0002c0001t0001g0259 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1096+5174C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199442 | ||||||
| chr8:100199481
|
T | C | 2 | a0001c0009t0001g0312a0002c0001t0001g0318 | 2 | NA18969.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1096+5213T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199481 | ||||||
| chr8:100199571
|
A | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1096+5303A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199571 | ||||||
| chr8:100199594
|
C | T | 4 | a0001c0003t0001g0255a0001c0003t0001g0258a0008c0014t0001g0256others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5326C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199594 | ||||||
| chr8:100199670
|
C | T | 1 | a0003c0004t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1096+5402C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199670 | ||||||
| chr8:100199960
|
T | A | 2 | a0001c0009t0001g0329a0010c0023t0001g0080 | 2 | HG02717.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1096+5692T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100199960 | ||||||
| chr8:100200342
|
A | G | 1 | a0001c0008t0002g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1096+6074A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200342 | ||||||
| chr8:100200349
|
A | T | 5 | a0003c0004t0001g0068a0003c0004t0001g0069a0003c0004t0001g0071others(2): Show | 5 | HG01071.hp1 HG01074.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096+6081A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200349 | ||||||
| chr8:100200582
|
A | G | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1096+6314A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200582 | ||||||
| chr8:100200717
|
A | G | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1096+6449A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200717 | ||||||
| chr8:100200791
|
GTTGT | G | 118 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(115): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1096+6530_1096+653 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100200791 | |||||
| chr8:100200870
|
GC | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1096+6603delC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200870 | ||||||
| chr8:100200998
|
T | A | 2 | a0001c0003t0001g0078a0001c0003t0001g0079 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1096+6730T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100200998 | ||||||
| chr8:100201037
|
A | G | 1 | a0003c0004t0001g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1096+6769A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201037 | ||||||
| chr8:100201296
|
T | A | 3 | a0003c0004t0001g0250a0003c0004t0005g0254a0009c0017t0001g0249 | 3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1096+7028T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201296 | ||||||
| chr8:100201605
|
G | A | 279 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(276): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1096+7337G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201605 | ||||||
| chr8:100201672
|
A | T | 1 | a0002c0001t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1096+7404A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201672 | ||||||
| chr8:100201741
|
C | G | 5 | a0002c0007t0001g0190a0002c0007t0001g0191a0002c0007t0001g0192others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096+7473C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201741 | ||||||
| chr8:100201788
|
A | T | 2 | a0001c0002t0001g0138a0001c0002t0001g0144 | 2 | HG00735.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1096+7520A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201788 | ||||||
| chr8:100201961
|
A | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1096+7693A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100201961 | ||||||
| chr8:100202013
|
C | T | 1 | a0002c0001t0001g0336 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1096+7745C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202013 | ||||||
| chr8:100202342
|
T | TA | 97 | a0001c0002t0001g0147a0001c0003t0001g0016a0001c0003t0001g0017others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1096+8085dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202342 | |||||
| chr8:100202432
|
C | T | 29 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(26): Show | 29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1096+8164C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202432 | ||||||
| chr8:100202437
|
G | A | 30 | a0001c0008t0002g0004a0001c0008t0002g0243a0001c0008t0002g0244others(27): Show | 31 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(28): Show |
intron_variant | MODIFIER | c.1096+8169G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202437 | ||||||
| chr8:100202448
|
T | G | 29 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(26): Show | 29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1096+8180T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202448 | ||||||
| chr8:100202506
|
C | T | 162 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(159): Show | 166 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1096+8238C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202506 | ||||||
| chr8:100202567
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+8299G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202567 | ||||||
| chr8:100202583
|
G | A | 30 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(27): Show | 30 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1096+8315G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202583 | ||||||
| chr8:100202591
|
T | C | 115 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(112): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1096+8323T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202591 | ||||||
| chr8:100202649
|
G | C | 10 | a0001c0009t0001g0329a0002c0001t0001g0222a0002c0001t0001g0320others(7): Show | 10 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096+8381G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202649 | ||||||
| chr8:100202666
|
C | T | 40 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(37): Show | 42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1096+8398C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202666 | ||||||
| chr8:100202709
|
C | CA | 61 | a0001c0002t0001g0120a0001c0002t0001g0124a0001c0002t0001g0126others(58): Show | 62 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1096+8470dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
C | CAA | 9 | a0001c0003t0001g0260a0001c0008t0002g0219a0001c0008t0008g0246others(6): Show | 9 | HG02055.hp2 HG02738.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8469_1096+847 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
C | CAAA | 5 | a0001c0008t0002g0004a0001c0008t0002g0243a0001c0008t0002g0244others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096+8468_1096+847 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
CA | C | 9 | a0001c0002t0001g0099a0001c0002t0001g0165a0002c0001t0001g0007others(6): Show | 9 | HG01943.hp2 HG03041.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8470delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
CAA | C | 54 | a0002c0001t0001g0010a0003c0004t0001g0022a0003c0004t0001g0023others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1096+8469_1096+847 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
CAAAAAAA others(3): Show |
C | 1 | a0015c0025t0001g0263 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1096+8461_1096+847 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202709
|
CAAAAAAA others(5): Show |
C | 3 | a0002c0007t0001g0194a0002c0007t0001g0195a0002c0007t0001g0196 | 3 | HG02258.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1096+8459_1096+847 others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100202709 | |||||
| chr8:100202725
|
A | G | 1 | a0001c0002t0001g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1096+8457A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202725 | ||||||
| chr8:100202927
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1096+8659G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100202927 | ||||||
| chr8:100203238
|
C | T | 1 | a0002c0001t0001g0283 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1096+8970C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203238 | ||||||
| chr8:100203295
|
C | T | 1 | a0001c0003t0003g0114 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096+9027C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203295 | ||||||
| chr8:100203329
|
A | G | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1096+9061A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203329 | ||||||
| chr8:100203418
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1096+9150G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203418 | ||||||
| chr8:100203979
|
A | G | 1 | a0002c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097-9111A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100203979 | ||||||
| chr8:100204067
|
G | C | 1 | a0011c0022t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1097-9023G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204067 | ||||||
| chr8:100204267
|
A | G | 2 | a0001c0002t0001g0170a0001c0002t0007g0187 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1097-8823A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204267 | ||||||
| chr8:100204389
|
A | T | 1 | a0001c0002t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1097-8701A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204389 | ||||||
| chr8:100204403
|
T | A | 1 | a0001c0002t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1097-8687T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204403 | ||||||
| chr8:100204512
|
TA | T | 175 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1097-8566delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100204512 | |||||
| chr8:100204652
|
T | C | 1 | a0001c0009t0001g0271 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1097-8438T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204652 | ||||||
| chr8:100204816
|
G | T | 1 | a0002c0001t0001g0261 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1097-8274G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204816 | ||||||
| chr8:100204872
|
C | T | 1 | a0002c0007t0001g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1097-8218C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204872 | ||||||
| chr8:100204935
|
T | C | 12 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-8155T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100204935 | ||||||
| chr8:100205172
|
C | A | 118 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(115): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1097-7918C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205172 | ||||||
| chr8:100205481
|
C | T | 1 | a0002c0001t0001g0297 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1097-7609C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205481 | ||||||
| chr8:100205482
|
G | A | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1097-7608G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205482 | ||||||
| chr8:100205730
|
G | A | 4 | a0001c0008t0002g0217a0001c0008t0002g0218a0001c0008t0002g0219others(1): Show | 4 | HG03041.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-7360G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205730 | ||||||
| chr8:100205754
|
T | C | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1097-7336T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205754 | ||||||
| chr8:100205755
|
G | A | 1 | a0001c0003t0001g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1097-7335G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205755 | ||||||
| chr8:100205768
|
G | A | 43 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(40): Show | 45 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1097-7322G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205768 | ||||||
| chr8:100205788
|
G | A | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1097-7302G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205788 | ||||||
| chr8:100205798
|
C | T | 1 | a0003c0004t0001g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1097-7292C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100205798 | ||||||
| chr8:100206017
|
C | CA | 42 | a0001c0003t0001g0266a0001c0003t0001g0292a0001c0003t0001g0293others(39): Show | 43 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1097-7035dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
C | CAA | 19 | a0001c0003t0001g0107a0001c0003t0003g0104a0001c0003t0003g0105others(16): Show | 19 | HG00408.hp2 HG00423.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1097-7036_1097-703 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CA | C | 8 | a0001c0003t0005g0296a0001c0009t0001g0298a0002c0001t0001g0093others(5): Show | 8 | HG01099.hp2 HG01346.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097-7035delA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(1): Show |
C | 56 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1097-7042_1097-703 others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(3): Show |
C | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-7044_1097-703 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0003t0001g0018a0002c0001t0001g0300 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1097-7047_1097-703 others(17): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(7): Show |
C | 11 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0019others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1097-7048_1097-703 others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(12): Show |
C | 8 | a0001c0009t0001g0329a0002c0001t0001g0320a0002c0001t0001g0324others(5): Show | 8 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-7053_1097-703 others(23): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(13): Show |
C | 2 | a0001c0002t0001g0130a0001c0002t0001g0167 | 2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1097-7054_1097-703 others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(14): Show |
C | 156 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(153): Show | 160 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1097-7055_1097-703 others(25): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206017
|
CAAAAAAA others(15): Show |
C | 4 | a0002c0005t0002g0230a0002c0005t0002g0232a0002c0005t0002g0253others(1): Show | 4 | HG02630.hp1 HG02735.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-7056_1097-703 others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206017 | |||||
| chr8:100206052
|
A | G | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1097-7038A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206052 | ||||||
| chr8:100206052
|
A | T | 2 | a0002c0001t0001g0013a0002c0001t0001g0025 | 2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1097-7038A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206052 | ||||||
| chr8:100206083
|
C | T | 38 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(35): Show | 39 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1097-7007C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206083 | ||||||
| chr8:100206097
|
A | G | 2 | a0001c0003t0001g0078a0001c0003t0001g0079 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1097-6993A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206097 | ||||||
| chr8:100206126
|
G | A | 162 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(159): Show | 166 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1097-6964G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206126 | ||||||
| chr8:100206178
|
C | T | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1097-6912C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206178 | ||||||
| chr8:100206248
|
G | A | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1097-6842G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206248 | ||||||
| chr8:100206261
|
G | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0167 | 2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1097-6829G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206261 | ||||||
| chr8:100206409
|
A | G | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-6681A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206409 | ||||||
| chr8:100206464
|
T | G | 55 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1097-6626T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206464 | ||||||
| chr8:100206614
|
T | C | 1 | a0002c0001t0001g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1097-6476T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206614 | ||||||
| chr8:100206648
|
CAAGATAT others(17): Show |
C | 1 | a0002c0001t0001g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1097-6417_1097-639 others(28): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100206648 | |||||
| chr8:100206767
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-6323G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206767 | ||||||
| chr8:100206863
|
G | A | 1 | a0010c0023t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1097-6227G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100206863 | ||||||
| chr8:100207217
|
C | T | 1 | a0002c0007t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1097-5873C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207217 | ||||||
| chr8:100207289
|
A | G | 8 | a0004c0006t0001g0033a0004c0006t0001g0035a0004c0006t0001g0036others(5): Show | 8 | HG01943.hp1 NA18951.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-5801A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207289 | ||||||
| chr8:100207353
|
T | G | 1 | a0001c0003t0001g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-5737T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207353 | ||||||
| chr8:100207359
|
G | A | 1 | a0002c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097-5731G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207359 | ||||||
| chr8:100207438
|
C | T | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1097-5652C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207438 | ||||||
| chr8:100207461
|
G | A | 1 | a0001c0003t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1097-5629G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207461 | ||||||
| chr8:100207666
|
C | T | 8 | a0003c0004t0001g0024a0003c0004t0001g0049a0003c0004t0001g0050others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097-5424C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207666 | ||||||
| chr8:100207739
|
C | T | 1 | a0002c0001t0001g0302 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1097-5351C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207739 | ||||||
| chr8:100207782
|
G | A | 37 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(34): Show | 38 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(35): Show |
intron_variant | MODIFIER | c.1097-5308G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207782 | ||||||
| chr8:100207875
|
C | T | 1 | a0001c0008t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1097-5215C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207875 | ||||||
| chr8:100207914
|
A | T | 1 | a0002c0001t0001g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1097-5176A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207914 | ||||||
| chr8:100207950
|
G | A | 4 | a0001c0003t0001g0255a0001c0003t0001g0258a0008c0014t0001g0256others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-5140G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100207950 | ||||||
| chr8:100208536
|
A | G | 1 | a0002c0001t0001g0338 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1097-4554A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208536 | ||||||
| chr8:100208549
|
A | G | 1 | a0003c0004t0001g0030 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1097-4541A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208549 | ||||||
| chr8:100208577
|
C | T | 1 | a0001c0009t0001g0345 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1097-4513C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208577 | ||||||
| chr8:100208941
|
G | C | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-4149G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208941 | ||||||
| chr8:100208985
|
G | C | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-4105G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208985 | ||||||
| chr8:100208999
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1097-4091A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100208999 | ||||||
| chr8:100209025
|
C | G | 1 | a0004c0006t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1097-4065C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209025 | ||||||
| chr8:100209080
|
C | T | 1 | a0013c0019t0001g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1097-4010C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209080 | ||||||
| chr8:100209224
|
G | A | 1 | a0009c0017t0001g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-3866G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209224 | ||||||
| chr8:100209248
|
A | T | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1097-3842A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209248 | ||||||
| chr8:100209303
|
C | CAT | 59 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1097-3772_1097-377 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100209303 | |||||
| chr8:100209305
|
T | C | 1 | a0001c0003t0001g0294 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1097-3785T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209305 | ||||||
| chr8:100209560
|
T | C | 17 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1097-3530T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209560 | ||||||
| chr8:100209626
|
TAA | T | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-3463_1097-346 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209626 | ||||||
| chr8:100209633
|
T | C | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-3457T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209633 | ||||||
| chr8:100209917
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1097-3173A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100209917 | ||||||
| chr8:100210191
|
GT | G | 59 | a0001c0003t0001g0255a0002c0001t0001g0268a0002c0001t0001g0322others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1097-2885delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100210191 | |||||
| chr8:100210192
|
T | G | 1 | a0002c0001t0004g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1097-2898T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210192 | ||||||
| chr8:100210257
|
G | A | 1 | a0002c0001t0001g0261 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1097-2833G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210257 | ||||||
| chr8:100210271
|
A | G | 192 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1097-2819A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210271 | ||||||
| chr8:100210404
|
C | T | 4 | a0001c0003t0001g0266a0002c0001t0001g0264a0002c0001t0001g0265others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-2686C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210404 | ||||||
| chr8:100210639
|
T | C | 1 | a0001c0008t0002g0247 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1097-2451T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210639 | ||||||
| chr8:100210656
|
C | T | 40 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(37): Show | 42 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1097-2434C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210656 | ||||||
| chr8:100210866
|
C | T | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1097-2224C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210866 | ||||||
| chr8:100210920
|
C | T | 5 | a0001c0008t0002g0004a0001c0008t0002g0243a0001c0008t0002g0244others(2): Show | 6 | HG02109.hp1 HG02257.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-2170C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100210920 | ||||||
| chr8:100211080
|
C | T | 29 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(26): Show | 29 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1097-2010C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211080 | ||||||
| chr8:100211195
|
T | C | 1 | a0002c0007t0001g0191 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1097-1895T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211195 | ||||||
| chr8:100211410
|
C | A | 1 | a0002c0001t0001g0259 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1097-1680C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211410 | ||||||
| chr8:100211550
|
G | A | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1097-1540G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211550 | ||||||
| chr8:100211587
|
G | A | 1 | a0002c0001t0001g0313 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1097-1503G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211587 | ||||||
| chr8:100211784
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1097-1306T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211784 | ||||||
| chr8:100211846
|
G | C | 1 | a0001c0003t0005g0296 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1097-1244G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211846 | ||||||
| chr8:100211874
|
T | C | 1 | a0002c0001t0001g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1097-1216T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100211874 | ||||||
| chr8:100212103
|
G | A | 2 | a0002c0001t0001g0006a0002c0001t0001g0344 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1097-987G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212103 | ||||||
| chr8:100212269
|
A | C | 2 | a0002c0005t0002g0230a0002c0005t0002g0248 | 2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1097-821A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212269 | ||||||
| chr8:100212436
|
T | C | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1097-654T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212436 | ||||||
| chr8:100212535
|
G | T | 3 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209 | 3 | HG00639.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1097-555G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212535 | ||||||
| chr8:100212652
|
T | C | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1097-438T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212652 | ||||||
| chr8:100212784
|
G | T | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1097-306G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212784 | ||||||
| chr8:100212851
|
G | C | 7 | a0001c0002t0001g0100a0001c0002t0001g0130a0001c0002t0001g0167others(4): Show | 7 | HG00673.hp1 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097-239G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212851 | ||||||
| chr8:100212893
|
AG | A | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1097-192delG | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100212893 | |||||
| chr8:100212923
|
C | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1097-167C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212923 | ||||||
| chr8:100212989
|
A | G | 1 | a0001c0003t0001g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-101A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100212989 | ||||||
| chr8:100213013
|
C | CCCGCGGC others(2): Show |
238 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1097-60_1097-52dup others(9): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | |||||
| chr8:100213013
|
C | CCCGCGGC others(11): Show |
5 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097-69_1097-52dup others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | |||||
| chr8:100213013
|
C | CCCGCGGC others(20): Show |
1 | a0001c0003t0003g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-52_1097-51ins others(27): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | |||||
| chr8:100213013
|
CCCGCGGC others(2): Show |
C | 12 | a0001c0003t0001g0255a0001c0003t0001g0258a0003c0004t0001g0024others(9): Show | 12 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-60_1097-52del others(9): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 100213013 | |||||
| chr8:100213070
|
C | T | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1097-20C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 10/18 | chr8 | 100213070 | ||||||
| chr8:100213444
|
C | T | 3 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018 | 3 | HG02145.hp2 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1435+16C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213444 | ||||||
| chr8:100213480
|
C | A | 57 | a0001c0009t0001g0005a0001c0009t0001g0271a0001c0009t0001g0278others(54): Show | 58 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1435+52C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213480 | ||||||
| chr8:100213537
|
G | A | 1 | a0002c0007t0002g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1435+109G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213537 | ||||||
| chr8:100213610
|
C | G | 256 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1435+182C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213610 | ||||||
| chr8:100213666
|
G | A | 58 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1436-153G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213666 | ||||||
| chr8:100213782
|
T | A | 2 | a0008c0014t0001g0256a0008c0014t0001g0257 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1436-37T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 11/18 | chr8 | 100213782 | ||||||
| chr8:100214130
|
A | AC | 3 | a0001c0003t0001g0260a0002c0007t0001g0191a0013c0019t0001g0047 | 3 | HG00423.hp1 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1535+214dupC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214130 | |||||
| chr8:100214143
|
G | A | 5 | a0004c0006t0001g0033a0004c0006t0001g0037a0004c0006t0001g0038others(2): Show | 5 | HG01943.hp1 NA18954.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1535+225G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214143 | ||||||
| chr8:100214206
|
G | A | 17 | a0001c0003t0001g0107a0001c0003t0003g0102a0001c0003t0003g0103others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1535+288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214206 | ||||||
| chr8:100214215
|
A | G | 119 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1535+297A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214215 | ||||||
| chr8:100214485
|
A | G | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1535+567A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214485 | ||||||
| chr8:100214566
|
C | A | 2 | a0008c0014t0001g0256a0008c0014t0001g0257 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1535+648C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214566 | ||||||
| chr8:100214679
|
G | A | 1 | a0002c0001t0001g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1535+761G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214679 | ||||||
| chr8:100214796
|
A | T | 253 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1535+878A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214796 | ||||||
| chr8:100214810
|
T | C | 12 | a0001c0009t0001g0298a0002c0001t0001g0093a0002c0001t0001g0094others(9): Show | 12 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535+892T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214810 | ||||||
| chr8:100214885
|
C | G | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1535+967C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214885 | ||||||
| chr8:100214924
|
G | A | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1535+1006G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214924 | ||||||
| chr8:100214966
|
A | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1535+1048A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100214966 | ||||||
| chr8:100214988
|
C | CAT | 3 | a0002c0001t0001g0270a0002c0001t0001g0335a0002c0001t0006g0097 | 3 | HG01358.hp1 HG02155.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1535+1131_1535+113 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CAT | C | 3 | a0001c0002t0001g0210a0002c0001t0001g0324a0002c0001t0001g0356 | 3 | HG02027.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1535+1131_1535+113 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATAT | C | 19 | a0001c0002t0001g0128a0001c0002t0001g0162a0001c0002t0001g0166others(16): Show | 19 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1535+1129_1535+113 others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATAT | C | 21 | a0001c0002t0001g0087a0001c0002t0001g0099a0001c0002t0001g0122others(18): Show | 21 | HG00438.hp1 HG00544.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1535+1127_1535+113 others(10): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(1): Show |
C | 21 | a0001c0002t0001g0083a0001c0002t0001g0126a0001c0002t0001g0129others(18): Show | 21 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1535+1125_1535+113 others(12): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(3): Show |
C | 26 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0117others(23): Show | 26 | HG00609.hp1 HG01175.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.1535+1123_1535+113 others(14): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(5): Show |
C | 7 | a0001c0002t0001g0098a0001c0002t0001g0124a0001c0002t0001g0169others(4): Show | 7 | HG00673.hp2 HG01109.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535+1121_1535+113 others(16): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(7): Show |
C | 63 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0086others(60): Show | 65 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1535+1119_1535+113 others(18): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(9): Show |
C | 48 | a0001c0002t0001g0127a0001c0002t0001g0130a0001c0002t0001g0138others(45): Show | 49 | HG00597.hp2 HG00741.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1535+1117_1535+113 others(20): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(11): Show |
C | 23 | a0001c0002t0001g0144a0001c0002t0001g0147a0001c0002t0001g0158others(20): Show | 23 | HG00735.hp1 HG01255.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1535+1115_1535+113 others(22): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(13): Show |
C | 8 | a0001c0002t0001g0100a0001c0002t0001g0168a0001c0002t0001g0183others(5): Show | 8 | HG00673.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535+1113_1535+113 others(24): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(15): Show |
C | 3 | a0001c0003t0003g0102a0002c0001t0001g0340a0002c0001t0002g0341 | 3 | HG00733.hp2 HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1535+1111_1535+113 others(26): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(17): Show |
C | 3 | a0001c0003t0001g0260a0002c0001t0001g0317a0002c0001t0001g0355 | 3 | HG02055.hp2 HG02698.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1535+1109_1535+113 others(28): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(19): Show |
C | 1 | a0001c0003t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1535+1107_1535+113 others(30): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(23): Show |
C | 2 | a0001c0002t0001g0215a0002c0001t0001g0012 | 2 | NA18950.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1535+1103_1535+113 others(34): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(25): Show |
C | 1 | a0004c0006t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1535+1101_1535+113 others(36): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(27): Show |
C | 7 | a0002c0001t0001g0006a0002c0001t0001g0344a0003c0004t0001g0030others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535+1099_1535+113 others(38): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(29): Show |
C | 51 | a0001c0003t0003g0216a0002c0001t0001g0290a0002c0001t0001g0305others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1535+1097_1535+113 others(40): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(31): Show |
C | 6 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535+1095_1535+113 others(42): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(33): Show |
C | 1 | a0002c0005t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1535+1093_1535+113 others(44): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(35): Show |
C | 39 | a0001c0003t0003g0108a0001c0008t0002g0004a0001c0008t0002g0090others(36): Show | 41 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1535+1091_1535+113 others(46): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100214988
|
CATATATA others(39): Show |
C | 1 | a0003c0004t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1535+1087_1535+113 others(50): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100214988 | |||||
| chr8:100215104
|
G | C | 1 | a0011c0022t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1535+1186G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215104 | ||||||
| chr8:100215194
|
T | G | 181 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1535+1276T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215194 | ||||||
| chr8:100215620
|
G | A | 2 | a0002c0001t0001g0284a0002c0001t0001g0285 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1535+1702G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215620 | ||||||
| chr8:100215686
|
G | A | 39 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(36): Show | 41 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1535+1768G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215686 | ||||||
| chr8:100215816
|
G | A | 1 | a0001c0021t0001g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1535+1898G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215816 | ||||||
| chr8:100215854
|
T | A | 122 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1535+1936T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100215854 | ||||||
| chr8:100216140
|
T | C | 1 | a0002c0007t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1535+2222T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216140 | ||||||
| chr8:100216220
|
C | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1535+2302C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216220 | ||||||
| chr8:100216253
|
A | T | 1 | a0002c0007t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1535+2335A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216253 | ||||||
| chr8:100216255
|
C | G | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1535+2337C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216255 | ||||||
| chr8:100216302
|
C | T | 254 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1535+2384C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216302 | ||||||
| chr8:100216495
|
G | C | 1 | a0002c0007t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1535+2577G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216495 | ||||||
| chr8:100216563
|
C | T | 63 | a0001c0003t0001g0078a0001c0003t0001g0079a0002c0001t0001g0007others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1535+2645C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100216563 | ||||||
| chr8:100216931
|
CT | C | 22 | a0001c0002t0001g0130a0001c0002t0001g0137a0001c0002t0001g0185others(19): Show | 22 | HG00438.hp2 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1535+3036delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | |||||
| chr8:100216931
|
CTT | C | 188 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1535+3035_1535+303 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | |||||
| chr8:100216931
|
CTTT | C | 43 | a0001c0002t0001g0120a0001c0002t0001g0124a0001c0003t0001g0359others(40): Show | 45 | HG00323.hp2 HG01081.hp1 HG01516.hp2 others(42): Show |
intron_variant | MODIFIER | c.1535+3034_1535+303 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100216931 | |||||
| chr8:100217225
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1536-3054G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217225 | ||||||
| chr8:100217351
|
A | G | 256 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1536-2928A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217351 | ||||||
| chr8:100217366
|
A | G | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1536-2913A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217366 | ||||||
| chr8:100217399
|
G | A | 36 | a0001c0008t0002g0090a0001c0008t0002g0091a0001c0008t0002g0092others(33): Show | 37 | HG01081.hp1 HG02148.hp1 HG02280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536-2880G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217399 | ||||||
| chr8:100217661
|
A | G | 44 | a0001c0002t0001g0130a0001c0002t0001g0137a0001c0002t0001g0167others(41): Show | 46 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1536-2618A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217661 | ||||||
| chr8:100217689
|
C | T | 13 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1536-2590C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217689 | ||||||
| chr8:100217814
|
A | G | 1 | a0001c0002t0001g0149 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1536-2465A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217814 | ||||||
| chr8:100217828
|
G | A | 1 | a0002c0007t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1536-2451G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217828 | ||||||
| chr8:100217891
|
T | G | 1 | a0001c0008t0002g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1536-2388T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100217891 | ||||||
| chr8:100218035
|
A | G | 107 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(104): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1536-2244A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218035 | ||||||
| chr8:100218242
|
T | C | 1 | a0003c0004t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1536-2037T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218242 | ||||||
| chr8:100218247
|
C | A | 2 | a0003c0004t0001g0069a0003c0004t0001g0071 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1536-2032C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218247 | ||||||
| chr8:100218295
|
A | G | 244 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1536-1984A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218295 | ||||||
| chr8:100218306
|
T | A | 244 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1536-1973T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218306 | ||||||
| chr8:100218867
|
G | T | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1536-1412G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100218867 | ||||||
| chr8:100219091
|
A | G | 1 | a0001c0003t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1536-1188A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219091 | ||||||
| chr8:100219290
|
T | A | 356 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(353): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1536-989T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219290 | ||||||
| chr8:100219295
|
T | C | 4 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-984T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219295 | ||||||
| chr8:100219460
|
T | C | 1 | a0001c0012t0002g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1536-819T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219460 | ||||||
| chr8:100219539
|
T | G | 1 | a0005c0010t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1536-740T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219539 | ||||||
| chr8:100219579
|
G | A | 1 | a0001c0003t0005g0296 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1536-700G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100219579 | ||||||
| chr8:100220162
|
C | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0167 | 2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1536-117C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220162 | ||||||
| chr8:100220171
|
G | A | 4 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-108G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220171 | ||||||
| chr8:100220193
|
TCAGTACT others(1): Show |
T | 31 | a0001c0003t0001g0107a0001c0003t0001g0255a0001c0003t0001g0258others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1536-80_1536-73del others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 100220193 | |||||
| chr8:100220199
|
C | G | 1 | a0003c0004t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1536-80C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220199 | ||||||
| chr8:100220201
|
G | T | 1 | a0003c0004t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1536-78G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220201 | ||||||
| chr8:100220270
|
C | G | 4 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536-9C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 12/18 | chr8 | 100220270 | ||||||
| chr8:100220473
|
T | C | 245 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1688+42T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220473 | ||||||
| chr8:100220549
|
G | A | 8 | a0003c0004t0001g0024a0003c0004t0001g0049a0003c0004t0001g0050others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+118G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220549 | ||||||
| chr8:100220550
|
ATTGCCT | A | 8 | a0003c0004t0001g0024a0003c0004t0001g0049a0003c0004t0001g0050others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+121_1688+126d others(8): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 100220550 | |||||
| chr8:100220559
|
T | A | 8 | a0003c0004t0001g0024a0003c0004t0001g0049a0003c0004t0001g0050others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+128T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220559 | ||||||
| chr8:100220588
|
C | T | 1 | a0002c0001t0001g0310 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1688+157C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220588 | ||||||
| chr8:100220780
|
T | C | 238 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(235): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1688+349T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220780 | ||||||
| chr8:100220844
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1688+413G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220844 | ||||||
| chr8:100220870
|
C | T | 1 | a0002c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1688+439C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220870 | ||||||
| chr8:100220945
|
C | T | 1 | a0002c0001t0006g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1688+514C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100220945 | ||||||
| chr8:100221014
|
G | A | 2 | a0002c0001t0001g0308a0002c0001t0001g0311 | 2 | HG02040.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1688+583G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221014 | ||||||
| chr8:100221055
|
G | A | 1 | a0002c0001t0001g0299 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1688+624G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221055 | ||||||
| chr8:100221069
|
A | T | 245 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1688+638A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221069 | ||||||
| chr8:100221072
|
C | CAA | 4 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688+641_1688+642i others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221072 | ||||||
| chr8:100221073
|
C | A | 245 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1688+642C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221073 | ||||||
| chr8:100221178
|
T | C | 3 | a0001c0008t0002g0090a0001c0008t0002g0091a0001c0008t0002g0092 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1688+747T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221178 | ||||||
| chr8:100221383
|
C | T | 1 | a0009c0017t0001g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1688+952C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221383 | ||||||
| chr8:100221430
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1688+999C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221430 | ||||||
| chr8:100221668
|
T | C | 245 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1688+1237T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221668 | ||||||
| chr8:100221898
|
A | G | 248 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(245): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1688+1467A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100221898 | ||||||
| chr8:100222256
|
C | T | 1 | a0003c0004t0001g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1688+1825C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222256 | ||||||
| chr8:100222261
|
C | G | 4 | a0001c0008t0002g0217a0001c0008t0002g0218a0001c0008t0002g0219others(1): Show | 4 | HG03041.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1688+1830C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222261 | ||||||
| chr8:100222333
|
A | C | 1 | a0006c0011t0002g0252 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1688+1902A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222333 | ||||||
| chr8:100222357
|
C | T | 41 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010others(38): Show | 41 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1688+1926C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222357 | ||||||
| chr8:100222915
|
G | A | 1 | a0002c0007t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1689-2258G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100222915 | ||||||
| chr8:100223074
|
C | A | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1689-2099C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223074 | ||||||
| chr8:100223238
|
A | G | 1 | a0002c0001t0001g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1689-1935A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223238 | ||||||
| chr8:100223363
|
G | T | 1 | a0001c0002t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1689-1810G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223363 | ||||||
| chr8:100223580
|
CT | C | 127 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1689-1579delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 100223580 | |||||
| chr8:100223804
|
C | T | 1 | a0002c0001t0001g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1689-1369C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223804 | ||||||
| chr8:100223836
|
A | T | 1 | a0002c0001t0001g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1689-1337A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223836 | ||||||
| chr8:100223943
|
T | G | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689-1230T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100223943 | ||||||
| chr8:100224075
|
C | T | 1 | a0002c0001t0001g0309 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1689-1098C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224075 | ||||||
| chr8:100224219
|
C | A | 1 | a0002c0001t0001g0259 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1689-954C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224219 | ||||||
| chr8:100224283
|
C | G | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1689-890C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224283 | ||||||
| chr8:100224411
|
G | A | 37 | a0001c0003t0001g0260a0001c0003t0003g0102a0001c0003t0003g0103others(34): Show | 39 | HG00733.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1689-762G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224411 | ||||||
| chr8:100224528
|
T | C | 45 | a0001c0002t0001g0137a0001c0008t0002g0004a0001c0008t0002g0090others(42): Show | 47 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1689-645T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224528 | ||||||
| chr8:100224579
|
A | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1689-594A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224579 | ||||||
| chr8:100224884
|
T | G | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689-289T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224884 | ||||||
| chr8:100224979
|
G | A | 1 | a0011c0022t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1689-194G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 13/18 | chr8 | 100224979 | ||||||
| chr8:100225442
|
C | T | 1 | a0002c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1855+103C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225442 | ||||||
| chr8:100225516
|
C | T | 5 | a0003c0004t0001g0022a0003c0004t0001g0030a0003c0004t0001g0031others(2): Show | 5 | HG00099.hp1 HG00735.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+177C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225516 | ||||||
| chr8:100225573
|
C | T | 1 | a0001c0002t0001g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1855+234C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225573 | ||||||
| chr8:100225635
|
G | T | 3 | a0001c0002t0001g0151a0001c0002t0001g0213a0001c0003t0001g0016 | 3 | HG02280.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1855+296G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225635 | ||||||
| chr8:100225636
|
T | G | 28 | a0001c0002t0001g0137a0001c0015t0001g0224a0001c0015t0001g0228others(25): Show | 28 | HG01081.hp1 HG02148.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.1855+297T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225636 | ||||||
| chr8:100225689
|
G | T | 21 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(18): Show | 21 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1855+350G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225689 | ||||||
| chr8:100225714
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1855+375A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225714 | ||||||
| chr8:100225801
|
T | C | 1 | a0002c0001t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1855+462T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225801 | ||||||
| chr8:100225829
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1855+490G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225829 | ||||||
| chr8:100225881
|
G | A | 1 | a0001c0002t0001g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1855+542G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225881 | ||||||
| chr8:100225882
|
G | A | 1 | a0006c0011t0002g0003 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1855+543G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225882 | ||||||
| chr8:100225892
|
G | T | 203 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1855+553G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225892 | ||||||
| chr8:100225902
|
G | A | 17 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(14): Show | 19 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1855+563G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225902 | ||||||
| chr8:100225936
|
A | G | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+597A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100225936 | ||||||
| chr8:100225998
|
G | GT | 14 | a0001c0002t0001g0098a0001c0002t0001g0161a0001c0002t0001g0164others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+677dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100225998 | |||||
| chr8:100225998
|
GT | G | 6 | a0002c0001t0001g0113a0002c0007t0001g0190a0002c0007t0001g0191others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855+677delT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100225998 | |||||
| chr8:100226278
|
T | C | 1 | a0001c0002t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1855+939T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226278 | ||||||
| chr8:100226363
|
T | C | 1 | a0002c0001t0001g0272 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1855+1024T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226363 | ||||||
| chr8:100226912
|
T | C | 1 | a0001c0008t0008g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1855+1573T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100226912 | ||||||
| chr8:100227360
|
A | G | 6 | a0001c0003t0001g0260a0001c0003t0001g0357a0001c0003t0001g0358others(3): Show | 6 | HG01099.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1855+2021A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227360 | ||||||
| chr8:100227662
|
G | C | 37 | a0001c0003t0001g0260a0001c0003t0001g0357a0001c0003t0001g0358others(34): Show | 39 | HG00733.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1855+2323G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227662 | ||||||
| chr8:100227841
|
A | AT | 37 | a0001c0002t0001g0085a0001c0002t0001g0099a0001c0002t0001g0124others(34): Show | 37 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1855+2525dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | |||||
| chr8:100227841
|
A | ATT | 141 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(138): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1855+2524_1855+252 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | |||||
| chr8:100227841
|
A | ATTT | 70 | a0001c0002t0001g0086a0001c0002t0001g0137a0001c0002t0001g0153others(67): Show | 70 | HG00140.hp2 HG00544.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.1855+2523_1855+252 others(7): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100227841 | |||||
| chr8:100227872
|
G | T | 2 | a0001c0009t0001g0278a0002c0001t0001g0280 | 2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1855+2533G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227872 | ||||||
| chr8:100227980
|
G | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1855+2641G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100227980 | ||||||
| chr8:100228063
|
C | T | 1 | a0001c0003t0003g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1855+2724C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100228063 | ||||||
| chr8:100228159
|
A | G | 1 | a0001c0009t0001g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1855+2820A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100228159 | ||||||
| chr8:100228410
|
C | CA | 49 | a0001c0002t0001g0120a0001c0003t0001g0260a0001c0003t0001g0357others(46): Show | 51 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1856-2728dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100228410 | |||||
| chr8:100228410
|
C | CAA | 199 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1856-2729_1856-272 others(6): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100228410 | |||||
| chr8:100229063
|
C | T | 1 | a0002c0001t0001g0334 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1856-2093C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229063 | ||||||
| chr8:100229174
|
G | A | 2 | a0002c0007t0001g0191a0002c0007t0001g0192 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1856-1982G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229174 | ||||||
| chr8:100229387
|
G | A | 1 | a0002c0001t0001g0317 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1856-1769G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229387 | ||||||
| chr8:100229403
|
G | A | 14 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(11): Show | 15 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1856-1753G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229403 | ||||||
| chr8:100229418
|
C | T | 1 | a0001c0002t0001g0169 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1856-1738C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229418 | ||||||
| chr8:100229445
|
C | A | 1 | a0001c0002t0001g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1856-1711C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229445 | ||||||
| chr8:100229445
|
C | CA | 13 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1856-1702dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 100229445 | |||||
| chr8:100229497
|
T | A | 1 | a0010c0023t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1856-1659T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229497 | ||||||
| chr8:100229670
|
T | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1856-1486T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229670 | ||||||
| chr8:100229684
|
A | G | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856-1472A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229684 | ||||||
| chr8:100229940
|
T | C | 59 | a0001c0002t0001g0137a0001c0003t0003g0102a0001c0003t0003g0103others(56): Show | 61 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1856-1216T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100229940 | ||||||
| chr8:100230385
|
C | T | 32 | a0001c0003t0001g0107a0001c0003t0001g0255a0001c0003t0001g0258others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1856-771C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230385 | ||||||
| chr8:100230529
|
C | G | 175 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1856-627C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230529 | ||||||
| chr8:100230598
|
A | G | 1 | a0009c0017t0001g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1856-558A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230598 | ||||||
| chr8:100230748
|
C | T | 1 | a0002c0001t0001g0282 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1856-408C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230748 | ||||||
| chr8:100230863
|
C | T | 2 | a0003c0004t0001g0250a0009c0017t0001g0249 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1856-293C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230863 | ||||||
| chr8:100230868
|
G | A | 1 | a0001c0009t0001g0329 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1856-288G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230868 | ||||||
| chr8:100230910
|
T | C | 1 | a0002c0001t0001g0310 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1856-246T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100230910 | ||||||
| chr8:100231038
|
C | T | 4 | a0001c0009t0001g0005a0001c0009t0001g0288a0001c0009t0001g0291others(1): Show | 5 | HG01496.hp1 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856-118C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100231038 | ||||||
| chr8:100231119
|
A | G | 65 | a0001c0002t0001g0137a0001c0003t0001g0260a0001c0003t0001g0357others(62): Show | 67 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1856-37A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 14/18 | chr8 | 100231119 | ||||||
| chr8:100231350
|
TAA | T | 45 | a0001c0002t0001g0137a0001c0008t0002g0004a0001c0008t0002g0090others(42): Show | 47 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(44): Show |
intron_variant | MODIFIER | c.1988+63_1988+64del others(2): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231350 | ||||||
| chr8:100231465
|
G | A | 45 | a0001c0002t0001g0137a0001c0008t0002g0004a0001c0008t0002g0090others(42): Show | 47 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(44): Show |
intron_variant | MODIFIER | c.1988+177G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231465 | ||||||
| chr8:100231497
|
C | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0002t0001g0210others(1): Show | 4 | HG02738.hp2 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1988+209C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231497 | ||||||
| chr8:100231509
|
T | C | 1 | a0001c0009t0001g0345 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1988+221T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231509 | ||||||
| chr8:100231726
|
G | A | 1 | a0001c0003t0003g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1988+438G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231726 | ||||||
| chr8:100231833
|
G | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0167 | 2 | NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1988+545G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231833 | ||||||
| chr8:100231961
|
C | CA | 45 | a0001c0002t0001g0118a0001c0003t0001g0107a0001c0003t0001g0255others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1988+688dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 100231961 | |||||
| chr8:100231976
|
A | AAAT | 44 | a0001c0002t0001g0137a0001c0008t0002g0004a0001c0008t0002g0090others(41): Show | 46 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(43): Show |
intron_variant | MODIFIER | c.1988+688_1988+689i others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231976 | ||||||
| chr8:100231976
|
A | AAT | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1988+688_1988+689i others(4): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231976 | ||||||
| chr8:100231977
|
T | A | 59 | a0001c0002t0001g0137a0001c0003t0003g0102a0001c0003t0003g0103others(56): Show | 61 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1988+689T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231977 | ||||||
| chr8:100231987
|
G | T | 243 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1988+699G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100231987 | ||||||
| chr8:100232043
|
G | C | 1 | a0003c0004t0005g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1988+755G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232043 | ||||||
| chr8:100232225
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1988+937T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232225 | ||||||
| chr8:100232307
|
A | T | 1 | a0002c0001t0001g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1988+1019A>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232307 | ||||||
| chr8:100232660
|
A | G | 1 | a0002c0007t0001g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1989-751A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232660 | ||||||
| chr8:100232670
|
T | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1989-741T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232670 | ||||||
| chr8:100232748
|
C | T | 3 | a0003c0004t0001g0022a0003c0004t0001g0081a0003c0004t0001g0082 | 3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1989-663C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232748 | ||||||
| chr8:100232844
|
T | C | 1 | a0010c0023t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1989-567T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100232844 | ||||||
| chr8:100233014
|
G | A | 36 | a0002c0001t0001g0093a0002c0001t0001g0094a0002c0001t0001g0095others(33): Show | 36 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1989-397G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233014 | ||||||
| chr8:100233171
|
G | T | 1 | a0002c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1989-240G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233171 | ||||||
| chr8:100233210
|
C | G | 3 | a0001c0008t0002g0090a0001c0008t0002g0091a0001c0008t0002g0092 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1989-201C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 15/18 | chr8 | 100233210 | ||||||
| chr8:100233776
|
G | T | 1 | a0012c0020t0001g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2115+239G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100233776 | ||||||
| chr8:100234010
|
A | G | 1 | a0002c0001t0001g0286 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2115+473A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234010 | ||||||
| chr8:100234359
|
T | TA | 202 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2115+831dupA | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100234359 | |||||
| chr8:100234603
|
G | A | 1 | a0002c0001t0001g0327 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2115+1066G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234603 | ||||||
| chr8:100234707
|
T | C | 7 | a0001c0008t0002g0004a0001c0008t0002g0243a0001c0008t0002g0244others(4): Show | 8 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2115+1170T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234707 | ||||||
| chr8:100234709
|
T | G | 1 | a0002c0007t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2115+1172T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100234709 | ||||||
| chr8:100235092
|
T | C | 247 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2115+1555T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235092 | ||||||
| chr8:100235123
|
G | C | 1 | a0002c0005t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2115+1586G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235123 | ||||||
| chr8:100235258
|
G | A | 1 | a0002c0007t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2115+1721G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235258 | ||||||
| chr8:100235373
|
C | A | 1 | a0001c0003t0001g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2115+1836C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235373 | ||||||
| chr8:100235594
|
G | A | 1 | a0003c0004t0001g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2115+2057G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235594 | ||||||
| chr8:100235741
|
T | A | 1 | a0002c0001t0001g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2115+2204T>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235741 | ||||||
| chr8:100235761
|
C | T | 118 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(115): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2115+2224C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235761 | ||||||
| chr8:100235782
|
G | A | 2 | a0002c0001t0001g0261a0002c0001t0001g0323 | 2 | NA19002.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2115+2245G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235782 | ||||||
| chr8:100235888
|
C | T | 25 | a0001c0003t0001g0107a0003c0004t0001g0022a0003c0004t0001g0023others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2115+2351C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235888 | ||||||
| chr8:100235954
|
T | C | 1 | a0003c0004t0001g0043 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2115+2417T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235954 | ||||||
| chr8:100235965
|
G | A | 3 | a0001c0008t0002g0217a0001c0008t0002g0218a0001c0008t0002g0219 | 3 | HG03041.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2115+2428G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100235965 | ||||||
| chr8:100236054
|
C | T | 3 | a0001c0003t0001g0357a0001c0003t0001g0358a0001c0003t0001g0359 | 3 | HG02723.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2115+2517C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236054 | ||||||
| chr8:100236090
|
A | C | 6 | a0001c0003t0001g0260a0001c0003t0001g0357a0001c0003t0001g0358others(3): Show | 6 | HG01099.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+2553A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236090 | ||||||
| chr8:100236135
|
T | G | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2115+2598T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236135 | ||||||
| chr8:100236210
|
G | C | 1 | a0002c0001t0001g0300 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2115+2673G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236210 | ||||||
| chr8:100236283
|
G | A | 1 | a0002c0005t0002g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2115+2746G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236283 | ||||||
| chr8:100236298
|
A | G | 42 | a0001c0008t0002g0004a0001c0008t0002g0090a0001c0008t0002g0091others(39): Show | 44 | HG01081.hp1 HG02109.hp1 HG02148.hp1 others(41): Show |
intron_variant | MODIFIER | c.2115+2761A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236298 | ||||||
| chr8:100236542
|
C | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-2698C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236542 | ||||||
| chr8:100236712
|
T | C | 2 | a0001c0003t0001g0293a0001c0003t0001g0294 | 2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2116-2528T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100236712 | ||||||
| chr8:100237269
|
C | T | 14 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2116-1971C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237269 | ||||||
| chr8:100237346
|
G | C | 1 | a0001c0003t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2116-1894G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237346 | ||||||
| chr8:100237534
|
G | T | 205 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2116-1706G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237534 | ||||||
| chr8:100237543
|
T | C | 4 | a0002c0001t0001g0009a0002c0007t0001g0194a0002c0007t0001g0195others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-1697T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237543 | ||||||
| chr8:100237679
|
C | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-1561C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100237679 | ||||||
| chr8:100238007
|
A | G | 1 | a0002c0001t0001g0303 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2116-1233A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238007 | ||||||
| chr8:100238012
|
A | G | 1 | a0004c0006t0001g0058 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2116-1228A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238012 | ||||||
| chr8:100238190
|
C | T | 1 | a0001c0009t0001g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2116-1050C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238190 | ||||||
| chr8:100238288
|
TC | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-949delC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100238288 | |||||
| chr8:100238379
|
A | G | 1 | a0003c0004t0005g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2116-861A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238379 | ||||||
| chr8:100238517
|
T | C | 2 | a0002c0001t0001g0264a0002c0001t0001g0265 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2116-723T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238517 | ||||||
| chr8:100238623
|
A | G | 56 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0104others(53): Show | 58 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.2116-617A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238623 | ||||||
| chr8:100238679
|
C | T | 168 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2116-561C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238679 | ||||||
| chr8:100238741
|
A | G | 1 | a0001c0003t0001g0359 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2116-499A>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238741 | ||||||
| chr8:100238750
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2116-490T>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238750 | ||||||
| chr8:100238765
|
CTTA | C | 168 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2116-469_2116-467d others(5): Show |
SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100238765 | |||||
| chr8:100238857
|
C | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-383C>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100238857 | ||||||
| chr8:100239068
|
G | A | 1 | a0001c0002t0001g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2116-172G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239068 | ||||||
| chr8:100239137
|
G | GC | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2116-102dupC | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 100239137 | |||||
| chr8:100239138
|
C | A | 3 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209 | 3 | HG00639.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2116-102C>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239138 | ||||||
| chr8:100239196
|
C | T | 3 | a0001c0012t0002g0116a0006c0011t0002g0003a0006c0011t0002g0252 | 4 | HG02280.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-44C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 16/18 | chr8 | 100239196 | ||||||
| chr8:100239479
|
A | C | 1 | a0001c0002t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2280+75A>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239479 | ||||||
| chr8:100239707
|
G | A | 2 | a0001c0003t0001g0076a0001c0003t0001g0077 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2280+303G>A | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239707 | ||||||
| chr8:100239715
|
G | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0008a0002c0001t0001g0010 | 3 | HG02055.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2280+311G>C | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100239715 | ||||||
| chr8:100240234
|
C | T | 208 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0083others(205): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2281-169C>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 17/18 | chr8 | 100240234 | ||||||
| chr8:100240864
|
G | GT | 10 | a0001c0003t0001g0021a0001c0003t0001g0258a0001c0003t0001g0260others(7): Show | 11 | HG00438.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2650-12dupT | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 100240864 | |||||
| chr8:100240864
|
G | T | 1 | a0002c0001t0001g0325 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2650-27G>T | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | chr8 | 100240864 | ||||||
| chr8:100240871
|
T | G | 1 | a0001c0002t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2650-20T>G | SPAG1 | ENSG00000104450.13 | transcript | ENST00000388798.7 | protein_coding | 18/18 | chr8 | 100240871 |