| geneid | 54558 |
|---|---|
| ensemblid | ENSG00000132122.12 |
| hgncid | 18309 |
| symbol | SPATA6 |
| name | spermatogenesis associated 6 |
| refseq_nuc | NM_019073.4 |
| refseq_prot | NP_061946.1 |
| ensembl_nuc | ENST00000371847.8 |
| ensembl_prot | ENSP00000360913.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 48295373 |
| end | 48472204 |
| strand | - |
| ver | v1.2 |
| region | chr1:48295373-48472204 |
| region5000 | chr1:48290373-48477204 |
| regionname0 | SPATA6_chr1_48295373_48472204 |
| regionname5000 | SPATA6_chr1_48290373_48477204 |
| 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 | 1/0 | 488 | 223 | 66 | 36 | 96 | 9 | 15 | 72 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002 | 0/1 | 488 | 93 | 2 | 21 | 51 | 7 | 11 | 41 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0003 | 0/0 | 488 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0004 | 0/0 | 488 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0005 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| 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 | 1467 | 222 | 66 | 35 | 96 | 9 | 15 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| c0002 | 0/1 | 1467 | 93 | 2 | 21 | 51 | 7 | 11 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| c0003 | 0/0 | 1467 | 3 | 0 | 3 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| c0004 | 0/0 | 1467 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| c0005 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| c0006 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| 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 | 0/0 | 3535 | 52 | 1 | 11 | 34 | 4 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0002 | 0/0 | 3526 | 44 | 4 | 13 | 23 | 1 | 3 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0003 | 1/0 | 3537 | 42 | 9 | 5 | 23 | 2 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0004 | 0/0 | 3531 | 35 | 1 | 1 | 32 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0005 | 0/1 | 3537 | 34 | 1 | 6 | 16 | 2 | 8 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0006 | 0/0 | 3531 | 15 | 6 | 5 | 0 | 2 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0007 | 0/0 | 3545 | 11 | 0 | 5 | 1 | 3 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0008 | 0/0 | 3533 | 9 | 8 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0009 | 0/0 | 3535 | 9 | 3 | 3 | 3 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0010 | 0/0 | 3539 | 6 | 1 | 3 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0011 | 0/0 | 3537 | 6 | 6 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0012 | 0/0 | 3533 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0013 | 0/0 | 3532 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0014 | 0/0 | 3529 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0015 | 0/0 | 3551 | 3 | 0 | 2 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0016 | 0/0 | 3549 | 3 | 2 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0017 | 0/0 | 3531 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0018 | 0/0 | 3533 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0019 | 0/0 | 3539 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0020 | 0/0 | 3535 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0021 | 0/0 | 3528 | 2 | 1 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0022 | 0/0 | 3537 | 2 | 1 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0023 | 0/0 | 3535 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0024 | 0/0 | 3524 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0025 | 0/0 | 3539 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0026 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0027 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0028 | 0/0 | 3541 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0029 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0030 | 0/0 | 3533 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0031 | 0/0 | 3531 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0032 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0033 | 0/0 | 3537 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0034 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0035 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0036 | 0/0 | 3557 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0037 | 0/0 | 3547 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0038 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0039 | 0/0 | 3541 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0040 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0041 | 0/0 | 3529 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0042 | 0/0 | 3527 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0043 | 0/0 | 3551 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| t0044 | 0/0 | 3535 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1467 | 222 | 66 | 35 | 96 | 9 | 15 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0005 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002 | 0/1 | 1467 | 93 | 2 | 21 | 51 | 7 | 11 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0003c0003 | 0/0 | 1467 | 3 | 0 | 3 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0004c0004 | 0/0 | 1467 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0005c0006 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5001 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0002 | 0/0 | 4992 | 42 | 4 | 11 | 23 | 1 | 3 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0003 | 1/0 | 5003 | 38 | 9 | 1 | 23 | 2 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0004 | 0/0 | 4997 | 35 | 1 | 1 | 32 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0006 | 0/0 | 4997 | 15 | 6 | 5 | 0 | 2 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0007 | 0/0 | 5011 | 11 | 0 | 5 | 1 | 3 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0008 | 0/0 | 4999 | 9 | 8 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0009 | 0/0 | 5001 | 9 | 3 | 3 | 3 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0010 | 0/0 | 5005 | 6 | 1 | 3 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0011 | 0/0 | 5003 | 6 | 6 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0012 | 0/0 | 4999 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0013 | 0/0 | 4998 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0014 | 0/0 | 4995 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0015 | 0/0 | 5017 | 3 | 0 | 2 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0016 | 0/0 | 5015 | 3 | 2 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0017 | 0/0 | 4997 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0018 | 0/0 | 4999 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0020 | 0/0 | 5001 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0021 | 0/0 | 4994 | 2 | 1 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0022 | 0/0 | 5003 | 2 | 1 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0023 | 0/0 | 5001 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0024 | 0/0 | 4990 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0025 | 0/0 | 5005 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0026 | 0/0 | 5015 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0034 | 0/0 | 4995 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0035 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0036 | 0/0 | 5023 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0037 | 0/0 | 5013 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0038 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0039 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0040 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0041 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0042 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0043 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0001t0044 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0001c0005t0003 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0001 | 0/0 | 5001 | 50 | 1 | 11 | 33 | 3 | 2 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0005 | 0/1 | 5003 | 34 | 1 | 6 | 16 | 2 | 8 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0019 | 0/0 | 5005 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0027 | 0/0 | 5003 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0028 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0029 | 0/0 | 5003 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0030 | 0/0 | 4999 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0031 | 0/0 | 4997 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0032 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0002c0002t0033 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0003c0003t0003 | 0/0 | 5003 | 3 | 0 | 3 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0004c0004t0002 | 0/0 | 4992 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| a0005c0006t0001 | 0/0 | 5001 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | copy fasta | chr1 | 48290373 | 48477204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0012g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0012g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0012g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0014g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0015g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0015g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0015g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0016g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0017g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0017g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0017g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0018g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0018g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0018g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0020g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0020g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0021g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0022g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0022g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0023g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0024g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0024g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0025g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0025g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0026g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0026g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0034g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0035g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0036g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0037g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0038g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0039g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0040g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0041g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0042g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0043g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0001t0044g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0001c0005t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0019g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0019g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0027g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0028g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0029g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0030g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0031g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0032g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0002c0002t0033g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0003c0003t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0004c0004t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0004c0004t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| a0005c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0302 | EUR | GBR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00099 | hp2 | a0002 | c0002 | t0005 | g0069 | EUR | GBR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00140 | hp1 | a0002 | c0002 | t0005 | g0068 | EUR | GBR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0147 | EUR | GBR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | FIN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00280 | hp2 | a0002 | c0002 | t0027 | g0062 | EUR | FIN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | FIN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0119 | EUR | FIN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00597 | hp2 | a0001 | c0001 | t0024 | g0185 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00621 | hp1 | a0001 | c0001 | t0024 | g0182 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | CHS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0308 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00642 | hp1 | a0001 | c0005 | t0003 | g0223 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00642 | hp2 | a0002 | c0002 | t0019 | g0080 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0307 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00735 | hp2 | a0002 | c0002 | t0028 | g0086 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0085 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0320 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0072 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0304 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0312 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0206 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0303 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0146 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0319 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01099 | hp2 | a0002 | c0002 | t0005 | g0071 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01167 | hp1 | a0001 | c0001 | t0035 | g0160 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0228 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01168 | hp2 | a0002 | c0002 | t0019 | g0076 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01243 | hp1 | a0001 | c0001 | t0041 | g0212 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0321 | AMR | PUR | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0275 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0166 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01256 | hp2 | a0004 | c0004 | t0002 | g0098 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0226 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01258 | hp2 | a0004 | c0004 | t0002 | g0097 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01261 | hp1 | a0002 | c0002 | t0033 | g0063 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01261 | hp2 | a0003 | c0003 | t0003 | g0110 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0137 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0149 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01433 | hp2 | a0003 | c0003 | t0003 | g0111 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0046 | EUR | IBS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0301 | EUR | IBS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0300 | EUR | IBS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0084 | EUR | IBS | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0317 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01934 | hp1 | a0001 | c0001 | t0040 | g0193 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01934 | hp2 | a0002 | c0002 | t0005 | g0081 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0236 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01952 | hp2 | a0002 | c0002 | t0005 | g0070 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01993 | hp1 | a0003 | c0003 | t0003 | g0112 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02040 | hp1 | a0002 | c0002 | t0005 | g0022 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0163 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02055 | hp2 | a0001 | c0001 | t0025 | g0210 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02129 | hp2 | a0002 | c0002 | t0032 | g0060 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0214 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0235 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0103 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CDX | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CDX | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CDX | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CDX | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02257 | hp1 | a0001 | c0001 | t0026 | g0297 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0198 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02451 | hp1 | a0001 | c0001 | t0034 | g0101 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02602 | hp2 | a0002 | c0002 | t0005 | g0015 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02615 | hp1 | a0001 | c0001 | t0043 | g0298 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0252 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0234 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02698 | hp1 | a0001 | c0001 | t0015 | g0318 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02698 | hp2 | a0001 | c0001 | t0021 | g0159 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02723 | hp2 | a0001 | c0001 | t0017 | g0246 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02809 | hp1 | a0001 | c0001 | t0022 | g0294 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0157 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0237 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0161 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02922 | hp2 | a0001 | c0001 | t0025 | g0209 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0196 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03017 | hp2 | a0002 | c0002 | t0031 | g0075 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03041 | hp1 | a0001 | c0001 | t0026 | g0295 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0245 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0241 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0213 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03225 | hp1 | a0001 | c0001 | t0018 | g0315 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0247 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03239 | hp1 | a0002 | c0002 | t0005 | g0083 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03239 | hp2 | a0002 | c0002 | t0005 | g0058 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03491 | hp1 | a0002 | c0002 | t0005 | g0066 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03492 | hp1 | a0002 | c0002 | t0005 | g0073 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03492 | hp2 | a0001 | c0001 | t0037 | g0310 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0299 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0164 | AFR | ESN | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0238 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03579 | hp2 | a0001 | c0001 | t0018 | g0316 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03669 | hp1 | a0002 | c0002 | t0005 | g0004 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0139 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03710 | hp1 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03834 | hp1 | a0002 | c0002 | t0005 | g0088 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0309 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0150 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG04184 | hp2 | a0001 | c0001 | t0039 | g0129 | SAS | BEB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | STU | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG04204 | hp2 | a0001 | c0001 | t0022 | g0314 | SAS | STU | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0207 | EAS | CHB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18612 | hp2 | a0002 | c0002 | t0005 | g0064 | EAS | CHB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18940 | hp2 | a0002 | c0002 | t0005 | g0091 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18941 | hp1 | a0002 | c0002 | t0005 | g0094 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18943 | hp2 | a0001 | c0001 | t0012 | g0280 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18952 | hp2 | a0002 | c0002 | t0005 | g0082 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0117 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18964 | hp2 | a0002 | c0002 | t0005 | g0090 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18965 | hp2 | a0002 | c0002 | t0005 | g0092 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0078 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18972 | hp1 | a0002 | c0002 | t0005 | g0049 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18974 | hp1 | a0001 | c0001 | t0020 | g0113 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18979 | hp2 | a0001 | c0001 | t0012 | g0282 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18981 | hp1 | a0001 | c0001 | t0012 | g0255 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18987 | hp2 | a0001 | c0001 | t0012 | g0284 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18989 | hp1 | a0002 | c0002 | t0005 | g0093 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18989 | hp2 | a0001 | c0001 | t0036 | g0311 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19000 | hp1 | a0001 | c0001 | t0010 | g0132 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19004 | hp1 | a0001 | c0001 | t0016 | g0306 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0099 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0096 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19056 | hp2 | a0002 | c0002 | t0005 | g0021 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19058 | hp1 | a0001 | c0001 | t0038 | g0305 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19062 | hp1 | a0002 | c0002 | t0030 | g0065 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19064 | hp2 | a0002 | c0002 | t0005 | g0048 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19074 | hp2 | a0002 | c0002 | t0005 | g0095 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19080 | hp1 | a0002 | c0002 | t0005 | g0077 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19080 | hp2 | a0001 | c0001 | t0020 | g0114 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19081 | hp1 | a0002 | c0002 | t0005 | g0079 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19084 | hp1 | a0001 | c0001 | t0012 | g0271 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19084 | hp2 | a0002 | c0002 | t0005 | g0047 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19086 | hp2 | a0005 | c0006 | t0001 | g0032 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20129 | hp1 | a0001 | c0001 | t0044 | g0322 | AFR | ASW | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0244 | AFR | ASW | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0136 | EUR | TSI | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0144 | EUR | TSI | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20805 | hp2 | a0002 | c0002 | t0029 | g0061 | EUR | TSI | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG01123 | hp2 | a0002 | c0002 | t0005 | g0074 | AMR | CLM | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0059 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02109 | hp2 | a0001 | c0001 | t0042 | g0197 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG02559 | hp2 | a0001 | c0001 | t0016 | g0296 | AFR | ACB | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0240 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG06807 | hp1 | a0001 | c0001 | t0017 | g0248 | AFR | USA | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | USA | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0250 | AFR | USA | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0162 | AFR | USA | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0211 | AFR | LWK | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0005 | g0067 | REF | REF | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0222 | REF | REF | SPATA6_chr1_48290373_48477204 | SPATA6 | chr1 | 48290373 | 48477204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:48298747
|
C | T | 2 | a0002a0005 | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
missense_variant | MODERATE | c.1433G>A | p.Cys478Tyr | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1629/5003 | 1433/1467 | 478/488 | chr1 | 48298747 | ||
| chr1:48359683
|
G | A | 1 | a0003 | 3 | HG01261.hp2 HG01433.hp2 HG01993.hp1 |
missense_variant | MODERATE | c.997C>T | p.Arg333Trp | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/13 | 1193/5003 | 997/1467 | 333/488 | chr1 | 48359683 | ||
| chr1:48359697
|
G | A | 1 | a0005 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.983C>T | p.Ser328Leu | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/13 | 1179/5003 | 983/1467 | 328/488 | chr1 | 48359697 | ||
| chr1:48399449
|
C | T | 1 | a0004 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.682G>A | p.Glu228Lys | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/13 | 878/5003 | 682/1467 | 228/488 | chr1 | 48399449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:48355736
|
G | A | 1 | a0001c0005 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1128C>T | p.Cys376Cys | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/13 | 1324/5003 | 1128/1467 | 376/488 | chr1 | 48355736 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:48295482
|
T | A | 25 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(22): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*3231A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 3231 | chr1 | 48295482 | |||||
| chr1:48295590
|
G | C | 1 | a0001c0001t0040 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3123C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 3123 | chr1 | 48295590 | |||||
| chr1:48296018
|
CTTTA | C | 2 | a0001c0001t0008a0001c0001t0017 | 12 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2691_*2694delTAAA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 2691 | chr1 | 48296018 | |||||
| chr1:48296159
|
A | G | 1 | a0001c0001t0038 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2554T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 2554 | chr1 | 48296159 | |||||
| chr1:48296301
|
C | T | 1 | a0001c0001t0041 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2412G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 2412 | chr1 | 48296301 | |||||
| chr1:48296329
|
A | T | 3 | a0001c0001t0008a0001c0001t0011a0001c0001t0017 | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2384T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 2384 | chr1 | 48296329 | |||||
| chr1:48296818
|
G | C | 4 | a0002c0002t0027a0002c0002t0029a0002c0002t0031others(1): Show | 4 | HG00280.hp2 HG01261.hp1 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1895C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1895 | chr1 | 48296818 | |||||
| chr1:48296989
|
G | A | 1 | a0001c0001t0006 | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1724C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1724 | chr1 | 48296989 | |||||
| chr1:48297003
|
TCACAATG others(2): Show |
T | 7 | a0001c0001t0002a0001c0001t0013a0001c0001t0021others(4): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1701_*1709delCTCA others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1701 | chr1 | 48297003 | |||||
| chr1:48297125
|
G | GGT | 3 | a0001c0001t0010a0001c0001t0025a0002c0002t0019 | 10 | HG00642.hp2 HG01168.hp2 HG01243.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1586_*1587dupAC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGT | 3 | a0001c0001t0013a0001c0001t0039a0002c0002t0028 | 6 | HG00735.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1584_*1587dupACAC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGTGTG others(1): Show |
2 | a0001c0001t0007a0001c0001t0038 | 12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1580_*1587dupACAC others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0037 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1578_*1587dupACAC others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGTGTG others(5): Show |
2 | a0001c0001t0016a0001c0001t0026 | 5 | HG02257.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1576_*1587dupACAC others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGTGTG others(7): Show |
2 | a0001c0001t0015a0001c0001t0043 | 4 | HG00741.hp1 HG01081.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1574_*1587dupACAC others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
G | GGTGTGTG others(13): Show |
1 | a0001c0001t0036 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1568_*1587dupACAC others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1587 | chr1 | 48297125 | |||||
| chr1:48297125
|
GGT | G | 12 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(9): Show | 115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1586_*1587delAC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1586 | chr1 | 48297125 | |||||
| chr1:48297125
|
GGTGT | G | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0024others(1): Show | 11 | HG00597.hp2 HG00621.hp1 HG01891.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1584_*1587delACAC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1584 | chr1 | 48297125 | |||||
| chr1:48297125
|
GGTGTGT | G | 3 | a0001c0001t0004a0001c0001t0006a0002c0002t0031 | 51 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1582_*1587delACAC others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1582 | chr1 | 48297125 | |||||
| chr1:48297125
|
GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0014a0001c0001t0034a0001c0001t0041 | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1580_*1587delACAC others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1580 | chr1 | 48297125 | |||||
| chr1:48297125
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0042 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1578_*1587delACAC others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1578 | chr1 | 48297125 | |||||
| chr1:48297230
|
C | T | 1 | a0001c0001t0020 | 2 | NA18974.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1483G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1483 | chr1 | 48297230 | |||||
| chr1:48297651
|
C | T | 1 | a0001c0001t0035 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1062 | chr1 | 48297651 | |||||
| chr1:48297655
|
C | T | 1 | a0002c0002t0027 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 1058 | chr1 | 48297655 | |||||
| chr1:48297730
|
T | A | 1 | a0002c0002t0032 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 983 | chr1 | 48297730 | |||||
| chr1:48297757
|
A | G | 1 | a0001c0001t0034 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*956T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 956 | chr1 | 48297757 | |||||
| chr1:48298000
|
G | A | 1 | a0001c0001t0025 | 2 | HG02055.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*713C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 713 | chr1 | 48298000 | |||||
| chr1:48298048
|
T | A | 1 | a0002c0002t0033 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 665 | chr1 | 48298048 | |||||
| chr1:48298364
|
T | C | 2 | a0001c0001t0026a0001c0001t0043 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*349A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 13/13 | 349 | chr1 | 48298364 | |||||
| chr1:48472019
|
A | T | 12 | a0001c0001t0001a0002c0002t0001a0002c0002t0005others(9): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-11T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/13 | 11 | chr1 | 48472019 | |||||
| chr1:48472146
|
G | A | 1 | a0001c0001t0044 | 1 | NA20129.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-138C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/13 | chr1 | 48472146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:48298996
|
C | A | 36 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1287-103G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48298996 | ||||||
| chr1:48299163
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1287-270A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299163 | ||||||
| chr1:48299199
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1287-306G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299199 | ||||||
| chr1:48299516
|
G | GAAAA | 31 | a0001c0001t0002g0156a0001c0001t0002g0201a0001c0001t0002g0202others(28): Show | 31 | HG00099.hp1 HG01243.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.1287-627_1287-624d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAA | 65 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(62): Show | 65 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1287-628_1287-624d others(7): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAA | 14 | a0001c0001t0002g0100a0001c0001t0002g0158a0001c0001t0002g0171others(11): Show | 14 | HG02055.hp1 HG02083.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1287-629_1287-624d others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(1): Show |
13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(10): Show | 13 | HG00558.hp1 HG01167.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1287-631_1287-624d others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(2): Show |
67 | a0001c0001t0003g0115a0001c0001t0003g0118a0001c0001t0003g0119others(64): Show | 67 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1287-632_1287-624d others(11): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(3): Show |
54 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0107others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1287-633_1287-624d others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(4): Show |
9 | a0001c0001t0003g0106a0001c0001t0003g0109a0002c0002t0001g0002others(6): Show | 9 | HG00140.hp1 HG00597.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287-634_1287-624d others(13): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(5): Show |
20 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0037others(17): Show | 20 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1287-635_1287-624d others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(6): Show |
15 | a0002c0002t0001g0084a0002c0002t0005g0004a0002c0002t0005g0059others(12): Show | 15 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1287-636_1287-624d others(15): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(7): Show |
3 | a0002c0002t0005g0058a0002c0002t0005g0071a0002c0002t0005g0093 | 3 | HG01099.hp2 HG03239.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1287-637_1287-624d others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(8): Show |
6 | a0001c0001t0006g0144a0001c0001t0006g0166a0001c0001t0006g0234others(3): Show | 6 | HG00280.hp2 HG00741.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-638_1287-624d others(17): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(9): Show |
2 | a0001c0001t0006g0148a0001c0001t0006g0149 | 2 | HG01358.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1287-639_1287-624d others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(10): Show |
6 | a0001c0001t0006g0143a0001c0001t0006g0145a0001c0001t0006g0146others(3): Show | 6 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-640_1287-624d others(19): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GAAAAAAA others(11): Show |
3 | a0001c0001t0006g0150a0001c0001t0006g0230a0001c0001t0006g0231 | 3 | HG01891.hp2 HG04184.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1287-641_1287-624d others(20): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GGAAAAAA others(4): Show |
2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1287-624_1287-623i others(13): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299516
|
G | GGAAAAAA others(5): Show |
1 | a0002c0002t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1287-624_1287-623i others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299516 | ||||||
| chr1:48299781
|
G | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1287-888C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299781 | ||||||
| chr1:48299813
|
G | A | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1287-920C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299813 | ||||||
| chr1:48299870
|
T | C | 1 | a0001c0001t0004g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1287-977A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299870 | ||||||
| chr1:48299892
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-999A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299892 | ||||||
| chr1:48299960
|
G | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1067C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299960 | ||||||
| chr1:48299981
|
T | C | 2 | a0001c0001t0017g0241a0001c0001t0017g0248 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1287-1088A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48299981 | ||||||
| chr1:48300032
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-1139G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48300032 | ||||||
| chr1:48300273
|
G | A | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1287-1380C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48300273 | ||||||
| chr1:48300291
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1287-1398T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48300291 | ||||||
| chr1:48300555
|
C | A | 3 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01167.hp2 HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1287-1662G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48300555 | ||||||
| chr1:48300995
|
C | T | 4 | a0001c0001t0007g0313a0001c0001t0016g0306a0001c0001t0036g0311others(1): Show | 4 | NA18969.hp1 NA18989.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287-2102G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48300995 | ||||||
| chr1:48301284
|
T | C | 1 | a0001c0001t0006g0147 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1287-2391A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301284 | ||||||
| chr1:48301292
|
G | GA | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-2400dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301292 | ||||||
| chr1:48301349
|
T | C | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1287-2456A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301349 | ||||||
| chr1:48301546
|
C | A | 7 | a0001c0001t0011g0252a0001c0001t0014g0196a0001c0001t0014g0198others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-2653G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301546 | ||||||
| chr1:48301547
|
A | AC | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0010g0137 | 3 | HG01346.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1287-2655_1287-265 others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301547 | ||||||
| chr1:48301548
|
A | C | 126 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0004g0229others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1287-2655T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301548 | ||||||
| chr1:48301550
|
A | C | 1 | a0002c0002t0001g0038 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1287-2657T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301550 | ||||||
| chr1:48301572
|
G | A | 36 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1287-2679C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301572 | ||||||
| chr1:48301873
|
C | T | 2 | a0001c0001t0038g0305a0002c0002t0005g0022 | 2 | HG02040.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1287-2980G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301873 | ||||||
| chr1:48301915
|
G | A | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-3022C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301915 | ||||||
| chr1:48301958
|
T | C | 1 | a0001c0001t0003g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1287-3065A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48301958 | ||||||
| chr1:48302042
|
A | G | 1 | a0001c0001t0011g0240 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1287-3149T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302042 | ||||||
| chr1:48302152
|
A | T | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-3259T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302152 | ||||||
| chr1:48302166
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1287-3273G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302166 | ||||||
| chr1:48302246
|
G | A | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1287-3353C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302246 | ||||||
| chr1:48302272
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1287-3379G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302272 | ||||||
| chr1:48302399
|
C | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1286+3388G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302399 | ||||||
| chr1:48302513
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1286+3274T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302513 | ||||||
| chr1:48302527
|
C | A | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1286+3260G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302527 | ||||||
| chr1:48302675
|
T | G | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1286+3112A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302675 | ||||||
| chr1:48302776
|
G | A | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1286+3011C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302776 | ||||||
| chr1:48302977
|
G | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1286+2810C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48302977 | ||||||
| chr1:48303009
|
A | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0176 | 2 | HG02523.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1286+2778T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303009 | ||||||
| chr1:48303046
|
C | T | 1 | a0002c0002t0027g0062 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1286+2741G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303046 | ||||||
| chr1:48303121
|
T | C | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1286+2666A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303121 | ||||||
| chr1:48303248
|
A | C | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1286+2539T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303248 | ||||||
| chr1:48303327
|
T | A | 1 | a0001c0001t0041g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1286+2460A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303327 | ||||||
| chr1:48303372
|
C | A | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1286+2415G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303372 | ||||||
| chr1:48303374
|
T | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1286+2413A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303374 | ||||||
| chr1:48303485
|
C | G | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1286+2302G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303485 | ||||||
| chr1:48303960
|
C | T | 2 | a0001c0001t0025g0209a0001c0001t0025g0210 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1286+1827G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48303960 | ||||||
| chr1:48304063
|
T | C | 1 | a0001c0001t0010g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1286+1724A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304063 | ||||||
| chr1:48304146
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1286+1641T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304146 | ||||||
| chr1:48304154
|
C | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286+1633G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304154 | ||||||
| chr1:48304343
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1286+1444G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304343 | ||||||
| chr1:48304544
|
A | G | 1 | a0001c0005t0003g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1286+1243T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304544 | ||||||
| chr1:48304624
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1286+1163C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304624 | ||||||
| chr1:48304895
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1286+892G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304895 | ||||||
| chr1:48304925
|
A | G | 1 | a0002c0002t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1286+862T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48304925 | ||||||
| chr1:48305125
|
G | A | 1 | a0002c0002t0005g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1286+662C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305125 | ||||||
| chr1:48305206
|
T | C | 1 | a0002c0002t0019g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1286+581A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305206 | ||||||
| chr1:48305330
|
A | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+457T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305330 | ||||||
| chr1:48305382
|
C | G | 1 | a0001c0001t0013g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1286+405G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305382 | ||||||
| chr1:48305395
|
G | C | 6 | a0001c0001t0003g0118a0001c0001t0003g0124a0001c0001t0003g0130others(3): Show | 6 | HG00544.hp2 HG02015.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286+392C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305395 | ||||||
| chr1:48305427
|
A | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1286+360T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305427 | ||||||
| chr1:48305491
|
T | C | 1 | a0002c0002t0027g0062 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1286+296A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 12/12 | chr1 | 48305491 | ||||||
| chr1:48306025
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1195-147T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306025 | ||||||
| chr1:48306059
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1195-181T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306059 | ||||||
| chr1:48306174
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-296A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306174 | ||||||
| chr1:48306389
|
A | G | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1195-511T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306389 | ||||||
| chr1:48306687
|
A | G | 1 | a0001c0001t0039g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1195-809T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306687 | ||||||
| chr1:48306887
|
C | T | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1195-1009G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48306887 | ||||||
| chr1:48307074
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0003g0141 | 2 | NA19006.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1195-1196G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48307074 | ||||||
| chr1:48307614
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1195-1736C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48307614 | ||||||
| chr1:48307808
|
G | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-1930C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48307808 | ||||||
| chr1:48307942
|
T | C | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-2064A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48307942 | ||||||
| chr1:48307995
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1195-2117A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48307995 | ||||||
| chr1:48308401
|
T | C | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1195-2523A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48308401 | ||||||
| chr1:48308581
|
G | A | 1 | a0001c0001t0014g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1195-2703C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48308581 | ||||||
| chr1:48308843
|
C | A | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1195-2965G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48308843 | ||||||
| chr1:48308956
|
G | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1195-3078C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48308956 | ||||||
| chr1:48309161
|
T | G | 1 | a0001c0001t0002g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1195-3283A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48309161 | ||||||
| chr1:48309529
|
G | A | 15 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(12): Show | 15 | HG00558.hp2 NA18954.hp2 NA18967.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-3651C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48309529 | ||||||
| chr1:48309690
|
T | A | 1 | a0002c0002t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1195-3812A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48309690 | ||||||
| chr1:48310165
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1195-4287C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310165 | ||||||
| chr1:48310191
|
C | G | 1 | a0001c0001t0006g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1195-4313G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310191 | ||||||
| chr1:48310250
|
G | C | 1 | a0001c0001t0003g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1195-4372C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310250 | ||||||
| chr1:48310271
|
G | A | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-4393C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310271 | ||||||
| chr1:48310486
|
T | C | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1195-4608A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310486 | ||||||
| chr1:48310546
|
G | C | 2 | a0001c0001t0008g0249a0001c0001t0008g0250 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1195-4668C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310546 | ||||||
| chr1:48310636
|
C | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-4758G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310636 | ||||||
| chr1:48310892
|
T | A | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-5014A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48310892 | ||||||
| chr1:48311385
|
G | T | 1 | a0001c0001t0006g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1195-5507C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311385 | ||||||
| chr1:48311429
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-5551A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311429 | ||||||
| chr1:48311501
|
C | T | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1195-5623G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311501 | ||||||
| chr1:48311561
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1195-5683G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311561 | ||||||
| chr1:48311709
|
C | T | 3 | a0001c0001t0007g0313a0001c0001t0016g0306a0001c0001t0036g0311 | 3 | NA18969.hp1 NA18989.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1195-5831G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311709 | ||||||
| chr1:48311745
|
G | A | 3 | a0001c0001t0003g0121a0001c0001t0003g0125a0001c0001t0010g0132 | 3 | NA18979.hp1 NA18999.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1195-5867C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311745 | ||||||
| chr1:48311749
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1195-5871C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311749 | ||||||
| chr1:48311753
|
G | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-5875C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311753 | ||||||
| chr1:48311755
|
C | T | 52 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(49): Show | 52 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1195-5877G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311755 | ||||||
| chr1:48311770
|
C | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195-5892G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311770 | ||||||
| chr1:48311783
|
G | A | 1 | a0001c0001t0004g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1195-5905C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311783 | ||||||
| chr1:48311830
|
G | A | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-5952C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48311830 | ||||||
| chr1:48312027
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1195-6149C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312027 | ||||||
| chr1:48312316
|
C | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1195-6438G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312316 | ||||||
| chr1:48312321
|
G | C | 40 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(37): Show | 40 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1195-6443C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312321 | ||||||
| chr1:48312404
|
T | A | 2 | a0001c0001t0004g0260a0001c0001t0004g0283 | 2 | NA18961.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1195-6526A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312404 | ||||||
| chr1:48312507
|
T | A | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1195-6629A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312507 | ||||||
| chr1:48312577
|
T | A | 13 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(10): Show | 13 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1195-6699A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312577 | ||||||
| chr1:48312663
|
G | T | 2 | a0001c0001t0001g0089a0001c0001t0009g0206 | 2 | HG01070.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1195-6785C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312663 | ||||||
| chr1:48312670
|
AC | A | 4 | a0001c0001t0007g0313a0001c0001t0016g0306a0001c0001t0036g0311others(1): Show | 4 | NA18969.hp1 NA18989.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195-6793delG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312670 | ||||||
| chr1:48312678
|
C | T | 1 | a0001c0001t0011g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1195-6800G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312678 | ||||||
| chr1:48312742
|
C | T | 2 | a0001c0001t0014g0213a0001c0001t0014g0214 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1195-6864G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312742 | ||||||
| chr1:48312869
|
A | AT | 21 | a0001c0001t0004g0257a0001c0001t0004g0258a0001c0001t0004g0259others(18): Show | 21 | HG00621.hp2 HG02074.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.1195-6992_1195-699 others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312869 | ||||||
| chr1:48312958
|
T | C | 1 | a0001c0001t0011g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1195-7080A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312958 | ||||||
| chr1:48312985
|
T | C | 2 | a0001c0001t0003g0105a0001c0001t0003g0109 | 2 | NA19006.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1195-7107A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48312985 | ||||||
| chr1:48313068
|
T | C | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-7190A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313068 | ||||||
| chr1:48313118
|
C | A | 51 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(48): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1195-7240G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313118 | ||||||
| chr1:48313141
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1195-7263G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313141 | ||||||
| chr1:48313165
|
T | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-7287A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313165 | ||||||
| chr1:48313174
|
A | G | 1 | a0002c0002t0005g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1195-7296T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313174 | ||||||
| chr1:48313221
|
C | A | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1195-7343G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313221 | ||||||
| chr1:48313239
|
T | C | 1 | a0001c0001t0004g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1195-7361A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313239 | ||||||
| chr1:48313264
|
G | A | 1 | a0001c0001t0010g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1195-7386C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313264 | ||||||
| chr1:48313302
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0010g0137 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1195-7424C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313302 | ||||||
| chr1:48313433
|
C | T | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1195-7555G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313433 | ||||||
| chr1:48313447
|
C | T | 1 | a0001c0001t0014g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1195-7569G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313447 | ||||||
| chr1:48313473
|
C | T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-7595G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313473 | ||||||
| chr1:48313546
|
A | G | 1 | a0001c0001t0009g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1195-7668T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313546 | ||||||
| chr1:48313826
|
C | T | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-7948G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313826 | ||||||
| chr1:48313832
|
A | T | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-7954T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313832 | ||||||
| chr1:48313838
|
G | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1195-7960C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313838 | ||||||
| chr1:48313895
|
T | G | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1195-8017A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313895 | ||||||
| chr1:48313929
|
A | C | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1195-8051T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313929 | ||||||
| chr1:48313972
|
A | G | 2 | a0001c0001t0020g0113a0001c0001t0020g0114 | 2 | NA18974.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1195-8094T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313972 | ||||||
| chr1:48313991
|
C | G | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-8113G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48313991 | ||||||
| chr1:48314129
|
C | T | 1 | a0001c0001t0006g0147 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1195-8251G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314129 | ||||||
| chr1:48314143
|
G | A | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1195-8265C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314143 | ||||||
| chr1:48314187
|
A | G | 2 | a0001c0001t0010g0103a0003c0003t0003g0110 | 2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1195-8309T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314187 | ||||||
| chr1:48314235
|
T | C | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1195-8357A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314235 | ||||||
| chr1:48314292
|
T | C | 1 | a0001c0001t0008g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1195-8414A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314292 | ||||||
| chr1:48314399
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-8521C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314399 | ||||||
| chr1:48314491
|
A | G | 1 | a0002c0002t0030g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1195-8613T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314491 | ||||||
| chr1:48314492
|
A | G | 1 | a0001c0001t0036g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1195-8614T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314492 | ||||||
| chr1:48314724
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1195-8846C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314724 | ||||||
| chr1:48314757
|
G | A | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1195-8879C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314757 | ||||||
| chr1:48314770
|
A | G | 1 | a0002c0002t0001g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1195-8892T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314770 | ||||||
| chr1:48314789
|
C | T | 1 | a0001c0001t0009g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1195-8911G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314789 | ||||||
| chr1:48314870
|
G | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-8992C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314870 | ||||||
| chr1:48314875
|
G | C | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195-8997C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48314875 | ||||||
| chr1:48315084
|
C | T | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1195-9206G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48315084 | ||||||
| chr1:48315112
|
T | C | 7 | a0001c0001t0007g0303a0001c0001t0007g0304a0001c0001t0007g0307others(4): Show | 7 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-9234A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48315112 | ||||||
| chr1:48315629
|
C | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1195-9751G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48315629 | ||||||
| chr1:48315962
|
C | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-10084G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48315962 | ||||||
| chr1:48315969
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-10091T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48315969 | ||||||
| chr1:48316006
|
C | G | 1 | a0002c0002t0005g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1195-10128G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316006 | ||||||
| chr1:48316172
|
GA | G | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1195-10295delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316172 | ||||||
| chr1:48316179
|
C | G | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1195-10301G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316179 | ||||||
| chr1:48316180
|
T | C | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1195-10302A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316180 | ||||||
| chr1:48316201
|
A | C | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1195-10323T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316201 | ||||||
| chr1:48316213
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(53): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1195-10335G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316213 | ||||||
| chr1:48316302
|
C | A | 1 | a0001c0001t0013g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1195-10424G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316302 | ||||||
| chr1:48316336
|
T | C | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1195-10458A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316336 | ||||||
| chr1:48316420
|
C | T | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1195-10542G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316420 | ||||||
| chr1:48316444
|
A | G | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1195-10566T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316444 | ||||||
| chr1:48316744
|
C | T | 3 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0215 | 3 | HG00609.hp1 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1195-10866G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316744 | ||||||
| chr1:48316775
|
T | A | 2 | a0001c0001t0004g0260a0001c0001t0004g0283 | 2 | NA18961.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1195-10897A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48316775 | ||||||
| chr1:48317525
|
T | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-11647A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317525 | ||||||
| chr1:48317686
|
A | G | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1195-11808T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317686 | ||||||
| chr1:48317750
|
A | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-11872T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317750 | ||||||
| chr1:48317756
|
C | T | 36 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1195-11878G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317756 | ||||||
| chr1:48317789
|
G | A | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1195-11911C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317789 | ||||||
| chr1:48317921
|
A | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12043T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317921 | ||||||
| chr1:48317923
|
G | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12045C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317923 | ||||||
| chr1:48317924
|
C | A | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12046G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317924 | ||||||
| chr1:48317927
|
A | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12049T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317927 | ||||||
| chr1:48317929
|
T | G | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12051A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317929 | ||||||
| chr1:48317930
|
C | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12052G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317930 | ||||||
| chr1:48317931
|
C | G | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12053G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317931 | ||||||
| chr1:48317934
|
C | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12056G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317934 | ||||||
| chr1:48317935
|
A | G | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12057T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317935 | ||||||
| chr1:48317936
|
A | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12058T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317936 | ||||||
| chr1:48317937
|
G | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12059C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48317937 | ||||||
| chr1:48318010
|
C | A | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-12132G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48318010 | ||||||
| chr1:48318325
|
G | T | 1 | a0001c0001t0009g0207 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1195-12447C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48318325 | ||||||
| chr1:48318409
|
T | C | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1195-12531A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48318409 | ||||||
| chr1:48318737
|
C | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1195-12859G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48318737 | ||||||
| chr1:48318765
|
A | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-12887T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48318765 | ||||||
| chr1:48319051
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1195-13173G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319051 | ||||||
| chr1:48319223
|
C | A | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1195-13345G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319223 | ||||||
| chr1:48319272
|
A | C | 1 | a0001c0001t0002g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1195-13394T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319272 | ||||||
| chr1:48319336
|
A | G | 3 | a0001c0001t0014g0213a0001c0001t0014g0214a0001c0001t0041g0212 | 3 | HG01243.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1195-13458T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319336 | ||||||
| chr1:48319614
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1195-13736G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319614 | ||||||
| chr1:48319827
|
G | A | 1 | a0001c0001t0017g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1195-13949C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319827 | ||||||
| chr1:48319993
|
C | T | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1195-14115G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48319993 | ||||||
| chr1:48320016
|
G | A | 8 | a0001c0001t0002g0172a0001c0001t0002g0178a0001c0001t0002g0183others(5): Show | 8 | HG00639.hp1 HG01099.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1195-14138C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320016 | ||||||
| chr1:48320098
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1195-14220T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320098 | ||||||
| chr1:48320211
|
C | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1195-14333G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320211 | ||||||
| chr1:48320413
|
AAGCTGAC others(3): Show |
A | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-14545_1195-14 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320413 | ||||||
| chr1:48320593
|
C | A | 1 | a0001c0001t0006g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1195-14715G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320593 | ||||||
| chr1:48320729
|
C | T | 11 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0002g0178others(8): Show | 11 | HG00639.hp1 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1195-14851G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320729 | ||||||
| chr1:48320735
|
G | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-14857C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320735 | ||||||
| chr1:48320884
|
G | A | 2 | a0002c0002t0001g0027a0005c0006t0001g0032 | 2 | HG00544.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1195-15006C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48320884 | ||||||
| chr1:48321160
|
A | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-15282T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48321160 | ||||||
| chr1:48321254
|
C | A | 1 | a0001c0001t0006g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1195-15376G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48321254 | ||||||
| chr1:48321733
|
A | G | 1 | a0001c0001t0007g0307 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1195-15855T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48321733 | ||||||
| chr1:48321902
|
T | A | 1 | a0001c0001t0006g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1195-16024A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48321902 | ||||||
| chr1:48321926
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1195-16048T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48321926 | ||||||
| chr1:48322524
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1195-16646G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48322524 | ||||||
| chr1:48322656
|
T | C | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1195-16778A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48322656 | ||||||
| chr1:48322675
|
C | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-16797G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48322675 | ||||||
| chr1:48322780
|
C | G | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1195-16902G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48322780 | ||||||
| chr1:48323055
|
G | A | 3 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0003g0107 | 3 | HG00597.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1195-17177C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323055 | ||||||
| chr1:48323065
|
T | G | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195-17187A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323065 | ||||||
| chr1:48323259
|
T | C | 2 | a0001c0001t0007g0313a0001c0001t0036g0311 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1195-17381A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323259 | ||||||
| chr1:48323287
|
A | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-17409T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323287 | ||||||
| chr1:48323462
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-17584C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323462 | ||||||
| chr1:48323616
|
GA | G | 67 | a0001c0001t0002g0100a0001c0001t0002g0167a0001c0001t0002g0169others(64): Show | 67 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1195-17739delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323616 | ||||||
| chr1:48323616
|
GAA | G | 13 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(10): Show | 13 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1195-17740_1195-17 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323616 | ||||||
| chr1:48323672
|
T | C | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1195-17794A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323672 | ||||||
| chr1:48323934
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-18056A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48323934 | ||||||
| chr1:48324008
|
G | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-18130C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324008 | ||||||
| chr1:48324098
|
C | T | 1 | a0001c0001t0004g0285 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1195-18220G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324098 | ||||||
| chr1:48324205
|
G | A | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-18327C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324205 | ||||||
| chr1:48324260
|
G | A | 1 | a0001c0001t0037g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1195-18382C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324260 | ||||||
| chr1:48324567
|
G | A | 1 | a0001c0001t0009g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1195-18689C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324567 | ||||||
| chr1:48324600
|
C | T | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1195-18722G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324600 | ||||||
| chr1:48324615
|
C | T | 1 | a0001c0001t0007g0301 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1195-18737G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324615 | ||||||
| chr1:48324736
|
T | C | 1 | a0002c0002t0001g0005 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1195-18858A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324736 | ||||||
| chr1:48324820
|
A | G | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1195-18942T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48324820 | ||||||
| chr1:48325333
|
C | T | 19 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(16): Show | 19 | HG01070.hp2 HG01167.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1195-19455G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325333 | ||||||
| chr1:48325335
|
T | G | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-19457A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325335 | ||||||
| chr1:48325398
|
G | A | 1 | a0002c0002t0005g0021 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1195-19520C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325398 | ||||||
| chr1:48325564
|
T | A | 1 | a0001c0001t0004g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1195-19686A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325564 | ||||||
| chr1:48325595
|
A | G | 2 | a0001c0001t0016g0296a0001c0001t0016g0299 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1195-19717T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325595 | ||||||
| chr1:48325796
|
G | A | 1 | a0002c0002t0001g0014 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1195-19918C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48325796 | ||||||
| chr1:48326042
|
G | A | 2 | a0001c0001t0017g0241a0001c0001t0017g0248 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1195-20164C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326042 | ||||||
| chr1:48326048
|
C | A | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-20170G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326048 | ||||||
| chr1:48326089
|
G | A | 2 | a0001c0001t0007g0309a0002c0002t0005g0083 | 2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1195-20211C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326089 | ||||||
| chr1:48326124
|
C | T | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1195-20246G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326124 | ||||||
| chr1:48326157
|
A | C | 1 | a0001c0001t0003g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1195-20279T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326157 | ||||||
| chr1:48326213
|
G | A | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1195-20335C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326213 | ||||||
| chr1:48326325
|
A | T | 1 | a0003c0003t0003g0112 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1195-20447T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326325 | ||||||
| chr1:48326474
|
T | C | 1 | a0002c0002t0005g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1195-20596A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326474 | ||||||
| chr1:48326521
|
C | CA | 13 | a0001c0001t0002g0171a0001c0001t0002g0188a0001c0001t0004g0257others(10): Show | 13 | HG01515.hp1 HG01891.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1195-20644dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326521 | ||||||
| chr1:48326521
|
CA | C | 10 | a0001c0001t0009g0228a0002c0002t0001g0006a0002c0002t0001g0007others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1195-20644delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326521 | ||||||
| chr1:48326531
|
A | G | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1195-20653T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326531 | ||||||
| chr1:48326866
|
G | T | 3 | a0002c0002t0005g0003a0002c0002t0005g0059a0002c0002t0019g0076 | 3 | HG01168.hp2 HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1195-20988C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326866 | ||||||
| chr1:48326879
|
T | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-21001A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326879 | ||||||
| chr1:48326889
|
T | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-21011A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326889 | ||||||
| chr1:48326956
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1195-21078C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48326956 | ||||||
| chr1:48327052
|
G | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1195-21174C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327052 | ||||||
| chr1:48327055
|
A | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0019others(3): Show | 6 | HG02015.hp2 HG02074.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195-21177T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327055 | ||||||
| chr1:48327174
|
A | C | 15 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(12): Show | 15 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195-21296T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327174 | ||||||
| chr1:48327296
|
A | C | 1 | a0001c0001t0018g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1195-21418T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327296 | ||||||
| chr1:48327379
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1195-21501G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327379 | ||||||
| chr1:48327549
|
T | C | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195-21671A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327549 | ||||||
| chr1:48327794
|
T | C | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1195-21916A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48327794 | ||||||
| chr1:48328218
|
G | C | 1 | a0001c0001t0006g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1195-22340C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48328218 | ||||||
| chr1:48328552
|
T | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1195-22674A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48328552 | ||||||
| chr1:48328771
|
G | C | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1195-22893C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48328771 | ||||||
| chr1:48329088
|
A | G | 1 | a0001c0001t0006g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1195-23210T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329088 | ||||||
| chr1:48329435
|
A | T | 110 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1195-23557T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329435 | ||||||
| chr1:48329444
|
G | A | 1 | a0001c0001t0007g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1195-23566C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329444 | ||||||
| chr1:48329698
|
C | T | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1195-23820G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329698 | ||||||
| chr1:48329747
|
G | A | 1 | a0002c0002t0005g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1195-23869C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329747 | ||||||
| chr1:48329791
|
C | T | 2 | a0001c0001t0011g0237a0001c0001t0011g0238 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1195-23913G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329791 | ||||||
| chr1:48329840
|
C | A | 1 | a0001c0001t0004g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1195-23962G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329840 | ||||||
| chr1:48329883
|
C | T | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1195-24005G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329883 | ||||||
| chr1:48329982
|
C | T | 2 | a0002c0002t0001g0007a0002c0002t0001g0011 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1195-24104G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48329982 | ||||||
| chr1:48330135
|
G | T | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1195-24257C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330135 | ||||||
| chr1:48330302
|
C | T | 1 | a0002c0002t0005g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1195-24424G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330302 | ||||||
| chr1:48330333
|
C | T | 1 | a0002c0002t0005g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1195-24455G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330333 | ||||||
| chr1:48330339
|
C | T | 11 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(8): Show | 11 | HG01070.hp2 HG01167.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1195-24461G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330339 | ||||||
| chr1:48330426
|
C | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-24548G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330426 | ||||||
| chr1:48330448
|
C | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1195-24570G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330448 | ||||||
| chr1:48330664
|
T | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1195-24786A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330664 | ||||||
| chr1:48330722
|
C | T | 1 | a0002c0002t0005g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1195-24844G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330722 | ||||||
| chr1:48330851
|
G | A | 1 | a0001c0001t0007g0313 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1194+24819C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48330851 | ||||||
| chr1:48331114
|
C | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0053 | 3 | NA18948.hp2 NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1194+24556G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331114 | ||||||
| chr1:48331400
|
GA | G | 25 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0006g0144others(22): Show | 25 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1194+24269delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331400 | ||||||
| chr1:48331479
|
T | G | 2 | a0002c0002t0001g0030a0002c0002t0001g0035 | 2 | NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1194+24191A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331479 | ||||||
| chr1:48331507
|
TCAGACAA others(3): Show |
T | 1 | a0002c0002t0001g0039 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1194+24153_1194+24 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331507 | ||||||
| chr1:48331660
|
C | T | 12 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(9): Show | 12 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1194+24010G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331660 | ||||||
| chr1:48331695
|
C | A | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1194+23975G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331695 | ||||||
| chr1:48331743
|
CAAG | C | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1194+23924_1194+23 others(9): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331743 | ||||||
| chr1:48331776
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1194+23894G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48331776 | ||||||
| chr1:48332010
|
A | G | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1194+23660T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332010 | ||||||
| chr1:48332190
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1194+23480G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332190 | ||||||
| chr1:48332227
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1194+23443A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332227 | ||||||
| chr1:48332275
|
C | T | 1 | a0002c0002t0001g0056 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1194+23395G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332275 | ||||||
| chr1:48332369
|
T | A | 6 | a0002c0002t0005g0090a0002c0002t0005g0091a0002c0002t0005g0092others(3): Show | 6 | NA18940.hp2 NA18941.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194+23301A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332369 | ||||||
| chr1:48332701
|
G | A | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1194+22969C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332701 | ||||||
| chr1:48332873
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1194+22797G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48332873 | ||||||
| chr1:48333149
|
T | C | 1 | a0002c0002t0005g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1194+22521A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333149 | ||||||
| chr1:48333252
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | NA18941.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1194+22418G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333252 | ||||||
| chr1:48333290
|
G | C | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1194+22380C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333290 | ||||||
| chr1:48333605
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1194+22065C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333605 | ||||||
| chr1:48333629
|
T | C | 1 | a0002c0002t0027g0062 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1194+22041A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333629 | ||||||
| chr1:48333689
|
AAGTT | A | 3 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0164 | 3 | HG02896.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1194+21977_1194+21 others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48333689 | ||||||
| chr1:48334065
|
C | T | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1194+21605G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334065 | ||||||
| chr1:48334136
|
C | T | 3 | a0001c0001t0026g0295a0001c0001t0026g0297a0001c0001t0043g0298 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1194+21534G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334136 | ||||||
| chr1:48334327
|
A | C | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1194+21343T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334327 | ||||||
| chr1:48334333
|
A | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+21337T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334333 | ||||||
| chr1:48334685
|
C | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+20985G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334685 | ||||||
| chr1:48334686
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1194+20984T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334686 | ||||||
| chr1:48334719
|
G | A | 3 | a0001c0001t0010g0211a0001c0001t0025g0209a0001c0001t0025g0210 | 3 | HG02055.hp2 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1194+20951C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334719 | ||||||
| chr1:48334856
|
A | T | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+20814T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48334856 | ||||||
| chr1:48335090
|
T | G | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1194+20580A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48335090 | ||||||
| chr1:48335337
|
C | CA | 109 | a0001c0001t0004g0256a0001c0001t0006g0143a0001c0001t0006g0144others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1194+20332dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48335337 | ||||||
| chr1:48335436
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1194+20234C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48335436 | ||||||
| chr1:48336021
|
T | C | 1 | a0001c0001t0003g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1194+19649A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336021 | ||||||
| chr1:48336112
|
G | A | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1194+19558C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336112 | ||||||
| chr1:48336122
|
C | A | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1194+19548G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336122 | ||||||
| chr1:48336180
|
C | T | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1194+19490G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336180 | ||||||
| chr1:48336216
|
G | C | 1 | a0002c0002t0001g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1194+19454C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336216 | ||||||
| chr1:48336684
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0009g0206 | 2 | HG01070.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1194+18986G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48336684 | ||||||
| chr1:48337068
|
C | A | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1194+18602G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337068 | ||||||
| chr1:48337105
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+18565C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337105 | ||||||
| chr1:48337141
|
T | C | 1 | a0001c0001t0009g0207 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1194+18529A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337141 | ||||||
| chr1:48337643
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+18027G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337643 | ||||||
| chr1:48337687
|
G | A | 1 | a0002c0002t0005g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1194+17983C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337687 | ||||||
| chr1:48337697
|
T | A | 1 | a0001c0001t0006g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1194+17973A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337697 | ||||||
| chr1:48337818
|
T | C | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1194+17852A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337818 | ||||||
| chr1:48337933
|
C | A | 49 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1194+17737G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48337933 | ||||||
| chr1:48338057
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0199 | 2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1194+17613T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338057 | ||||||
| chr1:48338428
|
A | G | 1 | a0001c0001t0003g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1194+17242T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338428 | ||||||
| chr1:48338452
|
C | T | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1194+17218G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338452 | ||||||
| chr1:48338553
|
T | C | 1 | a0002c0002t0001g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1194+17117A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338553 | ||||||
| chr1:48338634
|
G | T | 1 | a0002c0002t0005g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1194+17036C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338634 | ||||||
| chr1:48338771
|
G | C | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1194+16899C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338771 | ||||||
| chr1:48338781
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+16889T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338781 | ||||||
| chr1:48338888
|
C | T | 1 | a0001c0001t0021g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1194+16782G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338888 | ||||||
| chr1:48338889
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+16781C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48338889 | ||||||
| chr1:48339024
|
C | A | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+16646G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48339024 | ||||||
| chr1:48339108
|
C | G | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1194+16562G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48339108 | ||||||
| chr1:48339563
|
A | G | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1194+16107T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48339563 | ||||||
| chr1:48339581
|
G | T | 1 | a0001c0001t0002g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1194+16089C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48339581 | ||||||
| chr1:48340174
|
A | G | 36 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1194+15496T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340174 | ||||||
| chr1:48340241
|
TA | T | 76 | a0001c0001t0001g0089a0001c0001t0002g0199a0001c0001t0004g0229others(73): Show | 76 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1194+15428delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAA | T | 98 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(95): Show | 98 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1194+15427_1194+15 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAAA | T | 13 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0107others(10): Show | 13 | HG01943.hp1 HG02055.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1194+15426_1194+15 others(9): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAAAAAAA others(3): Show |
T | 92 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1194+15419_1194+15 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAAAAAAA others(4): Show |
T | 2 | a0002c0002t0001g0001a0002c0002t0030g0065 | 2 | NA18959.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1194+15418_1194+15 others(17): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAAAAAAA others(5): Show |
T | 3 | a0001c0001t0004g0257a0001c0001t0004g0263a0001c0001t0004g0277 | 3 | NA18966.hp1 NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1194+15417_1194+15 others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340241
|
TAAAAAAA others(6): Show |
T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+15416_1194+15 others(19): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340241 | ||||||
| chr1:48340509
|
T | TA | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1194+15160dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340509 | ||||||
| chr1:48340509
|
TA | T | 14 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(11): Show | 14 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1194+15160delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340509 | ||||||
| chr1:48340524
|
T | C | 10 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | NA18954.hp2 NA18967.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.1194+15146A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340524 | ||||||
| chr1:48340620
|
T | C | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1194+15050A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340620 | ||||||
| chr1:48340723
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+14947T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340723 | ||||||
| chr1:48340785
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1194+14885C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340785 | ||||||
| chr1:48340960
|
C | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+14710G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48340960 | ||||||
| chr1:48341221
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1194+14449T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341221 | ||||||
| chr1:48341252
|
C | A | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1194+14418G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341252 | ||||||
| chr1:48341386
|
T | G | 5 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0026g0295others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194+14284A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341386 | ||||||
| chr1:48341436
|
C | G | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1194+14234G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341436 | ||||||
| chr1:48341485
|
C | T | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1194+14185G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341485 | ||||||
| chr1:48341540
|
T | G | 1 | a0001c0001t0011g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1194+14130A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341540 | ||||||
| chr1:48341597
|
C | G | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1194+14073G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341597 | ||||||
| chr1:48341908
|
C | T | 72 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(69): Show | 72 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1194+13762G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48341908 | ||||||
| chr1:48342076
|
G | A | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1194+13594C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342076 | ||||||
| chr1:48342131
|
A | G | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1194+13539T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342131 | ||||||
| chr1:48342154
|
T | C | 1 | a0002c0002t0001g0009 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1194+13516A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342154 | ||||||
| chr1:48342324
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1194+13346G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342324 | ||||||
| chr1:48342370
|
C | T | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1194+13300G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342370 | ||||||
| chr1:48342615
|
C | CA | 7 | a0001c0001t0003g0115a0001c0001t0009g0116a0001c0001t0009g0140others(4): Show | 7 | HG00558.hp1 NA18964.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+13054dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342615 | ||||||
| chr1:48342989
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1194+12681T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48342989 | ||||||
| chr1:48343265
|
T | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+12405A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48343265 | ||||||
| chr1:48343479
|
A | C | 3 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0039 | 3 | NA18957.hp1 NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1194+12191T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48343479 | ||||||
| chr1:48343841
|
A | T | 94 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1194+11829T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48343841 | ||||||
| chr1:48344095
|
T | C | 1 | a0001c0001t0007g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1194+11575A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48344095 | ||||||
| chr1:48344440
|
T | C | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1194+11230A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48344440 | ||||||
| chr1:48344828
|
T | C | 2 | a0001c0001t0004g0260a0001c0001t0004g0283 | 2 | NA18961.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1194+10842A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48344828 | ||||||
| chr1:48345070
|
T | C | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194+10600A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48345070 | ||||||
| chr1:48345654
|
G | A | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1194+10016C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48345654 | ||||||
| chr1:48346129
|
G | A | 2 | a0001c0001t0008g0249a0001c0001t0008g0250 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1194+9541C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346129 | ||||||
| chr1:48346312
|
T | A | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1194+9358A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346312 | ||||||
| chr1:48346485
|
C | T | 1 | a0001c0001t0004g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1194+9185G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346485 | ||||||
| chr1:48346691
|
A | C | 6 | a0001c0001t0003g0118a0001c0001t0003g0124a0001c0001t0003g0130others(3): Show | 6 | HG00544.hp2 HG02015.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194+8979T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346691 | ||||||
| chr1:48346790
|
C | T | 2 | a0002c0002t0001g0045a0002c0002t0001g0052 | 2 | HG00558.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1194+8880G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346790 | ||||||
| chr1:48346885
|
C | T | 1 | a0001c0001t0008g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1194+8785G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346885 | ||||||
| chr1:48346953
|
A | C | 2 | a0001c0001t0004g0270a0001c0001t0012g0255 | 2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1194+8717T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48346953 | ||||||
| chr1:48347066
|
T | C | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1194+8604A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347066 | ||||||
| chr1:48347084
|
A | T | 1 | a0002c0002t0005g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1194+8586T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347084 | ||||||
| chr1:48347117
|
C | A | 1 | a0001c0001t0021g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1194+8553G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347117 | ||||||
| chr1:48347281
|
G | T | 95 | a0001c0001t0010g0321a0002c0002t0001g0001a0002c0002t0001g0002others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1194+8389C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347281 | ||||||
| chr1:48347460
|
TATATA | T | 51 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(48): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1194+8205_1194+820 others(9): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347460 | ||||||
| chr1:48347493
|
TATGTATA others(4): Show |
T | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+8166_1194+817 others(15): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347493 | ||||||
| chr1:48347495
|
TG | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+8174delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347495 | ||||||
| chr1:48347535
|
GTAAT | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+8131_1194+813 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347535 | ||||||
| chr1:48347824
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+7846G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347824 | ||||||
| chr1:48347893
|
A | T | 1 | a0001c0001t0021g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1194+7777T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347893 | ||||||
| chr1:48347905
|
C | T | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194+7765G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347905 | ||||||
| chr1:48347998
|
C | G | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1194+7672G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48347998 | ||||||
| chr1:48348109
|
G | A | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1194+7561C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48348109 | ||||||
| chr1:48348276
|
C | T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+7394G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48348276 | ||||||
| chr1:48348421
|
A | G | 3 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0003g0107 | 3 | HG00597.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1194+7249T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48348421 | ||||||
| chr1:48348569
|
T | C | 1 | a0001c0001t0009g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1194+7101A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48348569 | ||||||
| chr1:48349084
|
G | A | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1194+6586C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48349084 | ||||||
| chr1:48349266
|
G | A | 2 | a0004c0004t0002g0097a0004c0004t0002g0098 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1194+6404C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48349266 | ||||||
| chr1:48349943
|
G | A | 2 | a0001c0001t0003g0142a0001c0001t0010g0137 | 2 | HG01346.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1194+5727C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48349943 | ||||||
| chr1:48350151
|
C | A | 1 | a0002c0002t0005g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1194+5519G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48350151 | ||||||
| chr1:48350255
|
A | G | 1 | a0001c0001t0003g0141 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1194+5415T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48350255 | ||||||
| chr1:48350413
|
G | A | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1194+5257C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48350413 | ||||||
| chr1:48350731
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1194+4939G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48350731 | ||||||
| chr1:48350831
|
C | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+4839G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48350831 | ||||||
| chr1:48351128
|
T | C | 7 | a0001c0001t0003g0205a0001c0001t0003g0216a0001c0001t0003g0217others(4): Show | 7 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1194+4542A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48351128 | ||||||
| chr1:48351562
|
A | T | 1 | a0002c0002t0005g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1194+4108T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48351562 | ||||||
| chr1:48351680
|
A | G | 1 | a0001c0001t0012g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1194+3990T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48351680 | ||||||
| chr1:48351848
|
T | A | 1 | a0002c0002t0005g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1194+3822A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48351848 | ||||||
| chr1:48352156
|
A | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0023 | 2 | NA18999.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1194+3514T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352156 | ||||||
| chr1:48352176
|
A | G | 1 | a0002c0002t0001g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1194+3494T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352176 | ||||||
| chr1:48352280
|
A | G | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1194+3390T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352280 | ||||||
| chr1:48352505
|
G | C | 1 | a0002c0002t0001g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1194+3165C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352505 | ||||||
| chr1:48352559
|
A | T | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1194+3111T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352559 | ||||||
| chr1:48352630
|
A | G | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1194+3040T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352630 | ||||||
| chr1:48352786
|
T | C | 17 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(14): Show | 17 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1194+2884A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352786 | ||||||
| chr1:48352903
|
C | CA | 181 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0107others(178): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1194+2766dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352903 | ||||||
| chr1:48352903
|
C | CAA | 11 | a0001c0001t0010g0132a0001c0001t0011g0240a0001c0001t0011g0245others(8): Show | 11 | HG01243.hp1 HG01934.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1194+2765_1194+276 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352903 | ||||||
| chr1:48352903
|
CA | C | 43 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(40): Show | 43 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1194+2766delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352903 | ||||||
| chr1:48352903
|
CAA | C | 47 | a0001c0001t0002g0100a0001c0001t0002g0170a0001c0001t0002g0171others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1194+2765_1194+276 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48352903 | ||||||
| chr1:48353131
|
A | G | 1 | a0001c0001t0006g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1194+2539T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353131 | ||||||
| chr1:48353247
|
T | C | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1194+2423A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353247 | ||||||
| chr1:48353253
|
A | G | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1194+2417T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353253 | ||||||
| chr1:48353339
|
C | T | 1 | a0002c0002t0005g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1194+2331G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353339 | ||||||
| chr1:48353434
|
GA | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+2235delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353434 | ||||||
| chr1:48353586
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1194+2084C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353586 | ||||||
| chr1:48353858
|
T | C | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1194+1812A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353858 | ||||||
| chr1:48353866
|
C | G | 2 | a0002c0002t0005g0021a0002c0002t0005g0022 | 2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1194+1804G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48353866 | ||||||
| chr1:48354622
|
C | T | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1194+1048G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354622 | ||||||
| chr1:48354714
|
T | C | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1194+956A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354714 | ||||||
| chr1:48354739
|
TTGTTAGA others(50): Show |
T | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1194+874_1194+930d others(59): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354739 | ||||||
| chr1:48354847
|
A | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+823T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354847 | ||||||
| chr1:48354901
|
T | C | 1 | a0001c0001t0004g0267 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1194+769A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354901 | ||||||
| chr1:48354909
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+761A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48354909 | ||||||
| chr1:48355014
|
C | G | 1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1194+656G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355014 | ||||||
| chr1:48355014
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1194+656G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355014 | ||||||
| chr1:48355125
|
A | C | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1194+545T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355125 | ||||||
| chr1:48355126
|
G | C | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1194+544C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355126 | ||||||
| chr1:48355219
|
C | A | 1 | a0002c0002t0005g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1194+451G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355219 | ||||||
| chr1:48355646
|
C | CA | 11 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(8): Show | 11 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1194+23dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 11/12 | chr1 | 48355646 | ||||||
| chr1:48355775
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.1095-6C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48355775 | ||||||
| chr1:48356202
|
G | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095-433C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356202 | ||||||
| chr1:48356298
|
T | G | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095-529A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356298 | ||||||
| chr1:48356396
|
GA | G | 51 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(48): Show | 51 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1095-628delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356396 | ||||||
| chr1:48356418
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095-649A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356418 | ||||||
| chr1:48356510
|
C | CT | 10 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(7): Show | 10 | HG01123.hp1 HG01358.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095-742dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356510 | ||||||
| chr1:48356510
|
CT | C | 8 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(5): Show | 8 | HG01070.hp1 HG02896.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095-742delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356510 | ||||||
| chr1:48356522
|
T | C | 2 | a0001c0001t0006g0143a0001c0001t0011g0252 | 2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1095-753A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356522 | ||||||
| chr1:48356554
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1095-785G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356554 | ||||||
| chr1:48356755
|
G | T | 1 | a0001c0001t0002g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1095-986C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356755 | ||||||
| chr1:48356925
|
T | C | 1 | a0001c0001t0011g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1095-1156A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48356925 | ||||||
| chr1:48357292
|
A | C | 1 | a0001c0001t0024g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1095-1523T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357292 | ||||||
| chr1:48357374
|
C | T | 2 | a0001c0001t0007g0313a0001c0001t0036g0311 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1095-1605G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357374 | ||||||
| chr1:48357375
|
A | G | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095-1606T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357375 | ||||||
| chr1:48357509
|
A | G | 1 | a0002c0002t0005g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1095-1740T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357509 | ||||||
| chr1:48357627
|
T | C | 6 | a0001c0001t0004g0264a0001c0001t0004g0270a0001c0001t0004g0278others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095-1858A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357627 | ||||||
| chr1:48357875
|
C | A | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1094+1711G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357875 | ||||||
| chr1:48357920
|
A | G | 12 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(9): Show | 12 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1094+1666T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48357920 | ||||||
| chr1:48358046
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1094+1540A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358046 | ||||||
| chr1:48358366
|
T | A | 1 | a0001c0001t0002g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1094+1220A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358366 | ||||||
| chr1:48358484
|
A | T | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1094+1102T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358484 | ||||||
| chr1:48358669
|
G | T | 1 | a0001c0001t0003g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1094+917C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358669 | ||||||
| chr1:48358672
|
GTTA | G | 16 | a0001c0001t0003g0131a0002c0002t0001g0002a0002c0002t0001g0040others(13): Show | 16 | HG00558.hp2 NA18954.hp2 NA18967.hp1 others(13): Show |
intron_variant | MODIFIER | c.1094+911_1094+913d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358672 | ||||||
| chr1:48358735
|
C | T | 51 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(48): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1094+851G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358735 | ||||||
| chr1:48358785
|
A | G | 1 | a0001c0001t0037g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1094+801T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358785 | ||||||
| chr1:48358799
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1094+787C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358799 | ||||||
| chr1:48358892
|
A | G | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1094+694T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358892 | ||||||
| chr1:48358911
|
C | T | 1 | a0001c0001t0009g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1094+675G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 10/12 | chr1 | 48358911 | ||||||
| chr1:48359808
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.910-38G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48359808 | ||||||
| chr1:48359871
|
GCA | G | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-103_910-102del others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48359871 | ||||||
| chr1:48360027
|
G | A | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.910-257C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360027 | ||||||
| chr1:48360129
|
T | G | 1 | a0002c0002t0001g0009 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.910-359A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360129 | ||||||
| chr1:48360275
|
TAAATGTA | T | 11 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(8): Show | 11 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-512_910-506del others(7): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360275 | ||||||
| chr1:48360331
|
G | C | 10 | a0001c0001t0003g0115a0001c0001t0003g0121a0001c0001t0003g0123others(7): Show | 10 | HG00558.hp1 HG02165.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-561C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360331 | ||||||
| chr1:48360337
|
T | A | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.910-567A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360337 | ||||||
| chr1:48360348
|
A | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.910-578T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360348 | ||||||
| chr1:48360547
|
TAGG | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(53): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.910-780_910-778del others(3): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360547 | ||||||
| chr1:48360887
|
G | A | 15 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(12): Show | 15 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.910-1117C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48360887 | ||||||
| chr1:48361055
|
T | C | 1 | a0001c0001t0003g0141 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.910-1285A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361055 | ||||||
| chr1:48361058
|
T | C | 11 | a0001c0001t0002g0172a0001c0001t0002g0175a0001c0001t0002g0178others(8): Show | 11 | HG00639.hp1 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-1288A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361058 | ||||||
| chr1:48361126
|
T | G | 1 | a0001c0001t0007g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.910-1356A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361126 | ||||||
| chr1:48361162
|
G | A | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.910-1392C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361162 | ||||||
| chr1:48361181
|
A | G | 9 | a0002c0002t0001g0084a0002c0002t0005g0058a0002c0002t0005g0085others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1411T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361181 | ||||||
| chr1:48361255
|
T | C | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.910-1485A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361255 | ||||||
| chr1:48361311
|
G | A | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-1541C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361311 | ||||||
| chr1:48361632
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.910-1862G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361632 | ||||||
| chr1:48361832
|
C | T | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.910-2062G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361832 | ||||||
| chr1:48361834
|
T | G | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.910-2064A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361834 | ||||||
| chr1:48361836
|
A | G | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.910-2066T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361836 | ||||||
| chr1:48361838
|
T | G | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.910-2068A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361838 | ||||||
| chr1:48361917
|
T | C | 1 | a0001c0001t0006g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.910-2147A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48361917 | ||||||
| chr1:48362120
|
A | G | 19 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.910-2350T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362120 | ||||||
| chr1:48362204
|
T | C | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-2434A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362204 | ||||||
| chr1:48362297
|
G | A | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.910-2527C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362297 | ||||||
| chr1:48362343
|
A | C | 218 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.910-2573T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362343 | ||||||
| chr1:48362656
|
A | C | 1 | a0001c0001t0004g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.910-2886T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362656 | ||||||
| chr1:48362676
|
G | GGAAA | 321 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.910-2910_910-2907d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362676 | ||||||
| chr1:48362728
|
C | T | 1 | a0001c0001t0007g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.910-2958G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362728 | ||||||
| chr1:48362777
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.910-3007A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362777 | ||||||
| chr1:48362904
|
T | A | 4 | a0001c0001t0003g0119a0003c0003t0003g0110a0003c0003t0003g0111others(1): Show | 4 | HG00323.hp2 HG01261.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3134A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362904 | ||||||
| chr1:48362914
|
C | T | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.910-3144G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362914 | ||||||
| chr1:48362952
|
G | A | 6 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0019others(3): Show | 6 | HG02015.hp2 HG02074.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-3182C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48362952 | ||||||
| chr1:48363041
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.910-3271T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363041 | ||||||
| chr1:48363170
|
G | C | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-3400C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363170 | ||||||
| chr1:48363187
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.910-3417C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363187 | ||||||
| chr1:48363231
|
C | A | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-3461G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363231 | ||||||
| chr1:48363574
|
G | C | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.910-3804C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363574 | ||||||
| chr1:48363661
|
T | A | 2 | a0002c0002t0001g0027a0005c0006t0001g0032 | 2 | HG00544.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.910-3891A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363661 | ||||||
| chr1:48363716
|
T | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.910-3946A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363716 | ||||||
| chr1:48363754
|
ACTT | A | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-3987_910-3985d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363754 | ||||||
| chr1:48363825
|
A | G | 3 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01167.hp2 HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.910-4055T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363825 | ||||||
| chr1:48363863
|
C | G | 1 | a0001c0001t0002g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.910-4093G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48363863 | ||||||
| chr1:48364223
|
C | G | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.910-4453G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364223 | ||||||
| chr1:48364296
|
T | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-4526A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364296 | ||||||
| chr1:48364371
|
C | T | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-4601G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364371 | ||||||
| chr1:48364390
|
A | G | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.910-4620T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364390 | ||||||
| chr1:48364562
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-4792C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364562 | ||||||
| chr1:48364710
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-4940T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364710 | ||||||
| chr1:48364722
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-4952G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364722 | ||||||
| chr1:48364733
|
A | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.910-4963T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364733 | ||||||
| chr1:48364739
|
T | G | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-4969A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364739 | ||||||
| chr1:48364752
|
T | A | 1 | a0001c0001t0003g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.910-4982A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364752 | ||||||
| chr1:48364772
|
T | A | 25 | a0001c0001t0004g0257a0001c0001t0004g0258a0001c0001t0004g0259others(22): Show | 25 | HG00621.hp2 HG01255.hp1 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.910-5002A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364772 | ||||||
| chr1:48364795
|
T | C | 1 | a0001c0001t0011g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.910-5025A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364795 | ||||||
| chr1:48364809
|
T | C | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.910-5039A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364809 | ||||||
| chr1:48364842
|
C | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.910-5072G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48364842 | ||||||
| chr1:48365026
|
G | C | 1 | a0001c0001t0007g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.910-5256C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365026 | ||||||
| chr1:48365114
|
T | C | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.910-5344A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365114 | ||||||
| chr1:48365118
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-5348A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365118 | ||||||
| chr1:48365202
|
C | T | 3 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0043 | 3 | NA18977.hp2 NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.910-5432G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365202 | ||||||
| chr1:48365274
|
C | T | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.910-5504G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365274 | ||||||
| chr1:48365277
|
T | C | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-5507A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365277 | ||||||
| chr1:48365345
|
A | G | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.910-5575T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365345 | ||||||
| chr1:48365406
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.910-5636G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365406 | ||||||
| chr1:48365653
|
G | A | 2 | a0002c0002t0001g0018a0002c0002t0001g0023 | 2 | NA18999.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.910-5883C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365653 | ||||||
| chr1:48365660
|
C | G | 1 | a0002c0002t0001g0035 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.910-5890G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365660 | ||||||
| chr1:48365707
|
G | A | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.910-5937C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365707 | ||||||
| chr1:48365740
|
C | G | 1 | a0001c0001t0039g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.910-5970G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365740 | ||||||
| chr1:48365770
|
C | T | 2 | a0002c0002t0005g0077a0002c0002t0005g0078 | 2 | NA18966.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.910-6000G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365770 | ||||||
| chr1:48365802
|
T | C | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.910-6032A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365802 | ||||||
| chr1:48365925
|
T | C | 3 | a0001c0001t0004g0261a0001c0001t0004g0262a0001c0001t0004g0276 | 3 | NA18971.hp2 NA19005.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.910-6155A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48365925 | ||||||
| chr1:48366005
|
C | G | 2 | a0001c0001t0014g0213a0001c0001t0014g0214 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.910-6235G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366005 | ||||||
| chr1:48366256
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.910-6486A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366256 | ||||||
| chr1:48366274
|
G | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.910-6504C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366274 | ||||||
| chr1:48366301
|
G | C | 4 | a0002c0002t0027g0062a0002c0002t0029g0061a0002c0002t0031g0075others(1): Show | 4 | HG00280.hp2 HG01261.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-6531C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366301 | ||||||
| chr1:48366326
|
A | T | 1 | a0001c0001t0010g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910-6556T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366326 | ||||||
| chr1:48366333
|
C | G | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.910-6563G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366333 | ||||||
| chr1:48366339
|
C | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.910-6569G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366339 | ||||||
| chr1:48366341
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.910-6571T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366341 | ||||||
| chr1:48366354
|
G | C | 1 | a0001c0001t0010g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910-6584C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366354 | ||||||
| chr1:48366439
|
G | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-6669C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366439 | ||||||
| chr1:48366632
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.910-6862C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366632 | ||||||
| chr1:48366690
|
T | G | 1 | a0001c0001t0004g0286 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.910-6920A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366690 | ||||||
| chr1:48366708
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.910-6938T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366708 | ||||||
| chr1:48366812
|
T | C | 1 | a0002c0002t0005g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.910-7042A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366812 | ||||||
| chr1:48366824
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-7054A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366824 | ||||||
| chr1:48366854
|
C | T | 1 | a0002c0002t0005g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.910-7084G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48366854 | ||||||
| chr1:48367070
|
G | A | 1 | a0002c0002t0005g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.910-7300C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367070 | ||||||
| chr1:48367124
|
C | T | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-7354G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367124 | ||||||
| chr1:48367161
|
C | T | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-7391G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367161 | ||||||
| chr1:48367202
|
T | A | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.910-7432A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367202 | ||||||
| chr1:48367228
|
T | C | 7 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(4): Show | 7 | HG00597.hp1 HG04184.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-7458A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367228 | ||||||
| chr1:48367231
|
C | T | 217 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.910-7461G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367231 | ||||||
| chr1:48367265
|
A | C | 1 | a0001c0001t0003g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.910-7495T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367265 | ||||||
| chr1:48367321
|
G | A | 56 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(53): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.910-7551C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367321 | ||||||
| chr1:48367329
|
G | A | 1 | a0003c0003t0003g0110 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.910-7559C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367329 | ||||||
| chr1:48367344
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.910-7574C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367344 | ||||||
| chr1:48367371
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-7601T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367371 | ||||||
| chr1:48367380
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-7610T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367380 | ||||||
| chr1:48367381
|
A | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-7611T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367381 | ||||||
| chr1:48367698
|
A | T | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.910-7928T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367698 | ||||||
| chr1:48367731
|
G | A | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-7961C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367731 | ||||||
| chr1:48367838
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.910-8068G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367838 | ||||||
| chr1:48367897
|
T | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.910-8127A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367897 | ||||||
| chr1:48367930
|
A | G | 1 | a0001c0001t0036g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.910-8160T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367930 | ||||||
| chr1:48367975
|
T | A | 1 | a0001c0001t0003g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.910-8205A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48367975 | ||||||
| chr1:48368014
|
T | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.910-8244A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368014 | ||||||
| chr1:48368029
|
G | C | 1 | a0002c0002t0005g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.910-8259C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368029 | ||||||
| chr1:48368052
|
T | G | 94 | a0001c0001t0001g0089a0001c0001t0003g0104a0001c0001t0003g0105others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.910-8282A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368052 | ||||||
| chr1:48368202
|
G | A | 1 | a0002c0002t0030g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.910-8432C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368202 | ||||||
| chr1:48368308
|
G | A | 35 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(32): Show | 35 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.910-8538C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368308 | ||||||
| chr1:48368440
|
C | T | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-8670G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368440 | ||||||
| chr1:48368489
|
C | T | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-8719G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368489 | ||||||
| chr1:48368507
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-8737A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368507 | ||||||
| chr1:48368587
|
C | A | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.910-8817G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368587 | ||||||
| chr1:48368623
|
C | T | 1 | a0002c0002t0030g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.910-8853G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368623 | ||||||
| chr1:48368769
|
T | C | 5 | a0001c0001t0004g0257a0001c0001t0004g0263a0001c0001t0004g0268others(2): Show | 5 | HG01255.hp1 NA18966.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-8999A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368769 | ||||||
| chr1:48368950
|
G | A | 1 | a0001c0001t0007g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.910-9180C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48368950 | ||||||
| chr1:48369015
|
C | A | 3 | a0001c0001t0006g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG01891.hp2 HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.910-9245G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369015 | ||||||
| chr1:48369041
|
G | A | 1 | a0001c0001t0009g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.910-9271C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369041 | ||||||
| chr1:48369094
|
C | G | 1 | a0001c0001t0011g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.910-9324G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369094 | ||||||
| chr1:48369120
|
C | T | 1 | a0001c0001t0003g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.910-9350G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369120 | ||||||
| chr1:48369122
|
C | T | 40 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(37): Show | 40 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.910-9352G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369122 | ||||||
| chr1:48369343
|
GCTGT | G | 7 | a0001c0001t0004g0256a0001c0001t0004g0274a0001c0001t0004g0279others(4): Show | 7 | HG02129.hp1 NA18943.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-9577_910-9574d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369343 | ||||||
| chr1:48369420
|
G | A | 1 | a0002c0002t0001g0005 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.910-9650C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369420 | ||||||
| chr1:48369429
|
C | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-9659G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369429 | ||||||
| chr1:48369439
|
C | T | 1 | a0001c0001t0004g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.910-9669G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369439 | ||||||
| chr1:48369509
|
G | A | 56 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(53): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.910-9739C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369509 | ||||||
| chr1:48369576
|
G | A | 1 | a0001c0001t0003g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.910-9806C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369576 | ||||||
| chr1:48369609
|
C | T | 1 | a0001c0001t0007g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.910-9839G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369609 | ||||||
| chr1:48369623
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.910-9853C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369623 | ||||||
| chr1:48369634
|
G | A | 3 | a0001c0001t0007g0307a0001c0001t0015g0319a0001c0001t0015g0320 | 3 | HG00735.hp1 HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.910-9864C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369634 | ||||||
| chr1:48369723
|
A | G | 218 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.910-9953T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369723 | ||||||
| chr1:48369764
|
G | A | 1 | a0001c0001t0036g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.910-9994C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369764 | ||||||
| chr1:48369847
|
A | C | 5 | a0002c0002t0001g0084a0002c0002t0005g0058a0002c0002t0005g0085others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-10077T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369847 | ||||||
| chr1:48369905
|
A | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.910-10135T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48369905 | ||||||
| chr1:48370012
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.910-10242C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370012 | ||||||
| chr1:48370086
|
C | T | 218 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.910-10316G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370086 | ||||||
| chr1:48370452
|
A | C | 1 | a0001c0001t0004g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.910-10682T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370452 | ||||||
| chr1:48370662
|
A | T | 1 | a0001c0001t0003g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.910-10892T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370662 | ||||||
| chr1:48370725
|
T | C | 2 | a0002c0002t0005g0021a0002c0002t0005g0022 | 2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.910-10955A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370725 | ||||||
| chr1:48370835
|
A | C | 2 | a0001c0001t0003g0124a0001c0001t0003g0134 | 2 | HG00544.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.910-11065T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48370835 | ||||||
| chr1:48371078
|
A | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0142 | 2 | NA19011.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.910-11308T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371078 | ||||||
| chr1:48371127
|
G | A | 1 | a0001c0001t0013g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.910-11357C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371127 | ||||||
| chr1:48371267
|
C | CTAGA | 8 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0156others(5): Show | 8 | HG00558.hp1 HG00621.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.910-11498_910-1149 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371267 | ||||||
| chr1:48371267
|
C | CTAGATAG others(5): Show |
2 | a0001c0001t0009g0102a0001c0001t0010g0137 | 2 | HG01346.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.910-11498_910-1149 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371267 | ||||||
| chr1:48371267
|
CTATA | C | 59 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0168others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.910-11501_910-1149 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371267 | ||||||
| chr1:48371270
|
T | G | 36 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0154others(33): Show | 36 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.910-11500A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
T | TATAG | 79 | a0001c0001t0003g0218a0001c0001t0004g0256a0001c0001t0004g0258others(76): Show | 79 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.910-11504_910-1150 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
T | TATAGATA others(1): Show |
27 | a0001c0001t0004g0257a0001c0001t0004g0272a0001c0001t0004g0278others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.910-11508_910-1150 others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
T | TATAGATA others(5): Show |
8 | a0001c0001t0003g0216a0001c0001t0004g0274a0001c0001t0004g0279others(5): Show | 8 | HG01346.hp1 HG02129.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.910-11512_910-1150 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
TATAG | T | 19 | a0001c0001t0001g0089a0001c0001t0003g0225a0001c0001t0006g0234others(16): Show | 19 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.910-11504_910-1150 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
TATAGATA others(1): Show |
T | 5 | a0001c0001t0009g0206a0001c0001t0009g0207a0001c0001t0009g0226others(2): Show | 5 | HG01070.hp2 HG01243.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-11508_910-1150 others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371270
|
TATAGATA others(5): Show |
T | 9 | a0001c0001t0004g0229a0001c0001t0009g0208a0001c0001t0009g0227others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-11512_910-1150 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371270 | ||||||
| chr1:48371272
|
T | C | 1 | a0001c0001t0006g0145 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.910-11502A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371272 | ||||||
| chr1:48371280
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.910-11510A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371280 | ||||||
| chr1:48371392
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.910-11622A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371392 | ||||||
| chr1:48371602
|
A | G | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.910-11832T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371602 | ||||||
| chr1:48371724
|
G | A | 5 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0219others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-11954C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371724 | ||||||
| chr1:48371725
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.910-11955G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371725 | ||||||
| chr1:48371782
|
C | A | 5 | a0002c0002t0001g0084a0002c0002t0005g0058a0002c0002t0005g0085others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-12012G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371782 | ||||||
| chr1:48371802
|
C | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.910-12032G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371802 | ||||||
| chr1:48371885
|
G | A | 3 | a0001c0001t0026g0295a0001c0001t0026g0297a0001c0001t0043g0298 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.910-12115C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48371885 | ||||||
| chr1:48372063
|
C | T | 1 | a0001c0001t0003g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.910-12293G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372063 | ||||||
| chr1:48372066
|
G | T | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0010g0117 | 3 | NA18954.hp1 NA19011.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.910-12296C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372066 | ||||||
| chr1:48372211
|
G | T | 1 | a0002c0002t0019g0080 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.910-12441C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372211 | ||||||
| chr1:48372253
|
A | C | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-12483T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372253 | ||||||
| chr1:48372332
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.910-12562A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372332 | ||||||
| chr1:48372397
|
T | C | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-12627A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372397 | ||||||
| chr1:48372502
|
C | T | 11 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.910-12732G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372502 | ||||||
| chr1:48372503
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.910-12733C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372503 | ||||||
| chr1:48372895
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.909+12414G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48372895 | ||||||
| chr1:48373124
|
C | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+12185G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373124 | ||||||
| chr1:48373249
|
T | C | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+12060A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373249 | ||||||
| chr1:48373330
|
C | G | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.909+11979G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373330 | ||||||
| chr1:48373610
|
A | T | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+11699T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373610 | ||||||
| chr1:48373722
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.909+11587C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373722 | ||||||
| chr1:48373972
|
T | C | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.909+11337A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373972 | ||||||
| chr1:48373986
|
A | G | 1 | a0001c0001t0007g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.909+11323T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48373986 | ||||||
| chr1:48374296
|
A | C | 1 | a0001c0001t0006g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+11013T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48374296 | ||||||
| chr1:48374311
|
T | TA | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0262others(10): Show | 13 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+10997dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48374311 | ||||||
| chr1:48374609
|
C | T | 1 | a0001c0001t0014g0214 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.909+10700G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48374609 | ||||||
| chr1:48374690
|
T | C | 4 | a0001c0001t0004g0257a0001c0001t0004g0263a0001c0001t0004g0275others(1): Show | 4 | HG01255.hp1 NA18966.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+10619A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48374690 | ||||||
| chr1:48374923
|
T | C | 1 | a0001c0001t0008g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.909+10386A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48374923 | ||||||
| chr1:48375067
|
G | C | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+10242C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48375067 | ||||||
| chr1:48375405
|
G | A | 1 | a0001c0001t0003g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.909+9904C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48375405 | ||||||
| chr1:48375505
|
C | T | 1 | a0001c0001t0009g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.909+9804G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48375505 | ||||||
| chr1:48375709
|
G | T | 1 | a0002c0002t0019g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.909+9600C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48375709 | ||||||
| chr1:48376111
|
C | G | 1 | a0001c0001t0006g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+9198G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376111 | ||||||
| chr1:48376143
|
C | A | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.909+9166G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376143 | ||||||
| chr1:48376166
|
T | C | 1 | a0001c0001t0008g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.909+9143A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376166 | ||||||
| chr1:48376422
|
C | T | 1 | a0002c0002t0005g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.909+8887G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376422 | ||||||
| chr1:48376635
|
C | T | 49 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.909+8674G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376635 | ||||||
| chr1:48376809
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.909+8500T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376809 | ||||||
| chr1:48376884
|
G | A | 1 | a0005c0006t0001g0032 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.909+8425C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376884 | ||||||
| chr1:48376911
|
T | C | 1 | a0002c0002t0019g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.909+8398A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48376911 | ||||||
| chr1:48377264
|
C | T | 2 | a0002c0002t0005g0074a0002c0002t0019g0080 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.909+8045G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48377264 | ||||||
| chr1:48377374
|
ACCAATAT others(14): Show |
A | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909+7914_909+7934d others(23): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48377374 | ||||||
| chr1:48377389
|
G | A | 1 | a0001c0001t0011g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.909+7920C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48377389 | ||||||
| chr1:48377499
|
C | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.909+7810G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48377499 | ||||||
| chr1:48378001
|
C | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+7308G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378001 | ||||||
| chr1:48378054
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.909+7255A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378054 | ||||||
| chr1:48378329
|
T | C | 40 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(37): Show | 40 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+6980A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378329 | ||||||
| chr1:48378516
|
A | G | 11 | a0001c0001t0002g0165a0001c0001t0006g0144a0001c0001t0006g0145others(8): Show | 11 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+6793T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378516 | ||||||
| chr1:48378556
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.909+6753C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378556 | ||||||
| chr1:48378588
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+6721C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378588 | ||||||
| chr1:48378603
|
G | C | 1 | a0001c0001t0002g0170 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.909+6706C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378603 | ||||||
| chr1:48378893
|
C | T | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.909+6416G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378893 | ||||||
| chr1:48378895
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+6414T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48378895 | ||||||
| chr1:48379051
|
C | G | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+6258G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379051 | ||||||
| chr1:48379134
|
C | T | 1 | a0001c0001t0011g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.909+6175G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379134 | ||||||
| chr1:48379467
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.909+5842A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379467 | ||||||
| chr1:48379782
|
G | A | 3 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0087 | 3 | HG01257.hp2 HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.909+5527C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379782 | ||||||
| chr1:48379836
|
A | AAAATACA others(23): Show |
1 | a0001c0001t0002g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.909+5443_909+5472d others(32): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379836 | ||||||
| chr1:48379960
|
A | C | 1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.909+5349T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48379960 | ||||||
| chr1:48380266
|
A | C | 1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.909+5043T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380266 | ||||||
| chr1:48380518
|
T | C | 1 | a0001c0001t0008g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.909+4791A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380518 | ||||||
| chr1:48380694
|
AAGATCAA others(5): Show |
A | 1 | a0001c0001t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.909+4603_909+4614d others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380694 | ||||||
| chr1:48380735
|
A | G | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.909+4574T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380735 | ||||||
| chr1:48380814
|
CCAGGCCT others(14): Show |
C | 1 | a0001c0001t0002g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.909+4474_909+4494d others(23): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380814 | ||||||
| chr1:48380866
|
TAAACACT others(17): Show |
T | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.909+4419_909+4442d others(26): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48380866 | ||||||
| chr1:48381071
|
G | A | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.909+4238C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381071 | ||||||
| chr1:48381235
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.909+4074C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381235 | ||||||
| chr1:48381580
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.909+3729G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381580 | ||||||
| chr1:48381587
|
G | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+3722C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381587 | ||||||
| chr1:48381594
|
A | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+3715T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381594 | ||||||
| chr1:48381640
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.909+3669A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381640 | ||||||
| chr1:48381648
|
C | CT | 69 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.909+3660dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381648 | ||||||
| chr1:48381648
|
C | CTT | 11 | a0001c0001t0007g0303a0001c0001t0007g0304a0001c0001t0007g0307others(8): Show | 11 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+3659_909+3660d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381648 | ||||||
| chr1:48381648
|
CT | C | 47 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0167others(44): Show | 47 | HG01167.hp2 HG01168.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.909+3660delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381648 | ||||||
| chr1:48381687
|
C | CT | 156 | a0001c0001t0002g0168a0001c0001t0002g0178a0001c0001t0002g0181others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.909+3621dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381687 | ||||||
| chr1:48381687
|
C | CTT | 140 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0153others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.909+3620_909+3621d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381687 | ||||||
| chr1:48381687
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.909+3622G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381687 | ||||||
| chr1:48381687
|
CTT | C | 12 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(9): Show | 12 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+3620_909+3621d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381687 | ||||||
| chr1:48381719
|
ATTGATCA others(44): Show |
A | 1 | a0001c0001t0002g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.909+3539_909+3589d others(53): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381719 | ||||||
| chr1:48381772
|
C | T | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909+3537G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381772 | ||||||
| chr1:48381908
|
T | C | 36 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(33): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.909+3401A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381908 | ||||||
| chr1:48381938
|
T | C | 1 | a0002c0002t0005g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.909+3371A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381938 | ||||||
| chr1:48381984
|
T | TGGACACA others(21): Show |
1 | a0001c0001t0002g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.909+3297_909+3324d others(30): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48381984 | ||||||
| chr1:48382006
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+3303C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382006 | ||||||
| chr1:48382018
|
G | T | 1 | a0002c0002t0001g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.909+3291C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382018 | ||||||
| chr1:48382247
|
G | C | 1 | a0001c0001t0006g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+3062C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382247 | ||||||
| chr1:48382283
|
C | T | 1 | a0001c0001t0016g0306 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.909+3026G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382283 | ||||||
| chr1:48382328
|
C | T | 5 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(2): Show | 5 | NA18961.hp2 NA18971.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+2981G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382328 | ||||||
| chr1:48382455
|
C | T | 1 | a0002c0002t0030g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.909+2854G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382455 | ||||||
| chr1:48382473
|
ACCTCCCT others(163): Show |
A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+2666_909+2835d others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382473 | ||||||
| chr1:48382488
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.909+2821C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382488 | ||||||
| chr1:48382600
|
ACCTCCCT others(36): Show |
A | 55 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(52): Show | 55 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.909+2666_909+2708d others(45): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382600 | ||||||
| chr1:48382607
|
TCCCGGAC others(37): Show |
T | 1 | a0002c0002t0005g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.909+2658_909+2701d others(46): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382607 | ||||||
| chr1:48382614
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.909+2695G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382614 | ||||||
| chr1:48382626
|
C | G | 2 | a0002c0002t0005g0071a0002c0002t0005g0072 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.909+2683G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382626 | ||||||
| chr1:48382629
|
A | AC | 51 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0156others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.909+2679dupG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382629 | ||||||
| chr1:48382629
|
A | ACC | 94 | a0001c0001t0001g0089a0001c0001t0002g0158a0001c0001t0002g0165others(91): Show | 94 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.909+2678_909+2679d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382629 | ||||||
| chr1:48382629
|
A | ACCC | 39 | a0001c0001t0002g0173a0001c0001t0002g0178a0001c0001t0002g0179others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.909+2677_909+2679d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382629 | ||||||
| chr1:48382629
|
A | ACCCC | 24 | a0001c0001t0002g0100a0001c0001t0002g0175a0001c0001t0002g0183others(21): Show | 24 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+2676_909+2679d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382629 | ||||||
| chr1:48382640
|
C | A | 1 | a0002c0002t0027g0062 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.909+2669G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382640 | ||||||
| chr1:48382641
|
C | T | 17 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(14): Show | 17 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.909+2668G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382641 | ||||||
| chr1:48382704
|
G | A | 1 | a0001c0001t0044g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+2605C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382704 | ||||||
| chr1:48382732
|
G | A | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.909+2577C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382732 | ||||||
| chr1:48382746
|
G | A | 4 | a0001c0001t0003g0119a0003c0003t0003g0110a0003c0003t0003g0111others(1): Show | 4 | HG00323.hp2 HG01261.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2563C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382746 | ||||||
| chr1:48382752
|
CGGGGGGC others(18): Show |
C | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2532_909+2556d others(27): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382752 | ||||||
| chr1:48382780
|
C | T | 6 | a0001c0001t0004g0264a0001c0001t0004g0270a0001c0001t0004g0278others(3): Show | 6 | HG00423.hp1 HG02071.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+2529G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382780 | ||||||
| chr1:48382789
|
C | T | 10 | a0001c0001t0003g0205a0001c0001t0003g0216a0001c0001t0003g0217others(7): Show | 10 | HG00642.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+2520G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382789 | ||||||
| chr1:48382791
|
G | A | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2518C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382791 | ||||||
| chr1:48382802
|
GGGGGGCT others(43): Show |
G | 70 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.909+2457_909+2506d others(52): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382802 | ||||||
| chr1:48382803
|
GGGGGCTG others(42): Show |
G | 1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.909+2457_909+2505d others(51): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382803 | ||||||
| chr1:48382811
|
AC | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.909+2497delG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382811 | ||||||
| chr1:48382812
|
CCCCCCCC others(42): Show |
C | 2 | a0001c0001t0002g0189a0001c0001t0013g0163 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.909+2448_909+2496d others(51): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382812 | ||||||
| chr1:48382813
|
C | T | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2496G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382813 | ||||||
| chr1:48382848
|
G | A | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2461C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382848 | ||||||
| chr1:48382852
|
A | G | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2457T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382852 | ||||||
| chr1:48382861
|
A | AC | 13 | a0001c0001t0002g0186a0001c0001t0003g0205a0001c0001t0004g0273others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+2447dupG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382861 | ||||||
| chr1:48382866
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.909+2443G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382866 | ||||||
| chr1:48382869
|
T | A | 4 | a0002c0002t0001g0084a0002c0002t0005g0058a0002c0002t0005g0085others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2440A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382869 | ||||||
| chr1:48382869
|
T | C | 1 | a0003c0003t0003g0110 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.909+2440A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382869 | ||||||
| chr1:48382872
|
C | T | 4 | a0002c0002t0001g0084a0002c0002t0005g0058a0002c0002t0005g0085others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2437G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382872 | ||||||
| chr1:48382875
|
C | G | 1 | a0001c0001t0002g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.909+2434G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382875 | ||||||
| chr1:48382880
|
G | A | 40 | a0001c0001t0002g0173a0001c0001t0004g0256a0001c0001t0004g0257others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.909+2429C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382880 | ||||||
| chr1:48382907
|
C | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.909+2402G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382907 | ||||||
| chr1:48382910
|
A | AC | 21 | a0001c0001t0004g0290a0001c0001t0008g0235a0001c0001t0008g0236others(18): Show | 21 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.909+2398dupG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382910 | ||||||
| chr1:48382934
|
G | T | 1 | a0001c0001t0026g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.909+2375C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382934 | ||||||
| chr1:48382960
|
C | T | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.909+2349G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382960 | ||||||
| chr1:48382961
|
C | T | 1 | a0002c0002t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.909+2348G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382961 | ||||||
| chr1:48382995
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+2314C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48382995 | ||||||
| chr1:48383041
|
C | T | 2 | a0002c0002t0005g0074a0002c0002t0019g0080 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.909+2268G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383041 | ||||||
| chr1:48383065
|
G | A | 1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+2244C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383065 | ||||||
| chr1:48383076
|
C | T | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.909+2233G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383076 | ||||||
| chr1:48383087
|
TCCCCCCA others(41): Show |
T | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909+2174_909+2221d others(50): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383087 | ||||||
| chr1:48383108
|
C | T | 1 | a0001c0001t0004g0266 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.909+2201G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383108 | ||||||
| chr1:48383109
|
GGGGCGGC others(41): Show |
G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.909+2152_909+2199d others(50): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383109 | ||||||
| chr1:48383125
|
C | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.909+2184G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383125 | ||||||
| chr1:48383135
|
ACCCCCCA others(42): Show |
A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+2125_909+2173d others(51): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383135 | ||||||
| chr1:48383185
|
C | A | 1 | a0002c0002t0001g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.909+2124G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383185 | ||||||
| chr1:48383219
|
GGGCAGAG others(163): Show |
G | 4 | a0001c0001t0007g0313a0001c0001t0016g0306a0001c0001t0036g0311others(1): Show | 4 | NA18969.hp1 NA18989.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1920_909+2089d others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383219 | ||||||
| chr1:48383283
|
C | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+2026G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383283 | ||||||
| chr1:48383297
|
GGGCGGGG others(162): Show |
G | 1 | a0001c0001t0002g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.909+1843_909+2011d others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383297 | ||||||
| chr1:48383301
|
G | A | 72 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(69): Show | 72 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.909+2008C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383301 | ||||||
| chr1:48383307
|
CTGACCCC others(11): Show |
C | 1 | a0001c0001t0013g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.909+1984_909+2001d others(20): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383307 | ||||||
| chr1:48383312
|
C | A | 1 | a0002c0002t0005g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.909+1997G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383312 | ||||||
| chr1:48383333
|
G | A | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.909+1976C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383333 | ||||||
| chr1:48383347
|
A | AC | 11 | a0001c0001t0006g0144a0001c0001t0006g0147a0001c0001t0006g0148others(8): Show | 11 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1961dupG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383347 | ||||||
| chr1:48383349
|
CG | C | 65 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(62): Show | 65 | HG00323.hp1 HG01071.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.909+1959delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383349 | ||||||
| chr1:48383350
|
G | C | 146 | a0001c0001t0001g0089a0001c0001t0003g0104a0001c0001t0003g0105others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.909+1959C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383350 | ||||||
| chr1:48383350
|
G | GC | 21 | a0001c0001t0002g0152a0001c0001t0002g0170a0001c0001t0002g0172others(18): Show | 21 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.909+1958dupG | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383350 | ||||||
| chr1:48383351
|
C | A | 1 | a0002c0002t0005g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.909+1958G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383351 | ||||||
| chr1:48383353
|
C | G | 103 | a0001c0001t0001g0089a0001c0001t0003g0104a0001c0001t0003g0105others(100): Show | 103 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.909+1956G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383353 | ||||||
| chr1:48383361
|
A | G | 293 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(290): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.909+1948T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383361 | ||||||
| chr1:48383449
|
C | A | 1 | a0001c0001t0004g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.909+1860G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383449 | ||||||
| chr1:48383450
|
G | A | 2 | a0001c0001t0020g0113a0001c0001t0020g0114 | 2 | NA18974.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.909+1859C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383450 | ||||||
| chr1:48383466
|
C | CG | 290 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(287): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.909+1842dupC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383466 | ||||||
| chr1:48383469
|
C | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0186 | 2 | HG01952.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.909+1840G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383469 | ||||||
| chr1:48383510
|
C | T | 10 | a0001c0001t0003g0205a0001c0001t0003g0216a0001c0001t0003g0217others(7): Show | 10 | HG00642.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+1799G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383510 | ||||||
| chr1:48383594
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.909+1715G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383594 | ||||||
| chr1:48383682
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0199 | 2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.909+1627C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383682 | ||||||
| chr1:48383747
|
C | G | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+1562G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383747 | ||||||
| chr1:48383757
|
C | A | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.909+1552G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383757 | ||||||
| chr1:48383796
|
GCGCTCCT others(33): Show |
G | 1 | a0001c0001t0002g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+1473_909+1512d others(42): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383796 | ||||||
| chr1:48383884
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.909+1425T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383884 | ||||||
| chr1:48383886
|
CCCAGACG others(17): Show |
C | 1 | a0001c0001t0002g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.909+1399_909+1422d others(26): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383886 | ||||||
| chr1:48383893
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.909+1416C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383893 | ||||||
| chr1:48383931
|
C | CG | 7 | a0001c0001t0002g0174a0001c0001t0002g0183a0001c0001t0002g0194others(4): Show | 7 | HG00621.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+1377dupC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383931 | ||||||
| chr1:48383962
|
C | T | 2 | a0002c0002t0005g0074a0002c0002t0019g0080 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.909+1347G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383962 | ||||||
| chr1:48383978
|
C | T | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.909+1331G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48383978 | ||||||
| chr1:48384064
|
G | A | 6 | a0002c0002t0005g0090a0002c0002t0005g0091a0002c0002t0005g0092others(3): Show | 6 | NA18940.hp2 NA18941.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+1245C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384064 | ||||||
| chr1:48384072
|
A | G | 8 | a0001c0001t0004g0256a0001c0001t0004g0274a0001c0001t0004g0279others(5): Show | 8 | HG00609.hp2 HG02129.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1237T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384072 | ||||||
| chr1:48384081
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.909+1228G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384081 | ||||||
| chr1:48384095
|
AG | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+1213delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384095 | ||||||
| chr1:48384115
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+1194G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384115 | ||||||
| chr1:48384171
|
C | CA | 21 | a0001c0001t0003g0105a0001c0001t0003g0205a0001c0001t0003g0225others(18): Show | 21 | HG00423.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.909+1137dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384171 | ||||||
| chr1:48384228
|
C | T | 1 | a0001c0001t0007g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.909+1081G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384228 | ||||||
| chr1:48384260
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.909+1049C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384260 | ||||||
| chr1:48384274
|
G | A | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.909+1035C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384274 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(568): Show |
1 | a0001c0001t0002g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(575): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(413): Show |
1 | a0001c0001t0002g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(420): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(588): Show |
1 | a0001c0001t0002g0169 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(595): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(538): Show |
1 | a0001c0001t0002g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(545): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(538): Show |
1 | a0001c0001t0002g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(545): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(683): Show |
1 | a0001c0001t0002g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(690): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(640): Show |
1 | a0001c0001t0002g0201 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(647): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(329): Show |
1 | a0001c0001t0040g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(336): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(353): Show |
1 | a0001c0001t0002g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(360): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(479): Show |
1 | a0001c0001t0002g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(486): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(491): Show |
1 | a0001c0001t0021g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(498): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(544): Show |
1 | a0001c0001t0002g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(551): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(515): Show |
1 | a0001c0001t0002g0177 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(522): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(533): Show |
1 | a0001c0001t0002g0170 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(540): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(539): Show |
1 | a0004c0004t0002g0097 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(546): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(551): Show |
2 | a0001c0001t0002g0158a0004c0004t0002g0098 | 2 | HG01256.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.909+983_909+984ins others(558): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(569): Show |
1 | a0001c0001t0002g0175 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(576): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(575): Show |
1 | a0001c0001t0002g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(582): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(587): Show |
1 | a0001c0001t0002g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(594): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(599): Show |
1 | a0001c0001t0002g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(606): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(635): Show |
2 | a0001c0001t0002g0156a0001c0001t0002g0176 | 2 | HG02523.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.909+983_909+984ins others(642): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(659): Show |
1 | a0001c0001t0002g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(666): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(695): Show |
1 | a0001c0001t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(702): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(701): Show |
1 | a0001c0001t0002g0174 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(708): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(707): Show |
1 | a0001c0001t0002g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(714): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(743): Show |
1 | a0001c0001t0002g0180 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(750): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(749): Show |
2 | a0001c0001t0002g0173a0001c0001t0024g0185 | 2 | HG00597.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.909+983_909+984ins others(756): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(785): Show |
1 | a0001c0001t0002g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.909+983_909+984ins others(792): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(546): Show |
1 | a0001c0001t0002g0202 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(553): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(456): Show |
1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(463): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
G | GGAGGGAG others(895): Show |
1 | a0001c0001t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.909+983_909+984ins others(902): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
GGAGGGAC others(29): Show |
G | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.909+948_909+983del others(36): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
GGAGGGAC others(35): Show |
G | 1 | a0001c0001t0017g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.909+942_909+983del others(42): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384325
|
GGAGGGAC others(41): Show |
G | 2 | a0001c0001t0008g0235a0001c0001t0023g0099 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.909+936_909+983del others(48): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384325 | ||||||
| chr1:48384326
|
G | GAGGGAC | 4 | a0001c0001t0001g0089a0001c0001t0003g0205a0001c0001t0003g0216others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+977_909+982dup others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384326 | ||||||
| chr1:48384326
|
G | GAGGGACA others(5): Show |
1 | a0001c0001t0003g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.909+971_909+982dup others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384326 | ||||||
| chr1:48384326
|
GAGGGAC | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0027a0005c0006t0001g0032 | 3 | HG00544.hp1 NA19070.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.909+977_909+982del others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384326 | ||||||
| chr1:48384327
|
A | AGGGAGGA others(913): Show |
1 | a0001c0001t0002g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.909+981_909+982ins others(920): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384327 | ||||||
| chr1:48384329
|
GGACAGGG others(37): Show |
G | 8 | a0001c0001t0008g0242a0001c0001t0008g0243a0001c0001t0008g0251others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+936_909+979del others(44): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384329 | ||||||
| chr1:48384329
|
GGACAGGG others(43): Show |
G | 8 | a0001c0001t0008g0236a0001c0001t0008g0239a0001c0001t0008g0244others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+930_909+979del others(50): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384329 | ||||||
| chr1:48384332
|
C | G | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.909+977G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384332 | ||||||
| chr1:48384332
|
CAGGGACA others(29): Show |
C | 6 | a0001c0001t0003g0118a0001c0001t0003g0124a0001c0001t0003g0130others(3): Show | 6 | HG00544.hp2 HG02015.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+941_909+976del others(36): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384332 | ||||||
| chr1:48384334
|
G | GGGAGAGG others(734): Show |
1 | a0001c0001t0002g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.909+974_909+975ins others(741): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384334 | ||||||
| chr1:48384337
|
A | AGAGGGGG others(35): Show |
1 | a0001c0001t0002g0191 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.909+971_909+972ins others(42): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384337 | ||||||
| chr1:48384337
|
A | AGAGGGGG others(90): Show |
1 | a0001c0001t0013g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+971_909+972ins others(97): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384337 | ||||||
| chr1:48384337
|
A | G | 1 | a0001c0001t0013g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.909+972T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384337 | ||||||
| chr1:48384338
|
C | CAGGGAGA others(23): Show |
1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.909+970_909+971ins others(30): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384338
|
C | G | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.909+971G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384338
|
CAGGGACA others(29): Show |
C | 15 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+935_909+970del others(36): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384338
|
CAGGGACA others(35): Show |
C | 6 | a0001c0001t0007g0304a0001c0001t0007g0308a0001c0001t0007g0309others(3): Show | 6 | HG00639.hp2 HG01069.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+929_909+970del others(42): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384338
|
CAGGGACA others(41): Show |
C | 5 | a0001c0001t0007g0313a0001c0001t0016g0306a0001c0001t0018g0316others(2): Show | 5 | HG03579.hp2 NA18969.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+923_909+970del others(48): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384338
|
CAGGGACA others(53): Show |
C | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.909+911_909+970del others(60): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384338 | ||||||
| chr1:48384343
|
A | AGGGGGAG others(57): Show |
1 | a0001c0001t0002g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.909+965_909+966ins others(64): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384343 | ||||||
| chr1:48384343
|
A | G | 3 | a0001c0001t0002g0191a0001c0001t0013g0162a0001c0001t0013g0163 | 3 | HG02055.hp1 NA19003.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+966T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384343 | ||||||
| chr1:48384344
|
C | CAGGGAGA others(17): Show |
1 | a0001c0001t0003g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+964_909+965ins others(24): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384344 | ||||||
| chr1:48384344
|
C | G | 55 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(52): Show | 55 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.909+965G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384344 | ||||||
| chr1:48384344
|
CAGGGACA others(5): Show |
C | 2 | a0001c0001t0006g0146a0002c0002t0001g0038 | 2 | HG01081.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.909+953_909+964del others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384344 | ||||||
| chr1:48384345
|
A | AGGGGGAG others(85): Show |
1 | a0001c0001t0035g0160 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.909+963_909+964ins others(92): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384345 | ||||||
| chr1:48384349
|
A | G | 4 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0162others(1): Show | 4 | HG02040.hp2 HG02055.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+960T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384349 | ||||||
| chr1:48384350
|
C | CAGGGACA others(5): Show |
1 | a0001c0001t0003g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.909+958_909+959ins others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
C | CAGGGACA others(11): Show |
1 | a0001c0005t0003g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.909+958_909+959ins others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
C | CAGGGACA others(17): Show |
1 | a0001c0001t0009g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.909+958_909+959ins others(24): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
C | CAGGGAGA others(5): Show |
1 | a0001c0001t0009g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.909+947_909+958dup others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
C | G | 58 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(55): Show | 58 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.909+959G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAG | C | 40 | a0001c0001t0003g0105a0001c0001t0004g0288a0001c0001t0004g0289others(37): Show | 40 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.909+953_909+958del others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(5): Show |
C | 36 | a0001c0001t0003g0225a0001c0001t0003g0254a0001c0001t0004g0256others(33): Show | 36 | HG00140.hp2 HG00423.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.909+947_909+958del others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(11): Show |
C | 79 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0003g0108others(76): Show | 79 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.909+941_909+958del others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(17): Show |
C | 22 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0003g0135others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.909+935_909+958del others(24): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(23): Show |
C | 6 | a0001c0001t0014g0213a0001c0001t0014g0214a0001c0001t0034g0101others(3): Show | 6 | HG01243.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+929_909+958del others(30): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(29): Show |
C | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.909+923_909+958del others(36): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384350
|
CAGGGAGA others(47): Show |
C | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18950.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.909+905_909+958del others(54): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384350 | ||||||
| chr1:48384351
|
A | AGGGAGAG others(719): Show |
1 | a0001c0001t0024g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.909+957_909+958ins others(726): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384351 | ||||||
| chr1:48384351
|
A | AGGGGGAG others(52): Show |
1 | a0001c0001t0013g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.909+957_909+958ins others(59): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384351 | ||||||
| chr1:48384351
|
A | G | 1 | a0001c0001t0035g0160 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.909+958T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384351 | ||||||
| chr1:48384352
|
G | GGGAGAGG others(836): Show |
1 | a0001c0001t0002g0215 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.909+956_909+957ins others(843): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384352 | ||||||
| chr1:48384355
|
A | G | 4 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0162others(1): Show | 4 | HG02040.hp2 HG02055.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+954T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384355 | ||||||
| chr1:48384356
|
G | C | 5 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0219others(2): Show | 5 | HG02258.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+953C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384356 | ||||||
| chr1:48384357
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+952T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384357 | ||||||
| chr1:48384358
|
G | GGGAGAGG others(698): Show |
1 | a0001c0001t0002g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.909+950_909+951ins others(705): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384358 | ||||||
| chr1:48384361
|
A | AGAGGGAG others(685): Show |
1 | a0001c0001t0002g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.909+947_909+948ins others(692): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384361 | ||||||
| chr1:48384361
|
A | G | 4 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0162others(1): Show | 4 | HG02040.hp2 HG02055.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+948T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384361 | ||||||
| chr1:48384362
|
G | C | 3 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01167.hp2 HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.909+947C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384362 | ||||||
| chr1:48384363
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+946T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384363 | ||||||
| chr1:48384367
|
A | AGAGGGAG others(1155): Show |
1 | a0001c0001t0002g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.909+941_909+942ins others(1162): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384367 | ||||||
| chr1:48384367
|
A | G | 4 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0162others(1): Show | 4 | HG02040.hp2 HG02055.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+942T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384367 | ||||||
| chr1:48384368
|
G | C | 5 | a0001c0001t0003g0225a0001c0001t0006g0143a0001c0001t0009g0226others(2): Show | 5 | HG01167.hp2 HG01257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+941C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384368 | ||||||
| chr1:48384369
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+940T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384369 | ||||||
| chr1:48384373
|
A | G | 4 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0163others(1): Show | 4 | HG02040.hp2 HG02055.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+936T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384373 | ||||||
| chr1:48384374
|
G | C | 12 | a0001c0001t0003g0225a0001c0001t0004g0257a0001c0001t0004g0263others(9): Show | 12 | HG01167.hp2 HG01255.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+935C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384374 | ||||||
| chr1:48384375
|
A | G | 4 | a0001c0001t0013g0162a0001c0001t0013g0164a0001c0001t0017g0246others(1): Show | 4 | HG01167.hp1 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+934T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384375 | ||||||
| chr1:48384377
|
G | GGAGAGGG others(992): Show |
1 | a0001c0001t0002g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909+931_909+932ins others(999): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384377 | ||||||
| chr1:48384379
|
A | G | 13 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0008g0242others(10): Show | 13 | HG02040.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+930T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384379 | ||||||
| chr1:48384380
|
G | A | 1 | a0001c0001t0013g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.909+929C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384380 | ||||||
| chr1:48384381
|
A | G | 5 | a0001c0001t0008g0235a0001c0001t0013g0162a0001c0001t0013g0164others(2): Show | 5 | HG01167.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+928T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384381 | ||||||
| chr1:48384385
|
A | G | 22 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0008g0236others(19): Show | 22 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.909+924T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384385 | ||||||
| chr1:48384386
|
G | C | 5 | a0001c0001t0014g0213a0001c0001t0014g0214a0001c0001t0034g0101others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+923C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384386 | ||||||
| chr1:48384387
|
A | C | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+922T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384387 | ||||||
| chr1:48384387
|
A | G | 3 | a0001c0001t0013g0164a0001c0001t0017g0246a0001c0001t0035g0160 | 3 | HG01167.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.909+922T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384387 | ||||||
| chr1:48384391
|
A | G | 23 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0008g0235others(20): Show | 23 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+918T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384391 | ||||||
| chr1:48384392
|
G | C | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.909+917C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384392 | ||||||
| chr1:48384393
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+916T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384393 | ||||||
| chr1:48384397
|
A | G | 24 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0008g0235others(21): Show | 24 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+912T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384397 | ||||||
| chr1:48384399
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+910T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384399 | ||||||
| chr1:48384403
|
A | G | 24 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0008g0235others(21): Show | 24 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+906T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384403 | ||||||
| chr1:48384405
|
A | AGGGAGAG others(561): Show |
1 | a0001c0001t0021g0159 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.909+903_909+904ins others(568): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384405 | ||||||
| chr1:48384405
|
A | G | 2 | a0001c0001t0013g0164a0001c0001t0035g0160 | 2 | HG01167.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.909+904T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384405 | ||||||
| chr1:48384406
|
G | GGAGAGGG others(524): Show |
1 | a0001c0001t0002g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.909+902_909+903ins others(531): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384406 | ||||||
| chr1:48384409
|
A | G | 23 | a0001c0001t0002g0253a0001c0001t0008g0235a0001c0001t0008g0236others(20): Show | 23 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+900T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384409 | ||||||
| chr1:48384411
|
A | G | 1 | a0001c0001t0013g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.909+898T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384411 | ||||||
| chr1:48384415
|
A | G | 23 | a0001c0001t0002g0253a0001c0001t0008g0235a0001c0001t0008g0236others(20): Show | 23 | HG01943.hp1 HG02040.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+894T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384415 | ||||||
| chr1:48384417
|
A | AGGGAGAG others(670): Show |
1 | a0001c0001t0002g0179 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.909+891_909+892ins others(677): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384417 | ||||||
| chr1:48384421
|
A | AGAGGGAG others(479): Show |
1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.909+887_909+888ins others(486): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384421 | ||||||
| chr1:48384421
|
A | AGAGGGAG others(389): Show |
1 | a0001c0001t0013g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.909+887_909+888ins others(396): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384421 | ||||||
| chr1:48384421
|
A | G | 7 | a0001c0001t0002g0191a0001c0001t0002g0253a0001c0001t0013g0162others(4): Show | 7 | HG02040.hp2 HG02055.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+888T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384421 | ||||||
| chr1:48384425
|
G | GGAGAGGA others(789): Show |
1 | a0001c0001t0002g0200 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.909+883_909+884ins others(796): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384425 | ||||||
| chr1:48384567
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.909+742G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384567 | ||||||
| chr1:48384739
|
A | G | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.909+570T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384739 | ||||||
| chr1:48384802
|
A | T | 1 | a0001c0001t0002g0200 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.909+507T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384802 | ||||||
| chr1:48384854
|
T | C | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.909+455A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384854 | ||||||
| chr1:48384867
|
C | T | 1 | a0001c0001t0006g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.909+442G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384867 | ||||||
| chr1:48384868
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.909+441T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384868 | ||||||
| chr1:48384882
|
CAGAA | C | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+423_909+426del others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48384882 | ||||||
| chr1:48385249
|
A | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.909+60T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 9/12 | chr1 | 48385249 | ||||||
| chr1:48385495
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.869-146A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48385495 | ||||||
| chr1:48385730
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.869-381G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48385730 | ||||||
| chr1:48386240
|
A | C | 2 | a0001c0001t0016g0296a0001c0001t0016g0299 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.869-891T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48386240 | ||||||
| chr1:48386364
|
C | G | 1 | a0002c0002t0001g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.869-1015G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48386364 | ||||||
| chr1:48386370
|
C | A | 3 | a0001c0001t0007g0307a0001c0001t0015g0319a0001c0001t0015g0320 | 3 | HG00735.hp1 HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.869-1021G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48386370 | ||||||
| chr1:48386589
|
G | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-1240C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48386589 | ||||||
| chr1:48386642
|
G | A | 1 | a0002c0002t0001g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.869-1293C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48386642 | ||||||
| chr1:48387039
|
C | A | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.869-1690G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387039 | ||||||
| chr1:48387039
|
C | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.869-1690G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387039 | ||||||
| chr1:48387403
|
C | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2054G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387403 | ||||||
| chr1:48387578
|
G | T | 3 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0001t0002g0156 | 3 | HG01943.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.869-2229C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387578 | ||||||
| chr1:48387632
|
C | G | 1 | a0002c0002t0005g0081 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.869-2283G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387632 | ||||||
| chr1:48387710
|
C | A | 1 | a0002c0002t0001g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.869-2361G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48387710 | ||||||
| chr1:48388240
|
C | CA | 47 | a0001c0001t0002g0186a0001c0001t0003g0109a0001c0001t0004g0256others(44): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.869-2892dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388240 | ||||||
| chr1:48388711
|
A | AT | 13 | a0001c0001t0002g0171a0001c0001t0002g0174a0001c0001t0002g0201others(10): Show | 13 | HG00642.hp1 HG01891.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.869-3363dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388711 | ||||||
| chr1:48388790
|
C | A | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.869-3441G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388790 | ||||||
| chr1:48388812
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.869-3463C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388812 | ||||||
| chr1:48388817
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.869-3468A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388817 | ||||||
| chr1:48388866
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-3517T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388866 | ||||||
| chr1:48388915
|
C | T | 1 | a0002c0002t0031g0075 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.869-3566G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48388915 | ||||||
| chr1:48389034
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.869-3685C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389034 | ||||||
| chr1:48389415
|
C | T | 1 | a0001c0001t0003g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.869-4066G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389415 | ||||||
| chr1:48389643
|
A | C | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.869-4294T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389643 | ||||||
| chr1:48389773
|
G | C | 1 | a0002c0002t0027g0062 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.869-4424C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389773 | ||||||
| chr1:48389849
|
A | T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-4500T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389849 | ||||||
| chr1:48389874
|
A | G | 15 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.869-4525T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48389874 | ||||||
| chr1:48390505
|
A | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+4762T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48390505 | ||||||
| chr1:48390710
|
G | A | 321 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.868+4557C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48390710 | ||||||
| chr1:48390809
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0156 | 2 | HG01943.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.868+4458G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48390809 | ||||||
| chr1:48390836
|
G | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | NA18941.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.868+4431C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48390836 | ||||||
| chr1:48391086
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.868+4181G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391086 | ||||||
| chr1:48391090
|
C | A | 1 | a0001c0001t0002g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.868+4177G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391090 | ||||||
| chr1:48391093
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.868+4174C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391093 | ||||||
| chr1:48391104
|
C | T | 1 | a0002c0002t0005g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.868+4163G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391104 | ||||||
| chr1:48391203
|
GA | G | 296 | a0001c0001t0001g0089a0001c0001t0002g0152a0001c0001t0002g0153others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.868+4063delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391203 | ||||||
| chr1:48391203
|
GAA | G | 9 | a0001c0001t0002g0189a0001c0001t0002g0201a0001c0001t0009g0102others(6): Show | 9 | HG00558.hp1 HG01168.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.868+4062_868+4063d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391203 | ||||||
| chr1:48391562
|
C | T | 1 | a0001c0001t0004g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.868+3705G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391562 | ||||||
| chr1:48391641
|
C | T | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.868+3626G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391641 | ||||||
| chr1:48391786
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.868+3481A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391786 | ||||||
| chr1:48391900
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.868+3367T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391900 | ||||||
| chr1:48391907
|
T | A | 321 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.868+3360A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391907 | ||||||
| chr1:48391960
|
C | A | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.868+3307G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391960 | ||||||
| chr1:48391998
|
G | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.868+3269C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48391998 | ||||||
| chr1:48392128
|
C | T | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.868+3139G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48392128 | ||||||
| chr1:48392628
|
A | T | 2 | a0001c0001t0015g0319a0001c0001t0015g0320 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.868+2639T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48392628 | ||||||
| chr1:48392647
|
A | C | 1 | a0001c0001t0004g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.868+2620T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48392647 | ||||||
| chr1:48392647
|
A | G | 5 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 5 | HG00621.hp2 HG02165.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+2620T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48392647 | ||||||
| chr1:48392999
|
G | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0130 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.868+2268C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48392999 | ||||||
| chr1:48393071
|
A | G | 107 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.868+2196T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393071 | ||||||
| chr1:48393123
|
A | T | 41 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.868+2144T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393123 | ||||||
| chr1:48393381
|
C | G | 1 | a0001c0001t0007g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.868+1886G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393381 | ||||||
| chr1:48393469
|
T | C | 4 | a0002c0002t0001g0018a0002c0002t0001g0023a0002c0002t0005g0021others(1): Show | 4 | HG02040.hp1 NA18999.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+1798A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393469 | ||||||
| chr1:48393482
|
C | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+1785G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393482 | ||||||
| chr1:48393610
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.868+1657C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48393610 | ||||||
| chr1:48394009
|
T | C | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.868+1258A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48394009 | ||||||
| chr1:48394132
|
C | G | 1 | a0001c0001t0003g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.868+1135G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48394132 | ||||||
| chr1:48394156
|
G | A | 1 | a0001c0001t0024g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.868+1111C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48394156 | ||||||
| chr1:48394256
|
AG | A | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+1010delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48394256 | ||||||
| chr1:48394974
|
G | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.868+293C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48394974 | ||||||
| chr1:48395142
|
G | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.868+125C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 8/12 | chr1 | 48395142 | ||||||
| chr1:48395380
|
A | C | 1 | a0001c0001t0004g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.781-26T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48395380 | ||||||
| chr1:48395634
|
C | T | 1 | a0002c0002t0005g0082 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.781-280G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48395634 | ||||||
| chr1:48395959
|
A | C | 15 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(12): Show | 15 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.781-605T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48395959 | ||||||
| chr1:48396249
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.781-895C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396249 | ||||||
| chr1:48396378
|
A | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.781-1024T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396378 | ||||||
| chr1:48396474
|
C | G | 11 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(8): Show | 11 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.781-1120G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396474 | ||||||
| chr1:48396518
|
T | C | 1 | a0001c0001t0009g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.781-1164A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396518 | ||||||
| chr1:48396545
|
AAATG | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-1195_781-1192d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396545 | ||||||
| chr1:48396555
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.781-1201G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396555 | ||||||
| chr1:48396560
|
A | G | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781-1206T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396560 | ||||||
| chr1:48396581
|
C | T | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.781-1227G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396581 | ||||||
| chr1:48396784
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.781-1430A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396784 | ||||||
| chr1:48396954
|
A | C | 2 | a0001c0001t0003g0141a0001c0001t0003g0142 | 2 | NA19011.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.781-1600T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48396954 | ||||||
| chr1:48397117
|
T | C | 14 | a0001c0001t0004g0256a0001c0001t0004g0264a0001c0001t0004g0270others(11): Show | 14 | HG00423.hp1 HG00609.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-1763A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48397117 | ||||||
| chr1:48397230
|
A | G | 1 | a0001c0001t0006g0233 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781-1876T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48397230 | ||||||
| chr1:48397693
|
A | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.780+1658T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48397693 | ||||||
| chr1:48397925
|
G | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+1426C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48397925 | ||||||
| chr1:48398067
|
T | G | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.780+1284A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398067 | ||||||
| chr1:48398237
|
A | C | 1 | a0001c0001t0004g0270 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.780+1114T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398237 | ||||||
| chr1:48398303
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.780+1048G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398303 | ||||||
| chr1:48398504
|
A | T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+847T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398504 | ||||||
| chr1:48398618
|
A | G | 2 | a0001c0001t0014g0196a0001c0001t0014g0198 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.780+733T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398618 | ||||||
| chr1:48398757
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.780+594A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48398757 | ||||||
| chr1:48399027
|
C | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+324G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 7/12 | chr1 | 48399027 | ||||||
| chr1:48399870
|
C | A | 1 | a0001c0001t0006g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.487-226G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48399870 | ||||||
| chr1:48399900
|
G | A | 1 | a0002c0002t0005g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487-256C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48399900 | ||||||
| chr1:48399969
|
GCAAAC | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.487-330_487-326del others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48399969 | ||||||
| chr1:48400868
|
C | T | 1 | a0002c0002t0005g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.487-1224G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48400868 | ||||||
| chr1:48400883
|
A | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.487-1239T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48400883 | ||||||
| chr1:48401002
|
A | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.487-1358T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401002 | ||||||
| chr1:48401012
|
TTC | T | 40 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(37): Show | 40 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.487-1370_487-1369d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401012 | ||||||
| chr1:48401199
|
G | A | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.487-1555C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401199 | ||||||
| chr1:48401218
|
T | C | 1 | a0001c0001t0037g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.487-1574A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401218 | ||||||
| chr1:48401276
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.487-1632T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401276 | ||||||
| chr1:48401722
|
A | G | 3 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0035 | 3 | NA18969.hp2 NA18973.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.487-2078T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401722 | ||||||
| chr1:48401754
|
C | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.486+2048G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401754 | ||||||
| chr1:48401755
|
TA | T | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.486+2046delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48401755 | ||||||
| chr1:48402108
|
C | A | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+1694G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402108 | ||||||
| chr1:48402165
|
A | C | 1 | a0001c0001t0012g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+1637T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402165 | ||||||
| chr1:48402313
|
C | T | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.486+1489G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402313 | ||||||
| chr1:48402385
|
C | T | 1 | a0001c0001t0009g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.486+1417G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402385 | ||||||
| chr1:48402447
|
A | G | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.486+1355T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402447 | ||||||
| chr1:48402460
|
AAAAC | A | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+1338_486+1341d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402460 | ||||||
| chr1:48402588
|
A | C | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.486+1214T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402588 | ||||||
| chr1:48402745
|
T | C | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.486+1057A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402745 | ||||||
| chr1:48402907
|
A | G | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.486+895T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402907 | ||||||
| chr1:48402921
|
G | C | 1 | a0001c0001t0003g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.486+881C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48402921 | ||||||
| chr1:48403069
|
AG | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+732delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403069 | ||||||
| chr1:48403075
|
C | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+727G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403075 | ||||||
| chr1:48403152
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.486+650C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403152 | ||||||
| chr1:48403286
|
T | G | 2 | a0001c0001t0025g0209a0001c0001t0025g0210 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.486+516A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403286 | ||||||
| chr1:48403366
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486+436A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403366 | ||||||
| chr1:48403372
|
C | T | 1 | a0002c0002t0005g0077 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.486+430G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403372 | ||||||
| chr1:48403534
|
G | A | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.486+268C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403534 | ||||||
| chr1:48403616
|
T | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.486+186A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403616 | ||||||
| chr1:48403737
|
C | T | 6 | a0001c0001t0003g0119a0001c0001t0003g0120a0001c0001t0003g0128others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+65G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 6/12 | chr1 | 48403737 | ||||||
| chr1:48404084
|
A | G | 2 | a0001c0001t0026g0295a0001c0001t0043g0298 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.406-202T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404084 | ||||||
| chr1:48404254
|
CATAT | C | 15 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(12): Show | 15 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-376_406-373del others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404254 | ||||||
| chr1:48404638
|
T | C | 2 | a0002c0002t0001g0007a0002c0002t0001g0011 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.406-756A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404638 | ||||||
| chr1:48404824
|
A | G | 1 | a0001c0001t0006g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.406-942T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404824 | ||||||
| chr1:48404866
|
C | T | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.406-984G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404866 | ||||||
| chr1:48404965
|
A | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.406-1083T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48404965 | ||||||
| chr1:48405114
|
C | T | 1 | a0001c0001t0025g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406-1232G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48405114 | ||||||
| chr1:48405191
|
C | G | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG02132.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.406-1309G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48405191 | ||||||
| chr1:48405267
|
A | G | 1 | a0001c0001t0013g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.406-1385T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48405267 | ||||||
| chr1:48405443
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.406-1561A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48405443 | ||||||
| chr1:48405680
|
A | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-1798T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48405680 | ||||||
| chr1:48406277
|
T | C | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.406-2395A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48406277 | ||||||
| chr1:48406337
|
A | G | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.406-2455T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48406337 | ||||||
| chr1:48406518
|
C | G | 3 | a0001c0001t0026g0295a0001c0001t0026g0297a0001c0001t0043g0298 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.406-2636G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48406518 | ||||||
| chr1:48406621
|
A | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.406-2739T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48406621 | ||||||
| chr1:48407515
|
T | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.406-3633A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48407515 | ||||||
| chr1:48407656
|
T | A | 3 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0035 | 3 | NA18969.hp2 NA18973.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.406-3774A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48407656 | ||||||
| chr1:48407825
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.405+3639G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48407825 | ||||||
| chr1:48407916
|
T | C | 1 | a0001c0001t0004g0275 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.405+3548A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48407916 | ||||||
| chr1:48407979
|
G | C | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.405+3485C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48407979 | ||||||
| chr1:48408457
|
A | G | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.405+3007T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48408457 | ||||||
| chr1:48408485
|
T | C | 218 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.405+2979A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48408485 | ||||||
| chr1:48408606
|
A | G | 1 | a0001c0001t0013g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+2858T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48408606 | ||||||
| chr1:48408778
|
G | T | 1 | a0001c0001t0004g0269 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.405+2686C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48408778 | ||||||
| chr1:48408810
|
T | C | 52 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(49): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.405+2654A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48408810 | ||||||
| chr1:48409156
|
C | T | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.405+2308G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409156 | ||||||
| chr1:48409348
|
G | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0187 | 2 | NA18940.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.405+2116C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409348 | ||||||
| chr1:48409360
|
C | T | 6 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0019others(3): Show | 6 | HG02015.hp2 HG02074.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.405+2104G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409360 | ||||||
| chr1:48409364
|
G | A | 1 | a0002c0002t0019g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.405+2100C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409364 | ||||||
| chr1:48409373
|
C | T | 1 | a0001c0001t0035g0160 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.405+2091G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409373 | ||||||
| chr1:48409575
|
G | A | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.405+1889C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409575 | ||||||
| chr1:48409995
|
T | C | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405+1469A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409995 | ||||||
| chr1:48409997
|
T | C | 28 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.405+1467A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48409997 | ||||||
| chr1:48410457
|
T | G | 3 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0053 | 3 | NA18948.hp2 NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.405+1007A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48410457 | ||||||
| chr1:48410522
|
C | A | 4 | a0002c0002t0005g0003a0002c0002t0005g0004a0002c0002t0005g0059others(1): Show | 4 | HG01168.hp2 HG02109.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+942G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48410522 | ||||||
| chr1:48410610
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.405+854T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48410610 | ||||||
| chr1:48410650
|
TCA | T | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.405+812_405+813del others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48410650 | ||||||
| chr1:48411064
|
A | G | 109 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.405+400T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 5/12 | chr1 | 48411064 | ||||||
| chr1:48411693
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-105G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48411693 | ||||||
| chr1:48411777
|
A | C | 7 | a0002c0002t0005g0066a0002c0002t0005g0067a0002c0002t0005g0068others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-189T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48411777 | ||||||
| chr1:48411842
|
TTTTG | T | 6 | a0001c0001t0008g0235a0001c0001t0008g0239a0001c0001t0008g0244others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-258_281-255del others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48411842 | ||||||
| chr1:48411901
|
T | C | 1 | a0002c0002t0001g0050 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.281-313A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48411901 | ||||||
| chr1:48412034
|
A | G | 3 | a0001c0001t0014g0213a0001c0001t0014g0214a0001c0001t0041g0212 | 3 | HG01243.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.281-446T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412034 | ||||||
| chr1:48412045
|
A | G | 3 | a0001c0001t0014g0213a0001c0001t0014g0214a0001c0001t0041g0212 | 3 | HG01243.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.281-457T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412045 | ||||||
| chr1:48412251
|
T | C | 1 | a0005c0006t0001g0032 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.281-663A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412251 | ||||||
| chr1:48412299
|
A | C | 1 | a0001c0001t0008g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.281-711T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412299 | ||||||
| chr1:48412618
|
T | C | 2 | a0002c0002t0005g0021a0002c0002t0005g0022 | 2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.280+492A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412618 | ||||||
| chr1:48412642
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280+468C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412642 | ||||||
| chr1:48412642
|
G | C | 1 | a0001c0001t0039g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+468C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412642 | ||||||
| chr1:48412743
|
C | T | 1 | a0001c0001t0006g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+367G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412743 | ||||||
| chr1:48412807
|
C | T | 1 | a0001c0001t0007g0307 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.280+303G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412807 | ||||||
| chr1:48412808
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+302C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48412808 | ||||||
| chr1:48413046
|
T | C | 10 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | NA18954.hp2 NA18967.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+64A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 4/12 | chr1 | 48413046 | ||||||
| chr1:48413288
|
T | C | 1 | a0001c0001t0004g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.239-137A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413288 | ||||||
| chr1:48413388
|
C | T | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-237G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413388 | ||||||
| chr1:48413456
|
C | CT | 84 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(81): Show | 84 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.239-306dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413456 | ||||||
| chr1:48413620
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.239-469T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413620 | ||||||
| chr1:48413671
|
T | C | 6 | a0002c0002t0005g0090a0002c0002t0005g0091a0002c0002t0005g0092others(3): Show | 6 | NA18940.hp2 NA18941.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-520A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413671 | ||||||
| chr1:48413835
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-684G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413835 | ||||||
| chr1:48413854
|
A | C | 1 | a0001c0001t0039g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239-703T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413854 | ||||||
| chr1:48413889
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239-738T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48413889 | ||||||
| chr1:48414115
|
C | T | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.239-964G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414115 | ||||||
| chr1:48414134
|
C | G | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239-983G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414134 | ||||||
| chr1:48414227
|
A | G | 1 | a0001c0001t0003g0123 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.239-1076T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414227 | ||||||
| chr1:48414235
|
T | A | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-1084A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414235 | ||||||
| chr1:48414542
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239-1391G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414542 | ||||||
| chr1:48414608
|
G | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.239-1457C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414608 | ||||||
| chr1:48414658
|
C | T | 3 | a0001c0001t0006g0145a0001c0001t0006g0147a0001c0001t0006g0151 | 3 | HG00140.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.239-1507G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414658 | ||||||
| chr1:48414680
|
T | C | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-1529A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48414680 | ||||||
| chr1:48415037
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-1886T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415037 | ||||||
| chr1:48415038
|
T | C | 1 | a0002c0002t0001g0051 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.239-1887A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415038 | ||||||
| chr1:48415162
|
GA | G | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-2012delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415162 | ||||||
| chr1:48415386
|
C | T | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-2235G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415386 | ||||||
| chr1:48415438
|
T | G | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.239-2287A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415438 | ||||||
| chr1:48415639
|
A | T | 2 | a0002c0002t0001g0026a0002c0002t0001g0033 | 2 | HG02258.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.239-2488T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415639 | ||||||
| chr1:48415644
|
GA | G | 107 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.239-2494delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415644 | ||||||
| chr1:48415713
|
G | A | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-2562C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415713 | ||||||
| chr1:48415738
|
G | GA | 12 | a0001c0001t0007g0308a0001c0001t0014g0196a0001c0001t0014g0198others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-2588dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48415738 | ||||||
| chr1:48416019
|
G | A | 5 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(2): Show | 5 | HG00621.hp2 HG02165.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-2868C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416019 | ||||||
| chr1:48416325
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-3174C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416325 | ||||||
| chr1:48416330
|
G | A | 1 | a0002c0002t0001g0014 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.239-3179C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416330 | ||||||
| chr1:48416342
|
C | CAT | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3193_239-3192d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416342 | ||||||
| chr1:48416419
|
A | T | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.239-3268T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416419 | ||||||
| chr1:48416526
|
A | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3375T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48416526 | ||||||
| chr1:48417254
|
A | G | 28 | a0001c0001t0007g0139a0001c0001t0007g0300a0001c0001t0007g0301others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.239-4103T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417254 | ||||||
| chr1:48417326
|
T | C | 1 | a0001c0001t0009g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-4175A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417326 | ||||||
| chr1:48417391
|
C | T | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-4240G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417391 | ||||||
| chr1:48417393
|
A | T | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-4242T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417393 | ||||||
| chr1:48417394
|
C | A | 1 | a0001c0001t0034g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-4243G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417394 | ||||||
| chr1:48417425
|
T | C | 9 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(6): Show | 9 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-4274A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417425 | ||||||
| chr1:48417556
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.239-4405G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417556 | ||||||
| chr1:48417755
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.239-4604G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417755 | ||||||
| chr1:48417887
|
G | T | 2 | a0001c0001t0003g0205a0001c0001t0003g0220 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.239-4736C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417887 | ||||||
| chr1:48417931
|
G | A | 1 | a0001c0001t0014g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.239-4780C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417931 | ||||||
| chr1:48417965
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239-4814G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48417965 | ||||||
| chr1:48418166
|
A | G | 1 | a0001c0001t0009g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.239-5015T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418166 | ||||||
| chr1:48418544
|
C | CA | 14 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0171others(11): Show | 14 | HG00423.hp1 HG00642.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-5394dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
C | CAA | 20 | a0001c0001t0003g0104a0001c0001t0003g0107a0001c0001t0003g0108others(17): Show | 20 | HG00544.hp2 HG01257.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-5395_239-5394d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
C | CAAA | 17 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0109others(14): Show | 17 | HG00597.hp1 HG00738.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-5396_239-5394d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
C | CAAAA | 8 | a0001c0001t0003g0118a0001c0001t0003g0125a0001c0001t0003g0135others(5): Show | 8 | HG00558.hp1 HG02015.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-5397_239-5394d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CA | C | 59 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.239-5394delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAA | C | 40 | a0001c0001t0004g0257a0001c0001t0004g0258a0001c0001t0004g0261others(37): Show | 40 | HG00621.hp2 HG01261.hp1 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.239-5395_239-5394d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAAA | C | 59 | a0001c0001t0004g0279a0001c0001t0006g0143a0001c0001t0006g0231others(56): Show | 59 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-5396_239-5394d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAAAA | C | 66 | a0001c0001t0004g0281a0001c0001t0006g0230a0001c0001t0006g0233others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.239-5397_239-5394d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0005g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-5406_239-5394d others(15): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAAAAAAA others(7): Show |
C | 2 | a0002c0002t0005g0059a0002c0002t0019g0076 | 2 | HG01168.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.239-5407_239-5394d others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418544
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-5410_239-5394d others(19): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418544 | ||||||
| chr1:48418615
|
A | G | 4 | a0002c0002t0005g0070a0002c0002t0005g0077a0002c0002t0005g0078others(1): Show | 4 | HG01952.hp2 NA18966.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-5464T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418615 | ||||||
| chr1:48418753
|
GAGGGAAG others(9): Show |
G | 19 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.239-5618_239-5603d others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418753 | ||||||
| chr1:48418795
|
AGGAAGGA others(1): Show |
A | 96 | a0001c0001t0010g0103a0001c0001t0010g0211a0002c0002t0001g0001others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.239-5652_239-5645d others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418795 | ||||||
| chr1:48418893
|
G | A | 1 | a0001c0001t0004g0279 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.239-5742C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418893 | ||||||
| chr1:48418894
|
A | G | 1 | a0001c0001t0004g0279 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.239-5743T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418894 | ||||||
| chr1:48418924
|
G | GA | 12 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(9): Show | 12 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-5774dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48418924 | ||||||
| chr1:48419490
|
G | T | 1 | a0001c0001t0002g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.239-6339C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48419490 | ||||||
| chr1:48419550
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-6399C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48419550 | ||||||
| chr1:48420007
|
T | C | 1 | a0001c0001t0006g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-6856A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420007 | ||||||
| chr1:48420065
|
C | G | 1 | a0001c0001t0010g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.239-6914G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420065 | ||||||
| chr1:48420260
|
G | A | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.239-7109C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420260 | ||||||
| chr1:48420294
|
T | C | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-7143A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420294 | ||||||
| chr1:48420398
|
C | T | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-7247G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420398 | ||||||
| chr1:48420435
|
G | A | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.239-7284C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420435 | ||||||
| chr1:48420454
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239-7303C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420454 | ||||||
| chr1:48420758
|
T | C | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.239-7607A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420758 | ||||||
| chr1:48420866
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.239-7715A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48420866 | ||||||
| chr1:48421017
|
T | G | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.239-7866A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421017 | ||||||
| chr1:48421056
|
G | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.239-7905C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421056 | ||||||
| chr1:48421125
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239-7974A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421125 | ||||||
| chr1:48421295
|
CAT | C | 17 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(14): Show | 17 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.239-8146_239-8145d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421295 | ||||||
| chr1:48421330
|
T | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0023 | 2 | NA18999.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.239-8179A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421330 | ||||||
| chr1:48421391
|
A | C | 1 | a0001c0001t0003g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.239-8240T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421391 | ||||||
| chr1:48421430
|
C | G | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.239-8279G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421430 | ||||||
| chr1:48421439
|
A | G | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.239-8288T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421439 | ||||||
| chr1:48421447
|
G | A | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.239-8296C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421447 | ||||||
| chr1:48421596
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239-8445A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421596 | ||||||
| chr1:48421909
|
ATAAAAT | A | 14 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(11): Show | 14 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-8764_239-8759d others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48421909 | ||||||
| chr1:48422103
|
G | A | 1 | a0001c0001t0022g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.239-8952C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422103 | ||||||
| chr1:48422283
|
T | C | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.239-9132A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422283 | ||||||
| chr1:48422304
|
G | A | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239-9153C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422304 | ||||||
| chr1:48422669
|
T | C | 1 | a0002c0002t0005g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-9518A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422669 | ||||||
| chr1:48422732
|
A | AG | 3 | a0001c0001t0026g0295a0001c0001t0026g0297a0001c0001t0043g0298 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.239-9582_239-9581i others(3): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422732 | ||||||
| chr1:48422819
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.239-9668G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422819 | ||||||
| chr1:48422935
|
C | T | 1 | a0001c0001t0011g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-9784G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48422935 | ||||||
| chr1:48423304
|
A | G | 1 | a0001c0001t0006g0147 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.239-10153T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423304 | ||||||
| chr1:48423364
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.239-10213C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423364 | ||||||
| chr1:48423374
|
G | A | 1 | a0002c0002t0005g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-10223C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423374 | ||||||
| chr1:48423462
|
G | GA | 21 | a0001c0001t0004g0264a0001c0001t0006g0144a0001c0001t0006g0145others(18): Show | 21 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.239-10312dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423462 | ||||||
| chr1:48423496
|
G | C | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.239-10345C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423496 | ||||||
| chr1:48423506
|
T | C | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-10355A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423506 | ||||||
| chr1:48423564
|
C | CT | 42 | a0001c0001t0003g0107a0001c0001t0003g0128a0001c0001t0003g0135others(39): Show | 42 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.239-10414dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423564 | ||||||
| chr1:48423564
|
C | CTT | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-10415_239-1041 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423564 | ||||||
| chr1:48423566
|
T | TTC | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0042others(6): Show | 9 | NA18954.hp2 NA18977.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-10416_239-1041 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423566 | ||||||
| chr1:48423567
|
T | TC | 84 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.239-10417_239-1041 others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423567 | ||||||
| chr1:48423568
|
T | C | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10417A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423568 | ||||||
| chr1:48423601
|
G | C | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10450C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423601 | ||||||
| chr1:48423602
|
C | G | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.239-10451G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423602 | ||||||
| chr1:48423793
|
T | A | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.239-10642A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423793 | ||||||
| chr1:48423806
|
C | T | 1 | a0001c0001t0003g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.239-10655G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423806 | ||||||
| chr1:48423818
|
A | T | 4 | a0002c0002t0001g0084a0002c0002t0005g0083a0002c0002t0005g0085others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-10667T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423818 | ||||||
| chr1:48423883
|
G | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0053 | 3 | NA18948.hp2 NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.239-10732C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423883 | ||||||
| chr1:48423927
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-10776T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48423927 | ||||||
| chr1:48424042
|
G | A | 2 | a0002c0002t0005g0074a0002c0002t0019g0080 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.239-10891C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424042 | ||||||
| chr1:48424054
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-10903T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424054 | ||||||
| chr1:48424135
|
C | A | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.239-10984G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424135 | ||||||
| chr1:48424244
|
T | C | 10 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | NA18954.hp2 NA18967.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-11093A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424244 | ||||||
| chr1:48424568
|
T | C | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.239-11417A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424568 | ||||||
| chr1:48424639
|
T | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-11488A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424639 | ||||||
| chr1:48424841
|
A | G | 2 | a0004c0004t0002g0097a0004c0004t0002g0098 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.239-11690T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424841 | ||||||
| chr1:48424994
|
A | C | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.239-11843T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48424994 | ||||||
| chr1:48425276
|
C | A | 1 | a0001c0001t0042g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.239-12125G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48425276 | ||||||
| chr1:48425480
|
A | T | 94 | a0001c0001t0001g0089a0001c0001t0003g0104a0001c0001t0003g0105others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.239-12329T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48425480 | ||||||
| chr1:48425737
|
C | T | 1 | a0001c0001t0007g0304 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.239-12586G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48425737 | ||||||
| chr1:48425777
|
T | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-12626A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48425777 | ||||||
| chr1:48426285
|
T | C | 109 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.239-13134A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426285 | ||||||
| chr1:48426318
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.239-13167C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426318 | ||||||
| chr1:48426349
|
C | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-13198G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426349 | ||||||
| chr1:48426645
|
A | T | 1 | a0001c0001t0006g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.239-13494T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426645 | ||||||
| chr1:48426646
|
T | A | 10 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | NA18954.hp2 NA18967.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-13495A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426646 | ||||||
| chr1:48426752
|
A | T | 1 | a0002c0002t0005g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.239-13601T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426752 | ||||||
| chr1:48426762
|
C | T | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG02132.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.239-13611G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426762 | ||||||
| chr1:48426951
|
G | T | 1 | a0001c0001t0038g0305 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.239-13800C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48426951 | ||||||
| chr1:48427138
|
G | C | 1 | a0001c0001t0003g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.239-13987C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427138 | ||||||
| chr1:48427180
|
C | T | 2 | a0001c0001t0011g0237a0001c0001t0011g0238 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.239-14029G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427180 | ||||||
| chr1:48427434
|
C | CA | 45 | a0001c0001t0002g0187a0001c0001t0002g0203a0001c0001t0003g0106others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.239-14284dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427434 | ||||||
| chr1:48427434
|
CA | C | 7 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0219others(4): Show | 7 | HG01433.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-14284delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427434 | ||||||
| chr1:48427694
|
C | T | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.239-14543G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427694 | ||||||
| chr1:48427912
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239-14761A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48427912 | ||||||
| chr1:48428092
|
A | G | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-14941T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428092 | ||||||
| chr1:48428135
|
T | C | 1 | a0002c0002t0005g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.239-14984A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428135 | ||||||
| chr1:48428160
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.239-15009A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428160 | ||||||
| chr1:48428177
|
G | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.239-15026C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428177 | ||||||
| chr1:48428617
|
A | G | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0010g0137 | 3 | HG01346.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.239-15466T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428617 | ||||||
| chr1:48428618
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0010g0137 | 3 | HG01346.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.239-15467A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428618 | ||||||
| chr1:48428701
|
C | T | 1 | a0001c0001t0016g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239-15550G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428701 | ||||||
| chr1:48428752
|
C | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-15601G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428752 | ||||||
| chr1:48428753
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239-15602C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428753 | ||||||
| chr1:48428762
|
T | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.239-15611A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428762 | ||||||
| chr1:48428775
|
A | ATG | 4 | a0001c0001t0002g0100a0001c0001t0003g0205a0001c0001t0003g0220others(1): Show | 4 | HG00621.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-15626_239-1562 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTG | 3 | a0001c0001t0002g0169a0001c0001t0002g0199a0001c0001t0013g0163 | 3 | HG00423.hp2 HG02055.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.239-15628_239-1562 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTG | 7 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0200others(4): Show | 7 | HG01099.hp1 HG01934.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-15630_239-1562 others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(1): Show |
25 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0173others(22): Show | 25 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-15632_239-1562 others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0002g0170a0001c0001t0002g0181a0001c0001t0002g0186others(1): Show | 4 | HG02083.hp1 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-15634_239-1562 others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG02809.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.239-15636_239-1562 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(7): Show |
3 | a0001c0001t0035g0160a0004c0004t0002g0097a0004c0004t0002g0098 | 3 | HG01167.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.239-15638_239-1562 others(18): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(9): Show |
2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG02683.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239-15640_239-1562 others(20): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(11): Show |
5 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0156others(2): Show | 5 | HG00280.hp1 HG01943.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-15642_239-1562 others(22): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | ATGTGTGT others(15): Show |
1 | a0001c0001t0002g0158 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.239-15646_239-1562 others(26): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
A | G | 1 | a0002c0002t0001g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.239-15624T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
ATGTG | A | 4 | a0001c0001t0003g0217a0001c0001t0004g0258a0001c0001t0004g0259others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-15628_239-1562 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428775
|
ATGTGTG | A | 5 | a0001c0001t0002g0195a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01123.hp1 HG01891.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-15630_239-1562 others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428775 | ||||||
| chr1:48428809
|
G | A | 50 | a0001c0001t0001g0089a0001c0001t0004g0256a0001c0001t0004g0257others(47): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.239-15658C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTA | 51 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.239-15660_239-1565 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTATATAT others(89): Show |
1 | a0003c0003t0003g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.239-15659_239-1565 others(100): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTA | 24 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0003g0127others(21): Show | 24 | HG01081.hp1 HG01243.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.239-15659_239-1565 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTATAT others(23): Show |
1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.239-15659_239-1565 others(34): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTGTA | 79 | a0001c0001t0007g0309a0001c0001t0007g0313a0001c0001t0008g0236others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.239-15659_239-1565 others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTGTGT others(1): Show |
23 | a0001c0001t0006g0143a0001c0001t0007g0301a0001c0001t0007g0302others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.239-15659_239-1565 others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTGTGT others(3): Show |
22 | a0001c0001t0007g0300a0001c0001t0007g0308a0002c0002t0001g0087others(19): Show | 22 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.239-15659_239-1565 others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428809
|
G | GTGTGTGT others(5): Show |
4 | a0001c0001t0044g0322a0002c0002t0005g0064a0002c0002t0005g0078others(1): Show | 4 | HG03017.hp2 NA18612.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-15659_239-1565 others(16): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428809 | ||||||
| chr1:48428813
|
A | ATGTATAT others(45): Show |
1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-15663_239-1566 others(56): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428813 | ||||||
| chr1:48428813
|
A | G | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.239-15662T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428813 | ||||||
| chr1:48428839
|
G | GTGTATAT others(13): Show |
1 | a0001c0001t0007g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.239-15708_239-1568 others(24): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428839 | ||||||
| chr1:48428855
|
GTA | G | 13 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(10): Show | 13 | HG00280.hp1 HG01167.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-15706_239-1570 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428855 | ||||||
| chr1:48428870
|
C | CGT | 13 | a0001c0001t0002g0100a0001c0001t0007g0309a0001c0001t0008g0239others(10): Show | 13 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-15721_239-1572 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428870 | ||||||
| chr1:48428870
|
CGT | C | 51 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0003g0105others(48): Show | 51 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.239-15721_239-1572 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428870 | ||||||
| chr1:48428870
|
CGTGT | C | 96 | a0001c0001t0003g0218a0001c0001t0011g0237a0002c0002t0001g0001others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.239-15723_239-1572 others(8): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428870 | ||||||
| chr1:48428877
|
G | A | 1 | a0001c0001t0011g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.239-15726C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428877 | ||||||
| chr1:48428893
|
T | G | 6 | a0001c0001t0004g0256a0001c0001t0004g0274a0001c0001t0004g0279others(3): Show | 6 | HG02129.hp1 NA18943.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-15742A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48428893 | ||||||
| chr1:48429008
|
G | A | 1 | a0001c0001t0006g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.239-15857C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429008 | ||||||
| chr1:48429154
|
C | A | 52 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(49): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.239-16003G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429154 | ||||||
| chr1:48429308
|
G | A | 1 | a0002c0002t0001g0012 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.239-16157C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429308 | ||||||
| chr1:48429373
|
T | C | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.239-16222A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429373 | ||||||
| chr1:48429395
|
G | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-16244C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429395 | ||||||
| chr1:48429443
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.239-16292G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429443 | ||||||
| chr1:48429590
|
T | A | 49 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.239-16439A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429590 | ||||||
| chr1:48429681
|
C | A | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.239-16530G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48429681 | ||||||
| chr1:48430020
|
C | T | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.239-16869G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48430020 | ||||||
| chr1:48430341
|
T | C | 2 | a0001c0001t0014g0213a0001c0001t0014g0214 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.239-17190A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48430341 | ||||||
| chr1:48430511
|
A | G | 3 | a0001c0001t0010g0211a0001c0001t0025g0209a0001c0001t0025g0210 | 3 | HG02055.hp2 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.239-17360T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48430511 | ||||||
| chr1:48430566
|
C | A | 1 | a0001c0001t0003g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.239-17415G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48430566 | ||||||
| chr1:48430884
|
T | C | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.239-17733A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48430884 | ||||||
| chr1:48431406
|
C | A | 15 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(12): Show | 15 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-18255G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48431406 | ||||||
| chr1:48431730
|
A | T | 10 | a0002c0002t0001g0002a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | NA18954.hp2 NA18967.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-18579T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48431730 | ||||||
| chr1:48432091
|
T | C | 1 | a0001c0001t0011g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.239-18940A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48432091 | ||||||
| chr1:48432309
|
G | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.239-19158C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48432309 | ||||||
| chr1:48432878
|
A | C | 1 | a0001c0001t0004g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.238+18674T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48432878 | ||||||
| chr1:48433029
|
A | T | 1 | a0002c0002t0005g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+18523T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48433029 | ||||||
| chr1:48433295
|
T | C | 1 | a0001c0001t0007g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238+18257A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48433295 | ||||||
| chr1:48433489
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+18063A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48433489 | ||||||
| chr1:48434066
|
T | C | 1 | a0002c0002t0028g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.238+17486A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434066 | ||||||
| chr1:48434128
|
A | C | 3 | a0001c0001t0004g0257a0001c0001t0004g0263a0001c0001t0004g0277 | 3 | NA18966.hp1 NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.238+17424T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434128 | ||||||
| chr1:48434198
|
C | T | 1 | a0003c0003t0003g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.238+17354G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434198 | ||||||
| chr1:48434259
|
G | GA | 105 | a0001c0001t0002g0100a0001c0001t0002g0181a0001c0001t0002g0189others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.238+17292dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434259 | ||||||
| chr1:48434259
|
G | GAA | 15 | a0001c0001t0001g0089a0001c0001t0009g0207a0001c0001t0009g0208others(12): Show | 15 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+17291_238+1729 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434259 | ||||||
| chr1:48434259
|
GA | G | 41 | a0001c0001t0002g0172a0001c0001t0003g0104a0001c0001t0003g0105others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.238+17292delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434259 | ||||||
| chr1:48434361
|
G | GA | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+17190dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434361 | ||||||
| chr1:48434545
|
T | G | 1 | a0001c0001t0003g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.238+17007A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434545 | ||||||
| chr1:48434565
|
T | C | 1 | a0002c0002t0031g0075 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+16987A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434565 | ||||||
| chr1:48434580
|
T | TGA | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.238+16970_238+1697 others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434580 | ||||||
| chr1:48434697
|
G | T | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+16855C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434697 | ||||||
| chr1:48434699
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238+16853A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48434699 | ||||||
| chr1:48435024
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238+16528A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435024 | ||||||
| chr1:48435146
|
A | T | 1 | a0001c0001t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.238+16406T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435146 | ||||||
| chr1:48435159
|
T | C | 1 | a0002c0002t0001g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.238+16393A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435159 | ||||||
| chr1:48435221
|
G | C | 1 | a0001c0001t0002g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.238+16331C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435221 | ||||||
| chr1:48435224
|
T | A | 1 | a0001c0001t0002g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.238+16328A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435224 | ||||||
| chr1:48435317
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+16235G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435317 | ||||||
| chr1:48435388
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+16164A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435388 | ||||||
| chr1:48435426
|
A | C | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+16126T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435426 | ||||||
| chr1:48435539
|
A | G | 310 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.238+16013T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435539 | ||||||
| chr1:48435539
|
A | T | 1 | a0001c0001t0007g0309 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238+16013T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435539 | ||||||
| chr1:48435724
|
G | A | 11 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+15828C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435724 | ||||||
| chr1:48435730
|
G | A | 6 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+15822C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435730 | ||||||
| chr1:48435743
|
T | C | 1 | a0001c0001t0004g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.238+15809A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435743 | ||||||
| chr1:48435757
|
C | T | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.238+15795G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435757 | ||||||
| chr1:48435795
|
G | A | 3 | a0001c0001t0036g0311a0002c0002t0001g0026a0002c0002t0001g0033 | 3 | HG02258.hp2 HG03017.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.238+15757C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435795 | ||||||
| chr1:48435823
|
C | T | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238+15729G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435823 | ||||||
| chr1:48435912
|
C | G | 4 | a0002c0002t0001g0084a0002c0002t0005g0083a0002c0002t0005g0085others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+15640G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48435912 | ||||||
| chr1:48436140
|
C | G | 1 | a0001c0001t0004g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.238+15412G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436140 | ||||||
| chr1:48436141
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0010g0137 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.238+15411C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436141 | ||||||
| chr1:48436295
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.238+15257A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436295 | ||||||
| chr1:48436438
|
G | A | 1 | a0001c0001t0004g0275 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.238+15114C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436438 | ||||||
| chr1:48436629
|
T | C | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.238+14923A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436629 | ||||||
| chr1:48436630
|
T | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+14922A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436630 | ||||||
| chr1:48436717
|
A | G | 2 | a0001c0001t0007g0309a0001c0001t0037g0310 | 2 | HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.238+14835T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436717 | ||||||
| chr1:48436754
|
G | A | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+14798C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436754 | ||||||
| chr1:48436880
|
G | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+14672C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436880 | ||||||
| chr1:48436887
|
T | G | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+14665A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436887 | ||||||
| chr1:48436952
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238+14600C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48436952 | ||||||
| chr1:48437305
|
G | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.238+14247C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437305 | ||||||
| chr1:48437612
|
C | T | 2 | a0001c0001t0024g0182a0001c0001t0024g0185 | 2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.238+13940G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437612 | ||||||
| chr1:48437787
|
A | G | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.238+13765T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437787 | ||||||
| chr1:48437792
|
C | CT | 93 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.238+13759dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437792 | ||||||
| chr1:48437800
|
T | A | 1 | a0001c0001t0003g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.238+13752A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437800 | ||||||
| chr1:48437801
|
A | T | 310 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.238+13751T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437801 | ||||||
| chr1:48437802
|
A | T | 1 | a0001c0001t0002g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.238+13750T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437802 | ||||||
| chr1:48437897
|
GA | G | 143 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.238+13654delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437897 | ||||||
| chr1:48437945
|
T | A | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+13607A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48437945 | ||||||
| chr1:48438018
|
G | A | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+13534C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48438018 | ||||||
| chr1:48438406
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.238+13146C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48438406 | ||||||
| chr1:48438691
|
G | A | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.238+12861C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48438691 | ||||||
| chr1:48438709
|
C | A | 1 | a0001c0001t0003g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+12843G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48438709 | ||||||
| chr1:48439011
|
A | G | 94 | a0001c0001t0001g0089a0001c0001t0003g0104a0001c0001t0003g0105others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+12541T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439011 | ||||||
| chr1:48439075
|
A | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+12477T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439075 | ||||||
| chr1:48439084
|
T | C | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.238+12468A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439084 | ||||||
| chr1:48439181
|
G | A | 1 | a0001c0001t0007g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+12371C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439181 | ||||||
| chr1:48439259
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.238+12293C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439259 | ||||||
| chr1:48439277
|
T | C | 318 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.238+12275A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439277 | ||||||
| chr1:48439397
|
A | C | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238+12155T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439397 | ||||||
| chr1:48439909
|
T | C | 1 | a0001c0001t0037g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.238+11643A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48439909 | ||||||
| chr1:48440184
|
G | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.238+11368C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48440184 | ||||||
| chr1:48440499
|
A | C | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+11053T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48440499 | ||||||
| chr1:48440630
|
T | C | 1 | a0002c0002t0005g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.238+10922A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48440630 | ||||||
| chr1:48441640
|
T | C | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+9912A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48441640 | ||||||
| chr1:48441779
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.238+9773T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48441779 | ||||||
| chr1:48441809
|
T | C | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.238+9743A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48441809 | ||||||
| chr1:48441981
|
A | G | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.238+9571T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48441981 | ||||||
| chr1:48442201
|
G | T | 1 | a0002c0002t0001g0016 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.238+9351C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442201 | ||||||
| chr1:48442321
|
C | A | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.238+9231G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442321 | ||||||
| chr1:48442358
|
G | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.238+9194C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442358 | ||||||
| chr1:48442407
|
G | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+9145C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442407 | ||||||
| chr1:48442489
|
C | T | 2 | a0001c0001t0016g0296a0001c0001t0016g0299 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.238+9063G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442489 | ||||||
| chr1:48442641
|
G | C | 1 | a0001c0001t0021g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.238+8911C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442641 | ||||||
| chr1:48442717
|
T | TA | 69 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0108others(66): Show | 69 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.238+8834dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442717 | ||||||
| chr1:48442717
|
T | TAA | 19 | a0001c0001t0003g0107a0001c0001t0003g0128a0001c0001t0003g0131others(16): Show | 19 | HG00099.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8833_238+8834d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442717 | ||||||
| chr1:48442717
|
TA | T | 99 | a0001c0001t0001g0089a0001c0001t0002g0152a0001c0001t0002g0153others(96): Show | 99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.238+8834delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442717 | ||||||
| chr1:48442717
|
TAA | T | 60 | a0001c0001t0002g0100a0001c0001t0002g0165a0001c0001t0002g0167others(57): Show | 60 | HG00609.hp1 HG00639.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+8833_238+8834d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442717 | ||||||
| chr1:48442717
|
TAAA | T | 6 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0199others(3): Show | 6 | HG00423.hp2 HG01243.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+8832_238+8834d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442717 | ||||||
| chr1:48442733
|
A | C | 1 | a0002c0002t0005g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.238+8819T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48442733 | ||||||
| chr1:48443056
|
G | GT | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+8495dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443056 | ||||||
| chr1:48443203
|
C | T | 1 | a0002c0002t0001g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.238+8349G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443203 | ||||||
| chr1:48443342
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+8210G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443342 | ||||||
| chr1:48443389
|
C | T | 5 | a0001c0001t0002g0100a0001c0001t0013g0161a0001c0001t0013g0162others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+8163G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443389 | ||||||
| chr1:48443498
|
C | A | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.238+8054G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443498 | ||||||
| chr1:48443571
|
C | T | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.238+7981G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443571 | ||||||
| chr1:48443811
|
C | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+7741G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48443811 | ||||||
| chr1:48444049
|
G | A | 74 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(71): Show | 74 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.238+7503C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48444049 | ||||||
| chr1:48444061
|
A | G | 1 | a0001c0001t0038g0305 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.238+7491T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48444061 | ||||||
| chr1:48444624
|
A | C | 1 | a0001c0001t0009g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238+6928T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48444624 | ||||||
| chr1:48444672
|
G | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.238+6880C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48444672 | ||||||
| chr1:48445030
|
T | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.238+6522A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445030 | ||||||
| chr1:48445304
|
G | A | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.238+6248C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445304 | ||||||
| chr1:48445346
|
T | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+6206A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445346 | ||||||
| chr1:48445358
|
G | A | 3 | a0001c0001t0002g0100a0001c0001t0023g0096a0001c0001t0023g0099 | 3 | HG02572.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.238+6194C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445358 | ||||||
| chr1:48445373
|
C | G | 12 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+6179G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445373 | ||||||
| chr1:48445391
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.238+6161A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445391 | ||||||
| chr1:48445440
|
A | G | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+6112T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445440 | ||||||
| chr1:48445619
|
C | T | 7 | a0001c0001t0014g0196a0001c0001t0014g0198a0001c0001t0014g0213others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+5933G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445619 | ||||||
| chr1:48445659
|
C | CA | 44 | a0001c0001t0001g0089a0001c0001t0003g0130a0001c0001t0003g0131others(41): Show | 44 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.238+5892dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
C | CAA | 55 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(52): Show | 55 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+5891_238+5892d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
C | CAAA | 29 | a0001c0001t0002g0100a0001c0001t0002g0156a0001c0001t0002g0165others(26): Show | 29 | HG01099.hp1 HG01496.hp2 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.238+5890_238+5892d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
C | CAAAA | 6 | a0001c0001t0002g0191a0001c0001t0002g0204a0001c0001t0008g0235others(3): Show | 6 | HG02145.hp2 HG03579.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+5889_238+5892d others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
CA | C | 50 | a0001c0001t0003g0109a0001c0001t0015g0319a0002c0002t0001g0001others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.238+5892delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
CAAA | C | 13 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(10): Show | 13 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+5890_238+5892d others(5): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
CAAAAAAA others(4): Show |
C | 37 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.238+5882_238+5892d others(13): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445659
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0009g0102a0001c0001t0044g0322 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.238+5881_238+5892d others(14): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445659 | ||||||
| chr1:48445704
|
C | T | 1 | a0002c0002t0001g0005 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.238+5848G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445704 | ||||||
| chr1:48445712
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238+5840T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445712 | ||||||
| chr1:48445758
|
C | T | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.238+5794G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48445758 | ||||||
| chr1:48446121
|
G | T | 9 | a0001c0001t0016g0296a0001c0001t0016g0299a0001c0001t0018g0315others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+5431C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48446121 | ||||||
| chr1:48446171
|
C | CT | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+5380dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48446171 | ||||||
| chr1:48446258
|
G | A | 1 | a0001c0001t0013g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238+5294C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48446258 | ||||||
| chr1:48446876
|
T | C | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.238+4676A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48446876 | ||||||
| chr1:48447278
|
T | G | 217 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.238+4274A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48447278 | ||||||
| chr1:48447344
|
C | T | 8 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(5): Show | 8 | HG00280.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+4208G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48447344 | ||||||
| chr1:48447552
|
T | C | 1 | a0001c0001t0044g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.238+4000A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48447552 | ||||||
| chr1:48447565
|
G | A | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.238+3987C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48447565 | ||||||
| chr1:48447630
|
A | T | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+3922T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48447630 | ||||||
| chr1:48448223
|
T | C | 1 | a0001c0001t0009g0226 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.238+3329A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448223 | ||||||
| chr1:48448250
|
G | A | 54 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(51): Show | 54 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.238+3302C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448250 | ||||||
| chr1:48448260
|
C | CA | 57 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(54): Show | 57 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.238+3291dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448260 | ||||||
| chr1:48448260
|
C | CAA | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.238+3290_238+3291d others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448260 | ||||||
| chr1:48448260
|
CA | C | 28 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.238+3291delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448260 | ||||||
| chr1:48448404
|
A | C | 4 | a0001c0001t0007g0303a0001c0001t0007g0304a0001c0001t0007g0312others(1): Show | 4 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+3148T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448404 | ||||||
| chr1:48448492
|
G | GA | 7 | a0001c0001t0002g0192a0001c0001t0003g0134a0001c0001t0004g0283others(4): Show | 7 | HG00544.hp2 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+3059dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448492 | ||||||
| chr1:48448492
|
GA | G | 94 | a0001c0001t0007g0313a0002c0002t0001g0001a0002c0002t0001g0002others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+3059delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448492 | ||||||
| chr1:48448681
|
A | G | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.238+2871T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448681 | ||||||
| chr1:48448947
|
G | A | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.238+2605C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48448947 | ||||||
| chr1:48449280
|
C | T | 10 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(7): Show | 10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+2272G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48449280 | ||||||
| chr1:48449281
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+2271C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48449281 | ||||||
| chr1:48449683
|
C | T | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.238+1869G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48449683 | ||||||
| chr1:48449704
|
C | T | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.238+1848G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48449704 | ||||||
| chr1:48449769
|
G | C | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.238+1783C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48449769 | ||||||
| chr1:48450221
|
T | C | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+1331A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450221 | ||||||
| chr1:48450257
|
A | C | 1 | a0002c0002t0032g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.238+1295T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450257 | ||||||
| chr1:48450340
|
GA | G | 222 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.238+1211delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450340 | ||||||
| chr1:48450639
|
G | C | 1 | a0002c0002t0005g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.238+913C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450639 | ||||||
| chr1:48450764
|
T | C | 1 | a0002c0002t0001g0038 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.238+788A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450764 | ||||||
| chr1:48450766
|
G | T | 1 | a0002c0002t0005g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.238+786C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450766 | ||||||
| chr1:48450946
|
C | T | 1 | a0001c0001t0014g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238+606G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48450946 | ||||||
| chr1:48451027
|
T | G | 4 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0042others(1): Show | 4 | NA18977.hp2 NA18982.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+525A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48451027 | ||||||
| chr1:48451255
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.238+297G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 3/12 | chr1 | 48451255 | ||||||
| chr1:48451920
|
G | A | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-320C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48451920 | ||||||
| chr1:48452253
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.190-653C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452253 | ||||||
| chr1:48452381
|
T | C | 2 | a0001c0001t0007g0303a0001c0001t0007g0312 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.189+613A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452381 | ||||||
| chr1:48452387
|
CT | C | 59 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(56): Show | 59 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.189+606delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452387 | ||||||
| chr1:48452402
|
TA | T | 17 | a0001c0001t0008g0236a0001c0001t0008g0239a0001c0001t0008g0242others(14): Show | 17 | HG01943.hp1 HG02257.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+591delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452402 | ||||||
| chr1:48452403
|
A | T | 1 | a0001c0001t0008g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189+591T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452403 | ||||||
| chr1:48452464
|
A | G | 1 | a0002c0002t0005g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.189+530T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452464 | ||||||
| chr1:48452524
|
T | C | 1 | a0001c0001t0007g0302 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189+470A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452524 | ||||||
| chr1:48452565
|
G | T | 52 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(49): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.189+429C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452565 | ||||||
| chr1:48452801
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.189+193C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452801 | ||||||
| chr1:48452813
|
A | T | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.189+181T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 2/12 | chr1 | 48452813 | ||||||
| chr1:48453299
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.52-168T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453299 | ||||||
| chr1:48453519
|
T | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.52-388A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453519 | ||||||
| chr1:48453540
|
TA | T | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-410delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453540 | ||||||
| chr1:48453546
|
C | A | 1 | a0001c0001t0009g0116 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.52-415G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453546 | ||||||
| chr1:48453644
|
A | C | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-513T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453644 | ||||||
| chr1:48453788
|
C | A | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.52-657G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453788 | ||||||
| chr1:48453950
|
GA | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-820delT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48453950 | ||||||
| chr1:48454007
|
CT | C | 6 | a0001c0001t0007g0313a0001c0001t0035g0160a0002c0002t0001g0001others(3): Show | 6 | HG01167.hp1 HG01168.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-877delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48454007 | ||||||
| chr1:48454012
|
T | G | 1 | a0001c0001t0002g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.52-881A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48454012 | ||||||
| chr1:48454533
|
G | A | 1 | a0002c0002t0005g0082 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52-1402C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48454533 | ||||||
| chr1:48455224
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-2093C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48455224 | ||||||
| chr1:48455446
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-2315C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48455446 | ||||||
| chr1:48455530
|
G | A | 1 | a0001c0001t0023g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.52-2399C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48455530 | ||||||
| chr1:48455840
|
T | C | 5 | a0002c0002t0001g0002a0002c0002t0001g0054a0002c0002t0001g0055others(2): Show | 5 | NA18954.hp2 NA18967.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-2709A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48455840 | ||||||
| chr1:48456018
|
T | C | 6 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0287others(3): Show | 6 | HG00621.hp2 HG02165.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-2887A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456018 | ||||||
| chr1:48456467
|
C | CAAAGAAA others(326): Show |
1 | a0002c0002t0005g0077 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.52-3337_52-3336ins others(333): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456467 | ||||||
| chr1:48456467
|
C | CAAAGAAA others(327): Show |
1 | a0002c0002t0005g0078 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52-3337_52-3336ins others(334): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456467 | ||||||
| chr1:48456467
|
C | CAAAGAAA others(331): Show |
1 | a0002c0002t0005g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.52-3337_52-3336ins others(338): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456467 | ||||||
| chr1:48456501
|
A | T | 3 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01167.hp2 HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.52-3370T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456501 | ||||||
| chr1:48456809
|
C | T | 5 | a0001c0001t0003g0115a0001c0001t0009g0116a0001c0001t0009g0140others(2): Show | 5 | HG00558.hp1 NA18964.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-3678G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456809 | ||||||
| chr1:48456881
|
C | T | 1 | a0003c0003t0003g0110 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.52-3750G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48456881 | ||||||
| chr1:48457056
|
G | A | 2 | a0002c0002t0005g0081a0002c0002t0005g0082 | 2 | HG01934.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.52-3925C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457056 | ||||||
| chr1:48457087
|
CT | C | 4 | a0001c0001t0013g0161a0001c0001t0013g0162a0001c0001t0013g0163others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-3957delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457087 | ||||||
| chr1:48457213
|
C | T | 1 | a0001c0001t0007g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.52-4082G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457213 | ||||||
| chr1:48457304
|
T | C | 1 | a0002c0002t0019g0080 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.52-4173A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457304 | ||||||
| chr1:48457475
|
C | G | 1 | a0001c0001t0006g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.52-4344G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457475 | ||||||
| chr1:48457682
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.52-4551A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457682 | ||||||
| chr1:48457763
|
T | G | 1 | a0001c0001t0004g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.52-4632A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457763 | ||||||
| chr1:48457997
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.52-4866T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48457997 | ||||||
| chr1:48458053
|
C | T | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.52-4922G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48458053 | ||||||
| chr1:48458452
|
T | C | 52 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0004g0256others(49): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.52-5321A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48458452 | ||||||
| chr1:48458453
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52-5322C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48458453 | ||||||
| chr1:48458590
|
T | C | 1 | a0002c0002t0001g0014 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.52-5459A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48458590 | ||||||
| chr1:48458658
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.52-5527C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48458658 | ||||||
| chr1:48459204
|
C | CA | 107 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.52-6074dupT | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48459204 | ||||||
| chr1:48459689
|
T | G | 2 | a0002c0002t0005g0081a0002c0002t0005g0082 | 2 | HG01934.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.52-6558A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48459689 | ||||||
| chr1:48459820
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.52-6689T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48459820 | ||||||
| chr1:48459905
|
T | G | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.52-6774A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48459905 | ||||||
| chr1:48459999
|
G | A | 1 | a0001c0001t0004g0291 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.52-6868C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48459999 | ||||||
| chr1:48460050
|
A | G | 1 | a0001c0001t0012g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.52-6919T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460050 | ||||||
| chr1:48460096
|
A | G | 4 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(1): Show | 4 | HG00099.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-6965T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460096 | ||||||
| chr1:48460196
|
G | T | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.52-7065C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460196 | ||||||
| chr1:48460241
|
C | A | 1 | a0001c0001t0022g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.52-7110G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460241 | ||||||
| chr1:48460600
|
GAAAT | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.52-7473_52-7470del others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460600 | ||||||
| chr1:48460655
|
A | T | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-7524T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460655 | ||||||
| chr1:48460717
|
AAAATATA others(21): Show |
A | 109 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.52-7614_52-7587del others(28): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48460717 | ||||||
| chr1:48461277
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-8146C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48461277 | ||||||
| chr1:48461456
|
GT | G | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.52-8326delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48461456 | ||||||
| chr1:48461723
|
A | G | 318 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.52-8592T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48461723 | ||||||
| chr1:48461886
|
C | T | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52-8755G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48461886 | ||||||
| chr1:48462208
|
C | G | 9 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-9077G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48462208 | ||||||
| chr1:48462250
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.52-9119G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48462250 | ||||||
| chr1:48462547
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.51+9411T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48462547 | ||||||
| chr1:48463024
|
G | T | 16 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(13): Show | 16 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.51+8934C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463024 | ||||||
| chr1:48463351
|
T | G | 7 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(4): Show | 7 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+8607A>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463351 | ||||||
| chr1:48463412
|
A | T | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.51+8546T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463412 | ||||||
| chr1:48463696
|
A | G | 1 | a0002c0002t0005g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.51+8262T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463696 | ||||||
| chr1:48463820
|
C | G | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+8138G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463820 | ||||||
| chr1:48463949
|
AT | A | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.51+8008delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48463949 | ||||||
| chr1:48464391
|
A | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7567T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464391 | ||||||
| chr1:48464598
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.51+7360G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464598 | ||||||
| chr1:48464620
|
G | A | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.51+7338C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464620 | ||||||
| chr1:48464720
|
T | C | 1 | a0001c0001t0008g0251 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+7238A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464720 | ||||||
| chr1:48464780
|
G | A | 38 | a0002c0002t0001g0084a0002c0002t0005g0003a0002c0002t0005g0004others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.51+7178C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464780 | ||||||
| chr1:48464837
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.51+7121A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464837 | ||||||
| chr1:48464917
|
G | A | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0010g0137 | 3 | HG01346.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.51+7041C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48464917 | ||||||
| chr1:48465019
|
A | C | 3 | a0003c0003t0003g0110a0003c0003t0003g0111a0003c0003t0003g0112 | 3 | HG01261.hp2 HG01433.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.51+6939T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48465019 | ||||||
| chr1:48465163
|
A | C | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+6795T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48465163 | ||||||
| chr1:48465777
|
C | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+6181G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48465777 | ||||||
| chr1:48465823
|
C | A | 1 | a0001c0001t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.51+6135G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48465823 | ||||||
| chr1:48466050
|
A | G | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+5908T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466050 | ||||||
| chr1:48466381
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.51+5577A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466381 | ||||||
| chr1:48466443
|
A | G | 1 | a0001c0001t0022g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.51+5515T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466443 | ||||||
| chr1:48466637
|
TG | T | 6 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(3): Show | 6 | HG00597.hp1 NA18998.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+5320delC | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466637 | ||||||
| chr1:48466656
|
GT | G | 52 | a0001c0001t0001g0089a0001c0001t0003g0225a0001c0001t0004g0229others(49): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.51+5301delA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466656 | ||||||
| chr1:48466799
|
A | G | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.51+5159T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466799 | ||||||
| chr1:48466816
|
C | T | 311 | a0001c0001t0001g0089a0001c0001t0002g0100a0001c0001t0002g0152others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.51+5142G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48466816 | ||||||
| chr1:48467100
|
C | G | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.51+4858G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467100 | ||||||
| chr1:48467132
|
T | C | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+4826A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467132 | ||||||
| chr1:48467295
|
G | C | 1 | a0001c0001t0009g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+4663C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467295 | ||||||
| chr1:48467300
|
A | T | 4 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+4658T>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467300 | ||||||
| chr1:48467302
|
G | A | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+4656C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467302 | ||||||
| chr1:48467647
|
G | A | 1 | a0001c0001t0006g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.51+4311C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467647 | ||||||
| chr1:48467660
|
C | T | 4 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0042others(1): Show | 4 | NA18977.hp2 NA18982.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+4298G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467660 | ||||||
| chr1:48467890
|
G | C | 1 | a0001c0001t0003g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.51+4068C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48467890 | ||||||
| chr1:48468064
|
G | T | 4 | a0002c0002t0001g0084a0002c0002t0005g0083a0002c0002t0005g0085others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+3894C>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468064 | ||||||
| chr1:48468259
|
T | C | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3699A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468259 | ||||||
| chr1:48468472
|
G | A | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3486C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468472 | ||||||
| chr1:48468643
|
G | A | 1 | a0002c0002t0005g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.51+3315C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468643 | ||||||
| chr1:48468791
|
C | G | 1 | a0001c0001t0010g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.51+3167G>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468791 | ||||||
| chr1:48468806
|
G | A | 1 | a0001c0001t0010g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+3152C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468806 | ||||||
| chr1:48468926
|
C | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.51+3032G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48468926 | ||||||
| chr1:48469009
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0004g0229a0001c0001t0009g0206others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2949C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469009 | ||||||
| chr1:48469215
|
A | G | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.51+2743T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469215 | ||||||
| chr1:48469377
|
T | C | 18 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2581A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469377 | ||||||
| chr1:48469472
|
TTA | T | 66 | a0001c0001t0001g0089a0001c0001t0002g0199a0001c0001t0002g0200others(63): Show | 66 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.51+2484_51+2485del others(2): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469472 | ||||||
| chr1:48469472
|
TTATA | T | 120 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.51+2482_51+2485del others(4): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469472 | ||||||
| chr1:48469472
|
TTATATA | T | 108 | a0001c0001t0002g0100a0001c0001t0002g0152a0001c0001t0002g0153others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.51+2480_51+2485del others(6): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469472 | ||||||
| chr1:48469472
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0006g0143a0001c0001t0006g0230a0001c0001t0006g0231others(2): Show | 5 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2476_51+2485del others(10): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469472 | ||||||
| chr1:48469472
|
TTATATAT others(5): Show |
T | 1 | a0002c0002t0001g0005 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.51+2474_51+2485del others(12): Show |
SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469472 | ||||||
| chr1:48469607
|
A | C | 42 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.51+2351T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469607 | ||||||
| chr1:48469628
|
G | A | 22 | a0001c0001t0006g0230a0001c0001t0006g0231a0001c0001t0006g0232others(19): Show | 22 | HG01891.hp2 HG01943.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.51+2330C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469628 | ||||||
| chr1:48469782
|
T | C | 3 | a0001c0001t0018g0315a0001c0001t0018g0316a0001c0001t0018g0317 | 3 | HG01891.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.51+2176A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469782 | ||||||
| chr1:48469795
|
T | C | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.51+2163A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469795 | ||||||
| chr1:48469799
|
G | GT | 7 | a0001c0001t0002g0100a0001c0001t0008g0235a0001c0001t0008g0236others(4): Show | 7 | HG01943.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2158dupA | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469799 | ||||||
| chr1:48469888
|
A | C | 2 | a0001c0001t0023g0096a0001c0001t0023g0099 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.51+2070T>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469888 | ||||||
| chr1:48469961
|
T | C | 6 | a0002c0002t0005g0090a0002c0002t0005g0091a0002c0002t0005g0092others(3): Show | 6 | NA18940.hp2 NA18941.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+1997A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48469961 | ||||||
| chr1:48470067
|
T | C | 1 | a0001c0001t0015g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.51+1891A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470067 | ||||||
| chr1:48470181
|
T | A | 1 | a0001c0001t0006g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.51+1777A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470181 | ||||||
| chr1:48470281
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0008g0239others(15): Show | 18 | HG01943.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+1677C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470281 | ||||||
| chr1:48470359
|
C | A | 2 | a0001c0001t0015g0319a0001c0001t0015g0320 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.51+1599G>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470359 | ||||||
| chr1:48470568
|
A | G | 2 | a0004c0004t0002g0097a0004c0004t0002g0098 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.51+1390T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470568 | ||||||
| chr1:48470747
|
T | A | 1 | a0001c0001t0002g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.51+1211A>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470747 | ||||||
| chr1:48470958
|
T | C | 1 | a0001c0001t0003g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.51+1000A>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48470958 | ||||||
| chr1:48471483
|
C | T | 1 | a0001c0001t0023g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+475G>A | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48471483 | ||||||
| chr1:48471543
|
G | A | 39 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.51+415C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48471543 | ||||||
| chr1:48471679
|
G | C | 27 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0007g0302others(24): Show | 27 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.51+279C>G | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48471679 | ||||||
| chr1:48471806
|
A | G | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.51+152T>C | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48471806 | ||||||
| chr1:48471858
|
G | A | 1 | a0001c0001t0010g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51+100C>T | SPATA6 | ENSG00000132122.12 | transcript | ENST00000371847.8 | protein_coding | 1/12 | chr1 | 48471858 |